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  • Springer  (65)
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  • 1
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    Springer
    Journal of inorganic and organometallic polymers and materials 2 (1992), S. 79-85 
    ISSN: 1572-8870
    Keywords: Phthalocyanines ; polymers ; siloxanes ; conductivity ; stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The author's work on the incorporation of phthalocyanines into inorganic polymers is reviewed. The synthesis of poly(siloxane phthalocyanines) and the synthesis and characterization of fluoro(phthalocyanine) Group III compounds and their conducting derivatives are described.
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  • 2
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    Journal of inorganic and organometallic polymers and materials 5 (1995), S. 217-236 
    ISSN: 1572-8870
    Keywords: Polysilane ; NMR ; pyrolysis ; randomization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Bimodal molecular weight distributions of alternating copolymers of the type (Me2Si−R2Si−SiMe2) n , where R=hexyl and butyl, were obtained by polymerization of BrSiMe2−R2Si−Me2SiBr, using the Wurtz coupling method. Analysis of the samples by pyrolysis GC MS and solution29Si NMR indicated that some randomization occurred, due to cleavage of the original Si−Si bonds in the monomer. The extent of randomization was significantly greater in the high molecular weight fractions. Based on the nature of the rings from the py MGC/MS traces and the number on nonads found in the29Si spectra, two types of randomization processes have been proposed, involving backbiting followed by (1) ring expulsion or (2) redistribution.
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  • 3
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    Journal of polymers and the environment 3 (1995), S. 199-203 
    ISSN: 1572-8900
    Keywords: Chemiluminescence ; oxidation ; stability ; acrylonitrile-butadiene-styrene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The thermal oxidative stability of various formulations based on emulsion-grade ABS was studied by the chemiluminescence technique. Emulsion products were found to be essentially less stable than ionic mass polymerization resins. Among the antioxidants studied, Santonox R is clearly more efficient than Irganox 1076 and Irganox 3114, and its superiority is reflected primarily in improved induction period values. The introduction of Tinuvin 770 and Tinuvin 328 UV stabilizers into emulsion resins does not change the durability of the products. In mixtures where both Irganox 1076 and UV stabilizers are present, a certain antagonistic effect was noted at high UV stabilizer concentrations.
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  • 4
    ISSN: 1572-8927
    Keywords: Chromium(III) ; β-diketones ; β-diketonates ; chelation ; complexation ; correlation ; stability ; equilibrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract It has been demonstrated that the logarithm of the stability constant of some monochelated chromium(III) compounds, with structurally similar 1,3-dicarbonylic species, is linearly related to the negative logarithm of the acid ionization constant of the ligand. Graphical and analytical correlations which could be useful in predicting equilibrium constants of chromium(III)-β-diketonates, as well as other first-row transition metal derivatives, have been developed. A quantitative evaluation of the complexes stability has been carried out, providing information about the effects of ligand substituents on the equilibrium constants.
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  • 5
    ISSN: 1572-8927
    Keywords: Crown ethers ; hydronium ion ; complexation ; molar conductance ; ion pairing ; NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A conductance study concerning the interaction between hydronium ion and several crown ethers in acetonitrile, nitrobenzene and 1,2-dichloroethane solutions has been carried out at 25°C. The stability constants of the resulting 1:1 complexes in acetonitrile and nitrobenzene solutions were determined from the molar conductance-mole ratio data and found to vary in the order 18C6〉DB30C10〉DC18C6〉DB18C6〉DB21C7〉DB24C8〉B15C5. In 1,2-dichloroethane solution, the complexation process results in the dissociation of ion pairs. There is an inverse relationship between the stabilities of the complexes and the Gutmann donicity of the solvents. In nitrobenzene solution, some evidence for the formation of a 2:1 sandwich adduct between the smaller crowns (i.e., B15C5 and 18-crowns) are observed from the molar conductance-mole ratio data which is supported by the1H NMR data.
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  • 6
    ISSN: 1572-8927
    Keywords: Hydrogen-1 ; carbon-13 ; nitrogen-15 ; NMR ; magnesiumisothiocyanate complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A hydrogen-1, carbon-13, and nitrogen-15 NMR study of magnesium(II)-isothiocyanate complexation in aqueous mixtures has been completed. At temperatures low enough to slow proton and ligand exchange, separate1H,13C, and15N NMR signals are observed for coordinated and bulk water molecules and anions. The1H NMR spectra reveal signals for the hexahydrate and the mono-through triisothiocyanato complexes, as well as two small signals attributed to [Mg(H2O)5(OH)]1+ and [Mg(H2O)4(OH)(NCS)]. Accurate hydration numbers were obtained from signal area integrations at each NCS− concentration. In the15N NMR spectra, signals also were observed for the mono-through triisothiocyanato complexes, and a small signal believed to be due to [Mg(H2O)4(OH)(NCS)]. Coordination number contributions for NCS− were measured from these spectra and when combined with the hydration numbers they totalled essentially six at each anion concentration. Signals for [Mg(H2O)5(NCS)]1+ through [Mg(H2O)3(NCS)3]1− also were observed in the13C NMR spectra and the area evaluations were comparable to the15N NMR results. An analysis of the magnitude and sign of the coordinated NCS− chemical shifts identified the nitrogen atom as the anion binding site. All spectra indicated [Mg(H2O)5(NCS)]1+ and [Mg(H2O)4(NCS)2] were the dominat isothiocyanato complexes over the entire range of anion concentrations. The inability to detect evidence for complexes higher than the triisothiocyanato reflects the competitive binding ability of water molecules and perhaps the decreased electrostatic interaction between NCS− and negatively charged higher complexes.
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  • 7
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    Catalysis letters 13 (1992), S. 261-266 
    ISSN: 1572-879X
    Keywords: Vanadia ; alumina ; grinding ; ESR ; NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ultrahigh intensity grinding of mechanical mixtures of V2O5 with γ-Al2O3 at ambient temperature was found to create vanadyl complexes with ESR spectral parameters identical to those of vanadia-alumina samples prepared by impregnation methods. No interaction was found after intensive grinding of γ-Al2O3 with V2O4.
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  • 8
    ISSN: 1572-879X
    Keywords: metal-oxygen cluster compounds ; heteropoly acids ; stability ; pH ; aqueous solutions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The stabilities of the solid superacids H3Mo12O40, H3PW12O40, H4SiMo12O40 and H4SiW12O40 in aqueous solution have been measured at various values of pH by use of ion chromatographic analyses. The aforementioned acids are completely decomposed at values of pH, 4.0, 5.2, 7.0 and 11.0, respectively. The stabilities in aqueous solution with respect to pH follow the order H4SiW12O40 〉 H3PW12O40 〉 H4SiMo12O40 〉 H3PMo12O40.
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  • 9
    ISSN: 1572-8927
    Keywords: Nitrogen-15 ; chlorine-35 ; NMR ; cerium nitrate ; complexation ; water acetone mixtures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A study of the complex formation which occurs between cerium(III) and nitrate ions in aqueous solvent mixtures has been carried out by a direct, low-temperature, nitrogen-15 (15N) NMR technique. At temperatures in the range of −95 to −110°C, ligand exchange is slow enough to permit the observation of separate15N NMR signals for bulk nitrate, and this anion in the cerium(III) principal coordination shell. In water-acetone-Freon-12 mixtures, the spectra reveal the nitrato complexes do not form consecutively. Rather, signals are observed for Ce(NO3)2+, Ce(NO3) 2 1+ , and only two other higher order complexes, even at very high NO 3 − to Ce(III) mole ratios. Signal area evaluations were used to identify the possible higher order complexes. At comparable salt concentrations in aqueous-methanol mixtures, only Ce(NO3)2+ and Ce(NO3) 2 1+ are formed, reflecting a decreased tendency for complexation in media of higher dielectric constant.
