Electrospun Scaffold-Enabled Bioreactor for Scalable Manufacturing of Mechanically Programmed Macrophage-Derived Extracellular Vesicles Targeting Aged Bone Defects

Lingfei Xiao , Huayi Huang , Yunxiang Ding , Ming Lei , Qingjian Lei , Feifei Yan , Chaoran Shi , Jianbin Xu , Lin Cai , Wanli Li

Advanced Fiber Materials ›› : 1 -28.

PDF
Advanced Fiber Materials ›› :1 -28. DOI: 10.1007/s42765-026-00733-y
Research Article
research-article
Electrospun Scaffold-Enabled Bioreactor for Scalable Manufacturing of Mechanically Programmed Macrophage-Derived Extracellular Vesicles Targeting Aged Bone Defects
Author information +
History +
PDF

Abstract

Extracellular vesicles (EVs) represent promising cell-free therapeutics for the regeneration of aged bone defects. Mechanical stimulation is critical in bone regeneration and significantly influences both EV secretion and cargo composition. Despite this, translating mechanically programmed EVs to clinically relevant doses remains a significant challenge. Most current scalable bioreactor systems has achieved high yields through high-density cell culture and fluid flow, yet they do not provide programmable or spatially consistent mechanical stimulation. In this study, an electrospun scaffold-enabled bioreactor was developed to integrate high-density three-dimensional macrophage culture with programmable cyclic stretching, enabling simultaneous EV scale-up and cargo programming. The interconnected fiber junction network transmits boundary-applied strain with enhanced spatial consistency, while the highly porous scaffold supports dense cell seeding and efficient EV release and collection. This approach increases EV yield by 13.8-fold compared to conventional two-dimensional culture. Fiber-mediated mechanical conditioning activates Piezo1-dependent Ca2+ signaling and integrin-associated mechanotransduction, promotes Yes-associated protein (YAP) nuclear translocation, and remodels EV cargo composition. The resulting mechanically stimulated EVs (ms-EVs) demonstrate concurrent pro-regenerative activities, including cellular rejuvenation, vascular repair, and osteogenic enhancement, and perform favorably compared to canonical interleukin-4 (IL-4)-polarized M2 macrophage-derived extracellular vesicles (M2-EVs). In aged rat femoral defects, ms-EV-functionalized scaffolds increase bone volume fraction by approximately 1.7-fold at 8 weeks, reduce p16+ senescent cells, and enhance CD31+ neovascularization. These findings establish electrospun scaffolds as scalable mechanobiological manufacturing substrates for the production of functionally programmed EV therapeutics.

Graphical Abstract

Keywords

Electrospun scaffold / Bioreactor / Extracellular vesicles / Bone regeneration / Mechanical stimulation

Cite this article

Download citation ▾
Lingfei Xiao, Huayi Huang, Yunxiang Ding, Ming Lei, Qingjian Lei, Feifei Yan, Chaoran Shi, Jianbin Xu, Lin Cai, Wanli Li. Electrospun Scaffold-Enabled Bioreactor for Scalable Manufacturing of Mechanically Programmed Macrophage-Derived Extracellular Vesicles Targeting Aged Bone Defects. Advanced Fiber Materials 1-28 DOI:10.1007/s42765-026-00733-y

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Xu GL, Jin J, Fu ZH, Wang GM, Lei XH, Xu J, Wang JZ. Extracellular vesicle-based drug overview: Research landscape, quality control and nonclinical evaluation strategies. Signal Transduct Target Ther, 2025, 10. ArticleID: 255

[2]

Elsharkasy OM, Nordin JZ, Hagey DW, de Jong OG, Schiffelers RM, Andaloussi SE, Vader P. Extracellular vesicles as drug delivery systems: why and how?. Adv Drug Deliv Rev, 2020, 159. ArticleID: 332

[3]

