Research progress of responsive electrospun dressings for precise monitoring and treatment of diabetic wounds

Chengkai Zhou , Yan Geng , Chenxi Zhang , Yuwei Hsu , Le Ma , Mengen Li , Ye Tang , Wei Guo , Ming Li , Yanhua Wang

Burns & Trauma ›› 2026, Vol. 14 ›› Issue (1) : tkaf049

PDF (5243KB)
Burns & Trauma ›› 2026, Vol. 14 ›› Issue (1) :tkaf049 DOI: 10.1093/burnst/tkaf049
Review
research-article
Research progress of responsive electrospun dressings for precise monitoring and treatment of diabetic wounds
Author information +
History +
PDF (5243KB)

Abstract

Chronic diabetic wounds pose a serious health and economic burden globally. In recent years, there has been widespread attention on the research of functional and even personalized wound dressings, among which responsive smart nanofiber dressings made using electrospinning technology have shown great potential. Nanofibers have advantages such as extremely fine pore size, high porosity, and large specific surface area. By combining electrospinning technology with responsive materials and integrating electronic engineering and other manufacturing techniques, it is possible to weave smart nanofibers that can respond to specific diabetic wound environments (such as low pH, high reactive oxygen species, high glucose concentration, and overexpressed enzymes) or external conditions (such as temperature, light, and magnetic fields). This allows for the monitoring of the wound microenvironment and/or the automatic release of drugs based on changes in the wound microenvironment. Compared with ordinary dressings, this dressing can not only predict the wound state, but also respond to the specific wound (such as diabetic wound) microenvironment to promote wound healing rapidly and accurately. This article outlines the characteristics of the chronic diabetic wound microenvironment, electrospinning technology, and its application in responding to the chronic diabetic wound microenvironment.

Keywords

Chronic diabetic wounds / Microenvironment / Electrospinning technology / Responsive dressing / Monitoring

Cite this article

Download citation ▾
Chengkai Zhou, Yan Geng, Chenxi Zhang, Yuwei Hsu, Le Ma, Mengen Li, Ye Tang, Wei Guo, Ming Li, Yanhua Wang. Research progress of responsive electrospun dressings for precise monitoring and treatment of diabetic wounds. Burns & Trauma, 2026, 14 (1) : tkaf049 DOI:10.1093/burnst/tkaf049

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Baltzis D, Eleftheriadou I, Veves A. Pathogenesis and treatment of impaired wound healing in diabetes mellitus: new insights. Adv Ther 2014; 31:817-36. https://doi.org/10.1007/s12325-014-0140-x.

[2]

Uccioli L, Izzo V, Meloni M, Vainieri E, Ruotolo V, Giurato L. Non-healing foot ulcers in diabetic patients: general and local interfering conditions and management options with advanced wound dressings. J Wound Care 2015; 24:35-42. https://doi.org/10.12968/jowc.2015.24.Sup4b.35.

[3]

McCarty SM, Cochrane CA, Clegg PD, Percival SL. The role of endogenous and exogenous enzymes in chronic wounds: a focus on the implications of aberrant levels of both host and bacterial proteases in wound healing. Wound Repair Regen 2012; 20:125-36. https://doi.org/10.1111/j.1524-475X.2012.00763.x.

[4]

Noor S, Khan RU, Ahmad J. Understanding diabetic foot infection and its management. Diabetes Metab Syndr 2017; 11:149-56. https://doi.org/10.1016/j.dsx.2016.06.023.

[5]

Jiang P, Li Q, Luo Y, Luo F, Che Q, Lu Z, et al. Current status and progress in research on dressing management for diabetic foot ulcer. Front Endocrinol (Lausanne) 2023; 14:1221705. https://doi.org/10.3389/fendo.2023.1221705.

[6]

Behroozi AH, Al-Shaeli M, Vatanpour V. Fabrication and modification of nanofiltration membranes by solution electrospinning technique: a review of influential factors and applications in water treatment. Desalination 2023; 558:116638. https://doi.org/10.1016/j.desal.2023.116638.

[7]

Yang T, Ma J, Zhen SJ, Huang CZ. Electrostatic assemblies of well-dispersed AgNPs on the surface of electrospun nanofibers as highly active SERS substrates for wide-range pH sensing. ACS Appl Mater Interfaces 2016; 8:14802-11. https://doi.org/10.1021/acsami.6b03720.

[8]

Teepoo S, Dawan P, Barnthip N. Electrospun chitosan-Gelatin biopolymer composite nanofibers for horseradish peroxidase immobilization in a hydrogen peroxide biosensor. Biosensors 2017; 7:47. https://www.mdpi.com/2079-6374/7/4/47.

[9]

Khalid A, Bai D, Abraham AN, Jadhav A, Linklater D, Matusica A, et al. Electrospun Nanodiamond-silk fibroin membranes: a multifunctional platform for biosensing and wound-healing applications. ACS Appl Mater Interfaces 2020; 12:48408-19. https://doi.org/10.1021/acsami.0c15612.

[10]

Ding S, Lou Y, Niu Z, et al. A biomimetic asymmetric structured intelligent wound dressing with dual-modality humidity-pressure sensing for non-invasive and real-time wound healing monitoring. Macromol Mater Eng 2022; 307:2200233. https://doi.org/10.1002/mame.202200233.

[11]

Li H, Sang Q, Wu J, Williams GR, Wang H, Niu S, et al. Dual-responsive drug delivery systems prepared by blend electrospinning. Int J Pharm 2018; 543:1-7. https://doi.org/10.1016/j.ijpharm.2018.03.009.

[12]

Zárate IA, Aguilar-Bolados H, Yazdani-Pedram M, Pizarro GDC, Neira-Carrillo A. In vitro hyperthermia evaluation of electrospun polymer composite Fibers loaded with reduced graphene oxide. Polymers (Basel) 2020; 12:2663. https://doi.org/10.3390/polym12112663.

[13]

Yun J, Im JS, Lee Y-S, Kim H-I. Electro-responsive transdermal drug delivery behavior of PVA/PAA/MWCNT nanofibers. Eur Polym J 2011; 47:1893-902. https://doi.org/10.1016/j.eurpolymj.2011.07.024.

[14]

Senneville É, Albalawi Z, van Asten SA, Abbas ZG, Allison G, Aragón-Sánchez J, et al. IWGDF/IDSA Guidelines on the Diagnosis and Treatment of Diabetes-related Foot Infections (IWGDF/IDSA 2023). Clinical Infectious Diseases, 2023;ciad527. https://doi.org/10.1093/cid/ciad527.

[15]

Armstrong DG, Boulton AJM, Bus SA. Diabetic foot ulcers and their recurrence. N Engl J Med 2017; 376:2367-75. https://doi.org/10.1056/NEJMra1615439.

[16]

Shah SA, Sohail M, Khan S, Minhas MU, de Matas M, Sikstone V, et al. Biopolymer-based biomaterials for accelerated diabetic wound healing: a critical review. Int J Biol Macromol 2019; 139:975-93. https://doi.org/10.1016/j.ijbiomac.2019.08.007.

