Hoeprich P D, Warshauer D M
Antimicrob Agents Chemother. 1974 Mar;5(3):330-6. doi: 10.1128/AAC.5.3.330.
Although meningococci are susceptible to the tetracyclines by testing in vitro, oxytetracycline (OC) and doxycycline (DC) have failed to eliminate carriage, whereas minocycline (MC) has been effective. Because these congeners differ in lipophilicity, they and tetracycline (TC) were studied in volunteers by assay of serum, saliva, and tears obtained after 5 days of treatment. OC and TC were undetectable or attained concentrations subinhibitory for meningococci in saliva and tears. The concentrations of MC in saliva and tears were equal to or greater than the average minimal inhibitory concentration as long as 12 h post-dose. Near inhibitory concentrations resulted with DC at 100 mg/day; yet, doubling the dose to 100 mg/12 h did not yield concentrations that exceeded the average minimal inhibitory concentration for meningococci. The previous reports of failure or meager entry of DC and MC into saliva probably reflected extraction of these drugs in the paraffin chewed by subjects to stimulate salivary flow. The efficiency of entry of the tetracyclines into the secretions of the noninflamed upper respiratory tract correlates with lipophilicity at physiological pH, enabling prediction of meningococcal chemoprophylactic efficacy.
虽然通过体外试验表明脑膜炎球菌对四环素类药物敏感,但土霉素(OC)和强力霉素(DC)未能消除带菌状态,而米诺环素(MC)则有效。由于这些同系物的亲脂性不同,因此在志愿者中进行了研究,通过测定治疗5天后获得的血清、唾液和眼泪来研究它们以及四环素(TC)。在唾液和眼泪中未检测到OC和TC,或者它们达到了对脑膜炎球菌亚抑制浓度。给药后长达12小时,唾液和眼泪中MC的浓度等于或大于平均最低抑菌浓度。100mg/天的DC产生接近抑制浓度;然而,将剂量加倍至100mg/12小时并没有产生超过脑膜炎球菌平均最低抑菌浓度的浓度。先前关于DC和MC进入唾液失败或进入量少的报道可能反映了这些药物在受试者咀嚼石蜡以刺激唾液分泌时被提取。四环素进入未发炎上呼吸道分泌物的效率与生理pH下的亲脂性相关,从而能够预测脑膜炎球菌化学预防的效果。