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Acidity and Glutathione Dual‐Responsive Polydopamine‐Coated Organic‐Inorganic Hybrid Hollow Mesoporous Silica Nanoparticles for Controlled Drug Delivery
Author(s) -
Chen Qi,
Chen Yunna,
Zhang Wenjing,
Huang Qianqian,
Hu Mengru,
Peng Daiyin,
Peng Can,
Wang Lei,
Chen Weidong
Publication year - 2020
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.202000263
Subject(s) - mesoporous silica , nanoparticle , mesoporous material , drug delivery , biodegradation , controlled release , tumor microenvironment , nanotechnology , materials science , adsorption , x ray photoelectron spectroscopy , chemistry , in vivo , chemical engineering , degradation (telecommunications) , biophysics , catalysis , tumor cells , organic chemistry , cancer research , engineering , telecommunications , microbiology and biotechnology , computer science , biology
Controversial biodegradability and nonspecific pre‐drug leakage are major limitations for inorganic nanoparticles in cancer treatment. To solve these problems, we developed organic‐inorganic hybridized hollow mesoporous silica nanoparticles with polydopamine modifications on the surface to simultaneously achieve enhanced biodegradability and controllable drug release. The morphology and chemical structure of the nanoparticles were characterized by TEM, N 2 adsorption‐desorption isotherms, TEM‐mapping and XPS. Moreover, the release behavior of nanoparticles under various pH conditions and the degradation behavior in the presence of GSH were evaluated. With effective controlled release, HMONs‐PTX@PDA were shown to significantly inhibit cancer cell proliferation and achieve antitumor effects in vivo through dual‐response release in the tumor microenvironment. Overall, this nanoplatform has significant potential to achieve tumor microenvironment‐responsive degradation and release to enhance tumor accumulation, which is very promising for cancer treatment.
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