| Literature DB >> 35211626 |
Binglong Li1,2, Meng Zhang3, Qunshan Lu1, Baoqing Zhang1, Zhuang Miao1, Lei Li1, Tong Zheng1, Peilai Liu1.
Abstract
3D printing, also known as additive manufacturing, is a technology that uses a variety of adhesive materials such as powdered metal or plastic to construct objects based on digital models. Recently, 3D printing technology has been combined with digital medicine, materials science, cytology, and other multidisciplinary fields, especially in the field of orthopedic built-in objects. The development of advanced 3D printing materials continues to meet the needs of clinical precision medicine and customize the most suitable prosthesis for everyone to improve service life and satisfaction. This article introduces the development of 3D printing technology and different types of materials. We also discuss the shortcomings of 3D printing technology and the current challenges, including the poor bionics of 3D printing products, lack of ideal bioinks, product safety, and lack of market supervision. We also prospect the future development trends of 3D printing.Entities:
Mesh:
Year: 2022 PMID: 35211626 PMCID: PMC8863440 DOI: 10.1155/2022/8759060
Source DB: PubMed Journal: Biomed Res Int Impact factor: 3.411
Figure 1Main 3D printing techniques: (a) vat photopolymerization, (b) fused deposition modeling, (c) selective laser sintering, and (d) bioprinting.
Figure 2(a) Scheme of bottom-up and top-down stereolithography setups. (a1) The bottom-up setup shown is an example of a system whereby the laser scans the surface for the curing of the photosensitive material. (a2) In the example of the top-down setup, dynamic light projection technology is used to cure a complete 2D layer at once [9]. (b) Fused deposition modeling process [5]. (c) Schematic representation of the EBM process [27]. (d1) Schematic of a bioprinting system and basic patterning of a 3D architecture. (d2) Introduction of basic patterning of 3D architecture including multiple cell-laden hydrogels and supporting PCL polymers [24]. Used with permission from Elsevier and Nature America Publishing.
Summary of 3D printing techniques.
| 3DP techniques | Materials | Advantages | Disadvantages | References |
|---|---|---|---|---|
| Vat photopolymerization | Photopolymers, ceramics, composites | (i) High building accuracy | (i) High shrinkage | [ |
| Directed energy deposition | Metals, ceramics, polymeric, composites | (i) Supporting a wide range of materials | (i) Residual stress | [ |
| Binder jetting | Ceramics, metals | (i) Low cost | (i) Low resolution output | [ |
| Fused deposition modeling | Thermoplastic polymers, composites, low-melting temperature metal alloys | (i) Simplicity | (i) Thermal degradation of ingredients | [ |
| Powder bed fusion | Polymers, ceramics, metals | (i) Components exhibit excellent mechanical properties | (i) An expensive process | [ |
Figure 3(a) Shows optical and FESEM micrographs of the bone-implant interface 5 weeks postimplantation. (b) Shows optical and FESEM micrographs of the bone-implant interface 12 weeks postimplantation. (c) Shows the histomorphometric plots of OS/BS% for 5 weeks and 12 weeks of histology data, respectively [49]. Used with permission from Elsevier.
Figure 4The application of 3D printing in orthopedics.
Figure 5Biocompatibility of the 3D printed scaffolds seeded with BMSCs. (a) Morphology of the cells seeded on the surface of the scaffolds observed by SEM: (A) PCL, (B) PCL/DCPD, and (C) PCL/DCPD/nanoZIF-8. Arrows point to the BMSCs adhering to the surface of scaffolds. (b) Representative images of cell spatial distribution on PCL/DCPD/nanoZIF-8 scaffolds using LSCM. (c) Cell apoptosis rate examined by Annexin V assay: (A) PCL, (B) PCL/DCPD, and (C) PCL/DCPD/nanoZIF-8. (d) Cell viability measured by CCK-8 assays on days 1, 3, 5, and 7. Significant differences were marked among a series of points for each group, respectively. Data were shown as mean ± SD, ∗∗∗p < 0.001 (n = 4) [70]. Used with permission from the Royal Society of Chemistry.
Summary of additive manufacturing materials: advantages and disadvantages.
| Material types | Composition | Advantages | Disadvantages | Ref. |
|---|---|---|---|---|
| Metal | Titanium alloy, copper alloy, Ti6Al4V alloys, CoCrMo alloys | (i) Good toughness | (i) Pure titanium easily leads to a stress barrier | [ |
| Bioceramics | Hydroxyapatite (HA), calcium phosphate (CaPs), tricalcium phosphate, MgP, alumina, zirconia | (i) Good biocompatibility | (i) Ceramic stents need to be printed at high temperatures, and stents cannot be simultaneously coated with bioactive molecules that promote bone formation or anti-infective drugs | [ |
| Polymer materials | Polycaprolactone, polylactic acid-glycolic acid, polyglycolic acid, collagen, alginate, silk fibroin, chitosan | (i) Biocompatibility | (i) Natural polymer materials are difficult to obtain in large quantities, degrade quickly, and have insufficient biomechanical strength | [ |
| Composite materials | Polylactic acid-glycolic acid; copolymer/tertiary calcium phosphate; PCL/DCPD/nanoZIF-8; polycaprolactone mixed with | Combined with the advantages of the above materials | [ |