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健康成年人禁食和进食状态下胃肠道胆汁盐浓度:基于生理药代动力学(PBPK)模型机制的系统评价和荟萃分析

Gastrointestinal Bile Salt Concentrations in Healthy Adults Under Fasted and Fed Conditions: A Systematic Review and Meta-Analysis for Mechanistic Physiologically-Based Pharmacokinetic (PBPK) Modelling.

作者信息

Santos Laura G Al-Amiry, Musther Helen, Bala Neeru, Deferm Neel, Patel Gaurangkumar, Brouwers Joachim, Turner David B

机构信息

Certara UK Limited, Level 2, Acero, 1 Concourse Way, Sheffield, S1 2BJ, UK.

Katholieke Universiteit, Louvain, Belgium.

出版信息

AAPS J. 2025 Jan 22;27(1):31. doi: 10.1208/s12248-025-01016-x.

Abstract

Bile salts are biosurfactants released into the intestinal lumen which play an important role in the solubilisation of fats and certain drugs. Their concentrations vary along the gastrointestinal tract (GIT). This is significant for implementation in physiologically based pharmacokinetic (PBPK) modelling to mechanistically capture drug absorption. The aims of this meta-analysis were to collate all appropriate data on intestinal bile salt concentrations in healthy adults across all GIT segments in fasted and fed states for the purpose of PBPK modelling. Terms relating to bile composition were searched in PubMed and Google Scholar from inception to May 2024. Selected studies included aspirated intestinal fluid collected via gastric tubes or colonoscopy. Results showed high variability across studies and a time-dependency for the fed state. Data were rich for the duodenum, which showed a two-fold increase for the fed state versus the fasted state within multiple studies. Peaks and troughs in bile salt concentrations along the GIT were observed for both fasted and fed states, likely due to segmental water absorption differences. The highest between subject variability was observed for the duodenum in the fasted and fed state and the fed proximal jejunum, distal ileum, and colon. The findings from this meta-analysis can be used for the purpose of PBPK modelling to capture segmental drug solubilisation and absorption in fasted and fed states. However, data are lacking under different fed conditions, especially following low-fat meals, so the impact of different fat content associated with different meals on bile salt concentrations cannot be discerned.

摘要

胆汁盐是释放到肠腔中的生物表面活性剂,在脂肪和某些药物的溶解中起重要作用。它们在胃肠道(GIT)中的浓度各不相同。这对于基于生理的药代动力学(PBPK)建模以机械地捕捉药物吸收具有重要意义。本荟萃分析的目的是整理所有关于健康成年人在禁食和进食状态下整个GIT段肠道胆汁盐浓度的适当数据,以用于PBPK建模。从开始到2024年5月,在PubMed和谷歌学术中搜索了与胆汁成分相关的术语。选定的研究包括通过胃管或结肠镜检查收集的吸出肠液。结果显示,各研究之间存在高度变异性,且进食状态具有时间依赖性。十二指肠的数据丰富,多项研究表明,进食状态下十二指肠胆汁盐浓度比禁食状态增加了两倍。在禁食和进食状态下,沿GIT均观察到胆汁盐浓度的峰值和谷值,这可能是由于各段水吸收差异所致。在禁食和进食状态下的十二指肠以及进食状态下的空肠近端、回肠远端和结肠中,观察到个体间变异性最高。本荟萃分析的结果可用于PBPK建模,以捕捉禁食和进食状态下各段药物的溶解和吸收情况。然而,不同进食条件下的数据,尤其是低脂餐后的数据缺乏,因此无法辨别不同餐食中不同脂肪含量对胆汁盐浓度的影响。

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