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Block Copolymers of Polyacrilamide and Poly(ethylene oxide) as Nanocarriers for Drug Delivery: Micellization and Bulk Structure

机译:聚丙酰胺和聚(环氧乙烷)的嵌段共聚物作为用于药物递送的纳米载体:胶束化和散装结构

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The self-assembly of diblock copolymers series (DBC) of polyacrylamide and methoxypoly(ethylen oxide) (MOPEO-b-PAAm) with a variable length of both the blocks were studied in water and water-ethanol solutions. The tendency of DBCs to micellization in water-ethanol mixture grew with increased molecular weights of the blocks. The addition of NaCl resulted in increase of micellar stability, while the introduction of dimethylformamide (DMF) destructed DBC micelles. In DBC bulk structure, MOPEO blocks either lost or considerably reduced their ability of crystallization due to interaction with PAAm blocks. DBC micelles encapsulated anticancer drug doxorubicin (DOX) that led to lowering the crytical micellization concentration.
机译:在水和水 - 乙醇溶液中研究了聚丙烯酰胺和甲氧基聚酯系列(甲氧基)和甲氧基聚合物(乙烯氧化物)(MOPEO-B-PAAM)的自组装,其具有可变长度的嵌段和水 - 乙醇溶液。 DBC在水 - 乙醇混合物中胶丝化的趋势随着嵌段的分子量增加而增长。添加NaCl导致胶束稳定性的增加,同时引入二甲基甲酰胺(DMF)破坏的DBC胶束。在DBC散装结构中,由于与PAAM块的相互作用,MOPEO块丢失或显着降低其结晶能力。 DBC胶束包封抗癌药物多柔比星(DOX),导致降低丧耳胶束化浓度。

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