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The solubilisation of some hydrophobic drugs using tapered statistical block copolymers

机译:使用锥形统计嵌段共聚物增溶某些疏水性药物

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The ability of poly(oxyalkylene) (POA) block copolymers to form micelles at low concentration has led to these structures being studied for their potential as carriers for novel and existing drugs~1. The amphiphilic nature of POA copolymers also allows them to circulate in the body for extended periods as a result of their avoidance of the reticuloendothelial system (RES)~2. POA copolymers also have potential in the solubilisation of hydrophobic drug substances and have been investigated for use in drug delivery forms~3. However, traditional diblock and triblock POA copolymer micelles have been found to be relatively poor solubilisers, a characteristic which has been attributed to the location of solubilised drugs at the hydrophobic/hydrophilic interface~4, and to their small size.
机译:聚(氧化烯)(POA)嵌段共聚物在低浓度下形成胶束的能力已导致对这些结构作为新型药物和现有药物的载体的潜力进行了研究[1]。由于避免了网状内皮系统(RES)〜2,POA共聚物的两亲性质也使它们可以在体内长时间循环。 POA共聚物在疏水性药物物质的增溶方面也具有潜力,并且已被研究用于药物递送形式[3]。然而,已经发现传统的二嵌段和三嵌段POA共聚物胶束是相对较差的增溶剂,该特征归因于增溶的药物在疏水/亲水界面处的位置〜4,以及它们的小尺寸。

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