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Search Results (236)

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Keywords = photocrosslinkers

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15 pages, 7562 KiB  
Article
Unnatural Amino Acid Photo-Crosslinking Sheds Light on Gating of the Mechanosensitive Ion Channel OSCA1.2
by Scarleth Duran-Morales, Rachel Reyes-Lizana, German Fernández, Macarena Loncon-Pavez, Yorley Duarte, Valeria Marquez-Miranda and Ignacio Diaz-Franulic
Int. J. Mol. Sci. 2025, 26(15), 7121; https://doi.org/10.3390/ijms26157121 - 23 Jul 2025
Viewed by 347
Abstract
Mechanosensitive ion channels such as OSCA1.2 enable cells to sense and respond to mechanical forces by translating membrane tension into ionic flux. While lipid rearrangement in the inter-subunit cleft has been proposed as a key activation mechanism, the contributions of other domains to [...] Read more.
Mechanosensitive ion channels such as OSCA1.2 enable cells to sense and respond to mechanical forces by translating membrane tension into ionic flux. While lipid rearrangement in the inter-subunit cleft has been proposed as a key activation mechanism, the contributions of other domains to OSCA gating remain unresolved. Here, we combined the genetic encoding of the photoactivatable crosslinker p-benzoyl-L-phenylalanine (BzF) with functional Ca2+ imaging and molecular dynamics simulations to dissect the roles of specific residues in OSCA1.2 gating. Targeted UV-induced crosslinking at positions F22, H236, and R343 locked the channel in a non-conducting state, indicating their functional relevance. Structural analysis revealed that these residues are strategically positioned: F22 interacts with lipids near the activation gate, H236 lines the lipid-filled cavity, and R343 forms cross-subunit contacts. Together, these results support a model in which mechanical gating involves a distributed network of residues across multiple channel regions, allosterically converging on the activation gate. This study expands our understanding of mechanotransduction by revealing how distant structural elements contribute to force sensing in OSCA channels. Full article
(This article belongs to the Special Issue Ion Channels as a Potential Target in Pharmaceutical Designs 2.0)
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24 pages, 738 KiB  
Review
Photocuring in Lithium-Ion Battery Fabrication: Advances Towards Integrated Manufacturing
by Zihao Li, Yanlong Li, Mengting Chen, Weishan Li and Xiaoming Wei
Batteries 2025, 11(8), 282; https://doi.org/10.3390/batteries11080282 - 23 Jul 2025
Viewed by 397
Abstract
Photocuring, including photopolymerization and photocrosslinking, has emerged as a transformative manufacturing paradigm that enables the precise, rapid, and customizable fabrication of advanced battery components. This review first introduces the principles of photocuring and vat photopolymerization and their unique advantages of high process efficiency, [...] Read more.
Photocuring, including photopolymerization and photocrosslinking, has emerged as a transformative manufacturing paradigm that enables the precise, rapid, and customizable fabrication of advanced battery components. This review first introduces the principles of photocuring and vat photopolymerization and their unique advantages of high process efficiency, non-contact fabrication, ambient-temperature processing, and robust interlayer bonding. It then systematically summarizes photocured battery components, involving electrolytes, membranes, anodes, and cathodes, highlighting their design strategies. This review examines the impact of photocured materials on the battery’s properties, such as its conductivity, lithium-ion transference number, and mechanical strength, while examining how vat-photopolymerization-derived 3D architectures optimize ion transport and electrode–electrolyte integration. Finally, it discusses current challenges and future directions for photocuring-based battery manufacturing, emphasizing the need for specialized energy storage resins and scalable processes to bridge lab-scale innovations with industrial applications. Full article
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15 pages, 2303 KiB  
Article
Octacalcium Phosphate/Calcium Citrate/Methacrylated Gelatin Composites: Optimization of Photo-Crosslinking Conditions and Osteogenic Potential Evaluation
by Yuejun Wang, Taishi Yokoi, Masaya Shimabukuro and Masakazu Kawashita
Int. J. Mol. Sci. 2025, 26(14), 6889; https://doi.org/10.3390/ijms26146889 - 17 Jul 2025
Viewed by 251
Abstract
Bone grafting is essential for the regeneration of bone defects where natural healing is inadequate. Octacalcium phosphate (OCP)/calcium citrate (CC)/pig gelatin (pig Gel) composites promote hydroxyapatite (HAp) formation in simulated body fluid (SBF); however, the rapid degradation of pig Gel leads to their [...] Read more.
