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聚氧乙烯蓖麻油:药物制剂载体选择的优缺点

Cremophor EL: the drawbacks and advantages of vehicle selection for drug formulation.

作者信息

Gelderblom H, Verweij J, Nooter K, Sparreboom A

机构信息

Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek), The Netherlands.

出版信息

Eur J Cancer. 2001 Sep;37(13):1590-8. doi: 10.1016/s0959-8049(01)00171-x.

DOI:10.1016/s0959-8049(01)00171-x
PMID:11527683
Abstract

Cremophor EL (CrEL) is a formulation vehicle used for various poorly-water soluble drugs, including the anticancer agent paclitaxel (Taxol). In contrast to earlier reports, CrEL is not an inert vehicle, but exerts a range of biological effects, some of which have important clinical implications. Its use has been associated with severe anaphylactoid hypersensitivity reactions, hyperlipidaemia, abnormal lipoprotein patterns, aggregation of erythrocytes and peripheral neuropathy. The pharmacokinetic behaviour of CrEL is dose-independent, although its clearance is highly influenced by duration of the infusion. This is particularly important since CrEL can affect the disposition of various drugs by changing the unbound drug concentration through micellar encapsulation. In addition, it has been shown that CrEL, as an integral component of paclitaxel chemotherapy, modifies the toxicity profile of certain anticancer agents given concomitantly, by mechanisms other than kinetic interference. A clear understanding of the biological and pharmacological role of CrEL is essential to help oncologists avoid side-effects associated with the use of paclitaxel or other agents using this vehicle. With the present development of various new anticancer agents, it is recommended that alternative formulation approaches should be pursued to allow a better control of the toxicity of the treatment and the pharmacological interactions related to the use of CrEL.

摘要

聚氧乙烯蓖麻油(CrEL)是一种用于多种水溶性差的药物的制剂载体,包括抗癌药物紫杉醇(泰素)。与早期报道不同,CrEL不是一种惰性载体,而是具有一系列生物学效应,其中一些具有重要的临床意义。其使用与严重的类过敏超敏反应、高脂血症、异常脂蛋白模式、红细胞聚集和周围神经病变有关。CrEL的药代动力学行为与剂量无关,尽管其清除率受输注持续时间的影响很大。这一点尤为重要,因为CrEL可以通过胶束包封改变游离药物浓度,从而影响各种药物的处置。此外,研究表明,作为紫杉醇化疗的一个组成部分,CrEL通过动力学干扰以外的机制改变了某些同时给予的抗癌药物的毒性特征。清楚了解CrEL的生物学和药理学作用对于帮助帮助肿瘤学家避免与使用紫杉醇或其他使用该载体的药物相关的副作用至关重要。随着目前各种新型抗癌药物的开发,建议采用替代制剂方法,以便更好地控制治疗毒性以及与使用CrEL相关的药理相互作用。

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Cremophor EL: the drawbacks and advantages of vehicle selection for drug formulation.聚氧乙烯蓖麻油:药物制剂载体选择的优缺点
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