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Performance evaluation of a MIP for the MISPE-LC determination of p-[18F]MPPF and a potential metabolite in human plasma.
Lecomte, F; Aerts, J; Plenevaux, A; Defraiteur, C; Chapuis-Hugon, F; Rozet, E; Chiap, P; Luxen, A; Pichon, V; Hubert, Ph; Hubert, C.
Afiliación
  • Lecomte F; University of Liège (ULiege), CIRM, Laboratory of Pharmaceutical Analytical Chemistry, Liège, Belgium.
  • Aerts J; University of Liège (ULiege), GIGA-CRC In VIVO Imaging, Liège, Belgium.
  • Plenevaux A; University of Liège (ULiege), GIGA-CRC In VIVO Imaging, Liège, Belgium.
  • Defraiteur C; University of Liège (ULiege), GIGA-CRC In VIVO Imaging, Liège, Belgium.
  • Chapuis-Hugon F; Dept of Analytical, Bioanalytical Sciences and Miniaturization (LSABM), UMR CBI 8231 (CNRS-ESPCI Paris), ESPCI Paris, PSL University, Paris, France.
  • Rozet E; Pharmalex, Mont-St-Guibert, Belgium.
  • Chiap P; Academic Hospital of Liège, Department of Toxicology, GLP-AEPT Unit, CIRM, Liège, Belgium.
  • Luxen A; University of Liège (ULiege), GIGA-CRC In VIVO Imaging, Liège, Belgium.
  • Pichon V; Dept of Analytical, Bioanalytical Sciences and Miniaturization (LSABM), UMR CBI 8231 (CNRS-ESPCI Paris), ESPCI Paris, PSL University, Paris, France; Sorbonne Université, Paris, France.
  • Hubert P; University of Liège (ULiege), CIRM, Laboratory of Pharmaceutical Analytical Chemistry, Liège, Belgium.
  • Hubert C; University of Liège (ULiege), CIRM, Laboratory of Pharmaceutical Analytical Chemistry, Liège, Belgium. Electronic address: chubert@uliege.be.
J Pharm Biomed Anal ; 180: 113015, 2020 Feb 20.
Article en En | MEDLINE | ID: mdl-31865206
ABSTRACT
Within the family of serotonin (5-HT) receptors, the 5-HT1A subtype is particularly interesting as it may be involved in various physiological processes or psychological disorders. The p-[18F]MPPF, a highly selective 5-HT1A antagonist, is used for in vivo studies in human or animal by means of positron emission tomography (PET) [1]. In order to selectively extract p-[18F]MPPF and its main metabolites from plasma, molecularly imprinted polymer (MIP) was prepared against these compounds by using the p-MPPF as template. For the control of the selectivity, non-imprinted polymer (NIP) was also synthesized without template. The MIP sorbent, packed in disposable extraction cartridges (DECs), was then evaluated as molecularly imprinted solid-phase extraction (MISPE) prior to the LC determination. The conditions of extraction were evaluated in order to obtain the highest selective retention of the p-[18F]MPPF and its metabolites on this MIP. The MIP selectivity was exploited in the loading and washing steps by adjusting the pH of plasma samples at a suitable value and by selecting mixtures for the washing step to limit the contribution of non-specific interactions. Other important parameters involved in the conditioning and elution steps were also studied. Finally, a pre-validation was carried out with optimal extraction conditions to demonstrate the performance of this MISPE-LC method as a generic method in the context of evaluation of new MISPE for p-[18F]MPPF and its potential for metabolites extraction from human plasma.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piperazinas / Polímeros / Benzamidas / Radioisótopos de Flúor / Receptor de Serotonina 5-HT1A / Antagonistas del Receptor de Serotonina 5-HT1 / Aminopiridinas Límite: Humans Idioma: En Revista: J Pharm Biomed Anal Año: 2020 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piperazinas / Polímeros / Benzamidas / Radioisótopos de Flúor / Receptor de Serotonina 5-HT1A / Antagonistas del Receptor de Serotonina 5-HT1 / Aminopiridinas Límite: Humans Idioma: En Revista: J Pharm Biomed Anal Año: 2020 Tipo del documento: Article País de afiliación: Bélgica