Functional Biomaterials Research Articles

Bioactive Three-Dimensional Chitosan-Based Scaffolds Modified with Poly(dopamine)/CBD@Pt/Au/PVP Nanoparticles as Potential NGCs Applicable in Nervous Tissue Regeneration—Preparation and Characterization

Tissue engineering of nervous tissue is a promising direction in the treatment of neurological diseases such as spinal cord injuries or neuropathies. Thanks to technological progress and scientific achievements; the use of cells; artificial scaffolds; and growth factors are becoming increasingly common. Despite challenges such as the complex structure of this tissue, regenerative medicine appears as a promising future approach to improve the quality of life of patients with nervous injuries. Until now; most functional biomaterials used for this purpose were based on decellularized extra cellular matrix (ECM) or nanofibrous materials, whereas current clinically verified ones in most cases do not exhibit bioactivity or the possibility for external stimulation. The aim of this research was to develop a new type of bioactive, chitosan-based 3D materials applicable as nerve guide conduits (NGCs) modified with poly(dopamine), Au/Pt coated with PVP nanoparticles, and cannabidiol. The NGCs were prepared under microwave-assisted conditions and their chemical structure was studied using the FT-IR method. Next, this study will discuss novel biomaterials for morphology and swelling abilities as well as susceptibility to biodegradation in the presence of collagenase and lysozyme. Finally, their potential in the field of nervous tissue engineering has been verified via a cytotoxicity study using the 1321N1 human astrocytoma cell line, which confirmed their biocompatibility in direct contact studies.

Bioinspired orthogonal-shaped protein-biometal nanocrystals enable oral protein absorption.

With the growing number of marketed biological drugs, the development of technological strategies for their oral systemic absorption, becomes increasingly important. The harsh gastrointestinal environment and low permeability of the intestinal epithelium, represent a huge challenge for their systemic delivery. Herein, bioinspired in the physiological insulin-Zn interaction, the design of orthogonal-shaped protein-biometal hybrid nanocrystals, further enveloped by a bilayer of functional biomaterials, is reported. The nanocrystals exhibited a size of 80 nm, a neutral surface charge and a high insulin loading. In vitro studies showed the capacity of the nanocomplexes to control the release of the associated insulin, while preserving its stability. In vivo evaluation showed sustained blood glucose reductions in both healthy and diabetic rats (up to 40 % and 80 %, respectively), while chronic immunotoxicity studies in mice indicated no toxicity effect. Preliminary efficacy studies in healthy awake pigs following oral capsule administration showed over 20 % absolute bioavailability.

Abstract 4138380: Cardiac protection of hiPSC-CMs loaded chitosan cardiac patch in myocardial infarcted swine

Background: The low grafting rate of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) following direct injection into the myocardium limits the efficacy of cardiac repair after myocardial infarction (MI). Chitosan-based scaffolds have emerged as functional biomaterials for designing delivery systems in cardiac therapies. This study aimed to enhance the potency of cardiac repair using a hiPSC-CMs loaded chitosan cardiac muscle patch (hCCMP). Methods: The patches were fabricated using chitosan. Characterization of the chitosan patches involved assessing their swelling rate and porosity. The biocompatibility of the hCCMP was analyzed through scanning electron microscopy (SEM) and the CCK8 assay. 16 Yorkshire swine (15-20 kg, 45-50 days of age) were randomly divided into 4 groups (n=4 per group): Sham, MI without further intervention, MI with an empty patch (without hiPSC-CMs), and MI with hCCMP implantation. One and four weeks post-MI, heart function, Infarction size, myocardial perfusion and metabolism were evaluated via cardiac PET-MRI. Engraftment was assessed through human cardiac troponin T staining. Histological analysis including left ventricular anterior wall thickness, cardiac remodeling, angiogenesis, arterialization, and apoptosis in the infarct border area were analyzed using immunofluorescence. Results: SEM showed that the chitosan patch had regular pore size and good 3D structure; porosity was about (96.7±0.37)%. On day3, the patch swelling rate was about (715±64.55)%. SEM, CCK8 assay showed a normal cells growth in the chitosan patch. The hiPSC-CMs grafted well with chitosan patch delivery systems and was associated with significantly improvement in LV function, infarction size, angiogenesis and cardiomyocyte apoptosis in pigs 4 weeks after MI. Conclusions: The 3D chitosan cardiac patch with hiPSC-CMs loaded can enhance the potency of cardiac repair in pigs after MI and present a novel and promising therapic strategy.

