2023
DOI: 10.1016/j.pmatsci.2023.101124
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Biofunctionalized 3D printed structures for biomedical applications: A critical review of recent advances and future prospects

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Cited by 20 publications
(7 citation statements)
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“…3D printing in tissue engineering was first designed as a scaffold for cell culture, 278 and with the development of technology and materials, 3D printing in tissue repair gradually evolved into bioprinting. 279–281 Bioprinting is the precise three-dimensional structural design and integration of biomaterials, cells and bioactive molecules to fabricate implantable materials to which tissue cells can adhere and proliferate. Polyurethanes, 176 poly(glycerol sebacate), 282 polycitrate, 283,284 polycaprolactone, 285 and LCE 286 have shown extremely strong potential for tissue repair applications.…”
Section: Structures and Processing Advantages Of Elastomers For Tissu...mentioning
confidence: 99%
“…3D printing in tissue engineering was first designed as a scaffold for cell culture, 278 and with the development of technology and materials, 3D printing in tissue repair gradually evolved into bioprinting. 279–281 Bioprinting is the precise three-dimensional structural design and integration of biomaterials, cells and bioactive molecules to fabricate implantable materials to which tissue cells can adhere and proliferate. Polyurethanes, 176 poly(glycerol sebacate), 282 polycitrate, 283,284 polycaprolactone, 285 and LCE 286 have shown extremely strong potential for tissue repair applications.…”
Section: Structures and Processing Advantages Of Elastomers For Tissu...mentioning
confidence: 99%
“…Nevertheless, the surface properties of the polymers are frequently critical, necessitating the meticulous identification and acquisition of these characteristics. Non-thermal plasma exposure is commonly used to alter the surface characteristics of polymers [1][2][3][4][5][6][7][8][9], even for biofunctionalizing 3D-printed structures [10].…”
Section: Introductionmentioning
confidence: 99%
“…In contrast, methods for covalent linkage to an implant surface allow for sustained biological activity. [17][18][19][20][21][22] Covalent attachment of bioactive molecules on surfaces has been traditionally achieved using methods relying on wetchemical steps. [16] Examples of these approaches include linker chemistry methods based on salinization, [23] PEGylation, [24] and heparinization.…”
Section: Introductionmentioning
confidence: 99%
“…In contrast, methods for covalent linkage to an implant surface allow for sustained biological activity. [ 17–22 ]…”
Section: Introductionmentioning
confidence: 99%