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http://hdl.handle.net/10603/373093
Title: | Design and Evaluation of Press Coated Tablets |
Researcher: | Jadhav Suryakant Bapurao |
Guide(s): | Kawtikwar, P. S. and Wadher, S. J. |
Keywords: | Clinical Pre Clinical and Health Pharmacology and Pharmacy Pharmacology and Toxicology |
University: | Swami Ramanand Teerth Marathwada University |
Completed Date: | 2022 |
Abstract: | The 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 |
Pagination: | 205p |
URI: | http://hdl.handle.net/10603/373093 |
Appears in Departments: | Department of Pharmacy |
Files in This Item:
File | Description | Size | Format | |
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01_ title.pdf | Attached File | 115.07 kB | Adobe PDF | View/Open |
02_ certificates.pdf | 215.27 kB | Adobe PDF | View/Open | |
03_ abstract.pdf | 10.01 kB | Adobe PDF | View/Open | |
04_ declaration.pdf | 152.93 kB | Adobe PDF | View/Open | |
05_ acknowledgment.pdf | 300.49 kB | Adobe PDF | View/Open | |
06_ content.pdf | 155.22 kB | Adobe PDF | View/Open | |
07_ list of tables.pdf | 335.13 kB | Adobe PDF | View/Open | |
08_ list of figures.pdf | 277.77 kB | Adobe PDF | View/Open | |
09_ abbrevations.pdf | 145.4 kB | Adobe PDF | View/Open | |
10_ chapter 01.pdf | 711.39 kB | Adobe PDF | View/Open | |
11_ chapter 02.pdf | 424.56 kB | Adobe PDF | View/Open | |
12_ chapter 03.pdf | 268.08 kB | Adobe PDF | View/Open | |
13_ chapter 04.pdf | 147.95 kB | Adobe PDF | View/Open | |
14_ chapter 05.pdf | 646.44 kB | Adobe PDF | View/Open | |
15_ chapter 06.pdf | 788.17 kB | Adobe PDF | View/Open | |
16_ chapter 07.pdf | 7.48 MB | Adobe PDF | View/Open | |
17_ chapter 08.pdf | 408.75 kB | Adobe PDF | View/Open | |
18_ chapter 09.pdf | 612.55 kB | Adobe PDF | View/Open | |
80_recommendation.pdf | 361.96 kB | Adobe PDF | View/Open |
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