Reverson
Fernandes Quero
a,
Dosil Pereira de
Jesus
ab and
José Alberto
Fracassi da Silva
*ab
aInstitute of Chemistry, State University of Campinas, Campinas, SP 13083-861, Brazil. E-mail: fracassi@unicamp.br
bInstituto Nacional de Ciência e Tecnologia em Bioanalítica (INCTBio), Campinas, SP, Brazil
First published on 7th July 2023
Advances in the instrumentation and materials for photopolymerization 3D printing aided the use of this powerful technique in the fabrication of microfluidic devices. The costs of printers and supplies have been reduced to the point where this technique becomes attractive for prototyping microfluidic systems with good resolution. With all the development of multi-material 3D printers, most of the microfluidic devices prepared by photopolymerization 3D printing are based on a single substrate material. We developed a digital light processing multi-material 3D printer where two or more resins can be used to prepare complex objects and functional microfluidic devices. The printer is based on a vat inclination system and embedded peristaltic pumps that allow the injection and removal of resins and cleaning step between material changes. Although we have built the whole system, the modification can be incorporated into commercially available printers. Using a high-resolution projector, microfluidic channels as narrow as 43 μm were obtained. We demonstrate the printing of multi-material objects containing flexible, rigid, water-soluble, fluorescent, phosphorescent, and conductive (containing PEDOT or copper nanoparticles) resins. An example of a microfluidic chip containing electrodes for electrochemical detection is also presented.
In the context of the fabrication of microfluidic devices, additive manufacturing (or 3D printing) is very promising, as it enables the generation of objects with high structural complexity. In this way, the integration of connectors and cavities for coupling different parts (for example, tubes, optical fibers, and electrodes) is natural and can be incorporated into the manufacturing process. As expected, the use of 3D printing has accelerated in recent years due to improvements in printers, development of new materials, and introduction of new printing methodologies. Many groups have demonstrated the capabilities of 3D printing for the production of microfluidic devices,6–24 including the comparison of different printing techniques.25,26 The use of 3D printing in microfluidics has also been reviewed.1,26–31
Although microfluidic devices can be successfully created in a single material substrate, the use of multi-material printing allows the addition of features to the devices, promoting more functionality to them. Complete lab-on-a-chip devices could be one-step printed in order to incorporate conductive tracks for electric field application and electrochemical sensing, porous materials for filtration, preconcentration and separation, flexible membranes for valve actuation and pumping, among other applications. Fused deposition modeling (FDM) is a straightforward way to implement devices containing multi-materials32–34 since two or more extruders can be combined to deposit different materials. Print pausing has been used to introduce parts during the printing process,35 but this method cannot be named a truly multi-material printing. In spite of the fact that some progress has been made to improve the resolution of FDM 3D printing,12,24,36 it is still challenging to produce devices containing channels with dimensions below 100 μm. Inkjet37 and direct ink writing38 are also prone to multi-material deposition, but due to the vertical direction of deposition and the fluidity of the inks, a sacrificial material is necessary to create embedded channels and chambers. This fact itself is not a problem, but the removal of these sacrificial layers in the microscale can be troublesome, leading to clogged microchannels.25 Additionally, the resolution of these techniques is the limit to produce channels with dimensions below 100 μm, and the roughness of the microchannels is impaired by the removal of the sacrificial layer. Conversely, digital light processing (DLP) offers a suitable resolution level to produce microfluidic devices, as demonstrated by the research groups of Woolley and Nordin from Brigham Young University,15–21 where the production of microchannels as narrow as 20 μm was demonstrated.20
