Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/447635
Title: Implementation of Quality by design in formulation and development
Researcher: Desai, Nilesh Shirish
Guide(s): Purohit, Ravindra
Keywords: Clinical Pre Clinical and Health
Quality Assurance Techniques
University: Bharati Vidyapeeth Deemed University
Completed Date: 2019
Abstract: Quality by Design (QbD) concept for formulation development has been recently newlineimplemented by USFDA and it is being brought into practice worldwide gradually. newlineThe elements of QbD are still not very well understood and are going through scrutiny newlineby all major researchers, research institutes and industry. However, there is no dispute newlineon the fact that the QbD approach, if planned judiciously and followed appropriately newlineshall result in a robust product. In the current work, we have attempted to use the newlinebasic principles of QbD for the development of new formulations. newlineWe decided to develop various novel formulations of Clopidogrel bisulfate (CLB). newlineCLB is a potent antiplatelet agent that reduces the risk for thrombotic events in newlinepatients with atherothrombotic diseases. The anti-thrombotic activity of this drug newlinemakes it a potential candidate for being developed as a delayed release formulation. newlineSo that effective plasma concentrations of the drug can be achieved and maintained at newlineall times, including the early morning hours, when there are highest chances of heart newlineattack. Following is the summary of the current work newline8.1.1. Pre-formulation Studies newlinePre-formulation studies were carried out for CLB as well as all potential excipients, to newlineget an idea about their physical and chemical properties. Various analytical techniques newlinewere used for characterization and they included DSC, FTIR, HPLC and so on. CLB newlineexhibited good flow properties and good solubility in 0.1 N HCl, so this medium was newlinechosen for dissolution studies. All potential excipients were checked for their newlinecompatibility with CLB and it was found compatible. The risk assessment was carried newlineout to assess impact of CLB and excipients over formulation development.The pre-formulation studies revealed that CLB is stable in acidic pH, poorly soluble newlinein alkaline pH and has a narrow absorption window. Based on these findings, it was newlinespeculated that, CLB could be designed to remain in the stomach for more time and newlinethus be formulated into gastroretentive systems. newline newline
Pagination: All Pages
URI: http://hdl.handle.net/10603/447635
Appears in Departments:Faculty of Pharmaceutical Sciences

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02_prelim pages.pdf2.15 MBAdobe PDFView/Open
03_contents.pdf.pdf437.96 kBAdobe PDFView/Open
04_abstract.pdf130.65 kBAdobe PDFView/Open
05_chapter1.pdf.pdf1.08 MBAdobe PDFView/Open
06_chapter2.pdf.pdf365.69 kBAdobe PDFView/Open
07_chapter3.pdf.pdf418.26 kBAdobe PDFView/Open
08_chapter4.pdf.pdf1.44 MBAdobe PDFView/Open
09_chapter5.pdf.pdf1.02 MBAdobe PDFView/Open
10_chapter6.pdf.pdf1.65 MBAdobe PDFView/Open
11_chapter7.pdf.pdf1.8 MBAdobe PDFView/Open
80_recommendation.pdf604.41 kBAdobe PDFView/Open
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