Mattos Filho Thales Rocha, Junqueira Marcelo de Souza, Groppo Francisco Carlos, Motta Rogério Heládio Lopes, Perazzo Fábio Ferreira
Department of Pharmacology, Anesthesiology and Therapeutics, Piracicaba Dental School - UNICAMP, SP, Brazil.
J Appl Oral Sci. 2006 Oct;14(5):319-23. doi: 10.1590/s1678-77572006000500004.
Antimicrobial agents in combination with anti-inflammatory drugs have been usually prescribed in both Medicine and Dentistry. However, few scientific reports support this clinical practice. The aim of this study was to evaluate the effect of betamethasone and diclofenac sodium on serum and tissue concentration of amoxicillin in rats.
Four polyurethane sponges were implanted in the back skin of 48 rats. After seven days the animals were divided into 6 groups (n=8). Group 1: amoxicillin (25 mg/kg); G2: diclofenac sodium (2.5 mg/kg); G3: betamethasone (0.1 mg/kg); G4: diclofenac sodium and amoxicillin; G5: betamethasone and amoxicillin; and G6: 0.9% sodium chloride solution (1.0 mL - control group). All drugs were administered in a single dose. After 90 minutes, the granulomatous tissues of each animal were surgically removed and weighed. Blood was collected from cervical plexus, centrifuged and 10microL of serum was placed on paper discs. In order to estimate amoxicillin concentration, serum and granulomatous tissues were separately submitted to microbiological assay, which used 10(8)cfu/mL of Staphylococcus aureus ATCC 25923 (penicillin-susceptible strain). After incubation (18 hours, 37 degrees C) the inhibition zones were measured and compared to a regression curve.
No inhibition zones were observed for groups 2, 3 and 6. Tissue and serum concentrations of both G1 (4.14microg/g and 2.06microg/mL, respectively) and G5 (3.87microg/g and 1.70microg/mL, respectively) showed statistically significant differences (Kruskal-Wallis, p<0.05) in comparison to G4 (1.45microg/g and 0.41microg/mL, respectively). G1 and G5 did not differ significantly (p>0.05).
Considering single doses, betamethasone did not interfere with amoxicillin levels but diclofenac sodium reduced both tissue and serum levels of amoxicillin in rats.
在医学和牙科领域,抗菌药物通常会与抗炎药物联合使用。然而,很少有科学报告支持这种临床做法。本研究的目的是评估倍他米松和双氯芬酸钠对大鼠血清和组织中阿莫西林浓度的影响。
在48只大鼠的背部皮肤植入4块聚氨酯海绵。7天后,将动物分为6组(n = 8)。第1组:阿莫西林(25mg/kg);第2组:双氯芬酸钠(2.5mg/kg);第3组:倍他米松(0.1mg/kg);第4组:双氯芬酸钠和阿莫西林;第5组:倍他米松和阿莫西林;第6组:0.9%氯化钠溶液(1.0mL - 对照组)。所有药物均单次给药。90分钟后,手术切除每只动物的肉芽肿组织并称重。从颈丛采集血液,离心后将10μL血清置于纸片上。为了估计阿莫西林浓度,血清和肉芽肿组织分别进行微生物测定,该测定使用10⁸cfu/mL的金黄色葡萄球菌ATCC 25923(青霉素敏感菌株)。孵育(18小时,37℃)后,测量抑菌圈并与回归曲线进行比较。
第2组、第3组和第6组未观察到抑菌圈。与第4组(分别为1.45μg/g和0.41μg/mL)相比,第1组(分别为4.14μg/g和2.06μg/mL)和第5组(分别为3.87μg/g和1.70μg/mL)的组织和血清浓度显示出统计学显著差异(Kruskal - Wallis检验,p < 0.05)。第1组和第5组无显著差异(p > 0.05)。
考虑单次给药,倍他米松不干扰阿莫西林水平,但双氯芬酸钠降低了大鼠阿莫西林的组织和血清水平。