Literature DB >> 11248467

Guidance for robustness/ruggedness tests in method validation.

Y Vander Heyden1, A Nijhuis, J Smeyers-Verbeke, B G Vandeginste, D L Massart.   

Abstract

This paper is intended to give guidance in setting-up and interpreting a robustness test. The different steps in a robustness test are discussed and illustrated with examples. The recommendations given for the different steps are based on approaches found in the literature, several case studies performed by the authors and discussions of the authors within a commission of the French SFSTP (Société Française des Sciences et Techniques Pharmaceutiques). In the end of the paper a worked-out example is given of a robustness test case study set up and interpreted according to the guidelines.

Mesh:

Year:  2001        PMID: 11248467     DOI: 10.1016/s0731-7085(00)00529-x

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  26 in total

1.  Analysis of process parameters affecting spray-dried oily core nanocapsules using factorial design.

Authors:  Tao Zhang; Bi-Botti C Youan
Journal:  AAPS PharmSciTech       Date:  2010-09-15       Impact factor: 3.246

2.  Comparative biophysical properties of tenofovir-loaded, thiolated and nonthiolated chitosan nanoparticles intended for HIV prevention.

Authors:  Jianing Meng; Tao Zhang; Vivek Agrahari; Miezan J Ezoulin; Bi-Botti C Youan
Journal:  Nanomedicine (Lond)       Date:  2014-01-10       Impact factor: 5.307

3.  Engineering tenofovir loaded chitosan nanoparticles to maximize microbicide mucoadhesion.

Authors:  Jianing Meng; Timothy F Sturgis; Bi-Botti C Youan
Journal:  Eur J Pharm Sci       Date:  2011-06-17       Impact factor: 4.384

4.  Quality by design I: Application of failure mode effect analysis (FMEA) and Plackett-Burman design of experiments in the identification of "main factors" in the formulation and process design space for roller-compacted ciprofloxacin hydrochloride immediate-release tablets.

Authors:  Raafat Fahmy; Ravikanth Kona; Ramesh Dandu; Walter Xie; Gregg Claycamp; Stephen W Hoag
Journal:  AAPS PharmSciTech       Date:  2012-09-20       Impact factor: 3.246

5.  In Vitro Permeation Studies on Carvedilol Containing Dissolving Microarray Patches Quantified Using a Rapid and Simple HPLC-UV Analytical Method.

Authors:  Qonita Kurnia Anjani; Akmal Hidayat Bin Sabri; Mary B McGuckin; Huanhuan Li; Khuriah Abdul Hamid; Ryan F Donnelly
Journal:  AAPS PharmSciTech       Date:  2022-10-04       Impact factor: 4.026

6.  Development and Validation of an HPLC Method Using an Experimental Design for Analysis of Amlodipine Besylate and Enalapril Maleate in a Fixed-dose Combination

Authors:  Diren Sarısaltık Yaşın; Alev Arslantürk Bingül; Alptuğ Karaküçük; Zeynep Şafak Teksin
Journal:  Turk J Pharm Sci       Date:  2021-06-18

7.  Validation of a flow cytometry based binding assay for evaluation of monoclonal antibody recognizing EGF receptor.

Authors:  Mercedes Cedeño-Arias; Javier Sánchez-Ramírez; Rancés Blanco-Santana; Enrique Rengifo-Calzado
Journal:  Sci Pharm       Date:  2011-07-03

8.  Micellar electrokinetic chromatographic study of the separation of an aromatase inhibitor and a tryciclic antidepressant in the breast cancer treatment.

Authors:  J Rodríguez Flores; A M Contento Salcedo; L Muñoz Fernández
Journal:  Anal Chem Insights       Date:  2008-08-13

9.  Experimental Design and Response Surface Methodology Applied to Graphene Oxide Reduction for Adsorption of Triazine Herbicides.

Authors:  Martina Foschi; Paola Capasso; Maria Anna Maggi; Fabrizio Ruggieri; Giulia Fioravanti
Journal:  ACS Omega       Date:  2021-06-23

10.  Bioanalytical method validation: An updated review.

Authors:  Gaurav Tiwari; Ruchi Tiwari
Journal:  Pharm Methods       Date:  2010-10
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