Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/15220
Title: Novel strategies in formulation development And evaluation of dispersible tablets
Researcher: Chinmay Anand
Guide(s): G. Vidyasagar
Keywords: Pharmaceutical Sciences
Upload Date: 20-Jan-2014
University: Shri Jagdishprasad Jhabarmal Tibarewala University
Completed Date: 02-08-2013
Abstract: The basic aim behind development of any drug delivery system (DDS) is to achieve a safe and effective therapy for the human being. The dispersible tablet provides a utility dosage form, reducing the need for multiple formulations of the same drug. The novel concept of Rapid dispersible drug delivery system emerged from the desire to provide patient with conventional mean of taking their medication. In recent days major concentration for development work is laid down on the development of organoleptically elegant such as good in taste and patient friendly drug delivery system for the usage of pediatric and geriatric patients. The greater bioavailability of a drug from Rapid dispersible and or dissolving formulations also make it preferable dose as compare to conventional oral dosage forms. newline newlineThe main aim of this study is to develop new concept for the formulation of rapid dispersible tablets or Fast dissolving tablets using novel concepts such as solubility enhancement of active for fast and better release of drug to achieve better bioavailability of active in vivo, taste masking of active with various techniques to improve organoleptic properties and patience compliance. The design of formulation was basically developed for the pediatric and geriatric patients. Paracetamol and Tolfenamic Acid were used as model drugs in formulation study. The present study is an attempt towards application of some novel concepts in formulation of Rapid Dispersible Tablets. On the basis of preformulation study and characterization of active, development of rapid dispersible tablets of Tolfenamic acid initiated with concept of co-micronization with diluents requires. The rapid release of formulation was the basic behind the experimental study. Optimization of formulation parameters was completed to achieve the balance between various physical properties such as disintegration and dispersion time and analytical properties such as release profile of tablets. newline newline
Pagination: 
URI: http://hdl.handle.net/10603/15220
Appears in Departments:Faculty of Pharmacy

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01_title.pdfAttached File28.22 kBAdobe PDFView/Open
02_declaration.pdf5.17 kBAdobe PDFView/Open
03_certificate.pdf18.5 kBAdobe PDFView/Open
04_acknowledgement.pdf6.69 kBAdobe PDFView/Open
05_contents.pdf19.96 kBAdobe PDFView/Open
06_list of tables.pdf18.7 kBAdobe PDFView/Open
07_list of figures.pdf12.14 kBAdobe PDFView/Open
08_list of graphs.pdf15.66 kBAdobe PDFView/Open
09_list of abbreviations.pdf15.71 kBAdobe PDFView/Open
10_abstracts.pdf47.58 kBAdobe PDFView/Open
11_chapter - 1.pdf215.97 kBAdobe PDFView/Open
12_chapter - 2.pdf71.93 kBAdobe PDFView/Open
13_chapter - 3.pdf1.44 MBAdobe PDFView/Open
14_chapter - 4.pdf297.67 kBAdobe PDFView/Open
15_chapter - 5.pdf177.87 kBAdobe PDFView/Open
16_chapter - 6.pdf682.09 kBAdobe PDFView/Open
17_chapter - 7.pdf2.24 MBAdobe PDFView/Open
18_chapter - 8.pdf71.95 kBAdobe PDFView/Open
19_references.pdf92.55 kBAdobe PDFView/Open
20_annexure.pdf39.87 kBAdobe PDFView/Open
21_annexure-1.pdf43.45 kBAdobe PDFView/Open
22_annexure-2.pdf67.22 kBAdobe PDFView/Open
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