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  • 1
    Electronic Resource
    Electronic Resource
    Curves of osmotic fragility calculated from the isotonic areas and volumes of individual human erythrocytesThis investigation was supported by a grant from the Life Insurance Medical Research Fund. (1969)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 74 (1969), S. 203-211 
    Details
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Theoretical osmotic fragility curves were calculated and drawn by computer using the van't Hoff equation and the isotonic areas and volumes of 1000 individual erythrocytes. We studied the influence on the calculated curves of theoretically altering the fraction of the volume which was osmotically active from 50 to 70%, and of altering the permissible stretch before hemolysis from zero to 10%. With the two assumptions-that the membrane does not stretch before hemolysis, and that the osmotically active fraction of the cell volume is 0.58-it was possible to duplicate the general shape of the standard fragility curve; the exact NaCl concentration, however, at which there was 50% hemolysis was approximately 0.1 gm/100 ml higher than found in vitro. The calculated osmotic fragility curves can be made quantitatively similar to in vitro ones if the following statements are true: the osmotically active volume is 58%, the permissible stretch of the membrane without lysis is 6%, the cell membrane resists a slight osmotic pressure gradient of approximately 0.1 atmospheres, and hemolysis is an all or nothing phenomenon. This set of values for the relevant factors is sufficient but not unique in causing the superposition of the calculated and experimental curves. The frequency distribution of the cells according to the hemolytic salt concentrations (the sodium chloride concentration at which an individual cell just hemolyzes) was skewed positively and was leptokurtic for each of the seven normal subjects studied.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jcp.1040740212
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  • 2
    Electronic Resource
    Electronic Resource
    Sedimentation of single human red blood cells. Differences between normal and glutaraldehyde fixed cellsResearch supported by The Medical Research Council of Canada and The Alberta Heart Foundation. (1972)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 80 (1972), S. 367-372 
    Details
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The sedimentation behaviour of single human red blood cells fixed with glutaraldehyde at pH 7.4 and 6.4 was studied and compared to resiflts previously reported for normal fresh cells. The cells fixed at pH 7.4 were observed to have normal shapes while those fixed at pH 6.4 were more spherical and less disc-like. Fixation of glutaraldehyde removed “membrane flicker,” resulting in increased stability as indicated by a decrease in the number of orientation changes per minute from 2.93 ± 0.16 (SEM) to 1.74 ± 0.10 (SEM). An orientation change was defined as a change of 45° in any direction. Fixation also increased the edge-to-flat time preference ratio from 2.5 to 4.7, and increased the sedimentation velocities in all three orientations, despite a measured 2.5% decrease in mean cell density.Fixation of cells at pH 6.4 showed that the decrease in stability and preference for the on-edge orientation was associated with an increase in the sphericity of the cell.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jcp.1040800307
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  • 3
    Electronic Resource
    Electronic Resource
    The rate of sedimentation of individual human red blood cellsThis investigation was supported by a grant from the Medical Research Council of Canada. (1971)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 78 (1971), S. 319-331 
    Details
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The sedimentation of individual cells was investigated in the context of the Stokes' equation for sedimenting spheres. Blood obtained from a finger prick was diluted 104 times by volume in Tris buffered Ringer solution (pH 7.4, 310 milliosmolar). A small sample of the suspension was put in a plastic, flat bottomed depression slide which was then closed with a coverslip. Thirty-six runs were done in which a cell was kept in focus on an inverted microscope. The 250 μm descent was monitored on a two channel chart recorder. The orientation, determined by the observer as edge, oblique, or flat, and the verticle displacement, indicated by a ten turn potentiometer connected to the fine focussing knob, were recorded simultaneously. The cells studied indicated that cells are more frequently in the edge-on orientation, that larger cells sediment faster than smaller cells despite the lower density for larger cells, and that cells wobble considerably. The biconcave cells made approximately three orientation changes per minute where one change in orientation was considered to be a rotation of 45° in any direction. Brownian motion is thought to be responsible for the wobble, or random rotations of the sedimenting cell. The edge-to-flat velocity ratio was 1.38 ± 0.30 S.D. which is significantly less than 1.5, the theoretical and experimental value for thin discs. There was a moderate dependence of sedimentation velocity on the square of the diameter (R = +0.5) in accordance with Stokes' Law. The variance in this relation can be accounted for by the known variation of cellular density within a normal population of red cells, and by the inherent errors of measurement.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jcp.1040780302
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  • 4
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    The CAESAR New Frontiers Mission: 1. Expected Nature of the Returned Comet Sample (2019)
    In:  CASI
    Details
    Publication Date: 2019-07-20
    Description: Comets are time capsules from the birth of our Solar System that record pre-solar history, the initial stages of planet formation, and the sources of prebiotic organics and volatiles for the origin of life. These capsules can only be opened in laboratories on Earth. CAESAR (Comet Astrobiology Exploration Sample Return)s sample analysis objectives are to understand the nature of Solar System starting materials and how these components came together to form planets and give rise to life. Examination of these comet nucleus surface samples in laboratories around the world will also provide ground truth to remote observations of the innumerable icy bodies of the Solar System.