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  • 10
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    Monatshefte für Chemie 126 (1995), S. 233-239 
    ISSN: 1434-4475
    Keywords: Enaminoketones ; Lupin alkaloid ; Multiflorine ; NMR ; Nucleophilic methylation ; Stereospecificity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Multiflorin (1), ein Lupin-Nebenalkaloid, ergibt bei Umsetzung mit Methyllithium oder Methylmagnesiumiodid 4S-4-Hydroxy-4-methyl-2,3-didehydrospartein (2) und 2S-2-Methyl-4-oxospartein (3) als Hauptprodukte. Ihre NMR-spektroskopisch (1H und13C) aufgeklärte räumliche Struktur weist auf eine Stereoselektivität der erwähnten Reaktionen hin. Die beobachteten nucleophilen 1,2- und 1,4-Additionen zeigen, daß sich die Regiospezifität der Einwirkung von MeLi oder MeMgl auf Multiflorin von jener bis jetzt bekannter Alkylierungen von Enaminoketonen unterscheidet.
    Notes: Summary Multiflorine (1) — a minor lupine alkaloid — treated by methyl lithium or methyl magnesium iodide affords 4S-4-hydroxy-4-methyl-2,3-didehydrosparteine (2) and 2S-2-methyl-4-oxosparteine (3), respectively, as the dominating products. Their steric structure, determined by1H and13C NMR techniques, points to stereospecific preferences of these reactions. The observed nucleophilic 1,2- and 1,4-additions indicate that regiospecificity of the action of MeLi or MeMgI on multiflorine is different from that of the so far known similar alkylation of other enamino ketones.
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  • 11
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    Monatshefte für Chemie 126 (1995), S. 1011-1019 
    ISSN: 1434-4475
    Keywords: Precursors of strigol analogues ; Michael reaction ; NMR ; Molecular modelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung BasenkatalysierteMichael-Addition von 5-Nitropentan-2-on-ethylenketal (1) und Cyclohex-2-enon (2), anschließende Entfernung der Schutzgruppe und darauffolgende Aldolkondensation liefert isomer 8-Methyl-5-nitro-1-octalone (5a,b). Struktur, relative Konfiguration und Konformation von5a und5b wurden mittels1H- und13C-NMR-Spektroskopie aufgeklärt.
    Notes: Summary Base catalyzedMichael addition of 5-nitropentan-2-one ethylene ketal (1) and cyclohex-2-enone (2), subsequent deprotection, and intramolecular aldol condensation yields the 8-methyl-5-nitro-1-octalone isomers (5a,b). The structure, relative configuration, and conformation of5a and5b were elucidated utilizing the results of1H and13C NMR investigations
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  • 12
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    Catalysis letters 31 (1995), S. 267-272 
    ISSN: 1572-879X
    Keywords: MCM-41 synthesis ; NMR ; FTIR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The synthesis of MCM-41 mesoporous compounds with Si/Al ratios as low as 2 without observing the presence of octahedral Al in27AlMAS NMR is reported. FTIR spectra of chemisorbed pyridine indicated that MCM-41 materials in their protonated form exhibit both Brønsted and Lewis acid sites.
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  • 13
    ISSN: 1436-5073
    Keywords: stability ; chemical species ; solutions ; calibration ; interlaboratory studies ; measurement and testing programme
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The stability of chemical species in solution during storage is one of the critical aspect that has to be carefully studied e.g. for calibration purposes or prior to the organization of interlaboratory studies using synthetic solutions. The Measurements and Testing Programme (formerly BCR) is currently undertaking projects to improve the quality of speciation analysis for a variety of species (e.g. As, Hg, Sn, Pb, Cr). In all the cases the stability of these species was carefully studied in the solutions provided to the participants. This paper gives an overview of some of the results obtained in different BCR-projects on speciation analysis.
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  • 14
    ISSN: 1434-4475
    Keywords: Virus ; Peptide ; NMR ; Assignment ; Reverse Techniques ; Conformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Zwei Oligopeptide, die die native Spaltregion für die Proteinase2 A des humanen Rhinovirus von Serotyp 2 (HRV 22 A) beziehungsweise eine modifizierte Version repräsentieren, wurden mit Hilfe von homo- und heterokorrelierter 2 D-NMR-Spektroskopie untersucht. Protondetektierte C,H-Korrelationstechniken erwiesen sich als außerordentlich hilfreich bei der sequenziellen Zuordnung. In einem Fall konnte das gesamte Aminosäureskelett ohne Zuhilfenahme von NOESY-Spektren analysiert und damit die dieser Methode inhärenten Unsicherheiten bei der Zuordnung vermieden werden. In keinem der beiden Moleküle konnte eine definierte Tertiärstruktur der Spaltregion ermittelt werden. Eines der beiden Oligopeptide liegt jedoch zu einem sehr geringen Prozentsatz in einer von derrandom-coil Anordnung abweichenden Konformation vor.
    Notes: Summary Two oligopeptides representing a wild type and a modified version of the polyprotein cleavage region for proteinase2 A of the human rhinovirus type 2 (HRV 22 A) have been investigated using homo- and heterocorrelated 2 D NMR spectroscopy. Proton-detected C,H correlation techniques turned out to be extremely useful for sequential resonance assignment. In one case, the complete amino acid backbone could be analyzed without using NOESY spectra, thus avoiding ambiguities inherent to this method. No defined tertiary structure of the cleavage region could be detected in either molecule. However, one of the oligopeptides is present to a very low extent in a conformation different from therandom-coil arrangement.
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  • 15
    ISSN: 1432-2234
    Keywords: Direct ; CPHF ; GIAO ; Polarizability ; NMR ; Magnetic shielding ; Carbon ; C60 ; C70
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The ab initio SCF computation of second-order properties of large molecules (with 50 atoms or more) on workstation computers is demonstrated for static dipole polarizabilities and nuclear magneting shieldings. The magnetic shieldings are calculated on the basis of gauge including atomic orbitals (GIAO). Algorithmic advances (semi-direct algorithms with efficient integral pre-screening, and use of a quadratically convergent functional for the polarizabilities) are presented together with an illustrative application to the fullerenes C60 and C70.
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  • 16
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    Theoretical chemistry accounts 92 (1995), S. 61-65 
    ISSN: 1432-2234
    Keywords: NMR ; Nuclear spin coupling constant ; Maximum bond order hybrid orbital ; Phosphorus-carbon coupling ; Net atomic charge
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The novel generalized correlation of the nuclear spin-spin coupling constants with the atomic hybrids and net charges is employed to give a new relationship for calculating the directly bonded phosphorus-carbon coupling constants by use of the maximum bond order hybrid orbital procedure together with the extended Hückel molecular orbital calculation. The calculated coupling constants of phosphorus-carbon are all in good agreement with the experimental data, which shows that the new relationship obtained in the present paper is quite satisfactory for calculation of the phosphorus-carbon coupling constants.
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  • 17
    ISSN: 1572-8951
    Keywords: Protein engineering ; thermolysin ; activity ; stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermolysin mutants having a variety of amino acid at the 119th position are designed by considering electrostatic field effect upon the active area. The most activated mutant has five times higher hydrolytic activity than the wild type. Negative correlation between the activity and the thermal stability is observed. A combined effect of the flexibility of the substrate binding site and the negative electrostatic field around the site is suggested as a key to enhance the activity.
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  • 18
    ISSN: 1572-9001
    Keywords: NMR ; distance geometry ; cluster analysis ; absolute configuration ; fusaproliferin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The absolute configuration of fusaproliferin, a toxic metabolite produced byFusarium proliferation, was determined by the combined use of1H NMR and distance geometry. The configuration of double bonds has been determined in agreement with NOESY buildup data. An R configuration for C10 was determined using Mosher's method. Processing the constraints obtained from NOESY experiments with a distance geometry program, a limited number (80) of possible structures was derived. An agglomerative nonhierarchical method of clustering was used in order to place these structures into classes suggested by the data, and not previously defined in any way. This statistical method showed that indeed the structures could be grouped in four classes. One of these classes is represented by a single structure, with the highest sum of violations and was discarded. All other structures have the same chirality; respectively S for C14 and R for C15. In solution the overall conformation is quite well defined in the region of the five-member ring and the planes of double bonds C2–C3 and C11–C12, while near to C8 and C9 internal flexibility appears evident.
