首页> 外文期刊>Acta Cirurgica Brasileira >Metronidazole concentration in the bloodstream following its topical application, at different concentration levels, on experimental skin wounds during healing by secondary intention 1
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Metronidazole concentration in the bloodstream following its topical application, at different concentration levels, on experimental skin wounds during healing by secondary intention 1

机译:甲硝唑局部应用后在实验性皮肤伤口上以不同浓度水平局部应用甲硝唑后在血流中的浓度1

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Purpose: To characterize qualitatively and quantitatively the absorption of metronidazole solution, in greater concentrations and for longer periods, when applied topically to an experimental open skin wound model. Methods: An open skin wound, 2 cm in diameter and total skin thickness was prepared, under anesthetic, in the dorsal region of 108 Wistar rats weighing between 300 and 350 grams. The animals were allocated to groups of 18 animals in accordance with the concentration of metronidazole in the solution to be applied daily to the wound. In the control group (CG), 0.9% sodium chloride solution was used for application, and in the experimental groups (GI, GII, GIII, GIV and GV) metronidazole solution at 4%, 6%, 8%, 10% and 12%, respectively, was applied. After 3, 7 and 14 days of treatment. Blood samples collected through cardiac puncture were examined for the existence or non-existence of metronidazole, using high performance liquid chromatography (HPLC). Detected metronidazole values were compared statistically within each group (temporal analysis 3 days X 7 days X 14 days) and between the groups that used topical metronidazole (4% X 6% X 8% X 10% and 12%) using the Kruskal-Wallis test, considering a statistical significance of 95% (p0.05). Results: Metronidazole was detected in all the samples at all times in all the groups in which topical metronidazole was applied to the wounds. Characteristically, there was no significant difference between the doses obtained within each group over time (3 days X 7 days X 14 days) GI=0.461; GII=0.154; GIII=0.888; GIV= 0.264 and GV=0.152. In the evaluation between groups, a similar degree of absorption was found after 3 days (p=0.829) and 14 days (p=0.751). Conclusion: The serum concentration of metronidazole that was achieved was not influenced by the concentration of the solution applied to the skin wound, with similar extend, or by the duration of the application.
机译:目的:当将甲硝唑溶液局部应用于实验性开放性皮肤伤口模型时,以更高的浓度和更长的时间定性和定量地表征甲硝唑溶液的吸收。方法:在麻醉下,在108只体重在300至350克之间的Wistar大鼠的背侧区域准备一个直径为2厘米,皮肤总厚度为2厘米的开放性皮肤伤口。根据每天施加于伤口的溶液中甲硝唑的浓度,将动物分为18只动物。在对照组(CG)中,使用0.9%氯化钠溶液,在实验组(GI,GII,GIII,GIV和GV)中,甲硝唑溶液的浓度分别为4%,6%,8%,10%和12分别应用%。经过3、7和14天的治疗。使用高效液相色谱(HPLC)检查通过心脏穿刺收集的血液样本中甲硝唑的存在与否。使用Kruskal-Wallis在各组之间(时间分析3天X 7天X 14天)以及使用局部甲硝唑的组之间(4%X 6%X 8%X 10%和12%)对检测到的甲硝唑值进行统计学比较。检验的统计显着性为95%(p <0.05)。结果:在局部将甲硝唑应用于伤口的所有组中,所有时间都在所有样品中检测到甲硝唑。特征在于,随着时间的推移(3天X 7天X 14天),各组之间获得的剂量之间无显着差异GI = 0.461; GII = 0.154; GIII = 0.888; GIV = 0.264和GV = 0.152。在各组之间的评估中,在3天(p = 0.829)和14天(p = 0.751)之后发现相似的吸收程度。结论:甲硝唑的血清浓度不受皮肤伤口溶液浓度的影响,延长的时间或持续时间均不受其影响。

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