Photocurable Resin Research Articles

High-performing naphthalene-type photocurable resin: Tailored properties by the selection of di-functional acid chain extenders

Despite the significant progress in high thermal-resisting photocurable resin, the simultaneous achievement of robustness, stretchability, and dielectric properties in modified naphthalene-type photocurable resin remains a great challenge owing to intrinsic restrictions mediated by strong π-π stacking effect. Herein, a simple and feasible method is demonstrated to respectively introduce three selected di-functional acid chain extenders into 1,6-naphthalene diglycidyl ether (NDE), and prepare a series of naphthalene-type photocurable enhancement resin with excellent thermal/mechanical properties and low dielectric traits. Most importantly, the effect of the increase of succinic acid (SA) chain-extending segments on the thermal and mechanical properties of SA chain-extending NDE (S-NDE) resin is systematically investigated. An optimized synthesized route is presented by chain extension chemical strategy, which enables the improvement of the “seesaw” issue between high heat resistance and mechanical robustness. As a consequence, the optimized UV-curing S-NDE thin film exhibits robust tensile strength (75.45 ± 4.46 MPa), excellent heat resistance (Tg: 145.4 °C), high stretchability (7.22 ± 0.85 %), and desired dielectric constant (2.2). Meanwhile, the uncured S-NDE resin exhibited an excellent alkali elution property within 5 min. An actually printed circuit board (PCB) solder resistance coating/patterning application is further demonstrated based on the selective elution property of high-performance formulated S-NDE green ink, providing an efficient strategy for the design and fabrication of high-performance naphthalene-type photocurable materials.

Forces and moments generated during extrusion of a maxillary central incisor with clear aligners: an in vitro study

ObjectiveTo assess the possibility of extrusion of a maxillary central incisor with the use of buccal and lingual pressure columns in the absence of attachments, and to evaluate the forces and moments experienced by the teeth using both thermoformed and 3D-printed clear aligners.Materials and methodsA three-axis force and moment sensor (Aidin Robotics, Anyang, South Korea) was used to measure the forces and moments during extrusion of an upper left central incisor (UL1) and any forces experienced by the upper right central incisor (UR1) using thermoformed aligners and 3D-printed aligners. For the thermoformed aligners, the materials used were ATMOS® (American Orthodontics, Sheboygan, WI) and Zendura FLX® (Bay Materials LLC, Fremont, CA). 3D-printed aligners were fabricated using TC-85 clear photocurable resin (Graphy Inc., Seoul, South Korea). For each material type, three conditions were tested: Group 1: No attachment or pressure columns (control); Group 2: Attachment only; and Group 3: Pressure columns only. Each group was planned for 0.5 mm of extrusion on the UL1.ResultsAll force readings collected demonstrated statistically significant differences when compared by materials and when compared by groups, with a P value of < 0.001. In the absence of attachment or pressure columns (Group 1), ATMOS® and TC-85 groups exerted extrusive force on the UL1. However, significantly lower forces and moments were exerted by the TC-85 group in comparison to the ATMOS® and Zendura FLX® groups. In the presence of attachment (Group 2), all three ATMOS®, Zendura FLX® and TC-85 groups exerted extrusive force on the UL1, with the TA group showing different directions of faciolingual force, mesiodistal force and faciolingual inclination on the UR1 when compared to the other two thermoformed groups. Whereas in the presence of pressure columns (Group 3), only the TC-85 3D-printed aligner group exerted extrusive force. Thermoformed aligners generated significantly higher mean forces and moments than 3D-printed aligners. Significant levels of unintended forces and moments were present in all groups.ConclusionsForce levels generated during extrusion with clear aligners are significantly lower with those 3D-printed using TC-85 than with those thermoformed using ATMOS® or Zendura FLX®. Attachments consistently generated extrusive forces, and may be an effective adjunct in achieving extrusion of incisors. Extrusion may be achieved without the use of attachments by utilizing pressure columns in 3D-printed aligners using TC-85. While different strategies can generate extrusive forces, there are significant unintended forces and moments.

