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制备丙烯基异硫氰酸酯纳米粒子及其对 RAW 264.7 巨噬细胞的抗炎活性和对 HT1376 膀胱癌细胞的抗增殖作用。

Preparation of allyl isothiocyanate nanoparticles, their anti-inflammatory activity towards RAW 264.7 macrophage cells and anti-proliferative effect on HT1376 bladder cancer cells.

机构信息

Department of Food Science, Fu Jen Catholic University, New Taipei City, Taiwan.

出版信息

J Sci Food Agric. 2019 Apr;99(6):3106-3116. doi: 10.1002/jsfa.9524. Epub 2019 Jan 25.

Abstract

BACKGROUND

Allyl isothiocyanate (AITC), a volatile and water-insoluble compound present in several cruciferous vegetables, has been shown to possess several biological qualities such as anti-bacterial, anti-fungal, and anti-cancer activity. In this study, water-soluble allyl isothiocyanate nanoparticles (AITC-NPs) were prepared by oil dispersed in water (O/W) microemulsion and complex coacervation techniques and evaluated for their anti-inflammatory activity towards macrophage cell RAW 264.7 and anti-cancer effect on human bladder cancer cell HT1376.

RESULTS

The AITC-NPs with a particle size of 9.4 nm were stable during heating up to 110 °C or three freeze-thawing cycles. No significant cytotoxicity was shown on Caco-2 and intestine epithelial IEC-6 cells at AITC-NP doses ranging from 0.25 to 2 g L (8.75-70 mg L AITC). However, at 2 g L dosage, AITC-NPs could inhibit the growth of human bladder cancer cells HT1376 by 90%, while their low dosage at 0.25 g L could inhibit migration ability by 83.7, 71.3, 58.4 and 31.4% after 4, 8, 12, and 24 h of incubation, respectively. Compared to AITC and NPs, AITC-NPs showed a better inhibition on lipopolysaccharide (LPS)-induced TNF-α, IL-6, NO and iNOS production in RAW 264.7 macrophage cells.

CONCLUSION

The results demonstrate the potential of AITC-NPs as therapeutic agents for the treatment of bladder cancer and the enhancement of immune function. © 2018 Society of Chemical Industry.

摘要

背景

丙烯基异硫氰酸酯(AITC)是几种十字花科蔬菜中存在的一种挥发性和水溶性差的化合物,具有多种生物学特性,如抗菌、抗真菌和抗癌活性。在这项研究中,通过油分散在水中(O/W)微乳液和复凝聚技术制备了水溶性 AITC 纳米颗粒(AITC-NPs),并评价了它们对 RAW 264.7 巨噬细胞的抗炎活性和对人膀胱癌 HT1376 细胞的抗癌作用。

结果

AITC-NPs 的粒径为 9.4nm,在加热至 110°C 或经历三个冻融循环时保持稳定。在 AITC-NP 剂量为 0.25 至 2g/L(8.75-70mg/L AITC)时,对 Caco-2 和肠上皮 IEC-6 细胞没有显示出显著的细胞毒性。然而,在 2g/L 剂量下,AITC-NPs 可以抑制人膀胱癌 HT1376 细胞的生长,抑制率为 90%,而在低剂量 0.25g/L 时,孵育 4、8、12 和 24h 后,其迁移能力分别抑制了 83.7%、71.3%、58.4%和 31.4%。与 AITC 和 NPs 相比,AITC-NPs 对 LPS 诱导的 RAW 264.7 巨噬细胞中 TNF-α、IL-6、NO 和 iNOS 的产生具有更好的抑制作用。

结论

结果表明,AITC-NPs 有潜力作为治疗膀胱癌和增强免疫功能的治疗剂。© 2018 化学工业协会。

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