Natural Polymers for Organ 3D Bioprinting
Open accessAbstract
Three-dimensional (3D) bioprinting, known as a promising technology for bioartificial organ manufacturing, has provided unprecedented versatility to manipulate cells and other biomaterials with precise control their locations in space. Over the last decade, a number of 3D bioprinting technologies have been explored. Natural polymers have played a central role in supporting the cellular and biomolecular activities before, during and after the 3D bioprinting processes. These polymers have been widely used as effective cell-loading hydrogels for homogeneous/heterogeneous tissue/organ formation, hierarchical vascular/neural/lymphatic network construction, as well as multiple biological/biochemial/physiological/biomedical/pathological functionality realization. This review aims to cover recent progress in natural polymers for bioartificial organ 3D bioprinting. It is structured as introducing the important properties of 3D printable natural polymers, successful models of 3D tissue/organ construction and typical technologies for bioartificial organ 3D bioprinting.
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Natural polymers are obtained from natural materials and provide a guarantee of natural structure, biomimetic and bioactive nature.
“Natural polymers (biopolymers) are obtained from natural materials and provide a guarantee of natural structure, biomimetic and bioactive nature [42].”
From Resorbable Biomaterials Used for 3D Scaffolds in Tissue Engineering: A Review (2023) · cites this paper as [42]
Section 2, “Properties of Natural Polymers” (page unavailable), says natural polymers occur in nature and that their solutions or hydrogels can provide a mild biomimetic environment and facilitate cellular activities. It does not say that natural origin guarantees a natural structure or that every natural polymer is inherently biomimetic and bioactive. (LLM, conf=0.87)
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Printing three-dimensional tissue analogues with decellularized extracellular matrix bioink
Pati, F., Jang, J., Ha, D.-H., Won Kim, S., Rhie, J.-W., Shim, J.-H., Kim, D.-H., & Cho, D.-W. (2014) · Nature Communications · doi:10.1038/ncomms4935 · Cited by 1,904 · see citing works
Direct 3D bioprinting of perfusable vascular constructs using a blend bioink
Jia, W., Gungor-Ozkerim, P. S., Zhang, Y. S., Yue, K., Zhu, K., Liu, W., Pi, Q., Byambaa, B., Dokmeci, M. R., Shin, S. R., et al. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.07.038 · Cited by 922 · see citing works
The burden of musculoskeletal diseases in the United States
Yelin, E., Weinstein, S., & King, T. (2016) · Seminars in Arthritis and Rheumatism · doi:10.1016/j.semarthrit.2016.07.013 · Cited by 537 · see citing works
Bioprinting Cellularized Constructs Using a Tissue-specific Hydrogel Bioink
Skardal, A., Devarasetty, M., Kang, H.-W., Seol, Y.-J., Forsythe, S. D., Bishop, C., Shupe, T., Soker, S., & Atala, A. (2016) · Journal of Visualized Experiments · doi:10.3791/53606 · Cited by 65 · see citing works
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Research works printed but not linked: 140
- [1]Widmaier E.P. Raff H. Strang K.T. The Mechanisms of Body Function Vander’s Human Physiology McGraw-Hill New York, NY, USA 2012 250 291
- [2]Allemani C. Weir H.K. Carreira H. Harewood R. Spika D. Wang X.S. Bannon F. Ahn J.V. Johnson C.J. Bonaventure A. CONCORD Working Group. Global surveillance of cancer survival 1995–2009: Analysis of individual data for 25,676,887 patients from 279 population-based registries in 67 countries (CONCORD-2) Lancet 2015 385 977 1010 10.1016/S0140-6736(14)62038-9 25467588 PMC4588097 · DOI · Paper page
- [3]Patrick C.W. Jr. Adipose tissue engineering: The future of breast and soft tissue reconstruction following tumor resection Semin. Surg. Oncol. 2000 19 302 311 10.1002/1098-2388(200010/11)19:3<302::AID-SSU12>3.0.CO;2-S 11135487 · DOI
- [4]Vasir B. Reitz P. Xu G. Sharma A. Bonner W.S. Weir G.C. Effects of diabetes and hypoxia on gene markers of angiogenesis (HGF, cMET, uPA and uPAR, TGF-α, TGF-β, bFGF and Vimentin) in cultured and transplanted rat islets Diabetologia 2000 43 763 768 10.1007/s001250051374 10907122 · DOI
- [6]Dalal A.R. Philosophy of organ donation: Review of ethical facets World J. Transplant. 2015 24 44 51 10.5500/wjt.v5.i2.44 26131406 PMC4478599 · DOI
