4.6 Article

Anticancer Drug Release System Based on Hollow Silica Nanocarriers Triggered by Tumor Cellular Microenvironments

期刊

ACS OMEGA
卷 6, 期 1, 页码 553-558

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.0c05032

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资金

  1. National Natural Science Foundation of China [22074029, 51802082]
  2. Training Plan for University's Young Backbone Teachers of Henan Province [2019GGJS170]
  3. Program for Science & Technology Innovation Talents in Universities of Henan Province [21HATIT016]
  4. Science and Technology Research Project of Henan Provincial Science and Technology Department [142102210047]
  5. New Century Excellent Talent Support Program for Colleges and Universities in Henan Province [2006HANCET-01]
  6. Key Scientific Research Project of Education Department of Henan Province [17A150027]

向作者/读者索取更多资源

The article introduces a pH-responsive drug delivery system using in situ amino-functionalized hollow mesoporous silica nanoparticles as carriers, which can intelligently and targetedly release anticancer drugs in tumor microenvironments. The system shows efficient drug loadings and targeted release, with nearly 100% release of zorubicin hydrochloride at a buffer pH of 5.0, demonstrating great potential in anticancer therapy.
Targeted release of anticancer drugs to tumor sites has a pivotal role in clinical oncology. pH-responsive drug delivery systems, with an intelligent and targeted release of anticancer drugs in a controllable manner based on sensitivities to the weakly acidic environments of tumor cellular microenvironments, are desirable. Herein, the design of such a pH-responsive drug delivery system is detailed using in situ amino-functionalized hollow mesoporous silica nanoparticles as carriers. The drug release behavior of the pH-responsive delivery system was evaluated under an in vitro simulation of tumor cellular microenvironments. The drug delivery system has efficient drug loadings and targeted release. Zorubicin hydrochloride releasing percentage is almost up to 100% at a buffer pH of 5.0. The drug release systems described demonstrating great potential in anticancer therapy.

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