跳到主要导航 跳到搜索 跳到主要内容

A salt-assisted acid etching strategy for hollow mesoporous silica/organosilica for pH-responsive drug and gene co-delivery

  • Meiying Wu
  • , Yu Chen
  • , Lingxia Zhang
  • , Xiaoyu Li
  • , Xiaojun Cai
  • , Yanyan Du
  • , Linlin Zhang
  • , Jianlin Shi*
  • *此作品的通讯作者
  • CAS - Shanghai Institute of Ceramics

科研成果: 期刊稿件文章同行评审

摘要

A salt-assisted acid etching (SAAE) strategy has been developed to construct rattle/hollow mesoporous silica/organosilica nanovehicles (R/HMSVs or R/HMOVs), which settles the drawbacks of traditional silica etching approaches, such as undesirable by-products, by alkaline etching and strong corrosion of the HF etching process. The hollow structure and phenylene-bridged framework of HMOVs were found to be responsible for the high cargo-loading capacity and pH-responsive drug releasing behavior, respectively, based on the special cargo-framework interaction. Especially, the molecularly organic-inorganic hybrid HMOVs have been, for the first time, successfully engineered to concurrently deliver anticancer drugs and P-gp-associated shRNA molecules for enhancing the intracellular drug concentrations and reversing the multidrug resistance (MDR) of cancer cells. On the basis of this special SAAE strategy, a wide range of mesoporous silica-based hollow nanostructures are anticipated to be synthesized to satisfy the strict requirements in various nano-catalytic and biomedical applications.

源语言英语
页(从-至)766-775
页数10
期刊Journal of Materials Chemistry B
3
5
DOI
出版状态已出版 - 7 2月 2015
已对外发布

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

学术指纹

探究 'A salt-assisted acid etching strategy for hollow mesoporous silica/organosilica for pH-responsive drug and gene co-delivery' 的科研主题。它们共同构成独一无二的学术指纹。

引用此