Physiologically based pharmacokinetic (PBPK) modelling of oral drug absorption in older adults-an AGePOP review

被引:12
|
作者
Demeester, Cleo [1 ,2 ]
Robins, Donnia [3 ,4 ]
Edwina, Angela Elma [5 ]
Tournoy, Jos [5 ,6 ]
Augustijns, Patrick [2 ]
Ince, Ibrahim [1 ]
Lehmann, Andreas [3 ]
Vertzoni, Maria [4 ]
Schlender, Jan Frederik [1 ,7 ]
机构
[1] Bayer AG, Syst Pharmacol & Med, Pharmaceut, D-51373 Leverkusen, Germany
[2] Katholieke Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Drug Delivery & Disposit, Gasthuisberg O&N 2, Leuven, Belgium
[3] Merck KGaA, Global CMC Dev, Frankfurter Str 250, Darmstadt, Germany
[4] Natl & Kapodistrian Univ Athens, Sch Hlth Sci, Dept Pharm, Zografos, Greece
[5] Univ Leuven, KU Leuven, Dept Publ Hlth & Primary care, Gerontol & Geriatr Unit, Leuven, Belgium
[6] Univ Hosp Leuven, Dept Geriatr Med, Leuven, Belgium
[7] Novartis Inst Biomed Res, Basel, Switzerland
基金
欧盟地平线“2020”;
关键词
PBPK modelling; Absorption; Older people; Elderly; Peroral; In silico; Clinical pharmacology; Oral drug development; GASTRIC-ACID-SECRETION; HELICOBACTER-PYLORI INFECTION; GASTROINTESTINAL TRANSIT; ELDERLY-PATIENTS; FRAILTY INDEX; SERUM GASTRIN; YOUNG-ADULTS; HEALTHY-MEN; FOOD; HIV;
D O I
10.1016/j.ejps.2023.106496
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The older population consisting of persons aged 65 years or older is the fastest-growing population group and also the major consumer of pharmaceutical products. Due to the heterogenous ageing process, this age group shows high interindividual variability in the dose-exposure-response relationship and, thus, a prediction of drug safety and efficacy is challenging. Although physiologically based pharmacokinetic (PBPK) modelling is a wellestablished tool to inform and confirm drug dosing strategies during drug development for special population groups, age-related changes in absorption are poorly accounted for in current PBPK models. The purpose of this review is to summarise the current state-of-knowledge in terms of physiological changes with increasing age that can influence the oral absorption of dosage forms. The capacity of common PBPK platforms to incorporate these changes and describe the older population is also discussed, as well as the implications of extrinsic factors such as drug-drug interactions associated with polypharmacy on the model development process. The future potential of this field will rely on addressing the gaps identified in this article, which can subsequently supplement in-vitro and in-vivo data for more robust decision-making on the adequacy of the formulation for use in older adults and inform pharmacotherapy.
引用
收藏
页数:16
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