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  • 19
    ISSN: 1573-1561
    Keywords: Pheromone ; aggregation ; hydrocarbon ; tetraene ; triene ; NMR ; mass spectra ; dried-fruit beetle ; Carpophilus hemipterus ; Coleoptera ; Nitidulidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Males ofCarpophilus hemipterus (L.), the dried-fruit beetle, (Coleoptera: Nitidulidae) were found to emit nine all-E tetraene and one all-E triene hydrocarbons in addition to two pheromonally active tetraenes that had been reported previously. The previously known compounds are (2E,4E,6E,8E)-3,5,7-trimethyl-2,4,6,8-decatetraene(1) and (2E,4E,6E,8E)-3, 5,7-trimethyl-2,4,6,8-undecatetraene(2). The new tetraenes were all related to structure1 by having one additional carbon at either one or two of the following four locations: at carbon 1 of the chain, at carbon 10 of the chain, at the 5-alkyl branch, or at the 7-alkyl branch. (Structure 2 also fits within this pattern.) The triene inC. hemipterus is (2E,4E,6E)-5-ethyl-3-methyl-2, 4,6-nonatriene. Also identified from volatile collections from the beetles were the 2Z and 4Z isomers of1. All structures were proven by synthesis, with NMR and mass spectral data for the compounds provided. Two of the newly discovered compounds, (2E,4E,6E,8E)-7-ethyl-3,5-dimethyl-2,4,6,8-decatetraene and (2E,4E,6E,8E)-7-ethyl-3,5-dimethyl-2,4,6,8-undecatetraene, were quite active in the wind-tunnel bioassay, but others, such as (2E,4E,6E,8E)-5-ethyl-3,7-dimethyl-2,4,6,8-decatetraene and (2E,4E,6E,8E)-4,6,8-trimethyl-2,4,6,8-undecatetraene were not. Structureactivity relationships are explored among the natural compounds and additional, synthetic analogs, which were never detected from the beetles. Some of these analogs, such as (2E,4E,6E,8E)-3,5-dimethyl-7-propyl-2,4,6,8-undecatetraene, were quite active in the bioassay. The biosynthesis of the beetle-derived compounds is discussed. A single biosynthetic scheme that lacks complete enzyme specificity at four specific steps could account for the entire series of compounds found in the beetles and their relative proportions. The definition of “pheromone” is discussed in relation to these hydrocarbons.
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  • 20
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    The protein journal 11 (1992), S. 265-274 
    ISSN: 1573-4943
    Keywords: NMR ; peptide ; hormone ; systemin ; proton assignments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Complete proton NMR assignments have been made for a synthetic 18-amino acid peptide named systemin, which functions as a wound-induced polypeptide hormone in tomato plants, and three of its derivatives. The wild-type peptide and this synthetic homolog have equivalent activities in their functional roles as systemic inducing signals in tomato plants. Proton NMR studies were carried out to characterize the solution properties of systemin. A variety of homonuclear proton NMR experiments at both 500 and 600 MHz were utilized in making these assignments, which have resulted in additional structural information. Whereas these results provide no evidence for persistence of common secondary (helix, sheet) or tertiary structural elements in the systemin polypeptide, there is evidence for two distinct molecular conformations at the carboxy terminus.
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  • 21
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    Bioscience reports 12 (1992), S. 143-187 
    ISSN: 1573-4935
    Keywords: Fourier transform ; nuclear magnetic resonance ; NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The development and current status of Fourier transform spectroscopy is described.
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  • 22
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    Bioscience reports 15 (1995), S. 55-63 
    ISSN: 1573-4935
    Keywords: water transport mechanisms ; NMR ; rat erythrocytes ; tritium effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The inhibition of water diffusion across the rat erythrocyte membrane was studied by NMR using two basically different types of inhibitory agents: PCMB andin vivo irradiation. The contribution of lipid and protein to water permeability revealed the inhibitory effect of each pathway. Internal contamination with tritium (25–115 mGy) reduces water permeability due to protein modifications; for doses higher than 100 mGy the lipid mediated mechanism seems also to be impaired. The same procedure enables one to assess the extent to which the higher water permeability of rat, compared to human, erythrocyte is due to one of the two pathways.
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  • 23
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    Journal of sol gel science and technology 4 (1995), S. 151-162 
    ISSN: 1573-4846
    Keywords: sol-gel transition ; rheology ; siloxane ; NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ormosils are well-known organic-inorganic sol-gel derived materials also called heteropolysiloxanes. This paper presents two basic heteropolysiloxane structures where the organic part is either a short organic chain bridging two silicon atoms for the first material or an organic polymer backbone for the second. Their synthesis is detailed and a variety of experimental techniques (IR, 13C and 29Si NMR and CP-MAS NMR, GPC) have been employed to investigate the chemical structure of these new materials. Their mechanical properties, more precisely their viscoelastic behaviour, have been evaluated using dynamic rheological techniques. The storage and loss moduli have been followed during the sol-gel transition at fixed and variable oscillation frequencies. The results have been correlated to the 29Si CP-MAS NMR informations concerning the network polycondensation and compared to a pure inorganic sol-gel material prepared from tetraethoxysilane.
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  • 24
    ISSN: 1573-5001
    Keywords: α-DNA ; NMR ; Parallel-stranded hybrid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The unnatural duplex oligonucleotide α-d(CGCAATTCGC)·β-d(GCGTTAAGCG) was analyzed by high-resolution NMR methods. All of the exchangeable imino and nonexchangeable protons of the duplex were assigned. Detection of all 10 of the exchangeable imino protons confirms that a parallel, unsymmetrical duplex is formed. The thermal stability of the parallel duplex is similar to the analogous antiparallel β-β duplex. The right handedness of the helix is confirmed by inter-residue [H8/H6-H1′] and [H8/H6-H2″] NOEs to the 5′-neighbor in the β-strand and [H8/H6-H1′] NOEs to the 3′-neighbor in the α-strand. Intra-residue and inter-residue distances between base protons and deoxyribose protons in both strands were determined using the isolated spin-pair approximation for NOESY cross peaks acquired with mixing times 50 ms or less. The NOE data are consistent with a B-form geometry adopted by the α/β hybrid decamer.
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  • 25
    ISSN: 1573-5001
    Keywords: Scorpion ; Toxin ; NMR ; Assignment ; Structure ; Protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary 1H NMR has been applied to a3.5 mM, pH 5.4, solution of toxin III (64 amino acids) from venom of the scorpionAndroctonus australis Hector. The resonance assignment strategy began by applying a generalized main-chain directed method for rapid identification and resonance assignments of secondary structures. The remaining resonances were assigned by the sequential method. Major structural features include a helix of 2 1/2 turns (residues 20–28) which is linked by two disulfide bridges to the central strand of a triple-stranded antiparallel β-sheet. Turns were identified at residues 15–17, 47–49 and also at residues 51–53. Numerous NOEs have been observed between hydrophobic residues which suggest the presence of a hydrophobic core; these include Leu37, Leu23, Val47, Tyr14, Trp45 and Tyr5. The Trp45 and Tyr5 rings lie orthogonal to one another. No crystal structure has been solved for this AaH III toxin. Comparisons are made with other members of the scorpion toxin family.
