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Updated: May 27, 2025

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Urushiol-dextran SPIONs magnetic recyclable nanoparticles immobilizing vancomycin (V@DU@Fe) for antibacterial
Xingying Xue1, Zhiwen Qi2, Zhihong Wang3
1National Engineering Lab. for Biomass Chemical Utilization, Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, Jiangsu, People's Republic of China; College of Materials Science and Technology, Beijing Forestry University, Beijing 100083, People's Republic of China; Key Lab. of Biomass Energy and Material, Chinese Academy of Forestry, Nanjing 210042, Jiangsu, People's Republic of China.
Abstract:
In this study, magnetic nanocarriers (DU@Fe, Davg = 281.6 nm, zeta potential -28.0 mV) were fabricated using dextran, urushiol as the shell and superparamagnetic iron oxide nanoparticles (SPIONs) as the core. Subsequently, the specific ligand Lys-D-Ala-D-Ala of vancomycin (Van) was grafted onto the surface of DU@Fe, which generated nanoparticles (Lys-D-Ala-D-Ala@DU@Fe) with an average particle size of 385.5 nm and a zeta potential of -16.8 mV via specific and robust interaction. Ultimately, the immobilization capacity of Van reached up to 294.1 mg·g-1 for efficient antibacterial properties. Moreover, the assembly process adhered to the pseudo-second-order kinetics model (R2 = 0.998-0.999) and the Langmuir adsorption isotherm model (R2 = 0.999, 30 °C). Notably, V@DU@Fe effectively adhered to the cell envelopes of both Gram-negative and Gram-positive bacteria, achieving rapid bactericidal effects within 1 h. Furthermore, it maintained over 85.0 % of its initial antibacterial efficiency against S. aureus and S. epidermidis even after six recycles. Therefore, this study provides strategies and methods for the development of urushiol-dextran intelligent SPIONs nanomedicines.
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