Bone grafting is essential for the regeneration of bone defects where natural healing is inadequate. Octacalcium phosphate (OCP)/calcium citrate (CC)/pig gelatin (pig Gel) composites promote hydroxyapatite (HAp) formation in simulated body fluid (SBF); however, the rapid degradation of pig Gel leads to their degradation in SBF within 7 d. To address this, we developed a 35% OCP/35% CC/30% methacrylated gelatin (GelMA) composite by leveraging the tuneable photo-crosslinking ability of GelMA to enhance the initial structural stability in SBF. However, the optimal synthetic photo-crosslinking conditions and the apatite-forming abilities of the OCP/CC/GelMA composite require investigation. In this study, we employed photo-crosslinking to synthesize homogeneous OCP/CC/GelMA composites with initial structural stability in SBF and evaluated their HAp-forming ability in SBF as an indicator of osteogenic potential, in comparison with the OCP/CC/pig Gel composites. Both GelMA- and pig Gel-based composites were prepared and immersed in SBF for 7 d to assess HAp formation. Although the OCP/CC/GelMA composite showed reduced HAp nucleation compared to the OCP/CC/pig Gel composites, it exhibited enhanced initial structural stability in SBF while retaining its HAp-forming ability. These findings highlight the OCP/CC/GelMA composite as a stable and promising scaffold for bone regeneration, laying the groundwork for further research. Full article
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15 pages, 1994 KiB  
Article
An Integrated PMA Pretreatment Instrument for Simultaneous Quantitative Detection of Vibrio parahaemolyticus and Vibrio cholerae in Aquatic Products
by Yulong Qin, Rongrong Xiong, Yong Zhao, Zhaohuan Zhang and Yachang Yin
Foods 2025, 14(13), 2166; https://doi.org/10.3390/foods14132166 - 21 Jun 2025
Viewed by 323
Abstract
Traditional hazard identification techniques for Vibrio parahaemolyticus often neglect the distinction between viable and nonviable bacteria in aquatic products, leading to overestimated disease risks and uncertainties in risk assessments. To address this limitation, we developed an automated PMA pretreatment instrument that integrates dark [...] Read more.
Traditional hazard identification techniques for Vibrio parahaemolyticus often neglect the distinction between viable and nonviable bacteria in aquatic products, leading to overestimated disease risks and uncertainties in risk assessments. To address this limitation, we developed an automated PMA pretreatment instrument that integrates dark incubation and photo-crosslinking into a unified workflow, allowing customizable parameters such as incubation time, light exposure duration, and mixing speed while maintaining stable temperatures (<±1 °C fluctuation) to preserve bacterial DNA integrity. Leveraging this system, a duplex qPCR assay was optimized for simultaneous quantitative detection of V. parahaemolyticus and V. cholerae in aquatic products and environmental samples. The assay demonstrated robust performance with 90–110% amplification efficiencies across diverse matrices, achieving low limits of detection (LODs) of 101–102 CFU/mL in shrimp farming environment water and 102–103 CFU/g in shrimp (Litopenaeus vannamei) and oyster (Crassostrea gigas). Notably, it effectively discriminated viable bacteria from 106 CFU/mL(g) nonviable cells and showed strong correlation with ISO-standard methods in real-world sample validation. This integrated platform offers a rapid, automated solution for accurate viable bacterial quantification, with significant implications for food safety, pathogen surveillance, and risk management in aquatic industries. Full article
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18 pages, 1809 KiB  
Article
A Photo-Crosslinked Casein-Tannic Acid System for Enhanced Hair Protection: A Green Chemistry Approach
by Sujin Kyung, Won-Gun Koh and Hyun Jong Lee
Polymers 2025, 17(12), 1585; https://doi.org/10.3390/polym17121585 - 6 Jun 2025
Viewed by 903
Abstract
Hair is continuously exposed to various damaging factors in daily life, necessitating effective protective strategies that balance efficacy with environmental sustainability. In this study, we developed an environmentally friendly hair protective coating using casein proteins crosslinked with tannic acid via riboflavin phosphate-mediated photo-initiation. [...] Read more.
