FORMULATION AND COMPARATIVE EVALUATION OF ONDANSETR ON HYDROCHLORIDE MOUTH DISSOLVING TABLETS IN INDIA (Record no. 11134)

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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200210105126.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200210b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12044
Author Abdul Raheem T.
245 ## - TITLE STATEMENT
Title FORMULATION AND COMPARATIVE EVALUATION OF ONDANSETR ON HYDROCHLORIDE MOUTH DISSOLVING TABLETS IN INDIA
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(9)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. Innovare Academic Sciences Pvt Ltd
Year 2019
300 ## - PHYSICAL DESCRIPTION
Pagination 57-64p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective: <br/>The aim of the present study was to prepare the ond<br/>ansetron hydrochloride Mouth Dissolving Tablets (MD<br/>Ts) followed by its <br/>comparison with ethical and non-ethical (generic) m<br/>arketed tablets. <br/>Methods: <br/>Prior to the formulation, drug excipient compatibil<br/>ity study was carried out by FTIR spectroscopy. The<br/> λ<br/>max <br/>was determined by UV <br/>spectroscopy. The ondansetron hydrochloride MDTs we<br/>re prepared by direct compression method using Sodi<br/>um Starch Glycolate (SSG) as super <br/>disintegrant and camphor as a sublimating agent. Th<br/>en the prepared MDTs were subjected to evaluation o<br/>f post compression parameters such as <br/>thickness and diameter, weight variation, wetting t<br/>ime, hardness, friability, disintegration and disso<br/>lution. The results obtained were compared <br/>with that of ethical and non-ethical marketed ondan<br/>setron hydrochloride 4 mg tablets. <br/>Results: <br/>The λ<br/>max <br/>was found at 310 nm. FTIR<br/>study revealed that excipients used in the prepared<br/> formulations are compatible with the drug. The <br/>thickness and diameter was in the range of 2.646 to<br/> 3.27 mm and 6.0 to 8.12 mm, respectively. Friabili<br/>ty was in the range of 0.43 to 0.88 % and had <br/>a slightly higher friability (1.27%) for sublimated<br/> tablets. Wetting time and disintegration time were<br/> in the range of 15 to 40 sec and 23 to 50 sec, <br/>respectively. The 100 % drug release was found with<br/>in 180 sec for all the codes. These results were th<br/>en compared with non-ethical film coated <br/>ondansetron marketed tablets. <br/>Conclusion: <br/>Ondansetron hydrochloride MDT 4 mg tablets prepared<br/> in the laboratory were under specified IP limits. <br/>The experimental findings <br/>demonstrated that any of these ethical and non-ethi<br/>cal tablets of ondansetron hydrochloride can be sel<br/>ected, advised by the physician or <br/>pharmacist, as per the patient’s need and economica<br/>l status.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 12045
Co-Author Singh, Ranjeet
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
International Standard Serial Number 2656-0097
Title International journal of pharmacy and pharmaceutical science
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/33840/20641
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 10/02/2020   2020874 10/02/2020 10/02/2020 Articles Abstract Database
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