Applications of bio-composites in electronics

Abstract Functional biomaterials are being used in many promising industries to improve human quality of life and advance environmental objectives. Consideration has been given to many applications in the domains of medical, electronics, food, and pharmaceuticals. The use of bio-inspired materials enables the creation of more sustainable alternatives that strive to advance environmental preservation while simultaneously ensuring customer satisfaction. It was discovered that biopolymers are used in a number of different industries for the production of a wide range of functional bio-products. These bio-products include organic thin film transistors, organic phototransistors, emitting diodes, photodiodes, photovoltaic solar cells, hybrid dental resins, sustainable medicines, and consumer food packaging. A growth of this magnitude makes it possible to conduct substantial research in order to more inspection of the limitless requests and uses of bio-based composites. In order to fulfill the needs of certain applications, it is necessary to adjust and reassess attributes and parameters– such as hardness, durability, crack toughness, binding, solubility, polarization, plasticity, hydrogen bonding, thermal characteristics, and dielectric behavior. By virtue of their electronic and electrical properties, bio-composites and biopolymers have been put to use in a variety of applications; some includes organic thin-film transistors, electrical applications, electromagnetic insulation, energy harvesting, and thermoelectric processes. Substantial proportions of electronic waste, also referred to as E-waste, are regularly released into the environment due to the continuous growth in the production of electronic devices. Consequently, this leads to substantial environmental and ecological problems caused by the release of non-degradable polymers, hazardous compounds, and toxic heavy metals into the environment. The advancement of biodegradable polymers has significant potential for effectively reducing the environmental burden, since they may be decomposed or absorbed into the surrounding environment without generating any toxic effects. Hence, the purpose of this study is to illustrate the creation of biocompatible composites and their prospective uses in electrical applications.

Fresh insights into structure-function-integrated self-antibacterial Cu-containing Al alloys: giving Al alloys a new function.

Contact infection by bacteria and viruses is a serious concern to human health. The increasing occurrence of public health problems has stimulated the urgent need for the development of antibacterial materials. Al alloys are the fastest-growing mass-produced material group, a prerequisite for the lightweight design of vehicles, food containers and storage, as well as civil-engineering structures. In this work, the structure-function-integrated concept was used to design and produce self-antibacterial Al-xCu (x = 2.8 and 5.7) alloys for the first time ever. The antibacterial tests indicated that Al-2.8Cu and Al-5.7Cu alloys provided a stable and efficient bacteriostatic rate against S. aureus and E. coli, which was 87% for Al-2.8Cu and 100% for Al-5.7Cu against S. aureus at 24 h, and 89% for Al-2.8Cu and 94% for Al-5.7Cu against E. coli at 24 h. The antibacterial effect was similar to the commonly-used antibacterial materials with a similar Cu content. Furthermore, the mechanical properties and corrosion resistance of Al-2.8Cu and Al-5.7Cu were comparable to those of the current commonly-used commercial casting Al-Cu alloys. Structural insights into the performance and biomedical function by Cu-rich precipitates provided understanding of the mechanisms of these structure-function-integrated self-antibacterial Cu-containing Al alloys: (i) the Cu-rich precipitates produced strengthening, and (ii) the immediate contact with Cu-rich precipitates and the Cu2+ caused a synergistic action in improving antibacterial activity. This work gives Al alloys a new function and inspires fresh insights into structure-function-integrated antibacterial Al alloys.

Heterogeneous multiple soft millirobots in three-dimensional lumens.

Miniature soft robots offer opportunities for safe and physically adaptive medical interventions in hard-to-reach regions. Deploying multiple robots could further enhance the efficacy and multifunctionality of these operations. However, multirobot deployment in physiologically relevant three-dimensional (3D) tubular structures is limited by the lack of effective mechanisms for independent control of miniature magnetic soft robots. This work presents a framework leveraging the shape-adaptive robotic design and heterogeneous resistance from robot-lumen interactions to enable magnetic multirobot control. We first compute influence and actuation regions to quantify robot movement. Subsequently, a path planning algorithm generates the trajectory of a permanent magnet for multirobot navigation in 3D lumens. Last, robots are controlled individually in multilayer lumen networks under medical imaging. Demonstrations of multilocation cargo delivery and flow diversion manifest their potential to enhance biomedical functions. This framework offers a solution to multirobot actuation benefiting applications across different miniature robotic devices in complex environments.

