3D printed 2D materials for tissue engineering applications

Muhammad Bagas Ananda , Maradhana Agung Marsudi , Indra Jaya Budiarso , Akfiny Hasdi Aimon , Ferry Iskandar , Cian Vyas , Glen Cooper , Paulo J.D.S. Bartolo , Arie Wibowo

ChemPhysMater ›› 2025, Vol. 4 ›› Issue (3) : 251 -273.

PDF (4224KB)
ChemPhysMater ›› 2025, Vol. 4 ›› Issue (3) :251 -273. DOI: 10.1016/j.chphma.2024.12.004
Review Article
research-article
3D printed 2D materials for tissue engineering applications
Author information +
History +
PDF (4224KB)

Abstract

The field of tissue engineering has witnessed significant progress with the emergence of three-dimensional (3D) printing technologies. The ability to fabricate precise structures with complex geometries combined with the integration of two-dimensional (2D) materials, including graphene, graphene oxide, and transition metal dichalcogenides, has provided novel opportunities. This integration enables the fabrication of functional structures with tailored properties, leveraging the exceptional mechanical, electrical, and chemical characteristics of these materials, in conjunction with the design flexibility offered by 3D printing. Herein, we review the recent advancements in the selection of appropriate 2D materials, diverse 3D printing methods employed for integration, and characterization techniques used to evaluate the performance of the resulting constructs. The successful integration of 3D printing and 2D materials holds immense potential for advancing tissue engineering and paving the way for personalized medicine, regenerative therapies, and point-of-care diagnostics.

Keywords

3D printing / 2D materials / Biomaterials / Tissue engineering / Scaffold

Cite this article

Download citation ▾
Muhammad Bagas Ananda, Maradhana Agung Marsudi, Indra Jaya Budiarso, Akfiny Hasdi Aimon, Ferry Iskandar, Cian Vyas, Glen Cooper, Paulo J.D.S. Bartolo, Arie Wibowo. 3D printed 2D materials for tissue engineering applications. ChemPhysMater, 2025, 4 (3) : 251-273 DOI:10.1016/j.chphma.2024.12.004

登录浏览全文

4963

注册一个新账户 忘记密码

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

CRediT authorship contribution statement

Muhammad Bagas Ananda: Writing – review & editing, Writing – original draft, Methodology. Maradhana Agung Marsudi: Writing – original draft, Methodology. Indra Jaya Budiarso: Writing – original draft, Methodology. Akfiny Hasdi Aimon: Writing – review & editing, Methodology. Ferry Iskandar: Writing – review & editing, Methodology. Cian Vyas: Writing – review & editing, Methodology, Conceptualization. Glen Cooper: Writing – review & editing, Methodology, Conceptualization. Paulo J.D.S. Bartolo: Writing – review & editing, Conceptualization. Arie Wibowo: Writing – review & editing, Supervision, Resources, Project administration, Methodology, Funding acquisition, Conceptualization.

Acknowledgement

The authors acknowledge the ITB Research Fund 2023 scheme of the Institut Teknologi Bandung (PN-6-02-2023).

References

[1]

G.L. Koons, M. Diba, A.G. Mikos, Materials design for bone-tissue engineering, Nat. Rev. Mater. 5 (2020) 584-603, doi: 10.1038/s41578-020-0204-2.

[2]

N. Rohaizad, C.C. Mayorga-Martinez, M. Fojtů, N.M. Latiff, M. Pumera, Two-dimensional materials in biomedical, biosensing and sensing applications, Chem. Soc. Rev. 50 (2021) 619-657, doi: 10.1039/D0CS00150C.

[3]

W. Zhu, X. Ma, M. Gou, D. Mei, K. Zhang, S. Chen, 3D printing of functional biomaterials for tissue engineering, Curr. Opin. Biotechnol. 40 (2016) 103-112, doi: 10.1016/j.copbio.2016.03.014.

[4]

N. Shahrubudin, T.C. Lee, R. Ramlan, An overview on 3D printing technology: Technological, materials, and applications, Procedia Manuf. 35 (2019) 1286-1296, doi: 10.1016/j.promfg.2019.06.089.

[5]

P.F. Egan, Integrated design approaches for 3D printed tissue scaffolds: Review and outlook, Materials 12 (2019) 2355, doi: 10.3390/ma12152355.

[6]

C. Wang, W. Huang, Y. Zhou, L. He, Z. He, Z. Chen, X. He, S. Tian, J. Liao, B. Lu, 3D printing of bone tissue engineering scaffolds, Bioact. Mater. 5 (2020) 82-91, doi: 10.1016/j.bioactmat.2020.01.004.

[7]

T. Marew, G. Birhanu, Three dimensional printed nanostructure biomaterials for bone tissue engineering, Regener. Ther. 18 (2021) 102-111, doi: 10.1016/j.reth.2021.05.001.

[8]

M. Das, R.S. Ambekar, S.K. Panda, S. Chakraborty, C.S. Tiwary, 2D nanomaterials in 3D/4D-printed biomedical devices, J. Mater. Res. 36 (2021) 4024-4050, doi: 10.1557/s43578-021-00287-2.

[9]

P.K. Chakraborty, J. Azadmanjiri, C.L.P. Pavithra, X. Wang, S.H. Masood, S.R. Dey, J. Wang, Advancements in therapeutics via 3D printed multifunctional architectures from dispersed 2D nanomaterial inks, Small 16 (2020) 2004900, doi: 10.1002/smll.202004900.

[10]

N.Z. Laird, T.M. Acri, J.L. Chakka, J.C. Quarterman, W.I. Malkawi, S. Elangovan, A.K. Salem, Applications of nanotechnology in 3D printed tissue engineering scaffolds, Eur. J. Pharm. Biopharm. 161 (2021) 15-28, doi: 10.1016/j.ejpb.2021.01.018.

[11]

K.S. Novoselov, A.K. Geim, S.V. Morozov, D. Jiang, Y. Zhang, S.V. Dubonos, I.V. Grigorieva, A.A. Firsov, Electric field effect in atomically thin carbon films, Science 306 (2004) 666-669, doi: 10.1126/science.1102896.

[12]

C. Chung, Y.K. Kim, D. Shin, S.R. Ryoo, B.H. Hong, D.H. Min, Biomedical applications of graphene and graphene oxide, Acc. Chem. Res. 46 (2013) 2211-2224, doi: 10.1021/ar300159f.

[13]

B. Deng, Z. Liu, H. Peng, Toward mass production of CVD graphene films, Adv. Mater. 31 (2019) 1800996, doi: 10.1002/adma.201800996.

[14]

W.C.Lee Kenry, K.P. Loh, C.T. Lim, When stem cells meet graphene: Opportunities and challenges in regenerative medicine, Biomaterials 155 (2018) 236-250, doi: 10.1016/j.biomaterials.2017.10.004.

[15]

H.P. Bei, Y. Yang, Q. Zhang, Y. Tian, X. Luo, M. Yang, X. Zhao, Graphene-based nanocomposites for neural tissue engineering, Molecules 24 (2019) 658, doi: 10.3390/molecules24040658.

[16]

A. Sharma, S. Gupta, T. Sampathkumar, R.S. Verma, Modified graphene oxide nanoplates reinforced 3D printed multifunctional scaffold for bone tissue engineering, Biomater. Adv. 134 (2022) 112587, doi: 10.1016/j.msec.2021.112587.

[17]

A. Ivanoska-Dacikj, G. Bogoeva-Gaceva, A. Krumme, E. Tarasova, C. Scalera, V. Stojkovski, I. Gjorgoski, T. Ristoski, Biodegradable polyurethane/graphene oxide scaffolds for soft tissue engineering: In vivo behavior assessment, Int. J. Polym. Mater. Polym. Biomater. 69 (2020) 1101-1111, doi: 10.1080/00914037.2019.1655754.

[18]

G. Liao, F. He, Q. Li, L. Zhong, R. Zhao, H. Che, H. Gao, B. Fang, Emerging graphitic carbon nitride-based materials for biomedical applications, Prog. Mater Sci. 112 (2020) 100666, doi: 10.1016/j.pmatsci.2020.100666.

[19]

X. Kong, X. Liu, Y. Zheng, P.K. Chu, Y. Zhang, S. Wu, Graphitic carbon nitride-based materials for photocatalytic antibacterial application, Mater. Sci. Eng.: R: Rep. 145 (2021) 100610, doi: 10.1016/j.mser.2021.100610.

[20]

J.A.S. Syed, X.Y. Zhang, W.J. Ding, A.D. Li, An overview of the current progress of graphitic carbon nitride and its multifunctional applications, J. Environ. Chem. Eng. 10 (2022) 108745, doi: 10.1016/j.jece.2022.108745.

[21]

A.A. Sadek, M. Abd-Elkareem, H.N. Abdelhamid, S. Moustafa, K. Hussein, Repair of critical-sized bone defects in rabbit femurs using graphitic carbon nitride (g-C3N4) and graphene oxide (GO) nanomaterials , Sci. Rep. 13 (2023) 5404, doi: 10.1038/s41598-023-32487-7.

[22]

M. Zhang, Q. Wang, Y. Xu, L. Guo, Z. Lai, Z. Li, Graphitic carbon nitride quantum dots as analytical probe for viewing sialic acid on the surface of cells and tissues, Anal. Chim. Acta 1095 (2020) 204-211, doi: 10.1016/j.aca.2019.10.031.

[23]

M. Ahmadi, O. Zabihi, S. Jeon, M. Yoonessi, A. Dasari, S. Ramakrishna, M. Naebe, 2D transition metal dichalcogenide nanomaterials: Advances, opportunities, and challenges in multi-functional polymer nanocomposites, J. Mater. Chem. A 8 (2020) 845-883, doi: 10.1039/C9TA10130F.

