User profiles for Jaymin C. Shah

Jaymin C Shah

Research Fellow, Pfizer Research and Development
Verified email at pfizer.com
Cited by 3135

Cubic phase gels as drug delivery systems

JC Shah, Y Sadhale, DM Chilukuri - Advanced drug delivery reviews, 2001 - Elsevier
Lipids have been used extensively for drug delivery in various forms such as liposomes,
and solid-matrices. The focus of this review is evaluation of liquid crystalline cubic phases, …

Delineating the role of cooperativity in the design of potent PROTACs for BTK

…, J Chen, M Niosi, S Luthra, JC Shah… - Proceedings of the …, 2018 - National Acad Sciences
Proteolysis targeting chimeras (PROTACs) are heterobifunctional small molecules that
simultaneously bind to a target protein and an E3 ligase, thereby leading to ubiquitination and …

Hydrolysis in pharmaceutical formulations

…, J Hong, MS Landis, F Lombardo, JC Shah… - Pharmaceutical …, 2002 - Taylor & Francis
This literature review presents hydrolysis of active pharmaceutical ingredients as well as the
effects on dosage form stability due to hydrolysis of excipients. Mechanisms and …

Biodegradable polyanhydride devices of cefazolin sodium, bupivacaine, and taxol for local drug delivery: preparation, and kinetics and mechanism of in vitro release

ES Park, M Maniar, JC Shah - Journal of Controlled Release, 1998 - Elsevier
The overall objective was to design and evaluate biodegradable implants for local drug
delivery in clinical conditions and/or diseases described below, which are currently treated with …

Assessing and predicting physical stability of emulsion-based topical semisolid products: a review

AZM Badruddoza, T Yeoh, JC Shah, T Walsh - Journal of Pharmaceutical …, 2023 - Elsevier
The emulsion-based topical semisolid dosage forms present a high degree of complexity
due to their microstructures which is apparent from their compositions comprising at least two …

Prediction of vitreal half-life based on drug physicochemical properties: quantitative structure–pharmacokinetic relationships (QSPKR)

C Durairaj, JC Shah, S Senapati, UB Kompella - Pharmaceutical research, 2009 - Springer
Purpose The aim of this study was to develop quantitative structure pharmacokinetic relationships
(QSPKR) to correlate drug physicochemical properties (molecular weight, lipophilicity, …

Preformulation study of etoposide: II. Increased solubility and dissolution rate by solid-solid dispersions

JC Shah, JR Chen, D Chow - International Journal of Pharmaceutics, 1995 - Elsevier
Etoposide, an anticancer drug, has low and erratic oral bioavailability which is due to low
aqueous solubility, slow dissolution rate and instability in acidic pH. The study objective was to …

Preformulation study of etoposide: identification of physicochemical characteristics responsible for the low and erratic oral bioavailability of etoposide

JC Shah, JR Chen, D Chow - Pharmaceutical research, 1989 - Springer
Preformulation studies of etoposide, including pH–solubility profile, partition coefficient, pH–stability
profile, and in vitro dissolution kinetics, were conducted to identify the responsible …

Stabilization of insulin against agitation-induced aggregation by the GMO cubic phase gel

Y Sadhale, JC Shah - International journal of pharmaceutics, 1999 - Elsevier
The main objective of the study was to evaluate if the liquid crystalline cubic phase gel of
glyceryl monooleate (GMO) protects insulin from agitation induced aggregation. The …

Pharmacokinetics of oxytetracycline in the white shrimp, Litopenaeus setiferus

LA Reed, TC Siewicki, JC Shah - Aquaculture, 2004 - Elsevier
Shrimp are among the most highly valued seafood in the US, and a large proportion are
cultured. At least seven species of Vibrio bacteria and other pathogens often infect shrimp …