Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Cássia Virginia Garcia"'
Autor:
Camila F. A. Giordani, Sarah Campanharo, Nathalie R. Wingert, Lívia M. Bueno, Joanna W. Manoel, Barbara Costa, Shanda Cattani, Marcelo Dutra Arbo, Solange Cristina Garcia, Cássia Virginia Garcia, Nádia Maria Volpato, Elfrides Eva Scherman Schapoval, Martin Steppe
Publikováno v:
BMC Pharmacology and Toxicology, Vol 20, Iss S1, Pp 1-9 (2019)
Abstract Background The presence of impurities in some drugs may compromise the safety and efficacy of the patient’s treatment. Therefore, establishing of the biological safety of the impurities is essential. Diabetic patients are predisposed to ti
Externí odkaz:
https://doaj.org/article/309282526c4a4abfa0da457f364e5a43
Autor:
Caren Gobetti, Andressa da Silva Bitencourt, Márcio Vinícius Ayres, Ana Lucia Peixoto de Freitas, Andreas Sebastian Loureiro Mendez, Cássia Virginia Garcia
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 57 (2021)
Tizanidine hydrochloride is a centrally acting skeletal muscle relaxant, used in the management of spasticity. This drug is commercially available only as tablets, which highlights the need to develop oral liquid formulations. In the hospital environ
Externí odkaz:
https://doaj.org/article/15d05df64cc547cf949b225dc60392b6
Autor:
Nadia Maria Volpato, Joanna Wittckind Manoel, Camila Ferrazza Alves Giordani, Elfrides Eva Sherman Schapoval, Cássia Virginia Garcia, Lívia Maronesi Bueno, Martin Steppe, Sarah Chagas Campanharo
Publikováno v:
Current Pharmaceutical Analysis. 17:564-572
Introduction: Impurity analysis is an important step in the quality control of pharmaceutical ingredients and the final product. Impurities can arise from drug synthesis or excipients and even at small concentrations may affect product efficacy and s
Autor:
Sarah Chagas Campanharo, Martin Steppe, Lívia Maronesi Bueno, Nathalie Ribeiro Wingert, Cássia Virginia Garcia, Gabrielle D. Iop, Paola A. Mello, Elfrides Eva Scherman Schapoval, Joanna Wittckind Manoel, Erico M.M. Flores, Camila Ferrazza Alves Giordani, Nadia Maria Volpato
Publikováno v:
Journal of Chromatographic Science. 58:718-725
Vildagliptin (VLG) corresponds to a drug used for the treatment of diabetes mellitus. This disease requires continuous treatment, and so the control of impurities present in it is important to assure the quality of this drug. Thus, it is necessary to
Publikováno v:
Current Pharmaceutical Analysis. 16:55-63
Background: Ambrisentan is a drug used to treat the pulmonary arterial hypertension symptoms, commercialized as coated tablets. Drug quality control is an essential part for the development and release of drugs for consumption; however, there are few
Autor:
Martin Steppe, Nadia Maria Volpato, Nathalie Ribeiro Wingert, Cássia Virginia Garcia, Jéssica B. Ellwanger, Elfrides Eva Scherman Schapoval
Publikováno v:
Chromatographia. 83:65-75
Quality by Design (QbD) is a systematic approach that takes predefined objectives and emphasizes process understanding and control. Analytical QbD (AQbD) is widely used when it comes to the development and optimization of analytical methods. Since im
Autor:
Márcio Vinícius Ayres, Ana Lúcia Peixoto de Freitas, Andressa da Silva Bitencourt, Caren Gobetti, Andreas Sebastian Loureiro Mendez, Cássia Virginia Garcia
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 57 (2021)
Brazilian Journal of Pharmaceutical Sciences, Volume: 57, Article number: e18896, Published: 11 OCT 2021
Brazilian Journal of Pharmaceutical Sciences, Volume: 57, Article number: e18896, Published: 11 OCT 2021
Tizanidine hydrochloride is a centrally acting skeletal muscle relaxant, used in the management of spasticity. This drug is commercially available only as tablets, which highlights the need to develop oral liquid formulations. In the hospital environ
Autor:
Cássia Virginia Garcia, Sendy Sales Oliveira, Andreas Sebastian Loureiro Mendez, Andressa da Silva Bitencourt, Caren Gobetti
Publikováno v:
Journal of AOAC International. 104(4)
Background Posaconazole is a triazole antifungal drug that was approved by the U.S. Food and Drug Administration in 2006. No bioassay of it is available in the literature nor official codes for potency determination in bulk. Objective To conduct an a
Autor:
Nathalie Ribeiro Wingert, Silvia Helena Oliveira de Almeida, Cássia Virginia Garcia, Márcio Vinícius Ayres, Caren Gobetti, Maria Eduarda Balsan, Elisa de Saldanha Simon, Tercio Paschke Oppe
Publikováno v:
AAPS PharmSciTech. 21
Tizanidine hydrochloride is a centrally acting skeletal muscle relaxant used in the treatment of spasticity. This drug is sold only as tablets or capsules, which highlights the need to develop oral liquid formulations that allow administration to chi
Autor:
Leticia Malgarim Cordenonsi, Rafaela Martins Sponchiado, Alexandre Meneghello Fuentefria, Cássia Virginia Garcia, Martin Steppe, Andreas Sebastian Loureiro Mendez, Julia Medeiros Sorrentino
Publikováno v:
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Drug Analytical Research, Vol 4, Iss 1, Pp 44-48 (2020)
Drug Analytical Research; v. 4, n. 1 (2020); 44-48
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Drug Analytical Research, Vol 4, Iss 1, Pp 44-48 (2020)
Drug Analytical Research; v. 4, n. 1 (2020); 44-48
Drug biotransformation studies appear as an alternative to pharmacological investigations of metabolites, development of new drug candidates with reduced investment and most efficient production. The objective of this study was to evaluate the capaci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b39cc1f52edf5d6f49925502afb102