Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/373093
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dc.coverage.spatialPress Coated Tablets
dc.date.accessioned2022-04-11T06:46:10Z-
dc.date.available2022-04-11T06:46:10Z-
dc.identifier.urihttp://hdl.handle.net/10603/373093-
dc.description.abstractThe primary goal of study is to establish whether compression coating used to produce tablets that provide maximal medication plasma concentration of Six to Eight hrs after an evening dose given around 22:00. The essential concept behind the to-be-developed dosage form is that coat of polymer should control medication release from core containing medicine. newlineHypertension, asthma, gastric ulcers, arthritis, and other diseases are affected by circadian rhythm of body. In rheumatoid arthritis, for example, pain normally increases in morning which reduces as day goes on. Cardiovascular illnesses like hypertension and angina, as good as chest pain, have a clear circadian pattern. newlineFast dispersible core tablets which contain Aceclofenac and Diltiazem Hydrochloride were prepared by using superdisintegrants such as Ac-Di-Sol, Crospovidone, and Sodium starch glycolate; assessed for a variety of parameters utilizing wet granulation process. The release of drug from interior core of the produced press-coated tablets is implicit to begin when outer shield is removed by dissolving or erosion of hydrophilic polymers on the core surfaces. As a result, the desired lag time should be achieved, which can be done by blending various viscosity grade polymers. A three-factor, two-level, complete factorial design was applied in optimization process. Independent factors were quantity of HPMC K4 M in coating (X1 in mg), HPMC K100 M (X2, mg), and amount of sodium alginate (X3 in mg), whereas dependent variables were lag time (Y1, minutes) and amount of drug released in 450 minutes. (Y2, percent) During dissolution test on optimized press coated formulation of Diltiazem hydrochloride and Aceclofenac, lag time was calculated. This demonstrated the expected lag time in various dissolution media and at various rational speeds. A comparative dissolution analysis of an improved formulation including Aceclofenac compared to formulations commercially available yielded positive results. newlineOverall, the findings imply that press coated tablets which con
dc.format.extent205p
dc.languageEnglish
dc.relation234b
dc.rightsuniversity
dc.titleDesign and Evaluation of Press Coated Tablets
dc.title.alternative
dc.creator.researcherJadhav Suryakant Bapurao
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.description.note
dc.contributor.guideKawtikwar, P. S. and Wadher, S. J.
dc.publisher.placeNanded
dc.publisher.universitySwami Ramanand Teerth Marathwada University
dc.publisher.institutionDepartment of Pharmacy
dc.date.registered2011
dc.date.completed2022
dc.date.awarded2022
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Pharmacy

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01_ title.pdfAttached File115.07 kBAdobe PDFView/Open
02_ certificates.pdf215.27 kBAdobe PDFView/Open
03_ abstract.pdf10.01 kBAdobe PDFView/Open
04_ declaration.pdf152.93 kBAdobe PDFView/Open
05_ acknowledgment.pdf300.49 kBAdobe PDFView/Open
06_ content.pdf155.22 kBAdobe PDFView/Open
07_ list of tables.pdf335.13 kBAdobe PDFView/Open
08_ list of figures.pdf277.77 kBAdobe PDFView/Open
09_ abbrevations.pdf145.4 kBAdobe PDFView/Open
10_ chapter 01.pdf711.39 kBAdobe PDFView/Open
11_ chapter 02.pdf424.56 kBAdobe PDFView/Open
12_ chapter 03.pdf268.08 kBAdobe PDFView/Open
13_ chapter 04.pdf147.95 kBAdobe PDFView/Open
14_ chapter 05.pdf646.44 kBAdobe PDFView/Open
15_ chapter 06.pdf788.17 kBAdobe PDFView/Open
16_ chapter 07.pdf7.48 MBAdobe PDFView/Open
17_ chapter 08.pdf408.75 kBAdobe PDFView/Open
18_ chapter 09.pdf612.55 kBAdobe PDFView/Open
80_recommendation.pdf361.96 kBAdobe PDFView/Open


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