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Microsequential injection analysis/lab-on-valve system for the automatic evaluation of acetylcholinesterase inhibitors.
Ndongo, Thierno Moussa; Passos, Marieta L C; Durães, Fernando; Resende, Diana I S P; Pinto, Madalena; Sousa, Emília; Saraiva, Maria Lúcia M F S.
Afiliação
  • Ndongo TM; LAQV, REQUIMTE, Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, Porto University, Porto, Portugal.
  • Passos MLC; Faculté des sciences et techniques, Le Mans Université, Le Mans, France.
  • Durães F; LAQV, REQUIMTE, Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, Porto University, Porto, Portugal.
  • Resende DISP; Laboratório de Química Orgânica e Farmacêutica, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal.
  • Pinto M; Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR/CIMAR), Universidade do Porto, Matosinhos, Portugal.
  • Sousa E; Laboratório de Química Orgânica e Farmacêutica, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal.
  • Saraiva MLMFS; Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR/CIMAR), Universidade do Porto, Matosinhos, Portugal.
Arch Pharm (Weinheim) ; 354(10): e2100150, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34105191
ABSTRACT
A miniaturized microsequential injection/lab-on-valve (µSIA-LOV) system was developed and shown to be a useful alternative to perform inhibitory studies on acetylcholinesterase. These studies are essential for the evaluation of the potential therapeutic effect of drugs commonly used in the treatment of Alzheimer's disease. Donepezil, galantamine, and rivastigmine were tested, in addition to compounds based on the xanthone scaffold. Four of these xanthone derivatives were identified as having EC50 values between 676 and 4466 µmol/l, showing a potential inhibitory effect higher than the clinical agent rivastigmine. The developed automatic system added advantages of reduction of reagents and sample consumption (around 55 µl per analysis), lower cost per analysis, and the generation of less waste (around 1.2 ml per analysis). The µSIA-LOV system is also a robust, rapid, reliable, and simple system to use. Docking studies suggested a possible mode of interaction with the target acetylcholinesterase protein.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores da Colinesterase / Xantonas / Simulação de Acoplamento Molecular Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores da Colinesterase / Xantonas / Simulação de Acoplamento Molecular Idioma: En Ano de publicação: 2021 Tipo de documento: Article