Photothermally Triggered Control of the Drug Delivery System Using Doxorubicin-Loaded Mesoporous Silica for Effective Killing of Human Hepatoma Cells

Ming Li, Yu Han Huang, Yingqiang Qin, Bo Ren, Hong Yu Song, Yanhai Qi
{"title":"Photothermally Triggered Control of the Drug Delivery System Using Doxorubicin-Loaded Mesoporous Silica for Effective Killing of Human Hepatoma Cells","authors":"Ming Li, Yu Han Huang, Yingqiang Qin, Bo Ren, Hong Yu Song, Yanhai Qi","doi":"10.4028/p-g4xep4","DOIUrl":null,"url":null,"abstract":"Photothermal-temperature responsive [Ag nanoparticles-hollow mesoporous silica nanospheres–poly (N-isopropyl acrylamide-acrylic acid)] (Ag@HMSN@PNIPAM-AA) nanoparticles were designed and prepared, and the combination of Ag nanoparticles (AgNPs) and [poly (N-isopropyl acrylamide-acrylic acid)] (PNIPAM-AA) was used as a switch of the photothermal-temperature effect to control drug release. The results of cell culture in vitro showed that [mesoporous silica nanospheres–poly (N-isopropyl acrylamide-acrylic acid)] (MSN@PNIPAM-AA) and Ag@HMSN@PNIPAM-AA nanoparticles had good biocompatibility and less cytotoxicity, and Ag@HMSN@PNIPAM-AA nanoparticles had higher cell inhibition under 808 nm near-infrared light. The combination of near-infrared light and doxorubicin showed higher drug release efficiency and a stronger inhibitory effect on HepG2 cell growth. These characteristics indicate that Ag@HMSN@PNIPAM-AA nanoparticles have great potential for treatment. This study also proved the universal applicability of Ag@HMSN@PNIPAM-AA nanoparticles. Different model drugs and nanoparticles can play different roles and have development potential.","PeriodicalId":7271,"journal":{"name":"Advanced Materials Research","volume":"22 1","pages":"91 - 98"},"PeriodicalIF":0.0000,"publicationDate":"2022-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4028/p-g4xep4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Photothermal-temperature responsive [Ag nanoparticles-hollow mesoporous silica nanospheres–poly (N-isopropyl acrylamide-acrylic acid)] (Ag@HMSN@PNIPAM-AA) nanoparticles were designed and prepared, and the combination of Ag nanoparticles (AgNPs) and [poly (N-isopropyl acrylamide-acrylic acid)] (PNIPAM-AA) was used as a switch of the photothermal-temperature effect to control drug release. The results of cell culture in vitro showed that [mesoporous silica nanospheres–poly (N-isopropyl acrylamide-acrylic acid)] (MSN@PNIPAM-AA) and Ag@HMSN@PNIPAM-AA nanoparticles had good biocompatibility and less cytotoxicity, and Ag@HMSN@PNIPAM-AA nanoparticles had higher cell inhibition under 808 nm near-infrared light. The combination of near-infrared light and doxorubicin showed higher drug release efficiency and a stronger inhibitory effect on HepG2 cell growth. These characteristics indicate that Ag@HMSN@PNIPAM-AA nanoparticles have great potential for treatment. This study also proved the universal applicability of Ag@HMSN@PNIPAM-AA nanoparticles. Different model drugs and nanoparticles can play different roles and have development potential.
利用负载阿霉素的介孔二氧化硅光热触发控制药物传递系统有效杀伤人肝癌细胞
设计并制备了光热-温度响应的[Ag纳米颗粒-中空介孔二氧化硅纳米球-聚(n -异丙基丙烯酰胺-丙烯酸)](Ag@HMSN@PNIPAM-AA)纳米颗粒,并利用Ag纳米颗粒(AgNPs)与[聚(n -异丙基丙烯酰胺-丙烯酸)](PNIPAM-AA)的组合作为光热-温度效应的开关来控制药物释放。体外细胞培养结果表明,[介孔二氧化硅纳米球-聚(n -异丙基丙烯酰胺-丙烯酸)](MSN@PNIPAM-AA)和Ag@HMSN@PNIPAM-AA纳米颗粒在808 nm近红外光下具有良好的生物相容性和较小的细胞毒性,Ag@HMSN@PNIPAM-AA纳米颗粒在808 nm近红外光下具有较高的细胞抑制作用。近红外光联合阿霉素对HepG2细胞的释放效率更高,抑制作用更强。这些特征表明Ag@HMSN@PNIPAM-AA纳米颗粒具有很大的治疗潜力。该研究也证明了Ag@HMSN@PNIPAM-AA纳米颗粒的普遍适用性。不同的模型药物和纳米颗粒可以发挥不同的作用,具有开发潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信