Literature DB >> 12066569

Hydrolysis in pharmaceutical formulations.

Kenneth C Waterman1, Roger C Adami, Karen M Alsante, Amy S Antipas, Dan R Arenson, Rebecca Carrier, Jinyang Hong, Margaret S Landis, Franco Lombardo, Jaymin C Shah, Evgenyi Shalaev, Scott W Smith, Hai Wang.   

Abstract

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 measurement methods are discussed and recommendations for formulation stabilization are listed.

Mesh：

Substances：

Year:  2002        PMID： 12066569     DOI： 10.1081/pdt-120003494

Source DB:  PubMed          Journal:  Pharm Dev Technol        ISSN： 1083-7450            Impact factor:   3.133


  12 in total

Review 1.  Impact of excipient interactions on solid dosage form stability.

Authors:  Ajit S Narang; Divyakant Desai; Sherif Badawy
Journal:  Pharm Res       Date:  2012-06-16       Impact factor: 4.200

Review 2.  Pharmaceutical Cocrystals: Regulatory and Strategic Aspects, Design and Development.

Authors:  Dipak Dilip Gadade; Sanjay Sudhakar Pekamwar
Journal:  Adv Pharm Bull       Date:  2016-12-22

3.  ChemStable: a web server for rule-embedded naïve Bayesian learning approach to predict compound stability.

Authors:  Zhihong Liu; Minghao Zheng; Xin Yan; Qiong Gu; Johann Gasteiger; Johan Tijhuis; Peter Maas; Jiabo Li; Jun Xu
Journal:  J Comput Aided Mol Des       Date:  2014-07-17       Impact factor: 3.686

Review 4.  Best Practices in Stability Indicating Method Development and Validation for Non-clinical Dose Formulations.

Authors:  Teresa R Henry; Lara D Penn; Jason R Conerty; Francesca E Wright; Gregory Gorman; Brian W Pack
Journal:  AAPS J       Date:  2016-09-06       Impact factor: 4.009

5.  Measuring Biomolecular DSC Profiles with Thermolabile Ligands to Rapidly Characterize Folding and Binding Interactions.

Authors:  Robert W Harkness V; Philip E Johnson; Anthony K Mittermaier
Journal:  J Vis Exp       Date:  2017-11-21       Impact factor: 1.355

6.  Biodegradation of cefdinir by a novel yeast strain, Ustilago sp. SMN03 isolated from pharmaceutical wastewater.

Authors:  A Selvi; Jaseetha Abdul Salam; Nilanjana Das
Journal:  World J Microbiol Biotechnol       Date:  2014-08-03       Impact factor: 3.312

7.  Preparation of alginate beads containing a prodrug of diethylenetriaminepentaacetic acid.

Authors:  Yu-Tsai Yang; Anthony J Di Pasqua; Weiling He; Tsuimin Tsai; Katsuhiko Sueda; Yong Zhang; Michael Jay
Journal:  Carbohydr Polym       Date:  2012-11-30       Impact factor: 9.381

8.  Control of Drug-Excipient Particle Attributes with Droplet Microfluidic-based Extractive Solidification Enables Improved Powder Rheology.

Authors:  Denise Z L Ng; Arif Z Nelson; Gareth Ward; David Lai; Patrick S Doyle; Saif A Khan
Journal:  Pharm Res       Date:  2022-02-04       Impact factor: 4.200

9.  Modeling the Distribution of Diprotic Basic Drugs in Liposomal Systems: Perspectives on Malaria Nanotherapy.

Authors:  Ernest Moles; Maria Kavallaris; Xavier Fernàndez-Busquets
Journal:  Front Pharmacol       Date:  2019-09-25       Impact factor: 5.810

10.  Estimation of sertraline by chromatographic (HPLC-UV273 nm) technique under hydrolytic stress conditions.

Authors:  Md Akhlaquer Rahman; Zeenat Iqbal; Mohd Aamir Mirza; Arshad Hussain
Journal:  Pharm Methods       Date:  2012-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.