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Metabolic stability In Vitro assay of new drug candidates for Tub | 44067
Journal of Pharmaceutical Care & Health Systems

Journal of Pharmaceutical Care & Health Systems
Open Access

ISSN: 2376-0419

+44 1300 500008

Metabolic stability In Vitro assay of new drug candidates for Tuberculosis


11th World Congress on Pharmaceutical sciences

September 28-29, 2018 | Montreal, Canada

Taisa Busaranho Franchin, Bruna Cristina Ulian Silva, Joao Paulo dos Santos Fernandes, Michel Leandro de Campos, Rosangela Goncalves Peccinini

Sao Paulo State University, Brazil
Pharmaceutical Sciences at Federal University of Sao Paulo, Brazil
Federal
University of Parana, Brazil

Scientific Tracks Abstracts: J Pharma Care Health Sys

Abstract :

Introduction: The development of new drugs is a complex process, with only 0.027% of newly synthesized molecules being approved by regulatory agencies. Inadequate pharmacokinetic properties and toxicity are responsible for half of the failures in this process and the in vitro screening of new molecules assists in the selection of the best candidates and to understand the results of in the in vivo studies. In the metabolic stability assay, the molecules are submitted to a microsomal system to evaluate their degradation by the microsomal enzymes. Considering that Tuberculosis is still responsible for millions of deaths and cases of bacterial resistance to the drugs used in the treatment only increase, esters of pyrazinoic acid, the active metabolite of pyrazinamide, have been developed as a novel alternative for this treatment, and the present work aimed to evaluate the metabolic stability of POAEt POAEtPOA and POAMe. Methodology: The compounds were incubated with 0.5mg/mL rat microsome for up to 120 minutes in buffer, with and without NADPH regenerating system. They were tested in concentrations of 2, 5 and 10μM. The samples were quantified by UHPLC, with previously developed methods. Diclofenac was used as a control of the system. Results: The control was adequate, indicating the system operation, showing a half-life of 33 minutes. The quantification was not possible in the 2μM, while the concentrations of 5 and 10μM presented the same profile, thus, the concentration of 5μM was chosen to perform the experiment. The compounds showed no decay in any of the situations referred to it, making it impossible to calculate the elimination half-life, and therefore the extrapolated clearance. Conclusion: It was observed that the three molecules were stable in this system and there was no activity of the microsomal enzymes on these compounds.

Biography :

Taisa Busaranho Franchin graduated in Pharmacy-Biochemistry from the São Paulo State University "Júlio de Mesquita Filho", Araraquara - SP. Currently in Master's degree in Pharmaceutical Sciences at the School of Pharmaceutical Sciences of Sao Paulo State University, Araraquara-UNESP in the Laboratory of Toxicology of the Department of Natural Active Principles and Toxicology (PANT) with emphasis on Pharmacokinetics and Toxicology of new substances and medicines. Her scientific initiation was with tuberculosis drug, following the same line in the master's degree, is also, part of this, the implementation of the in vitro laboratory.

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