Hair is continuously exposed to various damaging factors in daily life, necessitating effective protective strategies that balance efficacy with environmental sustainability. In this study, we developed an environmentally friendly hair protective coating using casein proteins crosslinked with tannic acid via riboflavin phosphate-mediated photo-initiation. Casein solutions containing tannic acid (0.05% w/v) and riboflavin phosphate (0.01–0.1% w/v) were prepared and applied to virgin Asian hair, followed by blue light irradiation to initiate crosslinking. The coating formation mechanism was investigated through rheological characterization, which confirmed successful network formation with optimal mechanical stability at a 0.05% tannic acid concentration. Chemical analysis using FTIR spectroscopy revealed subtle but meaningful interactions between the coating components, while SEM analysis demonstrated the coating’s integration with the hair surface. Mechanical property evaluations showed that the photo-crosslinked coating significantly enhanced hair tensile strength by approximately 21% compared to untreated hair, while maintaining appropriate elasticity. Region-specific analysis of stress–strain behavior indicated that the coating extended the initial Hookean region while preserving natural resistance in the post-yield region, creating a balanced enhancement in mechanical properties. This approach offers a promising alternative to conventional hair treatments by utilizing natural, food-grade components and mild processing conditions, addressing growing demands for sustainable hair care solutions that effectively protect against daily damage. Full article
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32 pages, 11077 KiB  
Article
Gelatin/Cerium-Doped Bioactive Glass Composites for Enhancing Cellular Functions of Human Mesenchymal Stem Cells (hBMSCs)
by Andrey Iodchik, Gigliola Lusvardi, Alfonso Zambon, Poh Soo Lee, Hans-Peter Wiesmann, Anne Bernhardt and Vera Hintze
Gels 2025, 11(6), 425; https://doi.org/10.3390/gels11060425 - 1 Jun 2025
Viewed by 762
Abstract
Delayed or non-healing of bone defects in an aging, multi-morbid population is still a medical challenge. Current replacement materials, like autografts, are limited. Thus, artificial substitutes from biodegradable polymers and bioactive glasses (BGs) are promising alternatives. Here, novel cerium-doped mesoporous BG microparticles (Ce-MBGs) [...] Read more.
