Biocompatible Matrix Research Articles

Acid-decorated chitosan-magnetic aluminum ferrite as a bionanocomposite catalyst for green synthesis of biologically active [4,3‑d]pyrido[1,2‑a]pyrimidin-6‑ones

In this study, a novel hybrid nanostructure consisting of acid-decorated chitosan and magnetic AlFeO3 nanoparticles was fabricated. The acid-decorated chitosan provided a stable and biocompatible matrix for the magnetic AlFeO3 nanoparticles. Various techniques including Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction patterns (XRD), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), specific surface area (BET), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to characterize and confirm the successful synthesis of the hybrid nanostructure. The newly prepared magnetic bio-nanocomposite (AlFeO3@CS-SO3H) was effectively employed in the synthesis of biologically active 7-aryl[4,3d]pyrido[1,2a]pyrimidin-6(7H)one derivatives in an aqueous medium, creating an environmentally friendly process. The desired products were manufactured in high yields (88–98%) without the formation of noticeable side products. This procedure offers numerous advantages, including short reaction times, the use of a green solvent, the ability to reuse the catalyst without a significant decrease in catalytic activity, and easy separation of the catalyst using an external magnet. The high yields and minimal side product formation indicate the efficiency and selectivity of this method, making it a promising strategy for the sustainable production of biologically active compounds.

Flexible Electronic Patch Utilizing Gelatin Film for Heart and Brain Signal Detection.

Flexible electronic patches have been widely studied in various fields. However, they still face serious challenges in cardio-brain signaling monitoring to achieve accurate adhesion and detection with compatibility in mildly humid environments. To tackle these challenges, we engineered a gelatin hydrogel film cross-linked with a biocompatible matrix factor and combined it with a blend of liquid metal and PVP to create the flexible electronic patch. The flexible patch has good biocompatibility and fatigue resistance due to the incorporation of liquid metal and natural gelatin, with the conductivity of liquid metal and minimal toxicity of the gelatin film. It is possible to securely insert it into the body for a duration of 3 weeks while maintaining monitoring functionality and withstanding 10 000 cycles of flexural fatigue. This research provides an innovative approach to the future advancement of flexible electronic patches.

Decellularized Liver Matrices for Expanding the Donor Pool-An Evaluation of Existing Protocols and Future Trends.

Liver transplantation is the only curative option for end-stage liver disease and is necessary for an increasing number of patients with advanced primary or secondary liver cancer. Many patient groups can benefit from this treatment, however the shortage of liver grafts remains an unsolved problem. Liver bioengineering offers a promising method for expanding the donor pool through the production of acellular scaffolds that can be seeded with recipient cells. Decellularization protocols involve the removal of cells using various chemical, physical, and enzymatic steps to create a collagenous network that provides support for introduced cells and future vascular and biliary beds. However, the removal of the cells causes varying degrees of matrix damage, that can affect cell seeding and future organ performance. The main objective of this review is to present the existing techniques of producing decellularized livers, with an emphasis on the assessment and definition of acellularity. Decellularization agents are discussed, and the standard process of acellular matrix production is evaluated. We also introduce the concept of the stepwise assessment of the matrix during decellularization through decellularization cycles. This method may lead to shorter detergent exposure times and less scaffold damage. The introduction of apoptosis induction in the field of organ engineering may provide a valuable alternative to existing long perfusion protocols, which lead to significant matrix damage. A thorough understanding of the decellularization process and the action of the various factors influencing the final composition of the scaffold is essential to produce a biocompatible matrix, which can be the basis for further studies regarding recellularization and retransplantation.

A novel water-soluble polymer nanocomposite containing ultra-small Fe3O4 nanoparticles with strong antibacterial and antibiofilm activity.

