A discriminatory and biorelevant dissolution test method for simvastatin drug products

Dissolution Technologies

Volumn 16, Issue 4, 2009, Pages 11-13

  Singla, N ^a   Gupta, G D ^b   Kohli, K ^c   Singla, A K ^d  

^a Institute of Pharmacy   (India)

^b Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy   (India)

^c HAMDARD UNIVERSITY   (India)

^d RANBAXY RESEARCH LABORATORIES   (India)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 71649102288     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT160409P11     Document Type: Article

References (9)

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4. Hörter, D.; Dressman, J. B. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. Adv. Drug Deliver. Rev. 2001, 46, 75-87.
5. Shah, V. P.; Konecny, J. J.; Everett, R. L.; McCullough, B.; Noorizadeh, A. C.; Skelly, J. P. In vitro dissolution profile of water-insoluble drug dosage forms in the presence of surfactants. Pharm. Res. 1989, 6, 612-618.
6. Zhao, F.; Malayev, V.; Rao, V.; Hussain, M. Effect of SLS in dissolution media on dissolution of hard gelatin capsule shells. Pharm. Res. 2004, 21 (1), 144-148.
7. Noory, C.; Tran, N.; Ouderkirk, L.; Shah, V. Steps for development of a dissolution test for sparingly water-soluble drug products. Dissolution Technol. 2000, 7 (1), 16-21.
8. Aburub, A.; Risley, D. S.; Mishra, D. A critical evaluation of fasted state simulating gastric fluid (FaSSGF) that contain sodium lauryl sulfate and proposal of a modified recipe. Int. J. Pharm. 2007, 347, 16-22.
9. Simvaststin Tablets Monograph. In United States Pharmacopeia and National Formulary USP 32-NF 27; The United States Pharmacopeial Convention, Inc.: Rockville, MD, 2009; p 3558.