Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pavan B. Rathi"'
Publikováno v:
Journal of Chemical & Engineering Data. 66:3745-3756
Autor:
Aashruti Agrawal, Rascón-Chu Agustín, Hanan B. Ahmed, Bhavna Alke, Sánchez-Villegas J. Alfonso, Sukumaran Anil, Balaprasad Ankamwar, Geeta Arya, Rajib Bandopadhyay, Raju Biswas, Mengna Cao, Soma Chakraborty, Norma B. D'Accorso, Pandurang A. Dalavi, Anurag Dutta, Hossam E. Emam, Shahira M. Ezzat, Ohlmaier-Delgadillo Federico, Gomez-Rodriguez Gabriel H., Dipak D. Gadade, Nancy Lis Garcia, Qing Gu, Félix-Arias K. Guadalupe, Nidhi Gupta, Surabhi Gupta, Yusuf Haggag, Urmi Halder, Xiuting Hu, Harsha Jain, Supriya Jain, M.V. Jithin, Renjith P. Johnson, Ashutosh Kabiraj, Deepak A. Kulkarni, Mikhail I. Kusayin, Moitri Let, Lara-Espinoza Claudia Lizeth, Jitender Madan, Krishnendu Majhi, Verónica E. Manzano, Shirui Mao, Ming Miao, D.B. Mondal, Sesha Subramanian Murugan, Fangfang Ni, Surendra Nimesh, Purva Pingle, Ashwini Prabhu, Namitha K. Preman, Pradipta Purkayastha, R. Raguavaran, Carlos Rodriguez Ramirez, Vinitha Rani, Anton B. Rasin, Pavan B. Rathi, Evangelina Repetto, Mohamed A. Salem, Jaiprakash N. Sangshetti, Sandesh G. Sanjeeva, Jayanta K. Sarmah, Sanjib Sarmah, D.K. Sharma, Lokesh Sharma, Saurabh Shrivastava, Yujiao Sun, Usman T. Syed, Chandrakant Tagad, Syed N. Taqui, Shareefraza J. Ukkund, Roland Ulber, Rosa V. Usoltseva, Jayachandran Venkatesan, Hujun Xie, Awesh K. Yadav, Narayani Yadav, Ahmed Zayed, Gomeztagle-Romero M. Zuleth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e76d93ca638052ec742a2a338b5b1673
https://doi.org/10.1016/b978-0-12-822351-2.00099-1
https://doi.org/10.1016/b978-0-12-822351-2.00099-1
Publikováno v:
Drug Delivery Letters. 9:240-247
Background and Objective: The top approach to deliver poorly soluble drugs is the use of a highly soluble form. The present study was conducted to enhance the solubility and dissolution of a poorly aqueous soluble drug nevirapine via a pharmaceutical
Publikováno v:
Journal of Chemical & Engineering Data. 63:321-330
Experimental molar solubility of etoricoxib (ETR) in monosolvents such as glycerin, methanol (MeOH), polyethylene glycol 200 (PEG 200), polyethylene glycol 400 (PEG 400), polyethylene glycol 600 (PEG 600), propylene glycol (PG), and their aqueous bin
Publikováno v:
Advanced Pharmaceutical Bulletin
Advanced Pharmaceutical Bulletin, Vol 7, Iss 3, Pp 399-408 (2017)
Advanced Pharmaceutical Bulletin, Vol 7, Iss 3, Pp 399-408 (2017)
Purpose: Cocrystallisation of drug with coformers is a promising approach to alter the solid sate properties of drug substances like solubility and dissolution. The objective of the present work was to prepare, formulate and evaluate the piroxicam co
Publikováno v:
Journal of Chemical & Engineering Data. 60:2128-2134
Models for predicting the solubility of drugs in monosolvents and their mixtures have a practical importance in design and development of new products in pharmaceutical industries. Thus, present investigation pertains to the utility of a correlative
Autor:
Kirti V. Deshpande, Pavan B. Rathi
Publikováno v:
Journal of Solution Chemistry. 43:1886-1903
Models for predicting the solubility of drugs in solvent mixtures have an important practical application in drug formulation. Etodolac is a non-steroidal anti-inflammatory agent whose physicochemical properties in solution have not been adequately s