Delayed or non-healing of bone defects in an aging, multi-morbid population is still a medical challenge. Current replacement materials, like autografts, are limited. Thus, artificial substitutes from biodegradable polymers and bioactive glasses (BGs) are promising alternatives. Here, novel cerium-doped mesoporous BG microparticles (Ce-MBGs) with different cerium content were included in photocrosslinkable, methacrylated gelatin (GelMA) for promoting cellular functions of human mesenchymal stem cells (hBMSCs). The composites were studied for intrinsic morphology and Ce-MBGs distribution by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). They were gravimetrically analyzed for swelling and stability, compressive modulus via Microsquisher® and bioactivity by Fluitest® calcium assay and inductively coupled plasma-optical emission spectrometry (ICP-OES), also determining silicon and cerium ion release. Finally, seeding, proliferation, and differentiation of hBMSCs was investigated. Ce-MBGs were evenly distributed within composites. The latter displayed a concentration-dependent but cerium-independent decrease in swelling, while mechanical properties were comparable. A MBG type-dependent bioactivity was shown, while an enhanced osteogenic differentiation of hBMSCs was achieved for Ce-MBG-composites and related to different ion release profiles. These findings show their strong potential in promoting bone regeneration. Still, future work is required, e.g., analyzing the expression of osteogenic genes, providing further evidence for the composites’ osteogenic effect. Full article
(This article belongs to the Special Issue Synthesis, Characterization and Applications of Collagen-Based Gels)
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16 pages, 2552 KiB  
Article
Development of a Photocrosslinkable Collagen–Bone Matrix Hydrogel for Bone Tissue Engineering
by Po-Hsun Chen and Wei-Bor Tsai
Polymers 2025, 17(7), 935; https://doi.org/10.3390/polym17070935 - 29 Mar 2025
Viewed by 741
Abstract
Bone tissue engineering aims to restore lost bone and create an environment conducive to new bone formation. To address this challenge, we developed a novel biomimetic hydrogel that combines maleic anhydride–modified type I collagen (ColME) with maleic anhydride–modified demineralized and decellularized porcine bone [...] Read more.
Bone tissue engineering aims to restore lost bone and create an environment conducive to new bone formation. To address this challenge, we developed a novel biomimetic hydrogel that combines maleic anhydride–modified type I collagen (ColME) with maleic anhydride–modified demineralized and decellularized porcine bone matrix particles (mDBMp), forming a composite ColME–mDBMp (CMB) hydrogel. Chemical modification of collagen resulted in a high degree of substitution, thereby enhancing its photocrosslinkability. Integration of mDBMp into the ColME hydrogel via photocrosslinking resulted in enhanced physiological stability, reduced shrinkage, and improved mechanical strength compared to gelatin methacrylate (GelMA)-based hydrogels. Moreover, mineralization of the CMB hydrogel promoted the formation of pure hydroxyapatite (HAp) crystals, providing superior stiffness while maintaining ductility relative to GelMA-based hydrogels. In vitro, human bone marrow mesenchymal stem cells (hBMSCs) encapsulated in CMB hydrogels exhibited enhanced proliferation, cell–matrix interactions, and osteogenic differentiation, as evidenced by increased calcium deposition and histological analysis. These results demonstrate that the CMB hydrogel, enriched with extracellular matrix (ECM) components, shows considerable promise over current GelMA-based hydrogels for bone tissue engineering. Full article
(This article belongs to the Special Issue Synthesis and Applications of Bio-Based Polymers)
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22 pages, 7846 KiB  
Article
A Novel Type II Photoinitiator with Self-Supplied Hydrogen for Anti-Creep Crosslinking Polyethylene Film
by Fei Yang, Zhaoyuan Jing, Yingqiu Wang and Guodong Jiang
Materials 2025, 18(6), 1313; https://doi.org/10.3390/ma18061313 - 16 Mar 2025
Cited by 1 | Viewed by 523
Abstract
Two macromolecular photoinitiators, bis(4-benzoylphenyl) malonate (BPMD) and bis(4-benzoylphenyl) 3,3’-(piperazine-1,4-diyl)bis(3-oxopropanoate) (DBPMD), were successfully synthesized from 4-hydroxybenzophenone (4-BP), malonyl chloride, and anhydrous piperazine. Structural characterization using Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance spectroscopy (1H NMR) confirmed the expected molecular [...] Read more.
