Evaluation of in-vitro cytotoxic effect of 5-FU loaded-chitosan nanoparticles against spheroid models.

Journal of nature and science Pub Date : 2018-10-01
Taylor Smith, Kevin Affram, Errol Bulumko, Edward Agyare
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Abstract

Purpose: The studies investigate the anticancer activity of 5-fluorouracil (5-FU)-hyaluronidase (Hase) enzyme-loaded chitosan nanoparticles (5-FUChnps) using three-dimensional (3D) spheroid HCT-116 culture. Hase-loaded nanoparticles (Chnps) have recently been used to improve the efficacy of chemotherapeutic drugs for cancer treatment. It has been found that administration of Hase improves tumor vessel densities and increase perfusion within tumor.

Methods: Particle size and zeta potential of the nanoparticles were determined using a particle size analyzer while Fourier transform infrared (FTIR) was used to investigate the interactions among the various components making up the chitosan nanoparticles. Cytotoxic effects of 5-FU and 5FUchnps against dimensional (2D) and 3D spheroid cultures were assessed using trypan blue assay.

Results: Low molecular weight chitosan (ChiL) nanoparticle size was determined to between 215 to 670 nm while medium molecular weight chitosan (ChiM) nanoparticle size ranged from 151 to 778 nm. All 5FUChnps exhibited a zeta potential value ranging from +4 to +37 mV. Among the 16 formulations prepared, formulation #7 (5-FUChnps7) was selected for the in-vitro cytotoxic studies based on its high 5-FU entrapment efficiency (59%). 5FUchnps treated 3D HCT-116 culture exhibited significant growth inhibition compared with 5-FU treated groups. Further, spheroids with significant growth inhibition exhibited high spheroid volume and non-spherical shapes.

Conclusion: 5-FUChnps were significantly cytotoxic to the 3D HCT-116 cultures than that of the free 5-FU. Chnps proved to have the ability to deliver and improve the anticancer activity of 5-FU in 3D HCT-116 culture studies.

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5-FU负载壳聚糖纳米颗粒对球体模型的体外细胞毒作用评价。
目的:通过三维(3D)球形HCT-116培养,研究5-氟尿嘧啶(5-FU)-透明质酸酶(Hase)负载壳聚糖纳米颗粒(5-FUChnps)的抗癌活性。装载酶的纳米颗粒(Chnps)最近被用于提高化疗药物治疗癌症的疗效。研究发现,Hase可改善肿瘤血管密度,增加肿瘤内灌注。方法:采用粒径分析仪测定壳聚糖纳米颗粒的粒径和zeta电位,利用傅里叶变换红外光谱(FTIR)研究壳聚糖纳米颗粒各组分之间的相互作用。采用台锥蓝法评估5-FU和5FUchnps对二维和三维球体培养物的细胞毒作用。结果:低分子量壳聚糖(ChiL)纳米颗粒粒径在215 ~ 670 nm之间,中分子量壳聚糖(ChiM)纳米颗粒粒径在151 ~ 778 nm之间。所有5fuchps的zeta电位值均在+4 ~ +37 mV之间。在制备的16个制剂中,选择制剂#7 (5-FUChnps7)进行体外细胞毒性研究,因为其具有较高的5-FU包封率(59%)。与5-FU处理组相比,5FUchnps处理3D HCT-116培养物表现出明显的生长抑制。此外,具有显著生长抑制的球体表现出高球体体积和非球形形状。结论:5-FUChnps对3D HCT-116培养物的细胞毒性显著高于游离5-FU。在3D HCT-116培养研究中,Chnps被证明具有传递和提高5-FU抗癌活性的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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