[24]

M. Srivastava, S. Banerjee, S. Bairagi, P. Singh, B. Kumar, P. Singh, R.D. Kale, D.M. Mulvihill, S.W. Ali, Recent progress in molybdenum disulfide (MoS2) based flexible nanogenerators: An inclusive review , Chem. Eng. J. 480 (2024) 147963, doi: 10.1016/j.cej.2023.147963.

[25]

F.G. Aras, A. Yilmaz, H.G. Tasdelen, A. Ozden, F. Ay, N.K. Perkgoz, A. Yeltik, A review on recent advances of chemical vapor deposition technique for monolayer transition metal dichalcogenides (MX2: Mo, W; S, Se, Te) , Mater. Sci. Semicond. Process. 148 (2022) 106829, doi: 10.1016/j.mssp.2022.106829.

[26]

G.P. Awasthi, V.K. Kaliannagounder, B. Maharjan, J.Y. Lee, C.H. Park, C.S. Kim, Albumin-induced exfoliation of molybdenum disulfide nanosheets incorporated polycaprolactone/zein composite nanofibers for bone tissue regeneration, Mater. Sci. Eng. C 116 (2020) 111162, doi: 10.1016/j.msec.2020.111162.

[27]

X. Wang, T. Li, H. Ma, D. Zhai, C. Jiang, J. Chang, J. Wang, C. Wu, A 3D-printed scaffold with MoS2 nanosheets for tumor therapy and tissue regeneration , NPG Asia Mater. 9 (2017) e376, doi: 10.1038/am.2017.47.

[28]

Y.W. Chen, M.Y. Shie, C.H. Hsiao, Y.C. Liang, B. Wang, I.W.P. Chen, Synthesis of high-quality monolayer tungsten disulfide with chlorophylls and its application for enhancing bone regeneration, npj 2D Mater. Appl. 4 (2020) 34, doi: 10.1038/s41699-020-00168-y.

[29]

J.K. Carrow, K.A. Singh, M.K. Jaiswal, A. Ramirez, G. Lokhande, A.T. Yeh, T.R. Sarkar, I. Singh, A.K. Gaharwar, Photothermal modulation of human stem cells using light-responsive 2D nanomaterials, Proc. Natl. Acad. Sci. U.S.A. 117 (2020) 13329-13338, doi: 10.1073/pnas.1914345117.

[30]

S. Anju, J. Ashtami, P. Mohanan, Black phosphorus, a prospective graphene substitute for biomedical applications, Mater. Sci. Eng. C 97 (2019) 978-993, doi: 10.1016/j.msec.2018.12.146.

[31]

X. Ge, Z. Xia, S. Guo, Recent advances on black phosphorus for biomedicine and biosensing, Adv. Funct. Mater. 29 (2019) 1900318, doi: 10.1002/adfm.201900318.

[32]

Q. Weng, X. Huang, Y. Chen, L. Zhang, D. Xie, X. Sheng, Black phosphorus nanosheets for advanced polymer coatings and films: Preparation, stability and applications, J. Mater. Sci. Technol. 216 (2025) 192-208, doi: 10.1016/j.jmst.2024.08.002.

[33]

Z. Li, X. Zhang, J. Ouyang, D. Chu, F. Han, L. Shi, R. Liu, Z. Guo, G.X. Gu, W. Tao, Ca2+-supplying black phosphorus-based scaffolds fabricated with microfluidic technology for osteogenesis , Bioact. Mater. 6 (2021) 4053-4064, doi: 10.1016/j.bioactmat.2021.04.014.

[34]

Y.a. Qing, R. Li, S. Li, Y. Li, X. Wang, Y. Qin, Advanced black phosphorus nanomaterials for bone regeneration, Int. J. Nanomed. 15 (2020) 2045-2058, doi: 10.2147/IJN.S246336.

[35]

Y. Xu, C. Xu, L. He, J. Zhou, T. Chen, L. Ouyang, X. Guo, Y. Qu, Z. Luo, D. Duan, Stratified-structural hydrogel incorporated with magnesium-ion-modified black phosphorus nanosheets for promoting neuro-vascularized bone regeneration, Bioact. Mater. 16 (2022) 271-284, doi: 10.1016/j.bioactmat.2022.02.024.

[36]

X. Liu, B. Gaihre, S. Park, L. Li, B. Dashtdar, M.D.A. Potes, A. Terzic, B.D. Elder, L. Lu, 3D-printed scaffolds with 2D hetero-nanostructures and immunomodulatory cytokines provide pro-healing microenvironment for enhanced bone regeneration, Bioact. Mater. 27 (2023) 216-230, doi: 10.1016/j.bioactmat.2023.03.021.

[37]

C. Xue, L. Sutrisno, M. Li, W. Zhu, Y. Fei, C. Liu, X. Wang, K. Cai, Y. Hu, Z. Luo, Implantable multifunctional black phosphorus nanoformulation-deposited biodegradable scaffold for combinational photothermal/chemotherapy and wound healing, Biomaterials 269 (2021) 120623, doi: 10.1016/j.biomaterials.2020.120623.

[38]

W. Li, S. Li, J. Zhang, H. Zhong, J. Liang, S. Huang, G. Liao, B. Zhang, C. Liu, Fabrication and evaluation of bone morphogenetic protein-2 microspheres coated black phosphorus nanosheets@ polylactic-glycolic acid copolymers scaffold: A multifunctional antibacterial photothermal scaffold for bone regeneration, Int. J. Biol. Macromol. 210 (2022) 350-364, doi: 10.1016/j.ijbiomac.2022.05.028.

[39]

Y. Li, H. Shao, Z. Lin, J. Lu, L. Liu, B. Duployer, P.O. Persson, P. Eklund, L. Hultman, M. Li, A general Lewis acidic etching route for preparing MXenes with enhanced electrochemical performance in non-aqueous electrolyte, Nat. Mater. 19 (2020) 894-899, doi: 10.1038/s41563-020-0657-0.

[40]

L. Mao, S. Hu, Y. Gao, L. Wang, W. Zhao, L. Fu, H. Cheng, L. Xia, S. Xie, W. Ye, Biodegradable and electroactive regenerated bacterial cellulose/MXene (Ti3C2Tx) composite hydrogel as wound dressing for accelerating skin wound healing under electrical stimulation , Adv. Healthc. Mater. 9 (2020) 2000872, doi: 10.1002/adhm.202000872.

[41]

J. Yin, Q. Han, J. Zhang, Y. Liu, X. Gan, K. Xie, L. Xie, Y. Deng, MXene-based hydrogels endow polyetheretherketone with effective osteogenicity and combined treatment of osteosarcoma and bacterial infection, ACS Appl. Mater. Interfaces 12 (2020) 45891-45903, doi: 10.1021/acsami.0c14752.

[42]

X. Mi, Z. Su, Y. Fu, S. Li, A. Mo, 3D printing of Ti3C2-MXene-incorporated composite scaffolds for accelerated bone regeneration , Biomed. Mater. 17 (2022) 035002, doi: 10.1088/1748-605X/ac5ffe.

[43]

S. Pan, J. Yin, L. Yu, C. Zhang, Y. Zhu, Y. Gao, Y. Chen, 2D MXene-integrated 3D-printing scaffolds for augmented osteosarcoma phototherapy and accelerated tissue reconstruction, Adv. Sci. 7 (2020) 1901511, doi: 10.1002/advs.201901511.

[44]

A. Merlo, V. Mokkapati, S. Pandit, I. Mijakovic, Boron nitride nanomaterials: Biocompatibility and bio-applications, Biomater. Sci. 6 (2018) 2298-2311, doi: 10.1039/C8BM00516H.

[45]

A.E. Naclerio, P.R. Kidambi, A review of scalable hexagonal boron nitride (h-BN) synthesis for present and future applications, Adv. Mater. 35 (2023) 2207374, doi: 10.1002/adma.202207374.

[46]

Y. Qian, Y. Xu, Z. Yan, Y. Jin, X. Chen, W.-E. Yuan, C. Fan, Boron nitride nanosheets functionalized channel scaffold favors microenvironment rebalance cocktail therapy for piezocatalytic neuronal repair, Nano Energy 83 (2021) 105779, doi: 10.1016/j.nanoen.2021.105779.

[47]

J. Yang, Y.W. Yang, Metal-organic frameworks for biomedical applications, Small 16 (2020) 1906846, doi: 10.1002/smll.201906846.

[48]

G. Qian, Y. Mao, Y. Shuai, Z. Zeng, S. Peng, C. Shuai, Enhancing bone scaffold interfacial reinforcement through in situ growth of metal-organic frameworks (MOFs) on strontium carbonate: Achieving high strength and osteoimmunomodulation, J. Colloid Interface Sci. 655 (2024) 43-57, doi: 10.1016/j.jcis.2023.10.133.

[49]

Y. You, C. Yang, X. Zhang, H. Lin, J. Shi, Emerging two-dimensional silicene nanosheets for biomedical applications, Mater. Today Nano 16 (2021) 100132, doi: 10.1016/j.mtnano.2021.100132.

[50]

N. Ni, M. Ge, R. Huang, D. Zhang, H. Lin, Y. Ju, Z. Tang, H. Gao, H. Zhou, Y. Chen, Thermodynamic 2D silicene for sequential and multistage bone regeneration, Adv. Healthc. Mater. 12 (2023) 2203107, doi: 10.1002/adhm.202203107.

[51]

W. Zheng, L.Y.S. Lee, Beyond sonication: Advanced exfoliation methods for scalable production of 2D materials, Matter 5 (2022) 515-545, doi: 10.1016/j.matt.2021.12.010.

