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一种用于少量血浆样本的精确儿茶酚胺测定法。

A precise catecholamine assay for small plasma samples.

作者信息

Diamant J, Byers S O

出版信息

J Lab Clin Med. 1975 Apr;85(4):678-93.

PMID:1120934
Abstract

The time, temperature, and pH of the trihydroxyindole reaction were controlled to minimize interference between norepinephrine (NE) and epinephrine (E) so that, in plasma catecholamine assay within normal human physiologic range, NE contributes less than 1 per cent to the fluorescence produced from E, and E contributes only 0.5 to 10 per cent to NE fluorescence; assay and blank measurements show superior stability. Elution from alumina and instrumental factors, such as optical filters, were optimized so that a single 5 ml. plasma sample sufficed for triplicate analyses of both NE and E, with duplicate blanks for each. This triplicate fluorescence assay was combined with duplicate recovery measurements of radioactive catecholamines added in tracer quantities to the plasma so as to make possible reliable estimates of the precision of measurement of each individual sample. The mean levels found for men aged 40 to 60 years from antecubital vein blood drawn during the subject's working hours (but after a brief rest) were, for NE 0.38 ng. per milliliter, range 0.15 to 0.54 ng. per millilter, and for E 0.09 ng./ml, range 0.01 to 0.27 ng. per millilter. The high precision and small amounts of blood required by this method made possible the measurement of basal plasma levels of E and NE in rats under two-stage phenobarbital anesthesia. The mean levels for 13 male and 4 female Long-Evans-stain rats weighing 250 to 350 grams were, for NE 0.26 ng. per millilter, range 0.16 to 0.37 ng. per millilter, and for E 0.36 ng. per millilter, range 0.14 to ng. per millilter. These rat values are called basal because they are only 1/5 to 1/10 as large as values obtained on plasma secured by single-stage pentobarbital anesthesia or from unanesthetized rats. Eight to 11 ml. of whole blood obtained from each rat were sufficient for individual analyses, an improvement over most other reported methods which require blood from a number of animals to be pooled. The average precision of an individual determination of NE was plus or minus 10 per cent in the range of 0.20 to 0.40 ng. per millilter. The average recovery for NE was 65 per cent and for E it was 55 per cent. Major factors influencing recovery were quantitatively investigated and discussed.

摘要

对三羟基吲哚反应的时间、温度和pH值进行控制,以尽量减少去甲肾上腺素(NE)和肾上腺素(E)之间的干扰,从而在正常人体生理范围内的血浆儿茶酚胺测定中,NE对E产生的荧光贡献小于1%,而E对NE荧光的贡献仅为0.5%至10%;测定和空白测量显示出卓越的稳定性。优化了从氧化铝上的洗脱过程以及诸如滤光片等仪器因素,使得一份5毫升的血浆样本足以对NE和E进行一式三份的分析,每份分析还带有一式两份的空白样本。这种一式三份的荧光测定法与对添加到血浆中的微量放射性儿茶酚胺进行一式两份的回收率测量相结合,从而能够可靠地估计每个个体样本测量的精密度。从40至60岁男性在工作时间(但经过短暂休息后)从肘前静脉抽取的血液中测得的平均水平,NE为每毫升0.38纳克,范围为每毫升0.15至0.54纳克,E为每毫升0.09纳克,范围为每毫升0.01至0.27纳克。该方法的高精度以及所需血量少使得在苯巴比妥两阶段麻醉下对大鼠血浆中E和NE的基础水平进行测量成为可能。对13只体重250至350克的雄性和4只雌性长-伊文斯品系大鼠测得的平均水平,NE为每毫升0.26纳克,范围为每毫升0.16至0.37纳克,E为每毫升0.36纳克,范围为每毫升0.14至[此处原文似乎有误,缺少具体数值]纳克。这些大鼠的值被称为基础值,因为它们仅为通过戊巴比妥单阶段麻醉获得的血浆值或未麻醉大鼠血浆值的1/5至1/10。从每只大鼠获取8至11毫升全血就足以进行个体分析,这相较于大多数其他报道的方法有所改进(那些方法需要汇集多只动物的血液)。在每毫升0.20至0.40纳克的范围内,对NE的个体测定平均精密度为正负10%。NE的平均回收率为65%,E的平均回收率为55%。对影响回收率的主要因素进行了定量研究和讨论。

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