A novel water-soluble polymer nanocomposite containing ultra-small iron oxide nanoparticles, intercalated into a biocompatible matrix of 1-vinyl-1,2,4-triazole and N-vinylpyrrolidone copolymer has been synthesized for the first time. The use of an original polymer matrix ensured effective stabilization of the crystalline phase of iron oxides at an early stage of its formation in an ultra-small (2-8 nm, average diameter is 4.8 nm) nanosized state due to its effective interaction with the functional groups of copolymer macromolecules. At the same time, the copolymer ensures the long-term stability of iron oxide nanoparticles in a nanosized dispersion. The structure and physicochemical properties of the copolymer and nanocomposite were studied by elemental analysis, 1H and 13C NMR spectroscopy, gel permeation chromatography, Fourier-transform infrared spectroscopy, transmission and scanning electron microscopy, dynamic light scattering, thermogravimetric analysis and differential scanning calorimetry. The nanocomposite exhibits high antibacterial and antibiofilm activity against both Gram-negative and Gram-positive bacteria. The nanocomposite at a concentration of 500 and 1000 μg mL-1 leads to complete death of Escherichia coli cells after 24 and 3 hours of incubation, respectively. The nanocomposite at a concentration of 100 μg mL-1 leads to complete death of Staphylococcus aureus cells after 24 hours of incubation. Which indicates the potential of using the nanocomposite for the treatment of superficial wounds and purulent-inflammatory complications.

Enhancing epithelial regeneration with gelatin methacryloyl hydrogel loaded with extracellular vesicles derived from adipose mesenchymal stem cells for decellularized tracheal patching.

Patch tracheoplasty offers an alternative approach to repairing congenital tracheal stenosis without tension but poses a higher risk of restenosis, granulation tissue formation, and tracheal collapse. The use of tissue-engineered patches for tracheoplasty has been proposed as a solution. Studies suggest that decellularization methods are effective in preparing tracheal patches; however, further research is necessary to improve their efficiency and safety. This study introduces a novel decellularization method using 3-[(3Cholamidopropyl)dimethylammonio]propanesulfonate (CHAPS) and DNase to create a biocompatible tracheal matrix. To enhance the regeneration of epithelial regions within decellularized tracheal scaffolds, this study conducted experimental validations at various levels, both in vivo and in vitro, by introducing extracellular vesicles derived from adipose mesenchymal stem cells as an intervention measure. The ability to promote epithelial regeneration was validated both in vitro and in vivo by incorporating a GelMA hydrogel loaded with adipose-derived mesenchymal stem cell extracellular vesicles (ADMSC-EVs). Evaluation of HBE cell proliferation on tracheal patches treated with varying concentrations of ADMSC-EVs, along with migration and invasion experiments on ADMSC-EV-treated HBE cells, demonstrated enhanced epithelialization in vitro. The inflammatory response and vascular regeneration were assessed via subcutaneous implantation in rats for two weeks. In a rabbit tracheal defect model, the hydrogel loaded with ADMSC-EVs accelerated re-epithelialization in the patch area. This approach shows promise as a novel material for tracheal patching in clinical applications.

Synthesis of rice husk-zinc oxide-chitosan-based sponge: A green and eco-friendly nanocomposite for enhanced antibacterial, hemostasis, and wound healing applications

Wounds are a serious health concern that is often made worse by conditions including bacterial infections, poor blood circulation, and decreased cell growth. This work presents a novel sustainable wound dressing sponge made of zinc oxide nanoparticles (ZnO-NPs), rice husk (RH), and chitosan (CS). CS functions as a biocompatible matrix that induces cell adhesion and proliferation, while ZnO-NPs provide their well-documented antibacterial activity, which is critical for wound infection prevention. RH, a natural and renewable resource, strengthens the structural integrity of the composite and offers further antioxidant advantages. CS/RH/ZnO nanocomposite was synthesized by the freeze-drying method, and its evaluation was done through various tests, including wound healing assays, antibacterial tests, and histological analysis. Antibacterial tests revealed substantial inhibition zones against Pseudomonas aeruginosa (24 mm) and Staphylococcus aureus (22 mm), which is comparable to other commonly used wound care materials, validating the material’s effectiveness in preventing infections. Within 14 days, in vivo testing showed a 75 % wound closure rate, which was far higher than the control group's 50 % closure rate. Histopathological analysis showed marked re-epithelialization and active tissue regeneration, evidenced by pronounced acanthosis in the epidermis. In addition to improving therapeutic effectiveness, this multipurpose approach to wound care lessens dependency on non-renewable resources. This study demonstrated that the development of a sponge wound dressing from rice husk, a natural agricultural byproduct, represents a sustainable approach to wound care. By reducing reliance on non-renewable resources and minimizing the environmental impact of medical waste, it offers an eco-friendly solution that enhances wound management.

