Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Yogesh Pore"'
Autor:
Priyanka Jadhav, Yogesh Pore
Publikováno v:
Bulletin of Faculty of Pharmacy Cairo University, Vol 55, Iss 1, Pp 147-154 (2017)
The interactions of poorly aqueous soluble endothelin receptor antagonist bosentan (BOS) with hydroxypropyl-β-cyclodextrin (HPβCD) were assessed in presence and absence of an amino acid l-arginine (ARG), to improve its physicochemical properties. I
Externí odkaz:
https://doaj.org/article/40ce97679af74bee91aad95417c602e3
Autor:
Sarika Sapte, Yogesh Pore
Publikováno v:
Journal of Pharmaceutical Analysis, Vol 6, Iss 5, Pp 300-306 (2016)
The inclusion complexes of poorly water-soluble cephalosporin, cefuroxime axetil (CFA), were prepared with β-cyclodextrin (βCD) with or without addition of l-arginine (ARG) to improve its physicochemical properties. We also investigated the effect
Externí odkaz:
https://doaj.org/article/288913fccda24961b8bd73fd633033d8
Autor:
George Chumburidze, E. Vijaya Sekhar, Tochukwu Uzoma Apugo-Nwosu, Ramaz Katsarava, Tofik Nagiev, Felix Osarumhense Aguele, Justice Agbonayinma Idiaghe, Keisham Surjit Singh, Luis J. del Valle, Nehad M. Gumgumji, S. Hema, Ranbir Kaur, Manisha Bansal, Yogesh Pore, Anand Mohan Jha, Sajal Kundu, Aisha M. Turkustani, Angélica Díaz, Milind Ubale, B.K. Sagar, Priyanka H. Jadhav, Vishwa Deepak Tripathi, María Teresa Casas, Mahesh G. Shioorkar, Mahesh Bhat, Rajjyoti Gogoi, Noel Rodrigo, Jordi Puiggalí, Abdulrahman S. Al Hajar, Kulvir Kaur, M. Supreeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe78b27f9901685133e4315f9a83cd2d
https://doi.org/10.9734/bpi/cpcs/v5
https://doi.org/10.9734/bpi/cpcs/v5
Autor:
Yogesh Pore, Priyanka H. Jadhav
Publikováno v:
Asian Journal of Chemistry. 29:2522-2530
Autor:
Yogesh Pore, Sarika Sapte
Publikováno v:
Journal of Pharmaceutical Analysis
Journal of Pharmaceutical Analysis, Vol 6, Iss 5, Pp 300-306 (2016)
Journal of Pharmaceutical Analysis, Vol 6, Iss 5, Pp 300-306 (2016)
The inclusion complexes of poorly water-soluble cephalosporin, cefuroxime axetil (CFA), were prepared with β-cyclodextrin (βCD) with or without addition of l-arginine (ARG) to improve its physicochemical properties. We also investigated the effect
Publikováno v:
Journal of Applied Pharmaceutical Science. :037-044
The main objective of the present investigation was to improve dissolution efficiency and stabilize amorphous form of itraconazole (ITR) through formulation of ternary solid dispersion system (SDs) with polyvinylpyrrolidone K30 (PVP K30) and sylysia
Publikováno v:
Scientia Pharmaceutica
Volume 83
Issue 2
Pages 243-267
Volume 83
Issue 2
Pages 243-267
The study of inflammatory pain has been one of the most rapidly advancing and expanding areas of pain research in recent years. Studies from our lab have demonstrated the chronic pain-modulating potential of the Phyllanthus species and their probable
Publikováno v:
Particulate Science and Technology. 32:512-519
In order to improve solubility and dissolution rate of poorly aqueous soluble telmisartan, its amorphous polymeric microparticles with PVP K30 were prepared with or without aid of adsorbent (Aerosil200/Sylysia350) using spray-drying technique. The pu
Publikováno v:
Journal of Pharmaceutical Investigation. 44:213-224
Spherical agglomerates of ezetimibe (EZT) were prepared with hydrophilic polymers; polyvinyl pyrrolidone K30 (PVP) and/or poloxamer 188 (poloxamer) at drug to polymer ratios of 1:1 (w/w) by spherical crystallization technique, in order to improve its
Publikováno v:
Carbohydrate Polymers. 98:1317-1325
In an attempt to improve the physicochemical properties of cefixime (CEF), its supramolecular inclusion compounds were prepared with β-cyclodextrin (βCD) and hydroxypropyl-β-cyclodextrin (HPβCD) in presence and/or absence of ternary component L-a