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含磷脂酰肌醇 3-激酶抑制剂(PIK75)的表面功能化纳米乳液增强卵巢癌细胞的药物传递、细胞毒性和促凋亡活性。

Phosphatidylinositol 3-kinase inhibitor (PIK75) containing surface functionalized nanoemulsion for enhanced drug delivery, cytotoxicity and pro-apoptotic activity in ovarian cancer cells.

机构信息

School of Pharmacy, Faculty of Medical & Health Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand.

出版信息

Pharm Res. 2012 Oct;29(10):2874-86. doi: 10.1007/s11095-012-0793-6. Epub 2012 Jun 1.

Abstract

PURPOSE

Ovarian cancer is a debilitating disease, which needs multi-pronged approach of targeted drug delivery and enhanced efficacy with the use of combination therapeutics. In this study, we have examined the anticancer activity of PIK75 incorporated in surface functionalized nanoemulsions for targeted delivery to SKOV-3 cells. A pro-apoptotic molecule C(6)-ceramide was also co-delivered to augment therapeutic efficacy.

METHODS

EGFR and FR functionalized nanoemulsions incorporating PIK75 and C(6)-ceramide were characterized for particle size, surface charge, entrapment efficiency and morphology. Fluorescence and quantitative uptake studies were conducted in SKOV-3 cells to determine intracellular distribution. Cell viability was assessed using MTT assay while mechanism of cytotoxicity was evaluated using capsase-3/7, TUNEL and hROS assay.

RESULTS

Cytotoxicity assay showed 57% decrease in IC(50) value of PIK75 following treatment with EGFR targeted nanoemulsion and 40% decrease following treatment with FR targeted nanoemulsion. Combination therapy with PIK75 and ceramide enhanced the cytotoxicity of PIK75 compared to therapy with individual formulations. The increase in cytotoxicity was attributed to increase in cellular apoptosis and hROS activity.

CONCLUSION

The results of this study showed that the targeted system improved cytotoxicity of PIK75 compared to the non-targeted system. Combination therapy with ceramide augmented PIK75's therapeutic activity.

摘要

目的

卵巢癌是一种使人虚弱的疾病,需要采用靶向药物输送和联合治疗的增强疗效的多管齐下的方法。在这项研究中,我们研究了掺入表面功能化纳米乳液中用于靶向递送至 SKOV-3 细胞的 PIK75 的抗癌活性。还共递送促凋亡分子 C(6)-神经酰胺以提高治疗效果。

方法

对 EGFR 和 FR 功能化纳米乳液进行了表征,以确定其粒径、表面电荷、包封效率和形态。在 SKOV-3 细胞中进行荧光和定量摄取研究,以确定细胞内分布。使用 MTT 测定法评估细胞活力,并用 caspase-3/7、TUNEL 和 hROS 测定法评估细胞毒性机制。

结果

细胞毒性测定表明,在用 EGFR 靶向纳米乳液处理后,PIK75 的 IC(50)值降低了 57%,在用 FR 靶向纳米乳液处理后降低了 40%。与单独使用制剂相比,PIK75 和神经酰胺联合治疗增强了 PIK75 的细胞毒性。细胞毒性的增加归因于细胞凋亡和 hROS 活性的增加。

结论

这项研究的结果表明,与非靶向系统相比,靶向系统提高了 PIK75 的细胞毒性。与神经酰胺联合治疗增强了 PIK75 的治疗活性。

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