Two macromolecular photoinitiators, bis(4-benzoylphenyl) malonate (BPMD) and bis(4-benzoylphenyl) 3,3’-(piperazine-1,4-diyl)bis(3-oxopropanoate) (DBPMD), were successfully synthesized from 4-hydroxybenzophenone (4-BP), malonyl chloride, and anhydrous piperazine. Structural characterization using Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance spectroscopy (1H NMR) confirmed the expected molecular framework. Ultraviolet (UV) absorption spectroscopy revealed that BPMD and DBPMD exhibited enhanced molar extinction coefficients and red-shifted absorption maxima compared to 4-BP. Migration studies in high-density polyethylene (HDPE) demonstrated significantly lower diffusion rates for BPMD and DBPMD than for 4-BP, with DBPMD exhibiting superior photoinitiation efficiency even in the absence of amine-based activators. Photoinitiation performance, photocrosslinking kinetics, and mechanical evaluations indicated that both BPMD and DBPMD enabled efficient UV-initiated crosslinking, leading to improved tensile strength and creep resistance in polyethylene films. These findings highlight the potential of BPMD and DBPMD as advanced photoinitiators for high-performance UV-crosslinked polyethylene systems. Full article
(This article belongs to the Section Polymeric Materials)
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14 pages, 2093 KiB  
Article
Enhanced Mechanical Stability of Water-Based Peel-Off Nail Polish Through Riboflavin Phosphate-Mediated Visible Light Photocrosslinking
by Minjin Kim, Youngran Park and Hyun Jong Lee
Polymers 2025, 17(6), 766; https://doi.org/10.3390/polym17060766 - 14 Mar 2025
Cited by 1 | Viewed by 745
Abstract
Water-based peel-off nail polishes offer environmental and safety advantages but often suffer from poor mechanical properties. This study investigated the effect of visible-light-induced photocrosslinking with riboflavin phosphate (RFP) on the mechanical properties and adhesion of water-based peel-off nail polish films. Polyurethane films that [...] Read more.
Water-based peel-off nail polishes offer environmental and safety advantages but often suffer from poor mechanical properties. This study investigated the effect of visible-light-induced photocrosslinking with riboflavin phosphate (RFP) on the mechanical properties and adhesion of water-based peel-off nail polish films. Polyurethane films that contained various concentrations of RFP (0–0.1%) were prepared by combining two commercial water-based polyurethane dispersions and characterized through tensile testing, rheological analysis, and adhesion measurements. Under large deformation, the photocrosslinked films showed significantly enhanced mechanical properties, with the highest RFP concentration (0.1%) exhibiting a 54% increase in tensile strength and a 94% increase in Young’s modulus compared with the control, which reflected a transition from physical to covalent network dominance. Rheological analysis under small deformation revealed the formation of complex network structures, where lower RFP concentrations maintained a higher chain mobility beneficial for adhesion, while higher concentrations created more stable networks with enhanced thermal stability, which maintained 50% of the initial storage modulus up to 100 °C. The films exhibited biocompatibility across all RFP concentrations in the cell viability tests, and the straightforward preparation process that used commercially available materials suggests immediate potential for industrial implementation. These results demonstrate that RFP-mediated visible light photocrosslinking offers a promising approach for developing high-performance, environmentally friendly nail polish formulations that combine enhanced durability with user safety and manufacturing practicality. Full article
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22 pages, 11811 KiB  
Review
Development of Hydrogels Fabricated via Stereolithography for Bioengineering Applications
by Youngjin Jeon, Minji Kim and Kwang Hoon Song
Polymers 2025, 17(6), 765; https://doi.org/10.3390/polym17060765 - 14 Mar 2025
Cited by 2 | Viewed by 1239
Abstract
The architectures of hydrogels fabricated with stereolithography (SLA) 3D printing systems have played various roles in bioengineering applications. Typically, the SLA systems successively illuminated light to a layer of photo-crosslinkable hydrogel precursors for the fabrication of hydrogels. These SLA systems can be classified [...] Read more.
