Bio-inspired natural fibers-derived e-skin equipped with intelligent drug-release system for advanced robustly-integrated melanoma therapy

Xinhua Liu , Yifan Fei , Boqiang Cui , Xing Chen , Jiamin Zhang , Ouyang Yue , Zhongxue Bai , Ling Wen , Huie Jiang

Collagen and Leather ›› 2025, Vol. 7 ›› Issue (1)

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Collagen and Leather ›› 2025, Vol. 7 ›› Issue (1) DOI: 10.1186/s42825-025-00210-z
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Bio-inspired natural fibers-derived e-skin equipped with intelligent drug-release system for advanced robustly-integrated melanoma therapy

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Abstract

Malignant melanoma, a highly aggressive malignancy, necessitates innovative therapeutic strategies integrating biomaterial innovation with multimodal treatment modalities. Herein, we report the development of a collagen-derived bioelectronic skin (c-ADM) nanoengineered via interfacial assembly of porcine acellular dermal matrix (ADM)—a natural collagen-rich scaffold—with conductive poly (3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and copper sulfide nanoparticles (CuS-NPs). This hybrid system synergizes photothermal ablation, stimuli-responsive drug delivery, and electrostimulation (ES) for comprehensive postoperative melanoma management and tissue regeneration. The c-ADM platform exhibits superior mechanical robustness, enzymatic resistance, and biocompatibility, enabling real-time motion monitoring while maintaining structural integrity in dynamic physiological environments. Leveraging the photothermal efficiency of CuS-NPs, localized hyperthermia (ΔT > 40 °C) under near-infrared (NIR) irradiation induces irreversible melanoma cell apoptosis. Concurrently, laser-triggered temperature-responsive drug release enables synchronized photothermal-chemotherapy, with sustained doxorubicin release profiles at tumor sites. Notably, pH-responsive Cu2⁺ liberation from CuS-NPs facilitates intelligent functional switching: bactericidal activity at tumor microenvironment pH (5.0–6.0) and pro-regenerative effects under physiological pH (7.4) for wound healing. In vitro/in vivo assessments confirm c-ADM’s dual therapeutic efficacy including ES-enhanced cancer cell death via mitochondrial dysfunction and accelerated full-thickness skin regeneration through collagen remodeling and angiogenesis modulation. This work establishes a collagen-based bioelectronic scaffold for personalized oncological care, integrating intraoperative tumor eradication, postoperative surveillance, and adaptive tissue reconstruction.

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Nature fibers / Acellular dermal matrix / Bioelectronic skin / Copper nanomaterials / Wound healing

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Xinhua Liu, Yifan Fei, Boqiang Cui, Xing Chen, Jiamin Zhang, Ouyang Yue, Zhongxue Bai, Ling Wen, Huie Jiang. Bio-inspired natural fibers-derived e-skin equipped with intelligent drug-release system for advanced robustly-integrated melanoma therapy. Collagen and Leather, 2025, 7(1): DOI:10.1186/s42825-025-00210-z

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References

[1]

ChenL, et al.. Skin to E-skin. Nat Nanotechnol, 2017, 121020.

[2]

SorgH, TilkornDJ, HagerS, HauserJ, MirastschijskiU. Skin wound healing: an update on the current knowledge and concepts. Eur Surg Res, 2016, 5881.

[3]

MoranB, SilvaR, PerryAS, GallagherWM. Epigenetics of malignant melanoma. Semin Cancer Biol, 2018, 5180.

[4]

RogersHW, WeinstockMA, HarrisAR, HinckleyMR, FeldmanSR, FleischerAB, ColdironBM. Coldiron, Incidence estimate of nonmelanoma skin cancer in the United States. Arch Dermatol, 2010, 146283.

[5]

TobinDJ. Biochemistry of human skin-our brain on the outside. Chem Soc Rev, 2006, 3552.