Hafnium dioxide obtained by atomic layer deposition possesses the ability to induce the formation of biological apatite

The research explored the spontaneous formation of the BAp precursor on surfaces of HfO2 films obtained by Atomic Layer Deposition (ALD). It has been found that a careful selection of ALD growth conditions, followed by rapid thermal annealing (RTP) is crucial to achieve bioactivity of the films. Simulated Body Fluid experiment was used as a reliable test of the film's functionality as bone implant coating. SEM, XRD and XPS investigations proved that amorphous calcium orthophosphate structures were formed on the HfO2 films. These structures are of importance for biomineralization of bones. Physical and chemical characterization of the films was an integral part of the research. Such approach allowed us to achieve biomaterial functionality while maintaining the films’ quality. The finding has significance for future progress in personalized traumatological medicine.

Dielectric characteristics of Mediterranean lignocellulosic fibers for functional biocomposite materials

Abstract The primary aim of this study is to investigate the dielectric properties of lignocellulosic fibers, a unique kind of natural fiber prevalent in the Mediterranean area. Comprehensive investigations were undertaken to determine the suitability of these fibers for functional biomaterials and to reveal their potential capabilities comparable to those commonly used in other parts of the world. More exploration of the electrical characteristics of agricultural waste fibers may lead to the development and improvement of a more comprehensive knowledge on their use in the production of practical eco-products. This will provide novel opportunities for ecologically conscious design. Based on the introduction of natural fibers and their advantages in biomaterials, this study will examine the parallel plate capacitor approach to assess the dielectric properties of biological fibers. Subsequently, the impact of maleic anhydride on the dielectric properties of natural fiber composites was demonstrated as a focused case study. Therefore, it is possible to develop a suitable database for the selection of visually appealing materials in order to enhance comprehensive knowledge of the intrinsic electrical properties and attributes of these materials. Consequently, this would result in the development of more practical strategies for designing environmentally friendly products in bio-electronics and the identification of novel biomaterials with potential applications in electronics.

Unlocking Genome Editing: Advances and Obstacles in CRISPR/Cas Delivery Technologies

CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats associated with protein 9) was first identified as a component of the bacterial adaptive immune system and subsequently engineered into a genome-editing tool. The key breakthrough in this field came with the realization that CRISPR/Cas9 could be used in mammalian cells to enable transformative genetic editing. This technology has since become a vital tool for various genetic manipulations, including gene knockouts, knock-in point mutations, and gene regulation at both transcriptional and post-transcriptional levels. CRISPR/Cas9 holds great potential in human medicine, particularly for curing genetic disorders. However, despite significant innovation and advancement in genome editing, the technology still possesses critical limitations, such as off-target effects, immunogenicity issues, ethical considerations, regulatory hurdles, and the need for efficient delivery methods. To overcome these obstacles, efforts have focused on creating more accurate and reliable Cas9 nucleases and exploring innovative delivery methods. Recently, functional biomaterials and synthetic carriers have shown great potential as effective delivery vehicles for CRISPR/Cas9 components. In this review, we attempt to provide a comprehensive survey of the existing CRISPR-Cas9 delivery strategies, including viral delivery, biomaterials-based delivery, synthetic carriers, and physical delivery techniques. We underscore the urgent need for effective delivery systems to fully unlock the power of CRISPR/Cas9 technology and realize a seamless transition from benchtop research to clinical applications.