The architectures of hydrogels fabricated with stereolithography (SLA) 3D printing systems have played various roles in bioengineering applications. Typically, the SLA systems successively illuminated light to a layer of photo-crosslinkable hydrogel precursors for the fabrication of hydrogels. These SLA systems can be classified into point-scanning types and digital micromirror device (DMD) types. The point-scanning types form layers of hydrogels by scanning the precursors with a focused light, while DMD types illuminate 2D light patterns to the precursors to form each hydrogel layer at once. Overall, SLA systems were cost-effective and allowed the fabrication of hydrogels with good shape fidelity and uniform mechanical properties. As a result, hydrogel constructs fabricated with the SLA 3D printing systems were used to regenerate tissues and develop lab-on-a-chip devices and native tissue-like models. Full article
(This article belongs to the Section Polymer Applications)
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18 pages, 3350 KiB  
Article
Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
by Krishi Patel, Derya Ozhava and Yong Mao
Gels 2025, 11(3), 199; https://doi.org/10.3390/gels11030199 - 13 Mar 2025
Cited by 3 | Viewed by 806
Abstract
Cartilage damage is common in sports injuries and cartilage-related diseases, such as degenerative joint and rheumatic disorders. Autologous chondrocyte implantation (ACI) is a widely used cell-based therapy for repairing cartilage damage in clinical practice. In this procedure, a patient’s chondrocytes are isolated, cultured [...] Read more.
Cartilage damage is common in sports injuries and cartilage-related diseases, such as degenerative joint and rheumatic disorders. Autologous chondrocyte implantation (ACI) is a widely used cell-based therapy for repairing cartilage damage in clinical practice. In this procedure, a patient’s chondrocytes are isolated, cultured in vitro to expand the cell population, and then implanted into the damaged site. However, in vitro expansion of chondrocytes on standard 2D culture surfaces leads to dedifferentiation (loss of the chondrocyte phenotype), and the delivery of detached cells has proven to be ineffective. To overcome these limitations, the matrix-assisted ACI (MACI) procedure was developed. In MACI, matrices such as hydrogels and microspheres are used as cell carriers or scaffolds to deliver expanded chondrocytes, enhancing cell viability and precision delivery. To streamline the two key steps of MACI—cell expansion and delivery—this study aims to investigate various configurations of gelatin-based hydrogels for their potential to support both cell expansion and delivery as a single step. This study evaluated gelatin microspheres (Gel MS), micronized photo-crosslinked GelMA microparticles (GelMA MP), and bulky GelMA hydrogels containing cells (GelMA HG). Cell growth, maintenance of the chondrocyte phenotype, and cartilage extracellular matrix (ECM) production were assessed in pellet cultures for cells grown on/in these carriers, compared with cells cultured on tissue culture-treated polystyrene (TCP). Our results demonstrate that normal human knee articular chondrocytes exhibit robust growth on Gel MS and form aggregates enriched with glycosaminoglycan-rich ECM. Gel MS outperformed both GelMA MP and GelMA HG as a cell carrier by both supporting long-term cell growth with reduced dedifferentiation and precision delivery. Full article
(This article belongs to the Special Issue Smart Hydrogel for Wound Healing and Tissue Repair)
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14 pages, 7452 KiB  
Article
Light-Intensity-Dependent Control of Collagen Hydrogel Properties via Riboflavin Phosphate-Mediated Photocrosslinking
by Seungyeop Yoo, Won-Gun Koh and Hyun Jong Lee
Materials 2025, 18(4), 828; https://doi.org/10.3390/ma18040828 - 14 Feb 2025
Cited by 2 | Viewed by 1049
Abstract
While photocrosslinked collagen hydrogels show promise in tissue engineering, conventional approaches for property control often require complex chemical modifications or concentration changes that alter their biochemical composition. Here, we present the first systematic investigation of light-intensity-dependent control in riboflavin phosphate (RFP)-mediated photocrosslinking as [...] Read more.
