Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Devang B. Sheth"'
Autor:
Ashok B. Patel, Bhumi K. Jinja, Amit Kumar J. Vyas, Nilesh K. Patel, Ajay I. Patel, Devang B. Sheth, Sunny R. Shah
Publikováno v:
Asian Journal of Pharmaceutical Research. :295-301
The United States Food and Drug Administration (US FDA) is a department of health and human services federal agency. If the FDA notices major violations of federal regulations, it sends warning letters to pharmaceutical makers, distributors, and clin
Autor:
Mukesh N. Kher, Sandip P. Dholakia, Grisha G. Shah, Dipen K. Sureja, Vaibhav D. Bhatt, Devang B. Sheth
Publikováno v:
Analytical Chemistry Letters. 12:576-585
Autor:
Ashok B. Patel, Avadhi R. Bundheliya, Rushali V. Zala, Amitkumar J. Vyas, Nilesh K. Patel, Ajay I. Patel, Devang B. Sheth
Publikováno v:
Asian Journal of Pharmaceutical Analysis. :127-134
Dissolution testing is a critical methodology; widely utilized in the development of a new pharmaceutical product. The test, in its simplest form, consists of placing the formulation in a dissolution apparatus containing suitable dissolution medium.
Publikováno v:
Asian Journal Of Research in Pharmaceutical Science. 11:41-44
Publikováno v:
International Journal of Advanced Research. 5:289-300
Autor:
Devang B. Sheth., Jayant Chavda, Hani R Prajapati, Sunny Shah, Moinuddin Soniwala, Amit J. Vyas, Ekta M Gondaliya
Publikováno v:
The Journal of pharmacy and pharmacologyReferences. 72(8)
Objectives The aim of this study was to develop and optimize levofloxacin loaded PLGA nanoparticles (LN) for pulmonary delivery employing screening and experimental design and evaluate their in-vitro and in-vivo performance. The objective was to achi