References
- Chua AW, Khoo YC, Tan BK, Tan KC, Foo CL, Chong SJ. Skin tissue engineering advances in severe burns: review and therapeutic applications. Burns Trauma. 2016;4:3. doi:10.1186/s41038-016-0027-y
- Xi Y, Ge J, Wang M, et al. Bioactive anti-inflammatory, antibacterial, antioxidative silicon-based nanofibrous dressing enables cutaneous tumor photothermo-chemo therapy and infection-induced wound healing. ACS Nano. 2020;14(3):2904–2916. doi:10.1021/acsnano.9b07173
- Xi Y, Ge J, Guo Y, Lei B, Ma PX. Biomimetic elastomeric polypeptide-based nanofibrous matrix for overcoming multidrug-resistant bacteria and enhancing full-thickness wound healing/skin regeneration. ACS Nano. 2018;12(11):10772–10784. doi:10.1021/acsnano.8b01152
- Chaudhari AA, Vig K, Baganizi DR, et al. Future prospects for scaffolding methods and biomaterials in skin tissue engineering: a review. Int J Mol Sci. 2016;17(12):1974. doi:10.3390/ijms17121974
- Cardona AF, Wilson SE. Skin and soft-tissue infections: a critical review and the role of telavancin in their treatment. Clin Infect Dis. 2015;61(Suppl 2):S69–S78. doi:10.1093/cid/civ528
- Herbst S, Lorkowski M, Sarenko O, Nguyen TKL, Jaenicke T, Hengge R. Transmembrane redox control and proteolysis of PdeC, a novel type of c-di-GMP phosphodiesterase. EMBO J. 2018;37(8). doi:10.15252/embj.201797825
- Huh AJ, Kwon YJ. “Nanoantibiotics”: a new paradigm for treating infectious diseases using nanomaterials in the antibiotics resistant era. J Control Release. 2011;156(2):128–145. doi:10.1016/j.jconrel.2011.07.002
- Hu Y, Ruan X, Lv X, et al. Biofilm microenvironment-responsive nanoparticles for the treatment of bacterial infection. Nano Today. 2022;46. doi:10.1016/j.nantod.2022.101602
- Si Y, Zhang Z, Wu W, et al. Daylight-driven rechargeable antibacterial and antiviral nanofibrous membranes for bioprotective applications. Sci Adv. 2018;4(3):eaar5931. doi:10.1126/sciadv.aar5931
- Huo J, Jia Q, Huang H, et al. Emerging photothermal-derived multimodal synergistic therapy in combating bacterial infections. Chem Soc Rev. 2021;50(15):8762–8789. doi:10.1039/d1cs00074h
- Taubes G. The bacteria fight back. Science. 2008;321(5887):356–361. doi:10.1126/science.321.5887.356
- Zhang Y, Wang D, Liu F, et al. Enhancing the drug sensitivity of antibiotics on drug-resistant bacteria via the photothermal effect of FeTGNPs. J Control Release. 2022;341:51–59. doi:10.1016/j.jconrel.2021.11.018
- Tang J, Wang S, Tai Y, et al. Evaluation of factors influencing annual occurrence, bioaccumulation, and biomagnification of antibiotics in planktonic food webs of a large subtropical river in South China. Water Res. 2020;170:115302. doi:10.1016/j.watres.2019.115302
- Marchant J. When antibiotics turn toxic. Nature. 2018;555(7697):431–433. doi:10.1038/d41586-018-03267-5
- Ye Y, Wu T, Jiang X, et al. Portable smartphone-based qds for the visual onsite monitoring of fluoroquinolone antibiotics in actual food and environmental samples. ACS Appl Mater Interfaces. 2020;12(12):14552–14562. doi:10.1021/acsami.9b23167
- Singh R, Smitha MS, Singh SP. The role of nanotechnology in combating multi-drug resistant bacteria. J Nanosci Nanotechnol. 2014;14(7):4745–4756. doi:10.1166/jnn.2014.9527
- Hu Y, Li S, Dong H, et al. Environment-responsive therapeutic platforms for the treatment of implant infection. Adv Healthc Mater. 2023:e2300985. doi:10.1002/adhm.202300985
- Cao J, Min L, Lansing B, Foxman B, Mody L. Multidrug-resistant organisms on patients’ hands: a missed opportunity. JAMA Intern Med. 2016;176(5):705–706. doi:10.1001/jamainternmed.2016.0142
- Yang Y, Qin Z, Zeng W, et al. Toxicity assessment of nanoparticles in various systems and organs. Nanotechnol Rev. 2017;6(3):279–289. doi:10.1515/ntrev-2016-0047
- Kandi V, Kandi S. Antimicrobial properties of nanomolecules: potential candidates as antibiotics in the era of multi-drug resistance. Epidemiol Health. 2015;37:e2015020. doi:10.4178/epih/e2015020
- Wang L, Hu C, Shao L. The antimicrobial activity of nanoparticles: present situation and prospects for the future. Int J Nanomedicine. 2017;12:1227–1249. doi:10.2147/IJN.S121956
