Zobrazeno 1 - 10
of 65
pro vyhledávání: '"S Selvamuthukumar"'
Publikováno v:
PLoS ONE, Vol 19, Iss 9, p e0310492 (2024)
Liposils, synthesized via the liposome templating method, offer a promising strategy for enhancing liposome stability by employing a silica coating. This study focuses on the development of nanocarriers utilizing silica-coated nanoliposomes for encap
Externí odkaz:
https://doaj.org/article/dcf6f32b9f0a420fbcf25c291f3268f8
Publikováno v:
Polymers; Volume 14; Issue 18; Pages: 3886
The main aim of this study was to optimize the formulation and process variables for the preparation of ibrutinib nanoliposomes and to evaluate the stability of nanoliposomes. The influence of four formulations and process parameters, namely, the pho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec1f3255acd97cf65b641650fa435f9
Akademický článek
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Akademický článek
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Publikováno v:
International Journal of Pharmaceutical Investigation. 10:279-285
Objectives: The present systematic research is to design, develop clarithromycin nasal mucoadhesive microspheres for the utilisation in respiratory tract infection as alternative route of drug delivery. Methods: Current study designed to formulate, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acac390566283f2e03b7e06244c2008b
https://doi.org/10.5530/ijpi.2020.3.51
https://doi.org/10.5530/ijpi.2020.3.51
Publikováno v:
Current drug delivery.
Purpose: To formulate and characterize tablets containing Pitavastatin that has been loaded with a self-nano emulsifying drug delivery system (SNEDDS). Methods: Pitavastatin SNEDDS were prepared with a variety of oils, surfactants, co-surfactants, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4f710b7a71acf41afef2c84c4b76f8
https://pubmed.ncbi.nlm.nih.gov/35585816
https://pubmed.ncbi.nlm.nih.gov/35585816
Publikováno v:
Journal of Drug Delivery Science and Technology. 52:55-64
The present study aims at the design of the transdermal co-delivery of curcumin (CUR) and resveratrol (RES) using cyclodextrin nanosponge based hydrogel. Cyclodextrin-based nanosponges (CDNS) were prepared by crosslinking cyclodextrin using pyromelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d1aa8d802dd08693845e9041d94b234
https://doi.org/10.1016/j.jddst.2019.04.025
https://doi.org/10.1016/j.jddst.2019.04.025
Publikováno v:
Current Computer-Aided Drug Design. 16
The article for the journal "Current Computer-Aided Drug Design" has been removed by the Publisher due to acute language inconsistencies and grammatical errors. Bentham Science apologizes to the readers of the journal for any inconvenience this may c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4efda8889a592fdbcec2579edb0672d
https://doi.org/10.2174/1573409916666201224153414
https://doi.org/10.2174/1573409916666201224153414
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 92:261-272
The purpose of the study was to explore the effect of different type of crosslinked cyclodextrins for the delivery of poorly soluble, photosensitive drug, resveratrol. Crosslinkers, diphenyl carbonate and pyromellitic dianhydride were used to prepare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f56d2445934363b91f53879187df37
https://doi.org/10.1007/s10847-018-0843-8
https://doi.org/10.1007/s10847-018-0843-8
Publikováno v:
Journal of Drug Delivery Science and Technology. 45:45-53
Curcumin (CUR) is a poorly water-soluble and photoreactive drug having potent anticancer activity. The purpose of the study is to fabricate cyclodextrin nanosponges, for the delivery of curcumin using two crosslinkers, diphenyl carbonate (DPC) and py
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad929c74396da64b2ea6282f506abd16
https://doi.org/10.1016/j.jddst.2018.03.004
https://doi.org/10.1016/j.jddst.2018.03.004