Welsh JA, Goberdhan DCI, O'Driscoll L, Buzas EI, Blenkiron C, Bussolati B, Cai H, Di Vizio D, Driedonks TAP, Erdbrugger U, Falcon-Perez JM, Fu QL, Hill AF, Lenassi M, Lim SK, Mahoney MG, Mohanty S, Moller A, Nieuwland R, Ochiya T, Sahoo S, Torrecilhas AC, Zheng L, Zijlstra A, Abuelreich S, Bagabas R, Bergese P, Bridges EM, Brucale M, Burger D, Carney RP, Cocucci E, Crescitelli R, Hanser E, Harris AL, Haughey NJ, Hendrix A, Ivanov AR, Jovanovic-Talisman T, Kruh-Garcia NA, Ku'ulei-Lyn Faustino V, Kyburz D, Lasser C, Lennon KM, Lotvall J, Maddox AL, Martens-Uzunova ES, Mizenko RR, Newman LA, Ridolfi A, Rohde E, Rojalin T, Rowland A, Saftics A, Sandau US, Saugstad JA, Shekari F, Swift S, Ter-Ovanesyan D, Tosar JP, Useckaite Z, Valle F, Varga Z, van der Pol E, van Herwijnen MJC, Wauben MHM, Wehman AM, Williams S, Zendrini A, Zimmerman AJConsortium MThery C, Witwer KW. Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches. J Extracell Vesicles, 2024, 13. ArticleID: e12404

[4]

Pu PJ, Wu SN, Zhang KJ, Xu H, Guan JN, Jin ZC, Sun W, Zhang HW, Yan B. Mechanical force induces macrophage-derived exosomal UCHL3 promoting bone marrow mesenchymal stem cell osteogenesis by targeting SMAD1. J Nanobiotechnol, 2023, 21. ArticleID: 88

[5]

Zhao HY, Liu WJ, Wang P, Zhang S, Xing X, Yan ZJ, Wang L, Wu DY, Wang FK, Yang S, Deng XT, Li XY, Li YL, Chen W, Wang J, Zhang YZ. Extracellular vesicles from mechanical loading stimulated-macrophages favor fracture healing through targeting Adrb2 of osteoblasts. Chem Eng J, 2025.

[6]

Kalukula Y, Ciccone G, Mohammed D, Proces A, Versaevel M, Deridoux A, Ergot L, Barbier Z, Mansy M, Aucouturier R, Tranzer R, Surin M, Gabriele S, Luciano M. Unlocking the therapeutic potential of cellular mechanobiology. Sci Adv, 2025, 11. ArticleID: eaea6817

[7]

Dupont S, Morsut L, Aragona M, Enzo E, Giulitti S, Cordenonsi M, Zanconato F, Le Digabel J, Forcato M, Bicciato S, Elvassore N, Piccolo S. Role of YAP/TAZ in mechanotransduction. Nature, 2011, 474. ArticleID: 179

[8]

Atcha H, Jairaman A, Holt JR, Meli VS, Nagalla RR, Veerasubramanian PK, Brumm KT, Lim HE, Othy S, Cahalan MD, Pathak MM, Liu WF. Mechanically activated ion channel Piezo1 modulates macrophage polarization and stiffness sensing. Nat Commun, 2021, 12. ArticleID: 3256

[9]

Engler AJ, Sen S, Sweeney HL, Discher DE. Matrix elasticity directs stem cell lineage specification. Cell, 2006, 126. ArticleID: 677

[10]

Halder G, Dupont S, Piccolo S. Transduction of mechanical and cytoskeletal cues by YAP and TAZ. Nat Rev Mol Cell Biol, 2012, 13. ArticleID: 591

[11]

Lenoir S, Thouvenot E, Gropplero G, Dec L, Loew D, Thery C, Perez JE, Wilhelm C. A hydrodynamic bioreactor for high-yield production of extracellular vesicles from stem cell spheroids with defined cargo profiling. Adv Sci, 2025, 13. ArticleID: e10607

[12]

Huang JJ, Chen HX, Li N, Liu PM, Yang JJ, Zhao YJ. Emerging technologies towards extracellular vesicles large-scale production. Bioact Mater, 2025, 52: 338

[13]

Ng CY, Kee LT, Al-Masawa ME, Lee QH, Subramaniam T, Kok D, Ng MH, Law JX. Scalable production of extracellular vesicles and its therapeutic values: a review. Int J Mol Sci, 2022, 23. ArticleID: 7986

[14]

Gobin J, Muradia G, Mehic J, Westwood C, Couvrette L, Stalker A, Bigelow S, Luebbert CC, Bissonnette FS, Johnston MJW, Sauve S, Tam RY, Wang L, Rosu-Myles M, Lavoie JR. Hollow-fiber bioreactor production of extracellular vesicles from human bone marrow mesenchymal stromal cells yields nanovesicles that mirrors the immuno-modulatory antigenic signature of the producer cell. Stem Cell Res Ther, 2021, 12. ArticleID: 127

