Synthesis and anchoring of antineoplastic ferrocene and phthalocyanine derivatives on water-soluble polymeric drug carriers derived from lysine and aspartic Acid.

M David Maree, Eberhard W Neuse, Elizabeth Erasmus, Jannie C Swarts
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引用次数: 9

Abstract

The general synthetic strategy towards water-soluble biodegradable drug carriers and the properties that they must have are discussed. The syntheses of water-soluble biodegradable copolymers of lysine and aspartic acid as potential drug-delivering devices, having amine-functionalised side chains are then described. Covalent anchoring of carboxylic acid derivatives of the antineoplastic ferrocene and photodynamically active phthalocyanine moieties to the amine-containing drug carrier copolymers under mild coupling conditions has been achieved utilising the coupling reagent O-benzotriazolyl-N,N,N('),N(')-tetramethyluronium hexafluorophosphate to promote formation of the biodegradable amide bond. Even though the parent antineoplastic ferrocene and phthalocyanine derivatives are themselves insoluble in water at pH < 7, the new carrier-drug conjugates that were obtained are well water-soluble.

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赖氨酸和天冬氨酸水溶性高分子药物载体上抗肿瘤二茂铁和酞菁衍生物的合成和锚定。
讨论了水溶性生物可降解药物载体的一般合成策略及其必须具备的性能。水溶性可生物降解的赖氨酸和天冬氨酸共聚物的合成作为潜在的药物传递装置,具有胺功能化的侧链,然后描述。利用偶联剂o -苯并三唑-N,N,N('),N(')-六氟磷酸四甲基脲铵,在温和偶联条件下实现了抗肿瘤二茂铁的羧酸衍生物和光动力活性酞菁部分与含胺药物载体共聚物的共价锚定,以促进生物可降解酰胺键的形成。尽管母体抗肿瘤二茂铁和酞菁衍生物本身在pH < 7时不溶于水,但获得的新的载体-药物偶联物具有良好的水溶性。
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