- [7]Langer R. Vacanti J.P. Tissue engineering Science 1993 260 920 926 10.1126/science.8493529 8493529 · DOI · Paper page
- [8]Wang X. Yan Y. Lin F. Xiong Z. Wu R. Zhang R. Lu Q. Preparation and characterization of a collagen/chitosan/heparin matrix for an implantable bioartificial liver J. Biomater. Sci. Polym. Ed. 2005 16 1063 1080 10.1163/1568562054798554 16231599 · DOI
- [9]Moniaux N. Faivre J.A. Reengineered liver for transplantation J. Hepatol. 2011 54 386 387 10.1016/j.jhep.2010.07.053 21112113 · DOI
- [10]Mao A.S. Mooney D.J. Regenerative medicine: Current therapies and future directions Proc. Natl. Acad. Sci. USA 2015 112 14452 14459 10.1073/pnas.1508520112 26598661 PMC4664309 · DOI
- [11]Hanauer N. Latreille P.L. Alsharif S. Banquy X. 2D, 3D and 4D active compound delivery in tissue engineering and regenerative medicine Curr. Pharm. Des. 2015 21 1506 1516 10.2174/1381612821666150115153417 25594405 · DOI
- [12]Wang X. Yan Y. Zhang R. Rapid prototyping as tool for manufacturing bioartificial livers Trends Biotechnol. 2007 25 505 513 10.1016/j.tibtech.2007.08.010 17949840 · DOI
- [13]Wang X. Intelligent freeform manufacturing of complex organs Artif. Org. 2012 36 951 961 10.1111/j.1525-1594.2012.01499.x 22888830 · DOI
- [14]Wang X. Yan Y. Zhang R. Recent trends and challenges in complex organ manufacturing Tissue Eng. Part B 2010 16 189 197 10.1089/ten.teb.2009.0576 19824803 · DOI
- [15]Ott H.C. Matthiesen T.S. Goh S.K. Black L.D. Kren S.M. Netoff T.I. Taylor D.A. Perfusion-decellularized matrix: Using nature’s platform to engineer a bioartificial heart Nat. Med. 2008 14 213 221 10.1038/nm1684 18193059 · DOI · Paper page
- [16]Wang X. Huang Y.W. Liu C. A combined rotational mold for manufacturing a functional liver system J. Bioact. Compat. Polym. 2015 39 436 451 10.1177/0883911515578872 · DOI
- [17]Lei M. Wang X. Biodegradable polymers and stem cells for bioprinting Molecules 2016 21 539 10.3390/molecules21050539 27136526 PMC6274354 · DOI
- [18]Bonandrini B. Figliuzzi M. Papadimou E. Morigi M. Perico N. Casiraghi F. Sangalli F. Conti S. Benigni A. Remuzzi A. Recellularization of well-preserved acellular kidney scaffold using embryonic stem cells Tissue Eng. Part A 2014 20 1486 10.1089/ten.tea.2013.0269 24320825 PMC4011423 · DOI · Paper page
- [19]Ozbolat I.T. Hospodiuk M. Current advances and future perspectives in extrusion-based bioprinting Biomaterials 2016 76 321 343 10.1016/j.biomaterials.2015.10.076 26561931 · DOI
- [20]Liu F. Liu C. Chen Q. Ao Q. Tian X. Fan J. Tong H. Wang X. Progress in organ 3D bioprinting Int. J. Bioprint. 2018 4 1 15 10.18063/ijb.v4i1.128 PMC7582006 33102911 · DOI
- [22]Wang X. Yan Y. Zhang R. Gelatin-based hydrogels for controlled cell assembly Biomedical Applications of Hydrogels Handbook Ottenbrite R.M. Springer New York, NY, USA 2010 269 284
- [23]Nair L.S. Laurencin C.T. Biodegradable polymers as biomaterials Prog. Polym. Sci. 2007 32 762 798 10.1016/j.progpolymsci.2007.05.017 · DOI · Paper page
- [24]Derby B. Printing and prototyping of tissues and scaffolds Science 2012 338 921 926 10.1126/science.1226340 23161993 · DOI
- [25]Toh W.S. Loh X.J. Advances in hydrogel delivery systems for tissue regeneration Mater. Sci. Eng. C Mater. Biol. Appl. 2014 45 690 697 10.1016/j.msec.2014.04.026 25491878 · DOI
- [26]Hou R. Nie L. Du G. Xiong X. Fu J. Natural polysaccharides promote chondrocyte adhesion and proliferation on magnetic nanoparticle/PVA composite hydrogels Colloids Surf. B 2015 132 146 154 10.1016/j.colsurfb.2015.05.008 26037704 · DOI
- [27]Billiet T. Vandenhaute M. Schelfhout J. Van Vlierberghe S. Dubruel P. A review of trends and limitations in hydrogel-rapid prototyping for tissue engineering Biomaterials 2015 33 6020 6041 10.1016/j.biomaterials.2012.04.050 22681979 · DOI
- [28]Li C. Faulkner-Jones A. Dun A.R. Jin J. Chen P. Xing Y. Yang Z. Li Z. Shu W. Liu D. Rapid formation of a supramolecular polypeptide–DNA hydrogel for in situ three-dimensional multilayer bioprinting Angew. Chem. Int. Ed. Engl. 2015 54 3957 3961 10.1002/anie.201411383 25656851 · DOI · Paper page
- [29]Doppalapudi S. Jain A. Domb A.J. Khan W. Biodegradable polymers for targeted delivery of anti-cancer drugs Expert Opin. Drug Deliv. 2016 13 891 909 10.1517/17425247.2016.1156671 26983898 · DOI
