Method Development and Validation for …
Journal of Analytical & Pharmaceutical Research Method Development and Validation for Fingolimod by HPLC/UV in Immediate-Release Oral Capsule and Study the Effect of Excipients on Solubility and Dissolution Behavior Volume 2 Issue 1 - 2016 1Pharmaceutical chemistry Department, Dublin City University, Ireland2Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt*Corresponding author: Islam A Osman, Pharmaceutical chemistry Department, Dublin City University, Al-Obour, Cairo, Egypt, Tel: +201003420050; Email: Received: August 17, 2015 | Published: January 28, 2016Research ArticleAbbreviations: RP: Reverse Phase; HPLC: High-Performance Liquid Chromatography; UV: Ultra Violet; LC: Liquid Chromatography; MS: Mass Spectrometry; DAD: Diode Array Detectors; LOD: Limit of Detection; LOQ: Limit of Quantification; RSD: Reflex Sympathetic Dystrophy; DSC: Differential scanning Calorimetry; FT-IR Infrared SpectroscopyIntroduction Fingolimod (2-amino-2-[2-(4-octylphenyl) ethyl] propane-1, 3)
Journal of Analytical & Pharmaceutical Research Method Development and Validation for Fingolimod by HPLC/UV in Immediate-Release Oral Capsule and Study
Download Method Development and Validation for …
Information
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document:
Related search queries
Complimentary WEBINAR Wednesday, December, Complimentary WEBINAR Wednesday, December 12, Development and Validation of In Vitro Release, Development and validation, Stability indicating quantitative, Method, Particle, GUIDELINES ON VALIDATION APPENDIX 4, GUIDELINES ON VALIDATION – APPENDIX 4, METHOD VALIDATION