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  • 26
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    The protein journal 14 (1995), S. 115-126 
    ISSN: 1573-4943
    Keywords: NMR ; high-potential iron protein ; 15N assignment ; heteronuclear correlation ; paramagnetic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The15N resonances in reduced and oxidizedChromatium vinosum high-potential iron protein have been assigned by use of1H-1H COSY spectra and1H-15N HMQC, HMQC-COSY, and HMQC-NOESY spectra. Unambiguous assignment of 70 of 85 backbone15N resonances in the reduced protein and 62 of 85 resonances in the oxidized protein are made, as are 12 of 21 side-chain15N resonances.
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  • 27
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    Journal of biomolecular NMR 2 (1992), S. 349-360 
    ISSN: 1573-5001
    Keywords: NMR ; NOESY ; Relaxation matrix refinement ; Build-up curves ; Linear prediction ; R-factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The structural determination of biological molecules in solution by NMR relies on the determination of a set of interatomic distances obtained by measurement of intramolecular nuclear Overhauser effects (NOE). It is shown in this paper that it is possible to obtain the accurate relaxation rate (and hence the interatomic distance) from the direct measurement of a single NOE signal. The precise analysis of a NOESY peak evolution with respect to the mixing time allows the evaluation of the relaxation parameters for the pair of spins under consideration. This is done without any assumption on the relaxation of unmeasured spins, or on the movement of the molecule. The theoretical basis of this method is presented. In order to evaluate the proposed method, a simulated case on the protein BPTI is studied, which shows that the method performs very well even in the case of noisy data sets.
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  • 28
    ISSN: 1573-4943
    Keywords: Follicle-stimulating hormone ; FSH peptide ; NMR ; peptide structure
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The receptor binding surface of human follicle-stimulating hormone (hFSH) is mimicked by synthetic peptides corresponding to the hFSH-β chain amino acid sequences 33–53 [Santa-Coloma, T. A., Dattatreyamurty, D., and Reichert, L. E., Jr. (1990),Biochemistry 29, 1194–1200], 81–95 [Santa-Coloma, T. A., and Reichert, L. E., Jr. (1990),J. Biol. Chem. 265, 5037–5042], and the combined sequence (33–53)–(81–95) [Santa-Coloma, T. A., Crabb, J. W., and Reichert, L. E., Jr. (1991),Mol. Cell. Endocrinol. 78, 197–204]. These peptides have been shown to inhibit binding of hFSH to its receptor. Circular dichroism (CD) and nuclear magnetic resonance (NMR) spectroscopy were used to determine the structure of the first peptide in this series, the 21 amino acid peptide hFSH-β-(33–53), H2N-YTRDLVYKDPARPKIQKTCTF-COOH. Analysis of CD data indicated the presence of approximately equal amounts of antiparallel β-pleated sheet, turns including a β-turn, “other” structures, and a small amount ofa-helix. The major characteristics of the structure were found to be relatively stable at acidicpH and the predominant effect of increased solvent polarity was a small increase ina-helical content. One- and two-dimensional NMR techniques were used to obtain full proton and carbon signal assignments in aqueous solution atpH 3.1. Analysis of NMR results confirmed the presence of the structural features revealed by CD analysis and provided a detailed picture of the secondary structural elements and global folding pattern in hFSH-β-(33–53). These features included an antiparallel β-sheet (residues 38–51 and 46–48), turns within residues 41–46, and 50–52 (a β-turn) and a small N-terminal helical region comprised of amino acids 34–36. One of the turns is facilitated by prolines 42 and 45. Proline-45 was constrained to thetrans conformation, whereas proline-42 favored thetrans conformer (∼70%) over thecis (∼30%). Two resonances were observed for the single alanine residue (A-43) sequentially proximal to P-42, but the rest of the structure was minimally affected by the isomerization at proline-42. The major population of molecules, containingtrans-42 andtrans-45 prolines, presented 120 NOEs. Distance geometry calculations with 140 distance constraints and energy minimization refinements were used to derive a moderately well-defined model of the peptide's structure. The hFSH-β-(33–53) structure has a highly polar surface composed of six cationic amino acid (arginie-35, lysine-40, arginine-44, lysine-46, glutamine-48, and lysine-49) and two anionic residues (aspartate-36 and aspartic acid-41). A hydrophobic region in the structure is composed of residues in the antiparallel β-sheet and β-turn which fold to produce a distorted “hairpin.” The structure of this domain, together with the protruding and positively charged region in the vicinity of residues 42–45, may mimic the surface of hFSH that binds to the receptor.
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  • 29
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    Journal of biomolecular NMR 2 (1992), S. 83-98 
    ISSN: 1573-5001
    Keywords: Protein ; NMR ; Chemical shift
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The chemical shifts of CαH protons have been calculated for 9 proteins, based on coordinates taken from high-resolution crystal structures. Chemical shifts were calculated using ring-current shifts, shifts arising from magnetic anisotropies of bonds, and shifts arising from the polarizing effect of polar atoms on the Cα-H bond. The parameters used were refined iteratively to give the best fit to (experimental — random coil) shifts over the set of 9 proteins. A further small correction was made to the averaged Gly CαH shift. The calculated shifts match observed shifts with correlation coefficients varying between 0.45 and 0.86, with a standard deviation of about 0.3 ppm. The differences between calculated and observed shifts have been studied in detail, including an analysis of different crystal structures of the same protein, and indicate that most of the differences can be accounted for by small differences between the structure in solution and in the crystal. Calculations using NMR-derived structures give a poor fit. The calculations reproduce the experimentally observed differences between chemical shifts for CαH in α-helix and β-sheet. Most of the differentiation in secondary structure-dependent shifts arises from electric field effects, although magnetic anisotropy also makes a large contribution to the net shift. Applications of the calculations to assignment (including stereospecific assignment) and structure determination are discussed.
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  • 30
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    Russian chemical bulletin 41 (1992), S. 1384-1391 
    ISSN: 1573-9171
    Keywords: fluorophosphoranes ; phosphorus fluorides ; NMR ; pseudorotation ; restricted rotation ; rotational barrier ; hydrogen bonds ; conjugation
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Phenomena associated with stereochemical nonrigidity of five-coordinate phosphorus fluorides (Berry pseudorotation and restricted rotation of different functional groups about the bond with the central phosphorus atom) have been analyzed. The main cause of restricted rotation isp π d π bonding of unsharedp-electron pairs of substituents with vacantd-orbitals of the phosphorus. Additional stabilization of the molecule occurs when it is possible to form an H...F hydrogen bond between the liquid and an axial fluorine atom in the phosphorane. The relationship between pseudorotation and restricted rotation is considered.
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    Russian chemical bulletin 41 (1992), S. 462-467 
    ISSN: 1573-9171
    Keywords: deoxycholic acid ; ferrocene ; inclusion compounds ; molecular dynamics ; relaxation ; NMR
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Using solid-state 13 C NMR spectroscopy and also measurements of proton spin-lattice relaxation times T 1 and second moments M 2 , we have investigated molecular motion in solid inclusion compounds of deoxycholic acid with ferrocene in the interval 100–400 K. We have identified various dynamic processes occurring with participation of molecules of the matrix and the included molecules. We have shown that in addition to rapid reorientations of the cyclopentadienyl rings, the ferrocene molecules undergo 180° jumps about the C 2 axis. We have determined the parameters for all the molecular motions. We discuss the conformational state of the included molecules.
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  • 32
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    Russian chemical bulletin 41 (1992), S. 504-510 
    ISSN: 1573-9171
    Keywords: electronic structure ; geometry optimization ; electron affinity ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The electronic and geometric structures of the ground state and a number of excited states of the SF6 molecule and the SF 6 − anion have been calculated by the discrete-variation method of the local density-functionals. The anion was found to possess a number of states stable toward the outer electron detachment, and at least one excited state stable toward dissociation. The adiabatic electron affinity (EA) was determined as 3.46 eV at the highest level of theory. This result is correlated to the high EAs of the isovalent compound SeF6 and TeF6; however, it does not agree with the presently accepted experimental estimate of 1.0 ± 0.2 eV for the SF6EA value. The basic anion configuration is octahedral with a S-F bond length of 1.717 Å. The calculated limit for the highest dissociation channel of the ground state SF 6 − → SF 5 − + F is ≈ 1.5 eV lower than the minimum of the total energy of the neutral molecule; this is in good agreement with experimental estimates.
