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3D球体模型揭示了甘露糖修饰的纳米颗粒在结核病治疗中的增强疗效。

3D spheroid model reveals enhanced efficacy of mannose-decorated nanoparticles for TB treatment.

作者信息

Patil Suyash M, Daram Apoorva, Kunda Nitesh K

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, New York, NY, USA.

出版信息

Nanomedicine (Lond). 2025 Apr;20(8):777-789. doi: 10.1080/17435889.2025.2478806. Epub 2025 Mar 18.

Abstract

AIMS

Tuberculosis (TB), caused by remains a significant global health challenge aggravated by drug-resistant strains and prolonged treatment regimens. Innovative strategies to enhance treatment efficacy, improve patient adherence, and reduce adverse effects are urgently required.

METHODS

We explored a combination therapy using bedaquiline and pretomanid encapsulated in polymeric nanoparticles (pNPs). Further, active targeting was achieved through mannose-decorated nanoparticles (Man-pNPs) for macrophage-specific delivery. The drug-loaded pNPs and Man-pNPs were spray-dried into dry powder particles to improve drug solubility and enable local lung delivery inhalation. Man-pNPs were prepared to target macrophages, wherein TB bacteria reside.

RESULTS

Formulations exhibited high drug loading and excellent aerosolization performance (MMAD 1-5 µm, FPF > 75%) for pNPs and Man-pNPs. Man-pNPs formulation enhanced macrophage targeting receptor-mediated endocytosis and phagocytosis, improving bacterial inhibition. Man-pNPs demonstrated similar MIC and enhanced intracellular inhibition compared to free drug combination and pNPs. In addition, a TB spheroid model was developed for formulation screening, mimicking granulomas' physiological conditions. Man-pNPs formulation showed superior intracellular bacterial inhibition in TB spheroid model compared to free drug combination and pNPs.

CONCLUSION

This research underscores the potential of combination therapy, particulate-based inhaled drug delivery, and active targeting to advance efficient and patient-friendly TB treatments.

摘要

目的

由[病原体名称未给出]引起的结核病仍然是一项重大的全球健康挑战,耐药菌株和延长的治疗方案使其更加严峻。迫切需要创新策略来提高治疗效果、改善患者依从性并减少不良反应。

方法

我们探索了一种联合疗法,使用包裹在聚合物纳米颗粒(pNPs)中的贝达喹啉和普瑞玛胺。此外,通过用甘露糖修饰的纳米颗粒(Man-pNPs)实现主动靶向,以实现巨噬细胞特异性递送。将载药的pNPs和Man-pNPs喷雾干燥成干粉颗粒,以提高药物溶解度并实现肺部局部递送(吸入)。制备Man-pNPs以靶向巨噬细胞,结核杆菌寄生于其中。

结果

pNPs和Man-pNPs制剂表现出高载药量和出色的雾化性能(质量中值空气动力学直径1 - 5μm,细颗粒分数>75%)。Man-pNPs制剂通过受体介导的内吞作用和吞噬作用增强了巨噬细胞靶向性,改善了细菌抑制效果。与游离药物组合和pNPs相比,Man-pNPs表现出相似的最低抑菌浓度(MIC)并增强了细胞内抑制作用。此外,开发了一种结核球模型用于制剂筛选,模拟肉芽肿的生理条件。与游离药物组合和pNPs相比,Man-pNPs制剂在结核球模型中表现出优异的细胞内细菌抑制作用。

结论

本研究强调了联合疗法、基于颗粒的吸入药物递送和主动靶向在推进高效且患者友好的结核病治疗方面的潜力。

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In Vitro Miniaturized Tuberculosis Spheroid Model.体外小型化结核球模型
Biomedicines. 2021 Sep 13;9(9):1209. doi: 10.3390/biomedicines9091209.

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