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使用51Cr的单同位素技术测定储存红细胞的活力。有效性分析。

Measurement of the viability of stored red cells by the single-isotope technique using 51Cr. Analysis of validity.

作者信息

Beutler E, West C

出版信息

Transfusion. 1984 Mar-Apr;24(2):100-4. doi: 10.1046/j.1537-2995.1984.24284173337.x.

Abstract

A single-isotope 51Cr method often is used to evaluate the viability of stored red cells. In this technique, the red cell mass is measured by back-extrapolation to time zero (t0) of the radioactivity of the blood between 5 and 20 minutes after infusion of the sample. If there is early destruction of stored cells, this method provides an overestimate of the red cell mass and, hence, of the viability of the stored cells. Freshly drawn red cells from normal donors were labeled with 99mTc, and cells from the same donor which had been stored in citrate-phosphate-dextrose-adenine-one (CPDA-1) for periods ranging from 7 to 49 days were labeled with 51Cr. A comparison of the "true red cell mass" as determined with 99mTc with the back-extrapolated red cell mass from stored 51Cr-labeled cells has made it possible to define the magnitude of error introduced by early loss of red cells. The overestimation of red cell mass and viability was diminished if only the 51Cr radioactivity between 5 and 15 minutes after infusion was used in back-extrapolating to t0. The degree of overestimation of red cell mass was greatest when the red cell viability had declined to very low levels. However, in the entire range of 10 to 80 percent viability, the overestimate of viability was usually less than 4 percent. The overestimate of viability proved to be quite similar for all samples and may be taken into account when using the single-isotope technique for measurement of red cell viability.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

单同位素51Cr法常被用于评估储存红细胞的活力。在该技术中,通过对输注样本后5至20分钟血液放射性外推至时间零点(t0)来测量红细胞量。如果储存细胞早期被破坏,该方法会高估红细胞量,进而高估储存细胞的活力。从正常供体新鲜采集的红细胞用99mTc标记,而来自同一供体且已在枸橼酸盐 - 磷酸盐 - 葡萄糖 - 腺嘌呤 - 1(CPDA - 1)中储存7至49天的细胞用51Cr标记。将用99mTc测定的“真正红细胞量”与从储存的51Cr标记细胞外推得到的红细胞量进行比较,得以确定红细胞早期损失所引入的误差大小。如果在外推至t0时仅使用输注后5至15分钟之间的51Cr放射性,则红细胞量和活力的高估会减少。当红细胞活力降至非常低的水平时,红细胞量的高估程度最大。然而,在10%至80%活力的整个范围内,活力的高估通常小于4%。事实证明,所有样本的活力高估非常相似,在使用单同位素技术测量红细胞活力时可予以考虑。(摘要截短至250字)

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