Integrating AI with Chemical Engineering for Rapid Biomaterial Development in Health Applications

This research presents an innovative approach to healthcare biomaterial development by integrating AI with chemical engineering methodologies. This study combines AI’s predictive power with the precision of chemical engineering to accelerate the discovery and optimization of biomaterials tailored for health applications while focusing on biocompatibility, adaptability, and stringent biomedical functionality. By using machine learning frameworks and advanced simulation software, the project developed predictive models that streamline biomaterial synthesis. This reduced experimental cycles by up to 40% and shortened development timelines by over 30%. Through neural networks and hybrid AI models, material properties such as degradation rate, strength, and biocompatibility can be accurately predicted, which minimizes in vivo testing and accelerates the transition from laboratory research to clinical trials. Protocols optimized through AI-driven insights enhance biomaterial production’s reproducibility and scalability while reducing material costs by 20%, which supports economically viable synthesis methods for large-scale applications. This research contributes a customizable AI framework for health-focused biomaterial solutions and impacts areas such as regenerative medicine, drug delivery, and implantable devices. Future directions include integrating real-time clinical feedback into AI models to improve safety and adaptability, thus advancing sustainable and personalized approaches to biomaterial development. This interdisciplinary framework demonstrates how AI-enhanced chemical engineering workflows can yield adaptive biomaterials suited to specific biomedical needs and offers unprecedented precision in material selection. The model’s high predictive accuracy in biocompatibility screening, achieving over 90%, enables focused experimental validation while reducing the need to rely on animal studies, which fosters ethical research practices. The sustainability impact of this project is significant, as AI-driven optimization reduces resource consumption and waste and aligns with eco-friendly biomaterial development practices. Ultimately, this research paves the way for rapid, efficient, and sustainable innovations in healthcare materials and sets a foundation for future advancements in personalized medical applications.

Nondestructively Assemble Cell Membrane-Coated Nanoparticles by Host-Guest Interactions for Efficient Capture of Bioactive Compounds.

Cell membrane-coated nanoparticles (CNPs) have emerged as an attractive nanomedical tool. The basic premise is that the surface properties of natural cells can be integrated with the physical and chemical properties of nanoparticles by coating them with cell membranes. However, the degree of preservation of membrane proteins on nanoparticles, a key indicator related to the biomedical function of these biomimetic systems, is largely affected by the coating process. Herein, we report a supramolecular cell membrane conjugation strategy mediated by host-guest interactions to assemble CNPs without compromising protein activities. β-cyclodextrin (β-CD) was rapidly and stably inserted into the cell membrane by a lipid anchor without affecting the function of membrane proteins, thus attaching host-guest sites to the membrane surface. By harnessing the excellent binding affinity between β-CD attached to the membrane surface and adamantane, a supramolecular cell membrane-magnetic nanoparticle conjugate (CDM@AMNPs) was synthesized. Thanks to the nondestructive assembly of this strategy, CDM@AMNPs were endowed with a greater number of active binding sites, exhibiting efficient adsorption performance. This supramolecular conjugation strategy mediated by nonreceptor site-based host-guest interactions proposes a scalable and cell-friendly strategy for the development of highly efficient CNPs.

Osteogenic Potential and Long-Term Enzymatic Biodegradation of PHB-based Scaffolds with Composite Magnetic Nanofillers in a Magnetic Field.

Millions of people worldwide suffer from musculoskeletal damage, thus using the largest proportion of rehabilitation services. The limited self-regenerative capacity of bone and cartilage tissues necessitates the development of functional biomaterials. Magnetoactive materials are a promising solution due to clinical safety and deep tissue penetration of magnetic fields (MFs) without attenuation and tissue heating. Herein, electrospun microfibrous scaffolds were developed based on piezoelectric poly(3-hydroxybutyrate) (PHB) and composite magnetic nanofillers [magnetite with graphene oxide (GO) or reduced GO]. The scaffolds' morphology, structure, mechanical properties, surface potential, and piezoelectric response were systematically investigated. Furthermore, a complex mechanism of enzymatic biodegradation of these scaffolds is proposed that involves (i) a release of polymer crystallites, (ii) crystallization of the amorphous phase, and (iii) dissolution of the amorphous phase. Incorporation of Fe3O4, Fe3O4-GO, or Fe3O4-rGO accelerated the biodegradation of PHB scaffolds owing to pores on the surface of composite fibers and the enlarged content of polymer amorphous phase in the composite scaffolds. Six-month biodegradation caused a reduction in surface potential (1.5-fold) and in a vertical piezoresponse (3.5-fold) of the Fe3O4-GO scaffold because of a decrease in the PHB β-phase content. In vitro assays in the absence of an MF showed a significantly more pronounced mesenchymal stem cell proliferation on composite magnetic scaffolds compared to the neat scaffold, whereas in an MF (68 mT, 0.67 Hz), cell proliferation was not statistically significantly different when all the studied scaffolds were compared. The PHB/Fe3O4-GO scaffold was implanted into femur bone defects in rats, resulting in successful bone repair after nonperiodic magnetic stimulation (200 mT, 0.04 Hz) owing to a synergetic influence of increased surface roughness, the presence of hydrophilic groups near the surface, and magnetoelectric and magnetomechanical effects of the material.

