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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >ZnO Q-dots as a potent therapeutic nanomedicine for in vitro cytotoxicity evaluation of mouth KB44, breast MCF7, colon HT29 and HeLa cancer cell lines, mouse ear swelling tests in vivo and its side effects using the animal model
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ZnO Q-dots as a potent therapeutic nanomedicine for in vitro cytotoxicity evaluation of mouth KB44, breast MCF7, colon HT29 and HeLa cancer cell lines, mouse ear swelling tests in vivo and its side effects using the animal model

机译:ZnO Q-Dots作为一种有效的治疗纳米肽,用于口腔KB44,乳腺MCF7,结肠HT29和HELA癌细胞系,小鼠肿胀试验,体内肿胀试验及其使用动物模型的副作用

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摘要

Nanoformulations derived from fine porous ZnO quantum dot nanoparticles (QD NPs) can offer strong potential medical applications; especially in cancer therapy. ZnO QD NPs was synthesized by sol-gel hydrothermal process, fast cold quenching and further smart surface functionalization methods to obtain ultrasmall size (1-4nm) NPs. ZnO nanopolymer, a wetting agent, PEG co-solvent and water/oil emulsion stabilizer were considered in our nanofluid formulation. The resulting nanofluid was characterized by SEM, FTIR, photoluminescence, band gap energy, zeta potential and UV-Vis spectroscopy. The cytotoxic effects on the growth of four cancer cell lines were evaluated by MTT assay. The IC50 (mu g/ml) values of 30, 41, 40 and 35 for KB44, MCF-7, HT29 and HeLa cells, respectively, after 48h of nanoformulation treatment suggested the cytotoxic effect of this nanoformulation on these cell lines in a concentration-dependent manner (p.05). ZnO nanofluid destroyed cancer cell lines more efficiently than the normal HFF-2 (IC50=105 mu g/ml). The reduction in cell viability in response to ZnO nanofluid treatment induced apoptosis in the cultured cells. Skin sensitization test plus antibacterial activity were also measured. Side effect tests on 70 white mice in vivo resulted in only 3-4 abnormal situations in hepatic tissue section possibly due to the idiosyncratic drug reactions.
机译:源自精细多孔ZnO量子点纳米颗粒(QD NPS)的纳米型族种类可以提供强大的潜在医疗应用;特别是在癌症治疗中。通过溶胶 - 凝胶水热法,快速冷淬火和进一步的智能表面官能化方法合成ZnO QD NP,以获得超大尺寸(1-4nm)NPS。在我们的纳米流体制剂中考虑了ZnO纳米聚合物,润湿剂,PEG共溶剂和水/油乳液稳定剂。所得纳米流体的特征在于SEM,FTIR,光致发光,带隙能量,Zeta电位和UV​​-Vis光谱。通过MTT测定评估对四种癌细胞系生长的细胞毒性作用。对于KB44,MCF-7,HT29和HeLa细胞的IC50(mu g / ml)值分别在48小时后,在纳米造型处理48h后提出了该纳米型在这些细胞系中的细胞毒性作用 - 依赖性方式(P <.05)。 ZnO纳米流体比正常HFF-2更有效地破坏了癌细胞系(IC50 =105μg/ ml)。响应于ZnO纳米流体处理诱导培养细胞凋亡的细胞活力的降低。还测量皮肤敏化试验加抗菌活性。在体内70张白癜风上的副作用测试导致肝脏组织部分仅为3-4个异常情况,可能是由于特质药物反应。

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