- Gao Y, Xiao Y, Mao K, et al. Thermoresponsive polymer-encapsulated hollow mesoporous silica nanoparticles and their application in insecticide delivery. Chem Eng J. 2020;383. doi:10.1016/j.cej.2019.123169
- Hossen S, Hossain MK, Basher MK, Mia MNH, Rahman MT, Uddin MJ. Smart nanocarrier-based drug delivery systems for cancer therapy and toxicity studies: a review. J Adv Res. 2019;15:1–18. doi:10.1016/j.jare.2018.06.005
- Liang Y, Fan C, Dong H, et al. Preparation of MSNs-Chitosan@Prochloraz nanoparticles for reducing toxicity and improving release properties of prochloraz. ACS Sustain Chem Eng. 2018;6(8):10211–10220. doi:10.1021/acssuschemeng.8b01511
- Wang C, Li L, Zhang S, et al. Carrier-free platinum nanomedicine for targeted cancer therapy. Small. 2020;16(49):e2004829. doi:10.1002/smll.202004829
- Tian Y, Tang G, Gao Y, et al. Carrier-free small molecular self-assembly based on berberine and curcumin incorporated in submicron particles for improving antimicrobial activity. ACS Appl Mater Interfaces. 2022;14(8):10055–10067. doi:10.1021/acsami.1c22900
- Huang X, Wang P, Li T, et al. Self-assemblies based on traditional medicine berberine and cinnamic acid for adhesion-induced inhibition multidrug-resistant Staphylococcus aureus. ACS Appl Mater Interfaces. 2020;12(1):227–237. doi:10.1021/acsami.9b17722
- Li Z, Xu X, Wang Y, Kong L, Han C. Carrier-free nanoplatforms from natural plants for enhanced bioactivity. J Adv Res. 2022. doi:10.1016/j.jare.2022.09.013
- Tian X, Wang P, Li T, et al. Self-assembled natural phytochemicals for synergistically antibacterial application from the enlightenment of traditional Chinese medicine combination. Acta Pharm Sin B. 2020;10(9):1784–1795. doi:10.1016/j.apsb.2019.12.014
- Li T, Wang P, Guo W, et al. Natural berberine-based Chinese herb medicine assembled nanostructures with modified antibacterial application. ACS Nano. 2019;13(6):6770–6781. doi:10.1021/acsnano.9b01346
- Wang P, Guo W, Huang G, et al. Berberine-based heterogeneous linear supramolecules neutralized the acute nephrotoxicity of aristolochic acid by the self-assembly strategy. ACS Appl Mater Interfaces. 2021;13(28):32729–32742. doi:10.1021/acsami.1c06968
- Cai D, Yang Y, Lu J, et al. Injectable carrier-free hydrogel dressing with anti-multidrug-resistant staphylococcus aureus and anti-inflammatory capabilities for accelerated wound healing. ACS Appl Mater Interfaces. 2022;14(38):43035–43049. doi:10.1021/acsami.2c15463
- Lin X, Huang X, Tian X, et al. Natural small-molecule-based carrier-free self-assembly library originated from Traditional Chinese Herbal Medicine. ACS Omega. 2022;7(48):43510–43521. doi:10.1021/acsomega.2c04098
- Feng R, Shou JW, Zhao ZX, et al. Transforming berberine into its intestine-absorbable form by the gut microbiota. Sci Rep. 2015;5:12155. doi:10.1038/srep12155
- Bhatia E, Sharma S, Jadhav K, Banerjee R. Combinatorial liposomes of berberine and curcumin inhibit biofilm formation and intracellular methicillin resistant Staphylococcus aureus infections and associated inflammation. J Mater Chem B. 2021;9(3):864–875. doi:10.1039/d0tb02036b
- Sun T, Li XD, Hong J, et al. Inhibitory effect of two traditional Chinese medicine monomers, berberine and matrine, on the quorum sensing system of antimicrobial-resistant Escherichia coli. Front Microbiol. 2019;10:2584. doi:10.3389/fmicb.2019.02584
- Xie -Y-Y, Zhang Y-W, Liu X-Z, et al. Aggregation-induced emission-active amino acid/berberine hydrogels with enhanced photodynamic antibacterial and anti-biofilm activity. Chem Eng J. 2021;413. doi:10.1016/j.cej.2020.127542
- Huang H, Gong W, Wang X, He W, Hou Y, Hu J. Self-assembly of naturally small molecules into supramolecular fibrillar networks for wound healing. Adv Healthc Mater. 2022;11(12):e2102476. doi:10.1002/adhm.202102476
- Park SG, Li MX, Cho WK, Joung YK, Huh KM. Thermosensitive gallic acid-conjugated hexanoyl glycol chitosan as a novel wound healing biomaterial. Carbohydr Polym. 2021;260:117808. doi:10.1016/j.carbpol.2021.117808