- [30]Fedorovich N.E. Swennen I. Girones J. Moroni L. van Blitterswijk C.A. Schacht E. Alblas J. Dhert W.J. Evaluation of photocrosslinked lutrol hydrogel for tissue printing applications Biomacromolecules 2009 10 1689 1696 10.1021/bm801463q 19445533 · DOI
- [31]Li S. Yan Y. Xiong Z. Weng C. Zhang R. Wang X. Gradient hydrogel construct based on an improved cell assembling system J. Bioact. Compat. Polym. 2009 24 84 99 10.1177/0883911509103357 · DOI
- [32]Zhang Y. Yu Y. Ozbolat I.T. Direct bioprinting of vessel-like tubular microfluidic channels J. Nanotechnol. Eng. Med. 2013 4 210011 210017 10.1115/1.4024398 · DOI
- [33]Markstedt K. Mantas A. Tournier I. Martínez Ávila H. Hägg D. Gatenholm P. 3D bioprinting human chondrocytes with nanocellulose-alginate bioink for cartilage tissue engineering applications Biomacromolecules 2015 16 1489 1496 10.1021/acs.biomac.5b00188 25806996 · DOI · Paper page
- [34]Ozbolat I.T. Chen H. Yu Y. Development of “Multi-arm Bioprinter” for hybrid biofabrication of tissue engineering constructs Robot. Comput. Integr. Manuf. 2014 30 295 304 10.1016/j.rcim.2013.10.005 · DOI
- [35]Xavier J.R. Thakur T. Desai P. Jaiswal M.K. Sears N. Cosgriff-Hernandez E. Kaunas R. Gaharwar A.K. Bioactive nanoengineered hydrogels for bone tissue engineering: A growth-factor-free approach ACS Nano 2015 9 3109 3118 10.1021/nn507488s 25674809 · DOI
- [36]Xu C. Zhang M. Huang Y. Ogale A. Fu J. Markwald R.R. Study of droplet formation process during drop-on-demand inkjetting of living cell-laden bioink Langmuir 2014 30 9130 9138 10.1021/la501430x 25005170 · DOI
- [37]Lee V. Lanzi A. Ngo H. Yoo S.-S. Vincent P. Dai G. Generation of multi-scale vascular network system within 3D hydrogel using 3D bio-printing technology Cell. Mol. Bioeng. 2014 7 460 472 10.1007/s12195-014-0340-0 25484989 PMC4251565 · DOI
- [38]Lee V.K. Kim D.Y. Ngo H. Lee Y. Seo L. Yoo S. Vincent P.A. Dai G. Creating perfused functional vascular channels using 3D bio-printing technology Biomaterials 2014 35 8092 8102 10.1016/j.biomaterials.2014.05.083 24965886 PMC4112057 · DOI · Paper page
- [39]Thein-Han W. Xu H.H.K. Prevascularization of a gas-foaming macroporous calcium phosphate cement scaffold via coculture of human umbilical vein endothelial cells and osteoblasts Tissue Eng. Part A 2013 19 1675 1685 10.1089/ten.tea.2012.0631 23470207 PMC3700173 · DOI
- [40]Rutz A.L. Hyland K.E. Jakus A.E. Burghardt W.R. Shah R.N. A multi-material bioink method for 3D printing tunable, cell-compatible hydrogels Adv. Mater. 2015 27 1607 1614 10.1002/adma.201405076 25641220 PMC4476973 · DOI
- [41]Huang T.Q. Qu X. Liu J. Chen S. 3D printing of biomimetic microstructures for cancer cell migration Biomed. Microdevices 2014 16 127 132 10.1007/s10544-013-9812-6 24150602 PMC3945947 · DOI
- [42]Pawar S.N. Edgar K.J. Alginate derivatization: A review of chemistry, properties and applications Biomaterials 2012 33 3279 3305 10.1016/j.biomaterials.2012.01.007 22281421 · DOI
- [43]Lee K.Y. Mooney D.J. Alginate: Properties and biomedical applications Prog. Polym. Sci. 2012 37 106 126 10.1016/j.progpolymsci.2011.06.003 22125349 PMC3223967 · DOI
- [44]Choi Y.-J. YI H.-G. Kim S.-W. Cho D.-W. 3D cell printed tissue analogues: A new platform for theranostics Theranostics 2017 7 3118 3137 10.7150/thno.19396 28839468 PMC5566110 · DOI
- [45]Tønnesen H.H. Karlsen J. Alginate in drug delivery systems Drug Dev. Ind. Pharm. 2002 28 621 630 10.1081/DDC-120003853 12149954 · DOI
- [46]Drury J.L. Dennis R.G. Mooney D.J. The tensile properties of alginate hydrogels Biomaterials 2004 25 3187 3199 10.1016/j.biomaterials.2003.10.002 14980414 · DOI
- [47]Stanton M.M. Samitier J. Sánchez S. Bioprinting of 3D hydrogels Lab Chip 2015 15 3111 3115 10.1039/C5LC90069G 26066320 · DOI
- [48]Axpe E. Oyen M.L. Applications of alginate-based bioinks in 3D bioprinting Int. J. Mol. Sci. 2016 17 10.3390/ijms17121976 27898010 PMC5187776 · DOI
- [50]Ahn S. Lee H. Bonassar L.J. Kim G. Cells (MC3T3-E1)-laden alginate scaffolds fabricated by a modified solid-freeform fabrication process suppliemented with an aerosol spraying Biomacromolecules 2012 13 2997 3003 10.1021/bm3011352 22913233 · DOI
- [51]Yan Y. Wang X. Xiong Z. Liu H. Liu F. Lin F. Wu R. Zhang R. Lu Q. Direct construction of a three-dimensional structure with cells and hydrogel J. Bioact. Compat. Polym. 2005 20 259 269 10.1177/0883911505053658 · DOI
- [52]Yao R. Zhang R. Wang X. Design and evaluation of a cell microencapsulating device for cell assembly technology J. Bioact. Compat. Polym. 2009 24 48 62 10.1177/0883911509103329 · DOI