Immunomodulatory Biomaterials: Tailoring Surface Properties to Mitigate Foreign Body Reaction and Enhance Tissue Regeneration.

The immune cells have demonstrated the ability to promote tissue repair by removing debris, breaking down the extracellular matrix, and regulating cytokine secretion profile. If the behavior of immune cells is not well directed, chronic inflammation and foreign body reaction (FBR) will lead to scar formation and loss of biomaterial functionality. The immunologic response toward tissue repair or chronic inflammation after injury and implantation can be modulated by manipulating the surface properties of biomaterials. Tailoring surface properties of biomaterials enables the regulation of immune cell fate such as adhesion, proliferation, recruitment, polarization, and cytokine secretion profile. This review begins with an overview of the role of immune cells in tissue healing and their interactions with biomaterials. It then discusses how the surface properties of biomaterials influence immune cell behavior. The core focus is reviewing surface modification methods to create innovative materials that reduce foreign body reactions and enhance tissue repair and regeneration by modulating immune cell activities. The review concludes with insights into future advancements in surface modification techniques and the associated challenges.

Mechanistic understanding of enhancing bioactivity via bio-ionic liquid functionalization of biomaterials

The selection of biomaterials is a pivotal criterion for designing tissue engineering scaffolds, crucial for diverse biomedical applications. While natural biomaterials offer inherent bioactivity and biocompatibility, fine-tuning their properties for specific applications poses challenges. Conversely, synthetic biomaterials, while highly customizable, are often bio-inert. Functionalizing materials with bioactive molecules can improve cell-material interactions. Prevailing approaches utilizing RGD peptides or natural/synthetic composites have drawbacks including cost and immunogenicity. Bio-ionic liquids (BILs), a class of biocompatible ionic liquids derived from natural or synthetic biomolecules, offer a potential alternative. Herein, we present the biofunctionalization of a bio-inert polyethylene glycol diacrylate (PEGDA) with an acrylated choline-based BIL (“BioPEG”) as a method for enhancing the bioactivity of biomaterials. Cell studies using mouse myoblast C2C12 and human mesenchymal stem cells (hMSCs) revealed the excellence of BioPEG hydrogels in promoting cell attachment, growth, proliferation, and differentiation. Computational molecular dynamics (MD) simulations elucidated the mechanism by which BIL facilitates cell interaction with PEGDA. 3D printability of BioPEG hydrogel was showcased using a digital light processing (DLP) bioprinter, with printed scaffolds demonstrating excellent cytocompatibility. Collectively, these findings present BIL as a versatile bioactive agent for augmenting cell adhesion to materials, thus enriching the repertoire of biomaterials for advanced tissue engineering.

All-aqueous microfluidic fabrication of calcium alginate/alkylated chitosan core-shell microparticles with time-sequential functions for promoting whole-stage wound healing

Wound healing comprises a series of complex physiological processes, including hemostasis, inflammation, cell proliferation, and tissue remodeling. Designing new functional biomaterials by biological macromolecules with tailored therapeutic effects to precisely match the unique requirements of each stage is cherished but rarely discussed. Here, we employ all-aqueous microfluidics to fabricate multifunctional core-shell microparticles aimed at promoting whole-stage wound healing. These microparticles feature a core comprising calcium alginate, cellulose nanocrystals and epidermal growth factor, surrounded by a shell made of alkylated chitosan, alginate, and ciprofloxacin (EGF + CNC@Ca-ALG/CIP@ACS core-shell microparticles, D-CSMP). Response surface methodology (RSM) with a combination of central composite rotatable design (CCRD) is used to meticulously optimize the fabrication processes, endowing the resulting D-CSMP with superior capabilities for efficiently encapsulating and controlled releasing CIP and EGF tailored to each stage aligning the healing timeline. The developed D-CSMP demonstrate notable time-sequential functionalities, including promoting blood coagulation, enhancing hemostasis, and exerting antibacterial effects. Furthermore, in a skin injury model, D-CSMP significantly expedite and enhance the chronic wound healing process. In conclusion, our core-shell microparticles with notable time-sequential functions present a versatile and robust approach for wound treatment and related biomedical applications.