    Keywords: Lunar and Planetary Science and Exploration
    Type: JSC-E-DAA-TN64974 , Lunar and Planetary Science Conference (LPSC 2019); 18ý22 Mar. 2019; The Woodlands, Texas; United States
    Format: application/pdf
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  • 5
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    Aseptic Operations for Post DHMR Processing of MOMA Mass Spectrometer (2018)
    In:  CASI
    Details
    Publication Date: 2019-07-13
    Description: Mars Organic Molecule Analyzer - Mass Spectrometer (MOMA-MS) is an instrument in the MOMA instrument suite for the European Space Agency (ESA) ExoMars 2020 Rover. The rover is Planetary Protection Mission Category IVb, the first IVb mission since the Viking missions in the 1970s. Within the sample path of the MOMA instrument suite, the hardware surfaces of the must be sanitized to a level of less than 0.03 spore/m sq. To meet this requirement, the MS sample path was subjected to Dry Heat Microbial Reduction (DHMR) to decrease the number of viable spores by 4 orders of magnitude from a measured 88 spores/m sq to 0.009 spores/m sq. Before DHMR, the hardware is handled using standard cleanroom practices. After DHMR, planetary protection filters protect the sample path for most of integration, but when sample path exposure is required, aseptic operations are instituted and exposure times are kept to an absolute minimum. The surface area of exposure is also taken into account to determine safe exposure times. Before work begins, the ISO class 5 aseptic workspace is cleaned and tested for surface and airborne bioburden, and all tools that will contact or be used near sample path surfaces are sterilized. During the exposure activity, sterile garments are worn, sterile gloves are changed as often as necessary, and the environment is monitored with active and passive fallout for bioburden and real time airborne particle counts. Sterile tools are handled by a two person team so that the operator touches only the tool and not the exterior surfaces of the sterilization pouch, and a sterile operating field is established as a safe place to organize tools or parts during the aseptic operations. In cases where aseptic operations are not feasible, localized DHMR is used after exposure. Any breach in the planetary protection cleanliness can necessitate repeating instrument level DHMR, which not only has significant cost and schedule implications, it also become a risk to hardware that is not rated for repeated long exposures to high temperatures.
    Keywords: Lunar and Planetary Science and Exploration
    Type: GSFC-E-DAA-TN58788 , COSPAR 2018; Jul 14, 2018 - Jul 22, 2018; Pasadena, CA; United States
    Format: application/pdf
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  • 6
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    Development and Implementation of Aseptic Operations for the MOMA-Mass Spectrometer (2018)
    In:  CASI
    Details
    Publication Date: 2019-07-13
    Description: The ExoMars 2020 Rover is a life detection mission, and is classified as Planetary Protection (PP) Mission Category IVb, the first IVb mission since the Viking missions. Mars Organic Molecule Analyzer Mass Spectrometer (MOMA-MS) is a life detection instrument for the rover. To meet the stringent bioburden requirement of 0.03 spore/m2, the MS is subjected to Dry Heat Microbial Reduction (DHMR) to decrease the bioburden from a measured 88 spores/m2 to 0.009 spores/m2. After DHMR, exposure of the sample path must be kept to an absolute minimum and requires aseptic operations. Aseptic operations include determining the safe exposure time based on the surface area of exposure and particle fallout expected in the aseptic ISO class 5 workspace, preparing an aseptic ISO class 5 workspace, and using sterile garments and tools. During the exposure activity the environment is monitored with active and passive fallout for bioburden and real time airborne particle counts. Sterile tools are handled by a two person team so the operator touches only the tool and not the exterior surfaces of the sterilization pouch, and a sterile operating field is established as a safe place to organize tools or parts during the aseptic operations. In cases where aseptic operations are not feasible, localized DHMR is used after exposure. Any breach in the PP cleanliness can necessitate repeating instrument level DHMR, which not only has significant cost and schedule implications, but also is a risk to hardware that is not rated for repeated long exposures to high temperatures.
    Keywords: Lunar and Planetary Science and Exploration
    Type: GSFC-E-DAA-TN60188 , SPIE Optics + Photonics 2018; Aug 19, 2018 - Aug 23, 2018; San Diego, CA; United States
    Format: application/pdf
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