[17]

Raziyeva K, Kim Y, Zharkinbekov Z, Kassymbek K, Jimi S, Saparov A. Immunology of acute and chronic wound healing. Biomolecules 2021; 11:700. https://doi.org/10.3390/biom11050700.

[18]

Strodtbeck F. Physiology of wound healing. Newborn Infant Nurs Rev 2001; 1:43-52. https://doi.org/10.1053/nbin.2001.23176.

[19]

Ellis S, Lin EJ, Tartar D. Immunology of wound healing. Curr Dermatol Rep 2018; 7:350-8. https://doi.org/10.1007/s13671-018-0234-9.

[20]

Rodrigues M, Kosaric N, Bonham CA, Gurtner GC. Wound healing: a cellular perspective. Physiol Rev 2019; 99:665-706. https://doi.org/10.1152/physrev.00067.2017.

[21]

Landén NX, Li D, Ståhle M. Transition from inflammation to proliferation: a critical step during wound healing. Cell Mol Life Sci 2016; 73:3861-85. https://doi.org/10.1007/s00018-016-2268-0.

[22]

Lansdown AB. Calcium: a potential central regulator in wound healing in the skin. Wound Repair Regen 2002; 10:271-85. https://doi.org/10.1046/j.1524-475x.2002.10502.xPMID:12406163.

[23]

van der Vliet A, Janssen-Heininger YM. Hydrogen peroxide as a damage signal in tissue injury and inflammation: murderer, mediator, or messenger? J Cell Biochem 2014; 115:427-35. https://doi.org/10.1002/jcb.2468.

[24]

Su Y, Richmond A. Chemokine regulation of neutrophil infiltration of skin wounds. Adv Wound Care (New Rochelle) 2015; 4:631-40. https://doi.org/10.1089/wound.2014.0559.

[25]

Banerjee K, Madhyastha R, Nakajima Y, Maruyama M, Madhyastha H. Nanoceutical adjuvants as wound healing material: precepts and prospects. Int J Mol Sci 2021; 22:4748. https://doi.org/10.3390/ijms22094748.

[26]

Sharifi S, Hajipour MJ, Gould L, Mahmoudi M. Nanomedicine in healing chronic wounds: opportunities and challenges. Mol Pharm 2021; 18:550-75. https://doi.org/10.1021/acs.molpharmaceut.0c00346.

[27]

Shen T, Dai K, Yu Y, Wang J, Liu C. Sulfated chitosan rescues dysfunctional macrophages and accelerates wound healing in diabetic mice. Acta Biomater 2020; 117:192-203. https://doi.org/10.1016/j.actbio.2020.09.035.

[28]

Pastar I, Stojadinovic O, Yin NC, Ramirez H, Nusbaum AG, Sawaya A, et al. Epithelialization in wound healing: a comprehensive review. Adv Wound Care (New Rochelle) 2014; 3:445-64. https://doi.org/10.1089/wound.2013.0473.

[29]

Kotwal GJ, Chien S. Macrophage differentiation in normal and accelerated wound healing. Results Probl Cell Differ 2017; 62:353-64. https://doi.org/10.1007/978-3-319-54090-0_14.

[30]

Nethi SK, Das S, Patra CR, Mukherjee S. Recent advances in inorganic nanomaterials for wound-healing applications. Biomater Sci 2019; 7:2652-74. https://doi.org/10.1039/C9BM00423H.

[31]

Xue M, Jackson CJ. Extracellular matrix reorganization during wound healing and its impact on abnormal scarring. Adv Wound Care (New Rochelle) 2015; 4:119-36. https://doi.org/10.1089/wound.2013.0485.

[32]

Martin P, Nunan R. Cellular and molecular mechanisms of repair in acute and chronic wound healing. Br J Dermatol 2015; 173:370-8. https://doi.org/10.1111/bjd.13954.

[33]

Lu Y, Li H, Wang J, Yao M, Peng Y, Liu T, et al. Engineering bacteria-activated multifunctionalized hydrogel for promoting diabetic wound healing. Adv Funct Mater 2021; 31:2105749. https://doi.org/10.1002/adfm.202105749.

[34]

Shao Z, Yin T, Jiang J, He Y, Xiang T, Zhou S. Wound microenvironment self-adaptive hydrogel with efficient angiogenesis for promoting diabetic wound healing. Bioact Mater 2023; 20:561-73. https://doi.org/10.1016/j.bioactmat.2022.06.018.

[35]

Zhang W, Chen L, Xiong Y, Panayi AC, Abududilibaier A, Hu Y, et al. Antioxidant therapy and antioxidant-related bionanomaterials in diabetic wound healing. Front Bioeng Biotechnol 2021; 9:707479. https://doi.org/10.3389/fbioe.2021.707479.

[36]

Shaikh-Kader A, Houreld NN, Rajendran NK, Abrahamse H . The link between advanced glycation end products and apoptosis in delayed wound healing. Cell Biochem Funct 2019; 37:432-42. https://doi.org/10.1002/cbf.3424.

[37]

Cano Sanchez M, Lancel S, Boulanger E, Neviere R . Targeting oxidative stress and mitochondrial dysfunction in the treatment of impaired wound healing: a systematic review. Antioxidants (Basel) 2018; 7:98. https://doi.org/10.3390/antiox7080098.

[38]

Fui LW, Lok MPW, Govindasamy V, Yong TK, Lek TK, Das AK. Understanding the multifaceted mechanisms of diabetic wound healing and therapeutic application of stem cells conditioned medium in the healing process. J Tissue Eng Regen Med 2019; 13:2218-33. https://doi.org/10.1002/term.2966.

[39]

Krzyszczyk P, Schloss R, Palmer A, Berthiaume F. The role of macrophages in acute and chronic wound healing and interventions to promote pro-wound healing phenotypes. Front Physiol 2018; 9:419. https://doi.org/10.3389/fphys.2018.00419.

[40]

de Oliveira S, Rosowski EE, Huttenlocher A. Neutrophil migration in infection and wound repair: going forward in reverse. Nat Rev Immunol 2016; 16:378-91. https://doi.org/10.1038/nri.2016.49.

[41]

Zhu Y, Zhang J, Song J, Yang J, Du Z, Zhao W, et al. A multifunctional pro-healing zwitterionic hydrogel for simultaneous optical monitoring of pH and glucose in diabetic wound treatment. Adv Funct Mater 2020; 30:1905493. https://doi.org/10.1002/adfm.201905493.

[42]

Li D, Chen T, Zhang Y, Xu Y, Niu H. Synergistical starvation and chemo-dynamic therapy for combating multidrug-resistant bacteria and accelerating diabetic wound healing. Adv Healthc Mater 2021; 10:e2100716. https://doi.org/10.1002/adhm.202100716.