[6]

Costa SvedmanF, SpanopoulosD, TaylorA, AmelioJ, HanssonJ. Surgical outcomes in patients with cutaneous malignant melanoma in Europe - a systematic literature review. J Eur Acad Dermatol Venereol, 2016, 31603.

[7]

ShiJ, KantoffPW, WoosterR, FarokhzadOC. Cancer nanomedicine: progress, challenges and opportunities. Nat Rev Cancer, 2016, 1720.

[8]

WangC. NIR/Thermoresponsive Injectable Self-Healing Hydrogels Containing Polydopamine Nanoparticles for Efficient Synergistic Cancer Thermochemotherapy. ACS Appl Mater Interfaces, 2020, 129118.

[9]

ZhangY. Nanozyme decorated metal-organic frameworks for enhanced photodynamic therapy. ACS Nano, 2018, 12615.

[10]

RomanoE, ScordoM, DuszaSW, CoitDG, ChapmanPB. (2010) Site and timing of first relapse in stage iii melanoma patients: implications for follow-up guidelines. J Clin Oncol: Official J Am Soc Clin Oncol., 2010, 283042.

[11]

MaHL, LiW, WangM, VarandaLC, PerussiJR, Shrike ZhangY, CarrilhoE. Hypericin-loaded oil-in-water nanoemulsion synthesized by ultrasonication process enhances photodynamic therapy efficiency. J Photochem Photobiol B Bio-Des Manuf., 2022, 5660

[12]

HammockML, ChortosA, TeeBCK, TokJBH, BaoZ. 25th anniversary article: the evolution of electronic skin (E-Skin): a brief history, design considerations, and recent progress. Adv Mater, 2013, 255997.

[13]

ZareiM, LeeG, LeeSG, ChoK. Achieving ultrasensitivity and high breathability in biodegradable piezoresistive electronic skins. Adv Mater, 2022, 1342203193.

[14]

DahiyaR. E-Skin: from humanoids to humans point of view. Proc IEEE, 2019, 107247.

[15]

LiuX. Nature-skin-derived e-skin as versatile “wound therapy-health monitoring” bioelectronic skin-scaffolds: skin to bio-e-skin. Adv Healthcare Mater, 2023, 1220.

[16]

DuS. Self-powered and photothermal electronic skin patches for accelerating wound healing. Nano Energy, 2021, 93. 106906

[17]

ZhangZ. Flexible tactile sensors with biomimetic microstructures: mechanisms, fabrication, and applications. Adv Coll Interface Sci, 2023, 320. 102988

[18]

YuH. 3D printed sodium alginate-gelatin skin scaffolds and their in vitro biocompatibility with fibroblasts. J Tissue Eng Reconstruct Surg., 2021, 17129705

[19]

MaM. An injectable photothermally active antibacterial composite hydroxypropyl chitin hydrogel for promoting the wound healing process through photobiomodulation. J Mater Chem B, 2021, 94567.

[20]

VedhanayagamM, Suresh kumarA, Unni NairB, JanardhananSK. Dendrimer-functionalized metal oxide nanoparticle-mediated self-assembled collagen scaffold for skin regenerative application: function of metal in metal oxides. Appl Biochem Biotechnol, 2021, 194266.

[21]

MogoşanuGD, GrumezescuAM. Natural and synthetic polymers for wounds and burns dressing. Int J Pharm, 2014, 463127.

[22]

BoatengJ, CatanzanoO. Advanced therapeutic dressings for effective wound healing-a review. J Pharm Sci, 2015, 1043653.

[23]

JinY. Self-supporting nanoclay as internal scaffold material for direct printing of soft hydrogel composite structures in air. ACS Appl Mater Interfaces, 2018, 1028361.

[24]

ZhaoH. 3D printing of artificial skin patches with bioactive and optically active polymer materials for anti-infection and augmenting wound repair. Mater Horiz, 2022, 9342.

