Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Srikanth Reddy Poreddy"'
Autor:
Nagaraju Ravouru, Rajeswari Surya Anusha Venna, Subhash Chandra Bose Penjuri, Saritha Damineni, Venkata Subbaiah Kotakadi, Srikanth Reddy Poreddy
Publikováno v:
Advanced Pharmaceutical Bulletin, Vol 8, Iss 3, Pp 419-427 (2018)
Purpose: The main aim of the present investigation was to enhance the solubility of poorly soluble Gliclazide by nanocrystallization. Methods: In present investigation gliclazide nanocrystals were prepared by sonoprecipitation using Pluronic F68, Pol
Externí odkaz:
https://doaj.org/article/5e9639944a81478e99132249923722f7
Autor:
Venkata Subbaiah Kotakadi, Rajeswari Surya Anusha Venna, Nagaraju Ravouru, Subhash Chandra Bose Penjuri, Saritha Damineni, Srikanth Reddy Poreddy
Publikováno v:
Advanced Pharmaceutical Bulletin
Advanced Pharmaceutical Bulletin, Vol 8, Iss 3, Pp 419-427 (2018)
Advanced Pharmaceutical Bulletin, Vol 8, Iss 3, Pp 419-427 (2018)
Purpose: The main aim of the present investigation was to enhance the solubility of poorly soluble Gliclazide by nanocrystallization. Methods: In present investigation gliclazide nanocrystals were prepared by sonoprecipitation using Pluronic F68, Pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c8e491f9847ff4420930fe20cb742e9
http://europepmc.org/articles/PMC6156478
http://europepmc.org/articles/PMC6156478
Publikováno v:
Turkish Journal of Pharmaceutical Sciences, Vol 14, Iss 2, Pp 108-119 (2017)
Turkish Journal of Pharmaceutical Sciences
Turkish Journal of Pharmaceutical Sciences
Objectives: The objective of the present study was to enhance the solubility, dissolution and hence anti-inflammatory activity of poorly soluble drug indomethacin (IMN) by formulating into self emulsifying systems. Materials and Methods: Self emulsif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c72272fe150c9d0b5a8da4083b04686d
https://doi.org/10.4274/tjps.60352
https://doi.org/10.4274/tjps.60352
Publikováno v:
Recent Patents on Drug Delivery & Formulation. 10:235-244
Background: The objective of this investigation was to develop a self emulsifying drug delivery system (SEDDS) of naproxen, a poorly water soluble drug, which could improve its solubility and oral bioavailability. Methods: The recent patents on SEDDS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe58b40ccfbcce8269061e18302c0389
https://doi.org/10.2174/1872211310666161020095721
https://doi.org/10.2174/1872211310666161020095721
Autor:
Saritha Damineni, Sailakshmi Bns, Srikanth Reddy Poreddy, Nagaraju Ravouru, Subhash Chandra Bose Penjuri
Publikováno v:
Turkish Journal of Pharmaceutical Sciences, Vol 13, Iss 3, Pp 304-310 (2016)
Lansoprazole is proton pump inhibitor which extensively degraded in acidic pH conditions. Lansoprazole loaded nanosponges were prepared by Emulsion solvent diffusion method using ethylcellulose, PVA and pluronic F-68 and dichloromethane as a solvent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63b41703916a8c9d75feff6ffc03d2a6
https://doi.org/10.4274/tjps.2016.04
https://doi.org/10.4274/tjps.2016.04
Autor:
Saritha Damineni, Subhash Chandra Bose Penjuri, Nagaraju Ravouru, Srikanth Reddy Poreddy, Raja Lakshmi Muni
Publikováno v:
Turkish Journal of Pharmaceutical Sciences, Vol 15, Iss 1, Pp 7-15 (2018)
Turkish Journal of Pharmaceutical Sciences
Turkish Journal of Pharmaceutical Sciences
Objectives: Ibuprofen, an anti-inflammatory drug, is characterized by poor water solubility, which limits its pharmacologic effects. The present work aimed to the study the effect of agglomeration on the micromeritic properties and dissolution of ibu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4595625241d74d0bcedc94a004336741
https://doi.org/10.4274/tjps.09609
https://doi.org/10.4274/tjps.09609
Publikováno v:
Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti. 66(1)
The goal of the present study was to develop a self-emulsifying drug delivery system for the oral poorly water-soluble drug ibuprofen and to evaluate its oral bioavailability. Phase diagrams were constructed to determine the phase behaviour of the mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6862f10fd02f1eb653fcb0024d9113f2
https://pubmed.ncbi.nlm.nih.gov/28569515
https://pubmed.ncbi.nlm.nih.gov/28569515