Yamaoka K, Nakagawa T, Uno T
J Pharm Pharmacol. 1983 Jan;35(1):19-22. doi: 10.1111/j.2042-7158.1983.tb04256.x.
Disposition kinetics of cefamandole, cefoperazone, cefotiam, cefmenoxime and cefmetazole following rapid intravenous injection into rats is investigated. The plasma concentrations of the antibiotics are determined by the high performance liquid chromatographic method, and the pharmacokinetic behaviours of the cephalosporins are evaluated by moment analysis which is a model-independent method. Analysis of variance (ANOVA) followed by the paired t-test reveals that cefmetazole and cefmenoxime have greater mean residence time (MRT) than cefotiam, cefamandole and cefoperazone, and that cefamandole and cefmetazole show larger steady-state volume of distribution (Vss) than the other cephalosporins. Cefamandole has the greatest total body clearance (40.2 ml kg-1 min-1) and cefmenoxime the smallest (7.72 ml kg-1 min-1).
研究了头孢孟多、头孢哌酮、头孢替安、头孢甲肟和头孢美唑快速静脉注射入大鼠后的处置动力学。通过高效液相色谱法测定抗生素的血浆浓度,并采用矩量法(一种与模型无关的方法)评估头孢菌素的药代动力学行为。方差分析(ANOVA)后进行配对t检验,结果显示头孢美唑和头孢甲肟的平均驻留时间(MRT)比头孢替安、头孢孟多和头孢哌酮更长,且头孢孟多和头孢美唑的稳态分布容积(Vss)比其他头孢菌素更大。头孢孟多的全身清除率最高(40.2 ml·kg⁻¹·min⁻¹),头孢甲肟最低(7.72 ml·kg⁻¹·min⁻¹)。