Urethane dimethacrylate-based photopolymerizable resins for stereolithography 3D printing: A physicochemical characterisation and biocompatibility evaluation

Vat photopolymerisation (VP) three-dimensional printing (3DP) has attracted great attention in many different fields, such as electronics, pharmaceuticals, biomedical devices and tissue engineering. Due to the low availability of biocompatible photocurable resins, its application in the healthcare sector is still limited. In this work, we formulate photocurable resins based on urethane dimethacrylate (UDMA) combined with three different difunctional methacrylic diluents named ethylene glycol dimethacrylate (EGDMA), di(ethylene glycol) dimethacrylate (DEGDMA) or tri(ethylene glycol) dimethacrylate (TEGDMA). The resins were tested for viscosity, thermal behaviour and printability. After printing, the 3D printed specimens were measured with a digital calliper in order to investigate their accuracy to the digital model and tested with FT-IR, TGA and DSC. Their mechanical properties, contact angle, water sorption and biocompatibility were also evaluated. The photopolymerizable formulations investigated in this work achieved promising properties so as to be suitable for tissue engineering and other biomedical applications.Graphical abstract

Photocurable resin as rapid in-situ protective coating for slag concrete against dry shrinkage

Slag concrete has the advantages of low hydration heat evolution and a low carbon footprint, but the impact of drying shrinkage will increase the risk of cracking concrete components. To achieve low-cracking performance, dry shrinkage was prevented against water evaporation by an in-situ coating of the concrete with a photocurable resin. In this study, polyurethane-acrylic resin was applied as an in-situ coating on the surface of slag concrete by UV polymerization for the first time. The purpose of the experiment is to explore the feasibility of using photocurable resin as a surface protective coating for general construction. The experimental results show that the drying shrinkage percentage of slag concrete samples after 28 days is reduced by 40%, the compressive strength of the test block increases by 1.67 times, and the tensile strength increases by 1.8 times. The photocurable resin in-situ protective coating can adhere tightly to the surface of the substrate, inhibiting water evaporation in the sample, and providing a moist internal curing environment that effectively alleviates shrinkage. Crack propagation on the concrete surface was also greatly prevented, resulting in a more deviated crack propagation behavior; therefore, the ductility of slag concrete is improved.

4D-printed needle panel meters coupled with enzymatic derivatization for reading urea and glucose concentrations in biological samples

On-site analytical techniques continue being developed with advances in modern technology. To demonstrate the applicability of four-dimensional printing (4DP) technologies in the direct fabrication of stimuli-responsive analytical devices for on-site determination of urea and glucose, we used digital light processing three-dimensional printing (3DP) and 2-carboxyethyl acrylate (CEA)–incorporated photocurable resins to fabricate all-in-one needle panel meters. When adding a sample having a value of pH above the pKa of CEA (ca. 4.6–5.0) into the fabricated needle panel meter, the [H+]-responsive layer of the needle, printed using the CEA-incorporated photocurable resins, swelled as a result of electrostatic repulsion among the dissociated carboxyl groups of the copolymer, leading to [H+]-dependent bending of the needle. When coupled with a derivatization reaction (urease-mediated hydrolysis of urea to decrease [H+]; glucose oxidase-mediated oxidization of glucose to increase [H+]), the bending of the needle allowed reliable quantification of urea or glucose when referencing pre-calibrated concentration scales. After method optimization, the method's detection limits for urea and glucose were 4.9 and 7.0 μM, respectively, within a working concentration range from 0.1 to 10 mM. We verified the reliability of this analytical method by determining the concentrations of urea and glucose in samples of human urine, fetal bovine serum, and rat plasma with spike analyses and comparing the results with those obtained using commercial assay kits. Our results confirm that 4DP technologies can allow the direct fabrication of stimuli-responsive devices for quantitative chemical analysis, and that they can advance the development and applicability of 3DP-enabling analytical methods.

Fabrication and characterization of light-curing soybean oil-based epoxy resin applied for LCD additive manufacturing

