Published by Scholars' Press Mrz 2021, 2021
ISBN 10: 6138933605 ISBN 13: 9786138933601
Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Aceclofenac can be successfully designed in tablets as sustained release formulation using melt granulation technique. The present study has demonstrated that stearic acid could be successfully employed as a meltable binder. It is worthy of mentioning that for controlling the release of poorly water-soluble drugs, the method is still advantageous.The prepared Aceclofenac compressed tablets were tested for weight variation, content uniformity, friability, tablet thickness and drug content and all the parameters were found to be within the Pharmacopoeial limits. In vitro drug dissolution tests were performed and dissolution profile of the selected batch was matched with that of standard release profile suggested by USP. Hence, the formulation was selected as optimized formulation. The tablets were further evaluated for studying the effect of storage temperature and pH on drug release. The release profiles show no significant difference in drug releases. This confirms the prepared tablets were robust. 72 pp. Englisch.
Published by Nirali Prakashan, 2018
Seller: dsmbooks, Liverpool, United Kingdom
Paperback. Condition: New. New. book.
Published by Scholars' Press, 2021
ISBN 10: 6138933605 ISBN 13: 9786138933601
Seller: AHA-BUCH GmbH, Einbeck, Germany
Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Aceclofenac can be successfully designed in tablets as sustained release formulation using melt granulation technique. The present study has demonstrated that stearic acid could be successfully employed as a meltable binder. It is worthy of mentioning that for controlling the release of poorly water-soluble drugs, the method is still advantageous.The prepared Aceclofenac compressed tablets were tested for weight variation, content uniformity, friability, tablet thickness and drug content and all the parameters were found to be within the Pharmacopoeial limits. In vitro drug dissolution tests were performed and dissolution profile of the selected batch was matched with that of standard release profile suggested by USP. Hence, the formulation was selected as optimized formulation. The tablets were further evaluated for studying the effect of storage temperature and pH on drug release. The release profiles show no significant difference in drug releases. This confirms the prepared tablets were robust.
Published by Scholars\' Press, 2021
ISBN 10: 6138933605 ISBN 13: 9786138933601
Seller: moluna, Greven, Germany
Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Sudke SureshProf.(Dr.) Suresh G. SudkeGaurishankar Education society, Satara college of pharmacy, Satara (Maharashtra) Prof.M.R.BhiseDr.Rajendra Gode college of Pharmacy, Malkapur (Maharashtra) Prof.Pramod V.BurakleDr.Rajendra Gode c.