纳米碳酸锌对白鼠模型的急性毒性

V. Koshevoy, S. Naumenko, O. Orobchenko, I. Bespalova
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摘要

锌基纳米颗粒(NPs)被成功用于满足动物和家禽对矿物质的需求,能够提高生长速度和饲料利用效率。氧化锌纳米颗粒被广泛使用,它在药理活性和生物利用率方面优于传统锌源,对生产力和抗氧化保护有积极影响,并能提高繁殖潜力。然而,对其毒理学参数的详细调查显示了其进入人体的风险,因此大量氧化锌 NPs 采用 "绿色化学 "方法合成,其主要缺点是方法复杂、成本高昂。我们以白鼠为模型,研究了碳酸锌纳米晶体胶体溶液的急性毒性。实验对象是 42 只雌性非线性白鼠,3-4 个月大,活体重 21-23 克,饲养条件最佳。根据类比原则,实验共分为 6 组:给小鼠注射纳米碳酸锌胶体溶液,剂量(按药物绝对重量计)分别为 15000.0、20000.0、25000.0、30000、35000.0 和 40000.0 毫克/千克体重;给小鼠注射纳米碳酸锌胶体溶液,剂量(按药物绝对重量计)分别为 15000.0、20000.0、25000.0、30000、35000.0 和 40000.0 毫克/千克体重。0毫克/千克体重,根据活性物质(纳米碳酸锌颗粒)的绝对重量为(37.5;50.0;62.5;75.0;87.5和100.0毫克/千克体重),使用食道-胃管口服。对照组小鼠则按照相同的方案注射体积为 0.2 立方厘米的蒸馏水。对实验动物的临床状况进行为期 14 天的观察,记录中毒临床症状的出现和发展、死亡时间或恢复到生理正常值的时间。动物死亡(诊断性屠宰)后,进行了病理解剖。临床观察结果表明,实验组 1-6 的小鼠一次胃内给药不会引起急性中毒。在 14 天的观察期内,没有观察到所有实验组的小鼠死亡,因此无法计算半数致死剂量指标。同时,纳米碳酸锌胶体溶液的最大注射剂量(按绝对重量计算)为 40,000.0 毫克/千克体重(按活性物质计算为 100.0 毫克/千克),这使得该药物被归入毒性 VI 级--相对无害物质(半数致死剂量大于 15,000.0 毫克/千克体重),根据危险程度被归入 IV 级--低危险物质(半数致死剂量大于 5,000.0 毫克/千克体重)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute toxicity of zinc carbonate nanocrystals on white mice model
Zinc-based nanoparticles (NPs) are successfully used to meet the mineral needs of animals and poultry, capable of increasing the growth rate and the efficiency of their use of feed. Nanoparticles of zinc oxide are widely used, which are superior to conventional sources of zinc in terms of pharmacological activity and bioavailability, have a positive effect on productivity and antioxidant protection, and increase reproductive potential. However, a detailed investigation of their toxicological parameters showed the risks of their introduction into the body, as a result of which a large number of zinc oxide NPs were synthesized by the methods of “green chemistry”, the main drawback of which is a complex methodology and a high level of costs. We investigated the acute toxicity of a colloidal solution of zinc carbonate nanocrystals in a model of white mice. The experiment was conducted on 42 female non-linear white mice, 3–4 months old, with a live weight of 21–23 g, kept under optimal vivarium conditions. According to the principle of analogues, 6 experimental groups were formed: mice were injected with a colloidal solution of zinc carbonate nanoparticles in doses (by absolute weight of the drug) of 15,000.0; 20000.0; 25000.0; 30000; 35000.0 and 40000.0 mg/kg of body weight based on the absolute weight of the drug, which according to the active substance (zinc carbonate nanoparticles) was (37.5; 50.0; 62.5; 75.0; 87.5 and 100, 0 mg/kg of body weight), orally using an esophageal-gastric tube. Mice of the control group were injected with distilled water in a volume of 0.2 cm3 according to the same protocol. The clinical condition of the experimental animals was observed for 14 days, noting the appearance and development of clinical signs of poisoning, the time of death or recovery to the physiological norm. After the death (diagnostic slaughter) of the animals, a pathological autopsy was performed. Clinical observations showed that a single intragastric administration of the drug to mice of experimental groups 1-6 did not cause acute poisoning. The deaths of mice in all experimental groups were not observed during the 14-day observation period, as a result of which the LD50 indicator could not be calculated. At the same time, the maximum possible injected dose of the colloidal solution of zinc carbonate nanoparticles (by absolute weight) was 40,000.0 mg/kg of body weight (100.0 mg/kg by active substance), which allows the drug to be assigned to the VI class of toxicity – substances are relatively harmless (LD50 > 15000.0 mg/kg of body weight), and according to the degree of danger up to IV class – low-hazardous substances (LD50 > 5000.0 mg/kg of body weight).
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