Abstract
Although hydrogels developed based on the decellularized amniotic membrane (dAM) hold great promise for tissue engineering and regenerative medicine, the development of printable bioinks faces serious limitations considering appropriate rheological behavior and shape fidelity after 3D printing. To improve the printability of dAM, we propose that hydroxyethyl cellulose (HEC) and silicate nanoplatelets (Laponite) can be used as a thickening agent and rheology modifier, respectively. It is shown that the Laponite operates as a physical crosslinking agent through reversible non-covalent interactions between nanoplatelets and the biopolymer matrix, thus improving the storage modulus of the bioink from 45 to 277 Pa at 1wt.% concentration. The decrease in pore size of the hydrogel network from 165 ± 45 to 130 ± 46 μm by the addition of 1 wt.% Laponite due to the increased crosslinking density is also observed. The enhanced crosslinking density and viscoelastic properties of hydrogels by the employment of nanoplatelets improved the printability of the bioinks. Nevertheless, the ion-containing HEC-dAM solution is prone to aggregate the silicate nanoplatelets, particularly at high concentrations, which may lead to degraded mechanical moduli (e.g., 125 Pa at 2 wt% concentration). The incorporation of 1 wt% Laponite offers improved biocompatibility by supporting the viability and proliferation of fibroblast cells. The developed nanocomposite bioinks also exhibit a promoting effect on the migration rate of fibroblast cells by about 2 times more than the Laponite-free counterpart, implying their in vitro wound healing potential. Overall, our nanoengineered formulation provides sufficient printability, structural stability, and biocompatibility for commensurate skin tissue engineering applications.
Graphical abstract
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Data availability
The raw/processed data required to reproduce these findings are available for sharing upon a reasonable request.
References
Aguado BA, Mulyasasmita W, Su J, Lampe KJ, Heilshorn SC (2012) Improving viability of stem cells during syringe needle flow through the design of hydrogel cell carriers. Tissue Eng Part A 18:806–815. https://doi.org/10.1089/ten.tea.2011.0391
Ahlfeld T, Cidonio G, Kilian D, Duin S, Akkineni A, Dawson J, Yang S, Lode A, Oreffo R, Gelinsky M (2017) Development of a clay based bioink for 3D cell printing for skeletal application. Biofabrication 9:034103. https://doi.org/10.1088/1758-5090/aa7e96
Antezana PE, Municoy S, Álvarez-Echazú MI, Santo-Orihuela PL, Catalano PN, Al-Tel TH, Kadumudi FB, Dolatshahi-Pirouz A, Orive G, Desimone MF (2022) The 3D bioprinted scaffolds for wound healing. Pharmaceutics 14:464. https://doi.org/10.3390/pharmaceutics14020464
Bhattacharjee M, Ivirico JLE, Kan HM, Bordett R, Pandey R, Otsuka T, Nair LS, Laurencin CT (2020) Preparation and characterization of amnion hydrogel and its synergistic effect with adipose derived stem cells towards IL1β activated chondrocytes. Sci Rep 10:18751. https://doi.org/10.1038/s41598-020-75921-w
Blaeser A, Duarte Campos DF, Puster U, Richtering W, Stevens MM, Fischer H (2016) Controlling shear stress in 3D bioprinting is a key factor to balance printing resolution and stem cell integrity. Adv Healthc Mater 5:326–333. https://doi.org/10.1002/adhm.201500677
Boekema BK, Vlig M, Olde Damink L, Middelkoop E, Eummelen L, Bühren AV, Ulrich MM (2014) Effect of pore size and cross-linking of a novel collagen-elastin dermal substitute on wound healing. J Mater Sci Mater Med 25:423–433. https://doi.org/10.1007/s10856-013-5075-2
Brokesh AM, Cross LM, Kersey AL, Murali A, Richter C, Gregory CA, Singh I, Gaharwar AK (2022) Dissociation of nanosilicates induces downstream endochondral differentiation gene expression program. Sci Adv 8:eabl9404. https://doi.org/10.1126/sciadv.abl9404