In this work, we developed a photocurable vegetable oil-based resin with suitable curing properties for use in 3D printing. The acrylated epoxidized soybean oil (AESO), which was synthesized by the catalytic ring-opening reaction of the epoxidized soybean oil (ESO) and acrylic acid (AA), replaced the oligomer in conventional light-curing petroleum-based resins. In order to optimize the various properties of the soybean oil-based epoxy resin, the performance parameters of the resin were analyzed by numerical simulation. It was also combined with the parameters of the printing equipment to better guide the 3D printing process of the resin. The results showed that the esterification rate of acrylic acid (AA) with epoxidized soybean oil (ESO) was higher than that of methacrylic acid (MAA) during the arylation of epoxidized soybean oil (ESO), and AESO had moderate viscosity and was suitable as an oligomer for 3D printing. When the diluent of the oligomer has an ACMO to HDDA ratio of 3:2, the cured parts exhibit the optimum mechanical properties, hydrophobic properties, and thermal stability. All properties of the resins were further improved and giving the formulation the best 3D printing performance when 10% of epoxy resin E44 was added to the soybean oil-based epoxy resin. In addition, the numerical simulations indicate that this soybean oil-based epoxy resin formulation has the highest printing efficiency when the single layer thickness of the cured layer is set to 0.2 mm with the exposure time of 4 s, where the wavelength of UV is 405 nm and the light intensity is 40 W/m2. In conclusion, the light-curing resin developed through the soybean oil-based epoxy resin exhibits excellent performance in all aspects. The optimal printing process was also derived by combining the results obtained from numerical simulations of the resin performance parameters with the device parameters, which significantly improved the efficiency of the 3D printing with the fabricated soybean oil-based epoxy resin, making it has great application potential for the biomedical materials.

Commercial 3D resin blended with TTA functionalized CaWO4:Eu (III), synthesis route and a luminescence study

Synthesis and characterization of calcium tungstate-based micro-nanophosphors are reported in the present work. These materials were synthesized by spray pyrolysis technique. According to Scanning Electron Microscopy measurements, CaWO4 and CaWO4:Eu (III) have quasi-spherical shape. CaWO4 presents blue luminescence whose origin is an electron transition within unperturbed WO42− complexes, while CaWO4:Eu (III) luminescent properties are generated by the presence of Eu (III) ions, which produced light emissions at 591, 615, 655, and 702 nm. Such emissions are due to radiative transitions from the excited state 5D0 to 7Fj (j = 1, 4) inter-level transitions within Eu (III) electronic energy states. These phosphors were blended with a commercial 3D print photocurable resin (Sain Smart 101-90-840TS) and their luminescent properties were transferred to resin. Besides in this case, blended 3D resin has an intrinsic blue luminescence due to its π and π* bonds which is activated under 380 nm excitation wavelength, however blended 3D resin can be also activated under 465 nm excitation which only activates Eu (III) ions producing a red emission 3D luminescent photocurable resin.

Elastomeric Porous Poly(glycerol sebacate) Methacrylate (PGSm) Microspheres as 3D Scaffolds for Chondrocyte Culture and Cartilage Tissue Engineering.

Cartilage defects can be difficult to treat; therefore, tissue engineering of cartilage is emerging as a promising potential therapy. One interesting area of research explores the delivery of cells to the cartilage defect via scaffold-based cell delivery vehicles and microsurgery. This study explores the use of novel poly(glycerol sebacate) methacrylate (PGSm)-polymerised high internal phase emulsion (polyHIPE) microspheres as scaffolds with embedded cells for cartilage tissue engineering. Porous microsphere scaffolds (100 µm-1 mm diameter) were produced from emulsions consisting of water and a methacrylate-based photocurable resin of poly(glycerol sebacate). These resins were used in conjunction with a T-junction fluidic device and an ultraviolet (UV) curing lamp to produce porous microspheres with a tuneable size. This technique produced biodegradable PGSm microspheres with similar mechanical properties to cartilage. We further explore these microspheres as scaffolds for three-dimensional culture of chondrocytes. The microspheres proved to be very efficient scaffolds for primary chondrocyte culture and were covered by a dense extracellular matrix (ECM) network during the culture period, creating a tissue disk. The presence of glycosaminoglycans (GAGs) and collagen-II was confirmed, highlighting the utility of the PGSm microspheres as a delivery vehicle for chondrocytes. A number of imaging techniques were utilised to analyse the tissue disk and develop methodologies to characterise the resultant tissue. This study highlights the utility of porous PGSm microspheres for cartilage tissue engineering.

Straightforward Manufacturing of 3D-Printed Metallic Structures toward Customized Electrical Components.

