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口服β-内酰胺类药物在人体所能达到的浓度下对青霉素敏感和耐药肺炎链球菌的体外活性及产生耐药性的可能性。

In vitro activities of oral beta-lactams at concentrations achieved in humans against penicillin-susceptible and -resistant pneumococci and potential to select resistance.

作者信息

Thorburn C E, Knott S J, Edwards D I

机构信息

SmithKline Beecham Pharmaceuticals, Brockham Park, Betchworth, Surrey RH3 7AJ, United Kingdom.

出版信息

Antimicrob Agents Chemother. 1998 Aug;42(8):1973-9. doi: 10.1128/AAC.42.8.1973.

Abstract

The beta-lactam susceptibilities of 65 strains of Streptococcus pneumoniae for which penicillin MICs covered a broad range were assessed. The order of potency was amoxicillin (AMX) = amoxicillin-clavulanate (AMC) > penicillin G > cefpodoxime (CPO) > cefuroxime (CXM) > cefprozil > cefaclor > loracarbef > cefixime. No decrease in susceptibility was seen following repeated subculture of two penicillin-susceptible strains of S. pneumoniae in AMX, AMC, cefaclor, or loracarbef, whereas repeated exposure to CPO and CXM resulted in 4- to 32-fold decreases in susceptibility for both strains. When one of these strains was exposed to concentrations of CPO, CXM, AMX, and AMC achieved in the serum of humans following the administration of an oral dose, all agents were rapidly bactericidal, with no decrease in susceptibility up to 72 h. This was consistent with antibiotic concentrations exceeding the MICs for 100% of the dosing interval. For a penicillin-resistant strain, MICs were exceeded for 29% of the 12-h dosing interval for 500 mg of AMX, 42% of the interval for AMC with 875 mg of AMX and 125 mg of clavulanate (875/125 mg of AMC) 21% of the interval for 500 mg of CXM, and 0% of the interval for 200 mg of CPO. Consequently, only 875/125 mg of AMC produced a sustained bactericidal effect. A four- to eightfold reduction in susceptibility to CPO and CXM and cross-resistance with cefotaxime, but not penicillin or AMC, were selected following exposure to simulated serum CPO and CXM concentrations. In addition, AMX and AMC were the only agents which consistently produced a >99% reduction in bacterial numbers in time-kill studies using concentrations of antibiotic achieved in middle ear fluid for all three strains of penicillin-resistant S. pneumoniae tested.

摘要

评估了65株肺炎链球菌的β-内酰胺敏感性,这些菌株的青霉素MIC覆盖了较宽范围。效力顺序为阿莫西林(AMX)=阿莫西林-克拉维酸(AMC)>青霉素G>头孢泊肟(CPO)>头孢呋辛(CXM)>头孢丙烯>头孢克洛>氯碳头孢>头孢克肟。两株青霉素敏感的肺炎链球菌在AMX、AMC、头孢克洛或氯碳头孢中反复传代培养后,未见敏感性降低,而反复暴露于CPO和CXM导致两株菌的敏感性降低4至32倍。当其中一株菌暴露于口服给药后人体血清中达到的CPO、CXM、AMX和AMC浓度时,所有药物均具有快速杀菌作用,直至72小时敏感性均未降低。这与抗生素浓度在整个给药间隔的100%时间内超过MIC一致。对于一株青霉素耐药菌株,500mg AMX在12小时给药间隔的29%时间内、875mg AMX和125mg克拉维酸(875/125mg AMC)在42%时间内、500mg CXM在21%时间内以及200mg CPO在0%时间内超过MIC。因此,只有875/125mg AMC产生持续杀菌作用。暴露于模拟血清CPO和CXM浓度后,对CPO和CXM的敏感性降低4至8倍,并与头孢噻肟产生交叉耐药,但与青霉素或AMC无交叉耐药。此外,在对所有三株青霉素耐药肺炎链球菌进行的时间杀菌研究中,使用中耳液中达到的抗生素浓度,AMX和AMC是唯一始终能使细菌数量减少>99%的药物。

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