Comparative assessment of different methods of studying skin toxicity of powder for wounds

V. Kushnir, I. Kushnir, B. Gutyj, O. Kutsan, S. Nychyk, M. Simonov, Z. Guta
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引用次数: 1

Abstract

The article provides data on the comparative assessment of the study of acute and subacute dermal toxicity of powder for wounds made based on iodoform by various methods. The research was conducted using the classic method and according to the methodology of the Organization for Economic Cooperation and Development (OECD No. 410). When studying acute skin toxicity using the traditional method, it was established that the drug under study belongs to the IV toxicity class (low-toxic substances) and, when determined by the way according to the UGS (GHS) – to category 5. During long-term dermal application of powder for wounds, no significant changes in hemoglobin concentration, hematocrit value, the average concentration of hemoglobin in erythrocytes (MCHC), the average volume of erythrocytes (MCV), the average content of hemoglobin in erythrocytes (MCH) and several platelets were established by the classical method. In addition, a slight increase in creatinine, urea, and the activity of ALT and AST was established against a slight decrease in the total protein content. When studying the acute toxicity of powder for wounds following the OECD method No. 410, it was confirmed that long-term dermal application of the investigated agent caused a slight increase in the weight coefficients of the liver, heart, and spleen and a probable increase in the weight coefficients of the kidneys against the background of a decrease in the body weight of animals. Also, in animals of all experimental groups, the number of erythrocytes increased by 0.6 %, 5.1 %, and 10.5 % (Р < 0.05), respectively, and the number of leukocytes decreased by 15.9 % (Р < 0.05), 21.8 % (Р < 0.05), 23.4 % (Р < 0.05), mean erythrocyte volume (MCV) by 2.4 %, 4.2 %, 9.2 % (Р < 0,05). When determining the biochemical indicators of blood serum, it was established that using the research product for 28 days caused a slight decrease in the total protein content in animals of the I, II, and III research groups. In addition, the animals of all experimental groups showed an increase in the level of creatinine, respectively, by – 10.6 % (Р < 0.05), 13.3 % (Р < 0.05), 15.4 % (Р < 0.05), urea at – 3.3 %, 7.3 % (Р < 0.05), 12.6 % (Р < 0.05).
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不同研究粉末对伤口皮肤毒性方法的比较评价
本文提供了用不同方法制备碘仿粉末对伤口急性和亚急性皮肤毒性研究的比较评估数据。这项研究采用了经典方法,并根据经济合作与发展组织(经合组织第410号)的方法进行。当使用传统方法研究急性皮肤毒性时,已确定所研究的药物属于IV毒性类别(低毒物质),当根据UGS(GHS)确定时,属于第5类。在长期皮肤应用粉末治疗伤口的过程中,通过经典方法确定血红蛋白浓度、红细胞比容值、红细胞中血红蛋白的平均浓度(MCHC)、红细胞的平均体积(MCV)、红红细胞中的血红蛋白的平均含量(MCH)和几个血小板没有显著变化。此外,肌酸酐、尿素、ALT和AST活性略有增加,而总蛋白质含量略有下降。根据OECD第410号方法研究粉末对伤口的急性毒性时,证实了长期经皮施用所研究的药剂会导致肝脏、心脏和脾脏的重量系数略有增加,并且在动物体重下降的背景下,肾脏的重量系数可能会增加。此外,在所有实验组的动物中,红细胞数量分别增加了0.6%、5.1%和10.5%(Р<0.05),白细胞数量减少了15.9%(Р<0.05)、21.8%(Р<0.005)、23.4%(Р=0.05),平均红细胞体积(MCV)减少了2.4%、4.2%、9.2%(Р<0,05)。在测定血清的生化指标时,确定使用研究产品28天会导致I、II和III研究组动物的总蛋白质含量略有下降。此外,所有实验组的动物的肌酸酐水平分别增加了-10.6%(Р<0.05)、13.3%(Р<0.05)和15.4%(Р=0.05),尿素水平增加了-3.3%、7.3%(РP<0.05)和12.6%(Рp<0.05)。
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