Engineering Functional Particles to Modulate T Cell Responses.

T cells play a critical role in adaptive immune responses. They work with other immune cells such as B cells to protect our bodies when the first line of defense, the innate immune system, is overcome by certain infectious diseases or cancers. Studying and regulating the responses of T cells, such as activation, proliferation, and differentiation, helps us understand not only their behavior in vivo but also their translation and application in the field of immunotherapy, such as adoptive T cell therapy and immune checkpoint therapy, the situations in which T cells cannot fight cancer alone and require external engineering regulation to help them. Nano- to micrometer-sized particulate biomaterials have achieved great progress in the assistance of T cell-based immunomodulation. For example, various types of microparticles decorated with T cell recognition and activation signals to mimic native antigen-presenting cells have shown successful ex vivo expansion of primary T cells and have been approved for clinical use in adoptive T cell therapy. Functional particles can also serve as vehicles for transporting cargos including small molecule drugs, cytokines, and antibodies. Especially for cargos with limited bioavailability and high repeat-dose toxicity, systemic administration in their free form is difficult. By using particle-assisted systems, the delivery can be tailored on demand, of which targeting and controlled release are two typical examples, ultimately aiding in the regulation of T cell responses. Furthermore, when T cells become overactive and behave in ways that contradict our expectations, such as attacking our own cells or innocuous foreign molecules, this can lead to a breakdown of immune tolerance. In such cases, particles to help reprogram those overactive T cells or suppress their activity are appreciated in vivo. The urgent need to introduce immune stimulation into the treatment of cancers, infectious diseases, and autoimmune diseases has driven recent advances in the engineering of functional particulate biomaterials that regulate T cell responses. In this Account, we will first cover a brief overview of the process of T cell-based immunomodulation from principle to development. It then outlines critical points in the design of functional particle platforms, including materials, size, morphology, surface engineering, and delivery of cargos, to modulate the features of T cells, and introduces selected work from our and other research groups with a focus on three major therapeutic applications: adoptive T cell therapy, immune checkpoint therapy, and immune tolerance restoration. Current challenges and future opportunities are also discussed.

Functions of Hemp-Induced Exosomes against Periodontal Deterioration Caused by Fine Dust.

Although fine dust is linked to numerous health issues, including cardiovascular, neurological, respiratory, and cancerous diseases, research on its effects on oral health remains limited. In this study, we investigated the protective effects of mature hemp stem extract-induced exosomes (MSEIEs) on periodontal cells exposed to fine dust. Using various methods, including microRNA profiling, PCR, flow cytometry, immunocytochemistry, ELISA, and Alizarin O staining, we found that MSE treatment upregulated key microRNAs, such as hsa-miR-122-5p, hsa-miR-1301-3p, and hsa-let-7e-5p, associated with vital biological functions. MSEIEs exhibited three primary protective functions: suppressing inflammatory genes while activating anti-inflammatory ones, promoting the differentiation of periodontal ligament stem cells (PDLSCs) into osteoblasts and other cells, and regulating LL-37 and MCP-1 expression. These findings suggest that MSEIEs have potential as functional biomaterials for applications in pharmaceuticals, cosmetics, and food industries.

Light-Armed Nitric Oxide-Releasing Micromotor In Vivo.

The delivery of NO at a high spatiotemporal precision is important but still challenging for existing NO-releasing platforms due to the lack of precise motion control and limited biomedical functions. In this work, we propose an alternative strategy for developing the light-armed nitric oxide-releasing micromotor (LaNorM), in which a main light beam was employed to navigate the microparticle and stimulate NO release and an auxiliary light beam was used to cooperate with the released NO to act as a remotely controlled scalpel for cell separation. Benefiting from the advantages of fully controlled locomotion, photostimulated NO release, and microsurgery ability at the single-cell level, the proposed LaNorM could enable a series of biomedical applications in vivo, including the separation of flowing emboli, selective removal of a specific thrombus, and inhibition of thrombus growth, which may provide new insight into the precise delivery of NO and the treatment of cardiovascular diseases.