Metalizing three-dimensional (3D)-printed polymers has been spotlighted in the field of manufacturing high-end and customized electrical components. Conventional metalization approaches that rely on the electroless plating (ELP) process typically require the use of noble metal-based catalysts or involve multistep processes, limiting their practical applications. Herein, we propose a straightforward yet effective approach to manufacture 3D-printed polymers with conductive metal layers through a thiol-mediated ELP process without involving an additional catalytic activation process. A photocurable ternary resin based on thiol-ene-acrylate monomers was precisely designed to induce excess thiol moieties on the surface of 3D-printed structures. These exposed thiol moieties served as active sites for metal ion complexion via strong metal-sulfur bonds, allowing the deposition of metal layers on the 3D-printed polymers through the ELP. Diverse metal layers, including Cu, Ag, and NiP, could be deposited onto virtually any 3D-printed structures with high uniformity and adhesion stability. To highlight the potential application of our approach, we fabricated fully functional glucose sensors through the deposition of the Cu layer on 3D-printed electrode models, and these sensors displayed excellent nonenzymatic glucose sensing performance. The proposed approach offers great insights for designing functional metallic structures and opens up new avenues for manufacturing lightweight, customized electrical components.

A Regression Approach to Model Refractive Index Measurements of Novel 3D Printable Photocurable Resins for Micro-Optofluidic Applications.

In this work, a quadratic polynomial regression model was developed to aid practitioners in the determination of the refractive index value of transparent 3D printable photocurable resins usable for micro-optofluidic applications. The model was experimentally determined by correlating empirical optical transmission measurements (the dependent variable) to known refractive index values (the independent variable) of photocurable materials used in optics, thus obtaining a related regression equation. In detail, a novel, simple, and cost-effective experimental setup is proposed in this study for the first time for collecting the transmission measurements of smooth 3D printed samples (roughness ranging between 0.04 and 2 μm). The model was further used to determine the unknown refractive index value of novel photocurable resins applicable in vat photopolymerization (VP) 3D printing techniques for manufacturing micro-optofluidic (MoF) devices. In the end, this study proved how knowledge of this parameter allowed us to compare and interpret collected empirical optical data from microfluidic devices made of more traditional materials, i.e., Poly(dimethylsiloxane) (PDMS), up to novel 3D printable photocurable resins suitable for biological and biomedical applications. Thus, the developed model also provides a quick method to evaluate the suitability of novel 3D printable resins for MoF device fabrication within a well-defined range of refractive index values (1.56; 1.70).

Development of Photo-curable Resin for 3D Printing Using Acrylic Monomers with Bisphenol Skeleton

Development of Photo-curable Resin for 3D Printing Using Acrylic Monomers with Bisphenol Skeleton

Development of polymeric/MXenes composites towards 3D printable electronics

3D printing is an emerging technology for many applications, including electronics. On the other hand, to gather the applications’ requirements with the possibility to produce complex 3-dimensional structures, the development of novel 3D printable materials is necessary. In this context, herein it is reported the synthesis of 3D printable photocurable resins embedding Ti3C2Tz-MXenes, a class of 2D layered materials with outstanding electrical and electronic properties. Stable inks suitable for Digital Light Processing 3D printing technology have been successfully synthesized and employed to fabricate complex 3D composite structures with high printing fidelity. To enhance the electrical conductivity of the material, annealing treatments have been performed, followed by a complete characterization of the so obtained materials. The results show that objects with improved electrical conductivity have been successfully obtained, opening new perspectives in towards the development of complex 3 dimensional electronic.

Laser Bioprinting with Cell Spheroids: Accurate and Gentle.

Laser printing with cell spheroids can become a promising approach in tissue engineering and regenerative medicine. However, the use of standard laser bioprinters for this purpose is not optimal as they are optimized for transferring smaller objects, such as cells and microorganisms. The use of standard laser systems and protocols for the transfer of cell spheroids leads either to their destruction or to a significant deterioration in the quality of bioprinting. The possibilities of cell spheroids printing by laser-induced forward transfer in a gentle mode, which ensures good cell survival ~80% without damage and burns, were demonstrated. The proposed method showed a high spatial resolution of laser printing of cell spheroid geometric structures at the level of 62 ± 33 µm, which is significantly less than the size of the cell spheroid itself. The experiments were performed on a laboratory laser bioprinter with a sterile zone, which was supplemented with a new optical part based on the Pi-Shaper element, which allows for forming laser spots with different non-Gaussian intensity distributions. It is shown that laser spots with an intensity distribution profile of the "Two rings" type (close to Π-shaped) and a size comparable to a spheroid are optimal. To select the operating parameters of laser exposure, spheroid phantoms made of a photocurable resin and spheroids made from human umbilical cord mesenchymal stromal cells were used.