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  • 33
    ISSN: 1573-8353
    Keywords: NMR ; 1H NMR ; 13C NMR ; 17O NMR ; 15N NMR ; aziridine-carboxylates ; configurational analysis ; conformational analysis
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    Topics: Chemistry and Pharmacology
    Notes: Abstract A confrgurational and conformational study of NH, N-acetyl- and N-sulfonylaziridine carboxylates is performed by1H ,13C,17O, and15N NMR spectroscopy. The presence of acetyl and su fonyl groups on the ring nitrogen atom seems to reduce greatly the configurational stability at nitrogen.
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  • 34
    ISSN: 1573-904X
    Keywords: proteins ; aggregation ; reconstitution ; lyophilization ; additives ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. Protein stabilization during lyophilization has previously focused on optimization of the formulation as well as the freezing and dehydration process parameters. However, the effect of the reconstitution medium has been largely neglected. We have investigated its effect on aggregate formation using recombinant keratinocyte growth factor (KGF). Methods. The protein was lyophilized under suboptimal conditions to induce aggregation and precipitation upon reconstitution with water. A series of additives were examined by UV spectrophotometry and size exclusion chromatography (SEC-HPLC) for their effects on decreasing the degree of KGF aggregation and precipitation by the increase in recovery of soluble monomer. Results. Several additives resulted in a significant reduction of aggregation, including sulfated polysaccharides, surfactants, polyphosphates, and amino acids. A similar effect was achieved by adjusting the ionic strength of the reconstitution medium. SEC-HPLC indicated that the amount of soluble monomer was also increased by these additives suggesting that the recovery of the soluble protein correlates with the native, monomeric protein. Conclusions. These results suggest that optimization of reconstitution conditions will be a useful methodology for increasing the recovery of soluble, active proteins and that for KGF, the recovery of the soluble protein correlates with the native, monomeric form.
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  • 35
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    Pharmaceutical research 12 (1995), S. 599-604 
    ISSN: 1573-904X
    Keywords: famotidine ; degradation ; isothermal ; nonisothermal ; kinetics ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The kinetics of hydrolysis of famotidine in aqueous solution was studied by isothermal and nonisothermal method over the pH range of 1.71 to 10.0. Nonisothermal kinetics was studied with the purpose of determining its use in the establishment of the expiration date of pharmaceutical preparations, particularly drugs in solutions and for assessment of stability characteristics of pharmaceutical formulations during the development stage. A comparison of isothermal (55, 70 and 85°C) and nonisothermal kinetics was performed. Aqueous solutions of famotidine were buffered at pH 1.71, 2.24, 2.66, 4.0, 8.5, 9.0 and 10.0 were used. In the nonisothermal studies, the temperature rate of the reaction was continuously varied throughout the experiment. The energies of activation were found to be in close agreement for isothermal and nonisothermal studies, indicating that nonisothermal studies may save considerable amount of time in the early stages of drug development and stability testing. Logk-pH profiles were constructed for 55, 70 and 85°C from the first-order rate constants obtained from isothermal studies at pH values ranging from 1.71 to 10.00. The pH-rate profile indicated that famotidine undergoes specific acid catalysis in the acidic region and general base catalysis in the alkaline region. Hydrolysis in the acidic and alkaline media resulted in the formation of four and five degradation products, respectively. A possible degradation pathway for the acidic and alkaline hydrolysis was discussed.
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  • 36
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    Pharmaceutical research 12 (1995), S. 1371-1375 
    ISSN: 1573-904X
    Keywords: prodrug ; bispilocarpic acid diester ; hydroxypropyl-β-cyclodextrin ; inclusion complex ; solubility ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The effects of 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) on the aqueous solubility and stability of two lipophilic bispilocarpine prodrugs were investigated at pH 7.4. Methods. The solubility of prodrugs was studied by phase-solubility method (0–72.5 mM HP-β-CD). The stability of one of the prodrugs was investigated as a function of temperature (40°C–70°C) and HP-β-CD concentration (0–72.5 mM). The apparent rate constants (k 1, k 2) for degradation of prodrug in 1:1 and 1:2 inclusion complexes and apparent stability constants (K 1:1, K l:2) were calculated by the curve-fitting method. Results. The phase-solubility diagrams were classified as Ap-type and the apparent stability constants (K l:l, K l:2) for 1:1- and 1:2-inclusion complexes were calculated to be 143–815 M−l and 29–825 M−1, respectively. The stability of prodrug increased as a function of HP-β-CD concentration over the studied temperature range. The shelf-life (t 90%, calculated by the Arrhenius equation) of the prodrug in 72.5 mM HP-β-CD solution increased 5.1-fold and 6.1-fold at 25°C and 4°C, respectively. Conclusions. The solubility of the prodrugs was shown to increase markedly in phase-solubility studies. The degradation rate of prodrug in stability studies was shown to be slower in the l:2-complex than in the l:l-complex and the relative amounts of complex species were found to be dependent on CD concentration.
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  • 37
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    Pharmaceutical research 12 (1995), S. 715-719 
    ISSN: 1573-904X
    Keywords: salbutamol base drug ; oleic acid ; propellant ; metered-dose inhaler ; stability ; adsorption
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The distribution of oleic acid between Salbutamol base drug and the solvent in metered-dose inhalers (MDI's) has been investigated. The equilibrium surfactant concentration in the drug dispersions has been determined using a colorimetric method. The samples examined contained Salbutamol base drug particles and oleic acid dispersed in different propellant blends of freon 11 and 12. The maximum equilibrium concentration observed depended on the propellant blend used. The propellant blend and the distribution of the surfactant affected the dispersion stability. The effect of the surfactant is illustrated by the adsorption isotherm for oleic acid onto the Salbutamol particles. The results are correlated with zeta-potentials and particle size measurements made on similar systems in order to characterize the properties of surfactant stabilized MDI's.
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  • 38
    ISSN: 1573-904X
    Keywords: 2′,3′,5′-triacetyl-6-azauridine ; prodrug ; hydrolysis ; pH-profile ; arrhenius plots ; CI-MS ; NMR ; liquid chromatography
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The purposes were to study the kinetics of hydrolysis of 2′,3′,5′-triacetyl-6-azauridine ( 1 ) in aqueous solution (µ = 0.5) and to identify the main intermediates and products of the reaction. Methods. A stability indicating isocratic LC assay was used to study the rate of degradation of 1 A gradient LC assay was used to study the time courses of the degradants. The products of hydrolysis were isolated by preparative liquid chromatography and identified by 1H-NMR and CI-MS. The pKa value was obtained by potentiometric titration. Results. At 36.8°C, the pH-rate profile of 1 in water was adequately described by a four-term rate equation. The intermediates were identified as the primary and secondary di-acetates, and the primary and secondary mono-acetates. The final product was 6-azauridine. Conclusions. A simplified kinetic scheme could be used to describe the concentration-time profiles of 1, the intermediates and the final product.