Emerging Cationic Nanovaccines.

Cationic vaccines of nanometric sizes can directly perform the delivery of antigen(s) and immunomodulator(s) to dendritic cells in the lymph nodes. The positively charged nanovaccines are taken up by antigen-presenting cells (APCs) of the lymphatic system often originating the cellular immunological defense required to fight intracellular microbial infections and the proliferation of cancers. Cationic molecules imparting the positive charges to nanovaccines exhibit a dose-dependent toxicity which needs to be systematically addressed. Against the coronavirus, mRNA cationic nanovaccines evolved rapidly. Nowadays cationic nanovaccines have been formulated against several infections with the advantage of cationic compounds granting protection of nucleic acids in vivo against biodegradation by nucleases. Up to the threshold concentration of cationic molecules for nanovaccine delivery, cationic nanovaccines perform well eliciting the desired Th 1 improved immune response in the absence of cytotoxicity. A second strategy in the literature involves dilution of cationic components in biocompatible polymeric matrixes. Polymeric nanoparticles incorporating cationic molecules at reduced concentrations for the cationic component often result in an absence of toxic effects. The progress in vaccinology against cancer involves in situ designs for cationic nanovaccines. The lysis of transformed cancer cells releases several tumoral antigens, which in the presence of cationic nanoadjuvants can be systemically presented for the prevention of metastatic cancer. In addition, these local cationic nanovaccines allow immunotherapeutic tumor treatment.

Plasticity variable collagen-PEG interpenetrating networks modulate cell spreading

The extracellular matrix protein collagen I has been used extensively in the field of biomaterials due to its inherent biocompatibility and unique viscoelastic and mechanical properties. Collagen I self-assembly into fibers and networks is environmentally sensitive to gelation conditions such as temperature, resulting in gels with distinct network architectures and mechanical properties. Despite this, collagen gels are not suitable for many applications given their relatively low storage modulus. We have prepared collagen-poly(ethylene glycol) [PEG] interpenetrating network (IPN) hydrogels to reinforce the collagen network, which also induces changes to network plasticity, a recent focus of study in cell-matrix interactions. Here, we prepare collagen/PEG IPNs, varying collagen concentration and collagen gelation temperature to assess changes in microarchitecture and mechanical properties of these networks. By tuning these parameters, IPNs with a range of stiffness, plasticity and pore size are obtained. Cell studies suggest that matrix plasticity is a key determinant of cell behavior, including cell elongation, on these gels. This work presents a natural/synthetic biocompatible matrix that retains the unique structural properties of collagen networks with increased storage modulus and tunable plasticity. The described IPN materials will be of use for applications in which control of cell spreading is desirable, as only minimal changes in sample preparation lead to changes in cell spreading and circularity. Additionally, this study contributes to our understanding of the connection between collagen self-assembly conditions and matrix structural and mechanical properties and presents them as useful tools for the design of other collagen based biomaterials. Statement of significanceWe developed a collagen-poly(ethylene glycol) interpenetrating network (IPN) platform that retains native collagen architecture and biocompatibility but provides higher stiffness and tunable plasticity. With minor changes in collagen gelation temperature or concentration, IPN gels with a range of plasticity, storage modulus, and pore size can be obtained. The tunable plasticity of the gels is shown to modulate cell spreading, with a greater proportion of elongated cells on the most plastic of IPNs, supporting the assertion that matrix plasticity is a key determinant of cell spreading. The material can be of use for situations where control of cell spreading is desired with minimal intervention, and the findings herein may be used to develop similar collagen based IPN platforms.

