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
相关论文
共 50 条
  • [41] Prediction of dolutegravir pharmacokinetics and dose optimization in neonates via physiologically based pharmacokinetic (PBPK) modelling
    Bunglawala, Fazila
    Rajoli, Rajith K. R.
    Mirochnick, Mark
    Owen, Andrew
    Siccardi, Marco
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2020, 75 (03) : 640 - 647
  • [42] Whole-body physiologically based pharmacokinetic population modelling of oral drug administration: inter-individual variability of cimetidine absorption
    Willmann, Stefan
    Edginton, Andrea N.
    Kleine-Besten, Marcus
    Jantratid, Ekarat
    Thelen, Kirstin
    Dressman, Jennifer B.
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2009, 61 (07) : 891 - 899
  • [43] PHYSIOLOGICALLY BASED PHARMACOKINETIC (PBPK) MODELING FOR PREDICTING TRANSPORTER-MEDIATED DRUG DISPOSITION IN HUMANS
    Watanabe, Takao
    Kusuhara, Hiroyuki
    Maeda, Kazuya
    Shitara, Yoshihisa
    Sugiyama, Yuichi
    DRUG METABOLISM REVIEWS, 2007, 39 : 98 - 98
  • [44] A Physiologically Based Pharmacokinetic (PBPK) Model for Predicting the Efficacy of Drug Overdose Treatment With Liposomes in Man
    Howell, Brett A.
    Chauhan, Anuj
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (08) : 3601 - 3619
  • [45] Food Effects on Oral Drug Absorption: Application of Physiologically-Based Pharmacokinetic Modeling as a Predictive Tool
    Cheng, Lisa
    Wong, Harvey
    PHARMACEUTICS, 2020, 12 (07) : 1 - 18
  • [46] Predictive Performance of Physiologically Based Pharmacokinetic Models for the Effect of Food on Oral Drug Absorption: Current Status
    Li, Mengyao
    Zhao, Ping
    Pan, Yuzhuo
    Wagner, Christian
    CPT-PHARMACOMETRICS & SYSTEMS PHARMACOLOGY, 2018, 7 (02): : 82 - 89
  • [47] PHYSIOLOGICALLY-BASED PHARMACOKINETIC MODELING (PBPK) OF PITAVASTATIN AND ATORVASTATIN TO PREDICT DRUG-DRUG INTERACTIONS (DDIS).
    Duan, P.
    Zhao, P.
    Zhang, L.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2015, 97 : S16 - S17
  • [48] Predicting pharmacodynamic effects through early drug discovery with artificial intelligence-physiologically based pharmacokinetic (AI-PBPK) modelling
    Wu, Keheng
    Li, Xue
    Zhou, Zhou
    Zhao, Youni
    Su, Mei
    Cheng, Zhuo
    Wu, Xinyi
    Huang, Zhijun
    Jin, Xiong
    Li, Jingxi
    Zhang, Mengjun
    Liu, Jack
    Liu, Bo
    FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [49] PHYSIOLOGICALLY-BASED PHARMACOKINETIC MODEL FOR ABSORPTION OF ORAL PARACETAMOL IN MAN
    CLEMENTS, JA
    NIMMO, WS
    HEADING, RC
    PRESCOTT, LF
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 1978, 30 : P60 - P60
  • [50] Investigating the Biodistribution of Anti-CD66 Antibody: Physiologically Based Pharmacokinetic (PBPK) Modelling and Radioimmunotherapy
    Kletting, P.
    Luster, M.
    Kull, T.
    Reske, S. N.
    Glatting, G.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2009, 36 : S290 - S290