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  • 39
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    Pharmaceutical research 12 (1995), S. 53-59 
    ISSN: 1573-904X
    Keywords: aerosol ; lactate dehydrogenase ; nebulizers ; proteins ; ultrasonic nebulization ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Ultrasonic nebulization of lactate dehydrogenase (LDH) was investigated using a DeVilbiss “Aerosonic” nebulizer. The enzyme (8ml, 0.025mg/ml Na2HPO4, pH 7.0) was completely inactivated after 20 minutes of operation. However, the inactivation profile observed during ultrasonic nebulization was different from that previously observed using air-jet nebulization. At least two mechanisms are involved, one associated with heating and the other with aerosol production. By preventing heating of the nebulizer fluid during operation, the denaturation profile was dramatically altered. By additionally including 0.01% w/v Tween 80 or l%w/v PEG 8000, almost all activity was retained. Similar results were obtained by preventing aerosol production and heating. However, 100% of activity was lost when heating was allowed to occur without aerosol formation. The results demonstrate that cooling in conjunction with a surfactant is one approach that could be used to stabilize proteins to ultrasonic nebulization. However, cooling also significantly reduced solute output from the nebulizer. When operated at 10°C output was negligible. At 50°C the output was 5× greater than that found at room temperature. The median droplet size (µm) was not significantly influenced by the operating temperature of the nebulizer fluid (3.6 ± 0.4, 21°C; 3.9 ± 0.2, 50°C, p = NS (n = 6)) although the size distribution was noted to increase at the higher temperature.
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  • 40
    ISSN: 1573-904X
    Keywords: acyl migration ; peptides ; cyclosporin ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The chemistry associated with the process of N,O-acyl migration was explored in both cyclic and linear peptides under aqueous acid conditions. The importance of backbone cyclization and N-methylation of the peptide bond on the kinetics of N,O-acyl migration in a series of linear and cyclic peptides related in structure to cyclosporin A (CsA) were examined. The similarity in the chemical reactivity of the cyclic peptide [MeLeu (3-OH)]1-CsA and the corresponding linear peptide [Val-MeLeu (3-OH)-Abu], suggested that for this series, cyclization of the peptide backbone may not play an important role in controlling the kinetics of N,O-acyl migration. In contrast, the disparity in the chemical reactivity of tripeptides [Val-MeLeu (3-OH)-Abu] and [Val-Leu (3-OH)-Abu], indicated that N-methylation of amide bond significantly impacted the kinetics. Various hypothesis are proposed to account for this observation.
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  • 41
    ISSN: 1573-904X
    Keywords: chimeric antibody ; protein ; immunoconjugate ; lyophilization ; freeze-drying ; stability ; aggregation
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Chimeric BR96-doxorubicin conjugate (BR96-DOX) is an immunoconjugate designed to specifically target and kill certain tumor cells. The linker between the chimeric BR96 antibody and DOX is an acid-labile hydrazone group which was designed to undergo lysosomal hydrolysis to release DOX in vivo. Stability studies indicated that acid-catalyzed hydrazone hydrolysis was the major degradation route in vitro. Even under optimal conditions of pH and temperature, the stability of BR96-DOX in solution was not acceptable for long-term storage. Lyophilization of BR96-DOX in the presence of added sugars, such as lactose or sucrose, and subsequent storage of the lyophile under refrigeration significantly improved the stability. Therefore lyophilization appears to be a viable approach for achieving long-term stabilization of BR96-DOX.
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  • 42
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    Pharmaceutical research 12 (1995), S. 305-308 
    ISSN: 1573-904X
    Keywords: RMP-7 ; bradykinin ; stability ; diketopiperazine
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  • 43
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    Colloid & polymer science 270 (1992), S. 747-752 
    ISSN: 1435-1536
    Keywords: FTIR ; amorphousorientation ; entropicelasticity ; NMR ; spin-spin ; relaxation ; solidecho ; hardelasticpolypropylene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The variation of amorphous orientation and crystalline regularity of hard elastic polypropylene (HEPP) films during cyclic deformation and stress relaxation processes were studied using a FTIR spectrometer. The result proves entropic elasticity and shows the orientational hysteresis in the amorphous region or within the microfibrils, and also shows that the amorphous orientation increases, but that the crystalline regularity decreases with the increase of extension rate. Three spin-spin relaxation timesT 2f,T 2m, andT 2s and associated mass fractionsF f,F m, andF s of HEPP fibers were measured with a solid echo of NMR method at different elongations and after relaxation or recovery for a long time A new possible interpretation was proposed that, while the microfibrils are formed in HEPP, the medium decay component should be ascribed to inner molecules of the microfibrils, and the slow decay component to the surface molecules of the microfibrils. According to this interpretation, the results implied that subfibrillation is the main process when HEPP is stretched up to 15% strain, and that at above 15% strain thinning and lengthening of the microfibrils become the main process. Thickening of the microfibrils was found in the recovery and relaxation processes.
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  • 44
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    Journal of bioenergetics and biomembranes 24 (1992), S. 139-146 
    ISSN: 1573-6881
    Keywords: Review ; NMR ; bacteriorhodopsin ; rhodopsin ; retinal ; opsin ; chromophore ; Schiff base
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    Topics: Biology , Chemistry and Pharmacology , Physics
    Notes: Abstract A review is given of the use of nuclear magnetic resonance (NMR) spectroscopy to study bacteriorhodopsin and bovine rhodopsin. Solution and solid-state approaches are included. The studies of the bacterial proton pump examine the chromophore, the peptide backbone, and the protein side chains. The studies of the bovine visual pigment are limited to the chromophore. Various forms of each pigment are considered. Both structural and dynamic features are addressed.
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  • 45
    ISSN: 1435-1536
    Keywords: Associative polymers ; NMR ; self-diffusion ; self-assembly
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The concentration and molecular weight dependence of the self-diffusion coefficient (D self) of associative polymers of HEUR-type in aqueous solution have been investigated using FT-PGSE-NMR technique. The idea of three-dimensional network formation as a result of aggregation of the hydrophobic end-groups of the polymer in junctions is supported through the observed dramatic lowering ofD self with increased concentration. The network-formation efficiency depends on the polymer molecular weight as well as the hydrophobicity of the end-groups. A double logarithmic dependence of the self-diffusion coefficient versus concentration (c) has been observed:D self∝c −a1,a2 . The first exponent,a 1, is valid at low concentration, 〈1% polymer per weight solution, and ranges from 0.5 to 1, whereas the second exponent,a 2, describing systems of higher concentration, ranges from 2 to 2.7.
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  • 46
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    Rheologica acta 34 (1995), S. 417-429 
    ISSN: 1435-1528
    Keywords: Electrorheology ; nonlinear ; simulations ; stability ; steady shear
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Particle-level simulations are employed to investigate the transition from linear to nonlinear rheological behavior for electrorheological suspensions under start-up of steady shear flow. This transition is found to first arise from the very slight rearrangement of structures, as opposed to the gross rupture of particulate columns. Linear stability analysis shows that these rearrangements occur when the structures are sheared into electrostatically unstable configurations. The rearrangements also produce a second type of relaxation phenomenon that appears at low frequencies and finite strain amplitudes. Incorporating more realistic force descriptions into the idealized simulation model shifts the transition to nonlinear deformation to smaller strain amplitudes, approaching experimentally observed values. The role of the rearrangement of unstable structures on the oscillatory shear flow response is investigated in the following paper, Part II.
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  • 47
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    Rheologica acta 34 (1995), S. 430-439 
    ISSN: 1435-1528
    Keywords: Electrorheology ; nonlinear ; simulations ; stability ; viscoelasticity
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract In the preceding paper, Part 1, the transition from linear to nonlinear behavior for electrorheological (ER) suspensions under start-up of steady shear flow was found to first arise from the slight rearrangement of unstable structures. In this paper, we investigate the transition to nonlinear behavior for ER suspensions under oscillatory shear flow, focusing on the role of the rearrangement of unstable structures, and employing experimental and simulation results. Again, we find that nonlinear deformation first arises from these rearrangements, as opposed to the gross rearrangement or rupture of particulate chains. The Fourier transform of the simulated time-dependent shear stress is employed to quantify the dependence of the critical strain on the deformation frequency and electric field strength. The predicted behavior is consistent with experimental trends. Methods for verifying the predictions are discussed, as well as possible avenues for exploiting this information in improved operating strategies and improved ER fluids.
