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纳米碳酸钙在Sprague-Dawley大鼠中的理化分析及重复给药90天口服毒性研究。

Physicochemical analysis and repeated-dose 90-days oral toxicity study of nanocalcium carbonate in Sprague-Dawley rats.

作者信息

Sung Jae Hyuck, Park Soo Jin, Jeong Min Sook, Song Kyung Seuk, Ahn Kyu Sup, Ryu Hyun Ryol, Lee Han, Song Mi Ryoung, Cho Myung-Haing, Kim Jun Sung

机构信息

Laboratory of Toxicology, College of Veterinary Medicine, Seoul National University , Seoul , Republic of Korea .

出版信息

Nanotoxicology. 2015;9(5):603-12. doi: 10.3109/17435390.2014.958587. Epub 2014 Sep 18.

Abstract

In our previous studies of nanocalcium carbonate, in which we performed physicochemical analysis, genotoxicity, acute single-dose and repeated-dose 14-day oral toxicity testings in Sprague-Dawley (SD) rats, nanocalcium carbonate did not show a difference in toxicity compared to vehicle control. Here, we provide the first report of a repeated-dose 90-day oral toxicity test of nanocalcium carbonate in Sprague-Dawley rats, with physicochemical comparison of micro and nanocalcium carbonate. We find that the two particles differ in size, hydrodynamic size, and specific surface area, with no differences in components, crystalline structure and radical production. In terms of ionization ability, nanocalcium carbonate was slightly more ionized within 1% than microcalcium carbonate at pH 5 and pH 7. In the repeated-dose 90-day oral toxicity test of nanocalcium carbonate, there was no significant toxicity, and similar blood concentrations of Ca(2+) compared to the vehicle control group. Based on our results, although nanocalcium carbonate has different physicochemical properties, nanocalcium carbonate does not differ from microcalcium carbonate in terms of toxicity. Based on the results, we suggest that the no-observed-adverse-effect level (NOAEL) of nanocalcium carbonate is 1000 mg kg(-1) day(-1) in SD rats according to the maximum dose (OECD guideline 408). However, the NOAEL might be higher than 1000 mg kg(-1) day(-1) because there were no adverse effects revealed by consistent pathological findings or biochemical parameter changes. To justify a safe concentration of nanocalcium carbonate, which is a low toxicity chemical, more data is required on dose levels above 1000 mg kg(-1). Our findings may be useful for creating safety guidelines for the use nanocalcium carbonate.

摘要

在我们之前对纳米碳酸钙的研究中,我们对其进行了物理化学分析、遗传毒性、急性单剂量和重复剂量14天口服毒性测试(针对Sprague-Dawley,即SD大鼠),纳米碳酸钙与赋形剂对照组相比,在毒性方面未显示出差异。在此,我们首次报告了纳米碳酸钙在SD大鼠中的重复剂量90天口服毒性测试,并对微米和纳米碳酸钙进行了物理化学比较。我们发现,这两种颗粒在尺寸、流体动力学尺寸和比表面积方面存在差异,但在成分、晶体结构和自由基产生方面没有差异。就离子化能力而言,在pH 5和pH 7时,纳米碳酸钙在1%范围内的离子化程度比微米碳酸钙略高。在纳米碳酸钙的重复剂量90天口服毒性测试中,未发现明显毒性,与赋形剂对照组相比,血液中Ca(2+)浓度相似。基于我们的结果,尽管纳米碳酸钙具有不同的物理化学性质,但在毒性方面,纳米碳酸钙与微米碳酸钙并无差异。基于这些结果,我们建议,根据最大剂量(经合组织准则408),纳米碳酸钙在SD大鼠中的未观察到有害作用水平(NOAEL)为1000 mg kg(-1) day(-1)。然而,NOAEL可能高于1000 mg kg(-1) day(-1),因为一致的病理结果或生化参数变化未显示出有害影响。为了确定低毒性化学品纳米碳酸钙的安全浓度,需要更多关于高于1000 mg kg(-1)剂量水平的数据。我们的研究结果可能有助于制定纳米碳酸钙使用的安全指南。

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