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  • block copolymer  (2)
  • 75.25+z  (1)
  • Springer  (3)
  • American Association for the Advancement of Science (AAAS)
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  • Springer  (3)
  • American Association for the Advancement of Science (AAAS)
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  • 1
    ISSN: 1090-6487
    Keywords: 75.50.Ee ; 75.70.Cn ; 75.30.Kz ; 75.25+z
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The characteristic features of phase transitions induced by an external magnetic field and of the corresponding changes in the relative orientations of the spins in the ferromagnetic CoNiCu layers of a multilayer film, which are coupled by an antiferromagnetic exchange interaction via nonmagnetic Cu interlayers, are studied using a magnetooptic method for visualizing the fringing fields. It is established that the magnetization reversal process in this nanocomposite material proceeds by a spin-flop orientational phase transition on account of the formation and motion of specific domain walls as well as by incoherent rotation of the spins toward the applied field. It is shown that, depending on the direction of the external magnetic field with respect to the easy axis, asymmetric canted phases also arise as a result of such transitions.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-904X
    Keywords: block copolymer ; cancer ; multidrug resistance ; Pluronic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. Using monolayers of human pancreatic adenocarcinoma cells (Panc-1) that express multidrug resistance-associated protein (MRP), the present work investigates the effects of Pluronic block copolymers on the functional activity of MRP. Methods. The studies examined the accumulation and efflux of the MRP selective probe fluorescein (FLU) in Panc-1 cell monolayers with and without Pluronic P85 (P85), Pluronic L81 (L81) and Pluronic F108 (F108). Results. Treatment of Panc-1 cells with P85 resulted in concentration-dependent increases in FLU accumulation and elimination of FLU sequestration in vesicular compartments in these cells. The effects of P85 were selective for FLU in the Panc-1 cell monolayers. Inhibition of MRP-mediated transport was dependent on the composition of Pluronic block copolymer: the more hydrophobic copolymer had the greater effect on FLU uptake in Panc-1 monolayers (L81 〉 P85 〉 F108). Conclusions. This paper demonstrates for the first time that Pluronic block copolymers inhibit multidrug resistance-associated protein (MRP). The similarities in the effects of Pluronic block copolymers on MRP and P-glycoprotein drug efflux systems suggest that a single unifying mechanism may explain the inhibition observed.
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  • 3
    ISSN: 1573-904X
    Keywords: block copolymer ; intestinal delivery ; drug ; micelles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The present work characterizes the effects of Pluronic copolymers on the transport of a P-gp-dependent probe, rhodamine 123 (R123) in Caco-2 cell monolayers. Methods. The accumulation and efflux studies were performed on the confluent Caco-2 monolayers using fluorescent probes with and without Pluronic copolymers. Results. At concentrations below the critical micelle concentration single chains ("unimers”) of Pluronic P85 enhanced the accumulation and inhibited the efflux of R123 in Caco-2 monolayers. The transport of the P-gp-independent probe, rhodamine 110 was not altered under these conditions. In contrast the micelles increased R123 accumulation to a much lower extent when compared to the unimers and enhanced R123 efflux in Caco-2 monolayers. Conclusions. Pluronic P85 unimers increase accumulation of a P-gp-dependent drug in Caco-2 monolayers through inhibition of the P-gp efflux system. The mechanism of the micelle effect is not known, however, it is very similar to the micelle effects in BBMEC. This has been previously shown to involve vesicular transport of the micelle-incorporated drug. The study suggests that Pluronic copolymers can be useful in increasing oral absorption of select drugs.
    Type of Medium: Electronic Resource
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