[43]

Schneider LA, Korber A, Grabbe S, Dissemond J. Influence of pH on wound-healing: a new perspective for wound-therapy? Arch Dermatol Res 2007; 298:413-20. https://doi.org/10.1007/s00403-006-0713-x.

[44]

Kruse CR, Nuutila K, Lee CC, Kiwanuka E, Singh M, Caterson EJ, et al. The external microenvironment of healing skin wounds. Wound Repair Regen 2015; 23:456-64. https://doi.org/10.1111/wrr.12303.

[45]

Liang Y, Li M, Yang Y, Qiao L, Xu H, Guo B. pH/glucose dual responsive metformin release hydrogel dressings with adhesion and self-healing via dual-dynamic bonding for athletic diabetic foot wound healing. ACS Nano 2022; 16:3194-207. https://doi.org/10.1021/acsnano.1c11040.

[46]

Dissemond J, Witthoff M, Brauns TC, Haberer D, Goos M. pH values in chronic wounds. Evaluation during modern wound therapy. Hautarzt 2003; 54:959-65.

[47]

Alves PM, Barrias CC, Gomes P, Martins MCL. Smart biomaterial-based systems for intrinsic stimuli-responsive chronic wound management. Mater Today Chem 2021; 22:100623. https://doi.org/10.1016/j.mtchem.2021.100623.

[48]

Yao Y, Zhang H, Wang Z, Ding J, Wang S, Huang B, et al. Reactive oxygen species (ROS)-responsive biomaterials mediate tissue microenvironments and tissue regeneration. J Mater Chem B 2019; 7:5019-37. https://doi.org/10.1039/C9TB00847K.

[49]

Yang L, Liang F, Zhang X, Jiang Y, Duan F, Li L, et al. Remodeling microenvironment based on MOFs-hydrogel hybrid system for improving diabetic wound healing. Chem Eng J 2022; 427:131506. https://doi.org/10.1016/j.cej.2021.131506.

[50]

Dinh T, Tecilazich F, Kafanas A, Doupis J, Gnardellis C, Leal E, et al. Mechanisms involved in the development and healing of diabetic foot ulceration. Diabetes 2012; 61:2937-47. https://doi.org/10.2337/db12-0227.

[51]

Chang M, Nguyen TT. Strategy for treatment of infected diabetic foot ulcers. Acc Chem Res 2021; 54:1080-93. https://doi.org/10.1021/acs.accounts.0c00864.

[52]

Caley MP, Martins VL, O’Toole EA. Metalloproteinases and wound healing. Adv Wound Care (New Rochelle) 2015; 4:225-34. https://doi.org/10.1089/wound.2014.0581.

[53]

Das S, Baker AB. Biomaterials and nanotherapeutics for enhancing skin wound healing. Front Bioeng Biotechnol 2016; 4:82. https://doi.org/10.3389/fbioe.2016.00082.

[54]

Castleberry SA, Almquist BD, Li W, Reis T, Chow J, Mayner S, et al. Self-assembled wound dressings silence MMP-9 and improve diabetic wound healing in vivo. Adv Mater 2016; 28:1809-17. https://doi.org/10.1002/adma.201503565.

[55]

Liu Y, Min D, Bolton T, Nubé V, Twigg SM, Yue DK, et al. Increased matrix metalloproteinase-9 predicts poor wound healing in diabetic foot ulcers. Diabetes Care 2009; 32:117-9. https://doi.org/10.2337/dc08-0763.

[56]

Gao M, Nguyen TT, Suckow MA, Wolter WR, Gooyit M, Mobashery S, et al. Acceleration of diabetic wound healing using a novel protease-anti-protease combination therapy. Proc Natl Acad Sci USA 2015; 112:15226-31. https://doi.org/10.1073/pnas.1517847112.

[57]

Louiselle AE, Niemiec SM, Zgheib C, Liechty KW. Macrophage polarization and diabetic wound healing. Transl Res 2021; 236:109-16. https://doi.org/10.1016/j.trsl.2021.05.006.

[58]

Zhao H, Huang J, Li Y, Lv X, Zhou H, Wang H, et al. ROS-scavenging hydrogel to promote healing of bacteria infected diabetic wounds. Biomaterials 2020; 258:120286. https://doi.org/10.1016/j.biomaterials.2020.120286.

[59]

Pitocco D, Spanu T, Di Leo M, Vitiello R, Rizzi A, Tartaglione L, et al. Diabetic foot infections: a comprehensive overview. Eur Rev Med Pharmacol Sci 2019; 23:26-37. https://doi.org/10.26355/eurrev_201904_17471.

[60]

Zhang Z, Zhang W, Xu Y, Liu D. Efficacy of hyperbaric oxygen therapy for diabetic foot ulcers: an updated systematic review and meta-analysis. Asian J Surg 2022; 45:68-78. https://doi.org/10.1016/j.asjsur.2021.07.047.

[61]

Sharma R, Sharma SK, Mudgal SK, Jelly P, Thakur K. Efficacy of hyperbaric oxygen therapy for diabetic foot ulcer, a systematic review and meta-analysis of controlled clinical trials. Sci Rep 2021; 11:2189. https://doi.org/10.1038/s41598-021-81886-1.

[62]

Liu H, Li ZH, Zhao Y, Feng YB, Zvyagin AV, Wang JC, et al. Novel diabetic foot wound dressing based on multifunctional hydrogels with extensive temperature-tolerant, durable, adhesive, and intrinsic antibacterial properties. ACS Appl Mater Interfaces 2021; 13:26770-81. https://doi.org/10.1021/acsami.1c05514.

[63]

Chastain CA, Klopfenstein N, Serezani CH, Aronoff DM. A clinical review of diabetic foot infections. Clin Podiatr Med Surg 2019; 36:381-95. https://doi.org/10.1016/j.cpm.2019.02.004.

[64]

Martin JM, Zenilman JM, Lazarus GS. Molecular microbiology: new dimensions for cutaneous biology and wound healing. J Invest Dermatol 2010; 130:38-48. https://doi.org/10.1038/jid.2009.221.

[65]

Pouget C, Dunyach-Remy C, Pantel A, Schuldiner S, Sotto A, Lavigne JP. Biofilms in diabetic foot ulcers: significance and clinical relevance. Microorganisms 2020; 8:1580. https://doi.org/10.3390/microorganisms8101580.

[66]

Percival SL, McCarty SM, Lipsky B. Biofilms and wounds: An overview of the evidence. Adv Wound Care 2015; 4:373-81. https://doi.org/10.1089/wound.2014.0557.

[67]

Johnson TR, Gómez BI, McIntyre MK, Dubick MA, Christy RJ, Nicholson SE, et al. The cutaneous microbiome and wounds: new molecular targets to promote wound healing. Int J Mol Sci 2018; 19:2699. https://doi.org/10.3390/ijms19092699.

[68]

Ding J, Gao B, Chen Z, Mei X. An NIR-triggered Au nanocage used for photo-thermo therapy of chronic wound in diabetic rats through bacterial membrane destruction and skin cell mitochondrial protection. Front Pharmacol 2021; 12:779944. https://doi.org/10.3389/fphar.2021.779944.

