References
- Dasari V, Donthireddy S, Nikku M, Garapati H. Optimization of medium constituent for cephalosporin C production using response surface methodology and artificial neural networks. J Biochem Tech 2009;3:69–74
- Huang Y, Khanvilkar K, Moore A, Hilliard-Lott M. Effects of manufacturing process variables on in vitro dissolution characteristics of extended-release tablets formulated with hydroxypropyl methyl cellulose. Drug Dev Ind Pharm 2003;29:79–88
- Idris A, Assubaie F, Sultan S. Experimental design optimization of a sequential injection method for promazine assay in bulk and pharmaceutical formulations. J Autom Method Manag 2007;2007:32470 . doi: 10.1155/2007/32470
- Nair R, Sevukarajan M, Vishnu K, Kumar K. Response surface methodology for the optimization of ethylcellulose microspheres. Int J ChemTech Res 2011;3:775–83
- Hansuld E, Briens L, Sayani A, McCann J. The effect of process parameters on audible acoustic emissions from high-shear granulation. Drug Dev Ind Pharm 2013;39:331–41
- Malakar J, Nayak A, Goswami S. Use of response surface methodology in the formulation and optimization of bisoprolol fumarate matrix tablets for sustained drug release. ISRN Pharm 2012;2012:1–10
- Rao M, Gogad V, Sonar G. Preparation and evaluation of immediate release tablet of metoclopramide HCl using simplex centroid mixture design. Int J PharmTech Res 2010;2:1105–11
- Murtaza G, Shahzad M, Ubaid M. Formulation and optimization of celecoxib-loaded microspheres using response surface methodology. Trop J Pharm Res 2012;11:695–702
- Shahzad Y, Afreen U, Nisar Hussain Shah S. Applying response surface methodology to optimize nimesulide permeation from topical formulation. Pharm Dev Technol 2012;18:1391--8
- London J, Shaw L, Theodorsen L, Stromme J. Application of response surface methodology to the assay of gamma-glutamyltransferase. Clin Chem 1982;28:1140–3
- Dey S, Pramanik S, Malgope A. Formulation and optimization of sustained release stavudine microspheres using response surface methodology. ISRN Pharm 2011;2011:627623 . doi: 10.5402/2011/627623
- Weheba G, Sanchez-Marsa A. Using response surface methodology to optimize the stereolithography process. Rapid Prototyping J 2006;12:72–7
- Fauzee A. Development, manufacture and assessment of clobetasol 17-propionate cream formulations. MSc thesis, Rhodes University Library, Grahamstown, South Africa; 2010:1–291
- Li L, Zhao X, Yang C, et al. Preparation and optimization of doxorubicin-loaded albumin nanoparticles using response surface methodology. Drug Dev Ind Pharm 2011;37:1170–80
- Lashmar U, Richardson J, Erbod A. Correlation of physical parameters of an oil-in-water emulsion with manufacturing procedures and stability. Int J Pharm 1995;125:315–25
- Gordon M. The role of clobetasol propionate emollient 0.05% in the treatment of patients with dry, scaly, corticosteroid-responsive dermatoses. Clin Ther 2001;20:26–39
- Tsai J-C. Content and transdermal delivery of clobetasol 17-propionate from commercial creams and ointments. J Food Drug Anal 2001;10:7–12
- Yawalkar S, Wiesenberg-Boettcher I, Gibson J, et al. Dermatopharmacologic investigations of halobetasol propionate in comparison with clobetasol 17-propionate. J Am Acad Dermatol 1991;25:1137–44
- Feldman S. Relative efficacy and interchangeability of various clobetasol propionate vehicles in the management of steroid-responsive dermatoses. Curr Ther Res 2005;66:154–71
- Hull C, McKenough M, Sebastian K, et al. Valacyclovir and topical clobetasol gel for the episodic treatment of herpes labialis: a patient-initiated, double-blind, placebo-controlled trial. J Eur Acad Dermatol Venereol 2009;23:263--7
- Senyigit T, Sonvico F, Barbieri S, et al. Lecithin/chitosan nanoparticles of clobetasol 17-propionate capable of accumulation in pig skin. J Control Release 2009;142:368--73
- Mauger J, Chilko D, Howard S. On the analysis of dissolution data. Drug Dev Ind Pharm 1986;12:969–92
- Polli J, Rekhi G, Augsburger L, Shah V. Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets. J Pharm Sci 1997;86:690–700
- Costa P, Sousa Lobo J. Modeling and comparison of dissolution profiles. Eur J Pharm Sci 2001;13:123–33
- Costa P. An alternative method to the evaluation of similarity factor in dissolution testing. Int J Pharm 2001;220:77–83
- Dissolution Testing of Immediate Release Solid Oral Dosage Forms; Guidance for Industry; Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Washington, DC: U.S. Government Printing Office; 1997
- Gohel M, Panchal C. Novel use of similarity factors f2 and Sd for the development of diltiazem HCl modified-release tablets using a 32 factorial design. Drug Dev Ind Pharm 2002;28:77–87
- Sharma R, Walker R, Pathak K. Evaluation of the kinetics and mechanism of drug release from econazole nitrate nanosponge loaded carbapol hydrogen. Indian J Pharm Educ Res 2011;45:25–31
- Tan I, Ahmad A, Hameed B. Preparation of activated carbon from coconut husk: optimization study on removal of 2,4,6-trichlorophenol using response surface methodology. J Hard Mater 2008;153:709–17
- Ahuja M, Yadav M, Kumar S. Application of response surface methodology to formulation of ionotropically gelled gum cordial/gellan beads. Carbohydr Polym 2010;80:161–7
- Deyhimi F, Salamat-Ahangari R, Arabieth M, Parvin L. Application of response surface methodology for modelling the enzymatic assay of hydrogen peroxide by Emerson-Trinder reaction using 4-iodophenol. Int J Environ Anal Chem 2006;86:1151–63