Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/572338
Title: Formulation and Characterization of Bilayer Tablets of Gliclazide as Sustained Release and Sitagliptin as Immediate Release
Researcher: Rubina Reichal C
Guide(s): Gopal Rao M and Bagyalakshmi J
Keywords: Bilayer Tablets
Characterization
Formulation
Gliclazide
Immediate Release
Sitagliptin
Sustained Release
University: The Tamil Nadu Dr. M.G.R. Medical University
Completed Date: 2016
Abstract: Sitagliptin Phosphate and Gliclazide are selected based on the literature survey. The drugs are useful in the management of Type-2 Diabetes Mellitus. The results of FTIR study and DSC study confirmed that there is no chemical interaction or no incompatibility between the drugs and excipients. The values of Angle of Repose, Bulk Density, Tapped Bulk Density, Carr s Index and Hausner s, ratio were found to be within the pharmacopoeial limit. The granules of all formulations (F1S-F6S) and (F1G-F6G) have excellent flow properties and were suitable for compression. The Immediate release tablets of Sitagliptin Phosphate were successfully prepared by wet granulation method using various proportions and combinations of superdisintegrants. Gliclazide is poorly water soluble drug. For increasing the solubility and dissolution behavior, Gliclazide was prepared as solid dispersion with B-Cyclodextrin (1:5) ratio. Gliclazide sustained release tablets were prepared by the wet granulation method with solid dispersion of Gliclazide B CD; (1:5) using different concentrations of rate controlling polymer HPMC K4 MCR and other tableting excipients. For all the formulations, the Postcompression evaluation results of Friability, Hardness, Drug content uniformity and Weight variation were within pharmacopoeial limit. Among all the IR tablets of Sitagliptin Phosphate, F6S was selected, because it showed quick disintegration and higher amount of drug released 100.64% within 30 minutes. In Gliclazide SR trial tablets, the in vitro results FSG showed that the highest % of drug release (maximum release 85% at 12 hrs) than other batches. Hence, F5G was selected for bilayer formulation. The bilayer tablet (FBS6G5) was developed with the selected formulation of Sitagliptin IR (F6S) and Gliclazide SR (F5G) tablets. The results of post compression evaluation of the optimized bilayer tablets were within the pharmacopoeial limit. newline
Pagination: 216
URI: http://hdl.handle.net/10603/572338
Appears in Departments:Department of Pharmacy

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02_prelim pages.pdf2.83 MBAdobe PDFView/Open
03_content.pdf618.91 kBAdobe PDFView/Open
05_chapter 1.pdf2.64 MBAdobe PDFView/Open
06_chapter 2.pdf951.11 kBAdobe PDFView/Open
07_chapter 3.pdf4.79 MBAdobe PDFView/Open
08_chapter 4.pdf496.86 kBAdobe PDFView/Open
09_chapter 5.pdf3.52 MBAdobe PDFView/Open
10_annexures.pdf6.36 MBAdobe PDFView/Open
10_chapter 6.pdf954.85 kBAdobe PDFView/Open
11_chapter 7.pdf5.89 MBAdobe PDFView/Open
12_chapter 8.pdf7.74 MBAdobe PDFView/Open
13_chapter 9.pdf2.59 MBAdobe PDFView/Open
80_recommendation.pdf1.55 MBAdobe PDFView/Open
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