Synthesis and in vitro drug release studies on substituted polyphosphazene conjugates of lumefantrine.

Sahil Kumar, Alka Sharma, R. Singh, D. Prasad, T. Bhardwaj
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引用次数: 1

Abstract

The present study pertains to the delivery of antimalarial drug (Lumifantrine). In this, polyphosphazene has been used in the synthesis of polyphosphazene-linked conjugates of Lumifantrine. These polymer-linked Conjugates have been synthesized and characterized by modern analytical techniques. The in-vitro drug release of Lumifantrine drug conjugates: p -Amino benzoic acid ester substituted polyphosphazene drug conjugate (15) and Glycine methyl ester substituted polyphosphazene drug conjugate (21) have been found to be 6.00 % and 5.96% (pH 1.2), 88.52% and 79.86% (pH 7.4), respectively. These drug conjugate may prove an effective delivery system for the treatment of malaria.
甲基苯胺取代聚磷腈缀合物的合成及体外释药研究。
本研究涉及抗疟疾药物(鲁米曲明)的给药。在本研究中,聚磷腈被用于合成聚磷腈连接的鲁米芬汀缀合物。这些聚合物连接的共轭物已经被合成并通过现代分析技术进行了表征。对氨基苯甲酸酯取代聚磷腈药物偶联物(15)和甘氨酸甲酯取代聚磷腈药物偶联物(21)的体外释放度分别为6.00%和5.96% (pH值1.2)、88.52%和79.86% (pH值7.4)。这些药物偶联物可能被证明是治疗疟疾的有效给药系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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