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ROS/Electro 双响应性纳米凝胶靶向癫痫病灶重塑异常回路和炎症微环境

ROS/Electro Dual-Reactive Nanogel for Targeting Epileptic Foci to Remodel Aberrant Circuits and Inflammatory Microenvironment.

机构信息

Department of Pharmaceutics, School of Pharmacy, Fudan University, Key Laboratory of Smart Drug Delivery, Ministry of Education, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai 201203, People's Republic of China.

出版信息

ACS Nano. 2023 Apr 25;17(8):7847-7864. doi: 10.1021/acsnano.3c01140. Epub 2023 Apr 11.

Abstract

Medicinal treatment against epilepsy is faced with intractable problems, especially epileptogenesis that cannot be blocked by clinical antiepileptic drugs (AEDs) during the latency of epilepsy. Abnormal circuits of neurons interact with the inflammatory microenvironment of glial cells in epileptic foci, resulting in recurrent seizures and refractory epilepsy. Herein, we have selected phenytoin (PHT) as a model drug to derive a ROS-responsive and consuming prodrug, which is combined with an electro-responsive group (sulfonate sodium, SS) and an epileptic focus-recognizing group (α-methyl-l-tryptophan, AMT) to form hydrogel nanoparticles (i.e., a nanogel). The nanogel will target epileptic foci, release PHT in response to a high concentration of reactive oxygen species (ROS) in the microenvironment, and inhibit overexcited circuits. Meanwhile, with the clearance of ROS, the nanogel can also reduce oxidative stress and alleviate microenvironment inflammation. Thus, a synergistic regulation of epileptic lesions will be achieved. Our nanogel is expected to provide a more comprehensive strategy for antiepileptic treatment.

摘要

抗癫痫药物治疗面临着诸多难题,特别是在癫痫潜伏期,临床抗癫痫药物(AEDs)无法阻断癫痫发生。神经元异常回路与癫痫灶中神经胶质细胞的炎症微环境相互作用,导致反复发作和难治性癫痫。在此,我们选择苯妥英(PHT)作为模型药物,设计了一种 ROS 响应性消耗型前药,它与电响应基团(磺酸钠,SS)和癫痫灶识别基团(α-甲基-l-色氨酸,AMT)结合,形成水凝胶纳米颗粒(即纳米凝胶)。纳米凝胶将靶向癫痫灶,在微环境中高浓度活性氧(ROS)的作用下释放 PHT,抑制过度兴奋的回路。同时,随着 ROS 的清除,纳米凝胶还可以减轻氧化应激和炎症微环境。因此,可以实现对癫痫病变的协同调节。我们的纳米凝胶有望为抗癫痫治疗提供更全面的策略。

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