He Junhui, Yang Li, Li Dongmei, Xie Jiaxiu, Zhou Guili, Zhou Rongfei, Li Yi, Wei Guining, Gong Zhiqiang, Li Li, Lai Kedao, Zhou Juying
School of Chemistry and Chemical Engineering, Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission, Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products, Guangxi Minzu University, Nanning 530006, China; Guangxi Key Laboratory of Traditional Chinese Medicine Quality Standards, Guangxi Institute of Chinese Medicine and Pharmaceutical Science, Naning 530022, China.
Department of Pharmacology, Guangxi Medical University, Nanning 530021, Guangxi, China.
Int J Biol Macromol. 2025 Jan;286:138352. doi: 10.1016/j.ijbiomac.2024.138352. Epub 2024 Dec 4.
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for depression and bringing new hope for the return to the market of many first-line antidepressants that have been withdrawn.
血脑屏障(BBB)的局限性导致许多抗抑郁药疗效低且毒性高。然而,增强血脑屏障靶向性以提高抗抑郁药疗效和安全性的策略仍然具有挑战性。在本研究中,我们制备了转铁蛋白(Tf)功能化的壳聚糖(CS)-N,O-羧甲基壳聚糖(NOCMS)纳米系统(NPs)(NOCMS-CS-Tf NPs),其可在抑郁环境中增强血脑屏障靶向性,并使更多纳米颗粒进入大脑。实验表明,与正常环境相比,NOCMS-CS-Tf NPs在抑郁环境中具有增强的血脑屏障靶向性,且安全无毒。体外实验表明,NOCMS-CS-Tf NPs可靶向大脑中的多种细胞系,并且在神经炎症和神经元损伤环境中比在正常环境中具有更强的血脑屏障靶向性;体内实验表明,NOCMS-CS-Tf NPs在抑郁小鼠大脑中的血脑屏障靶向性比正常小鼠更强,且安全无毒。该纳米系统在抑郁症神经炎症和神经元损伤的情况下增强了血脑屏障靶向性,为抑郁症药物递送系统提供了一种有前景的方法,并为许多已撤市的一线抗抑郁药重返市场带来了新希望。