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紫杉醇及相关紫杉烷类化合物的生物技术生产:现状与展望

Biotechnological production of taxol and related taxoids: current state and prospects.

作者信息

Expósito O, Bonfill M, Moyano E, Onrubia M, Mirjalili M H, Cusidó R M, Palazón J

机构信息

Secció de Fisiologia Vegetal, Facultat de Farmacia, Universitat de Barcelona, Avda. Diagonal 643, E-08028 Barcelona, Spain.

出版信息

Anticancer Agents Med Chem. 2009 Jan;9(1):109-21. doi: 10.2174/187152009787047761.

Abstract

Taxol is one of the most effective anti-cancer drugs ever developed. The natural source of taxol is the inner bark of several Taxus species, but it accumulates at a very low concentration and with a prohibitively high cost of extraction. Another problem is that the use of inner bark for taxol production implies the destruction of yew trees. For all these reasons, the growing demand for taxol greatly exceeds the supply that can be sustained by isolation from its natural source and alternative sources of the drug are being sought. Although taxol has been prepared by total synthesis, the process is not commercially viable. Taxol can also be semisynthetically produced via the conversion of baccatin III or 10-deacethylbaccatinIII found in Taxus needles but the cost and difficulty of the extraction process of the semisynthetic precursors are also very high. The most promising approach for the sustainable production of taxol and related taxoids is provided by plant cell cultures at an industrial level. Taxol is currently being clinically used against different tumour processes but due to the difficulty of its extraction and formulation, as well as the growing demand for the compound, new taxol analogues with improved properties are being studied. In this revision we discuss current research in the design of new taxol-related compounds, the chemical structure/anti-cancer activity relationship and new formulations of the drug. We also consider the optimizing strategies to improve taxol and related taxoid production in cell cultures, as well as the current knowledge of taxol metabolism, all of which are illustrated with examples, some of them from our own research.

摘要

紫杉醇是有史以来开发出的最有效的抗癌药物之一。紫杉醇的天然来源是几种红豆杉属植物的内皮,但它的积累浓度非常低,且提取成本高得令人望而却步。另一个问题是,使用内皮生产紫杉醇意味着红豆杉树会遭到破坏。由于所有这些原因,对紫杉醇不断增长的需求大大超过了从其天然来源分离所能维持的供应,因此正在寻找该药物的替代来源。尽管紫杉醇已通过全合成制备,但该过程在商业上不可行。紫杉醇也可以通过转化红豆杉针叶中发现的巴卡亭III或10-去乙酰巴卡亭III进行半合成生产,但半合成前体的提取过程成本和难度也非常高。在工业水平上,植物细胞培养为紫杉醇及相关紫杉烷类化合物的可持续生产提供了最有前景的方法。紫杉醇目前正在临床上用于对抗不同的肿瘤过程,但由于其提取和制剂的难度,以及对该化合物不断增长的需求,正在研究具有改进特性的新紫杉醇类似物。在本综述中,我们讨论了当前在设计新的紫杉醇相关化合物、化学结构/抗癌活性关系以及该药物新制剂方面的研究。我们还考虑了优化细胞培养中紫杉醇及相关紫杉烷类化合物生产的策略,以及当前对紫杉醇代谢的认识,所有这些都通过实例进行说明,其中一些实例来自我们自己的研究。

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