Controlled-temperature photothermal and oxidative bacteria killing and acceleration of wound healing by polydopamine-assisted Au-hydroxyapatite nanorods.

Since skin wounds are subject to bacterial infection and tissue regeneration may be impeded, there is demand for biomaterials that possess rapid bactericidal and tissue repair capability. Herein we report in situ promotion of wound healing by a photothermal therapy (PTT) assisted nanocatalytic antibacterial system utilizing a polydopamine (PDA) coating on hydroxyapatite (HAp) incorporated with gold nanoparticles (Au-HAp). The PDA@Au-HAp NPs produce hydroxyl radicals (OH) via catalysis of a small concentration of H2O2 to render bacteria more vulnerable to the temperature change. The antibacterial efficacy against Escherichia coli and Staphylococcus aureus is 96.8% and 95.2%, respectively, at a controlled photo-induced temperature of 45 °C that causes no damage to normal tissues. By combining catalysis with near-infrared (NIR) photothermal therapy, the PDA@Au-HAp NPs provide safe, rapid, and effective antibacterial activity compared to OH or PTT alone. In addition, this system stimulates the tissue repairing-related gene expression to facilitate the formation of granulation tissues and collagen synthesis and thus accelerate wound healing. After the 10-day treatment of skin wounds in vivo, PDA@Au-HAp group exhibits quicker recovery than the control group and both sterilization and healing are completed after the 10-day treatment. This study presents in situ promotion of wound healing by a low-temperature photothermal therapy (PTT) assisted nanocatalytic antibacterial system utilizing a polydopamine (PDA) coating on hydroxyapatite (HAp) incorporated with gold nanoparticles (Au-HAp). The PDA@Au-HAp NPs produce hydroxyl radicals (OH) via catalysis of a small concentration of H2O2 to render bacteria more vulnerable to temperature change. After irradiation by 808 nm laser, the antibacterial efficacy against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) is 96.8% and 95.2%, respectively, at a low photo-induced temperature of 45 °C which causes no damage to normal tissues. In addition, this system stimulates the tissue repairing-related gene expression to facilitate the formation of granulation tissues and collagen synthesis and accelerate wound healing.

Xu X ，Liu X ，Tan L ，Cui Z ，Yang X ，Zhu S ，Li Z ，Yuan X ，Zheng Y ，Yeung KWK ，Chu PK ，Wu S ... -  《-》

Redox-Channeling Polydopamine-Ferrocene (PDA-Fc) Coating To Confer Context-Dependent and Photothermal Antimicrobial Activities.

Song J ，Liu H ，Lei M ，Tan H ，Chen Z ，Antoshin A ，Payne GF ，Qu X ，Liu C ... -  《-》

Magainin-modified polydopamine nanoparticles for photothermal killing of bacteria at low temperature.

Photothermal therapy (PTT) is a promising method to kill bacteria because of the broad-spectrum of antibacterial activity and the ability of spatiotemporal regulation. In the previously reported systems, light induced high temperature (˜70 °C) was essential for effectively killing of bacteria, which, however, would also damage nearby nontarget cells or tissues. Here we report photothermal nanoparticles (NPs) for more targeting and killing bacteria at a relative low temperature. Polydopamine (PDA) was chosen to prepare NPs because of its excellent capability of photothermal conversion. Magainin I (MagI) which is an antimicrobial peptide was used to modify NPs' surface because it can specifically interact with bacteria. We demonstrate that MagI-PEG@PDA NPs effectively killed E. coli at a low temperature of ˜45 °C upon near-infrared (NIR) light irradiation. In contrast, the native PDA NPs under light irradiation or the MagI-PEG@PDA NPs themselves showed no bacteria killing ability. This work highlights the importance of close interaction between the target bacteria and the photothermal materials and may promote the practical clinical applications of the PTT.

Fan XL ，Li HY ，Ye WY ，Zhao MQ ，Huang DN ，Fang Y ，Zhou BQ ，Ren KF ，Ji J ，Fu GS ... -  《-》

In situ assembly of well-dispersed Ag nanoparticles on the surface of polylactic acid-Au@polydopamine nanofibers for antimicrobial applications.

Nanofibrous membranes which exhibit bacteriostatic functions are a good strategy to prevent microorganisms from adhering to the surface of biomaterials. Here, we report the synthesis of such a nanofibrous membrane which can be applied to biological coatings to reduce bacteriostatic functionality. Ascorbic acid was utilized to reduced chloroauric acid to gold nanoparticles (AuNPs). Dopamine was then polymerized upon AuNP surfaces by ultrasound-assistance, to synthesize core-shell structured polydopamine-coated AuNPs (Au@PDA NPs). The Au@PDA NPs were then mixed with polylactic acid (PLA) for electrospinning into cylindrical nanofibers (136.6 nm diameter). PLA-Au@PDA nanofibrous membranes were finally immersed in silver nitrate for in situ reduction into a silver nanoparticle (AgNP) coating to yield PLA-Au@PDA@Ag nanofibers. The PLA-Au@PDA@Ag nanofibers were characterized based on field emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and contact angle analyses. The antibacterial properties of the PLA-Au@PDA@Ag nanofibers were examined based on the optical density absorbance of bacterial cell suspensions, traditional colony plate counts, zone inhibition analyses, and field-emission scanning electron microscopy. Escherichia coli and Staphylococcus aureaus respectively served as Gram negative and positive bacterial models of industrial relevance. The data conclusively illustrates the antimicrobial and biomedical applications of PLA-Au@PDA@Ag nanofibers.

Zhang Q ，Wang Y ，Zhang W ，Hickey ME ，Lin Z ，Tu Q ，Wang J ... -  《-》

Near-infrared light-responsive photothermal α-Fe(2)O(3)@Au/PDA core/shell nanostructure with on-off controllable anti-bacterial effects.

Xiong Q ，Fang Q ，Xu K ，Liu G ，Sang M ，Xu Y ，Hao L ，Xuan S ... -  《-》