TY - JOUR
T1 - Therapeutic Nanoplatform Integrating Photothermal Effect and Silver Nanoparticles for the Treatment of Intracellular Mycobacterium tuberculosis
AU - Tian, Na
AU - Liu, Bei
AU - Song, Peng
AU - Zhang, Fanling
AU - Xu, Wenzhao
AU - Sun, Zhaogang
AU - Zhang, Xiangyu
AU - Chu, Hongqian
AU - Chu, Naihui
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/3/25
Y1 - 2026/3/25
N2 - The global challenge of tuberculosis (TB), particularly in the context of rising drug resistance and intracellular bacterial persistence, highlights the need for innovative therapeutic strategies. In this study, we develop a multifunctional nanoplatform (CuS-Ag@FA) that integrates near-infrared (NIR)-responsive photothermal CuS, antimicrobial Ag nanoparticles (Ag NPs), and folate-receptor-mediated macrophage targeting for enhanced intracellular Mycobacterium tuberculosis (M.tb) clearance. Our work represents the first FA-functionalized CuS-Ag nanoplatform designed for dual-targeting of M.tb-infected macrophages and the first evaluation of this nanoplatform in an M.tb-infected animal model. FA functionalization markedly improves macrophage uptake, enabling precise intracellular delivery. Upon 808 nm irradiation, CuS-Ag@FA generates localized hyperthermia that synergizes with Ag NPs-induced oxidative and membrane-disruptive effects, resulting in potent intracellular bactericidal efficacy. Transcriptomic analysis reveals simultaneous inhibition of M.tb DNA replication, redox homeostasis, and metabolic pathways, supporting a multidimensional mechanism of action. In vivo studies confirm potent therapeutic efficacy, pulmonary accumulation, and favorable biosafety, establishing CuS-Ag@FA as a promising next-generation nanotherapeutic for combating drug-resistant and intracellular M.tb.
AB - The global challenge of tuberculosis (TB), particularly in the context of rising drug resistance and intracellular bacterial persistence, highlights the need for innovative therapeutic strategies. In this study, we develop a multifunctional nanoplatform (CuS-Ag@FA) that integrates near-infrared (NIR)-responsive photothermal CuS, antimicrobial Ag nanoparticles (Ag NPs), and folate-receptor-mediated macrophage targeting for enhanced intracellular Mycobacterium tuberculosis (M.tb) clearance. Our work represents the first FA-functionalized CuS-Ag nanoplatform designed for dual-targeting of M.tb-infected macrophages and the first evaluation of this nanoplatform in an M.tb-infected animal model. FA functionalization markedly improves macrophage uptake, enabling precise intracellular delivery. Upon 808 nm irradiation, CuS-Ag@FA generates localized hyperthermia that synergizes with Ag NPs-induced oxidative and membrane-disruptive effects, resulting in potent intracellular bactericidal efficacy. Transcriptomic analysis reveals simultaneous inhibition of M.tb DNA replication, redox homeostasis, and metabolic pathways, supporting a multidimensional mechanism of action. In vivo studies confirm potent therapeutic efficacy, pulmonary accumulation, and favorable biosafety, establishing CuS-Ag@FA as a promising next-generation nanotherapeutic for combating drug-resistant and intracellular M.tb.
KW - antimicrobial nanoplatform
KW - photothermal therapy
KW - silver nanoparticles
KW - targeted drug delivery
KW - tuberculosis
UR - https://www.scopus.com/pages/publications/105033759670
U2 - 10.1021/acsami.5c23795
DO - 10.1021/acsami.5c23795
M3 - Article
C2 - 41805320
AN - SCOPUS:105033759670
SN - 1944-8244
VL - 18
SP - 16101
EP - 16115
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 11
ER -