Cai Y, Chang SY, Gan SW, Ma S, Lu WF, Yen CC (2022) Nanocomposite bioinks for 3D bioprinting. Acta Biomater 151:45–69. https://doi.org/10.1016/j.actbio.2022.08.014
Daikuara LY, Chen X, Yue Z, Skropeta D, Wood FM, Fear MW, Wallace GG (2022) 3D bioprinting constructs to facilitate skin regeneration. Adv Funct Mater 32:2105080. https://doi.org/10.1002/adfm.202105080
Deus IA, Santos SC, Custódio CA, Mano JF (2022) Designing highly customizable human based platforms for cell culture using proteins from the amniotic membrane. Biomater Adv 134:112574. https://doi.org/10.1016/j.msec.2021.112574
Dias J, Baptista-Silva S, Sousa A, Oliveira A, Bártolo P, Granja P (2018) Biomechanical performance of hybrid electrospun structures for skin regeneration. Mater Sci Eng C 93:816–827. https://doi.org/10.1016/j.msec.2018.08.050
Dong L, Bu Z, Xiong Y, Zhang H, Fang J, Hu H, Liu Z, Li X (2021) Facile extrusion 3D printing of gelatine methacrylate/Laponite nanocomposite hydrogel with high concentration nanoclay for bone tissue regeneration. Int J Biol Macromol 188:72–81. https://doi.org/10.1016/j.ijbiomac.2021.07.199
Dong L, Han Z, Zhang H, Yang R, Fang J, Wang L, Li X (2022) Tea polyphenol/glycerol-treated double-network hydrogel with enhanced mechanical stability and anti-drying, antioxidant and antibacterial properties for accelerating wound healing. Int J Biol Macromol 208:530–543. https://doi.org/10.1016/j.ijbiomac.2022.03.128
Elkhenany H, El-Derby A, Abd Elkodous M, Salah RA, Lotfy A, El-Badri N (2022) Applications of the amniotic membrane in tissue engineering and regeneration: the hundred-year challenge. Stem Cell Res Ther 13:1–19. https://doi.org/10.1186/s13287-021-02684-0
Eslahi N, Simchi A, Mehrjoo M, Shokrgozar MA, Bonakdar S (2016) Hybrid cross-linked hydrogels based on fibrous protein/block copolymers and layered silicate nanoparticles: tunable thermosensitivity, biodegradability and mechanical durability. RSC Adv 6:62944–62957. https://doi.org/10.1039/C6RA08563F
Freeman FE, Kelly DJ (2017) Tuning alginate bioink stiffness and composition for controlled growth factor delivery and to spatially direct MSC fate within bioprinted tissues. Sci Rep 7:17042. https://doi.org/10.1038/s41598-017-17286-1
Gaharwar AK, Cross LM, Peak CW, Gold K, Carrow JK, Brokesh A, Singh KA (2019) 2D nanoclay for biomedical applications: regenerative medicine, therapeutic delivery, and additive manufacturing. Adv Mater 31:1900332. https://doi.org/10.1002/adma.201900332
Galante R, Pinto TJ, Colaço R, Serro AP (2018) Sterilization of hydrogels for biomedical applications: a review. J Biomed Mater Res B Appl Biomater 106:2472–2492. https://doi.org/10.1002/jbm.b.34048
Gao G, Lee JH, Jang J, Lee DH, Kong JS, Kim BS, Choi YJ, Jang WB, Hong YJ, Kwon SM (2017) Tissue engineered bio-blood-vessels constructed using a tissue-specific bioink and 3D coaxial cell printing technique: a novel therapy for ischemic disease. Adv Funct Mater 27:1700798. https://doi.org/10.1002/adfm.201700798
Ghadiri M, Chrzanowski W, Lee W, Rohanizadeh R (2014) Layered silicate clay functionalized with amino acids: wound healing application. RSC Adv 4:35332–35343. https://doi.org/10.1039/C4RA05216A
Gholipourmalekabadi M, Mozafari M, Salehi M, Seifalian A, Bandehpour M, Ghanbarian H, Urbanska AM, Sameni M, Samadikuchaksaraei A, Seifalian AM (2015) Development of a cost-effective and simple protocol for decellularization and preservation of human amniotic membrane as a soft tissue replacement and delivery system for bone marrow stromal cells. Adv Healthc Mater 4:918–926. https://doi.org/10.1002/adhm.201400704
