Robustness testing, using experimental design, of a flow-through dissolution method for a product where the actives have markedly differing solubility properties

M.S Bloomfield; W.C Butler

doi:10.1016/s0378-5173(00)00509-3

Robustness testing, using experimental design, of a flow-through dissolution method for a product where the actives have markedly differing solubility properties

International Journal of Pharmaceutics ◽

10.1016/s0378-5173(00)00509-3 ◽

2000 ◽

Vol 206 (1-2) ◽

pp. 55-61 ◽

Cited By ~ 15

Author(s):

M.S Bloomfield ◽

W.C Butler

Keyword(s):

Experimental Design ◽

Dissolution Method ◽

Robustness Testing ◽

Flow Through

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Validation and Experimental Design Assisted Robustness Testing of RPLC Method for the Simultaneous Analysis of Brinzolamide and Brimonidine Tartrate in an Ophthalmic Dosage Form

Indian Journal of Pharmaceutical Sciences ◽

10.4172/pharmaceutical-sciences.1000162 ◽

2016 ◽

Vol 78 (5) ◽

Cited By ~ 2

Author(s):

J R Christian ◽

Kalpana G Patel ◽

T R Gandhi

Keyword(s):

Experimental Design ◽

Dosage Form ◽

Simultaneous Analysis ◽

Robustness Testing ◽

Brimonidine Tartrate

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Experimental Design in Method Optimization and Robustness Testing

Chemometric Methods in Capillary Electrophoresis ◽

10.1002/9780470530191.ch2 ◽

2009 ◽

pp. 11-74 ◽

Cited By ~ 4

Author(s):

Bieke Dejaegher ◽

Alexandra Durand ◽

Yvan Vander Heyden

Keyword(s):

Experimental Design ◽

Robustness Testing ◽

Method Optimization

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Robustness Testing in HPLC Analysis of Clarithromycin, Norfloxacin, Doxycycline, Tinidazole and Omeprazole in Pharmaceutical Dosage forms Using Experimental Design

Current Pharmaceutical Analysis ◽

10.2174/157341291001140102111733 ◽

2014 ◽

Vol 10 (1) ◽

pp. 58-70 ◽

Cited By ~ 4

Author(s):

Mahmoud Elkhoudary ◽

Randa Salam ◽

Ghada Hadad

Keyword(s):

Experimental Design ◽

Hplc Analysis ◽

Dosage Forms ◽

Pharmaceutical Dosage Forms ◽

Robustness Testing

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In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution media

European Journal of Pharmaceutical Sciences ◽

10.1016/j.ejps.2004.11.007 ◽

2005 ◽

Vol 24 (4) ◽

pp. 305-313 ◽

Cited By ~ 108

Author(s):

Vibeke Hougaard Sunesen ◽

Betty Lomstein Pedersen ◽

Henning Gjelstrup Kristensen ◽

Anette Müllertz

Keyword(s):

Dissolution Method ◽

Biorelevant Dissolution ◽

Poorly Soluble ◽

Flow Through ◽

Poorly Soluble Drug ◽

Biorelevant Dissolution Media

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EXPERIMENTAL DESIGN STRATEGIES IN LC METHOD DEVELOPMENT AND IN ROBUSTNESS TESTING FOR REVERSIBLE CHOLINESTERASE INHIBITOR RIVASTIGMINE IN PHARMACEUTICAL FORMULATION

Journal of Liquid Chromatography &amp Related Technologies ◽

10.1080/10826070903439317 ◽

2009 ◽

Vol 33 (2) ◽

pp. 191-201 ◽

Cited By ~ 1

Author(s):

Mohammad H. Semreen ◽

Hassan Y. Aboul-Enein

Keyword(s):

Experimental Design ◽

Cholinesterase Inhibitor ◽

Method Development ◽

Pharmaceutical Formulation ◽

Design Strategies ◽

Robustness Testing

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Experimental design strategies in the optimization and robustness testing of adsorptive stripping voltammetric conditions for kynurenic acid determination

Journal of Pharmaceutical and Biomedical Analysis ◽

10.1016/s0731-7085(96)02029-8 ◽

1997 ◽

Vol 15 (9-10) ◽

pp. 1585-1594 ◽

Cited By ~ 18

Author(s):

S. Furlanetto ◽

S. Pinzauti ◽

P. Gratteri ◽

E. La Porta ◽

G. Calzeroni

Keyword(s):

Experimental Design ◽

Kynurenic Acid ◽

Design Strategies ◽

Robustness Testing ◽

Acid Determination

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The use of the Box–Behnken experimental design in the optimisation and robustness testing of a capillary electrophoresis method for the analysis of ethambutol hydrochloride in a pharmaceutical formulation

Journal of Pharmaceutical and Biomedical Analysis ◽

10.1016/s0731-7085(01)00659-8 ◽

2002 ◽

Vol 27 (6) ◽

pp. 995-1007 ◽

Cited By ~ 102

Author(s):

R Ragonese ◽

M Macka ◽

J Hughes ◽

P Petocz

Keyword(s):

Capillary Electrophoresis ◽

Experimental Design ◽

Pharmaceutical Formulation ◽

Robustness Testing ◽

Capillary Electrophoresis Method ◽

Electrophoresis Method

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Application of Flow-Through Dissolution Method for the Evaluation of Oral Formulations of Nifedipine

Drug Development and Industrial Pharmacy ◽

10.3109/03639049409050214 ◽

1994 ◽

Vol 20 (11) ◽

pp. 1869-1882 ◽

Cited By ~ 22

Author(s):

S. A. Qureshi ◽

G. Caillé ◽

R. Brien ◽

G. Piccirilli ◽

V. Yu ◽

...

Keyword(s):

Dissolution Method ◽

Oral Formulations ◽

Flow Through

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Factorial design used for ruggedness testing of flow through cell dissolution method by means of Weibull transformed drug release profiles

International Journal of Pharmaceutics ◽

10.1016/0378-5173(92)90300-q ◽

1992 ◽

Vol 88 (1-3) ◽

pp. 23-29 ◽

Cited By ~ 11

Author(s):

K. Jørgensen ◽

L. Jacobsen

Keyword(s):

Drug Release ◽

Factorial Design ◽

Dissolution Method ◽

Flow Through ◽

Ruggedness Testing ◽

Release Profiles

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The application of experimental design to the robustness testing of a method for the determination of drug-related impurities by capillary electrophoresis

Chromatographia ◽

10.1007/bf02274518 ◽

1994 ◽

Vol 39 (5-6) ◽

pp. 306-310 ◽

Cited By ~ 39

Author(s):

K. D. Altria ◽

S. D. Filbey

Keyword(s):

Capillary Electrophoresis ◽

Experimental Design ◽

Robustness Testing ◽

Related Impurities

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