[69]

Scalise A, Bianchi A, Tartaglione C, Bolletta E, Pierangeli M, Torresetti M, et al. Microenvironment and microbiology of skin wounds: the role of bacterial biofilms and related factors. Semin Vasc Surg 2015; 28:151-9. https://doi.org/10.1053/j.semvascsurg.2016.01.003.

[70]

Armstrong DG, Tan TW, Boulton AJM, Bus SA. Diabetic foot ulcers: a review. JAMA 2023; 330:62-75. https://doi.org/10.1001/jama.2023.10578.

[71]

Tavakoli S, Klar AS. Advanced hydrogels as wound dressings. Biomolecules 2020; 10:1169. https://doi.org/10.3390/biom10081169.

[72]

Pinho E, Soares G. Functionalization of cotton cellulose for improved wound healing. J Mater Chem B 2018; 6:1887-98. https://doi.org/10.1039/C8TB00052B.

[73]

Jones V, Grey JE, Harding KG. Wound dressings. BMJ 2006; 332:777-80. https://doi.org/10.1136/bmj.332.7544.777.

[74]

Vermeulen H, Ubbink D, Goossens A, de Vos R, Legemate D, Westerbos SJ, et al. Dressings and topical agents for surgical wounds healing by secondary intention. Cochrane Database Syst Rev 2004; 2004:CD003554. https://doi.org/10.1002/14651858.CD003554.pub2.

[75]

Richard Schreiber-Gastell, Anton Formhals . Process and apparatus for preparing artificial threads: US50028330A[P].1934-10-02.

[76]

Ji D, Lin Y, Guo X, et al. Electrospinning of nanofibres. Nat Rev Methods Primers 2024; 4:1. https://doi.org/10.1038/s43586-023-00278-z.

[77]

Buchko CJ, Chen LC, Shen Y, Martin DC. Processing and microstructural characterization of porous biocompatible protein polymer thin films. Polymer 1999; 40:7397-407. https://doi.org/10.1016/S0032-3861(98)00866-0.

[78]

Choktaweesap N, Arayanarakul K, Aht-ong D, et al. Electrospun Gelatin Fibers: effect of solvent system on morphology and Fiber diameters. Polym J 2007; 39:622-31. https://doi.org/10.1295/polymj.PJ2006190.

[79]

Yang GZ, Li HP, Yang JH, et al. Influence of working temperature on the formation of electrospun polymer nanofibers. Nanoscale Res Lett 2017; 12:55. https://doi.org/10.1186/s11671-016-1824-8.

[80]

Irantash S, Gholipour-Kanani A, Najmoddin N, et al. A hybrid structure based on silk fibroin/PVA nanofibers and alginate/gum tragacanth hydrogel embedded with cardamom extract. Sci Rep 2024; 14:14010. https://doi.org/10.1038/s41598-024-63061-4.

[81]

Meysam T, Le TT LF, Vinikoor T, Das R, Stevens JF, Mundrane C, et al. Highly piezoelectric, biodegradable, and flexible amino acid nanofibers for medical applications. Sci Adv 2023; 9:eadg6075. https://doi.org/10.1126/sciadv.adg6075.

[82]

Aderibigbe BA. Hybrid-based wound dressings: combination of synthetic and biopolymers. Polymers 2022; 14:3806. https://doi.org/10.3390/polym14183806.

[83]

Pasaribu KM, Mahendra IP, Sholeha NA, Masruchin N, Mardawati E, Karina M. Recent developments of the agroindustry byproducts utilization in bacterial cellulose production and its medical devices applications. In Lubis MAR, et al. (eds). Biomass Conversion and Sustainable Biorefinery. Green Energy and Technology. Springer, 2024. https://doi.org/10.1007/978-981-99-7769-7_10.

[84]

Nosrati H, Heydari M, Tootiaei Z, Ganjbar S, Khodaei M. Delivery of antibacterial agents for wound healing applications using polysaccharide-based scaffolds. J Drug Deliv Sci Technol 2023; 84:104516. https://doi.org/10.1016/j.jddst.2023.104516.

[85]

Ahmadian S, Ghorbani M, Mahmoodzadeh F. Silver sulfadiazine-loaded electrospun ethyl cellulose/polylactic acid/collagen nanofibrous mats with antibacterial properties for wound healing. Int J Biol Macromol 2020; 162:1555-65. https://doi.org/10.1016/j.ijbiomac.2020.08.059.

[86]

Razzaq A, Khan ZU, Saeed A, Shah KA, Khan NU, Menaa B, et al. Development of Cephradine-loaded Gelatin/polyvinyl alcohol electrospun nanofibers for effective diabetic wound healing: In-vitro and In-vivo assessments. Pharmaceutics 2021; 13:349. https://doi.org/10.3390/pharmaceutics13030349.

[87]

Astaneh ME, Fereydouni N. A focused review on hyaluronic acid contained nanofiber formulations for diabetic wound healing. Int J Biol Macromol 253. https://doi.org/10.1016/j.ijbiomac.2023.127607.

[88]

Charernsriwilaiwat N, Rojanarata T, Ngawhirunpat T, Sukma M, Opanasopit P. Electrospun chitosan-based nanofiber mats loaded with Garcinia mangostana extracts. Int J Pharm 2013; 452:333-43. https://doi.org/10.1016/j.ijpharm.2013.05.012.

[89]

Xiao J, Zhan B, He M, Qi X, Gong X, Yang J-L, et al. Interfacial Polarization Loss Improvement Induced by the Hollow Engineering of Necklace-like PAN/Carbon Nanofibers for Boosted Microwave Absorption. Adv Funct Mater 2025; 35:2316722. https://doi.org/10.1002/adfm.202316722.

[90]

Chen Y, Amiri A, Boyd JG, Naraghi M. Promising trade-offs between energy storage and load bearing in carbon nanofibers as structural energy storage devices. Adv Funct Mater 2019; 29:1901425. https://doi.org/10.1002/adfm.201901425.

[91]

Dong W, Wang Z, Zhang Q, et al. Polymer/block copolymer blending system as the compatible precursor system for fabrication of mesoporous carbon nanofibers for supercapacitors. J Power Sources 2019; 419:137-47. https://doi.org/10.1016/j.jpowsour.2019.02.070.

[92]

Townsend-Nicholson A, Jayasinghe SN. Cell electrospinning: a unique biotechnique for encapsulating living organisms for generating active biological microthreads/scaffolds. Biomacromolecules 2006; 7:3364-9. https://doi.org/10.1021/bm060649h.

[93]

Gopinathan J, Noh I. Recent trends in bioinks for 3D printing. Biomater Res 2018; 22:11. https://doi.org/10.1186/s40824-018-0122-1.

