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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >A new point-of-care portable immunosensor for non-invasive assessment of oro-ileal transit time by oral fluid tauroursodeoxycholate measurement after its oral load
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A new point-of-care portable immunosensor for non-invasive assessment of oro-ileal transit time by oral fluid tauroursodeoxycholate measurement after its oral load

机译:一种新型护理点便携式免疫传感器,通过口服负载牛磺去氧胆酸盐后口服测量无创评估口回肠传输时间

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A non-invasive test for oro-ileal transit time (OITT) evaluation was developed, based on the measurement of tauroursodeoxycholic acid (TUDCA) oral fluid concentration profile after its oral administration. Exploiting the fact that TUDCA is actively absorbed only in the ileum, OITT is measured as the time corresponding to TUDCA maximum oral fluid concentration (tmax).To measure oral fluid TUDCA concentration in a point-of-care setting, an ultrasensitive portable immunosensor was developed, based on a competitive chemiluminescent enzyme immunoassay (CL-EIA), using immobilized anti-TUDCA antibody and an ursodeoxycholic acid (UDCA)-peroxidase conjugate as tracer, detected by enhanced chemiluminescence employing a portable charge-coupled device (CCD)-based device. The test was validated in 24 healthy subjects before and after treatment with Loperamide, a drug that increases OITT.The developed CL-EIA was accurate and precise, with a LLOQ of 50pmolL-1. The measured OITT for healthy subjects (291±50min) was fairly well correlated with OITT values obtained by measuring TUDCA in serum (r=0.89). An increased OITT was observed in all the studied subjects after Loperamide treatment.The CL immunosensor can be employed directly in gastroenterology and paediatric units and it can thus represent a new non-invasive simple test for OITT evaluation in a point-of-care setting, with improved diagnostic utility.
机译:基于口服给药后牛磺去氧胆酸(TUDCA)口服液浓度分布的测量结果,开发了一种非侵入性的口服回肠时间(OITT)评估方法。利用TUDCA仅在回肠中被主动吸收这一事实,将OITT测量为对应于TUDCA最大口腔液浓度(tmax)的时间。要在即时护理环境中测量口腔液TUDCA浓度,需使用超灵敏便携式免疫传感器。基于竞争性化学发光酶免疫分析(CL-EIA)开发的技术,使用固定的抗-TUDCA抗体和熊去氧胆酸(UDCA)-过氧化物酶偶联物作为示踪剂,通过基于便携式电荷耦合器件(CCD)的增强化学发光法进行检测设备。该测试已在24名健康受试者中接受Loperamide(一种增加OITT的药物)治疗前后进行了验证。开发的CL-EIA准确准确,LLOQ为50 pmolL-1。健康受试者的OITT测量值(291±50分钟)与通过测量血清中的TUDCA获得的OITT值具有很好的相关性(r = 0.89)。洛哌丁胺治疗后,所有研究对象均观察到OITT升高。CL免疫传感器可直接用于肠胃病学和儿科单位,因此可以代表一种新的非侵入性简单测试,用于现场即时评估OITT,具有改进的诊断实用程序。

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