Geny F, Costa P, Bressolle F, Galtier M
Laboratoire de pharmacocinétique, Pharmacie Carémeau, Nîmes, France.
Biopharm Drug Dispos. 1993 Mar;14(2):161-9. doi: 10.1002/bdd.2510140207.
In a prospective study, the epididymal penetration of ceftriaxone was evaluated in order to use it in the treatment of orchi-epididymitis in men. A bolus intravenous dose of 1 g of ceftriaxone was administered to 15 patients hospitalized for surgery as part of treatment for prostatic adenoma or prostatic cancer. Nine successive blood samples were collected in the interval from 0 to 24 h after administration, and epididymis samples were taken 0.75 h after administration. Concentrations of drug in all samples were assayed by a reverse-phase-ion pairing high-performance liquid chromatography method with UV detection. The results showed that the pharmacokinetics of ceftriaxone in serum did not differ from those determined previously in healthy volunteers. The terminal half-life was 6.9 +/- 1.7 h, and the mean residence time 9.5 +/- 2.3 h. The volume of distribution was 0.144 +/- 0.018 1 kg-1 and the total body clearance 1.17 +/- 0.29 l h-1. The concentrations in tissue reached 27.2 +/- 6 micrograms g-1 in righ epididymis, and 25.4 +/- 6.2 micrograms g-1 in left epididymis. The tissue-versus-serum concentration ratios ranged from 0.175 to 0.545 (mean value, 0.295 +/- 0.099). The concentrations in serum and tissue observed in this study were in excess of the MICs for bacteria considered to be susceptible to ceftriaxone, particularly Neisseria gonorrhoeae and coliform bacteria.
在一项前瞻性研究中,对头孢曲松在附睾中的渗透情况进行了评估,以便将其用于男性睾丸炎-附睾炎的治疗。对15名因前列腺腺瘤或前列腺癌手术住院治疗的患者静脉注射1 g头孢曲松。给药后0至24小时内连续采集9份血样,给药后0.75小时采集附睾样本。采用反相离子对高效液相色谱法和紫外检测法测定所有样本中的药物浓度。结果表明,头孢曲松在血清中的药代动力学与先前在健康志愿者中测定的结果无差异。终末半衰期为6.9±1.7小时,平均驻留时间为9.5±2.3小时。分布容积为0.144±0.018 1 kg-1,全身清除率为1.17±0.29 l h-1。右侧附睾组织浓度达到27.2±6 μg g-1,左侧附睾组织浓度达到25.4±6.2 μg g-1。组织与血清浓度比在0.175至0.545之间(平均值为0.295±0.099)。本研究中观察到的血清和组织中的浓度超过了被认为对头孢曲松敏感细菌的最低抑菌浓度,尤其是淋病奈瑟菌和大肠菌。