[94]

Yeo MG, Kim GH. Fabrication of cell-laden electrospun hybrid scaffolds of alginate-based bioink and PCL microstructures for tissue regeneration. Chem Eng J 2015; 275:27-35. https://doi.org/10.1016/j.cej.2015.04.038.

[95]

Hong J, Yeo M, Yang GH, Kim G. Cell-electrospinning and its application for tissue engineering. Int J Mol Sci 2019; 20:6208. https://doi.org/10.3390/ijms20246208.

[96]

Kong B, Chen Y, Liu R, Liu X, Liu C, Shao Z, et al. Fiber reinforced GelMA hydrogel to induce the regeneration of corneal stroma. Nat Commun 2020; 11:1435. https://doi.org/10.1038/s41467-020-14887-9.

[97]

Gulfam M, Lee JM, Kim JE, Lim DW, Lee EK, Chung BG. Highly porous core-shell polymeric fiber network. Langmuir 2011; 27:10993-9. https://doi.org/10.1021/la201253z.

[98]

Yu T, Gleeson SE, Li CY, Marcolongo M. Electrospun poly(ε-caprolactone) nanofiber shish kebabs mimic mineralized bony surface features. J Biomed Mater Res B 2019; 107:1141-9. https://doi.org/10.1002/jbm.b.34207.

[99]

Zaarour B, Zhu L, Jin X. A review on the secondary surface morphology of electrospun nanofibers: formation mechanisms, characterizations, and applications. ChemistrySelect 2020; 5:1335-48. https://doi.org/10.1002/slct.201903981.

[100]

Yu DG, Li XY, Wang X, Yang JH, Bligh SW, Williams GR. Nanofibers fabricated using triaxial electrospinning as zero order drug delivery systems. ACS Appl Mater Interfaces 2015; 7:18891-7. https://doi.org/10.1021/acsami.5b06007.

[101]

Xue J, Wu T, Dai Y, Xia Y. Chem Rev 2019; 119:5298-415. https://doi.org/10.1021/acs.chemrev.8b00593.

[102]

Sultanova Z, Kaleli G, Kabay G, Mutlu M. Controlled release of a hydrophilic drug from coaxially electrospun polycaprolactone nanofibers. Int J Pharm 2016; 505:133-8. https://doi.org/10.1016/j.ijpharm.2016.03.032.

[103]

Pant B, Park M, Park S-J. Drug delivery applications of Core-sheath nanofibers prepared by coaxial electrospinning: a review. Pharmaceutics 2019; 11:305. https://doi.org/10.3390/pharmaceutics11070305.

[104]

Li H-N, Yang J, Xu Z-K. Asymmetric surface engineering for Janus membranes. Adv Mater Interfaces 2020; 7:1902064. https://doi.org/10.1002/admi.201902064.

[105]

Tian J, Ma Q, Wensheng Y, Li D, Dong X, Liu G, et al. Preparation of Janus microfibers with magnetic and fluorescence functionality via conjugate electro-spinning. Materials & Design 2019; 170:107701. https://doi.org/10.1016/j.matdes.2019.107701.

[106]

Xie X, Chen Y, Wang X, Xu X, Shen Y, Khan AR, et al. Electrospinning nanofiber scaffolds for soft and hard tissue regeneration. J Mater Sci Technol 2020; 59:243-61. https://doi.org/10.1016/j.jmst.2020.04.037.

[107]

Habibi S, Mohammadi T, Shirazi RHM, Atyabi F, Kiani M, Asadi AA. A bilayer mupirocin/bupivacaine-loaded wound dressing based on chitosan/poly(vinyl alcohol) nanofibrous mat: preparation, characterization, and controlled drug release. Int J Biol Macromol 2023; 240:124399. https://doi.org/10.1016/j.ijbiomac.2023.124399.

[108]

Figueira DR, Miguel SP, de Sá KD, Correia IJ. Production and characterization of polycaprolactone-hyaluronic acid/chitosan-zein electrospun bilayer nanofibrous membrane for tissue regeneration. Int J Biol Macromol 2016; 93:1100-10. https://doi.org/10.1016/j.ijbiomac.2016.09.080.

[109]

Ling Y, An T, Yap LW, Zhu B, Gong S, Cheng W. Disruptive, soft, wearable sensors. Adv Mater 2020; 32:e1904664. https://doi.org/10.1002/adma.201904664.

[110]

Correia TR, Antunes BP, Castilho PH, Nunes JC, Maria T, de Amorim P, et al. A bi-layer electrospun nanofiber membrane for plasmid DNA recovery from fermentation broths. Sep Purif Technol 2013; 112:20-5. https://doi.org/10.1016/j.seppur.2013.03.049.

[111]

Mao Y, Shen W, Wu S, Ge X, Ao F, Ning Y, et al. Electrospun polymers: using devices to enhance their potential for biomedical applications. React Funct Polym 2023; 186:105568. https://doi.org/10.1016/j.reactfunctpolym.2023.105568.

[112]

Feng X, Li J, Zhang X, Liu T, Ding J, Chen X. Electrospun polymer micro/nanofibers as pharmaceutical repositories for healthcare. J Control Release 2019; 302:19-41. https://doi.org/10.1016/j.jconrel.2019.03.020.

[113]

Zheng Q, Xi Y, Weng Y. Functional electrospun nanofibers: fabrication, properties, and applications in wound-healing process. RSC Adv 2024; 14:3359-78. https://doi.org/10.1039/d3ra07075a.

[114]

Sun Z, Zussman E, Yarin AL, Wendorff JH, Greiner A. Compound Core-Shell polymer nanofibers by Co-electrospinning†. Adv Mater 2003; 15:1929-32. https://doi.org/10.1002/adma.200305136.

[115]

Cai M, He H, Zhang X, Yan X, Li J, Chen F, et al. Efficient synthesis of PVDF/PI side-by-side bicomponent nanofiber membrane with enhanced mechanical strength and good thermal stability. Nanomaterials 2019; 9:39. https://doi.org/10.3390/nano9010039.

[116]

Li D, Xia Y. Direct fabrication of composite and ceramic hollow nanofibers by electrospinning. Nano Lett 2004; 4:933-8. https://doi.org/10.1021/nl049590f.

[117]

Jianxin L, Xuedi C, Xiaolei Z, Xicheng J, Yao Hengzhe F, Junlin R, et al. Review on functional electrospun nanofibers: Theory, application and fabrication. Materials Science and Engineering: B 2024; 307:117488. https://doi.org/10.1016/j.mseb.2024.117488.

[118]

Jin X, You-lo Hsieh . pH-responsive swelling behavior of poly(vinyl alcohol)/poly(acrylic acid) bi-component fibrous hydrogel membranes. Polymer 2005; 46:5149-60. https://doi.org/10.1016/j.polymer.2005.04.066.

[119]

Jedlovszky-Hajdu A, Molnar K, Nagy PM, Sinko K, Zrinyi M. Preparation and properties of a magnetic field responsive three-dimensional electrospun polymer scaffold. Colloids Surf A Physicochem Eng Asp 2016; 503:79-87. https://doi.org/10.1016/j.colsurfa.2016.05.036.

