Chinese Journal of Structural Chemistry, Год журнала: 2024, Номер unknown, С. 100398 - 100398
Опубликована: Июль 1, 2024
Язык: Английский
Chinese Journal of Structural Chemistry, Год журнала: 2024, Номер unknown, С. 100398 - 100398
Опубликована: Июль 1, 2024
Язык: Английский
Small, Год журнала: 2025, Номер unknown
Опубликована: Март 16, 2025
Abstract Conventional combinational antibacterial therapy requires the complicated assembly of multiple components that might cause a premature leak therapeutic agents. Thus one‐pot highly integrated multifunctional agents is desirable for treating multidrug‐resistant (MDR) bacteria. Herein, vancomycin‐derived carbon dots (Van‐CDs) are facilely developed as compact and powerful photodynamic nanozyme platform achieves augmented reactive oxygen species (ROS) generation accelerating bacterial elimination. By residual recognition groups vancomycin, red emissive Van‐CDs gain specific affinity toward bacteria with high binding constant 20 L g −1 , manifesting superior bacteria‐imaging ability. Meanwhile, encoded an excellent peroxidase‐mimicking (POD) activity mediating H 2 O ‐activated evolvement •OH, also endowed intrinsic property simultaneously producing singlet ( 1 ). Surprisingly, possesses auxiliary photothermal feature, which enables imaging‐guided hyperthermia‐reinforced in vivo. Furthermore, subcutaneous abscess model established to validate their pronounced biofilm eradication wound healing acceleration vivo through Van‐CDs‐promoted collagen deposition. Taken together, present all‐in‐one carbon‐derived functions represents promising competitive candidate diabetic infections clinical research.
Язык: Английский
Процитировано
0Chinese Journal of Structural Chemistry, Год журнала: 2024, Номер unknown, С. 100398 - 100398
Опубликована: Июль 1, 2024
Язык: Английский
Процитировано
0