- [54]Park J. Lee S.J. Chung S. Lee J.H. Kim W.D. Lee J.Y. Park S.A. Cell-laden 3D bioprinting hydrogel matrix depending on different compositions for soft tissue engineering: Characterization and evaluation Mater. Sci. Eng. C Mater. Biol. Appl. 2017 71 678 684 10.1016/j.msec.2016.10.069 27987760 · DOI
- [55]Kong H.J. Kaigler D. Kim K. Mooney D.J. Controlling rigidity and degradation of alginate hydrogels via molecular weight distribution Biomacromolecules 2004 5 1720 1727 10.1021/bm049879r 15360280 · DOI
- [56]Wong T.Y. Preston L.A. Schiller N.L. ALGINATE LYASE: Review of major sources and enzyme characteristics, structure-function analysis, biological roles, and applications Annu. Rev. Microbiol. 2000 54 289 340 10.1146/annurev.micro.54.1.289 11018131 · DOI · Paper page
- [57]Sui S. Wang X. Liu P. Yan Y. Zhang R. Cryopreservation of cells in 3D constructs based on controlled cell assembly processes J. Bioact. Compat. Polym. 2009 24 473 487 10.1177/0883911509338990 · DOI
- [58]Wang X. Paloheimo K.-S. Xu H. Liu C. Cryopreservation of cell/hydrogel constructs based on a new cell-assembling technique J. Bioact. Compat. Polym. 2010 25 634 653 10.1177/0883911510382571 · DOI
- [59]Wang X. Xu H. Incorporation of DMSO and dextran-40 into a gelatin/alginate hydrogel for controlled assembled cell cryopreservation Cryobiology 2010 61 345 351 10.1016/j.cryobiol.2010.10.161 21055398 · DOI
- [61]Xu M. Yan Y. Liu H. Yao Y. Wang X. Control adipose-derived stromal cells differentiation into adipose and endothelial cells in a 3-D structure established by cell-assembly technique J. Bioact. Compat. Polym. 2009 24 31 47 10.1177/0883911509102794 · DOI
- [62]Xu M. Wang X. Yan Y. Yao R. Ge Y. A cell-assembly derived physiological 3D model of the metabolic syndrome, based on adipose-derived stromal cells and a gelatin/alginate/fibrinogen matrix Biomaterials 2010 31 3868 3877 10.1016/j.biomaterials.2010.01.111 20153520 · DOI
- [63]Shim J.H. Lee J.S. Kim J.Y. Cho D.W. Bioprinting of a mechanically enhanced three-dimensional dual cell-laden construct for osteochondral tissue engineering using a multi-head tissue/organ building system J. Micromech. Microeng. 2012 22 085014 10.1088/0960-1317/22/8/085014 · DOI
- [64]Yu Y. Zhang Y. Martin J.A. Ozbolat I.T. Evaluation of cell viability and functionality in vessel-like bioprintable cell-laden tubular channels J. Biomech. Eng. 2013 135 91011 10.1115/1.4024575 23719889 PMC3708706 · DOI
- [65]Duan B. Hockaday L.A. Kang K.H. Butcher J.T. 3D bioprinting of heterogeneous aortic valve conduits with alginate/gelatin hydrogels J. Biomed. Mater. Res. Part A 2013 101A 1255 1264 10.1002/jbm.a.34420 23015540 PMC3694360 · DOI
- [66]Chung J.Y. Naficy S. Yue Z. Kapsa R. Quigley A. Moulton S. Wallace G. Bio-ink properties and printability for extrusion printing living cells Biomater. Sci. 2013 1 763 773 10.1039/c3bm00012e 32481829 · DOI
- [67]Wang X. He K. Zhang W. Optimizing the fabrication processes for manufacturing a hybrid hierarchical polyurethane-cell/hydrogel construct J. Bioact. Compat. Polym. 2013 28 303 319 10.1177/0883911513491359 · DOI
- [68]Huang Y. He K. Wang X. Rapid Prototyping of a hybrid hierarchical polyurethane-cell/hydrogel construct for regenerative medicine Mater. Sci. Eng. C 2013 33 3220 3229 10.1016/j.msec.2013.03.048 23706204 · DOI
- [69]Wang J. Development of a Combined 3D Printer and Its Application in Complex Organ Construction Master’s Thesis Tsinghua University Beijing, China 2014
- [70]Sarker B. Singh R. Silva R. Roether J.A. Kaschta J. Detsch R. Schubert D.W. Cicha I. Boccaccini A.R. Evaluation of fibroblasts adhesion and proliferation on alginate-gelatin crosslinked hydrogel PLoS ONE 2014 9 e107952 10.1371/journal.pone.0107952 25268892 PMC4182442 · DOI
- [71]Jia J. Richards D.J. Pollard S. Tan Y. Rodriguez J. Visconti R.P. Trusk T.C. Yost M.J. Yao H. Markwald R.R. Engineering alginate as bioink for bioprinting Acta Biomater. 2014 10 4323 4331 10.1016/j.actbio.2014.06.034 24998183 PMC4350909 · DOI
- [72]Zhang W. Lian Q. Li D. Wang K. Hao D. Bian W. He J. Jin Z. Cartilage repair and subchondral bone migration using 3D printing osteochondral composites: A one-year-period study in rabbit trochlea Biomed. Res. Int. 2014 5 23 28 10.1155/2014/746138 25177697 PMC4142181 · DOI
