Review of Curcumin and Its Different Formulations: Pharmacokinetics, Pharmacodynamics and Pharmacokinetic-Pharmacodynamic Interactions

Suchandra Goswami, Shivangi Saxena, Shalini Yadav, D. Goswami, K. Brahmachari, S. Karmakar, B. Pramanik, S. Brahmachari
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Abstract

Curcumin, the yellow principle of the Indian Turmeric, ‘Haldi’ has recently attracted renewed interest in the field of experimental medicine with pleiotropic activity. This review has emphasized three pharmaceutical studies of interest: the pharmacokinetics, pharmacology, and pharmacodynamics of curcumin. In this review, we attempted to review the general pharmacokinetics profile, pharmacokinetic interactions, and pharmacokinetic-pharmacodynamic interactions of curcumin and its formulations. Different species of turmeric in India, as well as their cultivars, different forms of curcumin, and harvesting methods have also been discussed. Furthermore, pharmacokinetic studies of the interaction of curcumin and its different formulations with efflux transporters such as P-glycoprotein, ABC-transporter protein, multidrug-resistant protein, and cytochrome p450 metabolism enzymes have been broadly explained following data from preclinical and clinical trials reported in the literature. A few interesting chemical interactions between curcumin and its metabolites with the receptor have also been described. The pharmacological activities of curcumin and its related formulations and products have been reviewed in a few targeted disease pathologies of national concern, such as cancer, gastroduodenal disorder, immunodeficiency, liver disease, ophthalmology, diabetes and osteoarthritis among other metabolic diseases, and microbial and viral infections. The pharmacodynamics of curcumin, especially regarding the potassium/calcium ion channel pathway, apoptosis, calcium signaling pathway, endoplasmic reticulum stress, and other intracellular signaling pathways, have been documented. Lastly, the use of curcumin as a cosmetic and the value chain analysis of turmeric products, as well as curcumin, have also been placed appropriately. A total of 174 publications were reviewed and, overall, this review tried to cover various important therapeutic aspects of curcumin, which can generate new research interest in general.
姜黄素及其不同制剂:药动学、药效学和药动学-药效学相互作用
姜黄素是印度姜黄的黄色成分,“Haldi”最近在具有多效性活性的实验医学领域重新引起了人们的兴趣。这篇综述强调了三项感兴趣的药物研究:姜黄素的药代动力学、药理学和药效学。在这篇综述中,我们试图综述姜黄素及其制剂的一般药代动力学概况、药代动力学相互作用和药代动力学-药效学相互作用。还讨论了印度不同种类的姜黄及其品种、不同形式的姜黄素和收获方法。此外,根据文献中报道的临床前和临床试验数据,对姜黄素及其不同制剂与外排转运蛋白(如P-糖蛋白、ABC转运蛋白、耐多药蛋白和细胞色素p450代谢酶)相互作用的药代动力学研究进行了广泛解释。姜黄素及其代谢产物与受体之间的一些有趣的化学相互作用也已被描述。姜黄素及其相关制剂和产品的药理活性已在一些全国关注的靶向疾病病理学中进行了综述,如癌症、胃十二指肠疾病、免疫缺陷、肝病、眼科、糖尿病和骨关节炎等代谢疾病,以及微生物和病毒感染。姜黄素的药效学,特别是关于钾/钙离子通道通路、细胞凋亡、钙信号通路、内质网应激和其他细胞内信号通路,已经有文献记载。最后,姜黄素作为化妆品的使用以及姜黄产品和姜黄素的价值链分析也得到了适当的重视。共对174篇出版物进行了综述,总的来说,这篇综述试图涵盖姜黄素的各种重要治疗方面,这可能会引起新的研究兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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