| Literature DB >> 30974757 |
Tao Han1, Sudip Kundu2, Anindya Nag3, Yongzhao Xu4.
Abstract
This paper showcases a substantial review on some of the significant work done on 3D printing of sensors for biomedical applications. The importance of 3D printing techniques has bloomed in the sensing world due to their essential advantages of quick fabrication, easy accessibility, processing of varied materials and sustainability. Along with the introduction of the necessity and influence of 3D printing techniques for the fabrication of sensors for different healthcare applications, the paper explains the individual methodologies used to develop sensing prototypes. Six different 3D printing techniques have been explained in the manuscript, followed by drawing a comparison between them in terms of their advantages, disadvantages, materials being processed, resolution, repeatability, accuracy and applications. Finally, a conclusion of the paper is provided with some of the challenges of the current 3D printing techniques about the developed sensing prototypes, their corresponding remedial solutions and a market survey determining the expenditure on 3D printing for biomedical sensing prototypes.Entities:
Keywords: 3D printed sensors; digital light processing; fused deposition modelling; inkjet; polyjet; selective laser sintering; stereolithography
Mesh:
Year: 2019 PMID: 30974757 PMCID: PMC6480222 DOI: 10.3390/s19071706
Source DB: PubMed Journal: Sensors (Basel) ISSN: 1424-8220 Impact factor: 3.576
Figure 1(A) Fused deposition modelling (B) Stereo-lithography (C) Polyjet Process (D) Selective laser sintering (E) 3D Inkjet printing (F) Digital light processing.
A summary of additive manufacturing techniques: principle, materials, resolution and 3D printed sensors in biomedical applications.
| 3D Printing Methods | Principle | Materials | Resolution Range (μm) | Application of 3D Printed Sensor in Biomedical |
|---|---|---|---|---|
| Fused deposition modelling | Extrusion of constant filament | ABS, PLA, Wax blend, Nylon | x: 100 | Lactate sensor [ |
| Stereolithography | UV initiated polymerisation cross section by cross section | Resin (Acrylate or Epoxy based with proprietary photoinitiator) | x: 10 | DNA imaging sensor [ |
| Polyjet | Deposition of the droplets of the photo-curable liquid material and cured | Polymer | x: 30 | Cell imaging sensor [ |
| Selective laser sintering | Laser-induced sintering of powder particles | Metallic powder, polyamide, PVC | x: 50 | Cell density sensor [ |
| 3D Inkjet printing | Extrusion of ink and powder liquid binding | Photo-resin or hydrogel | x: 10 | Bionic ear [ |
| Digital light processing | Photo-curing by a digital projector screen to project layers by squared voxels | Photopolymer and photo-resin | x: 25 | Piezoelectric acoustic sensor [ |
Comparative study of the 3D printing methods in terms of their advantages, disadvantages, accuracy and repeatability.
| 3D Printing Methods | Advantages | Disadvantages | Accuracy (µm) | Repeatability |
|---|---|---|---|---|
| Fused deposition modelling |
High speed High quality Used for a wide range of material Durable over time Less time |
Porous structure for the binder Weak mechanical properties Often required support | 350 | Fair |
| Stereolithography |
Large parts can be built easily High accuracy and surface finish Good for complex built Simple scalability Uncured material can be reused |
Not well-defined mechanical properties due to the usage of photopolymers Slow build process Expensive process Moisture, heat, and chemicals can reduce its durability Brittle structure | 25–150 | Good |
| Polyjet |
Multiple jetting heads are available to build materials Different levels of flexibility Allows using different coloured photopolymers More control over the accuracy High accuracy and smooth surface |
Vulnerable to heat and humidity Lose strength over time Relatively higher cost compared to others Sharp edges are often slightly rounded. | 10–20 | Good |
| Selective laser sintering |
High resolution No support structure is required High strength Less time Complex structures can be easily fabricated |
Only metal parts can be printed Finishing or post-processing required due to its grainy roughness Difficulty in the material changeover. | 300 | Good |
| 3D Inkjet printing |
Very good accuracy Very high surface finishes. |
Fragile parts Slow build process The grainy or rough appearance Post-processing is required to remove moisture Poor mechanical the properties. | 100 | Excellent |
| Digital light processing |
Excellent accuracy of laying High resolution Uncured photopolymer can be reused. |
Insecurity of the consumable material Difficult to print large structure Boxy surface finish due to its rectangular voxels. | 10–25 | Excellent |
Figure 2(a) A 3D printed smartphone adaptor depicting its (b) 3D printed cartridge being composed of reservoirs and sliding lid. (c) The assembled smartphone-based device for BL signal acquisition and analysis. Reproduced from Cevenini et al. [70].
Figure 3(a) Schematic illustration of separation of the captured bacteria by inertial focusing. (b) Representation of dean vortices in a channel with trapezoid cross-section. (c) Photograph of the 3D printed microfluidic device. Reproduced from Lee et al. [112].
Figure 4(A) The 3-D printed device has been modelled after the dimensions of a 96-well plate. (B) The inserting of the membrane is done into wells via a semi-permeable polyester membrane. (C) The channels are connected through threads, located at two ends of the channel. (D) A schematic cross-sectional view of the insertion of the channel and the membrane. (E) The locking of the device into the sample holder. Reproduced from Chen et al. [119].
Figure 5Continuous recalibration of the 3D-printed Control Unit Adaptive P controller. Reproduced from Ude et al. [127]. (A) The 3D printed flask is used to control the pH of the solution using defined algorithm. (B) The interior of th3 3D printed flask. (C) Variation in the amplitude, pH levels and intensity of the scattered light with time.
Figure 6Image of the (A) fabricated 3D printed bionic ear and (B) 3D printed bionic ear during its vitro culture. (C) The viability of chondrocyte at different stages during the printing process. (D) Deviation of the weight of the printed ear over time in culture, where the ear consisted of the chondrocyte-seeded alginate or only alginate shown in red and blue colour respectively. (E) Histologic analysis of chondrocyte morphology done using H&E staining. (F) Neocartilaginous tissue being Safranin O stained after 10 weeks of culture. Photographs (top) and fluorescent (bottom) images of (G) viability of the neo cartilaginous tissue being in contact with the antenna of the coil and (H) cross-section of the bionic ear showing the viability of the internal cartilaginous tissue in contact with the electrode. Reproduced from Mannoor et al. [82].
Figure 7Schematic diagram of the (a) 3D printed optics for universal coupling to cell phone camera and (b) 3D scheme of the unibody lab-on-a-chip (ULOC) device detailing the fluidic component. Reproduced from Comina et al. [135].