Advances in instrumentation have allowed multi-material printing in DLP. Recently, Shaukat et al. have published a comprehensive review on this topic.39 According to the authors, there are three main strategies for multi-material vat photopolymerization: (1) by changing resins in one or more vats, (2) by changing the light source to promote orthogonal photopolymerization reactions, and (3) by varying the light intensity. In the context of this work, it is important to describe the first strategy of multi-material vat photopolymerization 3D printing. According to Shaukat et al.,39 the first to describe multi-material stereolithography 3D printing was Maruo et al. in 2001.40 In 2004 and 2006, the research group of Ryan Wicker presented an automated multi-material stereolithography printer based on a rotating four-vat carousel,41,42 following publications in 2010 (ref. 43 and 44) and 2011 (ref. 45) and a review in 2012.46 The potential to incorporate conductive tracks and electronic parts into printed devices was also demonstrated in 2012 and 2014.47,48 The years that followed saw refinements to these basic ideas and examples of multi-material 3D printing applications. Ge et al. used the vat exchanging strategy to 3D print different tailored shape memory polymers (4D printing).49 Instead of using a “physical” vat, Wang et al. deposited resins over a delivery wheel mounted on a stepper motor.50 In 2018, Kowsari et al. used a similar approach by placing the resins in a linear stage made in borosilicate glass covered by a polytetrafluoroethylene film.51 In their approach, a high resolution was achieved (15 μm pixel size) by using a high-contrast digital microdisplay. Also, an air jet was delivered to the substrate after layer exposure for the removal of resin residues. Subsequently, Kowsari et al. studied the influence of the resin monomers on the quality of the printed objects. Outstanding roughness and transparency were achieved by using 1,6-hexanediol dimethacrylate (HDDMA).52 Other applications from this research group involve the production of multi-material 3D-printed stretchable hydrogels53 and pneumatic actuators for soft robots.54 In 2018, Kim et al. described the integration of porous membranes in a microfluidic chip by manually pausing a commercial printer at the desired layer and changing the resin vat.55 Changing vats was also the strategy employed by Khatri et al.,56 but in this case, the authors built their low-cost automated printer. In a different approach, Mao et al. developed an instrument containing printing heads to allow “coating, curing, cleaning, and post-curing” (C3P).57 Ahmed et al. pointed out that the time spent for the fabrication of a microfluidic chip was decreased from 6 to 2 h by applying a protocol of multi-material 3D printing when compared to the conventional 3D mold printing and polydimethylsiloxane replication.58 The authors used multi-material approach to combine flexible and rigid materials to integrate pneumatic valves into the microfluidic chips in a one-step process. Lipkowitz et al. introduced a modification of the Continuous Liquid Interface Production (CLIP) to allow the injection of the photo-resin in a process the authors called injection continuous liquid interface production (iCLIP).59 The injection of resin increased the printing velocity and also allowed the preparation of multi-material objects. Mayer et al.60 used 3D direct laser writing (DLW) with two-photon polymerization (2PP) and a microfluidic chamber to print 3D fluorescent-layered structures. The use of a flow controller and a multiport valve allowed the selection of up to seven liquids with an injection volume of about 0.5 mL. The 2PP processes guaranteed an outstanding resolution at the cost of small print volume. In a similar approach, Lamont et al. used 2PP-DLW to prepare a template for PDMS mold replication.61 Multi-material 3D printing was then conducted inside the PDMS microchannel.
From the previous examples, it is clear that multi-material DLP 3D printing is a powerful tool for the preparation of functional microfluidic devices. In this work, we describe an alternative approach to prepare multi-material objects by DLP 3D printing by changing the resins in a single vat. The instrumentation described here can be incorporated into commercial printers. To exemplify the potential of this approach, we demonstrate the fabrication of multi-component objects, which include fluorescent materials and conductive tracks for sensor applications. Microfluidic channels were also printed as narrow as 43 μm aiming for microchip electrophoresis applications.
The viscosity of the resins was measured with a model NDJ-8S rotational viscometer (Goyojo Instruments, Hangzhou, China).
The projector module is equipped with HDMI and DisplayPort connectors for video input, a USB connector, and I2C ports for digital control. The control of the status and light intensity was made through the board NanoDLP v1.4 (Hangzhou, China) and managed by using a microcontroller Raspberry Pi® running with the drive TMC2226 (Ncam Multitech, Goiânia, GO, Brazil). The NanoDLP board is used with open-source software under GNU Public License (GPL) v2.0 and configured with RepRap open-source firmware, available for download in the ESI.† The Raspberry Pi® executes the front-end NanoDLP and the control software (downloaded from https://www.nano3dtech.com/nanodlp-features/). The software allows the setting of the printing parameters and offers a slicer and web interface that can be accessed remotely. The software communicates with the NanoDLP board through the open-source firmware Marlin (under GPL v3.0 license) for the z-axis control.
