Impact of dendrimers on solubility of hydrophobic drug molecules

S Choudhary, L Gupta, S Rani, K Dave… - Frontiers in …, 2017 - frontiersin.org
Adequate aqueous solubility has been one of the desired properties while selecting drug
molecules and other bio-actives for product development. Often solubility of a drug …

Overcoming poor oral bioavailability using nanoparticle formulations–opportunities and limitations

PP Desai, AA Date, VB Patravale - Drug Discovery Today: Technologies, 2012 - Elsevier
Oral delivery of drugs with poor aqueous solubility and poor enzymatic and/or metabolic
stability is very challenging. However, the advent of nanotechnology has revolutionized the …

Recent trends of self-emulsifying drug delivery system for enhancing the oral bioavailability of poorly water-soluble drugs

P Tran, JS Park - Journal of pharmaceutical Investigation, 2021 - Springer
Background The oral route is the most popular route for the clinical administration of drugs to
treat various diseases. Before a drug is absorbed into the blood circulation, it must undergo …

[HTML][HTML] Design, optimization and evaluation of glipizide solid self-nanoemulsifying drug delivery for enhanced solubility and dissolution

RN Dash, H Mohammed, T Humaira… - Saudi Pharmaceutical …, 2015 - Elsevier
A solid self-nanoemulsifying drug-delivery system (solid SNEDDS) has been explored to
improve the solubility and dissolution profile of glipizide. SNEDDS preconcentrate was …

Development and in vitro/in vivo performance of self-nanoemulsifying drug delivery systems loaded with candesartan cilexetil

K AboulFotouh, AA Allam, M El-Badry… - European Journal of …, 2017 - Elsevier
Candesartan cilexetil is widely used in the management of hypertension and heart failure.
The drug delivery encounters obstacles of poor aqueous solubility, efflux by intestinal P …

Improving oral absorption via drug-loaded nanocarriers: absorption mechanisms, intestinal models and rational fabrication

MA Shahbazi, HA Santos - Current drug metabolism, 2013 - ingentaconnect.com
Although it is acknowledged that the main impediment of orally administered therapeutic
agents is their extensive and changeable pre-systemic metabolism, low absorption and …

Improving The oral absorption of nintedanib by a self-microemulsion drug delivery system: preparation and in vitro/in vivo evaluation

H Liu, J Mei, Y Xu, L Tang, D Chen, Y Zhu… - International Journal …, 2019 - Taylor & Francis
Objective Nintedanib (NDNB) is a triple receptor tyrosine kinase inhibitor with poor solubility
in neutral conditions and low bioavailability. A self-microemulsifying drug delivery system …

Dendrimer for solubility enhancement

B Gorain, M Pandey, H Choudhury, GK Jain… - Dendrimer-based …, 2021 - Elsevier
A drug is effective in their molecular form; thus solubility in the biological fluid is important.
Pharmaceutical researchers are continuously working on the improvement of solubility of …

Calculation of drug-polymer mixing enthalpy as a new screening method of precipitation inhibitors for supersaturating pharmaceutical formulations

DJ Price, A Nair, M Kuentz, J Dressman… - European Journal of …, 2019 - Elsevier
Supersaturating formulations are widely used to improve the oral bioavailability of poorly
soluble drugs. However, supersaturated solutions are thermodynamically unstable and such …

[PDF][PDF] Formulation and characterization of nimodipine nanoemulsion as ampoule for oral route

MM Ghareeb, AJ Neamah - International Journal of …, 2017 - researchgate.net
The aim of this study was to develop oil in water nanoemulsion of nimodipine intended for
oral use. Nimodipine is a calcium channel blocker that has poor oral bioavailability (3-30%) …