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功能化氧化石墨烯作为双重药物递送应用的纳米载体:槲皮素和吉非替尼对卵巢癌细胞的协同作用。

Functionalized graphene oxide as a nanocarrier for dual drug delivery applications: The synergistic effect of quercetin and gefitinib against ovarian cancer cells.

机构信息

Nanoscience and Nanotechnology Centre, Department of Chemistry, D.S.B. Campus, Kumaun University, Nainital, Uttarakhand, India.

Biotechnology Group, Biological Sciences and Technology Division, CSIR-North East Institute of Science and Technology, Academy of Scientific and Innovative Research, Jorhat, Assam, India.

出版信息

Colloids Surf B Biointerfaces. 2019 Jun 1;178:452-459. doi: 10.1016/j.colsurfb.2019.03.037. Epub 2019 Mar 18.

Abstract

Graphene Oxide (GO) has been extensively studied in the field of biomedical sciences as one of the most promising biomaterials due to its exceptional physiochemical properties. Experts have long favored anticancer drug cocktails over single drugs, given that the former may provide a more balanced molecular basis for novel chemotherapeutic strategies. Here, we investigated a combinatorial anticancer drug treatment involving the well-proven anticancer drugs quercetin and gefitinib and compared it with gefitinib and quercetin loaded separately onto polyvinylpyrrolidone (PVP)-functionalized graphene oxide (GO-PVP). The loading and cancer cell cytotoxicity of the individual drug systems and their combined loading onto GO-PVP nanovehicles were investigated in PA-1 ovarian cancer cells and compared to their effects on IOSE-364 ovarian epithelial cells. In this report, the combined drug system loaded on the GO-PVP nanovehicle was found to be significantly more toxic than the individual drug loaded systems, as well as the free drugs, toward PA-1 cells compared to the toxicity toward IOSE-364 cells. The combined drug system loaded on the GO-PVP nanovehicle is likely to be more successful than individual drug therapy, given the stronger impact of the combinatorial approach and the efficiency of chemotherapeutic delivery.

摘要

氧化石墨烯(GO)因其独特的物理化学性质,在生物医学科学领域被广泛研究,是最有前途的生物材料之一。鉴于前者可能为新的化疗策略提供更平衡的分子基础,专家们长期以来一直青睐抗癌药物鸡尾酒而非单一药物。在这里,我们研究了一种包含已被证实的抗癌药物槲皮素和吉非替尼的联合抗癌药物治疗方法,并将其与分别负载在聚乙烯吡咯烷酮(PVP)功能化氧化石墨烯(GO-PVP)上的吉非替尼和槲皮素进行了比较。在 PA-1 卵巢癌细胞中研究了各个药物系统的负载和癌细胞细胞毒性及其在 GO-PVP 纳米载体上的联合负载,并将其与对 IOSE-364 卵巢上皮细胞的作用进行了比较。在本报告中,与单独负载药物系统以及游离药物相比,载于 GO-PVP 纳米载体上的联合药物系统对 PA-1 细胞的毒性明显更大,而对 IOSE-364 细胞的毒性则较小。鉴于联合方法的更强影响和化疗药物递送的效率,载于 GO-PVP 纳米载体上的联合药物系统可能比单独药物治疗更成功。

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