Biopharmaceutical Factors Involved in the Disposition of Mycophenolic Acid: A Comprehensive Review of ADME Properties and Their Potential Impact on Mycophenolic Acid Plasma Exposure.

IF 1.8 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Eric Asare, Ting Du, Huan Xie, Dong Liang, Song Gao
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引用次数: 0

Abstract

Mycophenolic acid (MPA) is an approved drug widely used as an immunosuppressant agent for the prevention of rejection in organ transplant patients and for managing various autoimmune disorders. Pharma-cological studies have shown that the plasma exposure of MPA is critical to to maintaining its efficacy, leading to a significant focus on MPA therapeutic drug monitoring (TDM) in clinical practice. Additionally, many papers have been published regarding MPA's absorption, distribution, metabolism, and elimination (ADME) characteristics, which are the key disposition factors affecting the plasma exposure of MPA. In this paper, we synthesize the current data and information in the literature on the ADME properties of MPA and discuss their implications for MPA's TDM. We also analyze the disposition of MPA major metabolites mycophenolic acid-glucuronide (MPAG), and acyl-glucuronide (AcMPAG), highlighting the key factors that affect MPA plasma exposure, including the influence of transporters, namely Multidrug Resistance-Associated Protein 2 (MRP2), Breast Cancer Resistance Protein (BCRP), Organic Anion-Transporting Polypeptides (OATPs), metabolic en-zymes (i.e., UDP-Glucuronosyltransferases (UGTs)), enterohepatic recycling (EHR), and protein binding. We expect to provide researchers with a comprehensive understanding of factors that could affect MPA's TDM to ensure its efficacy.

参与霉酚酸处置的生物制药因素:ADME特性及其对霉酚酸血浆暴露的潜在影响的综合综述。
霉酚酸(MPA)是一种被批准的药物,广泛用作免疫抑制剂,用于预防器官移植患者的排斥反应和治疗各种自身免疫性疾病。药理学研究表明,MPA的血浆暴露对维持其疗效至关重要,因此在临床实践中对MPA治疗药物监测(TDM)的关注非常重要。此外,关于MPA的吸收、分布、代谢和消除(ADME)特性的研究也较多,这些特性是影响MPA血浆暴露的关键处置因素。在本文中,我们综合了目前关于MPA的ADME特性的数据和文献信息,并讨论了它们对MPA的TDM的影响。我们还分析了MPA主要代谢物霉酚酸-葡萄糖醛酸(MPAG)和酰基-葡萄糖醛酸(AcMPAG)的分布,强调了影响MPA血浆暴露的关键因素,包括转运体的影响,即多药耐药相关蛋白2 (MRP2)、乳腺癌耐药蛋白(BCRP)、有机阴离子转运多肽(OATPs)、代谢酶(即udp -葡萄糖醛酸基转移酶(UGTs))、肠肝再循环(EHR)和蛋白质结合。我们希望为研究者提供对影响MPA TDM的因素的全面了解,以确保其疗效。
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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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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