[15]

Cao JY, Wang B, Tang TT, Lv LL, Ding ZY, Li ZL, Hu RY, Wei Q, Shen AR, Fu YQ, Liu BC. Three-dimensional culture of MSCs produces exosomes with improved yield and enhanced therapeutic efficacy for cisplatin-induced acute kidney injury. Stem Cell Res Ther, 2020, 11. ArticleID: 206

[16]

Garcia SG, Sanroque-Munoz M, Clos-Sansalvador M, Font-Moron M, Monguio-Tortajada M, Borras FE, Franquesa M. Hollow fiber bioreactor allows sustained production of immortalized mesenchymal stromal cell-derived extracellular vesicles. Extracell Vesicles Circ Nucl Acids, 2024, 5. ArticleID: 201

[17]

Jakl V, Ehmele M, Winkelmann M, Ehrenberg S, Eiseler T, Friemert B, Rojewski MT, Schrezenmeier H. A novel approach for large-scale manufacturing of small extracellular vesicles from bone marrow-derived mesenchymal stromal cells using a hollow fiber bioreactor. Front Bioeng Biotechnol, 2023, 11. ArticleID: 1107055

[18]

Jeske R, Liu C, Duke L, Canonicco Castro ML, Muok L, Arthur P, Singh M, Jung S, Sun L, Li Y. Upscaling human mesenchymal stromal cell production in a novel vertical-wheel bioreactor enhances extracellular vesicle secretion and cargo profile. Bioact Mater, 2023, 25: 732

[19]

Ene J, Liu C, Syed F, Sun L, Berry D, Durairaj P, Liu ZL, Zeng CC, Jung S, Li Y. Biomanufacturing and lipidomics analysis of extracellular vesicles secreted by human blood vessel organoids in a vertical wheel bioreactor. Stem Cell Res Ther, 2025, 16. ArticleID: 207

[20]

Wu JG, Wu D, Wu GH, Bei HP, Li ZH, Xu H, Wang YM, Wu D, Liu H, Shi SY, Zhao C, Xu YB, He Y, Li J, Wang CY, Zhao X. Scale-out production of extracellular vesicles derived from natural killer cells via mechanical stimulation in a seesaw-motion bioreactor for cancer therapy. Biofabrication, 2022, 14. ArticleID: 045004

[21]

Huang HY, Xiao LF, Fang LC, Lei M, Liu ZB, Gao SJ, Lei QJ, Lei J, Wei RX, Lei YF, Xue LJ, Geng Z, Cai L, Yan FF. Static topographical cue combined with dynamic fluid stimulation enhances the macrophage extracellular vesicle yield and therapeutic potential for bone defects. ACS Nano, 2025, 19. ArticleID: 8667

[22]

Wang ZY, Maruyama K, Sakisaka Y, Suzuki S, Tada H, Suto M, Saito M, Yamada S, Nemoto E. Cyclic stretch force induces periodontal ligament cells to secrete exosomes that suppress IL-1β production through the inhibition of the NF-κB signaling pathway in macrophages. Front Immunol, 2019, 10. ArticleID: 1310

[23]

Dong LL, Song Y, Zhang YJ, Zhao WK, Wang CL, Lin HC, Al-Ani MK, Liu WQ, Xue RY, Yang L. Mechanical stretch induces osteogenesis through the alternative activation of macrophages. J Cell Physiol, 2021, 236. ArticleID: 6376

[24]

Liang W, Ding PB, Qian JY, Li G, Lu EH, Zhao ZM. Polarized M2 macrophages induced by mechanical stretching modulate bone regeneration of the craniofacial suture for midfacial hypoplasia treatment. Cell Tissue Res, 2021, 386. ArticleID: 585

[25]

Ballotta V, Driessen-Mol A, Bouten CVC, Baaijens FPT. Strain-dependent modulation of macrophage polarization within scaffolds. Biomaterials, 2014, 35. ArticleID: 4919

[26]

Wu J, Wang H, Sun T, Shi Q, Chen X, Qi YB, Tao S, Zhao JH, Liu DH. Force-controlled 3D mechanical stretching to enhance the exosome secretion of bone mesenchymal stem cells for bone repair. Bio-Des Manuf, 2025, 8. ArticleID: 442

[27]