[25]

FuXK, WangJ, Ramírez-PérezAC, ChoongC, LisakG. Flexible conducting polymer-based cellulose substrates for on-skin applications. Mater Sci Eng, C, 2020, 108. 110392

[26]

YaoQ. Recent development and biomedical applications of decellularized extracellular matrix biomaterials. Mater Sci Eng, C, 2019, 104. 109942

[27]

JiangA, YingL, ChengYS, ZhaiHF. Acellular dermal matrix in urethral reconstruction. Front Pediatr, 2024, 121342906

[28]

SongZ, YangD, YangJ, NieX, WuJ, SongH, et al.. Abdominal wall reconstruction following resection of large abdominal aggressive neoplasms using tensor fascia lata flap with or without mesh reinforcement. Hernia, 2018, 22(2): 333-341.

[29]

Xin ZC, Yang BC, Li M, Yuan YM, Cui WS, Tang Y, et al. 2019 Appllication of human acellular dermal matrix in surgical treatment of genitourinary disease. Beijing Da Xue Xue Bao Yi Xue Ban. 51(4):778–82. https://doi.org/10.19723/j.issn.1671-167X.2019.04.033.

[30]

KirsnerRS, BohnG, DriverVR, MillsJLSr, NanneyLB, WilliamsML, et al.. Human acellular dermal wound matrix: evidence and experience. Int Wound J, 2015, 12(6): 646-654.

[31]

FuQ, CaoYL. Use of tissue engineering in treatment of the male genitourinary tract abnormalities. J Sex Med, 2010, 7(5): 1741-1746.

[32]

ZhangX, YangJ, LiY, LiuS, LongK, ZhaoQ, et al.. Functional neovascularization in tissue engineering with porcine acellular dermal matrix and human umbilical vein endothelial cells. Tissue Eng Part C Methods, 2011, 17(4): 423-433.

[33]

YangJ, DangH, XuY. Recent advancement of decellularization extracellular matrix for tissue engineering and biomedical application. Artif Organs, 2022, 46(4): 549-567.

[34]

DingH, et al.. Platinum nanoenzyme functionalized black phosphorus nanosheets for photothermal and enhanced-photodynamic therapy. Chem Eng J, 2022, 4816085.

[35]

YangP. Hollow CuS nanoparticles equipped with hydroxyapatite/hyaluronic acid coating for NIR/pH dual-responsive drug delivery. Int J Biol Macromol, 2023, 253. 127150

[36]

SinghAP, BiswasA, Shukla AMaitiP. Targeted therapy in chronic diseases using nanomaterial-based drug delivery vehicles. Signal Transduct Target Ther, 2019, 421.

[37]

MendesBB, SousaDP, ConniotJ, CondeJ. Nanomedicine-based strategies to target and modulate the tumor microenvironment. Trends Cancer, 2021, 7847.

[38]

ZhengM. Nature-skin-based multi-responsive controlled-release electroactive scaffolds for integrated melanoma postoperative relapse prevention and wound therapy. J Mater Sci Technol, 2024, 188155

[39]

WangD. Scalable, flexible, durable, and salt-tolerant CuS/bacterial cellulose gel membranes for efficient interfacial solar evaporation. ACS Sustain Chem Eng, 2022, 89017.

[40]

LvR, YangP, HuB, XuJ, ShangW, HuiH. In situ growth strategy to integrate up-conversion nanoparticles with ultrasmall CuS for photothermal theranostics. ACS Nano, 2016, 111064.

[41]

LiangJ. pH/glutathione dual-responsive copper sulfide-coated organic mesoporous silica for synergistic chemo-photothermal therapy. J Colloid Interface Sci, 2024, 6571.

[42]

ZhaoZ. Developing fluorescent copper nanoclusters: Synthesis, properties, and applications. Colloids Surf, B, 2020, 195. 111244

[43]

RyanEJ, RyanAJ, González-VázquezA, PhilippartA, CiraldoFE, HobbsCNV, BoccacciniAR, KearneyCJ, O’BrienFJ. Collagen scaffolds functionalised with copper-eluting bioactive glass reduce infection and enhance osteogenesis and angiogenesis both in vitro and in vivo. Biomaterials, 2019, 197405.

