Biological voyage of solid lipid nanoparticles: a proficient carrier in nanomedicine

H Ali, SK Singh - Therapeutic delivery, 2016 - Taylor & Francis
This review projects the prospects and issues faced by solid lipid nanoparticles (SLNs) in
current scenarios, specially related to its clinical implementation and effectiveness. We re …

Molecular properties associated with transporter-mediated drug disposition

MV Varma, Y Lai, AF El-Kattan - Advanced Drug Delivery Reviews, 2017 - Elsevier
Membrane transporters play a key role in the absorption, distribution, clearance, elimination,
and transport of drugs. Understanding the drug properties and structure activity relationships …

[PDF][PDF] Molecular docking and pharmacokinetics study for selected leaf phytochemicals from Carica papaya Linn. against dengue virus protein, NS2B/NS3 protease

I Ghosh, P Talukdar - World Scientific News, 2019 - bibliotekanauki.pl
The Culex mosquito-transmitted dengue virus (DENV) under genus Flavivirus, a member of
Flaviviridae family, cause dengue fever worldwide also in many parts of India. At present …

Soluble polyphenols: Synthesis and bioavailability of 3, 4′, 5-tri (α-d-glucose-3-O-succinyl) resveratrol

L Biasutto, E Marotta, A Bradaschia, M Fallica… - Bioorganic & medicinal …, 2009 - Elsevier
We report the development of a chemical modification method of general applicability to
polyphenols, which increases solubility to influence absorption. Glucosyl groups were …

[PDF][PDF] Optimization of a dissolution method in early development based on IVIVC using small animals: Application to a BCS class II drug

S Deshmukh, A Avachat, A Garkal, N Khurana… - Dissolution …, 2016 - researchgate.net
The aim of the present study was to develop optimal dissolution conditions for a BCS Class II
drug in early development. The model drug efavirenz was formulated in two dosage forms: a …

Toward molecular design for hazard reduction—fundamental relationships between chemical properties and toxicity

AM Voutchkova, LA Ferris, JB Zimmerman, PT Anastas - Tetrahedron, 2010 - Elsevier
The relationship of in-silico predicted physical/chemical properties and human toxicity is
analyzed for a statistically significant sample size of chemical compounds. Results for …

Physiologically based absorption modeling to predict the bioequivalence of two cilostazol formulations

L Wang, P Zhao, T Luo, D Yang, Q Jiang… - Clinical and …, 2023 - Wiley Online Library
In vivo pharmacokinetic simulations and virtual bioequivalence (BE) evaluation of cilostazol
have not yet been described for humans. Here, we successfully developed a physiologically …

Metabolic profile and structure–activity relationship of resveratrol and its analogs in human bladder cancer cells

Y Yang, G Zhang, C Li, S Wang, M Zhu… - Cancer management …, 2019 - Taylor & Francis
Purpose: Resveratrol (RV), a promising anti-cancer candidate, is limited in application for its
poor bioavailability. However, the better bioavailability has been found in some RV …

Improvement of pharmacokinetics behavior of apocynin by nitrone derivatization: comparative pharmacokinetics of nitrone-apocynin and its parent apocynin in rats

K Wang, L Li, Y Song, X Ye, S Fu, J Jiang, S Li - PLoS One, 2013 - journals.plos.org
Apocynin, a potent inhibitor of NADPH-oxidase, was widely studied for activities in diseases
such as inflammation-mediated disorders, asthma and cardiovascular diseases. In our …

In vitro, in-vivo, and in-silico investigation of physicochemical interactions between pioglitazone and rifampicin

O Londhe, SS Mane, BU Hirlekar… - European Journal of …, 2023 - Elsevier
There is a possibility of in-situ physicochemical interactions between concomitantly
administered drugs. This study aimed to investigate such physicochemical interactions …