[52]

M.A. Marsudi, R.T. Ariski, A. Wibowo, G. Cooper, A. Barlian, R. Rachmantyo, P.J. Bartolo, Conductive polymeric-based electroactive scaffolds for tissue engineering applications: Current progress and challenges from biomaterials and manufacturing perspectives, Int. J. Mol. Sci. 22 (2021) 11543, doi: 10.3390/ijms222111543.

[53]

N. Nagarajan, A. Dupret-Bories, E. Karabulut, P. Zorlutuna, N.E. Vrana, Enabling personalized implant and controllable biosystem development through 3D printing, Biotechnol. Adv. 36 (2018) 521-533, doi: 10.1016/j.biotechadv.2018.02.004.

[54]

T. Kreller, T. Distler, S. Heid, S. Gerth, R. Detsch, A. Boccaccini, Physico-chemical modification of gelatine for the improvement of 3D printability of oxidized alginate-gelatine hydrogels towards cartilage tissue engineering, Mater. Des. 208 (2021) 109877, doi: 10.1016/j.matdes.2021.109877.

[55]

P. Szymczyk-Ziółkowska, M.B. Łabowska, J. Detyna, I. Michalak, P. Gruber, A review of fabrication polymer scaffolds for biomedical applications using additive manufacturing techniques, Biocybern. Biomed. Eng. 40 (2020) 624-638, doi: 10.1016/j.bbe.2020.01.015.

[56]

X. Mu, T. Bertron, C. Dunn, H. Qiao, J. Wu, Z. Zhao, C. Saldana, H.J. Qi, Porous polymeric materials by 3D printing of photocurable resin, Mater. Horiz. 4 (2017) 442-449, doi: 10.1039/C7MH00084G.

[57]

K. Hassan, M.J. Nine, T.T. Tung, N. Stanley, P.L. Yap, H. Rastin, L. Yu, D. Losic, Functional inks and extrusion-based 3D printing of 2D materials: A review of current research and applications, Nanoscale 12 (2020) 19007-19042, doi: 10.1039/D0NR04933F.

[58]

A.P.M. Madrid, S.M. Vrech, M.A. Sanchez, A.P. Rodriguez, Advances in additive manufacturing for bone tissue engineering scaffolds, Mater. Sci. Eng. C 100 (2019) 631-644, doi: 10.1016/j.msec.2019.03.037.

[59]

D.G. O’Shea, C.M. Curtin, F.J. O’Brien, Articulation inspired by nature: A review of biomimetic and biologically active 3D printed scaffolds for cartilage tissue engineering, Biomater. Sci. 10 (2022) 2462-2483, doi: 10.1039/D1BM01540K.

[60]

S. Bom, A.M. Martins, H.M. Ribeiro, J. Marto, Diving into 3D (bio) printing: A revolutionary tool to customize the production of drug and cell-based systems for skin delivery, Int. J. Pharm. 605 (2021) 120794, doi: 10.1016/j.ijpharm.2021.120794.

[61]

K. Liu, L. Yan, R. Li, Z. Song, J. Ding, B. Liu, X. Chen, 3D printed personalized nerve guide conduits for precision repair of peripheral nerve defects, Adv. Sci. 9 (2022) 2103875, doi: 10.1002/advs.202103875.

[62]

Z. Jiang, B. Diggle, M.L. Tan, J. Viktorova, C.W. Bennett, L.A. Connal, Extrusion 3D printing of polymeric materials with advanced properties, Adv. Sci. 7 (2020) 2001379, doi: 10.1002/advs.202001379.

[63]

J.K. Placone, A.J. Engler, Recent advances in extrusion-based 3D printing for biomedical applications, Adv. Healthc. Mater. 7 (2018) 1701161, doi: 10.1002/adhm.201701161.

[64]

N. Bhattacharjee, A. Urrios, S. Kang, A. Folch, The upcoming 3D-printing revolution in microfluidics, Lab. Chip 16 (2016) 1720-1742, doi: 10.1039/C6LC00163G.

[65]

W. Liao, X. Duan, F. Xie, D. Zheng, P. Yang, X. Wang, Z. Hu, 3D-bioprinted double-crosslinked angiogenic alginate/chondroitin sulfate patch for diabetic wound healing, Int. J. Biol. Macromol. 236 (2023) 123952, doi: 10.1016/j.ijbiomac.2023.123952.

[66]

Z. Bashiri, M.R. Fomeshi, H.G. Hamidabadi, D. Jafari, S. Alizadeh, M.N. Bojnordi, G. Orive, A. Dolatshahi-Pirouz, M. Zahiri, R.L. Reis, 3D-printed placental-derived bioinks for skin tissue regeneration with improved angiogenesis and wound healing properties, Mater. Today Bio. 20 (2023) 100666, doi: 10.1016/j.mtbio.2023.100666.

[67]

A.E. Jakus, E.B. Secor, A.L. Rutz, S.W. Jordan, M.C. Hersam, R.N. Shah, Three-dimensional printing of high-content graphene scaffolds for electronic and biomedical applications, ACS Nano 9 (2015) 4636-4648, doi: 10.1021/acsnano.5b01179.

[68]

Q. Shi, K. Yu, X. Kuang, X. Mu, C.K. Dunn, M.L. Dunn, T. Wang, H.J. Qi, Recyclable 3D printing of vitrimer epoxy, Mater. Horiz. 4 (2017) 598-607, doi: 10.1039/C7MH00043J.

[69]

C.B. Highley, C.B. Rodell, J.A. Burdick, Direct 3D printing of shear-thinning hydrogels into self-healing hydrogels, Adv. Mater. 27 (2015) 5075-5079, doi: 10.1002/adma.201501234.

[70]

H. Lee, S. Ahn, L.J. Bonassar, G. Kim, Cell (MC3T3-E1)-printed poly (𝜖-caprolactone)/alginate hybrid scaffolds for tissue regeneration , Macromol. Rapid Commun. 34 (2013) 142-149, doi: 10.1002/marc.201200524.

[71]

A.A. Aldana, F. Valente, R. Dilley, B. Doyle, Development of 3D bioprinted GelMA-alginate hydrogels with tunable mechanical properties, Bioprinting 21 (2021) e00105, doi: 10.1016/j.bprint.2020.e00105.

[72]

N.A. Sather, H. Sai, I.R. Sasselli, K. Sato, W. Ji, C.V. Synatschke, R.T. Zambrotta, J.F. Edelbrock, R.R. Kohlmeyer, J.O. Hardin, 3D printing of supramolecular polymer hydrogels with hierarchical structure, Small 17 (2021) 2005743, doi: 10.1002/smll.202005743.

[73]

B. Rankouhi, S. Javadpour, F. Delfanian, T. Letcher, Failure analysis and mechanical characterization of 3D printed ABS with respect to layer thickness and orientation, J. Fail. Anal. Prev. 16 (2016) 467-481, doi: 10.1007/s11668-016-0113-2.

[74]

R.F. Pereira, B.N. Lourenço, P.J. Bártolo, P.L. Granja, Bioprinting a multifunctional bioink to engineer clickable 3D cellular niches with tunable matrix microenvironmental cues, Adv. Healthc. Mater. 10 (2021) 2001176, doi: 10.1002/adhm.202001176.

[75]

T. Guo, T.R. Holzberg, C.G. Lim, F. Gao, A. Gargava, J.E. Trachtenberg, A.G. Mikos, J.P. Fisher, 3D printing PLGA: A quantitative examination of the effects of polymer composition and printing parameters on print resolution, Biofabrication 9 (2017) 024101, doi: 10.1088/1758-5090/aa6370.

[76]

S. Balasubramanian, M.E. Aubin-Tam, A.S. Meyer, 3D printing for the fabrication of biofilm-based functional living materials, ACS Synth. Biol. 8 (2019) 1564-1567, doi: 10.1021/acssynbio.9b00192.

[77]

Z. Bashiri, M. Gholipourmalekabadi, R. Falak, I. Amiri, H. Asgari, N.P.S. Chauhan, M. Koruji, In vitro production of mouse morphological sperm in artificial testis bioengineered by 3D printing of extracellular matrix, Int. J. Biol. Macromol. 217 (2022) 824-841, doi: 10.1016/j.ijbiomac.2022.07.127.

[78]

C. Yu, J. Schimelman, P. Wang, K.L. Miller, X. Ma, S. You, J. Guan, B. Sun, W. Zhu, S. Chen, Photopolymerizable biomaterials and light-based 3D printing strategies for biomedical applications, Chem. Rev. 120 (2020) 10695-10743, doi: 10.1021/acs.chemrev.9b00810.

[79]

S.R. Shin, B. Aghaei-Ghareh-Bolagh, T.T. Dang, S.N. Topkaya, X. Gao, S.Y. Yang, S.M. Jung, J.H. Oh, M.R. Dokmeci, X. Tang, Cell-laden microengineered and mechanically tunable hybrid hydrogels of gelatin and graphene oxide, Adv. Mater. 25 (2013) 6385-6391, doi: 10.1002/adma.201301082.

[80]

J. Zhang, Q. Hu, S. Wang, J. Tao, M. Gou, Digital light processing based three-dimensional printing for medical applications, Int. J. Bioprint. 6 (2019) 242, doi: 10.18063/ijb.v6i1.242.

[81]

P. Soman, P.H. Chung, A.P. Zhang, S. Chen, Digital microfabrication of user-defined 3D microstructures in cell-laden hydrogels, Biotechnol. Bioeng. 110 (2013) 3038-3047, doi: 10.1002/bit.24957.

[82]

C. Shuai, X. Yuan, W. Yang, S. Peng, G. Qian, Z. Zhao, Synthesis of a mace-like cellulose nanocrystal@Ag nanosystem via in-situ growth for antibacterial activities of poly-L-lactide scaffold, Carbohydr. Polym. 262 (2021) 117937, doi: 10.1016/j.carbpol.2021.117937.

