An overview of in vitro, ex vivo and in vivo models for studying the transport of drugs across intestinal barriers

Y Xu, N Shrestha, V Préat, A Beloqui - Advanced Drug Delivery Reviews, 2021 - Elsevier
Oral administration is the most commonly used route for drug delivery owing to its cost-
effectiveness, ease of administration, and high patient compliance. However, the absorption …

Biomedical application of mesoporous silica nanoparticles as delivery systems: A biological safety perspective

S Hosseinpour, LJ Walsh, C Xu - Journal of Materials Chemistry B, 2020 - pubs.rsc.org
The application of mesoporous silica nanoparticles (MSNs) as drug delivery systems to
deliver drugs, proteins, and genes has expanded considerably in recent years, using in vitro …

INFOGEST static in vitro simulation of gastrointestinal food digestion

A Brodkorb, L Egger, M Alminger, P Alvito… - Nature protocols, 2019 - nature.com
Developing a mechanistic understanding of the impact of food structure and composition on
human health has increasingly involved simulating digestion in the upper gastrointestinal …

[HTML][HTML] In vitro and in vivo correlation for lipid-based formulations: Current status and future perspectives

Y Huang, Q Yu, Z Chen, W Wu, Q Zhu, Y Lu - Acta Pharmaceutica Sinica B, 2021 - Elsevier
Lipid-based formulations (LBFs) have demonstrated a great potential in enhancing the oral
absorption of poorly water-soluble drugs. However, construction of in vitro and in vivo …

[HTML][HTML] Overview of the detection methods for equilibrium dissociation constant KD of drug-receptor interaction

W Ma, L Yang, L He - Journal of pharmaceutical analysis, 2018 - Elsevier
Drug-receptor interaction plays an important role in a series of biological effects, such as cell
proliferation, immune response, tumor metastasis, and drug delivery. Therefore, the …

Enhancing oral bioavailability of poorly soluble drugs with mesoporous silica based systems: Opportunities and challenges

KE Bremmell, CA Prestidge - Drug development and industrial …, 2019 - Taylor & Francis
Porous silica-based drug delivery systems have shown considerable promise for improving
the oral delivery of poorly water-soluble drugs. More specifically, micro-and meso-porous …

[HTML][HTML] Characterization of gastrointestinal transit and luminal conditions in pigs using a telemetric motility capsule

LJ Henze, NJ Koehl, H Bennett-Lenane, R Holm… - European Journal of …, 2021 - Elsevier
Within preclinical research, the pig has become an important model in regulatory toxicology
and pharmacokinetics, to assess oral dosage forms and to compare different formulation …

The pig as a preclinical model for predicting oral bioavailability and in vivo performance of pharmaceutical oral dosage forms: a PEARRL review

LJ Henze, NJ Koehl, JP O'Shea… - Journal of pharmacy …, 2019 - academic.oup.com
Objectives In pharmaceutical drug development, preclinical tests in animal models are
essential to demonstrate whether the new drug is orally bioavailable and to gain a first …

Mesoporous silica nanorods for improved oral drug absorption

N Zheng, J Li, C Xu, L Xu, S Li, L Xu - Artificial Cells, Nanomedicine …, 2018 - Taylor & Francis
Mesoporous silica nanoparticles (MSNs) have been widely used in biomedical applications.
However, most studies have been limited to spherical MSNs, while non-spherical MSNs …

Enhanced solubility, permeability and anticancer activity of vorinostat using tailored mesoporous silica nanoparticles

AK Meka, LJ Jenkins, M Dàvalos-Salas, N Pujara… - Pharmaceutics, 2018 - mdpi.com
Suberoylanilide hydroxamic acid (SAHA) or vorinostat (VOR) is a potent inhibitor of class I
histone deacetylases (HDACs) that is approved for the treatment of cutaneous T-cell …