A photoactivatable and phenylboronic acid-functionalized nanoassembly for combating multidrug-resistant gram-negative bacteria and their biofilms

Author:

Zhou Xiaoqing1,Dong Lanlan2,Zhao Baohua2,Hu Guangyun2,Huang Can2,Liu Tengfei3,Lu Yifei2,Zheng Mengxue1,Yu Yanlan1,Yang Zengjun1,Cheng Shaowen4,Xiong Yan5ORCID,Luo Gaoxing2,Qian Wei2ORCID,Yin Rui1ORCID

Affiliation:

1. Army Medical University (Third Military Medical University) Department of Dermatology, Southwest Hospital, , No. 29 Gaotanyan Road, Shapingba District, Chongqing 400038 , China

2. Southwest Hospital, Army Medical University (Third Military Medical University) Institute of Burn Research, State Key Laboratory of Trauma, Burn and Combined Injury, Key Laboratory of Disease Proteomics of Chongqing, , No. 29 Gaotanyan Road, Shapingba District, Chongqing 400038 , China

3. No. 906 Hospital of Joint Logistic Support Force of PLA Department of Burn and Plastic Sugery, , No. 377 Zhongshan East Road, Yinzhou District, Ningbo 315100 , China

4. the First Affiliated Hospital of Hainan Medical University Department of Wound Repair, , No. 31 Longhua Road, Haikou 570102 , China

5. Army Medical University (Third Military Medical University) Department of Orthopaedics, Daping Hospital, , No. 10 Changjiang Branch Road, Yuzhong District, Chongqing 400042 , China

Abstract

Abstract Background Multidrug-resistant (MDR) gram-negative bacteria-related infectious diseases have caused an increase in the public health burden and mortality. Moreover, the formation of biofilms makes these bacteria difficult to control. Therefore, developing novel interventions to combat MDR gram-negative bacteria and their biofilms-related infections are urgently needed. The purpose of this study was to develop a multifunctional nanoassembly (IRNB) based on IR-780 and N, N′-di-sec-butyl-N, N′- dinitroso-1,4-phenylenediamine (BNN6) for synergistic effect on the infected wounds and subcutaneous abscesses caused by gram-negative bacteria. Methods The characterization and bacteria-targeting ability of IRNB were investigated. The bactericidal efficacy of IRNB against gram-negative bacteria and their biofilms was demonstrated by crystal violet staining assay, plate counting method and live/dead staining in vitro. The antibacterial efficiency of IRNB was examined on a subcutaneous abscess and cutaneous infected wound model in vivo. A cell counting kit-8 assay, Calcein/PI cytotoxicity assay, hemolysis assay and intravenous injection assay were performed to detect the biocompatibility of IRNB in vitro and in vivo. Results Herein, we successfully developed a multifunctional nanoassembly IRNB based on IR-780 and BNN6 for synergistic photothermal therapy (PTT), photodynamic therapy (PDT) and nitric oxide (NO) effect triggered by an 808 nm laser. This nanoassembly could accumulate specifically at the infected sites of MDR gram-negative bacteria and their biofilms via the covalent coupling effect. Upon irradiation with an 808 nm laser, IRNB was activated and produced both reactive oxygen species (ROS) and hyperthermia. The local hyperthermia could induce NO generation, which further reacted with ROS to generate ONOO−, leading to the enhancement of bactericidal efficacy. Furthermore, NO and ONOO− could disrupt the cell membrane, which converts bacteria to an extremely susceptible state and further enhances the photothermal effect. In this study, IRNB showed a superior photothermal-photodynamic-chemo (NO) synergistic therapeutic effect on the infected wounds and subcutaneous abscesses caused by gram-negative bacteria. This resulted in effective control of associated infections, relief of inflammation, promotion of re-epithelization and collagen deposition, and regulation of angiogenesis during wound healing. Moreover, IRNB exhibited excellent biocompatibility, both in vitro and in vivo. Conclusions The present research suggests that IRNB can be considered a promising alternative for treating infections caused by MDR gram-negative bacteria and their biofilms.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Critical Care and Intensive Care Medicine,Dermatology,Biomedical Engineering,Emergency Medicine,Immunology and Allergy,Surgery

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