- [73]Ahn S.H. Lee H.J. Lee J.S. Yoon H. Chun W. Kim G.H. A novel cell-printing method and its application to hepatogenic differentiation of human adipose stem cell-embedded mesh structures Sci. Rep. 2015 5 13427 10.1038/srep13427 26293341 PMC4544022 · DOI
- [74]Kundu J. Shim J.H. Jang J. Kim S.W. Cho D.W. An additive manufacturing-based PCL-alginate-chondrocyte bioprinted scaffold for cartilage tissue engineering J. Tissue Eng. Regen. Med. 2015 9 1286 1297 10.1002/term.1682 23349081 · DOI
- [75]Colosi C. Shin S.R. Manoharan V. Massa S. Costantini M. Barbetta A. Dokmeci M.R. Dentini M. Khademhosseini A. Microfluidic bioprinting of heterogeneous 3D tissue constructs using low-viscosity bioink Adv. Mater. 2016 28 677 684 10.1002/adma.201503310 26606883 PMC4804470 · DOI · Paper page
- [76]Zhao X. Wang X. Preparation of an adipose-derived stem cell/fibrin-poly(dl-lactic-co-glycolic acid) construct based on a rapid prototyping technique J. Bioact. Compat. Polym. 2013 28 191 203 10.1177/0883911513481892 · DOI
- [77]Zhao X. Du S. Chai L. Xu Y. Liu L. Zhou X. Wang J. Zhang W. Liu C.-H. Wang X. Anti-cancer drug screening based on an adipose-derived stem cell/hepatocyte 3D printing technique J. Stem Cell Res. Ther. 2015 5 10.4172/2157-7633.1000273 · DOI
- [79]Izadifar Z. Chang T. Kulyk W. Chen X. Eames B.F. Analyzing biological performance of 3D-printed, cell-impregnated hybrid constructs for cartilage tissue engineering Tissue Eng. Part C Methods 2016 22 173 188 10.1089/ten.tec.2015.0307 26592915 · DOI
- [80]Daly A.C. Cunniffe G.M. Sathy B.N. Jeon O. Alsberg E. Kelly D.J. 3D bioprinting of developmentally inspired templates for whole bone organ engineering Adv. Healthc. Mater. 2016 5 2353 2362 10.1002/adhm.201600182 27281607 · DOI
- [83]Luo Y.X. Luo G.L. Gelinsky M. Huang P. Ruan C.S. 3D bioprinting scaffold using alginate/polyvinyl alcohol bioinks Mater. Lett. 2017 189 295 298 10.1016/j.matlet.2016.12.009 · DOI
- [84]Bendtsen S.T. Quinnell S.P. Wei M. Development of a novel alginate-polyvinyl alcohol-hydroxyapatite hydrogel for 3D bioprinting bone tissue engineered scaffolds J. Biomed. Mater. Res. Part A 2017 105 1457 1468 10.1002/jbm.a.36036 28187519 · DOI
- [85]Bendtsen S.T. Wei M. In vitro evaluation of 3D bioprinted tri-polymer network scaffolds for bone tissue regeneration J. Biomed. Mater. Res. Part A 2017 105 3262 3272 10.1002/jbm.a.36184 28804996 · DOI
- [86]Yu H.Y. Ma D.D. Wu B.L. Gelatin/alginate hydrogel scaffolds prepared by 3D bioprinting promotes cell adhesion and proliferation of human dental pulp cells in vitro J. South. Med. Univ. 2017 37 668 PMC6780481 28539292
- [87]Müller M. Öztürk E. Arlov Ø. Gatenholm P. Zenobi-Wong M. Alginate sulfate-nanocellulose bioinks for cartilage bioprinting applications Ann. Biomed. Eng. 2017 45 210 223 10.1007/s10439-016-1704-5 27503606 · DOI
- [88]Nguyen D. Hägg D.A. Forsman A. Ekholm J. Nimkingratana P. Brantsing C. Kalogeropoulos T. Zaunz S. Concaro S. Brittberg M. Cartilage tissue engineering by the 3D bioprinting of iPS cells in a nanocellulose/alginate bioink Sci Rep. 2017 7 658 10.1038/s41598-017-00690-y 28386058 PMC5428803 · DOI
- [89]Wang X. Ao Q. Tian X. Fan J. Tong H. Hou W. Bai S. Gelatin-based hydrogels for organ 3D bioprinting Polymers 2017 9 401 10.3390/polym9090401 PMC6418925 30965706 · DOI
- [90]Madl C.M. Katz L.M. Heilshorn S.C. Bio-orthogonally crosslinked, engineered protein hydrogels with tunable mechanics and biochemistry for cell encapsulation Adv. Funct. Mater. 2016 26 3612 3620 10.1002/adfm.201505329 27642274 PMC5019573 · DOI · Paper page
- [91]Zhao X. Liu L. Wang J. Xu Y. Zhang W. Khang G. Wang X. In vitro vascularization of a combined system based on a 3D printing technique J. Tissue Eng. Regen. Med. 2016 10 833 842 10.1002/term.1863 24399638 · DOI
- [92]Kang H.-W. Sang J.L. Ko I.K. Kengla C. Yoo J.J. Atala A. A 3D bioprinting system to produce human-scale tissue constructs with structural integrity Nat. Biotechnol. 2016 34 312 319 10.1038/nbt.3413 26878319 · DOI · Paper page
- [93]Kolesky D.B. Homan K.A. Skylarscott M.A. Lewis J.A. Three-dimensional bioprinting of thick vascularized tissues Proc. Natl. Acad. Sci. USA 2016 113 3179 3184 10.1073/pnas.1521342113 26951646 PMC4812707 · DOI · Paper page
- [94]Grigore A. Sarker B. Fabry B. Boccaccini A.R. Detsch R. Behavior of encapsulated MG-63 cells in RGD and gelatine-modified alginate hydrogels Tissue Eng. Part A. 2014 20 2140 2150 10.1089/ten.tea.2013.0416 24813329 · DOI
