Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/19041
Title: Design and Evaluation of Floating Dosage Forms as Controlled Release Modules
Researcher: Dasari, Varun
Guide(s): Rao , Chandu Babu
Mukkanti,K
Keywords: Controlled
Design
Dosage
Evaluation
Floating
Modules
Upload Date: 9-Jun-2014
University: Jawaharlal Nehru Technological University, Hyderabad
Completed Date: 2012
Abstract: Human immunodeficiency virus (HIV) infection and acquired immune deficiency syndrome (AIDS), commonly referred to as HIV/AIDS, constitute one of the most serious infectious disease challenges to public health globally, and has had a crippling effect in certain parts of the world. There are currently 33.2 million people living with HIV/AIDS globally. newlineThe people suffering with HIV infection need to take more number of drugs with repeated administration. This is because of the structural changes of the viral gene inside the cell and less biological half lives of these drugs. This causes the patient non compliance and some time may lead to the severe adverse affects. Sustaining the drug release of these drugs may improve the patient compliance, reduce the plasma drug fluctuations and limit the adverse reactions. newlineIn the present study five anti retroviral drugs such as Stavudine, lamivudine, Lopinavir, Ritonavir and Valganciclovir were selected to develop the extended release formulations using various rate controlled polymers such as Lipoidal carriers, Methylacrylates and Polyethylene oxides. newlineIn the present proposed work lipid based controlled release dosage forms of selected antiretro viral drugs are designed employing novel floating system technology. The hydrodynamically balanced systems without the effervescent components are designed and compared with effervescent systems. Both single and multi unit dosage forms are designed and evaluated for the desired parameters. Different polymers and polymer combinations are employed with various Lipoidal excipients differing in their hydrophilic and lipophilic properties to evaluate their suitability for floating systems.
Pagination: 363 p.
URI: http://hdl.handle.net/10603/19041
Appears in Departments:Faculty of Pharmaceutical Sciences

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01_title.pdfAttached File154.13 kBAdobe PDFView/Open
02_certificate.pdf221.5 kBAdobe PDFView/Open
03_acknowledgement.pdf275.51 kBAdobe PDFView/Open
04_acknowledgement.pdf275.51 kBAdobe PDFView/Open
05_abstract.pdf160.93 kBAdobe PDFView/Open
06_contents.pdf469.75 kBAdobe PDFView/Open
07_list of tables & figures.pdf489.05 kBAdobe PDFView/Open
08_list of publication.pdf223.72 kBAdobe PDFView/Open
09_aim,scope and invitigation.pdf250.21 kBAdobe PDFView/Open
10_chapter 1.pdf605.34 kBAdobe PDFView/Open
11_chapter 2.pdf613.3 kBAdobe PDFView/Open
12_chapter 3.pdf397.8 kBAdobe PDFView/Open
13_chapter 4.pdf2 MBAdobe PDFView/Open
15_chapter 6.pdf2.15 MBAdobe PDFView/Open
16_chapter 7.pdf1.41 MBAdobe PDFView/Open
17_chapter 8.pdf739.91 kBAdobe PDFView/Open
18_chapter 9.pdf836.06 kBAdobe PDFView/Open
19_chapter 10.pdf329.02 kBAdobe PDFView/Open
20_references.pdf391.18 kBAdobe PDFView/Open


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