Patterning of tissue spheroids biofabricated from human fibroblasts on the surface of electrospun polyurethane matrix using 3D bioprinter

Organ printing is a computer-aided additive biofabrication of functional three-dimensional human tissue and organ constructs according to digital model using the tissue spheroids as building blocks. The fundamental biological principle of organ printing technology is a phenomenon of tissue fusion. Closely placed tissue spheroids undergo tissue fusion driven by surface tension forces. In order to ensure tissue fusion in the course of post-printing, tissue spheroids must be placed and maintained close to each other. We report here that tissue spheroids biofabricated from primary human fibroblasts could be placed and maintained on the surface of biocompatible electrospun polyurethane matrix using 3D bioprinter according to desirable pattern. The patterned tissue spheroids attach to polyurethane matrix during several hours and became completely spread during several days. Tissue constructions biofabricated by spreading of patterned tissue spheroids on the biocompatible electrospun polyurethane matrix is a novel technological platform for 3D bioprinting of human tissue and organs.

Cellulose‐enriched ascorbic acid for wound dressing application: Future medical textile

AbstractWounds infected by resistant microbes have become a cost and health problem worldwide. In modern wound care, healing mechanisms require particular strategies, such as adding natural antioxidants and antimicrobials in a biocompatible biopolymer matrix mimicking extracellular tissue such as cellulose. Here, ascorbic acid or Vitamin C is a promising bioactive as a topical drug loaded in a cellulose‐based composite matrix for skin tissue repair. Ascorbic acid, cellulose, or cellulose composites enriched with ascorbic acid have shown better biocompatibility and biological effects for accelerating wound healing, making them promising as sustainable medical textiles. Future challenges relate to the ideal engineered wound dressing design, raw material toxicity, and 3D printing technology.

Multi-compartmentalized electrochemical sensing platforms for monitoring cascade enzymatic reactions

Designing an electrochemical biosensor with the required features is a complex process involving multiple factors. For instance, nanocomposite materials used ensure the adaptation of the sensor to specific parameters on demand. But beyond making more versatile sensors, these materials likely offer excellent sensing platforms to mimic biological processes (e.g. cell communication) on the electrode surface. For this, developed methods are needed to integrate non-conductive nanoreactors for molecular communication into a biocompatible matrix on electrode surfaces with the request of spatially separated and controlled enzyme localization. Here, we present a novel reduced graphene oxide hybrid material to immobilize polymeric nanoreactors supported by an alginate network as a matrix on the electrode surface. The possibility of introducing cascade reactions in an electrochemical biosensor has the advantage of broadening the target substrates as well as their selectivity using enzymes in different nanocompartments (=compartmentalization). The polymeric vesicles allow the loading of enzymes or artificial enzymes, offering active center retention and long-term enzyme stability. Firstly, the inclusion of spatially separated polymeric active nanocompartments into the matrix on the electrode surface is used to monitor a simple enzyme reaction. However, the study’s accomplishment lies in its successful ability to monitor an enzyme cascade reaction, one producing and the other consuming hydrogen peroxide, hosting natural and artificial enzymes. This proof-of-concept generates an important contribution to the design of analytical platforms capable of detecting complex environments or even monitoring communication between cell-like structures, extremely useful for fields such as synthetic biology, biomimetics and advanced biosensors.

Zeolite-Loaded Hydrogels as Wound pH-Modulating Dressings for Diabetic Wound Healing.