[83]

W. Yang, C. Zhou, C. He, Y. Yang, W. Aiyiti, L. Xu, C. Shuai, Defect engineering synergistically boosts the catalytic activity of Fe-MoOv for highly efficient breast mesh antitumor therapy , J. Colloid Interface Sci. 678 (2025) 260-271, doi: 10.1016/j.jcis.2024.08.195.

[84]

A. Mazzoli, Selective laser sintering in biomedical engineering, Med. Biol. Eng. Comput. 51 (2013) 245-256, doi: 10.1007/s11517-012-1001-x.

[85]

X. Yuan, W. Zhu, Z. Yang, N. He, F. Chen, X. Han, K. Zhou, Recent advances in 3D printing of smart scaffolds for bone tissue engineering and regeneration, Adv. Mater. 36 (2024) 2403641, doi: 10.1002/adma.202403641.

[86]

C. Shuai, C. Gao, P. Feng, S. Peng, Graphene-reinforced mechanical properties of calcium silicate scaffolds by laser sintering, RSC Adv. 4 (2014) 12782-12788, doi: 10.1039/C3RA47862A.

[87]

C. Gao, T. Liu, C. Shuai, S. Peng, Enhancement mechanisms of graphene in nano-58S bioactive glass scaffold: Mechanical and biological performance, Sci. Rep. 4 (2014) 4712, doi: 10.1038/srep04712.

[88]

C. Shuai, Z. Zeng, Y. Yang, F. Qi, S. Peng, W. Yang, C. He, G. Wang, G. Qian, Graphene oxide assists polyvinylidene fluoride scaffold to reconstruct electrical microenvironment of bone tissue, Mater. Des. 190 (2020) 108564, doi: 10.1016/j.matdes.2020.108564.

[89]

L.C. Zhang, H. Attar, Selective laser melting of titanium alloys and titanium matrix composites for biomedical applications: A review, Adv. Eng. Mater. 18 (2016) 463-475, doi: 10.1002/adem.201500419.

[90]

X. Sun, S. Tong, S. Yang, S. Guo, The effects of graphene on the biocompatibility of a 3D-printed porous titanium alloy, Coatings 11 (2021) 1509, doi: 10.3390/coatings11121509.

[91]

S. Li, H. Lei, H. Liu, P. Song, S. Fan, L. Wu, D. Liao, G. Xian, L. Xiong, C. Zhou, Pulsed electrodeposition of MXenes/HAp multiple biological functional coatings on 3D printed porous Ti-6Al-4V bone tissue engineering scaffold, Surf. Coat. Technol. 464 (2023) 129532, doi: 10.1016/j.surfcoat.2023.129532.

[92]

Y.C. Zhao, Y. Tang, M.C. Zhao, C. Liu, L. Liu, C.D. Gao, C. Shuai, A. Atrens, Study on Fe- x GO composites prepared by selective laser melting: Microstructure, hardness, biodegradation and cytocompatibility , JOM 72 (2020) 1163-1174, doi: 10.1007/s11837-019-03814-z.

[93]

M.N. Collins, G. Ren, K. Young, S. Pina, R.L. Reis, J.M. Oliveira, Scaffold fabrication technologies and structure/function properties in bone tissue engineering, Adv. Funct. Mater. 31 (2021) 2010609, doi: 10.1002/adfm.202010609.

[94]

L. Zhang, G. Yang, B.N. Johnson, X. Jia, Three-dimensional (3D) printed scaffold and material selection for bone repair, Acta Biomater. 84 (2019) 16-33, doi: 10.1016/j.actbio.2018.11.039.

[95]

Z. Li, L. Wang, Y. Li, Y. Feng, W. Feng, Carbon-based functional nanomaterials: Preparation, properties and applications, Compos. Sci. Technol. 179 (2019) 10-40, doi: 10.1016/j.compscitech.2019.04.028.

[96]

C. Zhang, X. Wang, S. Fan, P. Lan, C. Cao, Y. Zhang, Silk fibroin/reduced graphene oxide composite mats with enhanced mechanical properties and conductivity for tissue engineering, Colloid. Surf., B 197 (2021) 111444, doi: 10.1016/j.colsurfb.2020.111444.

[97]

H. Rastin, B. Zhang, A. Mazinani, K. Hassan, J. Bi, T.T. Tung, D. Losic, 3D bioprinting of cell-laden electroconductive MXene nanocomposite bioinks, Nanoscale 12 (2020) 16069-16080, doi: 10.1039/D0NR02581J.

[98]

A. Fathi, M. Ahmed, M. Afifi, A. Menazea, V. Uskoković, Taking hydroxyapatite-coated titanium implants two steps forward: Surface modification using graphene mesolayers and a hydroxyapatite-reinforced polymeric scaffold, ACS Biomater. Sci. Eng. 7 (2020) 360-372, doi: 10.1021/acsbiomaterials.0c01105.

[99]

A.M. Deliormanli, M. Ensoylu, G. ALMisned, H. Tekin, Two-dimensional molybdenum disulfide/polymer-coated bioactive glass scaffolds for tissue engineering: Fabrication, structural, mechanical, bioactivity, and radiation interaction properties, Ceram. Int. 49 (2023) 22861-22874, doi: 10.1016/j.ceramint.2023.04.110.

[100]

S. Jeon, J.H. Lee, H.J. Jang, Y.B. Lee, B. Kim, M.S. Kang, Y.C. Shin, D.M. Shin, S.W. Hong, D.W. Han, Spontaneously promoted osteogenic differentiation of MC3T3-E1 preosteoblasts on ultrathin layers of black phosphorus, Mater. Sci. Eng., C 128 (2021) 112309, doi: 10.1016/j.msec.2021.112309.

[101]

R. Guo, M. Xiao, W. Zhao, S. Zhou, Y. Hu, M. Liao, S. Wang, X. Yang, R. Chai, M. Tang, 2D Ti3C2Tx MXene couples electrical stimulation to promote proliferation and neural differentiation of neural stem cells , Acta Biomater. 139 (2022) 105-117, doi: 10.1016/j.actbio.2020.12.035.

[102]

A. Seyedsalehi, L. Daneshmandi, M. Barajaa, J. Riordan, C.T. Laurencin, Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds, Sci. Rep. 10 (2020) 22210, doi: 10.1038/s41598-020-78977-w.

[103]

H. Belaid, S. Nagarajan, C. Teyssier, C. Barou, J. Barés, S. Balme, H. Garay, V. Huon, D. Cornu, V. Cavailles, Development of new biocompatible 3D printed graphene oxide-based scaffolds, Mater. Sci. Eng. C 110 (2020) 110595, doi: 10.1016/j.msec.2019.110595.

[104]

M. Malaki, R.S. Varma, Mechanotribological aspects of MXene-reinforced nanocomposites, Adv. Mater. 32 (2020) 2003154, doi: 10.1002/adma.202003154.

[105]

U. Yadav, H. Mishra, V. Singh, S. Kashyap, A. Srivastava, S. Yadav, P.S. Saxena, Enhanced osteogenesis by molybdenum disulfide nanosheet reinforced hydroxyapatite nanocomposite scaffolds, ACS Biomater. Sci. Eng. 5 (2019) 4511-4521, doi: 10.1021/acsbiomaterials.9b00227.

[106]

H. Nazari, A. Heirani-Tabasi, M. Hajiabbas, M. Khalili, M. Shahsavari Alavijeh, S. Hatamie, A. Mahdavi Gorabi, E. Esmaeili, S.H. Ahmadi Tafti, Incorporation of two-dimensional nanomaterials into silk fibroin nanofibers for cardiac tissue engineering, Polym. Adv. Technol. 31 (2020) 248-259, doi: 10.1002/pat.4765.

[107]

P.X. Ma, Biomimetic materials for tissue engineering, Adv. Drug Deliv. Rev. 60 (2008) 184-198, doi: 10.1016/j.addr.2007.08.041.

[108]

M. Ensoylu, A.M. Deliormanlı, H. Atmaca, Tungsten disulfide nanoparticle-containing PCL and PLGA-coated bioactive glass composite scaffolds for bone tissue engineering applications, J. Mater. Sci. 56 (2021) 18650-18667, doi: 10.1007/s10853-021-06494-w.

[109]

G. Lalwani, A.M. Henslee, B. Farshid, P. Parmar, L. Lin, Y.X. Qin, F.K. Kasper, A.G. Mikos, B. Sitharaman, Tungsten disulfide nanotubes reinforced biodegradable polymers for bone tissue engineering, Acta Biomater. 9 (2013) 8365-8373, doi: 10.1016/j.actbio.2013.05.018.

[110]

A. Maleki, M. Ghomi, N. Nikfarjam, M. Akbari, E. Sharifi, M.A. Shahbazi, M. Kermanian, M. Seyedhamzeh, E. Nazarzadeh Zare, M. Mehrali, Biomedical applications of MXene-integrated composites: Regenerative medicine, infection therapy, cancer treatment, and biosensing, Adv. Funct. Mater. 32 (2022) 2203430, doi: 10.1002/adfm.202203430.

[111]

G.A. Asaro, M. Solazzo, M. Suku, D. Spurling, K. Genoud, J.G. Gonzalez, F.J.O. Brien, V. Nicolosi, M.G. Monaghan, MXene functionalized collagen biomaterials for cardiac tissue engineering driving iPSC-derived cardiomyocyte maturation, npj 2D Mater. Appl. 7 (2023) 44, doi: 10.1038/s41699-023-00409-w.

[112]

Z. Xu, Y. Zhang, H. Dai, Y. Wang, Y. Ma, S. Tan, B. Han, 3D printed MXene (Ti2AlN)/polycaprolactone composite scaffolds for in situ maxillofacial bone defect repair , J. Ind. Eng. Chem. 114 (2022) 536-548, doi: 10.1016/j.jiec.2022.07.042.