The vat, as well as the printing platform, was made in castable resin (Cerâmica, Melting 3D, Louveira, SP, Brazil) using a commercial Anycubic M3 MAX DLP printer. After printing, the part was post-processed at 200 °C to improve the mechanical resistance, material compatibility, and ease of cleaning. The design of the vat includes lateral channels to allow the filling of the vat with different resins and cleaning solvents. In our printer prototype, as a proof of concept, we included two peristaltic pumps to inject different resins into the vat. This way, it is possible to inject two resins automatically. For more than two different materials, the resin reservoir must be manually replaced. Although this seems a limitation, additional reservoirs and channels may be designed to accommodate the automatic replacement of more materials.
Quick fittings were used to connect 2 mm i.d. polypropylene tubes (Fig. S3 and S4 in ESI†). Flexible couplers to connect the stepper motor and vat screw nuts axes were also included in the design. This avoided unnecessary tension in these parts during the inclination of the vat. The design and final assembled part can be seen in Fig. S4.† Designs of vats that fit in some commercial printers are also available in ESI.†
A system of accommodation of the fluorinated ethylene propylene (FEP) (Anycubic FEP Photon Mono X-1200 × 280 cm, Quanton3D, Brazil) film was included in the vat to improve the printing performance. The film was cut into the desired dimensions and held in place in the bottom of the vat through 14 screws (see ESI† S4). The FEP film is a consumable part and must be substituted periodically to assure a good printing quality, but it usually lasts several months. The vat sat directly over the glass window on the Bene5 mono msla structure.
The build plate, where the printed part adhered during the printing, was also designed to allow easy cleaning and material exchange. The design in angle (Fig. S5 in ESI†) allows the use of up to 50 mL of resin without soiling the plate support, which facilitates the cleaning between material switching. The STL file of the built plate is available for download in the ESI.†
The printing protocol is depicted in Fig. 2 and is based on the following steps: (1) the first material is injected into the vat by using a peristaltic pump; (2) the layers are formed by exposure of the material 1 (as normally is done in single material printers); (3) the built plate is elevated, the vat is tilted to the right and the same peristaltic pump is used to aspirate the resin to the respective reservoir; (4) the vat is placed on the normal position, and a cleaning solvent is injected by a second peristaltic pump (we used ethanol in all our printings); a third peristaltic pump is used to drain the solvent residues; (5) after cleaning, the vat is set to the normal position and the second material is injected by using a fourth peristaltic pump. The vat washing procedure also allows the cleaning of the previously printed layers since the volume of solvent injected is enough to partially cover the building platform. Steps 1 to 5 are repeated until the whole object is printed. Also, more than two different materials can be combined just by changing the resin reservoirs. The whole protocol can be automated since the commands to actuate the inclination system and turn on–off the pumps can be added to the G code. Alternatively, the pumps and the stepper motors for the inclination of the vat can be independently accessed by pausing the printing. Having this option in mind, an additional control board and a panel were installed for manual operation. Examples of the G code generation for multi-material printing can be found in Fig. S6 and S7 in the ESI.† In this case, the printer must be used with slicer software and G code editing in a more intuitive way, in which we use the NanoDLP open source software. An example of the commands used is available in Fig. S6 in ESI.† Both software and all printer general control files are available from the ESI† and can be used under GNU General Public License v2.0. A video file exemplifying the whole process is also available for download in the ESI.†
We studied the flow time as a function of the inclination angle, according to the viscosity of the resins used in this work (Table S2 in the ESI†), to get a suitable time for resin removal with a minimum of residues left in the vat. We found that by using 5 mL of resin, an angle of 30°, and a flow time of 60 s, it was possible to recover 95% of the material in the vat (see Fig. S3 and S4 in ESI†). High-viscosity resins (>500 cps at 25 °C) favor the 3D printing of microfluidic channels and objects of complex geometries without the need of supports. However, vat filling and removal take longer and printing failure can occur due to incomplete filling between layers. Conversely, the use of low-viscosity resins (<300 cps at 25 °C) helps in filling the orifices between layers and makes the vat cleaning easier, but the printing parts tend to be more fragile.62,63
In Fig. 3A and B, a stylized yin-yang rod is illuminated by daylight (3A) and under 405 nm illumination. The rod was printed in clear resin GEM 1 (see Table S2 in ESI,† and the same GEM 1 resin modified with the blue fluorescent pigment XUK473/3019 supplied by Hycote (https://www.hycote.co.uk/wp-content/uploads/Fluorescent-Paints-v05-2013.pdf). Fig. 3C–E shows a two-component card also prepared in clear resin GEM 1 developed in this work and modified with fluorophores in resin powder pigment, TE3XWUJJJ, purchased from Corion (https://www.corionshop.com.br/po-glow). The device was illuminated by daylight (3C), 405 nm (3D), and daylight after UV exposure (3E) where it is possible to see the phosphorescence of the dye. Fig. 4A depicts a multi-material dice printed in flexible (Siraya Tech, Tenacious Flexible), rigid-clear (Siraya Tech, Blu-Tough Resin), and water-soluble (3Dresyn, IM-HT-WS) resins. In Fig. 4B, four concentric cubes were printed using (Siraya Tech, Tough Resin) resin containing dyes (3DLab, kit Pigments for 3D resins).