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  • 48
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    Pharmaceutical research 9 (1992), S. 1521-1523 
    ISSN: 1573-904X
    Keywords: salmon calcitonin ; stability ; kinetics ; peptide ; degradation ; pH–rate profile ; HPLC
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    Topics: Chemistry and Pharmacology
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  • 49
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    Pharmaceutical research 9 (1992), S. 406-409 
    ISSN: 1573-904X
    Keywords: centrifugation ; emulsification ; perfluorocarbon ; stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The effect of preparation temperature on the emulsification efficiency of perfluoro-3-butyltetrahydrofuran (FC-75) was investigated. Polyoxyethylene (POE) oleyl ether surfactants were used as the emulsifier(s) in a range of HLB values of 7.5 to 9.5. The emulsions were prepared by paddle mixing as a method of low-shear emulsification. After centrifugation of the resulting O/W emulsions, the volume of FC-75 which separated was utilized as a measure of the emulsification efficiency. In general, emulsions prepared at temperatures where the surfactant was in a lamellar-to-isotropic surfactant solution transition, Lα→ L3, displayed a better emulsification efficiency than those prepared with other surfactant phases.
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  • 50
    ISSN: 1573-904X
    Keywords: monoclonal antibody ; lyophilization ; freeze-drying ; stability ; formulation ; cyclodextrin
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of lyophilization on the stability of a monoclonal antibody (MN12) was investigated. MN12 was freeze-dried in different formulations [without lyoprotectant or in the presence of sucrose, dextran, or hydroxypropyl-β-cyclodextrin (HPβCD)] and under varying conditions (with or without secondary drying). Subsequently, the monoclonal antibody was stored for 18 or 32 days at various temperatures (4, 37, or 56°C). For comparison, solutions of MN12 were stored under the same conditions. Regardless of the lyoprotectant used, precipitation and a concomitant reduction of the antigen-binding capacity by about 10% were observed upon recon-stitution of lyophilized MN12. HPβCD proved to be the most effective stabilizer to prevent degradation of lyophilized MN12 during storage. Compared with MN12 solutions, HPβCD-containing lyophilized MN12 cakes were more resistant to heat-induced charge alterations and loss of antigen-binding capacity.
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  • 51
    ISSN: 1573-904X
    Keywords: glycosylation ; mass Spectrometry ; monoclonal antibody ; protein characterization ; stability
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  • 52
    ISSN: 1573-904X
    Keywords: submicron ; emulsion ; miconazole ; stability ; toxicity ; cryptococcosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Submicron emulsions of miconazole were stabilized by using a combination of three emulsifiers comprising phospholipids, poloxamer, and deoxycholic acid (DCA). The presence of DCA was vital for prolonged emulsion stability owing to its contribution to the elevated zeta potential of the emulsion. Further, the results by the phospholipid surface labelling colorimetric technique clearly suggested that poloxamer molecules interacted with phospholipid polar-head groups of the mixed DCA-phospholipid interfacial film, resulting in the stabilization of the emulsion by a steric enthalpic entropic mechanism. The plain emulsion vehicle was well tolerated up to a dose of 0.6 ml injected i.v. to BALB/c mice. The maximum tolerated dose of miconazole was 80 and 250 mg/kg in Daktarin® i.v. (a marketed product) and emulsion, respectively, showing an improved safety ratio of 1 to 3 in favor of the emulsion. These results tended to confirm that the adverse effects associated with Daktarin® i.v. injection should be associated with the vehicle rather than with the miconazole itself. In a murine cryptococcosis model, only one mouse out of ten remained alive by day 15 in the infected group treated with Daktarin® i.v., while in the miconazole emulsion treated group, mice began to die from day 16 up to day 25 post inoculation. Thus, the multiple-dose treatment with the miconazole emulsions improved the protection offered to the infected mice. However, the therapeutic levels of miconazole that were reached in the target organ (brain) were lower than those required for complete eradication of Cryptococcus neoformans, which is known to multiply preferentially in the brain.
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  • 53
    ISSN: 1573-904X
    Keywords: lyophilization ; interleukin-2 ; protein conformation ; infrared spectroscopy ; stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. Examination of the dried-state conformation of interleukin-2 (IL-2) was used to determine the pH conditions and stabilizers that provide optimal storage stability for the lyophilized product. Methods. Fourier-transform infrared spectroscopy and accelerated stability studies which examined solubility, aggregate formation, and covalent cross-linking were used. Results. Varying the pH in the absence of excipients resulted in dramatic differences in the dried state conformation of IL-2. At pH 7, IL-2 unfolds extensively upon lyophilization while at pH below 5 it remains essentially native. Additional unfolding was observed upon incubation at elevated temperatures. A strong direct correlation between the retention of the native (aqueous) structure during freeze-drying and enhanced stability is demonstrated. IL-2 prepared at pH 5 is approximately an order of magnitude more stable than at pH 7 with regard to formation of soluble and insoluble aggregates. A similar pH profile was observed in the presence of excipients, although the excipients alter the overall stability profile. Additional accelerated stability studies examined the stabilizers necessary for optimal stability. Conclusions. Excipients with the capacity to substitute for water upon dehydration better preserve the native structure resulting in enhanced stability. Those that have high glass transition temperatures provide the highest level of stability during storage, although they do not prevent dehydration induced unfolding.
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  • 54
    ISSN: 1573-904X
    Keywords: capillary gas chromatography ; analysis ; stability ; urea derivative ; capsules ; mass spectrometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A method for the analysis of hydroxyurea (HU) in solutions, powder, or capsules by use of capillary gas chromatography with N–P thermionic specific detection is described. Upon injection of an HU solution in a methanol and acetone mixture, the drug formed pyridine which was well separated from the internal standard (thiotepa) on a 30-m fused-silica, SE-30 capillary column with temperature programming. The peak height ratio versus concentration standard curves were linear with correlation coefficient ranging between 0.9942 and 0.9993. The coefficients of variation at 5, 25, and 50 µg/L were 7.2, 5.7, and 5.5%, respectively. Hydroxyurea was extracted from powder or capsule formulations with a mixture of methanol and acetone (50:50, v:v), and the percentage found of the label claim for 10 capsules ranged between 96.7 and 104.9 (mean = 100.1; CV = 2.7%). Further, this assay was used to examine the stability of hydroxyurea in aqueous solutions at 4, 23, and 45°C, and the apparent first-order rate constants observed at these temperatures were 0.06407, 0.08113, and 0.1293 day-1, respectively; the activation energy was 3011 cal · K-1 mol-1.
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  • 55
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    Pharmaceutical research 9 (1992), S. 312-315 
    ISSN: 1573-904X
    Keywords: controlled drug delivery system ; chronotherapeu-tics ; electrically modulated ; electrophoresis ; degradation of propranolol hydrochloride ; stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A number of factors affecting the stability of propranolol HC1 during electrophoretic control were investigated. It was found that significant degradation of propranolol HC1 and hydrolysis of water occurred when a current of 15 mA was used with platinized electrodes. This degradation was thought to be due to decomposition of propranolol HC1 at the electrodes. Degradation could be significantly reduced by using uncoated platinum electrodes and currents in the range of 0 to 2.5 mA, while still allowing control of drug delivery rates. Electrode reaction processes were found at high ionic strengths and high drug concentrations but were not thought to be associated with drug decomposition.
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  • 56
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    Pharmaceutical research 9 (1992), S. 939-944 
    ISSN: 1573-904X
    Keywords: calorimetry ; microcalorimetry ; stability ; kinetics, solid state ; degradation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new technique has been developed to calculate rapidly the solid-state room-temperature degradation rate of drugs and drug candidates. The technique utilizes measurements of the initial rate of heat output at several elevated temperatures by isothermal calorimetry and the degradation rate of the compound determined at a single elevated temperature by chromatography. The activation energies and degradation rates at 25°C calculated by conventional methods and by isothermal calorimetry are compared and discussed. The compounds studied were phenytoin, triamterene, digoxin, tetracycline, theophylline, diltiazem, and several proprietary ICI compounds.