[113]

G.P. Awasthi, V.K. Kaliannagounder, J. Park, B. Maharjan, M. Shin, C. Yu, C.H. Park, C.S. Kim, Assembly of porous graphitic carbon nitride nanosheets into electrospun polycaprolactone nanofibers for bone tissue engineering, Colloid. Surf. A: Physicochem. Eng. Asp. 622 (2021) 126584, doi: 10.1016/j.colsurfa.2021.126584.

[114]

L. Sutrisno, H. Chen, Y. Chen, T. Yoshitomi, N. Kawazoe, Y. Yang, G. Chen, Composite scaffolds of black phosphorus nanosheets and gelatin with controlled pore structures for photothermal cancer therapy and adipose tissue engineering, Biomaterials 275 (2021) 120923, doi: 10.1016/j.biomaterials.2021.120923.

[115]

J.S. Kim, J.S. Choi, Y.W. Cho, Cell-free hydrogel system based on a tissue-specific extracellular matrix for in situ adipose tissue regeneration, ACS Appl. Mater. Interface. 9 (2017) 8581-8588, doi: 10.1021/acsami.6b16783.

[116]

T.G. Kim, H. Shin, D.W. Lim, Biomimetic scaffolds for tissue engineering, Adv. Funct. Mater. 22 (2012) 2446-2468, doi: 10.1002/adfm.201103083.

[117]

M. Saadi, A. Maguire, N.T. Pottackal, M.S.H. Thakur, M.M. Ikram, A.J. Hart, P.M. Ajayan, M.M. Rahman, Direct ink writing: A 3D printing technology for diverse materials, Adv. Mater. 34 (2022) 2108855, doi: 10.1002/adma.202108855.

[118]

D. Ponnamma, Y. Yin, N. Salim, J. Parameswaranpillai, S. Thomas, N. Hameed, Recent progress and multifunctional applications of 3D printed graphene nanocomposites, Compos. B Eng. 204 (2021) 108493, doi: 10.1016/j.compositesb.2020.108493.

[119]

H. Li, S. Liu, L. Li, Rheological study on 3D printability of alginate hydrogel and effect of graphene oxide, Int. J. Bioprint. 2 (2016) 54-66, doi: 10.18063/IJB.2016.02.007.

[120]

C. Hu, Z. Chen, L. Tang, J. Liu, J. Yang, W.F. Lai, T. Wu, S. Liao, X. Zhang, H. Pan, A universally dispersible graphene-based ink modifier facilitates 3D printing of multi-functional tissue-engineered scaffolds, Mater. Des. 216 (2022) 110551, doi: 10.1016/j.matdes.2022.110551.

[121]

M. Shirzad, A. Zolfagharian, A. Matbouei, M. Bodaghi, Design, evaluation, and optimization of 3D printed truss scaffolds for bone tissue engineering, J. Mech. Behav. Biomed. Mater. 120 (2021) 104594, doi: 10.1016/j.jmbbm.2021.104594.

[122]

C. Xu, Y. Xu, M. Yang, Y. Chang, A. Nie, Z. Liu, J. Wang, Z. Luo, Black-phosphorus-incorporated hydrogel as a conductive and biodegradable platform for enhancement of the neural differentiation of mesenchymal stem cells, Adv. Funct. Mater. 30 (2020) 2000177, doi: 10.1002/adfm.202000177.

[123]

E.P. Nguyen, C.d.C.C. Silva, A. Merkoçi, Recent advancement in biomedical applications on the surface of two-dimensional materials: From biosensing to tissue engineering, Nanoscale 12 (2020) 19043-19067, doi: 10.1039/D0NR05287F.

[124]

N. Shadjou, M. Hasanzadeh, Graphene and its nanostructure derivatives for use in bone tissue engineering: Recent advances, J. Biomed. Mater. Res. A 104 (2016) 1250-1275, doi: 10.1002/jbm.a.35645.

[125]

W. Wang, J.R.P. Junior, P.R.L. Nalesso, D. Musson, J. Cornish, F. Mendonça, G.F. Caetano, P. Bártolo, Engineered 3D printed poly (ɛ-caprolactone)/graphene scaffolds for bone tissue engineering, Mater. Sci. Eng., C 100 (2019) 759-770, doi: 10.1016/j.msec.2019.03.047.

[126]

N. Dubey, R. Bentini, I. Islam, T. Cao, A.H. Castro Neto, V. Rosa, Graphene: A versatile carbon-based material for bone tissue engineering, Stem Cell. Int. 2015 (2015) 804213, doi: 10.1155/2015/804213.

[127]

E.I. Biru, M.I. Necolau, A. Zainea, H. Iovu, Graphene oxide-protein-based scaffolds for tissue engineering: Recent advances and applications, Polymers 14 (2022) 1032, doi: 10.3390/polym14051032.

[128]

G. Wang, C. He, W. Yang, F. Qi, G. Qian, S. Peng, C. Shuai, Surface-modified graphene oxide with compatible interface enhances poly-L-lactic acid bone scaffold, J. Nanomater. 2020 (2020) 1-11, doi: 10.1155/2020/5634096.

[129]

C. Gao, M. Yao, S. Li, P. Feng, S. Peng, C. Shuai, Highly biodegradable and bioactive Fe-Pd-bredigite biocomposites prepared by selective laser melting, J. Adv. Res. 20 (2019) 91-104, doi: 10.1016/j.jare.2019.06.001.

[130]

J. Su, Z. Du, L. Xiao, F. Wei, Y. Yang, M. Li, Y. Qiu, J. Liu, J. Chen, Y. Xiao, Graphene oxide coated titanium surfaces with osteoimmunomodulatory role to enhance osteogenesis, Mater. Sci. Eng., C 113 (2020) 110983, doi: 10.1016/j.msec.2020.110983.

[131]

B. Girase, J.S. Shah, R.D.K. Misra, Cellular mechanics of modulated osteoblasts functions in graphene oxide reinforced elastomers, Adv. Eng. Mater. 14 (2012) B101-B111, doi: 10.1002/adem.201180028.

[132]

S. Roy, K.A. Deo, K.A. Singh, H.P. Lee, A. Jaiswal, A.K. Gaharwar, Nano-bio interactions of 2D molybdenum disulfide, Adv. Drug Deliv. Rev. 187 (2022) 114361, doi: 10.1016/j.addr.2022.114361.

[133]

W. Dai, Y. Zheng, B. Li, F. Yang, W. Chen, Y. Li, Y. Deng, D. Bai, R. Shu, A 3D-printed orthopedic implant with dual-effect synergy based on MoS2 and hydroxyapatite nanoparticles for tumor therapy and bone regeneration , Colloid. Surf., B 228 (2023) 113384, doi: 10.1016/j.colsurfb.2023.113384.

[134]

B. Yuan, X. Zhou, Y. Li, Y. Zhao, M. Xue, Q. Guo, G. Zheng, X. Chen, H. Lin, X. Guo, Black-phosphorus-nanosheet-reinforced coating of implants for sequential biofilm ablation and bone fracture healing acceleration, ACS Appl. Mater. Interfaces 14 (2022) 47036-47051, doi: 10.1021/acsami.2c13566.

[135]

M. Heidari, S.H. Bahrami, M. Ranjbar-Mohammadi, P. Milan, Smart electrospun nanofibers containing PCL/gelatin/graphene oxide for application in nerve tissue engineering, Mater. Sci. Eng. C 103 (2019) 109768, doi: 10.1016/j.msec.2019.109768.

[136]

B. Ardeshirzadeh, N.A. Anaraki, M. Irani, L.R. Rad, S. Shamshiri, Controlled release of doxorubicin from electrospun PEO/chitosan/graphene oxide nanocomposite nanofibrous scaffolds, Mater. Sci. Eng. C 48 (2015) 384-390, doi: 10.1016/j.msec.2014.12.039.

[137]

A. Gautieri, S. Vesentini, A. Redaelli, M.J. Buehler, Hierarchical structure and nanomechanics of collagen microfibrils from the atomistic scale up, Nano Lett. 11 (2011) 757-766, doi: 10.1021/nl103943u.

[138]

H. San, M. Paresoglou, M. Minneboo, I.A. van Hengel, A. Yilmaz, Y. Gonzalez-Garcia, A.C. Fluit, P.L. Hagedoorn, L.E. Fratila-Apachitei, I. Apachitei, Fighting antibiotic-resistant bacterial infections by surface biofunctionalization of 3D-printed porous titanium implants with reduced graphene oxide and silver nanoparticles, Int. J. Mol. Sci. 23 (2022) 9204, doi: 10.3390/ijms23169204.

[139]

B. Yang, J. Yin, Y. Chen, S. Pan, H. Yao, Y. Gao, J. Shi, 2D-black-phosphorus-reinforced 3D-printed scaffolds: A stepwise countermeasure for osteosarcoma, Adv. Mater. 30 (2018) 1705611, doi: 10.1002/adma.201705611.

[140]

T.V. Patil, D.K. Patel, S.D. Dutta, K. Ganguly, K.T. Lim, Graphene oxide-based stimuli-responsive platforms for biomedical applications, Molecules 26 (2021) 2797, doi: 10.3390/molecules26092797.

[141]

Z. Weng, F. Yu, Q. Leng, S. Zhao, Y. Xu, W. Zhang, Z. Zhu, J. Ye, Q. Wei, X. Wang, Electrical and visible light dual-responsive ZnO nanocomposite with multiple wound healing capability, Mater. Sci. Eng. C 124 (2021) 112066, doi: 10.1016/j.msec.2021.112066.

