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使用五种商业放射免疫分析试剂盒对犬免疫反应性胰岛素进行定量分析。

Canine immunoreactive insulin quantitation using, five commercial radioimmunoassay kits.

作者信息

Stockham S L, Nachreiner R F, Krehbiel J D

出版信息

Am J Vet Res. 1983 Nov;44(11):2179-83.

PMID:6359984
Abstract

Five commercial radioimmunoassay (RIA) kits developed for quantitation of human immunoreactive insulin (IRI) were evaluated for their capability to quantitate canine IRI. Evaluation criteria included precision, dilutional parallelism, sensitivity, and comparison of IRI concentration in 4 control sera. One RIA kit had good dilutional parallelism, consistently good precision, and adequate sensitivity. Other RIA kits had poorer performance in dilutional parallelism or precision. No RIA kit quantitated the same IRI concentrations in all 4 control sera as did another. The results indicated that quantitation of canine IRI by some commercial RIA kits (for human use) may not be reliable. Variations in IRI concentrations quantitated indicated that reference intervals for healthy dogs should be established for each insulin RIA. At least 17 commercial radioimmunoassay (RIA) kits are available to quantitate human immunoreactive insulin (IRI). Two RIA kits have been used to quantitate canine IRI, but validation of assays to quantitate canine IRI were not reported. Evaluation of RIA validity should include assessment of specificity, precision, sensitivity, and accuracy. Two methods are recommended for assessing specificity: (i) demonstration of dilutional parallelism, and (ii) demonstration that related substances do not influence quantitation of analyte. Human insulin differs from canine insulin by having 1 amino acid substitution at the carboxyl-terminal of the B chain. Thus, it is possible that antibodies developed to react with human IRI will have cross immunoreactivity with canine IRI. Precision is affected by a variety of factors including technical steps and antigen-antibody interactions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为定量检测人免疫反应性胰岛素(IRI)而研发的5种商用放射免疫分析(RIA)试剂盒,对其定量检测犬IRI的能力进行了评估。评估标准包括精密度、稀释平行性、灵敏度以及4份对照血清中IRI浓度的比较。一种RIA试剂盒具有良好的稀释平行性、始终如一的良好精密度和足够的灵敏度。其他RIA试剂盒在稀释平行性或精密度方面表现较差。没有一种RIA试剂盒在所有4份对照血清中定量的IRI浓度与另一种试剂盒相同。结果表明,一些商用RIA试剂盒(供人使用)对犬IRI的定量检测可能不可靠。定量检测的IRI浓度存在差异,这表明应为每种胰岛素RIA建立健康犬的参考区间。至少有17种商用放射免疫分析(RIA)试剂盒可用于定量检测人免疫反应性胰岛素(IRI)。有两种RIA试剂盒已用于定量检测犬IRI,但未报道对犬IRI定量检测方法的验证情况。RIA有效性的评估应包括特异性、精密度、灵敏度和准确性的评估。推荐两种评估特异性的方法:(i)证明稀释平行性,(ii)证明相关物质不影响分析物的定量检测。人胰岛素与犬胰岛素的区别在于B链羧基末端有1个氨基酸取代。因此,针对人IRI产生反应的抗体有可能与犬IRI产生交叉免疫反应。精密度受多种因素影响,包括技术步骤和抗原-抗体相互作用。(摘要截短于250词)

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