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口服抗酸剂对静脉注射多西环素药代动力学的影响。

Effect of oral antacid administration on the pharmacokinetics of intravenous doxycycline.

作者信息

Nguyen V X, Nix D E, Gillikin S, Schentag J J

机构信息

State University of New York, Buffalo School of Pharmacy.

出版信息

Antimicrob Agents Chemother. 1989 Apr;33(4):434-6. doi: 10.1128/AAC.33.4.434.

Abstract

The effect of oral antacid administration on the pharmacokinetics of intravenous doxycycline was studied. In a randomized crossover design, six healthy male volunteers received an infusion of 200 mg of doxycycline hyclate on two occasions separated by 7 days. On one occasion, subjects were given 30 ml of aluminum hydroxide orally four times a day for 4 days, beginning 2 days prior to doxycycline dosing. Blood and urine samples were collected up to 48 and 96 h after the infusion, respectively, and were analyzed by a microbial assay. Values for volume of distribution at steady state, nonrenal clearance, urine recovery, and urine pH were not statistically different among treatment groups. With concomitant antacid therapy, the half-life of intravenous doxycycline was shortened from 16.2 +/- 2.6 to 11.2 +/- 1.2 h (P = 0.003), and total body clearance increased from 37.4 +/- 6.5 to 54.1 +/- 12.3 ml/min (P = 0.008). Area under the concentration-time curve for serum was decreased by 18 to 44%, with a 22 to 41% increase in renal clearance. Although the increase in nonrenal clearance ranged from 11 to 128%, the high variability led to a nonsignificant difference (P = 0.07). Concomitant oral antacid therapy may significantly enhance the clearance of intravenous doxycycline.

摘要

研究了口服抗酸剂对静脉注射多西环素药代动力学的影响。在随机交叉设计中,6名健康男性志愿者在两次间隔7天的情况下接受了200mg盐酸多西环素的输注。在一次试验中,受试者从多西环素给药前2天开始,每天口服30ml氢氧化铝,共4天。分别在输注后48小时和96小时采集血液和尿液样本,并通过微生物测定法进行分析。各治疗组之间的稳态分布容积、非肾清除率、尿回收率和尿pH值无统计学差异。同时进行抗酸治疗时,静脉注射多西环素的半衰期从16.2±2.6小时缩短至11.2±1.2小时(P = 0.003),全身清除率从37.4±6.5ml/min增加至54.1±12.3ml/min(P = 0.008)。血清浓度-时间曲线下面积降低了18%至44%,肾清除率增加了22%至41%。虽然非肾清除率的增加范围为11%至128%,但高变异性导致差异无统计学意义(P = 0.07)。同时口服抗酸剂治疗可能会显著提高静脉注射多西环素的清除率。

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本文引用的文献

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Pharmacokinetics of doxycycline reabsorption.
J Pharm Sci. 1980 Feb;69(2):204-7. doi: 10.1002/jps.2600690224.
4
Evidence for metabolic inertness of doxycycline.强力霉素代谢惰性的证据。
J Pharm Sci. 1981 Feb;70(2):226-8. doi: 10.1002/jps.2600700230.
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Doxycycline.多西环素
Ther Drug Monit. 1982;4(2):115-35. doi: 10.1097/00007691-198206000-00001.
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Effect of oral ferrous sulphate on the half-life of doxycycline in man.
Eur J Clin Pharmacol. 1974 Aug 23;7(5):361-3. doi: 10.1007/BF00558207.
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Metabolism of doxycycline and other tetracyclines.
Med Chir Dig. 1976 May 8;5(6):323-5.

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