Giachini P, Gupta S, Wang W, Wood D, Yunusa M, Baharlou E, Sitti M, Menges A (2020) Additive manufacturing of cellulose-based materials with continuous, multidirectional stiffness gradients. Sci Adv 6:eaay0929. https://doi.org/10.1126/sciadv.aay0929
Gillispie G, Prim P, Copus J, Fisher J, Mikos AG, Yoo JJ, Atala A, Lee SJ (2020) Assessment methodologies for extrusion-based bioink printability. Biofabrication 12:022003. https://doi.org/10.1088/1758-5090/ab6f0d
Golafshan N, Rezahasani R, Esfahani MT, Kharaziha M, Khorasani S (2017) Nanohybrid hydrogels of laponite: PVA-Alginate as a potential wound healing material. Carbohydr Polym 176:392–401. https://doi.org/10.1016/j.carbpol.2017.08.070
Gonzaga VdA, Poli AL, Gabriel JS, Tezuka DY, Valdes TA, Leitão A, Rodero CF, Bauab TM, Chorilli M, Schmitt CC (2020) Chitosan-laponite nanocomposite scaffolds for wound dressing application. J Biomed Mater Res B Appl Biomater 108:1388–1397. https://doi.org/10.1002/jbm.b.34487
Gospodinova A, Nankov V, Tomov S, Redzheb M, Petrov PD (2021) Extrusion bioprinting of hydroxyethylcellulose-based bioink for cervical tumor model. Carbohydr Polym 260:117793. https://doi.org/10.1016/j.carbpol.2021.117793
Han Y, Lian M, Wu Q, Qiao Z, Sun B, Dai K (2021) Effect of pore size on cell behavior using melt electrowritten scaffolds. Front Bioeng Biotechnol 9:629270. https://doi.org/10.3389/fbioe.2021.629270
Haraguchi K, Matsuda K (2005) Spontaneous formation of characteristic layered morphologies in porous nanocomposites prepared from nanocomposite hydrogels. Chem Mater 17:931–934. https://doi.org/10.1021/cm048093x
He P, Zhao J, Zhang J, Li B, Gou Z, Gou M, Li X (2018) Bioprinting of skin constructs for wound healing. Burns Trauma 6:5. https://doi.org/10.1186/s41038-017-0104-x
Hojabri M, Tayebi T, Kasravi M, Aghdaee A, Ahmadi A, Mazloomnejad R, Tarasi R, Shaabani A, Bahrami S, Niknejad H (2023) Wet-spinnability and crosslinked fiber properties of alginate/hydroxyethyl cellulose with varied proportion for potential use in tendon tissue engineering. Int J Biol Macromol 240:124492. https://doi.org/10.1016/j.ijbiomac.2023.124492
Huang S, Shuyi S, Gan H, Linjun W, Lin C, Danyuan X, Zhou H, Lin X, Qin Y (2019) Facile fabrication and characterization of highly stretchable lignin-based hydroxyethyl cellulose self-healing hydrogel. Carbohydr Polym 223:115080. https://doi.org/10.1016/j.carbpol.2019.115080
Jf P, Liu NH, Sun H, Xu F (2014) Preparation and characterization of electrospun PLCL/poloxamer nanofibers and dextran/gelatin hydrogels for skin tissue engineering. PLoS ONE 9:e112885. https://doi.org/10.1371/journal.pone.0112885
Kafili G, Tamjid E, Niknejad H, Simchi A (2022) Development of injectable hydrogels based on human amniotic membrane and polyethyleneglycol-modified nanosilicates for tissue engineering applications. Eur Polym J 179:111566. https://doi.org/10.1016/j.eurpolymj.2022.111566
Kafili G, Tamjid E, Niknejad H, Simchi A (2023) Development of printable nanoengineered composite hydrogels based on human amniotic membrane for wound healing application. J Mater Sci 58:12351–12372. https://doi.org/10.1007/s10853-023-08783-y
Kang B, Park Y, Hwang DG, Kim D, Yong U, Lim KS, Jang J (2022) Facile bioprinting process for fabricating size-controllable functional microtissues using light-activated decellularized extracellular matrix-based bioinks. Adv Mater Technol 7:2100947. https://doi.org/10.1002/admt.202100947
Kim BS, Kim H, Gao G, Jang J, Cho DW (2017) Decellularized extracellular matrix: a step towards the next generation source for bioink manufacturing. Biofabrication 9:034104. https://doi.org/10.1088/1758-5090/aa7e98
Kim BS, Das S, Jang J, Cho DW (2020) Decellularized extracellular matrix-based bioinks for engineering tissue-and organ-specific microenvironments. Chem Rev 120:10608–10661. https://doi.org/10.1021/acs.chemrev.9b00808
