Barkworth M F, Mangold B, Rehm K D, Schmieder G, Töberich H, Vinchenzo A, Weber J, Rübartsch C
Iphar-CRF Institut für Klinische Pharmakologie GmbHa, München.
Arzneimittelforschung. 1991 Aug;41(8):839-43.
A preliminary study revealed that similarly to the antibiotics amoxillin, thiamphenicol, erythromycin and doxycycline, the oral cephalosporin cefadroxil (CAS 66592-87-8) can be administered simultaneously with the mucolytic n-acetylcysteine (CAS 616-91-1). In the present study 12 healthy male volunteers received in a randomised cross-over design a single oral dose of 1000 mg cefadroxil or a single oral dose of 1000 mg cefadroxil (Bidocef) plus 200 mg n-acetylcysteine. The two study days were separated by a wash-out period of one week. To determine the pharmacokinetic profile of cefadroxil, plasma and sputum were analysed by HPLC at defined intervals. Regarding the bioavailability of cefadroxil, the free combination is bioequivalent to the individual component. After administration of cefadroxil plus n-acetylcysteine, a higher cefadroxil concentration was found in the sputum compared to an administration of cefadroxil alone. However, the difference was not statistically significant. According to the results, simultaneous administration of the oral cephalosporin cefadroxil and the mucolytic n-acetylcysteine is possible without changes in the bioavailability of cefadroxil being observed.
一项初步研究显示,与抗生素阿莫西林、甲砜霉素、红霉素和强力霉素类似,口服头孢菌素头孢羟氨苄(CAS 66592-87-8)可与黏液溶解剂n-乙酰半胱氨酸(CAS 616-91-1)同时给药。在本研究中,12名健康男性志愿者采用随机交叉设计,接受了1000毫克头孢羟氨苄的单次口服剂量,或1000毫克头孢羟氨苄(必度头孢)加200毫克n-乙酰半胱氨酸的单次口服剂量。两个研究日之间间隔一周的洗脱期。为了确定头孢羟氨苄的药代动力学特征,在规定的时间间隔通过高效液相色谱法分析血浆和痰液。关于头孢羟氨苄的生物利用度,游离组合与单个成分生物等效。与单独服用头孢羟氨苄相比,服用头孢羟氨苄加n-乙酰半胱氨酸后,痰液中头孢羟氨苄的浓度更高。然而,差异无统计学意义。根据结果,口服头孢菌素头孢羟氨苄和黏液溶解剂n-乙酰半胱氨酸同时给药是可行的,且未观察到头孢羟氨苄的生物利用度发生变化。