Abushhiwa Mohamed H, Salehi Nouria S, Whitton Robert C, Charles Jennifer A, Finnin Peter J, Lording Peter M, Parry Bruce W
Faculty of Veterinary Science, The University of Melbourne, Werribee, Vic. 3030, Australia.
Vet Radiol Ultrasound. 2009 Sep-Oct;50(5):545-9. doi: 10.1111/j.1740-8261.2009.01576.x.
Technetium-99m stannous colloid (9mTcSnC) has been used to radiolabel human leukocytes to investigate various inflammatory disorders. We investigated the in vitro behavior of feline leukocytes labeled in whole blood with 99mTcSnC. Heparinized blood samples were collected from healthy cats and divided into control and test aliquots. The latter were labeled with 99mTcSnC using a standard procedure. Leukocyte viability was determined for each sample using a trypan blue exclusion test. Labeling efficiency was determined for test aliquots. Test aliquots were layered onto Histopaque-1077 and centrifuged before measurement of radioactivity of the blood components. Leukocytes from radiolabeled and control samples were washed and incubated with opsonized zymosan particles to allow assessment of phagocytic function. Aliquots were taken from radiolabeled feline leukocyte samples at 1, 3, 4, and 7 h postlabelling. After centrifugation of each aliquot, radioactivity of the supernatant and pellet was measured and the labeling retention determined. Leukocyte viability in both radiolabeled and control samples was > 98%. The labeling efficiency was 95.2 +/- 0.14%. The distribution of radioactivity in feline blood was found to be 3.4 +/- 0.18% in plasma, 39.0 +/- 0.37% in erythrocytes, and 57.6 +/- 0.38% in leukocytes. Labeled feline leukocytes had phagocytic activity of 90.9 +/- 0.18% (control 91.3 +/- 0.15%). The radiolabeled leukocytes retained 93.4 +/- 0.19% of the radioactivity up to 7h postlabeling. 99TcSnC efficiently labeled feline leukocytes with no effect on viability and minimal effect on phagocytic function. The percentage retention of radioactivity by the leukocytes was still high at 7h postlabeling.
锝-99m 锡胶体(9mTcSnC)已被用于标记人类白细胞以研究各种炎症性疾病。我们研究了用 99mTcSnC 在全血中标记的猫白细胞的体外行为。从健康猫采集肝素化血样并分为对照和测试等分试样。后者使用标准程序用 99mTcSnC 进行标记。使用台盼蓝排斥试验测定每个样品的白细胞活力。测定测试等分试样的标记效率。在测量血液成分的放射性之前,将测试等分试样铺在 Histopaque-1077 上并离心。将放射性标记和对照样品中的白细胞洗涤并与调理的酵母聚糖颗粒孵育以评估吞噬功能。在标记后 1、3、4 和 7 小时从放射性标记的猫白细胞样品中取出等分试样。对每个等分试样离心后,测量上清液和沉淀的放射性并确定标记保留率。放射性标记和对照样品中的白细胞活力均>98%。标记效率为 95.2±0.14%。发现猫血液中放射性的分布为血浆中 3.4±0.18%,红细胞中 39.0±0.37%,白细胞中 57.6±0.38%。标记的猫白细胞的吞噬活性为 90.9±0.18%(对照为 91.3±0.15%)。放射性标记的白细胞在标记后长达 7 小时保留了 93.4±0.19%的放射性。99TcSnC 有效地标记了猫白细胞,对活力无影响,对吞噬功能影响最小。标记后 7 小时白细胞的放射性保留百分比仍然很高。