Kim H, Kang B, Cui X, Lee SH, Lee K, Cho DW, Hwang W, Woodfield TB, Lim KS, Jang J (2021) Light-activated decellularized extracellular matrix-based bioinks for volumetric tissue analogs at the centimeter scale. Adv Funct Mater 31:2011252. https://doi.org/10.1002/adfm.202011252
Kumar T, Shanmugasundaram N, Babu M (2003) Biocompatible collagen scaffolds from a human amniotic membrane: physicochemical and in vitro culture characteristics. J Biomater Sci Polym Ed 14:689–706. https://doi.org/10.1163/156856203322274941
Lansdown A, Sampson B, Rowe A (1999) Sequential changes in trace metal, metallothionein and calmodulin concentrations in healing skin wounds. J Anat 195:375–386. https://doi.org/10.1046/j.1469-7580.1999.19530375.x
Lee JY, Kim H, Ha DH, Shin JC, Kim A, Ko HS, Cho DW (2018) Amnion-analogous medical device for fetal membrane healing: a preclinical long-term study. Adv Healthc Mater 7:1800673. https://doi.org/10.1002/adhm.201800673
Lee J, Oh SJ, An SH, Kim WD, Kim SH (2020) Machine learning-based design strategy for 3D printable bioink: elastic modulus and yield stress determine printability. Biofabrication 12:035018. https://doi.org/10.1088/1758-5090/ab8707
Li X, Deng Q, Zhuang T, Lu Y, Liu T, Zhao W, Lin B, Luo Y, Zhang X (2020) 3D bioprinted breast tumor model for structure–activity relationship study. Biodes Manuf 3:361–372. https://doi.org/10.1007/s42242-020-00085-5
Li X, Deng Q, Wang S, Li Q, Zhao W, Lin B, Luo Y, Zhang X (2021) Hydroxyethyl cellulose as a rheological additive for tuning the extrusion printability and scaffold properties. 3D Print Addit Manuf 8:87–98. https://doi.org/10.1089/3dp.2020.0167
Li X, Li P, Wang C, Shang T, Han H, Tong Y, Kang Y, Fang J, Cui L (2022) A thermo-sensitive and injectable hydrogel derived from a decellularized amniotic membrane to prevent intrauterine adhesion by accelerating endometrium regeneration. Biomater Sci 10:2275–2286. https://doi.org/10.1039/D1BM01791H
Li J, Tian Z, Yang H, Duan L, Liu Y (2023) Infiltration of laponite: An effective approach to improve the mechanical properties and thermostability of collagen hydrogel. J Appl Polym Sci 140:e53366. https://doi.org/10.1002/app.53366
Lokhande G, Carrow JK, Thakur T, Xavier JR, Parani M, Bayless KJ, Gaharwar AK (2018) Nanoengineered injectable hydrogels for wound healing application. Acta Biomater 70:35–47. https://doi.org/10.1016/j.actbio.2018.01.045
Maia JR, Sobreiro-Almeida R, Cleymand F, Mano JF (2023) Biomaterials of human source for 3D printing strategies. J Phys Mater 6:012002. https://doi.org/10.1088/2515-367639/acada1
Mohanty RP, Joshi YM (2016) Chemical stability phase diagram of aqueous Laponite dispersions. Appl Clay Sci 119:243–248. https://doi.org/10.1016/j.clay.2015.10.021
Morariu S, Bercea M, Gradinaru LM, Rosca I, Avadanei M (2020) Versatile poly (vinyl alcohol)/clay physical hydrogels with tailorable structure as potential candidates for wound healing applications. Mater Sci Eng C 109:110395. https://doi.org/10.1016/j.msec.2019.110395
Nasiry D, Khalatbary AR, Abdollahifar MA, Amini A, Bayat M, Noori A, Piryaei A (2021) Engraftment of bioengineered three-dimensional scaffold from human amniotic membrane-derived extracellular matrix accelerates ischemic diabetic wound healing. Arch Dermatol Res 313:567–582. https://doi.org/10.1007/s00403-020-02137-3
Niknejad H, Peirovi H, Jorjani M, Ahmadiani A, Ghanavi J, Seifalian AM (2008) Properties of the amniotic membrane for potential use in tissue engineering. Eur Cells Mater 15:88–99
Nouri-Felekori M, Nezafati N, Moraveji M, Hesaraki S, Ramezani T (2021) Bioorthogonal hydroxyethyl cellulose-based scaffold crosslinked via click chemistry for cartilage tissue engineering applications. Int J Biol Macromol 183:2030–2043. https://doi.org/10.1016/j.ijbiomac.2021.06.005