[142]

Y. Li, X. Liu, L. Tan, Z. Cui, X. Yang, Y. Zheng, K.W.K. Yeung, P.K. Chu, S. Wu, Rapid sterilization and accelerated wound healing using Zn2+ and graphene oxide modified g-C3N4 under dual light irradiation , Adv. Funct. Mater. 28 (2018) 1800299, doi: 10.1002/adfm.201800299.

[143]

S. Wang, Z. Zhang, S. Wei, F. He, Z. Li, H.H. Wang, Y. Huang, Z. Nie, Near-infrared light-controllable MXene hydrogel for tunable on-demand release of therapeutic proteins, Acta Biomater. 130 (2021) 138-148, doi: 10.1016/j.actbio.2021.05.027.

[144]

E.H. Schemitsch, Size matters: Defining critical in bone defect size!, J. Orthop. Trauma 31 (2017) S20-S22, doi: 10.1097/BOT.0000000000000978.

[145]

H. Qu, H. Fu, Z. Han, Y. Sun, Biomaterials for bone tissue engineering scaffolds: A review, RSC Adv. 9 (2019) 26252-26262, doi: 10.1039/C9RA05214C.

[146]

M. Bez, D. Sheyn, W. Tawackoli, P. Avalos, G. Shapiro, J.C. Giaconi, X. Da, S.B. David, J. Gavrity, H.A. Awad, In situ bone tissue engineering via ultrasound-mediated gene delivery to endogenous progenitor cells in mini-pigs, Sci. Transl. Med. 9 (2017) eaal3128, doi: 10.1126/scitranslmed.aal3128.

[147]

Y. Liu, D. Luo, X.X. Kou, X.D. Wang, F.R. Tay, Y.L. Sha, Y.H. Gan, Y.H. Zhou, Hierarchical intrafibrillar nanocarbonated apatite assembly improves the nanomechanics and cytocompatibility of mineralized collagen, Adv. Funct. Mater. 23 (2013) 1404-1411, doi: 10.1002/adfm.201201611.

[148]

A. Ho-Shui-Ling, J. Bolander, L.E. Rustom, A.W. Johnson, F.P. Luyten, C. Picart, Bone regeneration strategies: Engineered scaffolds, bioactive molecules and stem cells current stage and future perspectives, Biomaterials 180 (2018) 143-162, doi: 10.1016/j.biomaterials.2018.07.017.

[149]

B. Charbonnier, M. Hadida, D. Marchat, Additive manufacturing pertaining to bone: Hopes, reality and future challenges for clinical applications, Acta Biomater. 121 (2021) 1-28, doi: 10.1016/j.actbio.2020.11.039.

[150]

J.S. Lee, H.D. Cha, J.H. Shim, J.W. Jung, J.Y. Kim, D.W. Cho, Effect of pore architecture and stacking direction on mechanical properties of solid freeform fabrication-based scaffold for bone tissue engineering, J. Biomed. Mater. Res. A 100 (2012) 1846-1853, doi: 10.1002/jbm.a.34149.

[151]

C.M. Murphy, M.G. Haugh, F.J. O’brien, The effect of mean pore size on cell attachment, proliferation and migration in collagen-glycosaminoglycan scaffolds for bone tissue engineering, Biomaterials 31 (2010) 461-466, doi: 10.1016/j.biomaterials.2009.09.063.

[152]

A. Wibowo, G.U. Tajalla, M.A. Marsudi, G. Cooper, L.A. Asri, F. Liu, H. Ardy, P.J. Bartolo, Green synthesis of silver nanoparticles using extract of Cilembu sweet potatoes (Ipomoea batatas L var. Rancing) as potential filler for 3D printed electroactive and anti-infection scaffolds, Molecules 26 (2021) 2042, doi: 10.3390/molecules26072042.

[153]

A. Wibowo, C. Vyas, G. Cooper, F. Qulub, R. Suratman, A.I. Mahyuddin, T. Dirgantara, P. Bartolo, 3D printing of polycaprolactone-polyaniline electroactive scaffolds for bone tissue engineering, Materials 13 (2020) 512, doi: 10.3390/ma13030512.

[154]

N.Y. Shim, J.S. Heo, Performance of the polydopamine-graphene oxide composite substrate in the osteogenic differentiation of mouse embryonic stem cells, Int. J. Mol. Sci. 22 (2021) 7323, doi: 10.3390/ijms22147323.

[155]

J. Prakash, D. Prema, K. Venkataprasanna, K. Balagangadharan, N. Selvamurugan, G.D. Venkatasubbu, Nanocomposite chitosan film containing graphene oxide/hydroxyapatite/gold for bone tissue engineering, Int. J. Biol. Macromol. 154 (2020) 62-71, doi: 10.1016/j.ijbiomac.2020.03.095.

[156]

V. Seleznev, V.Y. Prinz, Hybrid 3D-2D printing for bone scaffolds fabrication, Nanotechnology 28 (2017) 064004, doi: 10.1088/1361-6528/aa536f.

[157]

K. Markandan, I.P. Seetoh, C.Q. Lai, Mechanical anisotropy of graphene nanocomposites induced by graphene alignment during stereolithography 3D printing, J. Mater. Res. 36 (2021) 4262-4274, doi: 10.1557/s43578-021-00400-5.

[158]

X. Xie, K. Hu, D. Fang, L. Shang, S.D. Tran, M. Cerruti, Graphene and hydroxyapatite self-assemble into homogeneous, free standing nanocomposite hydrogels for bone tissue engineering, Nanoscale 7 (2015) 7992-8002, doi: 10.1039/C5NR01107H.

[159]

R. Balint, N.J. Cassidy, S.H. Cartmell, Conductive polymers: Towards a smart biomaterial for tissue engineering, Acta Biomater. 10 (2014) 2341-2353, doi: 10.1016/j.actbio.2014.02.015.

[160]

P.R.L. Nalesso, W. Wang, Y. Hou, L. Bagne, A.T. Pereira, J.V. Helaehil, T.A.M. de Andrade, G.B. Chiarotto, P. Bártolo, G.F. Caetano, In vivo investigation of 3D printed polycaprolactone/graphene electro-active bone scaffolds, Bioprinting 24 (2021) e00164, doi: 10.1016/j.bprint.2021.e00164.

[161]

D. Xu, X. He, E. Obeng, Z. Ye, J. Shen, X. Ding, Two-dimensional NbS2 nanosheets with hyperthermia for killing bacteria to promote infected wound healing , Mater. Des. 223 (2022) 111124, doi: 10.1016/j.matdes.2022.111124.

[162]

L. Zhou, H. Zheng, Z. Liu, S. Wang, Z. Liu, F. Chen, H. Zhang, J. Kong, F. Zhou, Q. Zhang, Conductive antibacterial hemostatic multifunctional scaffolds based on Ti3C2Tx MXene nanosheets for promoting multidrug-resistant bacteria-infected wound healing , ACS Nano 15 (2021) 2468-2480, doi: 10.1021/acsnano.0c06287.

[163]

S.X. Guan, T. Xu, J.Y. Zhang, Y.G. Luo, X. Zhai, N. Zhang, Y.Z. Fang, Q.F. Ke, Cu-MOFs based photocatalyst triggered antibacterial platform for wound healing: 2D/2D Schottky junction and DFT calculation, J. Hazard. Mater. 454 (2023) 131531, doi: 10.1016/j.jhazmat.2023.131531.

[164]

Y. Fang, S. Pei, L. Zhuo, P. Cheng, H. Yuan, L. Zhang, Phosphorus and sulfur codoped carbon nitride nanosheets with enhanced photocatalytic antibacterial activity and promotion of wound healing, Appl. Surf. Sci. 586 (2022) 152761, doi: 10.1016/j.apsusc.2022.152761.

[165]

S. Du, B. Liu, Z. Li, H. Tan, W. Qi, T. Liu, S. Qiang, T. Zhang, F. Song, X. Chen, A nanoporous graphene/nitrocellulose membrane beneficial to wound healing, ACS Appl. Bio Mater. 4 (2021) 4522-4531, doi: 10.1021/acsabm.1c00261.

[166]

X. Zhao, L.Y. Wang, C.Y. Tang, X.J. Zha, Y. Liu, B.H. Su, K. Ke, R.Y. Bao, M.B. Yang, W. Yang, Smart Ti3C2Tx MXene fabric with fast humidity response and joule heating for healthcare and medical therapy applications , ACS Nano 14 (2020) 8793-8805, doi: 10.1021/acsnano.0c03391.

[167]

Y. Shao, K. Dong, X. Lu, B. Gao, B. He, Bioinspired 3D-printed MXene and spidroin-based near-infrared light-responsive microneedle scaffolds for efficient wound management, ACS Appl. Mater. Interfaces 14 (2022) 56525-56534, doi: 10.1021/acsami.2c16277.

[168]

R. Luo, F. Li, Y. Wang, H. Zou, J. Shang, Y. Fan, H. Liu, Z. Xu, R. Li, H. Liu, MXene-modified 3D printed scaffold for photothermal therapy and facilitation of oral mucosal wound reconstruction, Mater. Des. 227 (2023) 111731, doi: 10.1016/j.matdes.2023.111731.

[169]

Z. Li, S. Xiang, Z. Lin, E.N. Li, H. Yagi, G. Cao, L. Yocum, L. Li, T. Hao, K.K. Bruce, Graphene oxide-functionalized nanocomposites promote osteogenesis of human mesenchymal stem cells via enhancement of BMP-SMAD1/5 signaling pathway, Biomaterials 277 (2021) 121082, doi: 10.1016/j.biomaterials.2021.121082.

[170]

S.F. Melo, S.C. Neves, A.T. Pereira, I. Borges, P.L. Granja, F.D. Magalhães, I.C. Gonçalves, Incorporation of graphene oxide into poly (ɛ-caprolactone) 3D printed fibrous scaffolds improves their antimicrobial properties, Mater. Sci. Eng., C 109 (2020) 110537, doi: 10.1016/j.msec.2019.110537.

