Zwitterionic meso-silica/polypeptide hybrid nanoparticles for efficient azithromycin delivery and photodynamic therapy for synergistic treatment of drug-resistant bacterial infection

被引:13
|
作者
Xiang, Ya-li [1 ]
Huang, Shuang-hui [1 ]
Hu, Qiu-hui [1 ]
Wang, Qiu-yue [1 ]
Zhao, Mei-qi [1 ]
Jiang, Yu-chen [1 ]
Chen, Xiao [1 ]
Lin, Juan [2 ]
Zhou, Qing-han [1 ,3 ]
机构
[1] Southwest Minzu Univ, Sch Chem & Environm, Natl Ethn Affairs Commiss, Key Lab Pollut Control Chem & Environm Funct Mat Q, First Ring Rd,4 Sect 16, Chengdu 610041, Sichuan, Peoples R China
[2] Chengdu Med Coll, Sch Biomed Sci & Technol, Xindu Rd 783, Chengdu 610500, Sichuan, Peoples R China
[3] Southwest Minzu Univ, Natl Ethn Affairs Commiss, Sch Chem & Environm, Key Lab Gen Chem, Chengdu 610041, Peoples R China
关键词
Nanocomposites; Chemo-photodynamic combined therapy; Antibacteria; NITRIC-OXIDE RELEASE; NANOCOMPOSITES;
D O I
10.1016/j.ijbiomac.2022.08.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The treatment of drug-resistant bacterial infections attributed to the overuse of antibiotics still remains a serious challenge globally. Herein, zwitterionic charge switchable meso-silica/polypeptide hybrid nanoparticles (MSPNs) were prepared for the synergistic chemo-photodynamic therapy in the treatment of drug-resistant bacterial infections. Subsequently, azithromycin (AZT) and methylene blue (MB) were loaded in the MSPNs to form the combined chemo-photodynamic therapeutic nanoparticles (MSPNs-AZT/MB) for the treatment of methicillin-resistant Staphylococcus aureus (MRSA). Remarkably, the as-prepared MSPNs-AZT/MB exhibited a negative surface charge of-5.2 mV at physiological pH while switching into positive surface charge of 24.7 mv in an acidic environment, leading to enhanced binding with bacterial surface. The lipase-triggered AZT release up to 77.9 % was achieved, and the loaded MB demonstrated efficient singlet oxygen (O-1(2)) generation for photodynamic therapy. The in vitro experimental results displayed an excellent antibacterial effect against MRSA in both planktonic and biofilm phenotypes. Additionally, the as-prepared MSPNs-AZT/MB exhibited synergistic and enhanced antibacterial infection effect up to 94 % comparing to monotherapy in a mice model. Considering the above advantages, the as-prepared combined chemo-photodynamic therapeutic nanoparticles showed promising biocompatibility and clinical potential for the efficient therapy of drug-resistant bacteria.
引用
收藏
页码:597 / 610
页数:14
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