Computational Fluid Dynamics Modeling of Top-Down Digital Light Processing Additive Manufacturing.

Digital light processing (DLP) as a vat photopolymerization technique is one of the most popular three-dimensional (3D) printing methods, where chains are formed between liquid photocurable resin molecules to crosslink them and solidify the liquid resin using ultraviolet light. The DLP technique is inherently complex and the part accuracy depends on the process parameters that have to be chosen based on the fluid (resin) properties. In the present work, computational fluid dynamics (CFD) simulations are presented for top-down DLP as photocuring 3D printing. The effects of fluid viscosity, travelling speed of build part, travelling speed ratio (ratio of the up-to-down traveling speeds of build part), printed layer thickness, and travel distance considering 13 various cases are scrutinized by the developed model to obtain a stability time of fluid interface. The stability time describes the time it takes for the fluid interface to show minimum fluctuations. According to the simulations, a higher viscosity leads to prints with higher stability time. However, lower stability times in the printed layers are caused by a higher traveling speed ratio (TSR). The variation in settling times with TSR is extremely small in comparison to that of viscosity and travelling speed variations. As a result, a declining trend can be detected for the stability time by increasing the printed layer thickness, while by enhancing the travel distance values, the stability time demonstrated a descending pattern. In total, it was revealed that it is essential to choose optimal process parameters for achieving practical results. Moreover, the numerical model can assist in the optimizing the process parameters.

Regulating copolymer architecture using photoiniferter polymerization to direct composite morphology

Due to mild conditions and straightforward synthetic routes, photoiniferter polymerization has received increasing use as a facile method for preparation of polymers with highly controlled structure. However, low quantum yields inherent to thiocarbonylthio species result in polymerization speeds that are considerably slower than traditional controlled radical polymerization techniques. To improve polymerization speed while maintaining high level control, it is critical to understand relationships between reaction parameters and ultimate polymer structure. In this work, initiating light intensity, reactant concentration, and monomer pendant groups were manipulated in the photoiniferter polymerization of acrylate monomers to explore the effect of these conditions on reaction kinetics and molecular weight control. Polymerization rate of n-butyl acrylate was significantly enhanced by increasing light intensity rivaling speeds of conventional thermally initiated RAFT polymerization while enabling more precise control over molecular weight. Interestingly, photoiniferter rate asymptotically approached saturation at relatively high light intensities. Moreover, degradation of trithiocarbonate species occurred at greater intensities, ultimately resulting in moderate increases in molecular weight. Increased reactant concentration enabled faster rates with bulk polymerization, possibly due to reduced macro radical mobility and termination. Additionally, comparing photoiniferter polymerization of methyl acrylate and hydroxyethyl acrylate showed that greater polarity considerably enhanced polymerization speeds. Finally, the utility of precisely controlling polymer structure was demonstrated by synthesizing and incorporating a series of amphiphilic block copolymers with increasing molecular weight into a photocurable epoxy resin. The well-defined block copolymer structures enabled controllable phase separation and thermomechanical properties in epoxy composites. This work showed that photoiniferter polymerization speeds could be significantly enhanced using elementary reaction conditions, and that these conditions enable facile production of well-defined copolymers allowing tailored composite morphology and properties.

Lignin nanoparticle-enhanced biobased resins for digital light processing 3D printing: Towards high resolution and tunable mechanical properties

The more widespread applicability of photopolymerization-based three-dimensional (3D) printing is limited by the availability of light-curable resins, most of which are based on fossil-derived compounds. We developed a biobased lignin-derivable resin by utilizing methacrylated derivatives of vanillin, vanillyl alcohol, and eugenol as aromatic monomers. Lignin nanoparticles (LNPs) were incorporated as functional fillers that enhance print resolution and material properties. The crosslinking degree, and thereby the tensile properties, was modulated through the use of mono- or dimethacrylated vanillin derivatives in the resin formulation. The LNPs acted as UV absorbers, conferring better control of the photopolymerization process by preventing light penetration across unintended layers, leading to enhanced print resolution. The LNPs showed excellent dispersion stability due to their size and morphology. The inclusion of up to 2 wt% of LNPs improved the ductility of the 3D printed nanocomposites through toughening mechanisms enabled by the rigid nanoparticles. Finally, exploiting the differences in crosslinking degree of the resin formulations, a multi-material model featuring both soft and rigid domains was fabricated. This study demonstrates a simple but effective strategy for the design of biobased photocurable resins with tailorable mechanical properties that are suitable for high-resolution and multi-material 3D printing.

