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Complex Formation of Cyclodextrins with Sulfasalazine in Buffer Solutions

机译:复合形成环糊精与磺基碱在缓冲溶液中

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摘要

Complex formation of alpha-, beta-, and gamma-cyclodextrins with sulfasalazine in biologically relevant buffer solutions (pH 1.2 and 7.4) was studied. Formation of inclusion complexes of 1 : 1 stoichiometry between the drug and cyclodextrins was revealed. The ionization state of sulfasalazine more strongly affects the complex formation than does the structure of cyclodextrins. Compared with a neutral molecule, sulfasalazine anionic species forms with cyclodextrins more stable complexes, which are essentially stabilized by possible surface interactions.
机译:研究了在生物学相关缓冲溶液(pH 1.2和7.4)中与磺基碱的α,β-和γ-环糊精的复杂形成。 揭示了药物和环糊精之间的1:1化学计量的包合物的形成。 磺基碱的电离状态更大地影响复杂的形成,而不是环糊精的结构。 与中性分子相比,磺基碱阴离子物质与环糊精形成更稳定的配合物,其基本上通过可能的表面相互作用稳定。

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