基于类黄酮复合物的凝胶组合物治疗正畸患者牙周病的临床前评估

IF 0.1 Q4 MEDICINE, GENERAL & INTERNAL Zaporozhye Medical Journal Pub Date : 2023-07-20 DOI:10.14739/2310-1210.2023.4.274894
О. В. Годований, Н. Л. Чухрай, О. І. Мрочко, О. І. Мартовлос, O. Hodovanyi, B. A
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引用次数: 0

摘要

这项工作的目的是临床前评估急性毒性、皮肤吸收、刺激效应、累积和过氧化氢酶活性,以及用于治疗正畸患者牙周病的局部凝胶组合物“Benzidaflaziverdine”(GCB)的致敏特性。材料和方法。119只动物参与了实验,被分为七个主要组和两个对照组。GCB以300 ~ 600 mg/kg的剂量灌胃,200 μg的剂量皮敷于耳外表面。将GCB天然溶液应用于鸡胚的皮肤和粘膜,并通过“亚慢性毒性”方法口服给药于绒毛膜-尿囊膜(CAM)表面。脂质过氧化(LPO)强度通过二烯偶联物(DCs)和丙二醛(MDA)水平来评估,抗氧化系统通过过氧化氢酶活性来评估。采用特异性白细胞聚集反应(SLAR)、特异性白细胞裂解反应和中性粒细胞损伤指标。大鼠和小鼠的致死中位数LD50均超过5000 mg/kg。GCB对粘膜的刺激作用在第2天表现为充血。经3-4天无药物干预刺激症状消失。在暴露于GCB后的第120秒两次观察中,对CAM血管的分析显示出血开始。在一项观察中,GCB在实验的第300秒引起了轻微的出血。结果发现,GCB刺激作用系数为5 (Me (Q1;Q3)为5 (4;5))。累积系数(Kcum)超过8.2。与对照组动物相比,过氧化氢酶活性、dc和LPO最终产物(如MDA)的中位数或平均值均无显著增加。SLAR试验表明,在1:10稀释的GCB影响下,发生了延迟型过敏反应。与对照组相比,稀释100倍后,主组的指标未发生显著变化。GCB属于第4类毒性物质——几乎无毒性物质,没有性别和物种敏感性,累积活性弱,对LPO系统的影响最小。GCB可推荐用于临床牙周学,为正畸患者提供医疗支持。
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Preclinical evaluation of a gel composition based on a flavonoid complex for the treatment of periodontal diseases in orthodontic patients
The aim of the work was a preclinical assessment of acute toxicity, skin resorptive, irritant effects, cumulative and catalase activity, as well as sensitizing properties of the local gel composition “Benzidaflaziverdine” (GCB) used for the treatment of periodontal diseases in orthodontic patients. Materials and methods. 119 animals were involved in the experiment, assigned to seven main and two control groups. GCB was administered intragastrically in doses of 300–600 mg/kg and intradermally of 200 μg into the outer surface of the ear. The native solution of GCB was applied to the skin and mucous membranes, administered orally by the method of “subchronic toxicity” and to the surface of the chorioallantoic membrane (CAM) of chicken embryos. The intensity of lipid peroxidation (LPO) was assessed by the level of diene conjugates (DCs) and malondialdehyde (MDA), and the antioxidant system by catalase activity. The specific leukocyte agglomeration reaction (SLAR), the specific leukocyte lysis reaction, and neutrophil damage indicators were used. Results. The median lethal dose LD50 for rats and mice of both sexes exceeded 5000 mg/kg. The irritant effect of GCB on the mucous membranes was manifested by hyperemia on the second day. Symptoms of irritation disappeared after 3–4 days without medical intervention. An analysis of the CAM blood vessels after exposure to GCB in two observations at the 120th second showed the beginning of hemorrhages. In one observation, GCB caused minor hemorrhages at the 300th second of the experiment. It was found that the coefficient of GCB irritant action was 5 (the mean score of Me (Q1; Q3) was 5 (4; 5)). The coefficient of cumulation (Kcum) exceeded 8.2. An insignificant increase in the median or mean values of catalase enzyme activity, DCs, and the amount of LPO end product such as MDA was observed compared to the control group animals. The SLAR test indicated the development of a delayed-type allergic reaction under the influence of GCB in a 1:10 dilution. One-hundred-fold dilution did not cause significant changes in the indicator in the main group compared to the control one. Conclusions. GCB belongs to the 4th class of toxicity – practically non-toxic substances, does not have sex- and species sensitivity, has weak cumulative activity, minimal effect on the system of LPO. GCB can be recommended for the use in clinical periodontology for medical support of orthodontic patients.
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Zaporozhye Medical Journal
Zaporozhye Medical Journal MEDICINE, GENERAL & INTERNAL-
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0.00%
发文量
72
审稿时长
8 weeks
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