D
Dipak K. Majumdar
Researcher at Delhi Institute of Pharmaceutical Sciences and Research
Publications - 81
Citations - 4313
Dipak K. Majumdar is an academic researcher from Delhi Institute of Pharmaceutical Sciences and Research. The author has contributed to research in topics: Self-healing hydrogels & Polyvinyl alcohol. The author has an hindex of 37, co-authored 81 publications receiving 3859 citations. Previous affiliations of Dipak K. Majumdar include University of Delhi & Apeejay Stya University.
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Eudragit®: a technology evaluation
TL;DR: In this review, the physicochemical characteristics and applications of different grades of Eudragit in colon-specific/enteric-coated/sustained release drug delivery and taste masking have been addressed.
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Preparation and characterization of polyvinyl alcohol-gelatin hydrogel membranes for biomedical applications.
TL;DR: The experimental results indicated that the hydrogels designed and developed by esterification of polyvinyl alcohol with gelatin could be tried for various biomedical applications and Hemocompatibility suggested that thehydrogel could be trying as wound dressing and as an implantable drug delivery system.
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Polymeric Hydrogels: Characterization and Biomedical Applications
TL;DR: Though far from extensive, this article has been devoted to study the common methods used for the characterization of the hydrogels and to review the range of applications of the same in health care.
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Topical Ocular Delivery of NSAIDs
TL;DR: Ocular penetration of NSAID demands an acidic ophthalmic solution where cyclodextrin could prevent precipitation of drug and minimize its ocular irritation potential, and the use of colloidal nanoparticle formulations and the potent COX 2 inhibitor bromfenac may enhance NSAID efficacy in eye preparations.
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Ketorolac entrapped in polymeric micelles: preparation, characterisation and ocular anti-inflammatory studies.
TL;DR: The formulation showed significant inhibition of lid closure up to 3 h and PMN migration up to 5 h compared to the suspension containing non-entrapped drug, which did not show any significant effect and the formulation was stable for 8-10 days at room temperature.