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采用黏附纳米聚集体实现抗结核药物经鼻-脑递送至大脑以有效治疗脑结核。

Effective cerebral tuberculosis treatment nose-to-brain transport of anti-TB drugs using mucoadhesive nano-aggregates.

机构信息

Pharmaceutical Nanotechnology lab, Institute of Nano Science and Technology (INST), Sector-81, Mohali, Punjab, 140306, India.

Experimental Animal Facility, ICMR-National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Tajganj, Agra, 282004, India.

出版信息

Nanoscale. 2024 Sep 12;16(35):16485-16499. doi: 10.1039/d4nr02621g.

DOI:10.1039/d4nr02621g
PMID:39135488
Abstract

Central nervous system tuberculosis (CNS-TB) is a severe form of extra-pulmonary tuberculosis with high mortality and morbidity rates. The standard treatment regimen for CNS-TB parallels that of pulmonary TB, despite the challenge posed by the blood-brain barrier (BBB), which limits the efficacy of first-line anti-TB drugs (ATDs). Nose-to-brain (N2B) drug delivery offers a promising solution for achieving high ATD concentrations directly at infection sites in the brain while bypassing the BBB. This study aimed to develop chitosan nanoparticles encapsulating ATDs, specifically isoniazid (INH) and rifampicin (RIF). These nanoparticles were further processed into micro-sized chitosan nano-aggregates (NA) spray drying. Both INH-NA and RIF-NA showed strong mucoadhesion and significantly higher permeation rates across RPMI 2650 cells compared to free ATDs. Intranasal administration of these NAs to TB-infected mice for four weeks resulted in a significant reduction of mycobacterial load by approximately ∼2.86 Log 10 CFU compared to the untreated group. This preclinical data highlights the efficacy of intranasal chitosan nano-aggregates in treating CNS-TB, demonstrating high therapeutic potential, and addressing brain inflammation challenges. To our knowledge, this study is the first to show nasal delivery of ATD nano-formulations for CNS-TB management.

摘要

中枢神经系统结核(CNS-TB)是一种严重的肺外结核形式,具有高死亡率和发病率。尽管血脑屏障(BBB)带来了挑战,限制了一线抗结核药物(ATD)的疗效,但 CNS-TB 的标准治疗方案与肺结核相似。鼻内(N2B)药物输送为实现高 ATD 浓度直接到达大脑感染部位,同时绕过 BBB 提供了有前途的解决方案。本研究旨在开发包载 ATD 的壳聚糖纳米粒,特别是异烟肼(INH)和利福平(RIF)。这些纳米粒进一步加工成微尺度壳聚糖纳米聚集体(NA)喷雾干燥。与游离 ATD 相比,INH-NA 和 RIF-NA 均表现出强烈的黏膜黏附性,并显著提高了穿透 RPMI 2650 细胞的渗透率。将这些 NAs 经鼻内给药给感染结核的小鼠 4 周,与未治疗组相比,细菌载量减少了约 2.86 Log10 CFU。这些临床前数据突出了鼻内壳聚糖纳米聚集体治疗 CNS-TB 的疗效,显示出高治疗潜力,并解决了脑炎症挑战。据我们所知,这是第一项展示用于 CNS-TB 管理的 ATD 纳米制剂鼻内递送的研究。

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