Oliveira SM, Alves NM, Mano JF (2014) Cell interactions with superhydrophilic and superhydrophobic surfaces. J Adhes Sci Technol 28:843–863. https://doi.org/10.1080/01694243.2012.697776
Orlando I, Basnett P, Nigmatullin R, Wang W, Knowles JC, Roy I (2020) Chemical modification of bacterial cellulose for the development of an antibacterial wound dressing. Front Bioeng Biotechnol 8:557885. https://doi.org/10.3389/fbioe.2020.557885
Ouyang L, Yao R, Zhao Y, Sun W (2016) Effect of bioink properties on printability and cell viability for 3D bioplotting of embryonic stem cells. Biofabrication 8:035020. https://doi.org/10.1088/1758-5090/8/3/035020
Peak CW, Stein J, Gold KA, Gaharwar AK (2018) Nanoengineered colloidal inks for 3D bioprinting. Langmuir 34:917–925. https://doi.org/10.1021/acs.langmuir.7b02540
Pettinelli N, Rodriguez-Llamazares S, Bouza R, Barral L, Feijoo-Bandin S, Lago F (2020) Carrageenan-based physically crosslinked injectable hydrogel for wound healing and tissue repairing applications. Int J Pharm 589:119828. https://doi.org/10.1016/j.ijpharm.2020.119828
Rathan S, Dejob L, Schipani R, Haffner B, Möbius ME, Kelly DJ (2019) Fiber reinforced cartilage ECM functionalized bioinks for functional cartilage tissue engineering. Adv Healthc Mater 8:1801501. https://doi.org/10.1002/adhm.201801501
Ryzhuk V, Xx Z, Wang X, Melnychuk V, Lankford L, Farmer D, Wang A (2018) Human amnion extracellular matrix derived bioactive hydrogel for cell delivery and tissue engineering. Mater Sci Eng C 85:191–202. https://doi.org/10.1016/j.msec.2017.12.026
Saldin LT, Cramer MC, Velankar SS, White LJ, Badylak SF (2017) Extracellular matrix hydrogels from decellularized tissues: structure and function. Acta Biomater 49:1–15. https://doi.org/10.1016/j.actbio.2016.11.068
Salem AK, Stevens R, Pearson R, Davies M, Tendler S, Roberts C, Williams P, Shakesheff K (2002) Interactions of 3T3 fibroblasts and endothelial cells with defined pore features. J Biomed Mater Res 61:212–217. https://doi.org/10.1002/jbm.10195
Sheikhi A, Afewerki S, Oklu R, Gaharwar AK, Khademhosseini A (2018) Effect of ionic strength on shear-thinning nanoclay–polymer composite hydrogels. Biomater Sci 6:2073–2083. https://doi.org/10.1039/C8BM00469B
Shen M, Li L, Sun Y, Xu J, Guo X, Prud’homme RK (2014) Rheology and adhesion of poly (acrylic acid)/laponite nanocomposite hydrogels as biocompatible adhesives. Langmuir 30:1636–1642. https://doi.org/10.1021/la4045623
Shin YJ, Shafranek RT, Tsui JH, Walcott J, Nelson A, Kim DH (2021) 3D bioprinting of mechanically tuned bioinks derived from cardiac decellularized extracellular matrix. Acta Biomater 119:75–88. https://doi.org/10.1016/j.actbio.2020.11.006
Stealey ST, Gaharwar AK, Zustiak SP (2023) Laponite-based nanocomposite hydrogels for drug delivery applications. Pharmaceuticals 16:821. https://doi.org/10.3390/ph16060821
Stoppel WL, White JC, Horava SD, Henry AC, Roberts SC, Bhatia SR (2014) Terminal sterilization of alginate hydrogels: efficacy and impact on mechanical properties. J Biomed Mater Res B Appl Biomater 102:877–884. https://doi.org/10.1002/jbm.b.33070
Tamjid E, Guenther BH (2010) Rheology and colloidal structure of silver nanoparticles dispersed in diethylene glycol. Powder Technol 197:49–53. https://doi.org/10.1016/j.powtec.2009.08.022
Tomás H, Alves CS, Rodrigues J (2018) Laponite®: a key nanoplatform for biomedical applications? Nanomed NBM 14:2407–2420. https://doi.org/10.1016/j.nano.2017.04.016
Tondera C, Akbar TF, Thomas AK, Lin W, Werner C, Busskamp V, Zhang Y, Minev IR (2019) Highly conductive, stretchable, and cell-adhesive hydrogel by nanoclay doping. Small 15:1901406. https://doi.org/10.1002/smll.201901406
