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1.
Rapid Commun Mass Spectrom ; 26(2): 133-40, 2012 Jan 30.
Artículo en Inglés | MEDLINE | ID: mdl-22173801

RESUMEN

Hollow fibre liquid-phase microextraction (LPME) and desorption electrospray ionization mass spectrometry (DESI-MS) were evaluated for the identification and quantification of basic drugs in human urine samples. The selective extraction capabilities of three-phase LPME provided a significant reduction in the matrix effects otherwise observed in direct DESI-MS analysis of urine samples. Aqueous LPME extracts (in 10 mM HCl) were deposited on porous Teflon, dried at room temperature, and the dried spots were then analyzed directly with DESI-MS in full scan mode. Pethidine, diphenhydramine, nortriptyline, and methadone were used as model compounds for identification, and their limits of identification were determined to be 100, 25, 100, and 30 ng/mL, respectively. In a reliability test with 19 spiked urine samples, 100% of the positive samples containing the model drugs in concentrations at or above the limit of identification were identified. Diphenhydramine was used as a model compound for quantitative analysis with diphenhydramine-d(5) as an internal standard. The calibration curve was linear in the range 50-2000 ng/mL (R(2) = 0.992) with a limit of quantification at approximately 140 ng/mL. The intra- and inter-day relative standard deviations were <9.5%. In a reliability test with six spiked urine samples, deviations between the measured and the true values for diphenhydramine were in the range 0.2-22.9%.


Asunto(s)
Microextracción en Fase Líquida/métodos , Preparaciones Farmacéuticas/orina , Espectrometría de Masa por Ionización de Electrospray/métodos , Difenhidramina/orina , Humanos , Límite de Detección , Modelos Lineales , Meperidina/orina , Metadona/orina , Nortriptilina/orina , Preparaciones Farmacéuticas/química , Preparaciones Farmacéuticas/clasificación , Reproducibilidad de los Resultados
2.
Anal Chem ; 83(9): 3256-9, 2011 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-21473636

RESUMEN

Secondary metabolites in plant material can be imaged in a simple and robust way by creating an imprint of the plant material on a porous Teflon surface. The Teflon surface serves to extract compounds from the plant material for enhanced desorption electrospray ionization imaging analysis, while maintaining the spatial information of the sample. The method, which remedies for limitations in mass spectrometry imaging of compounds embedded in plant material, was demonstrated on leaves and petals of Hypericum perforatum and leaves of Datura stramonium.


Asunto(s)
Magnoliopsida/metabolismo , Imagen Molecular/métodos , Espectrometría de Masa por Ionización de Electrospray/métodos , Componentes Aéreos de las Plantas/metabolismo , Reproducibilidad de los Resultados
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