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A biodegradable pH and glutathione dual-triggered drug delivery system based on mesoporous silica, carboxymethyl chitosan and oxidized pullulan
被引:25
|作者:
Rui, Qian
[1
]
Gao, Jun
[2
]
Yin, Zheng-Zhi
[3
]
Li, Junyao
[1
]
Cai, Wenrong
[1
,4
]
Wu, Datong
[1
]
Kong, Yong
[1
]
机构:
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Changzhou Municipal Hosp Tradit Chinese Med, Dept Orthoped, Changzhou 213003, Peoples R China
[3] Jiaxing Univ, Coll Biol Chem Sci & Engn, Jiaxing 314001, Peoples R China
[4] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Shandong Key Lab Biochem Anal, Qingdao 266042, Peoples R China
关键词:
Biodegradable mesoporous silica nanoparticles;
Carboxymethyl chitosan;
Oxidized pullulan;
Hydrogels;
Dual -triggered drug delivery;
GOLD NANOCAGES;
NANOPARTICLES;
ACID;
RELEASE;
REDOX;
D O I:
10.1016/j.ijbiomac.2022.10.215
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
A simple and smart drug controlled delivery system is developed in this work. Biodegradable mesoporous silica nanoparticles (BMSN) were first synthesized by introducing disulfide during the synthesis of mesoporous silica nanoparticles (MSN), which were used for the loading of methotrexate (MTX), an anti-cancer drug. The MTX loaded BMSN (BMSN-MTX) was then encapsulated in the hydrogels of carboxymethyl chitosan (CMCS)/oxidized pullulan (OPL) generated through Schiff base reaction. The acylhydrazone bonds (-N=CH-) between CMCS and OPL are prone to be hydrolyzed in acidic medium while the disulfide linkage (-S-S-) in the BMSN can be cleaved in the presence of glutathione (GSH), and thus the delivery of MTX from the BMSN-MTX-gel can be triggered by both pH and GSH. The results of release kinetics reveal that the delivery of MTX from the biodegradable hydrogels is controlled by Higuchi model. Finally, good biocompatibility and pronounced cytotoxicity of the developed BMSN-MTX-gel are confirmed by cytotoxicity test.
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页码:1294 / 1302
页数:9
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