- [95]Van Den Bulcke A.I. Bogdanov B. De Rooze N. Schacht E.H. Cornelissen M. Berghmans H. Structural and rheological properties of methacrylamide modified gelatin hydrogels Biomacromolecules 2000 1 31 38 10.1021/bm990017d 11709840 · DOI · Paper page
- [96]Wang X. Liu C. 3D bioprinting of adipose-derived stem cells for organ manufacturing Enabling Cutting Edge Technology for Regenerative Medicine, Khang, G., Ed. Springer Singapore 2018 1 16 30357615
- [97]Yan Y. Wang X. Pan Y. Liu H. Cheng J. Xiong Z. Lin F. Wu R. Zhang R. Lu Q. Fabrication of viable tissue-engineered constructs with 3D cell-assembly technique Biomaterials 2005 26 5864 5871 10.1016/j.biomaterials.2005.02.027 15949552 · DOI
- [98]Wang X. Yan Y. Pan Y. Xiong Z. Liu H. Cheng J. Liu F. Lin F. Wu R. Zhang R. Generation of three-dimensional hepatocyte/gelatin structures with rapid prototyping system Tissue Eng. 2006 12 83 90 10.1089/ten.2006.12.83 16499445 · DOI
- [99]Xu W. Wang X. Yan Y. Zheng W. Xiong Z. Lin F. Wu R. Zhang R. Rapid prototyping three-dimensional cell/gelatin/fibrinogen constructs for medical regeneration J. Bioact. Compat. Polym. 2007 22 363 377 10.1177/0883911507079451 · DOI
- [100]Zhang T. Yan Y. Wang X. Xiong Z. Lin F. Wu R. Zhang R. Three-dimensional gelatin and gelatin/hyaluronan hydrogel structures for traumatic brain injury J. Bioact. Compat. Polym. 2007 22 19 29 10.1177/0883911506074025 · DOI
- [101]Xu W. Wang X. Yan Y. Zhang R. A polyurethane-gelatin hybrid construct for the manufacturing of implantable bioartificial livers J. Bioact. Compat. Polym. 2008 23 409 422 10.1177/0883911508095517 · DOI
- [103]Skardal A. Zhang J. McCoard L. Xu X. Photocrosslinkable hyaluronan-gelatin hydrogels for two-step bioprinting Tissue Eng. A 2010 16 2675 2685 10.1089/ten.tea.2009.0798 20387987 PMC3135254 · DOI
- [104]Wüst S. Godla M.E. Müller R. Hofmann S. Tunable hydrogel composite with two-step processing in combination with innovative hardware upgrade for cell-based three-dimensional bioprinting Acta Biomater. 2014 10 630 640 10.1016/j.actbio.2013.10.016 24157694 · DOI
- [105]Hakam M.S. Imani R. Abolfathi N. Fakhrzadeh H. Sharifi A.M. Evaluation of fibrin-gelatin hydrogel as biopaper for application in skin bioprinting: An in-vitro study Biomed. Mater. Eng. 2016 27 669 682 10.3233/BME-161617 28234249 · DOI
- [106]Heris H.K. Rahmat M. Mongeau L. Characterization of a hierarchical network of hyaluronic acid/gelatin composite for use as a smart injectable biomaterial Macromol. Biosci. 2012 12 202 210 10.1002/mabi.201100335 22147507 PMC4490586 · DOI
- [108]Hemshekhar M. Thushara R.M. Chandranayaka S. Sherman L.S. Kemparaju K. Girish K.S. Emerging roles of hyaluronic acid bioscaffolds in tissue engineering and regenerative medicine Int. J. Biol. Macromol. 2016 86 917 928 10.1016/j.ijbiomac.2016.02.032 26893053 · DOI
- [109]Park Y.D. Tirelli N. Hubbell J.A. Photopolymerized hyaluronic acid-based hydrogels and interpenetrating networks Biomaterials 2003 24 893 900 10.1016/S0142-9612(02)00420-9 12504509 · DOI
- [110]Abbadessa A. Mouser V.H. Blokzijl M.M. Gawlitta D. Dhert W.J. Hennink W.E. Malda J. Vermonden T. A synthetic thermosensitive hydrogel for cartilage bioprinting and its biofunctionalization with polysaccharides Biomacromolecules 2016 17 2137 2147 10.1021/acs.biomac.6b00366 27171342 PMC4931898 · DOI
- [111]Camci-Unal G. Cuttica D. Annabi N. Demarchi D. Khademhosseini A. Synthesis and characterization of hybrid hyaluronic acid-gelatin hydrogels Biomacromolecules 2013 14 1085 1092 10.1021/bm3019856 23419055 PMC3643200 · DOI
- [112]Duan B. Kapetanovic E. Hockaday L.A. Butcher J.T. Three-dimensional printed trileaflet valve conduits using biological hydrogels and human valve interstitial cells Acta Biomater. 2014 10 1836 1846 10.1016/j.actbio.2013.12.005 24334142 PMC3976766 · DOI
- [113]Helary C. Bataille I. Abed A. Illoul C. Anglo A. Louedec L. Letourneur D. Meddahi-Pellé A. Giraud-Guille M.M. Concentrated collagen hydrogels as dermal substitutes Biomaterials 2010 31 481 490 10.1016/j.biomaterials.2009.09.073 19811818 · DOI
- [114]Nagel T. Kelly D.J. The composition of engineered cartilage at the time of implantation determines the likelihood of regenerating tissue with a normal collagen architecture Tissue Eng. Part A 2013 19 824 833 10.1089/ten.tea.2012.0363 23082998 · DOI
