Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Leonardo Santos Ribeiro Pinto"'
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
Interações medicamentosas envolvendo a glicoproteína-P (P-gp) intestinal e placentária são determinantes na disposição cinética e transferência placentária de medicamentos durante a gestação. A fexofenadina, fármaco anti-histamínico, es
Autor:
Howard Berger, Ricardo de Carvalho Cavalli, Leonardo Santos Ribeiro Pinto, Fernanda de Lima Moreira, Gideon Koren, Vera Lucia Lanchote, Priya Bapat, Angelika Lubetsky
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Fexofenadine is a well-identified in vivo probe substrate of P-glycoprotein (P-gp) and/or organic anion transporting polypeptide (OATP). This work aimed to investigate the transplacental pharmacokinetics of fexofenadine enantiomers with and without t
Autor:
Eduardo Barbosa Coelho, Fernanda de Lima Moreira, Maria Paula Marques, Leonardo Santos Ribeiro Pinto, Vera Lucia Lanchote, Ricardo de Carvalho Cavalli, Gabriel T. do Vale
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
This study shows the development and validation of two enantioselective LC-MS/MS methods for the determination of fexofenadine in biological matrices including the elution order determination. Plasma (200 µL) or urine (50 µL) aliquots were added to
Autor:
Paula Melo de Abreu Vieira, Israel Molina, Rodrigo Correa-Oliveira, Glauco Henrique Balthazar Nardotto, Luísa Perin, Cláudia Martins Carneiro, Kátia da Silva Fonseca, Leonardo Santos Ribeiro Pinto, Thaís Fernanda Rodrigues Bastos Mendes, Beatriz Oliveira Paiva
Publikováno v:
The Journal of antimicrobial chemotherapy. 75(8)
Objectives To evaluate the population pharmacokinetics of different benznidazole treatment regimens and the drug’s biodistribution in mice. Methods Two hundred mice were divided into five groups according to benznidazole dosing regimens: (1) 100 mg
Autor:
M. A. Artaza, L. Perin, Adrián Sánchez-Montalvá, Leonardo Santos Ribeiro Pinto, R. Moreno, A. Esquisabel, Fernando Salvador, Israel Molina, José Luis Pedraz
Publikováno v:
Antimicrobial agents and chemotherapy. 61(4)
Despite its toxicity and low efficacy in the chronic phase, benznidazole is the drug of choice in Chagas disease. Scarce information about pharmacokinetics and pharmacodynamics of benznidazole has been published. We performed a phase I, open-label, n
Autor:
Howard Berger, Leonardo Santos Ribeiro Pinto, Katarina Aleksa, Priya Bapat, Gideon Koren, Angelika Lubetsky, Shinya Ito
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 14(7)
UNLABELLED Essentials Apixaban is a novel oral anticoagulant that has not been studied in pregnant patients. Our objective was to determine the rate and extent of the placental transfer of apixaban. Apixaban rapidly crosses the ex vivo term human pla
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Interações medicamentosas envolvendo a glicoproteína-P (P-gp) intestinal e placentária são determinantes na disposição cinética e transferência placentária de medicamentos durante a gestação. A fexofenadina, fármaco anti-histamínico, es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b541cd53865e9e1716cd383d4cc5682
Publikováno v:
American Journal of Obstetrics and Gynecology. 213:710.e1-710.e6
Objective The purpose of this study was to determine the rate and extent of rivaroxaban transfer across the term human placenta and determine whether passive diffusion was the primary mechanism involved in this transfer. Study Design The transplacent