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Fedi, Arianna; Vitale, Chiara; Ponschin, Giulia; Ayehunie, Seyoum; Fato, Marco; Scaglione, Silvia
Journal of controlled release, 07/2021, Volume: 335Journal Article
Absorption, distribution, metabolism and excretion (ADME) studies represent a fundamental step in the early stages of drug discovery. In particular, the absorption of orally administered drugs, which occurs at the intestinal level, has gained attention since poor oral bioavailability often led to failures for new drug approval. In this context, several in vitro preclinical models have been recently developed and optimized to better resemble human physiology in the lab and serve as an animal alternative to accomplish the 3Rs principles. However, numerous models are ineffective in recapitulating the key features of the human small intestine epithelium and lack of prediction potential for drug absorption and metabolism during the preclinical stage. In this review, we provide an overview of in vitro models aimed at mimicking the intestinal barrier for pharmaceutical screening. After briefly describing how the human small intestine works, we present i) conventional 2D synthetic and cell-based systems, ii) 3D models replicating the main features of the intestinal architecture, iii) micro-physiological systems (MPSs) reproducing the dynamic stimuli to which cells are exposed in the native microenvironment. In this review, we will highlight the benefits and drawbacks of the leading intestinal models used for drug absorption and metabolism studies. Display omitted •Poor oral drug bioavailability is the primary cause of failures for new drugs approval.•Intestinal in vitro models include 2D traditional monolayers, complex 3D systems and emerging fluid-dynamic platforms.•Multicellular models display a good correlation between in vitro permability data and the fractions absorbed in humans.•Microphysiological systems closely recapitulate the intestinal physiological cues but still need to be standardized.
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