Your browser doesn't support javascript.
loading
GC-NPD analysis of topiramate in capillary dried plasma: assessing chemical dependency pharmacotherapy.
Ott, Isabela Ritter; Macali Oliveira, Debora Renata; Grando, Ana Paula; Frohlich, Klaus Vogel; Perassolo, Magda Susana; Linden, Rafael; Antunes, Marina Venzon.
Afiliação
  • Ott IR; Graduate Program on Toxicology & Analytical Toxicology, Feevale University, Novo Hamburgo, RS, 93525-075, Brazil.
  • Macali Oliveira DR; Toxicological Analysis Laboratory, Institute of Health Sciences, Feevale University, Novo Hamburgo, RS, 93525-080,Brazil.
  • Grando AP; Graduate Program on Toxicology & Analytical Toxicology, Feevale University, Novo Hamburgo, RS, 93525-075, Brazil.
  • Frohlich KV; Toxicological Analysis Laboratory, Institute of Health Sciences, Feevale University, Novo Hamburgo, RS, 93525-080,Brazil.
  • Perassolo MS; Toxicological Analysis Laboratory, Institute of Health Sciences, Feevale University, Novo Hamburgo, RS, 93525-080,Brazil.
  • Linden R; Toxicological Analysis Laboratory, Institute of Health Sciences, Feevale University, Novo Hamburgo, RS, 93525-080,Brazil.
  • Antunes MV; Graduate Program on Toxicology & Analytical Toxicology, Feevale University, Novo Hamburgo, RS, 93525-075, Brazil.
Bioanalysis ; 16(12): 603-613, 2024.
Article em En | MEDLINE | ID: mdl-39185792
ABSTRACT

Aim:

This study aimed to develop and validate a GC-NPD method for quantifying topiramate (TPM) in capillary dried plasma spots (DPS).Materials &

methods:

Extraction involved three 6 mm DPS with albumin 0.1%, alkaline liquid extraction with tert-Butyl methyl ether and TMAH methylation. The method was validated and applied to 15 paired samples of capillary DPS and venous plasma from chemical dependency patients.

Results:

The method was linear from 1 to 50 µg/ml (r >0.99), precise (CV% 3.62-8.29%) accurate (98.1-107.7%). TPM stability was confirmed in DPS stored at 4, 23 and 45°C for 21 days. DPS TPM measurements were highly correlated plasma concentrations (rs = 0.96), representing on average 102% of the venous plasma measurements.

Conclusion:

The method was fully validated, demonstrating potential for clinical application.
[Box see text].
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teste em Amostras de Sangue Seco / Topiramato Limite: Humans Idioma: En Revista: Bioanalysis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teste em Amostras de Sangue Seco / Topiramato Limite: Humans Idioma: En Revista: Bioanalysis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido