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锝-99m 巯基白蛋白作为锝-99m 标记红细胞的潜在替代物。

Technetium-99m mercaptoalbumin as a potential substitute or technetium-99m labelled red blood cells.

作者信息

Verbeke K A, Vanbilloen H P, De Roo M J, Verbruggen A M

机构信息

Laboratory of Radiopharmaceutical Chemistry, I.F.W., K.U. Leuven, Belgium.

出版信息

Eur J Nucl Med. 1993 Jun;20(6):473-82. doi: 10.1007/BF00175159.

Abstract

Technetium-99m labelled red blood cells (99mTc-RBCs) are far superior to 99mTc-labelled human serum albumin (99mTc-HSA) for radionuclide ventriculography, but their labelling is more complex, time consuming and risk bearing (in vitro labelling) or suffers from interference by some medications (in vivo labelling). We have now modified HSA by the introduction of mercapto groups with the purpose of preparing stable and practical 99mTc-mercaptoalbumin with long retention in the vascular system, that could replace 99mTc-RBCs. HSA was incubated with N-succinimidyl S-acetylthioacetate (SATA) or N-succinimidyl 2,3-di(S-acetylthio) propionate (SATP) to introduce a chain containing one or two protected sulfhydryl groups on some of the lysine amino groups. After purification by size-exclusion chromatography (SEC), the mercapto groups were deprotected by incubation at alkaline pH or by treatment with hydroxylamine. The reaction products were used with or without SEC purification for direct or exchange labelling experiments with 99mTc at neutral pH. SEC-HPLC was used to determine labelling yields and to isolate pure 99mTc-mercaptoalbumin. Stable 99mTc-mercaptoalbumin complexes could be formed in 90%-95% yield after coupling albumin with SATA or SATP in all molar ratios used followed by deacetylation in one of the mentioned conditions. The most favourable results were obtained after reaction of SATA or SATP with HSA in a 25:1 ratio and deprotection with NH2OH. The stability of the resulting 99mTc-mercaptoacetyl-albumin (99mTc-MA-HSA) and 99mTc-dimercaptopropionyl-albumin (99mTc-DMP-HSA) and their retention in vivo in plasma of mice and rabbits are clearly higher than that of conventional 99mTc-HSA preparations. 99mTc-DMP-HSA approaches the behaviour of 125I-HSA quite well in both animal species. A preliminary study with 99mTc-DMP-HSA in a volunteer showed a retention in the vascular compartment almost identical to that of 99mTc-RBCs and clearly higher than that of a common 99mTc-HSA preparation. The results indicate that these 99mTc-mercaptoalbumins and especially 99mTc-DMP-HSA are very promising as a practical alternative to 99mTc-RBCs.

摘要

锝-99m标记的红细胞(99mTc-RBCs)在放射性核素心室造影方面远优于99mTc标记的人血清白蛋白(99mTc-HSA),但其标记过程更为复杂、耗时且有风险(体外标记),或者会受到某些药物的干扰(体内标记)。我们现在通过引入巯基对人血清白蛋白进行了修饰,目的是制备在血管系统中保留时间长、稳定且实用的99mTc-巯基白蛋白,以替代99mTc-RBCs。将人血清白蛋白与N-琥珀酰亚胺基S-乙酰硫代乙酸酯(SATA)或N-琥珀酰亚胺基2,3-二(S-乙酰硫代)丙酸酯(SATP)孵育,在一些赖氨酸氨基上引入含一个或两个受保护巯基的链。通过尺寸排阻色谱法(SEC)纯化后,在碱性pH下孵育或用羟胺处理使巯基脱保护。反应产物在中性pH下用于直接或交换标记实验,标记实验使用或不使用SEC纯化后的产物与99mTc进行。SEC-HPLC用于测定标记产率并分离纯的99mTc-巯基白蛋白。在所有使用的摩尔比下,将白蛋白与SATA或SATP偶联,然后在上述条件之一中进行脱乙酰化后,可形成产率为90%-95%的稳定99mTc-巯基白蛋白复合物。SATA或SATP与HSA以25:1的比例反应并用NH2OH脱保护后,获得了最理想的结果。所得的99mTc-巯基乙酰白蛋白(99mTc-MA-HSA)和99mTc-二巯基丙酰白蛋白(99mTc-DMP-HSA)的稳定性及其在小鼠和兔子血浆中的体内保留率明显高于传统的99mTc-HSA制剂。在两种动物中,99mTc-DMP-HSA的行为与125I-HSA非常相似。对一名志愿者进行的99mTc-DMP-HSA初步研究表明,其在血管腔室中的保留率几乎与99mTc-RBCs相同,且明显高于普通的99mTc-HSA制剂。结果表明,这些99mTc-巯基白蛋白,尤其是99mTc-DMP-HSA,作为99mTc-RBCs的实用替代品非常有前景。

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