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姜黄素及其制剂:潜在的抗癌药物。

Curcumin and its formulations: potential anti-cancer agents.

机构信息

State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing, P. R.China.

出版信息

Anticancer Agents Med Chem. 2012 Mar;12(3):210-8. doi: 10.2174/187152012800228733.

Abstract

Curcumin, one of the most studied chemopreventive agents, is a natural compound extracted from Curcuma longa L. Extensive research over the last half century has revealed that curcumin can inhibit the proliferation of various tumor cells in culture, prevent carcinogen induced cancers in rodents and inhibit the growth of human tumors in xenotransplant or orthotransplant animal models. Several phase I and phase II clinical trials indicated that curcumin is quite safe and may exhibit therapeutic efficacy. The utility of curcumin is limited by its lack of water solubility and relatively low in vivo bioavailability. Multiple approaches including nanoparticles, liposomes, micelles and phospholipid complexes are being sought to overcome these limitations. This review describes the general properties of curcumin and its potential effect against cancer including evidences of its antitumor action in vitro, in vivo, clinically and the strategies to overcome its low bioavailability.

摘要

姜黄素是研究最多的化学预防剂之一,是从姜黄中提取的天然化合物。过去半个世纪的广泛研究表明,姜黄素可以抑制培养中的各种肿瘤细胞的增殖,预防致癌物诱导的啮齿动物癌症,并抑制异种移植或原位移植动物模型中人类肿瘤的生长。几项 I 期和 II 期临床试验表明,姜黄素相当安全,可能具有治疗效果。姜黄素的应用受到其缺乏水溶性和体内相对低生物利用度的限制。目前正在寻求多种方法,包括纳米粒子、脂质体、胶束和磷脂复合物,以克服这些限制。本综述描述了姜黄素的一般特性及其对癌症的潜在作用,包括其在体外、体内、临床抗肿瘤作用的证据以及克服其低生物利用度的策略。

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