Jones M M
Proc West Pharmacol Soc. 1984;27:163-7.
From a consideration of the donor preferences of toxic metals and the acceptor preferences of commonly used therapeutic chelating agents it is often possible to get a good estimate of the kinds of chelating agent which may be effective antagonists. The relative importance of extracellular vs. intracellular metal, however, introduces an important factor which can severely limit the utility of a given chelating agent with a toxic metal with which it forms very stable complexes. In general an effective antagonists of a specific toxic metal will be a chelating agent which can gain access to the metal in vivo and which forms a very stable complex, of modest toxicity with that metal ion which is rapidly excreted without damage to the kidney or liver. Such effective antagonists are not known for all metals.
从对有毒金属的供体偏好以及常用治疗性螯合剂的受体偏好的考虑出发,通常有可能对可能成为有效拮抗剂的螯合剂种类做出良好估计。然而,细胞外金属与细胞内金属的相对重要性引入了一个重要因素,这可能会严重限制给定螯合剂对与其形成非常稳定络合物的有毒金属的效用。一般来说,特定有毒金属的有效拮抗剂将是一种螯合剂,它能够在体内接触到该金属,并与之形成非常稳定的络合物,该络合物对该金属离子具有适度的毒性,且能迅速排出而不会损害肾脏或肝脏。并非所有金属都有这样的有效拮抗剂。