Transferrin-modified carboxymethyl chitosan-chitosan nanoparticles as an efficient delivery carrier for targeted therapy of depression

被引:0
|
作者
He, Junhui [1 ,2 ]
Yang, Li [3 ]
Li, Dongmei [2 ]
Xie, Jiaxiu [2 ]
Zhou, Guili [3 ]
Zhou, Rongfei [3 ]
Li, Yi [2 ]
Wei, Guining [2 ]
Gong, Zhiqiang [4 ]
Li, Li [2 ]
Lai, Kedao [2 ]
Zhou, Juying [1 ]
机构
[1] Guangxi Minzu Univ, Guangxi Collaborat Innovat Ctr Chem & Engn Forest, Sch Chem & Chem Engn, Key Lab Chem & Engn Forest Prod,Guangxi Key Lab Ch, Nanning 530006, Peoples R China
[2] Guangxi Inst Chinese Med & Pharmaceut Sci, Guangxi Key Lab Tradit Chinese Med Qual Stand, Naning 530022, Peoples R China
[3] Guangxi Med Univ, Dept Pharmacol, Nanning 530021, Guangxi, Peoples R China
[4] Guangxi Univ Chinese Med, Fac Chinese Med Sci, Nanning 530002, Peoples R China
基金
芬兰科学院;
关键词
Transferrin; Nanocarriers; Blood-brain barrier; LPS-INDUCED NEUROINFLAMMATION; ORAL DELIVERY; UP-REGULATION; RECEPTOR; CELLS; DRUG;
D O I
10.1016/j.ijbiomac.2024.138352
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
Limitations of the blood-brain barrier (BBB) are responsible for the low efficacy and high toxicity of many antidepressants. However, strategies to enhance BBB targeting to improve the efficacy and safety of antidepressants remain challenging. In this study, we prepared transferrin (Tf)-functionalized chitosan (CS)-N,O-carboxymethy chitosan (NOCMS) nanosystems (NPs) (NOCMS-CS-Tf NPs), which can enhance BBB targeting in the depressive environment and allow more NPs to enter the brain. Experiments demonstrated that NOCMS-CS-Tf NPs had enhanced BBB targeting in the depressed environment compared to the normal environment and were safe and non-toxic. In vitro experiments demonstrated that NOCMS-CS-Tf NPs could target multiple cell lines in the brain and had stronger BBB targeting in neuroinflammatory and neuronal injury environments than in normal environments; in vivo experiments demonstrated that NOCMS-CS-Tf NPs had stronger BBB targeting in the brains of depressed mice than in normal mice, and were safe and non-toxic. The nanosystem enhanced BBB targeting in the setting of neuroinflammation and neuronal damage in depression, providing a promising approach to drug delivery systems for depression and bringing new hope for the return to the market of many first-line antidepressants that have been withdrawn.
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页数:17
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