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脂质体紫杉醇制剂。

Liposomal paclitaxel formulations.

机构信息

Department of Toxicology, Pharmacology and Immunotherapy, Veterinary Research Institute, Brno, Czech Republic.

出版信息

J Control Release. 2012 Nov 10;163(3):322-34. doi: 10.1016/j.jconrel.2012.09.006. Epub 2012 Sep 15.

Abstract

Over the past three decades, taxanes represent one of the most important new classes of drugs approved in oncology. Paclitaxel (PTX), the prototype of this class, is an anti-cancer drug approved for the treatment of breast and ovarian cancer. However, notwithstanding a suitable premedication, present-day chemotherapy employing a commercial preparation of PTX (Taxol®) is associated with serious side effects and hypersensitivity reactions. Liposomes represent advanced and versatile delivery systems for drugs. Generally, both in vivo mice tumor models and human clinical trials demonstrated that liposomal PTX formulations significantly increase a maximum tolerated dose (MTD) of PTX which outperform that for Taxol®. Liposomal PTX formulations are in various stages of clinical trials. LEP-ETU (NeoPharm) and EndoTAG®-1 (Medigene) have reached the phase II of the clinical trials; Lipusu® (Luye Pharma Group) has already been commercialized. Present achievements in the preparation of various liposomal formulations of PTX, the development of targeted liposomal PTX systems and the progress in clinical testing of liposomal PTX are discussed in this review summarizing about 30 years of liposomal PTX development.

摘要

在过去的三十年中,紫杉烷类药物是肿瘤学领域批准的最重要的新药类别之一。紫杉醇(PTX)是该类药物的原型,是一种批准用于治疗乳腺癌和卵巢癌的抗癌药物。然而,尽管进行了适当的预处理,但目前使用紫杉醇商业制剂(Taxol®)进行的化疗与严重的副作用和过敏反应有关。脂质体是药物的先进且多功能的递药系统。一般来说,体内小鼠肿瘤模型和人体临床试验都表明,脂质体 PTX 制剂显著增加了 PTX 的最大耐受剂量(MTD),其效果优于 Taxol®。脂质体 PTX 制剂处于不同的临床试验阶段。LEP-ETU(NeoPharm)和 EndoTAG®-1(Medigene)已进入临床试验的第二阶段;Lipusu®(Luye Pharma Group)已经商业化。本文综述了近 30 年来脂质体 PTX 的制备、靶向脂质体 PTX 系统的发展以及脂质体 PTX 临床测试的进展,讨论了各种脂质体 PTX 制剂的制备、靶向脂质体 PTX 系统的发展以及脂质体 PTX 临床测试的进展。

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