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 …
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 …
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 …
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 …
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 …
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 …
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
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 …
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
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 …
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
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 …
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
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 …
dispersions (SD) to enhance solubility, dissolution, and bioavailability via hot-melt extrusion …