Preclinical Pharmacokinetics, pharmacokinetic/pharmacodynamic relationship study and Hepatic and Renal Safety Preliminary Evaluation of Phthalimide Derivative in rats.

• Grant number: 11/23007-5
• Support Opportunities: Scholarships in Brazil - Doctorate
• Start date: March 01, 2013
• End date: October 17, 2015
• Field of knowledge: Health Sciences - Pharmacy
• Principal Investigator: Rosangela Gonçalves Peccinini
• Grantee: Michel Leandro de Campos
• Host Institution: Faculdade de Ciências Farmacêuticas (FCFAR). Universidade Estadual Paulista (UNESP). Campus de Araraquara. Araraquara , SP, Brazil
• Associated scholarship(s): 14/01724-5 - Structural elucidation of metabolites from a phthalimide derivative (LAPDESF-SCD03) by high-resolution mass spectrometry (HRMS), BE.EP.DR

Abstract

Sickle cell disease is the most common monogenic disorder and severe throughout the world. It is characterized by acute illness and progressive organ damage. Results from a single mutation at position 6 of ² chain, with glutamate in hemoglobin to valine in hemoglobin S. Aiming to treat the symptoms of this disease, the phtalimide derivative LAPDESF-SCD03 was planned to have nitric oxide donor activity and anti-inflammatory activity, which has been demonstrated in published studies. Through this, it is proposed this project to perform preclinical pharmacokinetic evaluation, pharmacokinetic/pharmacodynamic relationship and preliminary evaluation of hepatic and renal safety. Will be developed and validated analytical and bioanalytical method for drug quantification in the proposed studies. The pharmacokinetics will be assessed in Wistar rats by oral and intravenous administration. This assay allows the calculation of pharmacokinetic parameters, including oral bioavailability. These pharmacokinetic parameters are important for calculating dosage regimens in further studies to meet the motion of the drug in the body. The test will determine pharmacodynamic action of the drug in vivo and its relation to plasma concentrations observed. Already the preliminary test designed to assess safety if drugs lead to liver or kidney changes that undermine the continuity of its development, which merit more detailed assessment immediately or allow them to continue their studies with these new molecules. All these tests are important information in preclinical development of new drug, which will be part of the justifications at the time of a clinical research protocol.

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

DE CAMPOS, MICHEL LEANDRO; OLIVEIRA, ISABELA JUNQUEIRA; DAVANCO, MARCELO GOMES; DOS SANTOS, JEAN LEANDRO; PECCININI, ROSANGELA GONCALVES. UHPLC Quantitation Method and In vitro Studies of Two New Phthalimide Derivatives Planned to Treat Sickle Cell Disease. CURRENT PHARMACEUTICAL ANALYSIS, v. 13, n. 4, p. 361-366, 2017. (11/23007-5, 14/01724-5)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

CAMPOS, Michel Leandro de. . 2015. Doctoral Thesis - Universidade Estadual Paulista (Unesp). Faculdade de Ciências Farmacêuticas. Araraquara Araraquara.