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Pharmacokinetics, Efficacy, and Safety Evaluation of Docetaxel/Hydroxypropyl-Sulfobutyl-β-Cyclodextrin Inclusion Complex

机译:多西他赛/羟丙基-磺丁基-β-环糊精包合物的药代动力学,功效和安全性评价

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摘要

Hydroxypropyl-sulfobutyl-β-cyclodextrin (HP-SBE-β-CD) inclusion complex was developed and used as a drug delivery system for DTX (DTX/HP-SBE-β-CD). The objective of the present study was to evaluate and compare the biological properties of DTX/HP-SBE-Β-CD with Taxotere®. The pharmacokinetics, biodistribution, antitumor efficacy in vivo and in vitro, and safety evaluation of DTX/HP-SBE-β-CD were studied. The most significant finding was that it was possible to prepare a Polysorbate-80-free inclusion complex for DTX. Studies based on pharmacokinetics, biodistribution, and antitumor efficacy indicated that DTX/HP-SBE-β-CD had similar pharmacokinetic properties and antitumor efficacy both in vitro and in vivo as Taxotere®. Fortunately, this new drug delivery system attenuated the side effects when used in vivo. As a consequence, DTX/HP-SBE-β-CD may be a promising alternative to Taxotere® for cancer chemotherapy treatment with reduced side effects. The therapeutic potential against a variety of human tumors and low toxicity demonstrated in a stringent study clearly warrant clinical investigation of DTX/HP-SBE-β-CD for possible use against human tumors.
机译:开发了羟丙基-磺丁基-β-环糊精(HP-SBE-β-CD)包合物,并将其用作DTX(DTX /HP-SBE-β-CD)的药物递送系统。本研究的目的是评估和比较DTX / HP-SBE-CD-CD与Taxotere®的生物学特性。研究了DTX /HP-SBE-β-CD的体内,体外药代动力学,生物分布,抗肿瘤效果以及安全性评价。最重要的发现是可以为DTX制备不含聚山梨酯80的包合物。基于药代动力学,生物分布和抗肿瘤功效的研究表明,DTX /HP-SBE-β-CD在体外和体内均具有与Taxotere®类似的药代动力学性质和抗肿瘤功效。幸运的是,这种新的药物递送系统在体内使用时可减轻副作用。因此,DTX /HP-SBE-β-CD可能是Taxotere®的有希望的替代品,可减少副作用,用于癌症化疗。一项严格的研究表明,针对多种人类肿瘤的治疗潜力和低毒性,显然需要对DTX /HP-SBE-β-CD进行临床研究,以可能用于对抗人类肿瘤。

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