Jackson P C, Pitcher E M, Davies J O, Davies E R, Sadowski C S, Staddon G E, Stirrat G M, Sunderland C A
Eur J Nucl Med. 1985;11(1):22-8. doi: 10.1007/BF00440956.
The biodistribution of a radiolabelled monoclonal antibody (123I-NDOG2) was studied in patients with ovarian tumour. It was found that the uptake patterns in known tumour sites was variable and that the clearance of the agent from the vascular pool was due to renal excretion of the radionuclide and the redistribution of the radioactively labelled compound into other compartments. The mean (+/- SD) plasma clearance time was 20.8 (+/- 2.3) h and the ratios of target (tumour) to background (thigh) ranged between 1.4 and 4.8. The ratio between the plasma radioactivity at either 3.5 or 20 h after administration was calculated relative to the initial plasma radioactivity. These values (0.79 and 0.48, respectively) were incorporated into an image-subtraction technique that allowed for redistribution outside the vascular pool. A whole-body dose equivalent to 16.3 mu Sv MBq-1 (60.4 mrem.mCi-1) was calculated.
对卵巢肿瘤患者研究了放射性标记单克隆抗体(¹²³I-NDOG2)的生物分布。发现已知肿瘤部位的摄取模式是可变的,且该制剂从血管池的清除是由于放射性核素经肾脏排泄以及放射性标记化合物重新分布到其他隔室。平均(±标准差)血浆清除时间为20.8(±2.3)小时,靶区(肿瘤)与本底(大腿)的比值在1.4至4.8之间。计算给药后3.5小时或20小时时的血浆放射性与初始血浆放射性的比值。这些值(分别为0.79和0.48)被纳入一种图像减法技术,该技术可考虑血管池外的重新分布。计算出全身剂量当量为16.3 μSv·MBq⁻¹(60.4 mrem·mCi⁻¹)。