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1.
J Chromatogr B Analyt Technol Biomed Life Sci ; 879(22): 2089-94, 2011 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-21684222

RESUMEN

We report in this manuscript, the use of direct ammonium persulfate-enhanced chemiluminescence (CL) imaging, to monitor changes to measure serum salbutamol concentration in subjects of different haptoglobin (Hp) phenotypes at different dosing time. It was noted that CL generated from Hp was decreased due to salbutamol's reducibility, which was used for monitoring salbutamol concentration in serum. The serum from the subjects treated by oral administration of salbutamol, was collected at different dosing time and was separated by polyacrylamide gel electrophoresis (PAGE) prior to the CL detection. According to CL images, samples were separated into three groups based on the Hp phenotypes. The curves of CL signal intensity versus time were obtained for each group, and we demonstrated that there were more significant variables on binding ability between groups. The maximum salbutamol concentration in the serum appeared after 4h, which was in agreement with the literature. In addition, the binding constants of salbutamol to Hp were determined by a fluorescence-based method, whose results were in agreement with the phenomenon of the greater salbutamol metabolism rate for Group Hp 1-1 than Group Hp 2-2. The presented method can monitor changes of salbutamol concentration in serum directly, making the procedures much simple, convenient, rapid and has the property of lower cost. It provided us with excellent reference information for the individual dosage regimen of different Hp groups, which hopefully could become a potential method for further pharmaceutical research.


Asunto(s)
Albuterol/sangre , Electroforesis en Gel de Poliacrilamida/métodos , Mediciones Luminiscentes/métodos , Espectrometría de Fluorescencia/métodos , Administración Oral , Adulto , Albuterol/administración & dosificación , Albuterol/metabolismo , Haptoglobinas/metabolismo , Humanos , Modelos Lineales , Masculino , Fenotipo , Unión Proteica , Reproducibilidad de los Resultados , Tilidina/administración & dosificación , Tilidina/sangre
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