[44]

WangN. Design of DOX-GNRs-PNIPAM@PEG-PLA micelle with temperature and light dual-function for potent melanoma therapy. Front Chem, 2021, 8. 599740

[45]

JiangZ. Nanomedicine potentiates mild photothermal therapy for tumor ablation. Asian J Pharm Sci, 2021, 16738.

[46]

LiD. Designed formation of Prussian Blue/CuS Janus nanostructure with enhanced NIR-I and NIR-II dual window response for tumor thermotherapy. J Colloid Interface Sci, 2022, 613671.

[47]

ZhangP. Theranostic nanoparticles with disease-specific administration strategies. Nano Today, 2022, 42. 101335

[48]

RobinsonJT, TabakmanSM, LiangY, WangH, Sanchez CasalongueH, VinhD, DaiH. Ultrasmall reduced graphene oxide with high near-infrared absorbance for photothermal therapy. J Am Chem Soc, 2011, 1336825.

[49]

LiuXY, DanNH, DanWH. Preparation and characterization of an advanced collagen aggregate from porcine acellular dermal matrix [J]. Int J Biol Macromol, 2016, 88: 179-188.

[50]

HouY, TianY, TianJ, ShiJ, ZhaoH, HuJ, ZhangY. Peptide-based double-network hydrogels for melanoma treatment and wound healing promotion. ACS Appl Mater Interfaces, 2023, 15: 29927-29938.

[51]

ZhongT. Core-shell structured nanospheres for photothermal ablation and pH-triggered drug delivery toward synergistic cancer therapy. RSC Adv, 2017, 726640.

[52]

Minceva-SukarovaB, NajdoskiM, GrozdanovI, ChunnilallCJ. Raman spectra of thin solid films of some metal sulfides. J Mol Struct, 1997, 267: 410-411.

[53]

ZhangM. Deng, highly electrically conductive PEDOT:PSS/SWCNT flexible thermoelectric films fabricated by a high-velocity non-solvent turbulent secondary doping approach. ACS Appl Mater Interfaces, 2023, 1510947.

[54]

ChenY. Quaternary ammonium salt modification of decellularised porcine dermal matrix. West Leather, 2013, 03524

[55]

HoYS, McKayG. The sorption of lead (II) ions on peat. Water Res, 1999, 33: 578-584.

[56]

GoestenkorsAP, LiuT, OkaforSS, SemarBA, AlvarezRM, MontgomerySK, FriedmanL, RutzAL. Manipulation of cross-linking in PEDOT:PSS hydrogels for biointerfacing. J Mater Chem B, 2023, 11: 11357-11371.

[57]

GaoX. Fabrication of porcine acellular dermal matrix and oxidized hyaluronic acid conductive composite hydrogels for accelerating skin wound healing under electrical stimulation. Int J Biol Macromol, 2024, 282: 137179-137179.

[58]

HadidiM, AghababaeiF, McClementsDJ. Enhanced alkaline extraction techniques for isolating and modifying plant-based proteins. Food Hydrocoll, 2023, 145. 109132

[59]

AlamHB, BurrisD, DaCortaJA, RheeP. Hemorrhage control in the battlefield: role of new hemostatic agents. Military Med, 2005, 170: 63-69.

[60]

WuSJ, YukH, WuJ, NabzdykCS, ZhaoX. A multifunctional origami patch for minimally invasive tissue sealing. Adv Mater, 2021, 332007667.

[61]

ZhaoF. H2S-activated ion-interference therapy: a novel tumor targeted therapy based on copper-overload-mediated cuproptosis and pyroptosis. Adv Func Mater, 2023, 3338.

[62]

TianQ. Hydrophilic flower-like CuS superstructures as an efficient 980 nm laser-driven photothermal agent for ablation of cancer cells. Adv Mater, 2011, 23: 3542-3547.

