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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 13 (1996), S. 1554-1558 
    ISSN: 1573-904X
    Keywords: rat intestinal permeability ; hydrophilic probe molecules ; probe geometry ; bile salt: fatty acid micelles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The relationship between rat intestinal permeability (Papp) of a range of hydrophilic probe molecules and probe geometry was examined. Methods. Molecules studied included mannitol, the polyethylene glycols (PEGs) 400, 900, and 4000, the dextran conjugated dye Texas Red® (MW 3000) and the polysaccharide inulin (MW 5500). Molecular surface area, volume and cross-sectional diameter for each probe were determined from computer models. The effect of the bile salt sodium cholate, and bile salt: fatty acid mixed micelles on probe intestinal permeability was also studied. Results. Of the size parameters tested, cross-sectional diameter correlated best with log intestinal permeability. The data was fitted to a relationship of the form Papp = P0 app exp(−Krca) where rca is the molecular cross sectional radius, P0 app and K are constants. Estimates of equivalent pore radii (R) were also made; the use of rca giving the most reasonable estimate of R. Absorption of all probes was enhanced by both simple and mixed micellar systems. Conclusions. For large hydrophilic probes, and possibly protein drugs, cross sectional diameter is a more important size parameter than volume based values for evaluating size-related retarded absorption. The relationship established may be used as a tool to assess absorption enhancement potential of excipients.
    Type of Medium: Electronic Resource
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