Technetium-99m labeled agents for skeletal imaging.

J H Thrall
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Abstract

Technetium-99m labeled radiopharmaceuticals are the currently accepted agents of choice for skeletal imaging. Their introduction in 1971 literally initiated a new era in clinical bone scanning. The development of techniques for reducing Tc(VII) with Sn(II) provided the means for complexing this useful radionuclide with various phosphorus-containing compounds which were already known to be avid bone seekers. Long chain polyphosphates were widely used at first, but have been superceded by pyrophosphate and its organic analogs, the diphosphonates. Pyrophosphate is characterized chemically by P--O--P bonds, and the diphosphonates by P--C--P bonds. The chemical forms of their complexes with tin and technetium are not known, but they behave in many respects as weak chelates. Labeling efficiencies for 99mTc of 95% or better are routinely obtainable with both "in house" preparations and commercial kits. Proper molar concentrations and ratios of phosphorus-compound to tin are necessary for both for good labeling and to achieve optimum tissue distribution. Unreacted TcO4- and reduced unbound 99mTc are both potential contaminants in these preparations and must be considered in radiochemical quality control. In vivo tissue distribution and kinetics of the 99mTc-Sn-phosphorus compounds differ with details of preparation, category of agent, and clinical status of the patient. Blood clearance is multi-exponential, with skeletal uptake and urinary clearance accounting for most of the activity. Scanning may be started in 2 1/2 to 4 hr, at which time skeletal activity is on the order of 40 to 50% of the injected dose. The primary indication for bone scanning remains the detection of metastases from extraskeletal malignancies, and the 99mTc labeled agents are more sensitive than either radiographs or Fluorine-18 for demonstrating active lesions. In addition, many new applications in evaluating benign bone disease have widened the clinical scope of skeletal imaging which is rapidly becoming one of the most important studies in nuclear medicine.

用于骨骼成像的锝-99m标记剂。
锝-99m标记的放射性药物是目前公认的骨骼成像选择剂。1971年,它们的问世开启了临床骨扫描的新纪元。用Sn(II)还原Tc(VII)的技术的发展为这种有用的放射性核素与各种含磷化合物络合提供了手段,这些化合物已经被认为是狂热的寻骨者。长链多磷酸盐最初被广泛使用,但已被焦磷酸盐及其有机类似物二磷酸盐所取代。焦磷酸盐的化学特征是P—O—P键,二磷酸盐的化学特征是P—C—P键。它们与锡和锝的配合物的化学形式尚不清楚,但它们在许多方面表现为弱螯合剂。99mTc的标记效率为95%或更高,通常可以通过“内部”制剂和商业试剂盒获得。适当的摩尔浓度和磷化合物与锡的比例对于良好的标记和实现最佳组织分布都是必要的。未反应的TcO4-和还原的未结合的99mTc都是这些制剂中的潜在污染物,必须在放射化学质量控制中加以考虑。99mtc - sn -磷化合物的体内组织分布和动力学随制剂、药物类别和患者临床状态的细节而异。血液清除是多指数的,骨骼摄取和尿液清除占大部分活动。扫描可在2 1/2至4小时内开始,此时骨骼活动约为注射剂量的40%至50%。骨扫描的主要指征仍然是检测骨骼外恶性肿瘤的转移,99mTc标记剂在显示活动性病变方面比x线片或氟-18更敏感。此外,在评估良性骨病方面的许多新应用拓宽了骨骼成像的临床范围,正迅速成为核医学最重要的研究之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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