[63]

SriramKN, AhmedABM. Cu vacancy and Sn doping effects on electronic and optical properties of cuprous oxide: Insights from DFT+ U calculations. Comput Mater Sci, 2025, 250113653

[64]

MutalikC, OkoroG, DyahIK, AchmadJ, ElfiQR, DwiR, HsuWT, KuoTR. Copper sulfide with morphology-dependent photodynamic and photothermal antibacterial activities. J Coll Interface Sci., 2021, 607: 1825-1835.

[65]

KarimiM. Temperature-responsive smart nanocarriers for delivery of therapeutic agents: applications and recent advances. ACS Appl Mater Interfaces, 2016, 8: 21107-21133.

[66]

KarimzadehM, SeyedtaghiaR, SahebkarH. CuS composite thermosensitive nanospheres for combined treatment of tumor photothermal and chemodynamic therapy[J]. Adv Modern Oncol, 2019, 216

[67]

ParkRJ, SonH, KimK, KimS, OhT. The effect of microcurrent electrical stimulation on the foot blood circulation and pain of diabetic neuropathy. J Phys Ther Sci, 2011, 23: 515-518.

[68]

FitzsimmonsRJ, StrongDD, MohanS, BaylinkDJ. Low-amplitude, low-frequency electric field-stimulated bone cell proliferation may in part be mediated by increased IGF-II release. J Cell Physiol, 1992, 150: 84-88.

[69]

SugimotoM. Optimum microcurrent stimulation intensity for galvanotaxis in human fibroblasts. J Wound Care, 2012, 21: 5-10

[70]

TandonN. Galvanic microparticles increase migration of human dermal fibroblasts in a wound-healing model via reactive oxygen species pathway. Exp Cell Res, 2014, 320: 79-91.

[71]

MartinF. Copper-dependent activation of hypoxia-inducible factor (HIF)-1: implications for ceruloplasmin regulation. Blood, 2005, 105: 4613-4619.

[72]

WuC. An injectable supramolecular polymer nanocomposite hydrogel for prevention of breast cancer recurrence with theranostic and mammoplastic functions. J Clin Investig, 2018, 1283425.

[73]

JiangW. Combination of biodegradable hydrogel and antioxidant bioadhesive for treatment of breast cancer recurrence and radiation skin injury. Oncol Lett, 2021, 1222.

[74]

LiQ. Supramolecular hydrogels based on poly (ethylene glycol)-poly (lactic acid) block copolymer micelles and α-cyclodextrin for potential injectable drug delivery system. ACS Biomater Sci Eng, 2019, 5768.

[75]

DaiY, XuC, SunX, ChenX. Nanoparticle design strategies for enhanced anticancer therapy by exploiting the tumor microenvironment. Chem Soc Rev, 2017, 46: 3830-3852.

[76]

ZhengM. Nature-skin-based multi-responsive controlled-release electroactive scaffolds for integrated melanoma postoperative relapse prevention and wound therapy. Res Square., 2023.

[77]

LiX. Research advances on tumor microenvironment responsive nano-preparations. Prog Pharma Sci, 2019, 43: 865-875

[78]

HuR, YangX, CuiW, LengL, ZhaoX, JiG, ZhaoJ, ZhuQ, JiaoZ. An ultrahigh stretchable and recyclable starch-based gel with multiple functions. Adv Mater, 2023.

[79]

RobbyAI, LeeG, LeeKD, JangYC, ParkSY. GSH-responsive self-healable conductive hydrogel of highly sensitive strain-pressure sensor for cancer cell detection. Nano Today, 2021, 39101178.

[80]

LiuX, TianS, XuS, LuW, ZhongC, LongY, MaY, YangK, ZhangL, YangJ. A pressure-resistant zwitterionic skin sensor for domestic real-time monitoring and pro-healing of pressure injury. Biosens Bioelectron, 2011, 214: 114528-114528.

Funding

National Natural Science Foundation of China(22278257)

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