Guex AG, Menzel U, Ladner Y, Armiento AR, Stoddart MJ. Mechanical stimulation of EV release from macrophages embedded in mineralized collagen hydrogels. Adv Healthc Mater, 2025, 14. ArticleID: e2500706

[28]

Humbert C, Cordier C, Drut I, Hamrick M, Wong J, Bellamy V, Flaire J, Bakshy K, Dingli F, Loew D, Larghero J, Fabreguettes JR, Menasche P, Renault NK, Churlaud G. GMP-compliant process for the manufacturing of an extracellular vesicles-enriched secretome product derived from cardiovascular progenitor cells suitable for a phase I clinical trial. J Extracell Vesicles, 2025, 14. ArticleID: e70145

[29]

Tieu A, Hu K, Gnyra C, Montroy J, Fergusson DA, Allan DS, Stewart DJ, Thebaud B, Lalu MM. Mesenchymal stromal cell extracellular vesicles as therapy for acute and chronic respiratory diseases: a meta-analysis. J Extracell Vesicles, 2021, 10. ArticleID: e12141

[30]

Kennedy KM, Bhaw-Luximon A, Jhurry D. Cell-matrix mechanical interaction in electrospun polymeric scaffolds for tissue engineering: implications for scaffold design and performance. Acta Biomater, 2017, 50. ArticleID: 41

[31]

Tang H, Wang XL, Qiu S, Wang YY, Zhang XN, Zhang YZ. Low-density electrospun fibrous network promotes mechanotransduction and matrix remodeling in fibroblasts. Biomater Adv, 2025, 174. ArticleID: 214316

[32]

Dalby MJ, Gadegaard N, Oreffo RO. Harnessing nanotopography and integrin-matrix interactions to influence stem cell fate. Nat Mater, 2014, 13. ArticleID: 558

[33]

Xiao LF, Liu HF, Huang HY, Wu SJ, Xue LJ, Geng Z, Cai L, Yan FF. 3D nanofiber scaffolds from 2D electrospun membranes boost cell penetration and positive host response for regenerative medicine. J Nanobiotechnol, 2024, 22. ArticleID: 322

[34]

Casajuana Ester M, Day RM. Production and utility of extracellular vesicles with 3D culture methods. Pharmaceutics, 2023, 15. ArticleID: 663

[35]

Cook K, Li H. Advancing extracellular vesicle production: improving physiological relevance and yield with 3D cell culture. Nanoscale, 2025, 17. ArticleID: 15110

[36]

Luo M, Zhao FK, Cheng H, Su M, Wang YM. Macrophage polarization: an important role in inflammatory diseases. Front Immunol, 2024, 15. ArticleID: 1352946

[37]

Murray PJ. Macrophage polarization. Annu Rev Physiol, 2017, 79. ArticleID: 541

[38]

Xu XJ, Xu PT, Shen GZ, Peng XS, Liu ZD, Chen CQ, Yu WH, Su ZP, Lin JJ, Zheng G, Ye GW, Wang P, Xie ZY, Wu YF, Shen HY, Li JT. Targeting macrophage polarization by inhibiting Pim2 alleviates inflammatory arthritis via metabolic reprogramming. Cell Mol Immunol, 2025, 22. ArticleID: 418

[39]

Khanmohammadi M, Mirzaalikhan Y, Baratchi S. Immunity in motion: the role of mechanics in macrophage biology. Cell Chem Biol, 2025, 32: 1442-1457.

[40]

Song LD. Effects of exercise or mechanical stimulation on bone development and bone repair. Stem Cells Int, 2022, 2022. ArticleID: 5372229

[41]

Lei JH, Xin ZJ, Liu N, Ning TX, Jing Y, Qiao YC, He Z, Jiang MM, Yang YH, Zhang ZY, Zhao LY, Li JY, Lv DL, Yan YP, Zhang H, Xiao LL, Zhang BH, Huang HY, Sun SH, Zheng FS, Jiang XY, Lu HF, Dong XD, Yue SS, Ma CC, Shuai JC, Ji ZJ, Liu FF, Ye YX, Yan KW, Hu QC, Xu G, Zhao Q, Wu RC, Cai YS, Fan YL, Jing YB, Wang QR, Reddy P, Lu XY, Zheng ZK, Liu BB, Haghani A, Ma S, Suzuki K, Esteban CR, Yang JY, Song MS, Horvath S, Zhang WQ, Li WL, Xiang AP, Zhu L, Fu XL, Zhao G, Belmonte JCI, Qu J, Wang S, Liu GH. Senescence-resistant human mesenchymal progenitor cells counter aging in primates. Cell, 2025, 188. ArticleID: 5039