Wang G, Maciel D, Wu Y, Rodrigues J, Shi X, Yuan Y, Liu C, Tomás H, Li Y (2014) Amphiphilic polymer-mediated formation of laponite-based nanohybrids with robust stability and pH sensitivity for anticancer drug delivery. ACS Appl Mater Interfaces 6:16687–16695. https://doi.org/10.1021/am5032874
Wang Y, Xu R, He W, Yao Z, Li H, Zhou J, Tan J, Yang S, Zhan R, Luo G (2015) Three-dimensional histological structures of the human dermis. Tissue Eng Part C Methods 21:932–944. https://doi.org/10.1089/ten.tec.2014.0578
Wang C, Niu H, Ma X, Hong H, Yuan Y, Liu C (2019) Bioinspired, injectable, quaternized hydroxyethyl cellulose composite hydrogel coordinated by mesocellular silica foam for rapid, noncompressible hemostasis and wound healing. ACS Appl Mater Interfaces 11:34595–34608. https://doi.org/10.1021/acsami.9b08799
Wang Y, Yuan X, Yao B, Zhu S, Zhu P, Huang S (2022) Tailoring bioinks of extrusion-based bioprinting for cutaneous wound healing. Bioact Mater 17:178–194. https://doi.org/10.1016/j.bioactmat.2022.01.024
Wang S, Yu P, Li X, Zhao Z, Dong Y, Li X (2023) Design and fabrication of functional hydrogels with specific surface wettability. Colloid Interface Sci Commun 52:100697. https://doi.org/10.1016/j.colcom.2023.100697
Wilson SA, Cross LM, Peak CW, Gaharwar AK (2017) Shear-thinning and thermo-reversible nanoengineered inks for 3D bioprinting. ACS Appl Mater Interfaces 9:43449–43458. https://doi.org/10.1021/acsami.7b13602
Xu R, Bai Y, Zhao J, Xia H, Kong Y, Yao Z, Yan R, Zhang X, Hu X, Liu M (2018) Silicone rubber membrane with specific pore size enhances wound regeneration. J Tissue Eng Regen Med 12:e905–e917. https://doi.org/10.1002/term.2414
Zhang K, Wang Y, Wei Q, Li X, Guo Y, Zhang S (2021a) Design and fabrication of sodium alginate/carboxymethyl cellulose sodium blend hydrogel for artificial skin. Gels 7:115. https://doi.org/10.3390/gels7030115
Zhang Y, Shen L, Cheng Y, Li G (2021b) Stable and biocompatible fibrillar hydrogels based on the self-crosslinking between collagen and oxidized chondroitin sulfate. Polym Degrad Stab 193:109742. https://doi.org/10.1016/j.polymdegradstab.2021.109742
Zhang X, Chen X, Hong H, Hu R, Liu J, Liu C (2022) Decellularized extracellular matrix scaffolds: recent trends and emerging strategies in tissue engineering. Bioact Mater 10:15–31. https://doi.org/10.1016/j.bioactmat.2021.09.014
Zhao Y, Li Y, Mao S, Sun W, Yao R (2015) The influence of printing parameters on cell survival rate and printability in microextrusion-based 3D cell printing technology. Biofabrication 7:045002. https://doi.org/10.1088/1758-5090/7/4/045002
Zhuang T, Li X, Deng Q, Zhao W, Lin B, Luo Y, Zhang X (2020) A GelMA/DECM/nanoclay composite biomaterial ink for printing 3D scaffolds for primary hepatocytes cultivation. Mater Lett 274:128034. https://doi.org/10.1016/j.matlet.2020.128034
Funding
The authors thank the Office of Research and Technology of the Sharif University of Technology for providing access to equipment and facilities.
Author information
Authors and Affiliations
Contributions
GK: Conceptualization, Data curation, Methodology, Investigation, Validation, Writing an original draft. ET: Supervision, Writing—review & editing. HN: Supervision, Writing—review & editing. AS: Conceptualization, Supervision, Data curation, Project administration, Funding acquisition, Resources, Writing—review & editing.
Corresponding author
Ethics declarations
Conflict of interest
The authors have no relevant financial or non-financial interests to disclose
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Kafili, G., Tamjid, E., Niknejad, H. et al. Development of bioinspired nanocomposite bioinks based on decellularized amniotic membrane and hydroxyethyl cellulose for skin tissue engineering. Cellulose 31, 2989–3013 (2024). https://doi.org/10.1007/s10570-024-05797-w
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10570-024-05797-w