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在两种动物模型中对体外标记的锝 Tc-99m 红细胞进行评估和测试,用于新生儿红细胞体积测定。

Evaluation and testing of in vitro labeled technetium Tc-99m red blood cells in two animal models for neonatal RBC volume determinations.

作者信息

Dirksen J W, Quaife M A, Paxson C L, Barton T P

出版信息

Pediatr Res. 1981 Jun;15(6):905-7. doi: 10.1203/00006450-198106000-00004.

Abstract

The present study was designed to evaluate the red blood cell (RBC) radiolabeling technique utilizing the short half-lived radionuclide technetium-99m and to compare the results with the well-recognized standard chromium-51 method. The procedure was evaluated in a canine and a newborn lamb model utilizing dual radionuclide labeling and counting techniques. With the express purpose of providing a significant radiation dose reduction, the procedure presented was adapted for utilization in a neonatal patient population. Statistical analysis of the data revealed that there was no significant difference in the radiolabeling efficiency for the two methods (Cr-51, 86.6%; Tc-99m, 92.4%). Assessment of the in vitro stability for technetium-99m RBCs showed that less than a 4% loss of radiolabel from the RBC was seen in a 4-hr time span in the canine model (15 min, 90.5%; 2 hr, 88.9%; 4 hr, 86.6%) when compared to the 15 min equilibrium sample. Evaluation of newborn lamb RBC volumes showed that the technetium-99m RBC volume did not significantly differ from the chromium-51 labeling technique (Cr-51, 24.0 ml/kg; Tc-99m, 23.2 ml/kg). Summarization of the whole-body radiation dose showed that greater than a 30-fold reduction in absorbed dose was achieved in the newborn (Cr-51, 30.0 mrad; Tc-99m, 0.9 mrad). The modified procedure presented for the radiolabeling of the RBC with the short half-lived radionuclide technetium-99m provides a technique comparable to the utilized standard chromium-51 RBC method, yet with a large reduction in absorbed radiation dose. This procedure is presented as a superior technique for the determination of pediatric RBC volumes.

摘要

本研究旨在评估利用短半衰期放射性核素锝-99m的红细胞(RBC)放射性标记技术,并将结果与公认的标准铬-51方法进行比较。该程序在犬和新生羔羊模型中利用双放射性核素标记和计数技术进行评估。为了显著降低辐射剂量,所提出的程序适用于新生儿患者群体。数据的统计分析表明,两种方法的放射性标记效率没有显著差异(铬-51为86.6%;锝-99m为92.4%)。对锝-99m红细胞的体外稳定性评估表明,与15分钟平衡样本相比,在犬模型中,4小时内红细胞放射性标记损失不到4%(15分钟时为90.5%;2小时时为88.9%;4小时时为86.6%)。对新生羔羊红细胞体积的评估表明,锝-99m红细胞体积与铬-51标记技术没有显著差异(铬-51为24.0 ml/kg;锝-99m为23.2 ml/kg)。全身辐射剂量总结表明,新生儿的吸收剂量降低了30倍以上(铬-51为30.0 mrad;锝-99m为0.9 mrad)。用短半衰期放射性核素锝-99m对红细胞进行放射性标记的改进程序提供了一种与使用的标准铬-51红细胞方法相当的技术,但吸收辐射剂量大幅降低。该程序是测定儿科红细胞体积的一种优越技术。

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