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Talanta ; 116: 403-8, 2013 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-24148422

RESUMEN

The use of Triton X surfactants in developing 1,1'-oxalylimidazole chemiluminescent enzyme immunoassays (ODI CEIs) with extended linear response range for the quantification of unconjugated estriol (uE3), alpha-fetoprotein (AFP), and human chorionic gonadotropin (hCG) is reported for the first time. The wider linear dynamic range in ODI CLEIA results from Triton X series (e.g., Triton X-100, -114, -405, -705) acting as an inhibitor in the interaction between Amplex Red (hydrophobic substrate) and horseradish peroxidase (hydrophilic enzyme) to produce resorufin (hydrophobic fluorescent dye). Triton X-100 acts as the appropriate inhibitor in ODI CLEIA. The maximum concentrations of AFP and hCG quantified with sandwich ODI CLEIA in the presence of Triton X-100 were 8 times higher than when analyzed with the same system in the absence of Triton X-100. In addition, the lowest concentration of uE3 determined using competitive ODI CLEIA in the presence of Triton X-100 was 20 times lower than that measured with competitive ODI CLEIA in the absence of Triton X-100. These results indicate that rapid quantification of AFP, uE3, and hCG using cost effective and highly sensitive ODI CLEIAs in the presence of Triton X-100 can be applied as an accurate, precise, and reproducible method to diagnose genetic disorders (e.g., trisomy 18 and trisomy 21) in fetuses.


Asunto(s)
Gonadotropina Coriónica/sangre , Síndrome de Down/diagnóstico , Estriol/sangre , Técnicas para Inmunoenzimas , Octoxinol/química , Trisomía/diagnóstico , alfa-Fetoproteínas/metabolismo , Calibración , Gonadotropina Coriónica/genética , Cromosomas Humanos Par 18/genética , Cromosomas Humanos Par 18/metabolismo , Síndrome de Down/genética , Síndrome de Down/metabolismo , Estriol/genética , Feto , Pruebas Genéticas , Peroxidasa de Rábano Silvestre/química , Humanos , Peróxido de Hidrógeno/química , Interacciones Hidrofóbicas e Hidrofílicas , Imidazoles/química , Límite de Detección , Mediciones Luminiscentes , Oxazinas/química , Trisomía/genética , Síndrome de la Trisomía 18 , alfa-Fetoproteínas/genética
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