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首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats
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Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats

机译:大鼠碳酸钙碳酸钙纳米钙皮下剂量的安全评估

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摘要

Calcium carbonate nanoparticles have shown promising potentials in the delivery of drugs and metabolites. There is however, a paucity of information on the safety of their intentional or accidental over exposures to biological systems and general health safety. To this end, this study aims at documenting information on the safety of subcutaneous doses of biogenic nanocrystals of aragonite polymorph of calcium carbonate derived from cockle shells (ANC) in Sprague-Dawley (SD) rats. ANC was synthesized using the top-down method, characterized using the transmission electron microscopy and field emission scanning electron microscope and its acute and repeated dose 28-day trial toxicities were evaluated in SD rats. The results showed that the homogenous 30 +/- 5 nm-sized spherical pure aragonite nanocrystals were not associated with mortality in the rats. Severe clinical signs and gross and histopathological lesions, indicating organ toxicities, were recorded in the acute toxicity (29,500 mg/m(2)) group and the high dose (5900 mg/m(2)) group of the repeated dose 28-day trial. However, the medium- (590 mg/m(2) body weight) and low (59 mg/m(2))-dose groups showed moderate to mild lesions. The relatively mild lesions observed in the low toxicity dosage group marked the safety margin of ANC in SD rats. It was concluded from this study that the toxicity of CaCO3 was dependent on the particulate size (30 +/- 5 nm) and concentration and the route of administration used.
机译:碳酸钙纳米粒子在递送药物和代谢物中显示了有希望的电位。然而,缺乏有关其故意或偶然的曝光对生物系统和一般健康安全的安全性的信息。为此,本研究旨在记录关于Sprague-Dawley(SD)大鼠的沟槽壳(ANC)的碳酸钙碳酸钙的虚拟纳米晶体的皮下纳米晶体的安全性的信息。使用自上而下的方法合成了ANC,其特征在于使用透射电子显微镜和场发射扫描电子显微镜及其急性和重复剂量的28天试验毒性在SD大鼠中评估。结果表明,均匀的30 +/- 5nm尺寸的球形纯的纯属纳米晶体与大鼠的死亡率无关。严重的临床症状和总体病理病变,表明器官毒性,急性毒性(29,500mg / m(2))组和高剂量(5900mg / m(2))重复剂量28天审判。然而,培养基(590mg / m(2)体重)和低(59mg / m(2)) - 剂量基团显示中等至温和病变。低毒性剂量组观察到的相对温和的病变标志着SD大鼠ANC的安全余量。从这项研究中得出结论,CaCO3的毒性依赖于颗粒尺寸(30 +/- 5nm)和浓度和使用的给药途径。

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