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Viscosity of heparin as a function of dielectric constant and of desulfation

✍ Scribed by L. Yuan; S. S. Stivala


Publisher
Wiley (John Wiley & Sons)
Year
1972
Tongue
English
Weight
645 KB
Volume
11
Category
Article
ISSN
0006-3525

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✦ Synopsis


Abstract

The effect of dielectric constant (D) of the solvent on the viscosity of heparin was examined using the relation \documentclass{article}\pagestyle{empty}\begin{document}$ \eta _{{\rm sp}} /c = [\eta ]_\infty (1 + k/\sqrt c) $\end{document}, where [Ξ·]~∞~ is the shielded intrinsic viscosity obtained by extrapolating \documentclass{article}\pagestyle{empty}\begin{document}$ \eta _{{\rm sp}} /c,{\rm vs}{\rm . },1/\sqrt c ) $\end{document} to infinite concentration, and k is an interaction parameter independent of the dielectric constant of the solvent. This equation was previously reported by the authors^9^ for describing the reduced viscosities of strong polyelectrolytes in salt‐free polar solvents. It was found that the [Ξ·]~∞~ of heparin increases linearly with increasing dielectric constant of the solvent whereas the k values were, within experimental error, independent of D in the range 54.7 < D < 93.2 examined. Graded hydrolysis of heparin from its acid form (heparinic acid) at 57Β°C resulted in samples of varying degree of desulfation with corresponding decrease in biological activity. It was found that both [Ξ·]~∞~ and k decrease with increasing desulfation.


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Self-Diffusion and Viscosity of Some Liquids as a Function of Temperature Self-diffusion coefficients of 15 liquids have been measured as a function of temperature between their melting and boiling points. The systems investigated were the benzenes, CBH5X where X = H, F, C1, Br, and I, n-paraffins,