Groppo F C, Mattos-Filho T R, Del-Fiol F S
Department of Physiological Sciences, Area of Pharmacology, Dentistry, School of Piracicaba, UNICAMP Brazil, Piracicaba-Sao Paulo.
Biol Pharm Bull. 2000 Sep;23(9):1033-5. doi: 10.1248/bpb.23.1033.
Few reports are available about tissue concentration of amoxicillin. The techniques used to measure tissue concentration usually require rupture and are expensive. The objective of the present study is to assess the utility of an animal model to predict tissue concentration of amoxicillin using induced granulomatous tissue. We used 160 rats with four polyurethane sponges previously implanted in their backs. At 7, 14, 21 and 28 d after sponge introduction, groups of eight animals each received 3.5, 7.0, 40.0 or 80.0 mg/kg of amoxicillin (p.o.) or 1 ml of 0.9% NaCl solution (control group). One hour after drug administration, 10 microl of serum and granulomatous tissue were obtained. Tissue and serum were placed on different plates containing Mueller Hinton agar inoculated with 10(8) cfu (colony forming unit) of Staphylococcus aureus (ATCC 25923), and the diameters of the inhibition zones were measured after 18 h of incubation. Analysis of variance showed no statistically significant differences (p>0.05) among time periods for the same dose of amoxicillin. These results suggest that the pharmacokinetics of amoxicillin did not change in relation to the development of granulomatous tissue; therefore this method is valid to measure the tissue concentration of amoxicillin.
关于阿莫西林的组织浓度,相关报道较少。用于测量组织浓度的技术通常需要破坏组织且成本高昂。本研究的目的是评估一种动物模型利用诱导性肉芽肿组织预测阿莫西林组织浓度的效用。我们使用了160只大鼠,它们的背部预先植入了四块聚氨酯海绵。在植入海绵后的第7、14、21和28天,每组8只动物分别接受3.5、7.0、40.0或80.0mg/kg的阿莫西林(口服)或1ml 0.9%氯化钠溶液(对照组)。给药1小时后,采集10微升血清和肉芽肿组织。将组织和血清分别置于含有接种了10(8)cfu(菌落形成单位)金黄色葡萄球菌(ATCC 25923)的Mueller Hinton琼脂的不同平板上,孵育18小时后测量抑菌圈直径。方差分析显示,相同剂量阿莫西林在不同时间段之间无统计学显著差异(p>0.05)。这些结果表明,阿莫西林的药代动力学与肉芽肿组织的发育无关;因此,该方法可有效测量阿莫西林的组织浓度。