[171]

V. Palmieri, M.C. Lauriola, G. Ciasca, C. Conti, M. De Spirito, M. Papi, The graphene oxide contradictory effects against human pathogens, Nanotechnology 28 (2017) 152001, doi: 10.1088/1361-6528/aa6150.

[172]

W. Weng, W. Nie, Q. Zhou, X. Zhou, L. Cao, F. Ji, J. Cui, C. He, J. Su, Controlled release of vancomycin from 3D porous graphene-based composites for dual-purpose treatment of infected bone defects, RSC Adv. 7 (2017) 2753-2765, doi: 10.1039/C6RA26062D.

[173]

Y. Xu, Z. Shi, X. Shi, K. Zhang, H. Zhang, Recent progress in black phosphorus and black-phosphorus-analogue materials: Properties, synthesis and applications, Nanoscale 11 (2019) 14491-14527, doi: 10.1039/C9NR04348A.

[174]

X. Liu, A.L. Miller, S. Park, M.N. George, B.E. Waletzki, H. Xu, A. Terzic, L. Lu, Two-dimensional black phosphorus and graphene oxide nanosheets synergistically enhance cell proliferation and osteogenesis on 3D printed scaffolds, ACS Appl. Mater. Interfaces 11 (2019) 23558-23572, doi: 10.1021/acsami.9b04121.

[175]

N. Goel, A. Kushwaha, M. Kumar, Two-dimensional MXenes: Recent emerging applications, RSC Adv. 12 (2022) 25172-25193, doi: 10.1039/D2RA04354H.

[176]

Q. Yang, H. Yin, T. Xu, D. Zhu, J. Yin, Y. Chen, X. Yu, J. Gao, C. Zhang, Y. Chen, Engineering 2D mesoporous Silica@ MXene-integrated 3D-printing scaffolds for combinatory osteosarcoma therapy and NO-augmented bone regeneration, Small 16 (2020) 1906814, doi: 10.1002/smll.201906814.

[177]

D. Chouhan, N. Dey, N. Bhardwaj, B.B. Mandal, Emerging and innovative approaches for wound healing and skin regeneration: Current status and advances, Biomaterials 216 (2019) 119267, doi: 10.1016/j.biomaterials.2019.119267.

[178]

Y. Ding, L. Xu, S. Chen, Y. Zhu, Y. Sun, L. Ding, B. Yan, S. Ramakrishna, J. Zhang, Y.Z. Long, Mxene composite fibers with advanced thermal management for inhibiting tumor recurrence and accelerating wound healing, Chem. Eng. J. 459 (2023) 141529, doi: 10.1016/j.cej.2023.141529.

[179]

Z. Miao, L. Fan, X. Xie, Y. Ma, J. Xue, T. He, Z. Zha, Liquid exfoliation of atomically thin antimony selenide as an efficient two-dimensional antibacterial nanoagent, ACS Appl. Mater. Interfaces 11 (2019) 26664-26673, doi: 10.1021/acsami.9b08320.

[180]

I. Altinbasak, R. Jijie, A. Barras, B. Golba, R. Sanyal, J. Bouckaert, D. Drider, R. Bilyy, T. Dumych, S. Paryzhak, Reduced graphene-oxide-embedded polymeric nanofiber mats: An “on-demand” photothermally triggered antibiotic release platform, ACS Appl. Mater. Interfaces 10 (2018) 41098-41106, doi: 10.1021/acsami.8b14784.

[181]

A. Shariati, S.M. Hosseini, Z. Chegini, A. Seifalian, M.R. Arabestani, Graphene-based materials for inhibition of wound infection and accelerating wound healing, Biomed. Pharmacother. 158 (2023) 114184, doi: 10.1016/j.biopha.2022.114184.

[182]

L. Jin, X. Guo, D. Gao, C. Wu, B. Hu, G. Tan, N. Du, X. Cai, Z. Yang, X. Zhang, NIR-responsive MXene nanobelts for wound healing, NPG Asia Mater. 13 (2021) 24, doi: 10.1038/s41427-021-00289-w.

[183]

S. Chen, J. Lu, T. You, D. Sun, Metal-organic frameworks for improving wound healing, Coord. Chem. Rev. 439 (2021) 213929, doi: 10.1016/j.ccr.2021.213929.

[184]

D. Luong, A.A. Yergeshov, M. Zoughaib, F.R. Sadykova, B.I. Gareev, I.N. Savina, T.I. Abdullin, Transition metal-doped cryogels as bioactive materials for wound healing applications, Mater. Sci. Eng. C 103 (2019) 109759, doi: 10.1016/j.msec.2019.109759.

[185]

M.A.M. Jahromi, P.S. Zangabad, S.M.M. Basri, K.S. Zangabad, A. Ghamarypour, A.R. Aref, M. Karimi, M.R. Hamblin, Nanomedicine and advanced technologies for burns: Preventing infection and facilitating wound healing, Adv. Drug Deliv. Rev. 123 (2018) 33-64, doi: 10.1016/j.addr.2017.08.001.

[186]

I.J. Budiarso, N.D. Rini, A. Tsalsabila, M.D. Birowosuto, A. Wibowo, Chitosan-based smart biomaterials for biomedical applications: Progress and perspectives, ACS Biomater. Sci. Eng. 9 (2023) 3084-3115, doi: 10.1021/acsbiomaterials.3c00216.

[187]

G.G. Chan, C.M. Koch, L.H. Connors, Blood proteomic profiling in inherited (ATTRm) and acquired (ATTRwt) forms of transthyretin-associated cardiac amyloidosis, J. Proteome Res. 16 (2017) 1659-1668, doi: 10.1021/acs.jproteome.6b00998.

[188]

P. Thangavel, R. Kannan, B. Ramachandran, G. Moorthy, L. Suguna, V. Muthuvijayan, Development of reduced graphene oxide (rGO)-isabgol nanocomposite dressings for enhanced vascularization and accelerated wound healing in normal and diabetic rats, J. Colloid Interface Sci. 517 (2018) 251-264, doi: 10.1016/j.jcis.2018.01.110.

[189]

N. Devi, J. Dutta, Preparation and characterization of chitosan-bentonite nanocomposite films for wound healing application, Int. J. Biol. Macromol. 104 (2017) 1897-1904, doi: 10.1016/j.ijbiomac.2017.02.080.

[190]

T. He, H. Wang, J. Wang, X. Tian, F. Wen, Q. Shi, J.S. Ho, C. Lee, Self-sustainable wearable textile nano-energy nano-system (NENS) for next-generation healthcare applications, Adv. Sci. 6 (2019) 1901437, doi: 10.1002/advs.201901437.

[191]

G. Qian, T. Wen, Y. Shuai, X. Wu, Z. Zeng, S. Peng, C. Shuai, Photothermal and photodynamic effects of g-C3N4 Nanosheet/Bi2S3 nanorod composites with antibacterial activity for tracheal injury repair , ACS Appl. Nano Mater. 5 (2022) 16528-16543, doi: 10.1021/acsanm.2c03569.

[192]

A.G. Tabriz, D. Douroumis, Recent advances in 3D printing for wound healing: A systematic review, J. Drug Deliv. Sci. Technol. 74 (2022) 103564, doi: 10.1016/j.jddst.2022.103564.

[193]

M. Mahmud, A.M. Rahman, K.S. Salem, M.L. Bari, H. Qiu, Architecting ultrathin graphitic C3N4 nanosheets incorporated PVA/Gelatin bionanocomposite for potential biomedical application: Effect on drug delivery, release kinetics, and antibacterial activity , ACS Appl. Bio Mater. 5 (2022) 5126-5139, doi: 10.1021/acsabm.2c00502.

[194]

A.N.T. Shabankareh, P.S. Pakchin, M. Hasany, H. Ghanbari, Development of a new electroconductive nanofibrous cardiac patch based on polyurethane-reduced graphene oxide nanocomposite scaffolds, Mater. Chem. Phys. 305 (2023) 127961, doi: 10.1016/j.matchemphys.2023.127961.

[195]

X.P. Li, K.Y. Qu, B. Zhou, F. Zhang, Y.Y. Wang, O.D. Abodunrin, Z. Zhu, N.P. Huang, Electrical stimulation of neonatal rat cardiomyocytes using conductive polydopamine-reduced graphene oxide-hybrid hydrogels for constructing cardiac microtissues, Colloid. Surf., B 205 (2021) 111844, doi: 10.1016/j.colsurfb.2021.111844.

[196]

G. Basara, M. Saeidi-Javash, X. Ren, G. Bahcecioglu, B.C. Wyatt, B. Anasori, Y. Zhang, P. Zorlutuna, Electrically conductive 3D printed Ti3C2Tx MXene-PEG composite constructs for cardiac tissue engineering , Acta Biomater. 139 (2022) 179-189, doi: 10.1016/j.actbio.2020.12.033.

[197]

C. Yang, R. Chen, C. Chen, F. Yang, H. Xiao, B. Geng, Y. Xia, Tissue engineering strategies hold promise for the repair of articular cartilage injury, BioMed. Eng. OnLine 23 (2024) 92, doi: 10.1186/s12938-024-01260-w.

[198]

F. Olate-Moya, L. Arens, M. Wilhelm, M.A. Mateos-Timoneda, E. Engel, H. Palza, Chondroinductive alginate-based hydrogels having graphene oxide for 3D printed scaffold fabrication, ACS Appl. Mater. Interfaces 12 (2020) 4343-4357, doi: 10.1021/acsami.9b22062.

