The evolution of commercial drug delivery technologies

AM Vargason, AC Anselmo, S Mitragotri - Nature biomedical …, 2021 - nature.com
Drug delivery technologies have enabled the development of many pharmaceutical
products that improve patient health by enhancing the delivery of a therapeutic to its target …

Nanonization techniques to overcome poor water-solubility with drugs

FLO Da Silva, MBDF Marques, KC Kato… - Expert opinion on drug …, 2020 - Taylor & Francis
Introduction Most drugs used in therapy have low water-solubility, a factor that could reduce
their dissolution rate and oral bioavailability, representing a challenge in pharmaceutical …

Effects of intestinal flora on pharmacokinetics and pharmacodynamics of drugs

A Džidić-Krivić, J Kusturica, EK Sher… - Drug Metabolism …, 2023 - Taylor & Francis
Gut microbiota is known as unique collection of microorganisms (including bacteria,
archaea, eukaryotes and viruses) that exist in a complex environment of the gut. Recently …

[HTML][HTML] Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa

JAC Barbosa, MSE Abdelsadig, BR Conway… - International journal of …, 2019 - Elsevier
A range of enteric polymers is used in pharmaceutical industry for developing gastro-
resistant formulations. It is generally implied that these coatings are interchangeable due to …

Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties

DM Mudie, N Samiei, DJ Marshall, GE Amidon… - The AAPS journal, 2020 - Springer
The rate and extent of drug dissolution in the gastrointestinal (GI) tract are highly dependent
upon drug physicochemical properties and GI fluid properties. Biorelevant dissolution media …

Coamorphous lurasidone hydrochloride–saccharin with charge-assisted hydrogen bonding interaction shows improved physical stability and enhanced dissolution …

S Qian, W Heng, Y Wei, J Zhang… - Crystal Growth & Design, 2015 - ACS Publications
Recently, coamorphous systems, composed of a drug and a guest molecule, have gained
increasing interest, due to their ability to overcome limitations associated with amorphous …

Hot-melt extruded amorphous solid dispersion for solubility, stability, and bioavailability enhancement of telmisartan

BR Giri, J Kwon, AQ Vo, AM Bhagurkar, S Bandari… - Pharmaceuticals, 2021 - mdpi.com
Telmisartan (TEL, an antihypertensive drug) belongs to Class II of the Biopharmaceutical
Classification System (BCS) because of its poor aqueous solubility. In this study, we …

Formulation and evaluation of self-nanoemulsifying drug delivery system derived tablet containing sertraline

AB Nair, B Singh, J Shah, S Jacob, B Aldhubiab… - Pharmaceutics, 2022 - mdpi.com
Being a biopharmaceutics classification system class II drug, the absorption of sertraline
from the gut is mainly limited by its poor aqueous solubility. The objective of this …

Improving dissolution behavior and oral absorption of drugs with pH-dependent solubility using ph modifiers: a physiologically realistic mass transport analysis

N Salehi, G Kuminek, J Al-Gousous… - Molecular …, 2021 - ACS Publications
Orally dosed drugs must dissolve in the gastrointestinal (GI) tract before being absorbed
through the epithelial cell membrane. In vivo drug dissolution depends on the GI tract's …

Formulation of aripiprazole-loaded pH-modulated solid dispersions via hot-melt extrusion technology: In vitro and in vivo studies

H McFall, S Sarabu, V Shankar, S Bandari… - International journal of …, 2019 - Elsevier
The objective of this study was to formulate aripiprazole (ARI)-loaded pH-modulated solid
dispersions (SD) to enhance solubility, dissolution, and bioavailability via hot-melt extrusion …