While photocrosslinked collagen hydrogels show promise in tissue engineering, conventional approaches for property control often require complex chemical modifications or concentration changes that alter their biochemical composition. Here, we present the first systematic investigation of light-intensity-dependent control in riboflavin phosphate (RFP)-mediated photocrosslinking as a novel, single-parameter approach to modulate hydrogel properties while preserving native biochemical environments. We systematically investigated the effects of varying light intensities (100 K, 50 K, and 10 K lux) during hydrogel fabrication through comprehensive structural, mechanical, and biological characterization. Scanning electron microscopy revealed unprecedented control over network architecture, where higher light intensities produced more uniform and compact networks, while swelling ratio analysis showed significant differences between 100 K lux (246 ± 2-fold) and 10 K lux (265 ± 4-fold) conditions. Most significantly, we discovered that intermediate intensity (50 K lux) uniquely optimized mechanical performance in physiological conditions, achieving storage modulus of about 220 Pa after 24 h swelling, compared to about 160 and 109 Pa for 100 K and 10 K lux conditions, respectively. Remarkably, cellular studies using NIH/3T3 fibroblasts demonstrated that lower light intensity (10 K lux) enhanced cell proliferation by 2.8-fold compared to 100 K lux conditions after 7 days of culture, with superior cell network formation in both 2D and 3D environments. This groundbreaking approach establishes light intensity as a powerful single parameter for precise control of both mechanical and biological properties, offering a transformative tool for tailoring collagen-based biomaterials in tissue engineering applications. Full article
(This article belongs to the Special Issue Advances in Bio-Polymer and Polymer Composites)
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19 pages, 9213 KiB  
Article
Direct Ink Writing and Photocrosslinking of Hydroxypropyl Cellulose into Stable 3D Parts Using Methacrylation and Blending
by Mehmet-Talha Yapa, Gopakumar Sivasankarapillai, Jacques Lalevée and Marie-Pierre Laborie
Polymers 2025, 17(3), 278; https://doi.org/10.3390/polym17030278 - 22 Jan 2025
Viewed by 1555
Abstract
Two 50% solid content solutions of methacrylated hydroxypropyl cellulose (MAHPC) with respective substitution degrees of 1.85 ± 0.04 (L_MAHPC) and 2.64 ± 0.04 (H_MAHPC) were screened for rheological properties, photocrosslinking kinetics and printability in relevance to direct ink writing (DIW). Photo-rheological and printability [...] Read more.
Two 50% solid content solutions of methacrylated hydroxypropyl cellulose (MAHPC) with respective substitution degrees of 1.85 ± 0.04 (L_MAHPC) and 2.64 ± 0.04 (H_MAHPC) were screened for rheological properties, photocrosslinking kinetics and printability in relevance to direct ink writing (DIW). Photo-rheological and printability studies reveal that the rheological properties of both MAHPC inks are better suited for DIW than those of hydroxypropyl cellulose (HPC) inks. Namely, methacrylate grafting improves shear dynamic moduli at low strain but also shear thinning and shear recovery. Both inks completely cure within 30 s upon shining UV light. Photocrosslinking is found to follow the phenomenological autocatalytic Sestak–Berggren kinetic model. However, prolonged exposure to UV light past full cure upon DIW leads to part fracture. The narrow UV-cure time window consequently precludes the production of multilayer parts using UV-assisted DIW for these neat MAHPC inks. In contrast, when blending MAHPC with HPC, an optimal balance between curing kinetics and DIW conditions is achieved, and stable, high-fidelity 150-layered parts are produced. Altogether this research highlights the need to design the content of photocrosslinkable moieties of cellulose derivatives to photoprint high fidelity and stable 3D parts from HPC inks. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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27 pages, 69684 KiB  
Article
Photo-Crosslinking Hydrogel Based on Porcine Small Intestinal Submucosa Decellularized Matrix/Fish Collagen/GelMA for Culturing Small Intestinal Organoids and Repairing Intestinal Defects
by Zihao Jia and Ziwei Wang
Int. J. Mol. Sci. 2025, 26(2), 663; https://doi.org/10.3390/ijms26020663 - 14 Jan 2025
Cited by 3 | Viewed by 1412
Abstract
Organoid technology, as an innovative approach in biomedicine, exhibits promising prospects in disease modeling, pharmaceutical screening, regenerative medicine, and oncology research. However, the use of tumor-derived Matrigel as the primary method for culturing organoids has significantly impeded the clinical translation of organoid technology [...] Read more.
