Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pedro M. Alva-Plasencia"'
Autor:
Lennin R. Rodriguez-Saavedra, Pedro M. Alva-Plasencia, Yuri F. Curo-Vallejos, Segundo F. Saavedra-Suárez, Luis A. Chávez-Abanto, Olga E. Caballero-Aquiño, Miriam E. Gutiérrez-Ramos, Junior F. Sánchez-Bautista
Publikováno v:
Journal of Pharmacy & Pharmacognosy Research, Vol 12, Iss 5, Pp 814-821 (2024)
Context: Ensuring the quality of a generic drug is essential for its commercialization. Propranolol hydrochloride is a drug in great demand on the market as it is widely used as an antihypertensive, antianginal, antiarrhythmic, and for the treatment
Externí odkaz:
https://doaj.org/article/5920b9fbf5d54996af5626b730315dfa
Autor:
Vanessa Saldaña-Bobadilla, Cintia P. Barreto-Villanueva, Frizzi J. Ganoza-Gasco, Enma Perez-Chauca, Olga E. Caballero-Aquiño, Ana E. Mantilla-Rodriguez, Pedro M. Alva-Plasencia, Maria S. Aurora-Prado
Publikováno v:
Journal of Pharmacy & Pharmacognosy Research, Vol 12, Iss 3, Pp 539-547 (2024)
Context: For regulatory reasons, a biowaiver is characterized as the substitution or exemption of bioavailability and/or bioequivalence research with in vitro dissolution tests, according to the Biopharmaceutical Classification System (BCS). These st
Externí odkaz:
https://doaj.org/article/f653e13f9df844069ef44027cdc520ef
Publikováno v:
Journal of Pharmacy & Pharmacognosy Research, Vol 10, Iss 5, Pp 847-856 (2022)
Context: In the development of a good analytical method, the selection of appropriate conditions for quantifying drugs is essential. The method validation should be determined before conducting the dissolution test. Aims: To develop and validate t
Externí odkaz:
https://doaj.org/article/637858c2845c43719d06d3040cb22138
Autor:
Antonella S. Araujo-Fernandez, José C. Uribe-Villarreal, Enma Perez-Chauca, Pedro M. Alva-Plasencia, Olga E. Caballero-Aquiño, Mayar L. Ganoza-Yupanqui
Publikováno v:
Journal of Pharmacy & Pharmacognosy Research, Vol 10, Iss 2, Pp 310-317 (2022)
Context: The validation of a method is synonymous with the quality of the obtained results. The dissolution test is an analytical technique to evaluate the quality and stability of drugs during their development. Aims: To evaluate whether the UV s
Externí odkaz:
https://doaj.org/article/af18ac10b010440b9dd83ec671de4a05