Brion M, Lambs L, Berthon G
Agents Actions. 1985 Dec;17(2):229-42. doi: 10.1007/BF01966597.
A series of studies was previously devoted to the dependence of the bioavailability of various tetracyclines on their coordination with calcium and magnesium ions. Several clinical investigations have also shown zinc to interfere with the gastrointestinal absorption of the drug in humans. On the other hand, the administration of tetracycline to rats was reported to result in the increase of the elimination rate of zinc, which could originate in zinc-tetracycline interactions in blood plasma. Formation constants for zinc complexes with tetracycline, oxytetracycline, doxycycline, minocycline, chlortetracycline and demethylchlortetracycline were thus determined at 37 degrees C in NaCl 0.15 mol. dm-3 aqueous medium. Computer simulations were then carried out to investigate the drug influence on the distribution of the low-molecular-weight fraction of zinc in human blood plasma. Zinc-tetracycline interactions in the gastrointestinal fluid were also simulated, using clinical data relative to fasting subjects as taken from the literature. No significant effect can be expected from tetracyclines on the distribution of zinc in plasma at the usual therapeutic levels. However, zinc-tetracycline interactions have been found to be determining factors for the bioavailabilities of the metal as well as of the antibiotic in the gastrointestinal fluid.
此前有一系列研究致力于各种四环素的生物利用度与其与钙和镁离子配位的关系。多项临床研究也表明,锌会干扰人体对该药物的胃肠道吸收。另一方面,据报道给大鼠服用四环素会导致锌的消除率增加,这可能源于血浆中锌与四环素的相互作用。因此,在37℃、0.15 mol·dm⁻³ NaCl 水溶液介质中测定了锌与四环素、土霉素、强力霉素、米诺环素、金霉素和去甲基金霉素形成配合物的形成常数。然后进行计算机模拟,以研究药物对人体血浆中低分子量锌组分分布的影响。还利用从文献中获取的关于空腹受试者的临床数据,模拟了胃肠液中锌与四环素的相互作用。在通常的治疗水平下,预计四环素对血浆中锌的分布不会有显著影响。然而,已发现锌与四环素的相互作用是胃肠液中金属以及抗生素生物利用度的决定性因素。