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新生儿和婴儿支气管肺泡灌洗液(BALF)中尿素氮测定的自动化方法描述

Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants.

作者信息

Pocino Krizia, Minucci Angelo, Manieri Rocco, Conti Giorgio, De Luca Daniele, Capoluongo Ettore Domenico

机构信息

Institute of Biochemistry and Clinical Biochemistry, Catholic University of the Sacred Heart, Rome, Italy

Institute of Biochemistry and Clinical Biochemistry, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

J Lab Autom. 2015 Dec;20(6):636-41. doi: 10.1177/2211068214567147. Epub 2015 Jan 13.

Abstract

Bronchoalveolar lavage (BAL) partially recovers both the instilled saline and the alveolar fluid, so-called epithelial lining fluid (ELF), but a correction for the dilution due to the BAL technique itself is needed to know the amount of recovered ELF. In this regard, urea nitrogen may be useful and has been proposed to calculate ELF. The aim of the present study was to develop and validate a new method to measure urea nitrogen in BAL fluid (BALF). We used 19 BALF samples obtained from neonates and infants with different respiratory conditions. The urea nitrogen assay was carried out on Cobas c311 analyzer (Roche Diagnostics). A validation study shows that the method is perfectly linear (R(2) = 0.999), sensitive (limit of detection = 0.055 mg/dL; limit of quantification = 0.16 mg/dL), repeatable (low = 0.15 ± 0.02, 13.3%; high = 1.80 ± 0.02, 1.1%), reproducible (low = 0.14 ± 0.02, 14.2 %; high = 1.76 ± 0.04, 2.2 %) with accuracy ranging between 93-96%. Our results support the robustness of validated procedure since the described method appears simple, precise, rapid, and suitable for routine analysis. Thus, it may be used to correct concentration of various noncellular BAL components and calculate their ELF amounts in neonates and infants.

摘要

支气管肺泡灌洗(BAL)可部分回收注入的生理盐水和肺泡液,即所谓的上皮衬液(ELF),但需要对BAL技术本身造成的稀释进行校正,以了解回收的ELF量。在这方面,尿素氮可能有用,并已被提议用于计算ELF。本研究的目的是开发并验证一种测量BAL液(BALF)中尿素氮的新方法。我们使用了从患有不同呼吸疾病的新生儿和婴儿身上获取的19份BALF样本。尿素氮测定在Cobas c311分析仪(罗氏诊断公司)上进行。一项验证研究表明,该方法具有完美的线性(R(2)=0.999)、灵敏(检测限=0.055mg/dL;定量限=0.16mg/dL)、可重复(低值=0.15±0.02,13.3%;高值=1.80±0.02,1.1%)、可再现(低值=0.14±0.02,14.2%;高值=1.76±0.04,2.2%),准确度在93%-96%之间。我们的结果支持了验证程序的稳健性,因为所描述的方法看起来简单、精确、快速且适用于常规分析。因此,它可用于校正新生儿和婴儿各种非细胞BAL成分的浓度,并计算其ELF量。

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