Photo-responsive degradable hollow mesoporous organosilica nanoplatforms for drug delivery

被引:32
|
作者
Fan, Jie [1 ]
Zhang, Zhipeng [1 ]
Wang, Yaru [1 ]
Lin, Shiting [1 ]
Yang, Shun [1 ]
机构
[1] Jiangsu Normal Univ, Sch Chem & Chem Engn, Xuzhou 221116, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Organosilica; Photo-responsive degradation; Drug delivery; Graphene oxide quantum dots; Hollow mesoporous materials; CO-GLYCOLIDE MICROPARTICLES; ENHANCED PERMEABILITY; PARTICLE-SIZE; NANOPARTICLES; POLYLACTIDE; NANOCARRIERS; CHEMOTHERAPY; THERAPY; RELEASE; AGENTS;
D O I
10.1186/s12951-020-00642-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Stimulus-responsive degradable mesoporous organosilica nanoparticles (MONs) have shown great promise as drug carriers via enhancing the efficiency of drug delivery and accelerating the degradation of nanocarriers. However, it remains a great challenge to develop novel light-enabled spatial and temporal degradable MONs with both superior responsiveness for efficient anti-cancer drug delivery and safe exocytosis. Results We report a novel photo-responsive degradable hollow mesoporous organosilica nanoplatform (HMONs@GOQD). The platform is based on organosilica nanoparticles (HMONs) containing singlet oxygen (O-1(2))-responsive bridged organoalkoxysilanes and wrapped graphene oxide quantum dots (GOQDs). The unique hollow mesoporous structure of the HMONs guarantees an excellent drug loading and release profile. During light irradiation,(1)O(2)produced by the GOQDs leads to the degradation of the organosilica nanoparticles, resulting in enhanced local drug release. Conclusions We carried out in vitro and in vivo experiments using DOX as a model drug; DOX-HMONs@GOQDs exhibited high biocompatibility, accelerated degradation, and superior therapeutic efficacy during light irradiation, indicating a promising platform for clinical cancer therapy.
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页数:14
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