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In vivo assessment of bone marrow toxicity by gold nanoparticle-based bioconjugates in Crl:CD1(ICR) mice

机译:基于金纳米粒子的生物缀合物在Crl:CD1(ICR)小鼠体内的骨髓毒性评估

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Introduction: The present study aimed at evaluating the biodistribution of Tween??20-gold nanoparticle (GNP) conjugates and their potential toxicity on the bone marrow before moving on to Phase I clinical trials. Materials and methods: Tween??20-conjugated GNPs were injected intravenously for 21?days in male Crl:CD1(ICR) mice. Body weight of the mice was evaluated each day. After the sub-chronic Tween??20-GNPs administration, blood samples were harvested, and a full blood count was done individually. Total Au quantity from all major organs was assessed using inductively coupled plasma mass spectrometry. One femur and the sternum obtained from each animal were used for histological assessment. Results: Our data showed that the Tween??20-GNP conjugates were found in large quantities in the bladder. Au was shown to accumulate in the hematopoietic bone tissue, with significant side effects such as leucopoiesis and megakaryopoiesis. The mice had a higher white blood cell and platelet count as opposed to the control group. This suggested that the previously described leukopenic effects of isoflurane were overridden by the leucopoietic effects of Tween??20-GNPs. Conclusion: It was uncertain whether the mice were reactive to Au as it is a foreign substance to the tissues or whether the side effects observed were a precursor condition of a more severe hematological condition. Au was found to be hepatotoxic, urging the need for further studies in order to achieve better in vivo compliance and exploit the immense potential of GNPs in cancer pharmacology.
机译:简介:本研究旨在评估Tween ??20金纳米粒子(GNP)缀合物的生物分布及其对骨髓的潜在毒性,然后再进行I期临床试验。材料与方法:在雄性Crl:CD1(ICR)小鼠中静脉注射Tween ??20偶联的GNP,持续21天。每天评估小鼠的体重。在亚慢性Tween →→20-GNPs给药后,采集血液样本,并分别进行全血细胞计数。使用电感耦合等离子体质谱法评估所有主要器官的总金含量。从每只动物获得的一个股骨和胸骨用于组织学评估。结果:我们的数据表明,在膀胱中大量发现了Tween ??20-GNP共轭物。已显示金在造血骨组织中积累,并具有明显的副作用,如白细胞生成和巨核生成。与对照组相比,小鼠的白细胞和血小板数量更高。这表明,先前所述的异氟烷的白细胞减少作用被吐温ββ20-GNP的促白细胞作用所取代。结论:尚不确定小鼠是否对Au产生反应,因为它是组织的异物,还是观察到的副作用是否是血液病更为严重的先兆。发现金具有肝毒性,敦促需要进一步研究,以实现更好的体内顺应性并开发GNP在癌症药理学中的巨大潜力。

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