唾液作为TDM矩阵及其在模型信息精确加药中的应用。

IF 2.3 4区 医学
Baohua Xu, Yujie Wen, Jinxia Lu, Maobai Liu, Xin Luo, Wei Huang, Helin Xie, Yu Cheng, Hongqiang Qiu, Xuemei Wu
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引用次数: 0

摘要

本文综述了唾液作为治疗药物监测(TDM)基质的主要观点、优点和局限性、唾液样本采集和检测方法、唾液TDM中药物的种类、唾液群体药代动力学(Pop PK)模型的建立方法,并总结了经验和局限性,为开展相关研究提供参考。我们系统地检索了PubMed数据库中关于唾液作为药物TDM基质的研究。按照建立的纳入和排除标准对文献进行筛选,提取并汇总相关资料。系统评价最终筛选了112篇文献,涉及73种药物的相关研究,其中53种药物的研究支持唾液作为TDM基质;对13种药物的研究不支持这一观点;七种药物的研究结果不一致,关于它们是否支持唾液TDM的结果相互矛盾。总结了基于唾液浓度的Pop PK建模的研究步骤,并列出了已建立血浆和唾液浓度混合的Pop PK模型的代表性药物。唾液TDM作为一种新的探索和尝试,在目前的研究中已经证实了部分药物的可行性,并有望在未来应用于临床;基于唾液TDM的Pop PK建模用于精准给药仅在部分药物上进行了初步尝试,其应用尚未在临床研究中得到验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Saliva as a TDM matrix and its application in the model-informed precision dosing.

This study reviews the main points of saliva as a therapeutic drug monitoring (TDM) matrix, its advantages and limitations, the methods of saliva sample collection and testing, the types of drugs in saliva TDM, and the methods of establishing saliva population pharmacokinetic (Pop PK) models, as well as summarizes the experiences and limitations, to provide references to carry out related studies. The PubMed database was systematically searched for studies on the topic of saliva as a matrix for drug TDM. The literature was screened according to the established inclusion and exclusion criteria, and relevant data were extracted and summarized. The systematic review ultimately screened 112 articles involving relevant studies on 73 drugs, of which studies on 53 drugs supported saliva as a matrix for TDM; studies on 13 drugs did not support it; and the results of studies on seven drugs were inconsistent, with conflicting results regarding whether they supported salivary TDM or not. The study steps for Pop PK modeling based on saliva concentrations are summarized, and representative drugs for which Pop PK models incorporating both plasma and saliva concentrations have been established are listed. Saliva TDM, as a new exploration and attempt, has been confirmed to be feasible for some drugs in the current study, and is expected to be applied to the clinic in the future; Pop PK modeling based on saliva TDM for precision drug delivery has only been initially attempted for some drugs, and its application has yet to be verified in clinical studies.

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来源期刊
Journal of Clinical Pharmacology
Journal of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
自引率
3.40%
发文量
0
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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