TY - JOUR
TI - Oral biopharmaceutics tools: Recent progress from partnership through the Pharmaceutical Education and Research with Regulatory Links collaboration
AU - O'Dwyer, P.J.
AU - Box, K.J.
AU - Dressman, J.
AU - Griffin, B.T.
AU - Henze, L.J.
AU - Litou, C.
AU - Pentafragka, C.
AU - Statelova, M.
AU - Vertzoni, M.
AU - Reppas, C.
JO - The Journal of pharmacy and pharmacology
PY - 2021
VL - 73
TODO - 4
SP - 437-446
PB - Oxford University Press
SN - null
TODO - 10.1093/jpp/rgaa055
TODO - animal;  bioavailability;  biological model;  drug development;  drug formulation;  drug research;  education;  food drug interaction;  gastrointestinal tract;  human;  intersectoral collaboration;  oral drug administration;  pharmaceutics;  pharmacokinetics;  physiology;  pig;  procedures, Administration, Oral;  Animals;  Biological Availability;  Biopharmaceutics;  Drug Compounding;  Drug Development;  Education, Pharmacy;  Food-Drug Interactions;  Gastrointestinal Tract;  Humans;  Intersectoral Collaboration;  Models, Biological;  Pharmaceutical Research;  Pharmacokinetics;  Swine
TODO - Objectives: To summarise key contributions of the Pharmaceutical Education and Research with Regulatory Links (PEARRL) project (2016-2020) to the optimisation of existing and the development of new biopharmaceutics tools for evaluating the in vivo performance of oral drug products during the development of new drugs and at the regulatory level. Key findings: Optimised biopharmaceutics tools: Based on new clinical data, the composition of biorelevant media for simulating the fed state conditions in the stomach was simplified. Strategies on how to incorporate biorelevant in vitro data of bio-enabling drug products into physiologically based pharmacokinetic (PBPK) modelling were proposed. Novel in vitro biopharmaceutics tools: Small-scale two-stage biphasic dissolution and dissolution-permeation setups were developed to facilitate understanding of the supersaturation effects and precipitation risks of orally administered drugs. A porcine fasted state simulated intestinal fluid was developed to improve predictions and interpretation of preclinical results using in vitro dissolution studies. Based on new clinical data, recommendations on the design of in vitro methodologies for evaluating the GI drug transfer process in the fed state were suggested. The optimized design of in vivo studies for investigating food effects: A food effect study protocol in the pig model was established which successfully predicted the food-dependent bioavailability of two model compounds. The effect of simulated infant fed state conditions in healthy adults on the oral absorption of model drugs was evaluated versus the fasted state and the fed state conditions, as defined by regulatory agencies for adults. Using PBPK modelling, the extrapolated fasted and infant fed conditions data appeared to be more useful to describe early drug exposure in infants, while extrapolation of data collected under fed state conditions, as defined by regulators for adults, failed to capture in vivo infant drug absorption. Summary: Substantial progress has been made in developing an advanced suite of biopharmaceutics tools for streamlining drug formulation screening and supporting regulatory applications. These advances in biopharmaceutics were achieved through networking opportunities and research collaborations provided under the H2020 funded PEARRL project. © 2021 The Author(s) 2021. Published by Oxford University Press on behalf of the Royal Pharmaceutical Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
ER -