Griffith R S, Black H R, Brier G L, Wolny J D
Antimicrob Agents Chemother. 1977 May;11(5):809-12. doi: 10.1128/AAC.11.5.809.
Two oral 0.5-g doses of probenecid given 7 and 1 h before a single 1-g intramuscular dose of cefamandole resulted in higher serum levels of cefamandole than when cefamandole was given alone: 37 versus 20 mug per ml of serum, respectively. Cefamandole was not measurable (<0.3 mug/ml) at 8 h when it was given alone, whereas an average 8-h value of 2.9 mug/ml was obtained after pretreatment with probenecid. By prolonging the duration of these high cefamandole levels, probenecid should permit the treatment of more serious clinical infections, including those due to relatively resistant organisms, or permit a reduction in either the dosage of cefamandole or the frequency of administration.
在单次肌内注射1g头孢孟多之前7小时和1小时分别口服0.5g丙磺舒,与单独使用头孢孟多相比,可使头孢孟多的血清水平更高:分别为每毫升血清37微克和20微克。单独使用头孢孟多时,8小时时无法测出头孢孟多(<0.3微克/毫升),而在丙磺舒预处理后,8小时的平均数值为2.9微克/毫升。通过延长这些高头孢孟多水平的持续时间,丙磺舒应能用于治疗更严重的临床感染,包括由相对耐药菌引起的感染,或者能减少头孢孟多的剂量或给药频率。