首页> 美国卫生研究院文献>Oncotarget >Temozolomide encapsulated and folic acid decorated chitosan nanoparticles for lung tumor targeting: improving therapeutic efficacy both in vitro and in vivo
【2h】

Temozolomide encapsulated and folic acid decorated chitosan nanoparticles for lung tumor targeting: improving therapeutic efficacy both in vitro and in vivo

机译:替莫唑胺封装和叶酸修饰的壳聚糖纳米颗粒用于靶向肺癌:在体内外均提高治疗效果

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Folic acid-conjugated temozolomide (TMZ)-loaded chitosan nanoparticles (CS-TMZ-FLA-NP) were developed to target lung cancer in the anticipation that folic acid would increase the affinity of nanoparticles for cancer cells. CS-TMZ-FLA-NP showed the highest anti-proliferative effect on the lung cancer cells in comparison to free TMZ and CS-TMZ-NP (nanoparticles without folic acid). A cellular uptake assay was performed on two different cell lines, L132 and A549. Cellular uptake efficiencies of CS-TMZ-NP and CS-TMZ-FLA-NP were found to be concentration-dependent in both cell lines. CS-TMZ-FLA-NP produced a 2.5 fold greater accumulation of TMZ than CS-TMZ-NP in both cell lines. CS-TMZ-FLA-NP maintained a significantly higher deposition of TMZ in lung tissue (approximately 7.5 μg/g of lung tissue) when compared to free TMZ and CS-TMZ-NP. Mice treated with CS-TMZ-FLA-NP had a 100% survival rate with significant suppression of tumor growth. Histopathological and immunohistochemical studies also demonstrated that CS-TMZ-FLA-NP had superior anticancer activity compared to the other two treatments. Our results indicate that CS-TMZ-FLA-NP can effectively facilitate targeting to human lung cancer cell lines in vitro and to lung tumors in vivo in a sustained manner and so improve the therapeutic efficacy of TMZ.
机译:由于预期叶酸会增加纳米颗粒对癌细胞的亲和力,因此开发了以叶酸偶联的替莫唑胺(TMZ)为载体的壳聚糖纳米颗粒(CS-TMZ-FLA-NP)。与游离TMZ和CS-TMZ-NP(不含叶酸的纳米颗粒)相比,CS-TMZ-FLA-NP对肺癌细胞显示出最高的抗增殖作用。在两种不同的细胞系L132和A549上进行了细胞摄取测定。发现CS-TMZ-NP和CS-TMZ-FLA-NP的细胞吸收效率在两种细胞系中均是浓度依赖性的。在两种细胞系中,CS-TMZ-FLA-NP产生的TMZ积累量比CS-TMZ-NP高2.5倍。与游离TMZ和CS-TMZ-NP相比,CS-TMZ-FLA-NP在肺组织中保持了更高的TMZ沉积(约7.5μg/ g肺组织)。用CS-TMZ-FLA-NP处理的小鼠的存活率为100%,并显着抑制了肿瘤的生长。组织病理学和免疫组织化学研究还表明,与其他两种治疗方法相比,CS-TMZ-FLA-NP具有更强的抗癌活性。我们的结果表明,CS-TMZ-FLA-NP可以有效地以持续的方式促进体外靶向人肺癌细胞系和体内靶向肺肿瘤,从而提高TMZ的治疗效果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号