[120]

Al-Shaeli M, Benkhaya S, Al-Juboori RA, Koyuncu I, Vatanpour V. pH-responsive membranes: mechanisms, fabrications, and applications. Sci Total Environ 946:173865. https://doi.org/10.1016/j.scitotenv.2024.173865.

[121]

Tan S, Han J, Yuan X, Song Z, Gao L, Jing Gao L, et al. Epigallocatechin gallate-loaded pH-responsive dressing with effective antioxidant, antibacterial and anti-biofilm properties for wound healing. Mater Des 2023; 227:111701. https://doi.org/10.1016/j.matdes.2023.111701.

[122]

Fan S, Lam Y, Yang J, Bian X, Xin JH. Development of photochromic poly(azobenzene)/PVDF fibers by wet spinning for intelligent textile engineering. Surf Interfaces 2022; 34:102383. https://doi.org/10.1016/j.surfin.2022.102383.

[123]

Babazadeh-Mamaqani M, Razzaghi D, Roghani-Mamaqani H, Babaie A, Rezaei M, Hoogenboom R, et al. Photo-responsive electrospun polymer nanofibers: mechanisms, properties, and applications. Prog Mater Sci 2024; 146:101312. https://doi.org/10.1016/j.pmatsci.2024.101312.

[124]

Keke W, Xiaoxian W, Chen M, Haoming W, Jiao Y, Zhou C, et al. H2O2-responsive smart dressing for visible H2O2 monitoring and accelerating wound healing. Chem Eng J 2020; 387:124127. https://doi.org/10.1016/j.cej.2020.124127.

[125]

Chen K, Li Y, Li Y, Tan Y, Liu Y, Pan W, et al. Stimuli-responsive electrospun nanofibers for drug delivery, cancer therapy, wound dressing, and tissue engineering. J Nanobiotechnol 2023; 21:237. https://doi.org/10.1186/s12951-023-01987-z.

[126]

Chen L-N, Chiu Y-C, Hung J-J, Kuo C-C, Chen W-C. Multifunctional electrospun nanofibers prepared from poly((N-isopropylacrylamide)-co-(N-hydroxymethylacrylamide)) and their blends with 1,2-Diaminoanthraquinone for NO gas detection. Macromol Chem Phys 2014; 215:286-94. https://doi.org/10.1002/macp.201300604.

[127]

Pawłowska S, Rinoldi C, Nakielski P, Ziai Y, Urbanek O, Li X, et al. Ultraviolet light-assisted electrospinning of Core-Shell fully cross-linked P(NIPAAm-co-NIPMAAm) hydrogel-based nanofibers for thermally induced drug delivery self-regulation. Adv Mater Interfaces 2020; 7:2000247. https://doi.org/10.1002/admi.202000247.

[128]

Haghparas Z, Kordrostami Z, Sorouri M, Rajabzadeh M, Khalifeh R. Highly sensitive non-enzymatic electrochemical glucose sensor based on dumbbell-shaped double-shelled hollow nanoporous CuO/ZnO microstructures. Sci Rep 2021; 11:344. https://doi.org/10.1038/s41598-020-79460-2.

[129]

Long L, Liu X, Chen L, Li D, Jia J. A hollow CuOx/NiOy nanocomposite for amperometric and non-enzymatic sensing of glucose and hydrogen peroxide. Microchim Acta 2019; 186:74. https://doi.org/10.1007/s00604-018-3183-x.

[130]

Huang W, Ding S, Chen Y, Hao W, Lai X, Peng J, et al. 3D NiO hollow sphere/reduced graphene oxide composite for high-performance glucose biosensor. Sci Rep 2017; 7:1-11. https://doi.org/10.1038/s41598-017-05528-1.

[131]

Tang T, Jiang H, Yu Y, He F, Ji S, Liu Y, et al. A new method of wound treatment: targeted therapy of skin wounds with reactive oxygen species-responsive nanoparticles containing SDF-1α. Int J Nanomedicine 2015; 10:6571-85. https://doi.org/10.2147/IJN.S88384.

[132]

Kim GJ, Kim KO. Novel glucose-responsive of the transparent nanofiber hydrogel patches as a wearable biosensor via electrospinning. Sci Rep 2020; 10:18858. https://doi.org/10.1038/s41598-020-75906-9.

[133]

Xue J, Wu T, Qiu J, Xia Y. Spatiotemporally controlling the release of biological effectors enhances their effects on cell migration and neurite outgrowth. Small Methods 2020; 4:2000125. https://doi.org/10.1002/smtd.202000125.

[134]

Shan Y, Wang E, Cui X, Xi Y, Ji J, Yuan J, et al. A biodegradable piezoelectric sensor for real-time evaluation of the motor function recovery after nerve injury. Adv Funct Mater 2024; 34:2400295. https://doi.org/10.1002/adfm.202400295.

[135]

Jang J, Hyun B, Ji S, Cho E, An BW, Cheong WH, et al. Rapid production of large-area, transparent and stretchable electrodes using metal nanofibers as wirelessly operated wearable heaters. NPG Asia Mater 2017; 9:e432. https://doi.org/10.1038/am.2017.172.

[136]

Park M, Tsai S-L, Chen W. Microbial biosensors: engineered microorganisms as the sensing machinery. Sensors 2013; 13:5777-95. https://doi.org/10.3390/s130505777.

[137]

Wang Z, Bai H, Yu W, Gao Z, Chen W, Yang Z, et al. Flexible bioelectronic device fabricated by conductive polymer-based living material. Sci Adv 2022; 8:eabo1458. https://doi.org/10.1126/sciadv.abo1458.

[138]

Ren X, Fan H, Zhao Y, Liu Z. Flexible lead-free BiFeO3/PDMS-based nanogenerator as piezoelectric energy harvester. ACS Appl Mater Interfaces 2016; 8:26190-7. https://doi.org/10.1021/acsami.6b04497.

[139]

Samadian H, Khastar H, Ehterami A, Salehi M. Bioengineered 3D nanocomposite based on gold nanoparticles and gelatin nanofibers for bone regeneration: in vitro and in vivo study. Sci Rep 2021; 11:13877. https://doi.org/10.1038/s41598-021-93367-6.

[140]

Mane PP, Ambekar RS, Kandasubramanian B. Electrospun nanofiber-based cancer sensors: a review. Int J Pharm 2020; 583:119364. https://doi.org/10.1016/j.ijpharm.2020.119364.

[141]

Kumar M, Hilles AR, Ge Y, Bhatia A, Mahmood S. A review on polysaccharides mediated electrospun nanofibers for diabetic wound healing: their current status with regulatory perspective. Int J Biol Macromol 2023; 234:123696. https://doi.org/10.1016/j.ijbiomac.2023.123696.