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  • 57
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    Journal of chemical ecology 21 (1995), S. 1191-1215 
    ISSN: 1573-1561
    Keywords: Ourebia ourebi ; Bovidae ; mammalian semiochemicals ; mammalian pheromones ; exocrine secretion ; preorbital secretion ; dimethyl disulfide derivatization ; skipped dienes ; chemical-ionization mass spectrometry ; NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Using gas chromatography-mass spectrometry in conjunction with ancillary techniques such as chemical ionization with different reactant gases, determination of the position of double bonds by means of dimethyl disulfide derivatization, and finally gas chromatographic and mass spectrometric comparison with authentic synthetic material, 75 constituents were identified in the preorbital secretion of the male oribi,Ourebia ourebi. The secretion contains compounds with long-chain, unbranched structures similar to those found in many other preorbital secretions but with a finite volatility range, in contrast to the seemingly endlessly increasing chain lengths typical of other preorbital secretions.
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  • 58
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    Journal of inclusion phenomena and macrocyclic chemistry 22 (1995), S. 99-105 
    ISSN: 1573-1111
    Keywords: DA15C5-iodine complex ; stoichiometry ; stability ; rate constant ; spectrophotometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The complex formation reaction between iodine and 1,7-diaza-15-crown-5 (DA15C5) has been studied spectrophotometrically in chloroform at 25°C. The resulting 1:2 (DA15C5:I2) molecular complex was formulated as (DA15C5...;I+)I 3 − . The spectrophotometric results, as well as the conductivity measurements, revealed that the gradual release of triiodide ion from its contact ion paired form in the molecular complex into the solution is the rate determining step of the reaction. The rate constant was calculated ask=(8.8±0.2)×10−3 min−1. The formation constant of the molecular complex was evaluated from the computer fitting of the absorbance-mole ratio data as logK f=6.89±0.09.
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  • 59
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    International journal of peptide research and therapeutics 2 (1995), S. 121-124 
    ISSN: 1573-3904
    Keywords: Backbone cyclization ; Substance P ; NMR ; Molecular dynamics ; Conformational analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Structure-activity relationships of cyclic substance P (SP) analogs were extensively studied in our laboratories utilizing the new concept of backbone cyclization. Employing the C-terminal hexapeptide SP6–11, we examined the influence of chemical changes in peptides containing backbone-to-amino-end cyclization. These changes in the ring have significant influence on activity, and should be carefully designed in order to optimize pharmacological feature.
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  • 60
    ISSN: 1573-3904
    Keywords: Biosurfactant ; Lipopeptide ; NMR ; Hydrophobic substitution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Bacillus subtilis coproduces several surfactin variants that are powerful biosurfactants and have potential applications in biology and industry. A single amino acid substitution in the heptapeptide moiety of surfactins strongly modifies their properties. To better establish structure-activity relationships and to search new variants with enhanced properties, Bacillus subtilis was grown into two modified culture media. Two new variants were isolated by chromatographic methods and studied by NMR spectroscopy. As planned, modifications consisted in the substitution of the l-valine residue at the fourth position by a more hydrophobic residue, i.e., leucine or isoleucine. These [Leu4]- and [Ile4]surfactins have a higher affinity for hydrophobic solvents and a twice improved surfactant power. Structure-property correlations were confirmed by analysis of the hydrophobic residue distribution in the three-dimensional model of the structure of surfactin in solution.
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  • 61
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    International journal of peptide research and therapeutics 2 (1995), S. 59-70 
    ISSN: 1573-3904
    Keywords: Opioid peptide ; NMR ; Enkephalins ; Micelles ; Dodecylphosphocholine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Opioid peptides are thought to interact with the cell membrane in their biological journey to the membrane-bound receptor. Both organic solvents and model membranes have been used previously to determine the stable solution conformations of peptide hormones. Leucine enkephalin has been studied in a number of different environments, but with limited resolution. Here it is shown that leucine enkephalin forms a stable type IV β-turn structure in dodecylphosphocholine micelles. We have observed a highly solvent-shielded amide proton with no evidence for a complementary hydrogen bond acceptor. The structural details of the peptide as determined by NMR spectroscopy in solution are described.
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  • 62
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    International journal of peptide research and therapeutics 2 (1995), S. 161-164 
    ISSN: 1573-3904
    Keywords: Cyclised peptide ; Dioxopiperazine ; Thiazolidine ; NMR ; Computer modelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Conformationally constrained peptidomimetics of the Lys-Pro sequence have been obtained using a new polycyclic structure. Bicyclic compounds containing a dioxopiperazine-thiazolidine fused ring have been synthesised starting from N-lysyl-4-ethoxycarbonylthiazolidine-2-carboxylic acid. The carboxyl group in either position 2 or 4 of the thiazolidine ring was reacted with the N-terminal amino group, giving different regioisomers. NMR and computer modelling were used to study the configuration of isomers and the lysine side-chain orientation with respect to the pseudoproline ring.
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  • 63
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    International journal of peptide research and therapeutics 2 (1995), S. 239-242 
    ISSN: 1573-3904
    Keywords: Pseudopeptide ; Triphosgene ; Beta-turn ; NMR ; FT-IR ; X-ray diffraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary For the sake of improving synthetic methods and evaluating the conformational perturbation induced by the substitution of AzAsx for the Asx residue in the cognate dipeptide R-CO-Asx-Pro-NHR′, we prepared the AzAsx-dipeptide sequence by making use of the crystalline triphosgene. This reagent allows, in situ and under very mild experimental conditions, both the carbonylation and the activation of the properly substituted and N-protected hydrazine before coupling with the proline partner. With regard to conformational behaviour, the azadipeptide sequence displays a β-fold, unlike the cognate dipeptide which adopts an Asx-turn.
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  • 64
    ISSN: 1573-9171
    Keywords: oligodienyl chain ; transition metals ; synthesis ; stability ; π-coordination ; IR spectra
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The results of investigations performed in the Laboratory of Organometallic Catalysis of the A. V. Topchiev Institute of Petrochemical Synthesis of the RAS are reviewed. The oligodienyl compounds of a series of transition metals, R n olM and R n olMXm (Rol= R′(diene)3–10, where R′ is an alkyl, allyl, alkenyl, or H; (diene)3–10 is an oligodienyl group with 3–10 monomeric diene units; M = Ti3+, Cr2+, Mn2+, Co2+, Ni2+, Nd3+, Pr3+, Sm3+, and Gd3+; X is a halogen or an electronegative group), have been synthesized for the first time and some of their properties have been studied. The stability of oligodienyl compounds is much higher than that of the corresponding π-alkenyl derivatives. The IR spectra of the compounds synthesized allowed us to conclude that their stability and some peculiarities of the reactions of these compounds can be explained by π-coordination of the isolated double bond of the oligodienyl chain to the transition metal.
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  • 65
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    Medical & biological engineering & computing 30 (1992), S. 427-432 
    ISSN: 1741-0444
    Keywords: Electrical scanning ; Magnetic focusing method ; NMR ; Nonlinear magnetic field gradient ; Spatial localisation ; Star-shaped focusing field
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The spatial localisation of NMR signals by the magnetic focusing method is examined and a method for electrical scanning of a spatially localised region is proposed. The small amount of signal from points of the star taper in static field focusing can almost be neglected, and the spatial localisation of the signal corresponds to the shape of a prolate spheroid in the centre region of the star-shaped focusing field. Electrical scanning of the focused region can be achieved at any position in the magnet system by superimposing linear field gradients on the focused field in the scanning direction. These are the inherent limitations of the static magnetic field focusing method. The embodiment of the scanning movement of the focused field is also confirmed.
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