首页> 外文期刊>Drug delivery. >Development of a docetaxel micellar formulation using poly(ethylene glycol)–polylactide–poly(ethylene glycol) (PEG–PLA–PEG) with successful reconstitution for tumor targeted drug delivery
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Development of a docetaxel micellar formulation using poly(ethylene glycol)–polylactide–poly(ethylene glycol) (PEG–PLA–PEG) with successful reconstitution for tumor targeted drug delivery

机译:使用聚(乙二醇)-聚丙交酯-聚(乙二醇)(PEG-PLA-PEG)成功开发出多西他赛胶束制剂,以成功地将其靶向肿瘤

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Abstract Docetaxel (DTX)-loaded polymeric micelles (DTBM) were formulated using the triblock copolymer, poly(ethylene glycol)–polylactide–poly(ethylene glycol) (PEG–PLA–PEG), to comprehensively study their pharmaceutical application as anticancer nanomedicine. DTBM showed a stable formulation of anticancer nanomedicine that could be reconstituted after lyophilization (DTBM-R) in the presence of PEG 2000 and D-mannitol (Man) as surfactant and protectant, respectively. DTBM-R showed a particle size less than 150?nm and greater than 90% of DTX recovery after reconstitution. The robustly formed micelles might minimize systemic toxicity due to their sustained drug release and also maximize antitumor efficacy through increased accumulation and release of DTX from the micelles. From the pharmaceutical development point of view, DTBM-R showing successful reconstitution could be considered as a potent nanomedicine for tumor treatment.
机译:摘要采用三嵌段共聚物聚乙二醇-聚丙交酯-聚乙二醇(PEG-PLA-PEG)配制载有多西他赛(DTX)的聚合物胶束(DTBM),以全面研究其在抗癌纳米药物中的应用。 DTBM显示了一种稳定的抗癌纳米药物制剂,可以在冻干(DTBM-R)后分别在PEG 2000和D-甘露醇(Man)作为表面活性剂和保护剂的情况下进行重构。重构后,DTBM-R的粒径小于150nm,DTX回收率大于90%。牢固形成的胶束可能会由于其持续释放药物而使全身毒性最小化,并且还会通过增加DTX从胶束的积累和释放来最大化抗肿瘤功效。从药物开发的角度来看,显示成功重构的DTBM-R可以被认为是治疗肿瘤的有效纳米药物。

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