[142]

Zhang Y, Zhang W, Hui S, Fan C, Sun J, Ying Z. Preparation of a super flexible Cu/carbon composite nanofiber film electrode for high-performance flexible all-solid-state supercapacitors. J Electron Mater 2020; 49:3165-73. https://doi.org/10.1007/s11664-020-08020-1.

[143]

Ramanan VV, Hribar KC, Katz JS, Burdick JA. Nanofiber-nanorod composites exhibiting light-induced reversible lower critical solution temperature transitions. Nanotechnology 2011; 22:494009. https://doi.org/10.1088/0957-4484/22/49/494009.

[144]

Wang M, Singh H, Hatton TA, Rutledge GC. Field-responsive superparamagnetic composite nanofibers by electrospinning. Polymer 2004; 45:5505-14. https://doi.org/10.1016/j.polymer.2004.06.013.

[145]

Burke L, Mortimer CJ, Curtis DJ, Lewis AR, Williams R, Hawkins K, et al. In-situ synthesis of magnetic iron-oxide nanoparticle-nanofibre composites using electrospinning. Mater Sci Eng 2017; 70:512-9. https://doi.org/10.1016/j.msec.2016.09.014.

[146]

Fang M, Grant PS, McShane MJ, Sukhorukov GB, Golub VO, Lvov YM. Magnetic bio/nanoreactor with multilayer shells of glucose oxidase and inorganic nanoparticles. Langmuir 2002; 18:6338-44. https://doi.org/10.1021/la025731m.

[147]

Hameed MMA, Khan SAPM, Thamer BM, Al-Enizi A, Aldalbahi A, El-Hamshary H, et al. Core-shell nanofibers from poly(vinyl alcohol) based biopolymers using emulsion electrospinning as drug delivery system for cephalexin drug. J Macromol Sci A 2021; 58:130-44. https://doi.org/10.1080/10601325.2020.1832517.

[148]

Wang X, Fan L, Zhang J, Sun X, Chang H, Yuan B, et al. Printed conformable liquid metal e-skin-enabled spatiotemporally controlled bioelectromagnetics for wireless multisite tumor therapy. Adv Funct Mater 2019; 29:1907063. https://doi.org/10.1002/adfm.201907063.

[149]

Kim M, Cho C, Shin W, Park JJ, Kim J, Won P, et al. Nanowire-assisted freestanding liquid metal thin-film patterns for highly stretchable electrodes on 3D surfaces. Npj Flex Electron 2022; 6:99. https://doi.org/10.1038/s41528-022-00232-1.

[150]

Ma J, Liu Z, Nguyen Q-K, Zhang P. Lightweight soft conductive composites embedded with liquid metal Fiber networks. Adv Funct Mater 2024; 34:2308128. https://doi.org/10.1002/adfm.202308128.

[151]

Liu Z, Wang J, Zhang Q, Li Z, Li Z, Cheng L, et al. Electrospinning silk fibroin/graphene nanofiber membrane used for 3D wearable pressure sensor. Polymers 2022; 14:3875. https://doi.org/10.3390/polym14183875.

[152]

Wei Z, Yang J, Long S, Zhang G, Wang X. Smart and in-situ formation electrospun fibrous membrane for the control of antimicrobial efficacy. Smart Mater Med 2021; 2:87-95. https://doi.org/10.1016/j.smaim.2021.02.001.

[153]

Nezhadghaffar-Borhani E, Abdollahi A, Roghani-Mamaqani H, Salami-Kalajahi M. Photoswitchable surface wettability of ultrahydrophobic nanofibrous coatings composed of spiropyran-acrylic copolymers. J Colloid Interface Sci 2021; 593:67-78. https://doi.org/10.1016/j.jcis.2021.03.012.

[154]

Wei Z, Lin Q, Yang J, Long S, Zhang G, Wang X, et al. Fabrication of novel dual thermo-and pH-sensitive poly(N-isopropylacrylamide-N-methylolacrylamide-acrylic acid) electrospun ultrafine fibres for controlled drug release. Mater Sci Eng C 2020; 115:111050. https://doi.org/10.1016/j.msec.2020.111050.

[155]

Soares JC, Iwaki LEO, Soares AC, Rodrigues VC, Melendez ME, Fregnani JHTG, et al. Immunosensor for pancreatic cancer based on electrospun nanofibers coated with carbon nanotubes or gold nanoparticles. ACS Omega 2017; 2:6975-83. https://doi.org/10.1021/acsomega.7b01029.

[156]

Sun J, Wang W, Yu D. NiCo2O4 nanosheet-decorated carbon nanofiber electrodes with high electrochemical performance for flexible supercapacitors. J Electron Mater 2019; 48:3833-43. https://doi.org/10.1007/s11664-019-07135-4.

[157]

Qi K, He J, Wang H, Zhou Y, You X, Nan N, et al. A highly stretchable nanofiber-based electronic skin with pressure-, strain-, and flexion-sensitive properties for health and motion monitoring. ACS Appl Mater Interfaces 2017; 9:42951-60. https://doi.org/10.1021/acsami.7b07935.

[158]

Zhang L, Belova V, Wang H, Dong W, Möhwald H. Controlled cavitation at nano/microparticle surfaces. Chem Mater 2014; 26:2244-8.

[159]

Luo G, Xie J, Liu J, Zhang Q, Luo Y, Li M, et al. Highly conductive, stretchable, durable, breathable electrodes based on electrospun polyurethane mats superficially decorated with carbon nanotubes for multifunctional wearable electronics. Chemical Engineering Journal 2023; 451:138549. https://doi.org/10.1016/j.cej.2022.138549.

[160]

Luo Y, Zhao L, Luo G, Dong L, Xia Y, Li M, et al. Highly sensitive piezoresistive and thermally responsive fibrous networks from the in situ growth of PEDOT on MWCNT-decorated electrospun PU fibers for pressure and temperature sensing. Microsyst Nanoeng 2023; 9:113. https://doi.org/10.1038/s41378-023-00593-1.

[161]

Wen P, Yang Y-Y, Yin W-J, Jian-Cheng H, Yu-Dong Shen Y, Wang Z-LX, et al. Preparation of an ultrasensitive electrochemical immunosensor for the rapid detection of 19-nortestosterone based on polyvinyl alcohol/polyacrylic acid electrospun nanofiber mat. Sensors Actuators B Chem 2022; 370:132450. https://doi.org/10.1016/j.snb.2022.132450.

[162]

Temoçin Z. Designing of a stable and selective glucose biosensor by glucose oxidase immobilization on glassy carbon electrode sensitive to H2O2 via nanofiber interface. J Appl Electrochem 2021; 51:283-93. https://doi.org/10.1007/s10800-020-01502-4.

[163]

Zhang LQ. Preparation of a healing dressing that can monitor wound humidity [D]. Chongqing: Chongqing Medical University, 2021. (in Chinese).

[164]

Ding S, Lou Y, Niu Z, Wang J, Jin X, Ma J, et al. A highly sensitive, breathable, and biocompatible wearable sensor based on nanofiber membrane for pressure and humidity monitoring. Macromol Mater Eng 2022; 307:2200233. https://doi.org/10.1002/mame.202200233.

