Tailoring gas-releasing nanoplatforms for wound treatment: An emerging approach

被引:29
作者
Wang, Zixin [1 ]
Rong, Fan [1 ]
Li, Zhao [1 ]
Li, Wei [1 ]
Kaur, Kuljeet [2 ,3 ]
Wang, Yin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Engn Res Ctr Cell & Therapeut Antibody, Sch Pharm, Shanghai 200240, Peoples R China
[2] Ecole Polytech Fed Lausanne EPFL, Inst Mat, Batiment MXD,Stn 12, CH-1015 Lausanne, Switzerland
[3] Inst Sci & Ingn Chim, Lab Polymeres, Batiment MXD,Stn 12, CH-1015 Lausanne, Switzerland
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Drug delivery; Gas signaling molecules; Gas therapy; Nanoplatform; Wound repair; CYSTATHIONINE-BETA-SYNTHASE; HYDROGEN-SULFIDE; NITRIC-OXIDE; CARBON-MONOXIDE; PHOTOTHERMAL THERAPY; PRUSSIAN BLUE; CHEMISTRY; GRAPHENE; DELIVERY; H2S;
D O I
10.1016/j.cej.2022.139297
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Wound treatment especially of coping with chronic wounds is a global health issue that challenges medical care and financial strength of every nation. In recent years, gas therapy emerges as a facile yet promising modality for wound healing given that gas signaling molecules (GSMs) participate in various physiological processes such as angiogenesis. In this review, we survey the recent advancements in the tailoring design and fabrication of GSM -releasing nanoplatforms for wound repair according to the specific wound microenvironment. We carefully analyze the different synthetic strategies for the preparation of nanoplatforms in terms of the different gas sources or donor types. Both single gas therapy (GT) and GT-based combined therapies are examined in this review thoroughly. Besides, given the synergetic effects of different GSMs in vivo, nanoplatforms capable of unleashing multiple gas molecules from a single vector are also included in this review. At the end, future outlooks and upcoming challenges of this promising treatment for wound closure are discussed.
引用
收藏
页数:16
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共 150 条
[1]  
Abe K, 1996, J NEUROSCI, V16, P1066
[2]   A Dual-Function Antibiotic-Transporter Conjugate Exhibits Superior Activity in Sterilizing MRSA Biofilms and Killing Persister Cells [J].
Antonoplis, Alexandra ;
Zang, Xiaoyu ;
Huttner, Melanie A. ;
Chong, Kelvin K. L. ;
Lee, Yu B. ;
Co, Julia Y. ;
Amieva, Manuel R. ;
Kline, Kimberly A. ;
Wender, Paul A. ;
Cegelski, Lynette .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (47) :16140-16151
[3]   Functional Composite Materials Based on Chemically Converted Graphene [J].
Bai, Hua ;
Li, Chun ;
Shi, Gaoquan .
ADVANCED MATERIALS, 2011, 23 (09) :1089-1115
[4]   Nitric-Oxide-Releasing aza-BODIPY: A New Near-Infrared J-Aggregate with Multiple Antibacterial Modalities [J].
Bao, Xinyao ;
Zheng, Shaoqiu ;
Zhang, Lei ;
Shen, Aizong ;
Zhang, Guoying ;
Liu, Shiyong ;
Hu, Jinming .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2022, 61 (32)
[5]   Nanomaterials in wound healing: From material sciences to wound healing applications [J].
Barroso, Andreia ;
Mestre, Henrique ;
Ascenso, Andreia ;
Simoes, Sandra ;
Reis, Catarina .
NANO SELECT, 2020, 1 (05) :443-460
[6]   A Novel Cryo-Reduction Method to Investigate the Molecular Mechanism of Nitric Oxide Synthases [J].
Bernad, Sophie ;
Brunel, Albane ;
Dorlet, Pierre ;
Sicard-Roselli, Cecile ;
Santolini, Jerome .
JOURNAL OF PHYSICAL CHEMISTRY B, 2012, 116 (19) :5595-5603
[7]  
BODEY GP, 1983, REV INFECT DIS, V5, P279
[8]   Neuropathic diabetic foot ulcers [J].
Boulton, AJM ;
Kirsner, RS ;
Vileikyte, L .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (01) :48-55
[9]   Carbon monoxide generated by heme oxygenase 1 suppresses endothelial cell apoptosis [J].
Brouard, S ;
Otterbein, LE ;
Anrather, J ;
Tobiasch, E ;
Bach, FH ;
Choi, AMK ;
Soares, MP .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (07) :1015-1025
[10]   Nitric oxide:: NO apoptosis or turning it ON? [J].
Brüne, B .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (08) :864-869