- Kang Y, Xu C, Meng L, Dong X, Qi M, Jiang D. Exosome-functionalized magnesium-organic framework-based scaffolds with osteogenic, angiogenic and anti-inflammatory properties for accelerated bone regeneration. Bioact Mater. 2022;18:26–41. doi:10.1016/j.bioactmat.2022.02.012
- De Fazio AF, Misatziou D, Baker YR, Muskens OL, Brown T, Kanaras AG. Chemically modified nucleic acids and DNA intercalators as tools for nanoparticle assembly. Chem Soc Rev. 2021;50(23):13410–13440. doi:10.1039/d1cs00632k
- Zheng X, Zhao Y, Jia Y, et al. Biomimetic co-assembled nanodrug of doxorubicin and berberine suppresses chemotherapy-exacerbated breast cancer metastasis. Biomaterials. 2021;271:120716. doi:10.1016/j.biomaterials.2021.120716
- Labastie MC, Poole TJ, Peault BM, Le Douarin NM. MB1, a quail leukocyte-endothelium antigen: partial characterization of the cell surface and secreted forms in cultured endothelial cells. Proc Natl Acad Sci U S A. 1986;83(23):9016–9020. doi:10.1073/pnas.83.23.9016
- Xie M, Wang L, Guo B, Wang Z, Chen YE, Ma PX. Ductile electroactive biodegradable hyperbranched polylactide copolymers enhancing myoblast differentiation. Biomaterials. 2015;71:158–167. doi:10.1016/j.biomaterials.2015.08.042
- Leavitt S, Freire E. Direct measurement of protein binding energetics by isothermal titration calorimetry. Curr Opin Struct Biol. 2001;11(5):560–566. doi:10.1016/s0959-440x(00)00248-7
- Zhang JP, Liao PQ, Zhou HL, Lin RB, Chen XM. Single-crystal X-ray diffraction studies on structural transformations of porous coordination polymers. Chem Soc Rev. 2014;43(16):5789–5814. doi:10.1039/c4cs00129j
- Bethke JH, Davidovich A, Cheng L, et al. Environmental and genetic determinants of plasmid mobility in pathogenic Escherichia coli. Sci Adv. 2020;6(4):eaax3173. doi:10.1126/sciadv.aax3173
- Stepanova E, Wang M, Severinov K, Borukhov S. Early transcriptional arrest at Escherichia coli rplN and ompX promoters. J Biol Chem. 2009;284(51):35702–35713. doi:10.1074/jbc.M109.053983
- Babina AM, Soo MW, Fu Y, Meyer MM. An S6:S18 complex inhibits translation of E. coli rpsF. RNA. 2015;21(12):2039–2046. doi:10.1261/rna.049544.115
- Wang J, Wang J, Wang Y, et al. iTRAQ(R)-based quantitative proteomics reveals the proteomic profiling of methicillin-resistant Staphylococcus aureus-derived extracellular vesicles after exposure to imipenem. Folia Microbiol. 2021;66(2):221–230. doi:10.1007/s12223-020-00836-y
- Nishi K, Muller M, Schnier J. Spontaneous missense mutations in the rplX gene for ribosomal protein L24 from Escherichia coli. J Bacteriol. 1987;169(10):4854–4856. doi:10.1128/jb.169.10.4854-4856.1987
- Fivenson DP, Faria DT, Nickoloff BJ, et al. Chemokine and inflammatory cytokine changes during chronic wound healing. Wound Repair Regen. 1997;5(4):310–322. doi:10.1046/j.1524-475X.1997.50405.x
- Song M, Chen L, Zhang L, et al. Cryptotanshinone enhances wound healing in type 2 diabetes with modulatory effects on inflammation, angiogenesis and extracellular matrix remodelling. Pharm Biol. 2020;58(1):845–853. doi:10.1080/13880209.2020.1803369
- Tombulturk FK, Todurga-Seven ZG, Huseyinbas O, Ozyazgan S, Ulutin T, Kanigur-Sultuybek G. Topical application of metformin accelerates cutaneous wound healing in streptozotocin-induced diabetic rats. Mol Biol Rep. 2022;49(1):73–83. doi:10.1007/s11033-021-06843-7
- Hose D, Moreaux J, Meissner T, et al. Induction of angiogenesis by normal and malignant plasma cells. Blood. 2009;114(1):128–143. doi:10.1182/blood-2008-10-184226
- Liu X, Jing X, Cheng X, et al. FGFR3 promotes angiogenesis-dependent metastasis of hepatocellular carcinoma via facilitating MCP-1-mediated vascular formation. Med Oncol. 2016;33(5):46. doi:10.1007/s12032-016-0761-9
- Jia T, Jacquet T, Dalonneau F, et al. FGF-2 promotes angiogenesis through a SRSF1/SRSF3/SRPK1-dependent axis that controls VEGFR1 splicing in endothelial cells. BMC Biol. 2021;19(1):173. doi:10.1186/s12915-021-01103-3
- Holzer-Geissler JCJ, Schwingenschuh S, Zacharias M, et al. The impact of prolonged inflammation on wound healing. Biomedicines. 2022;10(4):856. doi:10.3390/biomedicines10040856