McNulty C A, Dent J C, Ford G A, Wilkinson S P
Public Health Laboratory, Gloucestershire Royal Hospital, UK.
J Antimicrob Chemother. 1988 Nov;22(5):729-38. doi: 10.1093/jac/22.5.729.
Gastric mucosal concentrations of erythromycin, amoxycillin, ampicillin and ciprofloxacin were determined in patients at upper gastrointestinal endoscopy 38-480 min after a 500 mg dose of erythromycin ethyl succinate, erythromycin stearate, amoxycillin, pivampicillin or ciprofloxacin. All the agents attained concentrations greater than the MIC 90 for Campylobacter pylori. The macrolides attained the lowest concentrations. There was no significant difference between concentrations attained with erythromycin ethyl succinate and stearate. High concentrations were attained by amoxycillin (range 14.6-322 mg/kg) and pivampicillin (range 47.5-209 mg/kg). Ciprofloxacin attained very high concentrations (range 35-1762 mg/kg); inhibitory concentrations 35 mg/kg) were still present at 6 h after the dose. Ciprofloxacin and erythromycin are ineffective in vivo despite these high gastric mucosal concentrations. Penetration into the gastric mucus and crypts where C. pylori is found will be determined by physicochemical properties of the antimicrobials, such as pKa, stability, activity over a wide range of pH, and lipid solubility.
在给予500mg琥乙红霉素、硬脂酸红霉素、阿莫西林、匹氨西林或环丙沙星后38 - 480分钟,于上消化道内镜检查时测定患者胃黏膜中红霉素、阿莫西林、氨苄西林和环丙沙星的浓度。所有药物达到的浓度均高于幽门螺杆菌的MIC90。大环内酯类药物达到的浓度最低。琥乙红霉素和硬脂酸红霉素达到的浓度之间无显著差异。阿莫西林(范围为14.6 - 322mg/kg)和匹氨西林(范围为47.5 - 209mg/kg)达到高浓度。环丙沙星达到非常高的浓度(范围为35 - 1762mg/kg);给药后6小时仍存在抑制浓度(35mg/kg)。尽管胃黏膜中这些药物浓度很高,但环丙沙星和红霉素在体内无效。抗菌药物的物理化学性质,如pKa、稳定性、在广泛pH范围内的活性和脂溶性,将决定其渗透到发现幽门螺杆菌的胃黏液和隐窝中的情况。