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Methotrexate Gold Nanocarriers: Loading and Release Study: Its Activity in Colon and Lung Cancer Cells

机译:甲氨蝶呤金纳米载波:装载和释放研究:其在结肠癌和肺癌细胞中的活性

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摘要

In the present study, the synthesis of gold nanoparticles (AuNPs) loaded with methotrexate (MTX) has been carried out in order to obtain controlled size and monodispersed nanocarriers of around 20 nm. The characterization study shows metallic AuNPs with MTX polydispersed on the surface. MTX is linked by the replacement of citrate by the MTX carboxyl group. The drug release profiles show faster MTX release when it is conjugated, which leads to the best control of plasma concentration. Moreover, the enhanced release observed at pH 5 could take advantage of the pH gradients that exist in tumor microenvironments to achieve high local drug concentrations. AuNP–MTX conjugates were tested by flow cytometry against lung (A-549) and colon (HTC-116) cancer cell lines. Results for A-549 showed a weaker dose–response effect than for colon cancer ones. This could be related to the presence of folate receptors in line HTC-116 in comparison to line A-549, supporting the specific uptake of folate-conjugated AuNP–MTX by folate receptor positive tumor cells. Conjugates exhibited considerably higher cytotoxic effects compared with the effects of equal doses of free MTX. Annexin V-PI tests sustained the cell death mechanism of apoptosis, which is normally disabled in cancer cells.
机译:在本研究中,已经进行了用甲氨蝶呤(MTX)负载的金纳米颗粒(AUNP)的合成,以获得约20nm的受控尺寸和单分散的纳米载体。表征研究显示了具有MTX多分散在表面上的金属AUNP。 MTX通过MTX羧基替代柠檬酸盐来连接。当缀合时,药物释放型材显示出更快的MTX释放,这导致血浆浓度的最佳控制。此外,在pH5中观察到的增强释放可以利用肿瘤微环境中存在的pH梯度以实现高局部药物浓度。通过针对肺(A-549)和结肠(HTC-116)癌细胞系的流式细胞仪测试AUNP-MTX缀合物。 A-549的结果显示出比结肠癌患者的剂量 - 反应效果较弱。与线A-549相比,这可能与线HTC-116中叶酸受体的存在有关,并通过叶酸受体阳性肿瘤细胞支持叶酸缀合的AUNP-MTX的特异性摄取。与相等剂量的游离MTX的影响相比,缀合物表现出相当高的细胞毒性效果。 Annexin V-PI试验持续凋亡的细胞死亡机制,通常在癌细胞中丧失。

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