[HTML][HTML] Intranasal delivery of darunavir-loaded mucoadhesive in situ gel: Experimental design, in vitro evaluation, and pharmacokinetic studies

AB Nair, S Chaudhary, H Shah, S Jacob, V Mewada… - Gels, 2022 - mdpi.com
The clinical efficacy of antiretroviral therapy in NeuroAIDS is primarily limited by the low
perfusion of the drug to the brain. The objective of the current investigation was to design …

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 …

Co-crystallization: a green approach for the solubility enhancement of poorly soluble drugs

M Bhatia, S Devi - CrystEngComm, 2024 - pubs.rsc.org
Recently, the co-crystallization of pharmaceutical drugs is gaining consideration because it
is an environmentally friendly and potentially effective technique to improve the solubility …

Compression-coated pulsatile chronomodulated therapeutic system: QbD assisted optimization

HM Aldawsari, NR Naveen, NA Alhakamy… - Drug Delivery, 2022 - Taylor & Francis
Pulsatile drug delivery systems have drawn attention in contemporary research for
designing chronotherapeutic systems. The current work aims to design pulsatile ketorolac …

Quality-by-design-based development of rivaroxaban-loaded liquisolid compact tablets with improved biopharmaceutical attributes

P Shah, H Desai, B Vyas, M Lalan, M Kulkarni - AAPS PharmSciTech, 2023 - Springer
Rivaroxaban (RXN) finds use in the management of pulmonary embolism and deep vein
thrombosis. Its poor solubility (5–7 µg/mL) and P-gp-mediated efflux from intestinal lining …

Enhanced Solubility and Bioavailability of Dolutegravir by Solid Dispersion Method: In Vitro and In Vivo Evaluation—a Potential Approach for HIV Therapy

S Chaudhary, AB Nair, J Shah, B Gorain, S Jacob… - AAPS …, 2021 - Springer
Being a candidate of BCS class II, dolutegravir (DTG), a recently approved antiretroviral
drug, possesses solubility issues. The current research was aimed to improve the solubility …

Enhancement of ketoprofen dissolution rate by the liquisolid technique: Optimization and in vitro and in vivo investigations

S Devi, S Kumar, V Verma, D Kaushik, R Verma… - Drug Delivery and …, 2022 - Springer
The objective of the current study is to evaluate the prospective of liquisolid formulation to
improve the dissolution rate of ketoprofen and thereby the bioavailability. Different batches …

Liquisolid systems as a novel approach in formulation and manufacturing of solid dosage forms: Challenges and perspectives

I Aleksić, T Glišić, J Parojčić - Archives of Pharmacy, 2022 - aseestant.ceon.rs
Liquisolid systems are a novel, promising platform for the production of solid dosage forms
with a high liquid content, ie dispersion of the drug in a suitable, hydrophilic, non-volatile …

Design and optimization of liquisolid compact based vaginal sustained release tablet of antifungal agent for vaginal candidiasis

PS Kanojiya, PN Ghodake… - Journal of Dispersion …, 2024 - Taylor & Francis
Antifungal therapy is causing an alarming drug resistance problem during the treatment of
Vaginal Candidiasis and also many of the antifungal vaginal marketed formulations have …

Pharmacokinetics and tissue distribution of hydrazinocurcumin in rats

Satyavert, S Gupta, H Choudhury, S Jacob… - Pharmacological …, 2021 - Springer
Background Curcumin, a natural polyphenol from Curcuma longa, is known to possess
diversified pharmacological roles including anti-inflammatory, antioxidant, antiproliferative …