Wood xerogel for fabrication of high-performance transparent wood

Optically transparent wood has been fabricated by structure-retaining delignification of wood and subsequent infiltration of thermo- or photocurable polymer resins but still limited by the intrinsic low mesopore volume of the delignified wood. Here we report a facile approach to fabricate strong transparent wood composites using the wood xerogel which allows solvent-free infiltration of resin monomers into the wood cell wall under ambient conditions. The wood xerogel with high specific surface area (260 m2 g–1) and high mesopore volume (0.37 cm3 g–1) is prepared by evaporative drying of delignified wood comprising fibrillated cell walls at ambient pressure. The mesoporous wood xerogel is compressible in the transverse direction and provides precise control of the microstructure, wood volume fraction, and mechanical properties for the transparent wood composites without compromising the optical transmittance. Transparent wood composites of large size and high wood volume fraction (50%) are successfully prepared, demonstrating potential scalability of the method.

Interplay of photopolymerization and phase separation kinetics and the resulting structure-property relationship of photocurable resins

In this work we develop thermoset materials with heterogeneous microstructures on sub-micron scales by photopolymerization-induced phase separation (photo-PIPS). To this end, we designed a photo-curable resin based on pentaerythritol tetraacrylate (PETA), an acrylate monomer, combined with 2-ethylhexyl methacrylate (2-EHMA), a methacrylate diluent. Polypropylene glycol (PPG) was used as a phase separation agent. Phase separation was monitored by reactive light transmittance using a custom-built light transmission apparatus and through dynamic mechanical analysis (DMA). The photopolymerization kinetics and the microstructure morphology were characterized using real-time Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM), respectively. We observe double phase separation: PETA and 2-EHMA separate due to different reactivities, while PPG phase separates as the network develops due to immiscibility. A synergy is observed between the two processes: PPG phase separation leads to an enhanced separation of 2-EHMA. Phase separation leads to reduced transmittance due to scattering, which is primarily associated with the separation of 2-EHMA. Phase separation also causes the reduction of stiffness due to the formation of PPG subdomains. The kinetics is enhanced by increasing the PPG molecular weight and increasing the irradiation intensity.

Optical Imaging Methods for Volumetric Additive Manufacturing

Tomographic volumetric additive manufacturing (VAM) is a technique that enables light-induced curing of photoresins into complex 3D end use objects within a single step. This is made possible through projecting tomographically patterned light energy into a photo-curable resin volume within a rotating container. In order to monitor, quantify, and control curing during tomographic VAM, researchers need to visualize the curing parts in real-time. This may enable advancements toward dynamic, controlled and closedloop VAM methods in the future, as some researchers have shown. Herein we briefly review various optical imaging methods used to monitor printing in real-time, as well as provide some perspectives for future needs and considerations for imaging methods in VAM.

Design and Synthesis of CdHgSe/HgS/CdZnS Core/Multi-Shell Quantum Dots Exhibiting High-Quantum-Yield Tissue-Penetrating Shortwave Infrared Luminescence.

Cdx Hg1- x Se/HgS/Cdy Zn1- y S core/multi-shell quantum dots (QDs) exhibiting bright tissue-penetrating shortwave infrared (SWIR; 1000-1700nm) photoluminescence (PL) are engineered. The new structure consists of a quasi-type-II Cdx Hg1- x Se/HgS core/inner shell domain creating luminescent bandgap tunable across SWIR window and a wide-bandgap Cdy Zn1- y S outer shell boosting the PL quantum yield (QY). This compositional sequence also facilitates uniform and coherent shell growth by minimizing interfacial lattice mismatches, resulting in high QYs in both organic (40-80%) and aqueous (20-70%) solvents with maximum QYs of 87and 73%, respectively, which are comparable to those of brightest visible-to-near infrared QDs. Moreover, they maintain bright PL in a photocurable resin (QY 40%, peak wavelength≈1300nm), enabling the fabrication of SWIR-luminescent composites of diverse morphology and concentration. These composites are used to localize controlled amounts of SWIR QDs inside artificial (Intralipid) and porcine tissues and quantitatively evaluate the applicability as luminescent probes for deep-tissue imaging.