[42]

Liu JT, Zhang J, Lin X, Boyce BF, Zhang HW, Xing LP. Age-associated callus senescent cells produce TGF-β1 that inhibits fracture healing in aged mice. J Clin Invest, 2022, 132. ArticleID: e148073

[43]

Chen SQ, Yu YM, Xie SQ, Liang DN, Shi W, Chen SZ, Li GL, Tang W, Liu CS, He QJ. Local H2 release remodels senescence microenvironment for improved repair of injured bone. Nat Commun, 2023, 14. ArticleID: 7783

[44]

Wu HT, Zhang Q, Zhu JH, Wu LH, Xiao Y, Yang XC. Biomaterials targeting senescent cells for bone regeneration: state-of-the-art and future perspectives. Bioact Mater, 2025, 54: 686

[45]

Brunet A, Goodell MA, Rando TA. Ageing and rejuvenation of tissue stem cells and their niches. Nat Rev Mol Cell Biol, 2023, 24. ArticleID: 45

[46]

Thompson W, Papoutsakis ET. The role of biomechanical stress in extracellular vesicle formation, composition and activity. Biotechnol Adv, 2023, 66. ArticleID: 108158

[47]

Park H, Seo YK, Arai Y, Lee SH. Physicochemical modulation strategies for mass production of extracellular vesicle. Tissue Eng Regen Med, 2025, 22. ArticleID: 569

[48]

Bai CM, Ren HF, Zhang F, Li DD, Feng QY, Li Y, Chen T, Li CX, Xiao X, Zhang HR, Hu L. Normal stress on surface of mesenchymal stem cells boosts extracellular vesicle secretion and regenerative bioactivity. J Nanobiotechnol, 2025, 23. ArticleID: 476

[49]

Cai GH, Lu YH, Zhong WJ, Wang T, Li YY, Ruan XL, Chen HY, Sun L, Guan ZL, Li G, Zhang HW, Sun W, Chen ML, Zhang WB, Wang H. Piezo1-mediated M2 macrophage mechanotransduction enhances bone formation through secretion and activation of transforming growth factor-β1. Cell Prolif, 2023, 56. ArticleID: e13440

[50]

Tang Y, Zhao CX, Zhuang Y, Zhong AJ, Wang M, Zhang W, Zhu LQ. Mechanosensitive Piezo1 protein as a novel regulator in macrophages and macrophage-mediated inflammatory diseases. Front Immunol, 2023, 14. ArticleID: 1149336

[51]

Sun Z, Guo SS, Fässler R. Integrin-mediated mechanotransduction. J Cell Biol, 2016, 215. ArticleID: 445

[52]

Whitney NP, Lamb AC, Louw TM, Subramanian A. Integrin-mediated mechanotransduction pathway of low-intensity continuous ultrasound in human chondrocytes. Ultrasound Med Biol, 2012, 38. ArticleID: 1734

[53]

Panciera T, Azzolin L, Cordenonsi M, Piccolo S. Mechanobiology of YAP and TAZ in physiology and disease. Nat Rev Mol Cell Biol, 2017, 18: 758.

[54]

Aragona M, Panciera T, Manfrin A, Giulitti S, Michielin F, Elvassore N, Dupont S, Piccolo S. A mechanical checkpoint controls multicellular growth through YAP/TAZ regulation by actin-processing factors. Cell, 2013, 154: 1047.

[55]

Totaro A, Panciera T, Piccolo S. YAP/TAZ upstream signals and downstream responses. Nat Cell Biol, 2018, 20: 888.

[56]

Puhm F, Afonyushkin T, Resch U, Obermayer G, Rohde M, Penz T, Schuster M, Wagner G, Rendeiro AF, Melki I, Kaun C, Wojta J, Bock C, Jilma B, Mackman N, Boilard E, Binder CJ. Mitochondria are a subset of extracellular vesicles released by activated monocytes and induce type I IFN and TNF responses in endothelial cells. Circ Res, 2019, 125: 43.

[57]

Lenzini S, Bargi R, Chung G, Shin JW. Matrix mechanics and water permeation regulate extracellular vesicle transport. Nat Nanotechnol, 2020, 15: 217.

