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基于多萜醇的纳米乳液负载 TiO 和叶酸偶联壳聚糖纳米粒子的表征、细胞毒性和遗传毒性研究。

Characterization, Cytotoxicity, and Genotoxicity of TiO and Folate-Coupled Chitosan Nanoparticles Loading Polyprenol-Based Nanoemulsion.

机构信息

Institute of Chemical Industry of Forest Products, CAF, Nanjing, Jiangsu Province, 210042, China.

Research Institute of Forestry New Technology, CAF, Xiangshan Road, Beijing, 100091, China.

出版信息

Biol Trace Elem Res. 2018 Jul;184(1):60-74. doi: 10.1007/s12011-017-1184-y. Epub 2017 Oct 9.

Abstract

The structure and bioactivity of Ginkgo biloba leaves polyprenol (GBP) are similar to that of dolichol which widely exists in human and mammalian organs. GBP possesses potential pharmacological activities against cancer. This study involved oil-in-water type nanoemulsion (NE) loading GBP was prepared by dissolving polyprenol in nanoemulsion of sodium tripolyphosphate (TPP)/TiO solution, Triton X-100, and 1-octanol by inversed-phase emulsification (EIP) and ultrasonic emulsification (UE) method. Folic acid (FA)-coupled chitosan (CS) nanoparticles (NPs), GBP-FA-CS-NPs and GBP-TiO-FA-CS-NPs, were fabricated by ionic cross-linking of positively charged FA-CS conjugates and negatively charged nanoemulsion with TPP/TiO. And characterizations of them were investigated by TEM, SEM, FTIR, particle size, and zeta potential. The cytotoxic and genotoxic effects of GBP-TiO-FA-CS-NP treatment were higher than GBP-NE, GBP-FA-CS-NPs, TiO-NE, GBP-TiO-NE, TiO-FA-CS-NPs, and GBP-TiO-FA-CS-NP treatment at the same tested concentrations in HepG2 cells. GBP-TiO-FA-CS-NPs at low TiO concentration (from 1 to 2.5 μg/ml) showed good inhibition capacity on HepG2 cells and low cytotoxic and genotoxic effects on HL-7702 cells. The possible mechanism of cytotoxicity on GBP-TiO-FA-CS-NPs against HepG2 cells is by preventing excessive intracellular Ca into extracellular spaces via inhibiting Ca-ATPase and Ca/Mg-ATPase.

摘要

银杏叶多聚戊烯(GBP)的结构和生物活性与广泛存在于人和哺乳动物器官中的鲨烯类似。GBP 具有潜在的抗癌药理活性。本研究涉及载有 GBP 的油包水型纳米乳(NE)的制备,通过将多聚戊烯溶解在三聚磷酸钠(TPP)/TiO 溶液、Triton X-100 和 1-辛醇的纳米乳液中,采用相反相乳化(EIP)和超声乳化(UE)法制备。通过带正电荷的 FA-CS 缀合物与带负电荷的纳米乳液与 TPP/TiO 的离子交联,制备了叶酸(FA)偶联壳聚糖(CS)纳米颗粒(NPs)、GBP-FA-CS-NPs 和 GBP-TiO-FA-CS-NPs,并通过 TEM、SEM、FTIR、粒径和 Zeta 电位对其进行了表征。在 HepG2 细胞中,与 GBP-NE、GBP-FA-CS-NPs、TiO-NE、GBP-TiO-NE、TiO-FA-CS-NPs 和 GBP-TiO-FA-CS-NP 处理相同测试浓度相比,GBP-TiO-FA-CS-NP 处理的细胞毒性和遗传毒性作用更高。在低 TiO 浓度(1-2.5μg/ml)下,GBP-TiO-FA-CS-NPs 对 HepG2 细胞表现出良好的抑制能力,对 HL-7702 细胞的细胞毒性和遗传毒性作用较低。GBP-TiO-FA-CS-NPs 对 HepG2 细胞的细胞毒性作用的可能机制是通过抑制 Ca-ATPase 和 Ca/Mg-ATPase 阻止细胞内过多的 Ca 进入细胞外间隙。

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