简介概要

Synthesis of NaYF4:Yb,Er upconversion nanoparticle-based optomagnetic multifunctional composite for drug delivery system

来源期刊:JOURNAL OF RARE EARTHS2021年第5期

论文作者:Xuhua Liang Jun Fan Yanyan Zhao Ruyi Jin

文章页码:579 - 586

摘    要:Optomagnetic multifunctional composite has attracted much attention in recent years because of its promising application prospect in bioimaging,analysis,detection,disease diagnosis,and targeted drug delivery.To explore a dual-targeted therapy for cancer,a novel class of optomagnetic multifunctional composite(UCNP-Fe3 O4@MSNs-FA) was successfully synthesized by using upconversion nanoparticles(UCNPs) as nucleus,embedding Fe3 O4 nanoparticles into the SiO2 coating layer,and modifying the surface with folic acid(FA) to strengthen its tumor targeting performance.The properties of the composite were extensively studied.The obtained composite possesses excellent upconversion fluorescence,good dispersion,high specific surface area(229.347 m2/g),and saturation magnetization value(10.9 A m2/g).Its drug loading co ntent and encapsulation efficiency can reach as high as 14.2% and 47.3%,respectively,using doxorubicin hydrochloride(DOX) as model drug.The DOX-UCNP-Fe3 O4@MSNs-FA system shows excellent sustained drug release and strong pH-dependent performance,in which the drug release would be accelerated at the slightly acidic microenvironment in the tumor;thus,the system can realize the targeted treatment of cancers.The viability of L929 cells demonstrates the good biocompatibility of the composite.Furthermore,DOX-UCNP-Fe3 O4@MSNs-FA exhibits specific cytotoxicity to folate receptor(FR) positive tumor cells,whereas DOX has weak toxicity to FR-negative cells.Therefore,the as-prepared UCNP-Fe3 O4@MSNs-FA can potentially be used as an anti-cancer targeted drug delivery system and enhance the therapeutic efficacy against FR-positive tumor cells.

详情信息展示

Synthesis of NaYF4:Yb,Er upconversion nanoparticle-based optomagnetic multifunctional composite for drug delivery system

Xuhua Liang1,2,Jun Fan3,Yanyan Zhao1,Ruyi Jin4

1. College of Biology Pharmacy and Food Engineering,Shangluo University2. Shaanxi Qinling Industrial Technology Research Institute of Special Biological Resources3. College of Food Science and Technology,Northwest University4. College of Pharmacy,Shaanxi University of Chinese Medicine

摘 要:Optomagnetic multifunctional composite has attracted much attention in recent years because of its promising application prospect in bioimaging,analysis,detection,disease diagnosis,and targeted drug delivery.To explore a dual-targeted therapy for cancer,a novel class of optomagnetic multifunctional composite(UCNP-Fe3 O4@MSNs-FA) was successfully synthesized by using upconversion nanoparticles(UCNPs) as nucleus,embedding Fe3 O4 nanoparticles into the SiO2 coating layer,and modifying the surface with folic acid(FA) to strengthen its tumor targeting performance.The properties of the composite were extensively studied.The obtained composite possesses excellent upconversion fluorescence,good dispersion,high specific surface area(229.347 m2/g),and saturation magnetization value(10.9 A m2/g).Its drug loading co ntent and encapsulation efficiency can reach as high as 14.2% and 47.3%,respectively,using doxorubicin hydrochloride(DOX) as model drug.The DOX-UCNP-Fe3 O4@MSNs-FA system shows excellent sustained drug release and strong pH-dependent performance,in which the drug release would be accelerated at the slightly acidic microenvironment in the tumor;thus,the system can realize the targeted treatment of cancers.The viability of L929 cells demonstrates the good biocompatibility of the composite.Furthermore,DOX-UCNP-Fe3 O4@MSNs-FA exhibits specific cytotoxicity to folate receptor(FR) positive tumor cells,whereas DOX has weak toxicity to FR-negative cells.Therefore,the as-prepared UCNP-Fe3 O4@MSNs-FA can potentially be used as an anti-cancer targeted drug delivery system and enhance the therapeutic efficacy against FR-positive tumor cells.

关键词:

<上一页 1 下一页 >

有色金属在线官网  |   会议  |   在线投稿  |   购买纸书  |   科技图书馆

中南大学出版社 技术支持 版权声明   电话:0731-88830515 88830516   传真:0731-88710482   Email:administrator@cnnmol.com

互联网出版许可证:(署)网出证(京)字第342号   京ICP备17050991号-6      京公网安备11010802042557号