[199]

J. Malda, J. Groll, P.R. van Weeren, Rethinking articular cartilage regeneration based on a 250-year-old statement, Nat. Rev. Rheumatol. 15 (2019) 571-572, doi: 10.1038/s41584-019-0278-7.

[200]

C. Lyu, C. Cheng, Y. He, L. Qiu, Z. He, D. Zou, D. Li, J. Lu, Graphene hydrogel as a porous scaffold for cartilage regeneration, ACS Appl. Mater. Interfaces 14 (2022) 54431-54438, doi: 10.1021/acsami.2c11307.

[201]

S. He, J. Wu, S.H. Li, L. Wang, Y. Sun, J. Xie, D. Ramnath, R.D. Weisel, T.M. Yau, H.W. Sung, The conductive function of biopolymer corrects myocardial scar conduction blockage and resynchronizes contraction to prevent heart failure, Biomaterials 258 (2020) 120285, doi: 10.1016/j.biomaterials.2020.120285.

[202]

E.S. Fioretta, S.E. Motta, V. Lintas, S. Loerakker, K.K. Parker, F.P.T. Baaijens, V. Falk, S.P. Hoerstrup, M.Y. Emmert, Next-generation tissue-engineered heart valves with repair, remodelling and regeneration capacity, Nat. Rev. Cardiol. 18 (2021) 92-116, doi: 10.1038/s41569-020-0422-8.

[203]

K. Bashandeh, A. Amiri, A. Rafieerad, S. Rahman, W. Yan, S. Dhingra, A.A. Polycarpou, MXene-aromatic thermosetting copolyester nanocomposite as an extremely wear-resistant biocompatible implant material for osteoarthritis applications, Appl. Surf. Sci. 600 (2022) 154124, doi: 10.1016/j.apsusc.2022.154124.

[204]

I.H. Ali, A. Ouf, F. Elshishiny, M.B. Taskin, J. Song, M. Dong, M. Chen, R. Siam, W. Mamdouh, Antimicrobial and wound-healing activities of graphene-reinforced electrospun chitosan/gelatin nanofibrous nanocomposite scaffolds, ACS Omega 7 (2022) 1838-1850, doi: 10.1021/acsomega.1c05095.

[205]

R. Khalili, P. Zarrintaj, S.H. Jafari, H. Vahabi, M.R. Saeb, Electroactive poly (p-phenylene sulfide)/r-graphene oxide/chitosan as a novel potential candidate for tissue engineering, Int. J. Biol. Macromol. 154 (2020) 18-24, doi: 10.1016/j.ijbiomac.2020.03.029.

[206]

A. Ghasemi, R. Imani, M. Yousefzadeh, S. Bonakdar, A. Solouk, H. Fakhrzadeh, Studying the potential application of electrospun polyethylene terephthalate/graphene oxide nanofibers as electroconductive cardiac patch, Macromol. Mater. Eng. 304 (2019) 1900187, doi: 10.1002/mame.201900187.

[207]

M. Sekuła-Stryjewska, S. Noga, M. Dźwigońska, E. Adamczyk, E. Karnas, J. Jagiełło, A. Szkaradek, P. Chytrosz, D. Boruczkowski, Z. Madeja, Graphene-based materials enhance cardiomyogenic and angiogenic differentiation capacity of human mesenchymal stem cells in vitro-focus on cardiac tissue regeneration, Mater. Sci. Eng., C 119 (2021) 111614, doi: 10.1016/j.msec.2020.111614.

[208]

W. Lin, M. Chen, T. Qu, J. Li, Y. Man, Three-dimensional electrospun nanofibrous scaffolds for bone tissue engineering, J. Biomed. Mater. Res. B Appl. Biomater. 108 (2020) 1311-1321, doi: 10.1002/jbm.b.34479.

[209]

S.K. Asl, M. Rahimzadegan, R. Ostadrahimi, The recent advancement in the chitosan hybrid-based scaffolds for cardiac regeneration after myocardial infarction, Carbohydr. Polym. 300 (2022) 120266, doi: 10.1016/j.carbpol.2022.120266.

[210]

L. Jiang, D. Chen, Z. Wang, Z. Zhang, Y. Xia, H. Xue, Y. Liu, Preparation of an electrically conductive graphene oxide/chitosan scaffold for cardiac tissue engineering, Appl. Biochem. Biotechnol. 188 (2019) 952-964, doi: 10.1007/s12010-019-02967-6.

[211]

S. Saravanan, N. Sareen, E. Abu-El-Rub, H. Ashour, G.L. Sequiera, H.I. Ammar, V. Gopinath, A.A. Shamaa, S.S.E. Sayed, M. Moudgil, J. Vadivelu, S. Dhingra, Graphene oxide-gold nanosheets containing chitosan scaffold improves ventricular contractility and function after implantation into infarcted heart, Sci. Rep. 8 (2018) 15069, doi: 10.1038/s41598-018-33144-0.

[212]

C. Zhang, M.H. Hsieh, S.Y. Wu, S.H. Li, J. Wu, S.M. Liu, H.J. Wei, R.D. Weisel, H.W. Sung, R.K. Li, A self-doping conductive polymer hydrogel that can restore electrical impulse propagation at myocardial infarct to prevent cardiac arrhythmia and preserve ventricular function, Biomaterials 231 (2020) 119672, doi: 10.1016/j.biomaterials.2019.119672.

[213]

K. Diedkova, A.D. Pogrebnjak, S. Kyrylenko, K. Smyrnova, V.V. Buranich, P. Horodek, P. Zukowski, T.N. Koltunowicz, P. Galaszkiewicz, K. Makashina, Polycaprolactone-MXene nanofibrous scaffolds for tissue engineering, ACS Appl. Mater. Interfaces 15 (2023) 14033-14047, doi: 10.1021/acsami.2c22780.

[214]

C. Mancino, T. Hendrickson, L.V. Whitney, F. Paradiso, S. Abasi, E. Tasciotti, F. Taraballi, A. Guiseppi-Elie, Electrospun electroconductive constructs of aligned fibers for cardiac tissue engineering, Nanomed.: Nanotechnol. Biol. Med. 44 (2022) 102567, doi: 10.1016/j.nano.2022.102567.

[215]

M. Gasparotto, P. Bellet, G. Scapin, R. Busetto, C. Rampazzo, L. Vitiello, D.I. Shah, F. Filippini, 3D printed graphene-PLA scaffolds promote cell alignment and differentiation, Int. J. Mol. Sci. 23 (2022) 1736, doi: 10.3390/ijms23031736.

[216]

X. Zhang, H. Zhang, Y. Zhang, H. Huangfu, Y. Yang, Q. Qin, Y. Zhang, Y. Zhou, 3D printed reduced graphene oxide-GelMA hybrid hydrogel scaffolds for potential neuralized bone regeneration, J. Mater. Chem. B 11 (2023) 1288-1301, doi: 10.1039/D2TB01979E.

[217]

J. Long, Z. Yao, W. Zhang, B. Liu, K. Chen, L. Li, B. Teng, X.F. Du, C. Li, X.F. Yu, L. Qin, Y. Lai, Regulation of osteoimmune microenvironment and osteogenesis by 3D-printed PLAG/black phosphorus scaffolds for bone regeneration, Adv. Sci. 10 (2023) 2302539, doi: 10.1002/advs.202302539.

[218]

H. Wei, W. Chen, S. Chen, T. Zhang, X. Xiao, 3D printing of MOF-reinforced methacrylated gelatin scaffolds for bone regeneration, J. Biomater. Sci., Polym. Ed. 35 (2024) 443-462, doi: 10.1080/09205063.2023.2295057.

[219]

J.W. Ko, Graphitic carbon nitride as reinforcement of photopolymer resin for 3D printing, Polymers 16 (2024) 370, doi: 10.3390/polym16030370.

[220]

W. Guo, C. Liu, W. Bu, Y. Yang, F. Guo, J. Li, E. Wang, Y. Mao, H. Mai, H. You, Y. Long, 3D printing of polylactic acid/boron nitride bone scaffolds: Mechanical properties, biomineralization ability and cell responses, Ceram. Int. 49 (2023) 25886-25898, doi: 10.1016/j.ceramint.2023.05.137.

[221]

M.H. Mobarak, N. Hossain, A. Hossain, J.J. Mim, F. Khan, M.T. Rayhan, M.A. Islam, M.A. Chowdhury, Advances of graphene nanoparticles in dental implant applications-A review, Appl. Surf. Sci. Adv. 18 (2023) 100470, doi: 10.1016/j.apsadv.2023.100470.

[222]

Y. Bréchet, J.Y. Cavaillé, E. Chabert, L. Chazeau, R. Dendievel, L. Flandin, C. Gauthier, Polymer based nanocomposites: Effect of filler-filler and filler-matrix interactions, Adv. Eng. Mater. 3 (2001) 571-577, doi: 10.1002/1527-2648(200108)3:8%3C571::AID-ADEM571%3E3.0.CO;2-M.

[223]

M. Peng, Z. Wen, L. Xie, J. Cheng, Z. Jia, D. Shi, H. Zeng, B. Zhao, Z. Liang, T. Li, 3D printing of ultralight biomimetic hierarchical graphene materials with exceptional stiffness and resilience, Adv. Mater. 31 (2019) 1902930, doi: 10.1002/adma.201902930.

[224]

W. Zhao, C. Yue, L. Liu, Y. Liu, J. Leng, Research progress of shape memory polymer and 4D printing in biomedical application, Adv. Healthc. Mater. 12 (2023) 2201975, doi: 10.1002/adhm.202201975.

[225]

H. Kamata, X. Li, U.i. Chung, T. Sakai, Design of hydrogels for biomedical applications, Adv. Healthc. Mater. 4 (2015) 2360-2374, doi: 10.1002/adhm.201500076.

PDF (4224KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/