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Drug Development and Industrial Pharmacy Volume 21, 1995 - Issue 7
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Research Article

Degradation Rates of Captopril in Aqueous Medium Through Buffer-Catalysis Oxidation

David Chen Drug Delivery, Pharmaceutical R & D Laboratories, Development Center for Biotechnology, 81 Chang Hsing Street, Taipei, Taiwan
,
Huilan Chen Drug Delivery, Pharmaceutical R & D Laboratories, Development Center for Biotechnology, 81 Chang Hsing Street, Taipei, Taiwan
&
Hao Ku Drug Delivery, Pharmaceutical R & D Laboratories, Development Center for Biotechnology, 81 Chang Hsing Street, Taipei, Taiwan
Pages 781-792 | Published online: 20 Oct 2008

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Asim Sattwa Mandal, Sugata Chatterjee, Kazi Masud Karim, Nikhil Biswas, Arijit Guha, Mamata Behera & Ketousetuo Kuotsu. (2012) Fabrication and in vitro evaluation of bidirectional release and stability studies of mucoadhesive donut-shaped captopril tablets. Drug Development and Industrial Pharmacy 38:6, pages 706-717.
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Articles from other publishers (2)

M.A Khan, S.V Sastry, S.R Vaithiyalingam, V Agarwal, S Nazzal & I.K Reddy. (2000) Captopril gastrointestinal therapeutic system coated with cellulose acetate pseudolatex: evaluation of main effects of several formulation variables. International Journal of Pharmaceutics 193:2, pages 147-156.
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J. Liu, S. Y. Chan & P. C. Ho. (1999) Effects of sucrose, citric buffer and glucose oxidase on the stability of captopril in liquid formulations. Journal of Clinical Pharmacy and Therapeutics 24:2, pages 145-150.
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