Transcription of Development and validation of dissolution method for ...
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*Correspondence: Shah Riteshkumar R. Department of Pharmaceutics, Maliba Pharmacy College, Bardoli Mahuva Road, Dist- Surat -394 350 - State Guja-rat, India. E-mail: Journal of Pharmaceutical Sciencesvol. 47, n. 4, , 2011 Development and validation of dissolution method for carvedilol compression-coated tabletsRitesh Shah*, Sachin Patel, Hetal Patel, Sonia Pandey, Shailesh Shah, Dinesh ShahDepartment of Pharmaceutics, Maliba Pharmacy College, Bardoli, Surat, Gujarat, IndiaThe present study describes the Development and validation of a dissolution method for carvedilol compression-coated tablets. dissolution test was performed using a TDT-06T dissolution apparatus. Based on the physiological conditions of the body, hydrochloric acid was used as dissolution medium and release was monitored for 2 hours to verify the immediate release pattern of the drug in acidic pH, followed by pH in citric-phosphate buffer for 22 hours, to simulate a sustained release pattern in the intestine.
Development and validation of dissolution method for carvedilol compression-coated tablets 901 dissolution medium in a 25 ml volumetric flask and then
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Analytical Method Selection for Drug Product Dissolution, Dissolution, Method Validation in Pharmaceutical Analysis, Drug Product, Drug, And Quality by Design exemplified, Product, For drug, Dissolution Method Development for Immediate Release, ANALYTICAL METHOD, CHROMATOGRAPHIC METHOD FOR THE ESTIMATION, Guidelines on good manufacturing practices, TPI 2015; 4(5): 14-20, PHARMACEUTICAL DEVELOPMENT FOR, PHARMACEUTICAL DEVELOPMENT FOR MULTISOURCE (GENERIC) PHARMACEUTICAL