Scientific evaluation on biodegradable and biofunctional polyurethane incorporated chitosan/elastin electrospun membranes in compared with synthetic polymeric expanded polytetrafluoroethylene and polyethylene terephthalate vascular membranes

Cardiovascular disease is a life-threatening health problem. Employing vascular membranes is one of the treatment options in cardiovascular surgery to replace damaged vascular tissues. However, certain limitations associated with synthetic polymeric vascular membranes (expanded polytetrafluoroethylene (e-PTFE) and polyethylene terephthalate (PET)) such as low biodegradability and biofunctional, may lead to thrombosis, inflammatory response, and tissue necrosis. Polyurethane (PU) is commonly applied in vascular engineering, owing to its good biocompatibility and biodegradability. Incorporating chitosan (CS) and elastin (EL) into the PU matrix, specifically in the design of electrospun nanofibrous membrane, is expected to enhance the biological properties of PU. These improvements are crucial to overcome the limitations of synthetic vascular membranes. Previously, there was no scientific comparison between synthetic vascular membranes and the improved design of PU-based nanofibrous membranes. This scientific comparison is pivotal to allow more research exploration on biodegradable and biofunctional materials towards the fabrication of vascular membranes. Herein, the physicochemical, biodegradability, and biofunctional capability of the electrospun PU-based electrospun membranes and two synthetic membranes were compared. Both PU and PU/CS/ES electrospun membranes were annotated with N–H, C–H, and C–N groups with the appearance of elongated fibers. The –CF2 group was presented in the e-PTFE membranes with the view of expanded fibril structure and interconnecting nodes. Whereas for the PET membranes, C=C, C=O, and C–O groups were noticed with the appearance of homogeneous knitted morphology. The PU/CS/ES membranes were found to be more hydrophilic than the PU and the synthetic membranes. The incorporation of CS and EL in the matrix of electrospun PU has improved the PU's biodegradability up to 23.86 ± 5.86 % at 60 days of incubation with the view of swollen and degraded elongated fibers, following the degradation test. Both synthetic polymeric membranes were declared non-biodegradable with less than 7 % degradation at similar incubation timepoint. The PU/CS/ES membranes were also found biofunctional with the most 82 ± 0.49 % of cell viability, protruded cell filopodia, and 44.24 ± 13.99 % scratch cell closure within 24 h of incubation. The incorporation of CS and EL into the PU matrix has improved the biodegradability and biofunctionality compared to the pure PU and synthetic polymeric membranes. Thus, highlight the suitability of PU/CS/ES electrospun membranes to be applied in cardiovascular tissue engineering.

Electrospun Silk-ICG Composite Fibers and the Application toward Hemorrhage Control.

In trauma and surgery, efficient hemorrhage control is crucial to avert fatal blood loss and increase the likelihood of survival. There is a significant demand for novel biomaterials capable of promptly and effectively managing bleeding. This study aimed to develop flexible biocomposite fibrous scaffolds with an electrospinning technique using silk fibroin (SF) and indocyanine green (ICG). The FDA-approved ICG dye has unique photothermal properties. The water permeability, degradability, and biocompatibility of Bombyx mori cocoon-derived SF make it promising for biomedical applications. While as-spun SF-ICG fibers were dissolvable in water, ethanol vapor treatment (EVT) effectively induced secondary structural changes to promote β-sheet formation. This resulted in significantly improved aqueous stability and mechanical strength of the fibers, thereby increasing their fluid uptake capability. The enhanced SF-ICG interaction effectively prevented ICG leaching from the composite fibers, enabling them to generate heat under NIR irradiation due to ICG's photothermal properties. Our results showed that an SF-ICG 0.4% fibrous matrix can uptake 473% water. When water was replaced by bovine blood, a 25 s NIR irradiation induced complete blood coagulation. However, pure silk did not have the same effect. Additionally, NIR irradiation of the SF-ICG fibers successfully stopped the flow of blood in an in vitro model that mimicked a damaged blood vessel. This novel breakthrough offers a biotextile platform poised to enhance patient outcomes across various medical scenarios, representing a significant milestone in functional biomaterials.