Wound pH has emerged as a promising therapeutic target in diabetic foot ulcers (DFU). Here, we aimed to develop a microparticle-loaded hydrogel for pH modulation in wound fluid. In a screen of polymeric and inorganic microparticles, zeolites were identified as pH-modulating microparticles. Zeolites were encapsulated in a calcium cross-linked alginate hydrogel, a biocompatible matrix clinically used as a wound dressing. This hydrogel potently neutralized hydroxide ions in serum-containing simulated wound fluid. These findings encourage a further development of this pH-modulating device as a molecular therapeutic system for DFUs.

DESIGN AND DEVELOPMENT OF CURCUMIN LOADED CHIA SEED MUCILAGE BASED ELECTROSPRAYED NANOPARTICLES: IN VITRO-EX VIVO CHARACTERIZATION

Chia seed mucilage (CSM) has recently been reported as a biocompatible polymeric matrix for drug delivery. Curcumin (CUR), an active phytoconstituent widely recognized for managing colon and other types of cancer, faces limitations, such as poor water solubility and low bioavailability. Hence, this study focuses on developing CUR-loaded CSM-based electrosprayed nanoparticles (ENPs) using the electrospraying technology. The particle size and zeta potential of the optimized batch (F9) were measured at 82.20 nm and 22.39 mV, respectively. Solubility studies confirmed that the optimized CUR-ENPs exhibit higher solubility compared to bare CUR, with a 92.25% drug release in 12 h (pH 5.8). The designed CUR-ENPs showed good biocompatibility in normal FHC-CRL-1831 cell lines over the bare CUR. Moreover, CUR-ENPs demonstrated a reduction in % cell viability in the preferred HCT116 cell line as a colorectal cancer cell line over bare CUR. In conclusion, the designed electrosprayed CUR-ENPs demonstrate improved solubility of CUR.

Developing a gel-col heterogeneous network hydrogel scaffold for tissue-engineered skin with enhanced basement membrane formation

Tissue-engineered skin is constructed utilizing biocompatible matrix materials as scaffolds, and incorporating human epidermal keratinocytes (HEKs), dermal fibroblasts (HDFs), and bioactive molecules, addressing clinical issues such as skin graft rejection and donor scarcity. Conventional fabrication methods of tissue-engineered skin typically rely on homogeneous single-network scaffolds, which may not adequately address the distinct requirements of epidermal and dermal cells or the critical formation of the basement membrane, potentially impacting the development and functional integrity of the skin tissue. Cell culture studies employing GelMA hydrogels of varied concentrations have elucidated that epidermal cells exhibit increased viability on scaffolds with higher concentrations (15 %), whereas fibroblasts show increased proliferation within scaffolds of lower concentrations (5 %). Consequently, we have engineered a GelMA-collagen (Gel-Col) hydrogel scaffold with a heterogeneous network of dense and sparse matrices, conducive to the growth of both fibroblasts and epidermal cells. Culturing epidermal cells on this innovative scaffold, coupled with histological section staining, RT-PCR, and Western blot analyses, has demonstrated that the scaffold significantly enhances cellular adhesion and promotes the development of the epidermal basement membrane compared to single-network hydrogels. Mouse wound transplantation experiments have further confirmed the scaffold’s effectiveness in accelerating wound repair, supporting the development of the basement membrane, and enhancing epidermal regeneration. This research provides a reference for constructing tissue-engineered skin that more precisely emulates the intricate architecture and cellular dynamics of natural skin, propelling the advancement of tissue-engineered skin grafts in the clinical treatment of skin injuries.

