Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Swati C. Jagdale"'
Autor:
Priyanka S. Waghmare, Anuruddha R. Chabukswar, Kunal G. Raut, Bhagyashree Gaikwad-Pawar, Swati C. Jagdale
Publikováno v:
Exploration of Medicine, Vol 5, Iss 4, Pp 513-529 (2024)
The emergence and subsequent advancement of nanotechnology in recent years have greatly benefited the healthcare sector, particularly in the treatment of cancer. As per study, major fatalities are related to the lung cancer. For many years, oral tyro
Externí odkaz:
https://doaj.org/article/78ee4bae16f843b2b7a666939ae91d6c
Publikováno v:
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 35, Iss 1, Pp 29-39 (2014)
Drug-cyclodextrin complexes improve aqueous solubility and dissolution rate of poorly water-soluble drugs. Solubilisation followed by buccal delivery of poorly water-soluble drugs can be advantageous for increasing drug absorption. Darifenacin is
Externí odkaz:
https://doaj.org/article/b0386f0b9b0e46fc87c96c66c7e84956
Publikováno v:
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 33, Iss 1, Pp 83-94 (2012)
Clonazepam (CLZ) is an anticonvulsant benzodiazepine widely used in the treatment of epilepsy. CLZ is a BCS Class II drug and its bioavailability is thus dissolution limited. The objective of the present study was to prepare solid dispersions (SD
Externí odkaz:
https://doaj.org/article/53a33caad3f040db8403bd818acccd84
Publikováno v:
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 31, Iss 1, Pp 25-31 (2010)
Gabapentin is a high-dose drug widely used as an oral anti-epilepticagent. Due to high crystalline and has poor compaction properties it is difficult to form tablets by direct compression. The aim of this study was to develop gabapentin tablets, phar
Externí odkaz:
https://doaj.org/article/2b76f77929674d41b88fa75cfc7f105b
Publikováno v:
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 31, Iss 3 (2010)
The selection of a suitable superdisintegrant for a rapidly disintegrating dosage form is of the utmost importance, since disintegration time (DT) is a critical parameter. An experimental design was implemented, to find out the effects of superdisint
Externí odkaz:
https://doaj.org/article/00343a7bba064853b0f2dbbd4a47fc77
Autor:
Sunita Salunke Gawali, Kisan M. Kodam, Anurudhha Chabukswar, Savita R. Tapase, Digamber S Pawar, Vasant V. Chabukswar, Sabrina Dallavalle, Swati C. Jagdale, Pravin B Adhav, Balasaheb B Diwate
Publikováno v:
Medicinal Chemistry. 17:926-936
Background: Coumarins are naturally occurring biologically active heterocyclic molecules endowed with a wide range of biological properties, including antibacterial, antifungal, and antitumor activities. Objective: The present work aimed to synthesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baa674027290e1ef6d893f8f71e12424
https://doi.org/10.2174/1573406416666200817155056
https://doi.org/10.2174/1573406416666200817155056
Autor:
Rajesh Pawar, Swati C. Jagdale
Publikováno v:
Journal of Pharmaceutical Research International. :143-155
Aim: This research work was aimed to evaluate Metformin hydrochloride (MH) floating dosage form by In vitro evaluation/In vivo prediction and to evaluate it’s predictability through it’s application during the R&D using Insilico technique in WINO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9200b5927c8c8e5e859c6b710b3661da
https://doi.org/10.9734/jpri/2021/v33i40a32231
https://doi.org/10.9734/jpri/2021/v33i40a32231
Publikováno v:
Journal of Pharmaceutical Research International. :135-145
Background and Objective: Fluconazole (FLZ) is a novel triazole antifungistatic drug; topical administration of FLZ resulted in systemic absorption and skin inflammation, and thereby failed to achieve mycological eradication, resulting in low patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35ffbb52123909cbd7c10bd4482cc02d
https://doi.org/10.9734/jpri/2021/v33i38b32108
https://doi.org/10.9734/jpri/2021/v33i38b32108
Autor:
Swati C. Jagdale, Payal V Kothekar
Publikováno v:
Recent Patents on Anti-Infective Drug Discovery. 15:137-156
Aim:: To design controlled release topical delivery of mupirocin for the treatment of skin infection. Background:: Mupirocin is an antibacterial drug. Mupirocin works to kill the bacteria, which include strains of Staphylococcus aureus and Streptococ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c4d4f020d02277e3c6e474f6828cb17
https://doi.org/10.2174/1386207323999200819153404
https://doi.org/10.2174/1386207323999200819153404
Publikováno v:
International Journal of Pharmacy and Pharmaceutical Sciences. :62-71
Objective: The present study aimed to develop a new SR metformin hydrochloride (MH) gastroretentive formulation with novel excipient (NE), which has better floatation and can be prepared with more simple pharmaceutical techniques for the treatment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11a7ea63c11e0cf380146f396e0f19cc
https://doi.org/10.22159/ijpps.2020v12i10.38678
https://doi.org/10.22159/ijpps.2020v12i10.38678