Fig. 3 Example of two-component multi-material 3D printing. Stylized yin-yang rod illuminated under daylight (A) and 405 nm (B). The rod was printed in clear GEM 1 resin and the same resin containing a fluorescent pigment. Card printed in clear GEM 1 resin and the same resin containing phosphorescent pigment visualized under daylight (C), 405 nm (D), and daylight after UV exposure (E). Composition of the resins can be found in the ESI† Table S2. |
Fig. 4 Examples of complex multi-material objects. (A) Dice formed in flexible, rigid-clear, and water-soluble resins. (B) Concentric cubes prepared in clear resin containing dyes. |
Conductive parts and tracks are essential to build complete and autonomous sensor devices. Conductive materials play a central role in the development of electrochemical and physical sensors, actuation systems, electrodes for flow control (electroosmotic pumping) and electrophoretic separation, electromagnetic shielding, and embedded electronics. We have prepared two conductive-photopolymerizable resins based on PEDOT:PSS and copper nanoparticles (CuNP) dispersed in clear resin GEM 1. The electrical data of these conductive resins were evaluated in 300 μm thickness layers of the conductive material. We obtained resistivity of 35 and 85 Ω m and conductivity of 0.7 and 0.5 S m−1 for PEDOT:PSS and CuNP-based resins, respectively. Although we expect to develop applications in sensing using these conductive materials, here, we demonstrate as a proof-of-concept of the potential use of multi-material 3D printing on the construction of a printed circuit board containing tracks made in both PEDOT and CuNP (Fig. 5A) and flexible conductive tracks used to turn on a light emitting diode (Fig. 5B). Based on these examples, the potentiality of the printing system for applications involving wearable devices is clear.
As the ultimate goal of this work, we demonstrate the application of this high-resolution and affordable 3D printer in the fabrication of microfluidic channels. Fig. 6 depicts two microfluidic systems with typical cross-shaped channels to perform capillary microchip electrophoresis coupled with a pair of electrodes for contactless conductivity detection16 (Fig. 6A and C). Additionally, a single-straight channel surrounded by a spiral channel (Fig. 6B and D) was 3D printed. Optical microscopy was used to measure the cross-section of the printed microchannels, obtaining values of 43 μm (Fig. 6E).
Compared to previously reported works in the literature, our approach does not require changing the resin vat, allows large printing volume with a pixel size of 35 μm, with minimal waste of resin. Moreover, the vat inclination system can be implemented in commercial DLP printers and the ESI† (S8 and S9) lists the necessary components for the modification of two selected commercial printers (Nova3D Bene6 and Anycubic DLP D2). Our approach is also prone to fully automation, to allow the required number of materials to be printed. The iCLIP approach proposed by Lipkowitz et al.59 is also versatile in producing multi-material with accelerated printing speeds, but requires the use of viaducts in the design of the objects, which can make the production of microfluidic devices more difficult. This drawback is not found in our proposed peristaltic pumping and vat inclination systems for resin replacement and vat cleaning.
Multi-material 3D printing holds enormous potential for producing microfluidic devices in an unprecedented way. We described a simple procedure to produce objects containing combined materials in order to prepare complex objects and functional microfluidic devices. Although we have built the whole system, the modification can be incorporated into commercially available printers. By using a high resolution projector, we were able to produce microfluidic devices containing channels as narrow as 43 μm.
By adding fluorescent or phosphorescent molecules to the resin formulation, it is possible to design and 3D print optical sensors. The incorporation of conductive tracks to the microfluidic devices opens a wide range of possibilities to integrate electrochemical sensors, as well as electrodes for application of electric field for electrophoresis, dielectrophoresis, cell manipulation, and sorting.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3lc00356f |
This journal is © The Royal Society of Chemistry 2023 |