[165]

Ding S, Jin X, Guo J, Kou B, Chai M, Dou S, et al. A biomimetic asymmetric structured intelligent wound dressing with dual-modality humidity-pressure sensing for non-invasive and real-time wound healing monitoring. Adv Fiber Mater 2025; 7:156-71. https://doi.org/10.1007/s42765-024-00473-x.

[166]

Yang L, Li C, Wang X, Zhang X, Li Y, Liu S, et al. Electroactive nanofibrous membrane with temperature monitoring for wound healing. RSC Adv 2023; 13:14224-35. https://doi.org/10.1039/d3ra01665j.

[167]

ACS Appl. Mater. Interfaces 2022; 14:12984-3000.

[168]

Zhang S, Wang L, Xu T, Zhang X. Luminescent MOF-Based Nanofibers with Visual Monitoring and Antibacterial Properties for Diabetic Wound Healing. ACS Appl Mater Interfaces 2023; 15:9110-9119. https://doi.org/10.1021/acsami.2c21786.

[169]

Yang P, Zhu Z, Zhang T, Zhang W, Chen W, Cao Y, et al. Orange-emissive carbon quantum dots: toward application in wound pH monitoring based on colorimetric and fluorescent changing. Small 2019; 15:e1902823. https://doi.org/10.1002/smll.201902823.

[170]

Oh HH, Ko YG, Uyama H, Park WH, Cho D, Kwon OH. Fabrication and characterization of thermoresponsive polystyrene nanofibrous mats for cultured cell recovery. Biomed Res Int 2014; 2014:480694.

[171]

Safari S, Ehsani M, Zandi M. Stimuli-responsive electrospun nanofibers based on PNVCL-PVAc copolymer in biomedical applications. Prog Biomater 2021; 10:245-58. https://doi.org/10.1007/s40204-021-00168-1.

[172]

El-Husseiny HM, Mady EA, Hamabe L, Abugomaa A, Shimada K, Yoshida T, et al. Smart/stimuli-responsive hydrogels: cutting-edge platforms for tissue engineering and other biomedical applications. Mater Today Bio 2022; 13:100186. https://doi.org/10.1016/j.mtbio.2021.100186.

[173]

Kim YJ, Ebara M, Aoyagi T. Temperature-responsive electrospun nanofibers for ‘on-off’ switchable release of dextran. Sci Technol Adv Mater 2012; 13:064203. https://doi.org/10.1088/1468-6996/13/6/064203.

[174]

Huang Y, Song M, Li X, Du Y, Gao Z, Zhao YQ, et al. Temperature-responsive self-contraction nanofiber/hydrogel composite dressing facilitates the healing of diabetic-infected wounds. Materials Today Bio 2024; 28:101214. https://doi.org/10.1016/j.mtbio.2024.101214.

[175]

Cheng Y, Zhu M, Chi M, Lai Y, Li B, Qian R, et al. MXene/TPU hybrid fabrics enable smart wound management and Thermoresponsive drug delivery. ACS Appl Mater Interfaces 2024. https://doi.org/10.1021/acsami.3c19604.

[176]

Federico S, Martorana A, Pitarresi G, Palumbo FS, Fiorica C, Giammona G . Development of stimulus-sensitive electrospun membranes based on novel biodegradable segmented polyurethane as triggered delivery system for doxorubicin. Biomater Adv 2022; 136:212769. https://doi.org/10.1016/j.bioadv.2022.212769.

[177]

Lee H, Woo J, Son D, Kim M, Choi WI, Sung D. Electrospinning/electrospray of ferrocene containing copolymers to fabricate ROS-responsive particles and fibers. Polymers (Basel) 2020;12:12. https://doi.org/10.3390/polym12112520.

[178]

Jo YJ, Gulfam M, Jo SH, Gal YS, Oh CW, Park SH, et al. Multi-stimuli responsive hydrogels derived from hyaluronic acid for cancer therapy application. Carbohydr Polym 2022; 286:119303. https://doi.org/10.1016/j.carbpol.2022.119303.

[179]

Zhang J, Xiao C, Zhang X, Lin Y, Yang H, Zhang YS, et al. An oxidative stress-responsive electrospun polyester membrane capable of releasing anti-bacterial and anti-inflammatory agents for postoperative anti-adhesion. J Control Release 2021; 335:359-68. https://doi.org/10.1016/j.jconrel.2021.04.017.

[180]

Yao Y, Ding J, Wang Z, Zhang H, Xie J, Wang Y, et al. ROS-responsive polyurethane fibrous patches loaded with methylprednisolone (MP) for restoring structures and functions of infarcted myocardium in vivo. Biomaterials 2020; 232:119726. https://doi.org/10.1016/j.biomaterials.2019.119726.

[181]

Kwak M, Han L, Chen JJ, Fan R. Interfacing inorganic nanowire arrays and living cells for cellular function analysis. Small 2015; 11:5600-10. https://doi.org/10.1002/smll.201501236.

[182]

Singh B, Shukla N, Kim J, Kim K, Park MH. Stimuli-responsive nanofibers containing gold nanorods for on-demand drug delivery platforms. Pharmaceutics 2021; 13:1319. https://doi.org/10.3390/pharmaceutics13081319.

[183]

Lee HP, Gaharwar AK. Light-responsive inorganic biomaterials for biomedical applications. Adv Sci (Weinh) 2020; 7:2000863. https://doi.org/10.1002/advs.202000863.

[184]

Wen T, Xiong S, Zhao H, Wang J, Wang C, Long Z, et al. Polylactic acid-based dressing with oxygen generation and enzyme-like activity for accelerating both light-driven biofilm elimination and wound healing. Burns Trauma 2024; 12:tkae041. https://doi.org/10.1093/burnst/tkae041.

[185]

Chong Y, Ge C, Fang G, Wu R, Zhang H, Chai Z, et al. Light-enhanced antibacterial activity of graphene oxide, mainly via accelerated electron transfer. Environ Sci Technol 2017; 51:10154-61. https://doi.org/10.1021/acs.est.7b00663.

[186]

Murakami T, NakaHsuji H, Inada M, Matoba Y, Umeyama T, Hsujimoto M, et al. Photodynamic and Photothermal effects of semiconducting and metallic-enriched single-walled carbon nanotubes. J Am Chem Soc 2012; 134:17862-5. https://doi.org/10.1021/ja3079972.

[187]

Hu X, Liu S, Zhou G, Huang Y, Xie Z, Jing X. Electrospinning of polymeric nanofibers for drug delivery applications. J Control Release 2014; 185:12-21. https://doi.org/10.1016/j.jconrel.2014.04.018.

[188]

Chen M, Li YF, Besenbacher F. Electrospun nanofibers-mediated on-demand drug release. Adv Healthc Mater 2014; 3:1721-32. https://doi.org/10.1002/adhm.201400166.

PDF (5243KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