Near-infrared light activated rapidly separable polymeric microneedles for transdermal biologics delivery

Polymeric microneedles (PMNs) are an attractive transdermal drug delivery approach with minimal invasiveness and improved patient compliance. However, it is uncomfortable and inconvenient for patients to wear a PMN patch for hours or days until complete payload release. Here, we report a facile strategy to fabricate rapidly separable PMN arrays activated by near-infrared (NIR) light (NIR-RS-PMN) with enhanced mechanical strength through introduction of a photothermal-sensitive spacer integrating plasmonic gold nanorods into a biocompatible sodium hyaluronate matrix. Under NIR irradiation, the NIR-RS-PMN achieved rapid separation of the patch backing and microneedles within 1 min. The loaded bioactive therapeutics, e.g., insulin and RNA, were well-preserved during fabrication, NIR irradiation, and 20-day storage at room temperature. The NIR-RS-PMN was well tolerated by rats without skin irritation. Its feasibility for biologics delivery was further established by the treatment of diabetic rats with insulin encapsulated PMNs. The innovative PMNs increase ease of use and achieve effective and precise payload delivery, which may increase access to biopharmaceuticals and vaccines in remote and resource-limited communities.

Environmental-friendly, flexible silk fibroin-based film as dual-responsive shape memory material

Bio-based shape memory materials have attracted wide attention due to their biocompatibility, degradability and safety. However, designing and manufacturing wearable bio-based shape memory films with excellent flexibility and toughness is still a challenge. In this work, silk fibroin substrate with a β-sheet structure was combined with a tri-block shape memory copolymer to prepare a transparent composited shape memory film. The silk fibroin-based film showed a dual-responsive shape memory function, which can respond to both temperature and water stimuli. This film has a sensitive water-responsive shape memory, which starts deforming after exposure to water for 3 s and fully recovers in 30 s. In addition, the composite film shows highly stretchable (>300 %) and could maintain its high tensile properties after 5 cycles of regeneration. The films also exhibited rapid degradation ability. This study provides new insights for the design of dual-responsive shape memory materials by combining biocompatible matrix and multi-block SMP to simultaneously enhance the mechanical properties, which can be used for intelligent packaging, medical supplies, soft actuators and wearable devices.

Biocompatible adipose extracellular matrix and reduced graphene oxide nanocomposite for tissue engineering applications

Despite the immense need for effective treatment of spinal cord injury (SCI), no successful repair strategy has yet been clinically implemented. Multifunctional biomaterials, based on porcine adipose tissue-derived extracellular matrix (adECM) and reduced graphene oxide (rGO), were recently shown to stimulate in vitro neural stem cell growth and differentiation. Nevertheless, their functional performance in clinically more relevant in vivo conditions remains largely unknown. Before clinical application of these adECM-rGO nanocomposites can be considered, a rigorous assessment of the cytotoxicity and biocompatibility of these biomaterials is required. For instance, xenogeneic adECM scaffolds could still harbour potential immunogenicity following decellularization. In addition, the toxicity of rGO has been studied before, yet often in experimental settings that do not bear relevance to regenerative medicine. Therefore, the present study aimed to assess both the in vitro as well as in vivo safety of adECM and adECM-rGO scaffolds. First, pulmonary, renal and hepato-cytotoxicity as well as macrophage polarization studies showed that scaffolds were benign invitro. Then, a laminectomy was performed at the 10th thoracic vertebra, and scaffolds were implanted directly contacting the spinal cord. For a total duration of 6 weeks, animal welfare was not negatively affected. Histological analysis demonstrated the degradation of adECM scaffolds and subsequent tissue remodeling. Graphene-based scaffolds showed a very limited fibrous encapsulation, while rGO sheets were engulfed by foreign body giant cells. Furthermore, all scaffolds were infiltrated by macrophages, which were largely polarized towards a pro-regenerative phenotype. Lastly, organ-specific histopathology and biochemical analysis of blood did not reveal any adverse effects. In summary, both adECM and adECM-rGO implants were biocompatible upon laminectomy while establishing a pro-regenerative microenvironment, which justifies further research on their therapeutic potential for treatment of SCI.

In Vivo Evaluation of Innovative Gadolinium-Based Contrast Agents Designed for Bioimaging Applications.