[58]

Zhou TF, Gao B, Fan Y, Liu YC, Feng SH, Cong Q, Zhang XL, Zhou YX, Yadav PS, Lin JC, Wu N, Zhao L, Huang DS, Zhou SH, Su PQ, Yang YZ. Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-β-catenin. Elife, 2020, 9. ArticleID: e52779

[59]

Chen JX, Zhao Y, Ruan RJ, Feng X, Niu ZX, Pan L, Xia C, Gu QH, Feng W, Zhao LY, Fan Y, Lai FY, Zhao CC, Wang J, Zhang J, Sun Y. Bone morphogenetic protein-2-derived peptide-conjugated nanozyme-integrated photoenhanced hybrid hydrogel for cascade-regulated bone regeneration. ACS Nano, 2025, 19: 14707.

[60]

Lin HR, Jin XM, Cao Y, Ruan RJ, Liu CH, Huang SD, Xu J, Ding JX, Yang HH, Zhang J. Self-adaptive hydrogel with cascade microenvironments-responsiveness to inhibit osteosarcoma progression and augment bone reconstruction. Adv Funct Mater, 2025, 35: 2421470.

[61]

Al-Sharabi N, Mohamed-Ahmed S, Shanbhag S, Kampleitner C, Elnour R, Yamada S, Rana N, Birkeland E, Tangl S, Gruber R, Mustafa K. Osteogenic human MSC-derived extracellular vesicles regulate MSC activity and osteogenic differentiation and promote bone regeneration in a rat calvarial defect model. Stem Cell Res Ther, 2024, 15: 33.

[62]

Jiao Y, Liu YT, Du J, Xu JJ, Luo ZH, Liu Y, Guo LJ. Advances in the study of extracellular vesicles for bone regeneration. Int J Mol Sci, 2024, 25: 3480.

[63]

Rodriguez-Carballo E, Gamez B, Ventura F. p38 MAPK signaling in osteoblast differentiation. Front Cell Dev Biol, 2016, 4. ArticleID: 40

[64]

Lanna A, Henson SM, Escors D, Akbar AN. The kinase p38 activated by the metabolic regulator AMPK and scaffold TAB1 drives the senescence of human T cells. Nat Immunol, 2017, 18. ArticleID: 354

[65]

Wu ZB, Li WM, Jiang KL, Lin ZX, Qian C, Wu MZ, Xia Y, Li N, Zhang HT, Xiao HX, Bai JX, Geng DC. Regulation of bone homeostasis: signaling pathways and therapeutic targets. MedComm (2020), 2024, 5. ArticleID: e657

[66]

Li SQ, Cai XJ, Guo JH, Li XL, Li W, Liu Y, Qi MC. Cell communication and relevant signaling pathways in osteogenesis-angiogenesis coupling. Bone Res, 2025, 13. ArticleID: 45

[67]

Zhang J, Li FL, Gao X, Qiu WQ, Xia B, He SX, Zhang YF, Huang X, Liu B, Huang JH, Ding JX, Yang HH. Bamboo-inspired composite conduit accelerates peripheral nerve regeneration through synergistic oriented structure and piezoelectricity. Adv Mater, 2026, 38. ArticleID: e09425

[68]

Kumar MA, Baba SK, Sadida HQ, Marzooqi SA, Jerobin J, Altemani FH, Algehainy N, Alanazi MA, Abou-Samra AB, Kumar R, Akil ASA, Macha MA, Mir R, Bhat AA. Extracellular vesicles as tools and targets in therapy for diseases. Signal Transduct Target Ther, 2024, 9. ArticleID: 27

Funding

Fundamental Research Funds for Central Universities of the Central South University(2042022kf1121)

Innovative Research Group Project of the National Natural Science Foundation of China(32571566)

the National Natural Science Foundation of China(32371412)

Zhejiang Provincial Natural Science Foundation of China(LY24C100001)

Central Guidance on Local Science and Technology Development Fund of Zhejiang Province(2024ZY01033)

the National Natural Science Foundation of Chin(81472065)

Key R&D Project of Zhejiang Provincial Department of Science and Technology(2025C02164)

RIGHTS & PERMISSIONS

Donghua University, Shanghai, China

PDF

0

Accesses

0

Citation

Detail

Sections
Recommended

/