Organoid technology, as an innovative approach in biomedicine, exhibits promising prospects in disease modeling, pharmaceutical screening, regenerative medicine, and oncology research. However, the use of tumor-derived Matrigel as the primary method for culturing organoids has significantly impeded the clinical translation of organoid technology due to concerns about potential risks, batch-to-batch instability, and high costs. To address these challenges, this study innovatively introduced a photo-crosslinkable hydrogel made from a porcine small intestinal submucosa decellularized matrix (SIS), fish collagen (FC), and methacrylate gelatin (GelMA). The cost-effective hydrogel demonstrated excellent biocompatibility, tunable mechanical properties, rapid gelation properties, and low immunogenicity. Importantly, the proliferation and differentiation capacities of small intestinal organoids cultured in hydrogel were comparable to those in Matrigel, with no significant disparity observed. Furthermore, after one week of transplantation in nude mice, the hydrogel–organoid complex exhibited sustained structural and functional stability while preserving the differentiation characteristics of small intestinal organoids. Our study also demonstrated the effective potential of FC/SIS/GelMA hydrogel in accelerating the repair process of small intestinal defects, reducing the area of scar formation, and promoting the regeneration of both intestinal villi and smooth muscle tissue. In summary, this study presents a novel protocol for culturing small intestinal organoids, offering potential implications for future clinical applications and serving as an experimental foundation for the development of tissue-engineered intestines based on small intestinal organoids. Full article
(This article belongs to the Section Biochemistry)
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20 pages, 6417 KiB  
Article
Polydeoxynucleotide-Loaded Visible Light Photo-Crosslinked Gelatin Methacrylate Hydrogel: Approach to Accelerating Cartilage Regeneration
by Sunjae Park, Youngjun Son, Jonggyu Park, Soyoon Lee, Na-Hyeon Kim, Se-Na Jang, Tae-Woong Kang, Jeong-Eun Song and Gilson Khang
Gels 2025, 11(1), 42; https://doi.org/10.3390/gels11010042 - 7 Jan 2025
Cited by 3 | Viewed by 1419
Abstract
Articular cartilage faces challenges in self-repair due to the lack of blood vessels and limited chondrocyte concentration. Polydeoxyribonucleotide (PDRN) shows promise for promoting chondrocyte growth and cartilage regeneration, but its delivery has been limited to injections. Continuous PDRN delivery is crucial for effective [...] Read more.
Articular cartilage faces challenges in self-repair due to the lack of blood vessels and limited chondrocyte concentration. Polydeoxyribonucleotide (PDRN) shows promise for promoting chondrocyte growth and cartilage regeneration, but its delivery has been limited to injections. Continuous PDRN delivery is crucial for effective cartilage regeneration. This study explores using gelatin methacrylate (gelMA) hydrogel, crosslinked with visible light and riboflavin 5′-phosphate sodium (RF) as a photoinitiator, for sustained PDRN release. GelMA hydrogel’s synthesis was confirmed through spectrophotometric techniques, demonstrating successful methacrylate group incorporation. PDRN-loaded gelMA hydrogels displayed varying pore sizes, swelling ratios, degradation rates, and mechanical properties based on gelMA concentration. They showed sustained PDRN release and biocompatibility, with the 14% gelMA-PDRN composition performing best. Glycosaminoglycan (GAG) activity was higher in PDRN-loaded hydrogels, indicating a positive effect on cartilage formation. RT-PCR analysis revealed increased expression of cartilage-specific genes (COL2, SOX9, AGG) in gelMA-PDRN. Histological assessments in a rabbit cartilage defect model demonstrated superior regenerative effects of gelMA-PDRN hydrogels. This study highlights the potential of gelMA-PDRN hydrogels in cartilage tissue engineering, providing a promising approach for effective cartilage regeneration. Full article
(This article belongs to the Special Issue Hydrogel for Tissue Engineering and Biomedical Therapeutics)
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