The aim of this study was the investigation of biochemical and histological changes induced in different tissues, as a result of the subcutaneous administration of Gd nanohydrogels (GdDOTA⸦CS-TPP/HA) in a CD-1 mouse strain. The nanohydrogels were obtained by encapsulating contrast agents (GdDOTA) in a biocompatible polymer matrix composed of chitosan (CS) and hyaluronic acid (HA) through the ionic gelation process. The effects of Gd nanohydrogels on the redox status were evaluated by measuring specific activities of the antioxidant enzymes catalase (CAT), glutathione peroxidase (GPx), and superoxide dismutase (SOD), as well as oxidative stress markers, such as reduced glutathione (GSH), malondialdehyde (MDA), advanced oxidation protein products (AOPP), and protein-reactive carbonyl groups (PRCG), in the liver, kidney, and heart tissues. The nitrosylated proteins expression were analyzed with Western Blot and the serum biochemical markers were measured with spectrophotometric methods. Also, a histological analysis of CD-1 mouse tissues was investigated. These results indicated that Gd nanohydrogels could potentially be an alternative to current MRI contrast agents thanks to their low toxicity in vivo.

Glutenin-chitosan 3D porous scaffolds with tunable stiffness and systematized microstructure for cultured meat model

A glutenin (G)-chitosan (CS) complex (G-CS) was cross-linked by water annealing with aim to prepare structured 3D porous cultured meat scaffolds (CMS) here. The CMS has pore diameters ranging from 18 to 67 μm and compressive moduli from 16.09 to 60.35 kPa, along with the mixing ratio of G/CS. SEM showed the porous organized structure of CMS. FTIR and CD showed the increscent content of α-helix and β-sheet of G and strengthened hydrogen-bondings among G-CS molecules, which strengthened the stiffness of G-CS. Raman spectra exhibited an increase of G concentration resulted in higher crosslinking of disulfide-bonds in G-CS, which aggrandized the bridging effect of G-CS and maintained its three-dimensional network. Cell viability assay and immuno-fluorescence staining showed that G-CS effectively facilitated the growth and myogenic differentiation of porcine skeletal muscle satellite cells (PSCs). CLSM displayed that cells first occupied the angular space of hexagon and then ring-growth circle of PSCs were orderly formed on G-CS. The texture and color of CMS which loaded proliferated PSCs were fresh-meat like. These results showed that physical cross-linked G-CS scaffolds are the biocompatible and stable adaptable extracellular matrix with appropriate architectural cues and natural micro-environment for structured CM models.

Novel materials for radiation sensing in radiotherapy treatments: Development of luminescent YVO4:Eu3+ polymer-based nanocomposites

This scientific work explores the development of luminescent nanocomposite materials for radiation sensors in Fiber Optic Dosimetry (FOD). The study emphasizes the use of YVO4:Eu3+ as a scintillator material due to its high luminescent efficiency. However, the challenge arises from its higher effective atomic number compared to soft tissue. To address this issue, the work explores the dispersion of YVO4:Eu3+ as nanoparticles (NPs) in a biocompatible polymeric matrix, specifically considering poly(methyl methacrylate) (PMMA) and poly(ethylene glycol) dimethacrylate (PEGDMA). Both PMMA/YVO4:Eu3+@TMSPM and PEGDMA/YVO4:Eu3+@TMSPM formulations were synthesized with minimal impact on the glass transition temperatures of the polymers. Under UV and beta particle excitation, these formulations exhibit emission spectra characteristic of Eu3+ f-f transitions. The decay times of the main emission peak at 620 nm were 615 μs, 584 μs, and 567 μs for the NPs, PEGDMA- and PMMA-based polymeric nanocomposites (PNCs), respectively. These decay times fall within the range suitable for scintillators in LINAC pulsed radiation facilities. Also, PEGDMA- and PMMA-based PNCs with varying contents of YVO4:Eu3+ NPs showed radioluminescence spectra under beta particle irradiation. This work demonstrates the feasibility of developing PEGDMA- and PMMA-based PNCs containing dispersed YVO4:Eu3+ NPs for their application as scintillators in radiotherapy dosimetry.