- [115]Weadock K.S. Miller E.J. Keuffel E.L. Dunnl M.G. Effect of physical crosslinking methods on collagen-fiber durability in proteolytic solutions J. Biomed. Mater. Res. 1996 32 221 226 10.1002/(SICI)1097-4636(199610)32:2<221::AID-JBM11>3.0.CO;2-M 8884499 · DOI
- [116]Ren X. Wang F. Chen C. Gong X. Yin L. Yang L. Engineering zonal cartilage through bioprinting collagen type II hydrogel constructs with biomimetic chondrocyte density gradient BMC Musculoskelet. Disord. 2016 17 301 10.1186/s12891-016-1130-8 27439428 PMC4955200 · DOI
- [117]Chen C. Zhao M.L. Zhang R.K. Lu G. Zhao C.Y. Fu F. Sun H.T. Zhang S. Tu Y. Li X.H. Collagen/heparin sulfate scaffolds fabricated by a 3D bioprinter improved mechanical properties and neurological function after spinal cord injury in rats J. Biomed. Mater. Res. A 2017 105 1324 1332 10.1002/jbm.a.36011 28120511 · DOI
- [118]Cui T. Yan Y. Zhang R. Liu L. Xu W. Wang X. Rapid prototyping of a double layer polyurethane-collagen conduit for peripheral nerve regeneration Tissue Eng. Part C 2009 15 1 9 10.1089/ten.tec.2008.0354 18844602 · DOI
- [119]Cui T. Wang X. Yan Y. Zhang R. Rapid prototyping a new polyurethane-collagen conduit and its Schwann cell compatibility J. Bioact. Compat. Polym. 2009 24 5 17 10.1177/0883911509102349 · DOI
- [120]Wang X. Cui T. Yan Y. Zhang R. Peroneal nerve regeneration along a new polyurethane-collagen guide conduit J. Bioact. Compat. Polym. 2009 24 109 127 10.1177/0883911508101183 · DOI
- [121]Mosesson M.W. Fibrinogen and fibrin structure and functions J. Thromb. Haemost. 2005 3 1894 1904 10.1111/j.1538-7836.2005.01365.x 16102057 · DOI · Paper page
- [122]Wang X. Mäkitie A.A. Paloheimo K.-S. Tuomi J. Paloheimo M. Sui S. Zhang Q. Characterization of a PLGA sandwiched cell/fibrin tubular construct and induction of the adipose derived stem cells into smooth muscle cells Mater. Sci. Eng. C 2011 31 801 808 10.1016/j.msec.2010.10.007 · DOI
- [123]Wang X. Sui S. Liu C. Optimizing the step by step forming processes for fabricating a PLGA sandwiched cell/hydrogel construct J. Appl. Polym. Sci. 2011 120 1199 1207 10.1002/app.33093 · DOI
- [124]Wang X. Sui S. Pulsatile culture of a PLGA sandwiched cell/hydrogel construct fabricated using a step by step mold/extraction method Artif. Organs 2011 35 645 655 10.1111/j.1525-1594.2010.01137.x 21671960 · DOI
- [125]Gasperini L. Mano J.F. Reis R.L. Natural polymers for the microencapsulation of cells J. R. Soc. Interface 2014 11 20140817 10.1098/rsif.2014.0817 25232055 PMC4191114 · DOI
- [126]Rowe S.L. Lee S. Stegemann J.P. Influence of thrombin concentration on the mechanical and morphological properties of cell-seeded fibrin hydrogels Acta Biomater. 2007 3 59 67 10.1016/j.actbio.2006.08.006 17085089 PMC1852453 · DOI
- [129]Wang X. Ao Q. Tian X. Fan J. Wei Y. Hou W. Tong H. Bai S. 3D bioprinting technologies for hard tissue and organ engineering Materials 2016 9 802 10.3390/ma9100802 28773924 PMC5456640 · DOI
- [131]Skardal A. Mack D. Kapetanovic E. Atala A. Jackson J.D. Yoo J. Soker S. Bioprinted amniotic fluid-derived stem cells accelerate healing of large skin wounds Stem Cells Transl. Med. 2012 1 792 802 10.5966/sctm.2012-0088 23197691 PMC3659666 · DOI
- [132]Wang X. Ma J. Wang Y. He B. Structural characterization of phosphorylated chitosan and their applications as effective additives of calcium phosphate cements Biomaterials 2001 22 2247 2255 10.1016/S0142-9612(00)00413-0 11456064 · DOI
- [133]Wang X. Ma J. Wang Y. He B. Bone repair in radii and tibias of rabbits with phosphorylated chitosan reinforced calcium phosphate cements Biomaterials 2002 23 4167 4176 10.1016/S0142-9612(02)00153-9 12194519 · DOI
- [134]Wang X. Ma J. Feng Q. Cui F. Skeletal repair in of rabbits with calcium phosphate cements incorporated phosphorylated chitin reinforced Biomaterials 2002 23 4591 4600 10.1016/S0142-9612(02)00205-3 12322980 · DOI
- [135]Wang X. Li D. Wang W. Feng Q. Cui F. Xu Y. Song X. Covalent immobilization of chitosan and heparin on PLGA surface Int. J. Macromol. 2003 33 95 100 10.1016/S0141-8130(03)00072-2 14599590 · DOI
- [136]Wang X. Ma J. Feng Q. Cui F. The effects of S-chitosan on the physical properties of calcium phosphate cements J. Bioact. Compat. Polym. 2003 18 45 57 10.1177/0883911503018001005 · DOI
- [137]Wang X. Ma J. Feng Q. Cui F. In vivo testing of S-chitosan enhanced calcium phosphate cements J. Bioact. Compat. Polym. 2003 18 259 271 10.1177/088391103036042 · DOI
- [138]Wang X. Li D. Wang W. Feng Q. Cui F. Xu Y. Song X. van der Werf M. Crosslinked collagen/chitosan matrices for artificial livers Biomaterials 2003 24 3213 3220 10.1016/S0142-9612(03)00170-4 12763448 · DOI
- [139]Ma L. Gao C. Mao Z. Zhou J. Shen J. Hu X. Han C. Collagen/chitosan porous scaffolds with improved biostability for skin tissue engineering Biomaterials 2003 24 4833 4841 10.1016/S0142-9612(03)00374-0 14530080 · DOI
- [140]Fu X.T. Kim S.M. Agarase: Review of major sources, categories, purification method, enzyme characteristics and applications Mar. Drugs 2010 8 200 218 10.3390/md8010200 20161978 PMC2817930 · DOI
- [141]Panwar A. Tan L.P. Current status of bioinks for micro-extrusion-based 3D bioprinting Molecules 2016 21 685 10.3390/molecules21060685 27231892 PMC6273655 · DOI
- [142]Awad H.A. Wickham M.Q. Leddy H.A. Gimble J.M. Guilak F. Chondrogenic differentiation of adipose-derived adult stem cells in agarose, alginate, and gelatin scaffolds Biomaterials 2004 25 3211 3222 10.1016/j.biomaterials.2003.10.045 14980416 · DOI
- [143]Fan R. Piou M. Darling E. Cormier D. Sun J. Wan J. Bio-printing cell-laden matrigel-agarose constructs J. Biomater. Appl. 2016 31 684 692 10.1177/0885328216669238 27638155 PMC5603305 · DOI · Paper page
- [144]Chen R.N. Ho H.O. Tsai Y.T. Sheu M.T. Process development of an acellular dermal matrix (ADM) for biomedical applications Biomaterials 2004 25 2679 2686 10.1016/j.biomaterials.2003.09.070 14751754 · DOI
- [145]Freytes D.O. Martin J. Velankar S.S. Lee A.S. Badylak S.F. Preparation and rheological characterization of a gel form of the porcine urinary bladder matrix Biomaterials 2008 29 1630 1637 10.1016/j.biomaterials.2007.12.014 18201760 · DOI
- [147]Sellaro T.L. Ranade A. Faulk D.M. McCabe G.P. Dorko K. Badylak S.F. Strom S.C. Maintenance of human hepatocyte function in vitro by liver-derived extracellular matrix gels Tissue Eng. Part A 2010 16 1075 1082 10.1089/ten.tea.2008.0587 19845461 PMC2863084 · DOI
- [148]Wong S.Y. Tay C.Y. Wen F. Venkatraman S.S. Tan L.P. Engineered polymeric biomaterials for tissue engineering Curr. Tissue Eng. 2012 1 41 53 10.2174/2211542011201010041 · DOI
- [149]Wang X. Rijff B.L. Khang G. A building block approach into 3D printing a multi-channel organ regenerative scaffold J. Tissue Eng. Regen. Med. 2017 11 1403 1411 10.1002/term.2038 26123711 · DOI
- [150]Xu Y. Wang X. Fluid and cell behaviors along a 3D printed alginate/gelatin/fibrin channel Biotechnol. Bioeng. 2015 112 1683 1695 10.1002/bit.25579 25727058 · DOI
- [154]Wang X. Liu C. Fibrin hydrogels for endothelialized liver tissue engineering with a predesigned vascular network Polymers 2018 10 1084 10.3390/polym10101048 PMC6403613 30960973 · DOI
- [155]Wang X. Bioartificial organ manufacturing technologies Cell Transplant 2018 in press PMC6322143 30477315
- [156]Guarino V. Gloria A. Raucci M.G. Santis R.D. Ambrosio L. Bio-inspired composite and cell instructive platforms for bone regeneration Int. Mater. Rev. 2012 57 256 275 10.1179/0950660812Z.00000000021 · DOI
- [157]Reitmaier S. Shirazi-Adl A. Bashkuev M. Wilke H.-J. Gloria A. Schmidt H. In vitro and in silico investigations of disc nucleus replacement J. R. Soc. Interface 2012 9 1869 1879 10.1098/rsif.2012.0016 22337630 PMC3385764 · DOI
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- Authors
- Liu, F., Chen, Q., Liu, C., Ao, Q., Tian, X., Fan, J., Tong, H., & Wang, X.
- Affiliations
- China Medical University (CN)
- Corresponding author
- Wang, Xiaohong
- Venue
- Polymers
- Publisher
- MDPI AG
- Published
- 2018-11-16
- Volume
- 10
- Issue
- 11
- Pages
- 1278
- ISSN
- 2073-4360 (ISSN-L)
- PMC
- PMC6401941
- OpenAlex
- W2901587830
- Cited by
- 170
- References
- 4
- Citations by year
- 2026: 8 · 2025: 16 · 2024: 35 · 2023: 20 · 2022: 33 · 2021: 28 · 2020: 19 · 2019: 11
- FWCI
- 1.18
- Type
- journal article
- Language
- en
- Open access
- gold
- dx.doi.org
- Licence
- Locations
- Polymers (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- the 2017 Discipline Promotion Project of China Medical University (CMU) (3110117049)
- the National Natural Science Foundation of China (NSFC) (81571832 & 81271665 & 31600793 & 81571919)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- 3D bioprinting, natural polymers, bioartificial organs, hydrogels, cell loading, neural network construction, tissue engineering
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