Biomedical Applications Research Articles

Design approaches for 3D cell culture and 3D bioprinting platforms.

The natural habitat of most cells consists of complex and disordered 3D microenvironments with spatiotemporally dynamic material properties. However, prevalent methods of in vitro culture study cells under poorly biomimetic 2D confinement or homogeneous conditions that often neglect critical topographical cues and mechanical stimuli. It has also become increasingly apparent that cells in a 3D conformation exhibit dramatically altered morphological and phenotypical states. In response, efforts toward designing biomaterial platforms for 3D cell culture have taken centerstage over the past few decades. Herein, we present a broad overview of biomaterials for 3D cell culture and 3D bioprinting, spanning both monolithic and granular systems. We first critically evaluate conventional monolithic hydrogel networks, with an emphasis on specific experimental requirements. Building on this, we document the recent emergence of microgel-based 3D growth media as a promising biomaterial platform enabling interrogation of cells within porous and granular scaffolds. We also explore how jammed microgel systems have been leveraged to spatially design and manipulate cellular structures using 3D bioprinting. The advent of these techniques heralds an unprecedented ability to experimentally model complex physiological niches, with important implications for tissue bioengineering and biomedical applications.

Assessing the functional impact of protein binding site definition.

Many biomedical applications, such as classification of binding specificities or bioengineering, depend on the accurate definition of protein binding interfaces. Depending on the choice of method used, substantially different sets of residues can be classified as belonging to the interface of a protein. A typical approach used to verify these definitions is to mutate residues and measure the impact of these changes on binding. Besides the lack of exhaustive data, this approach also suffers from the fundamental problem that a mutation introduces an unknown amount of alteration into an interface, which potentially alters the binding characteristics of the interface. In this study we explore the impact of alternative binding site definitions on the ability of a protein to recognize its cognate ligand using a pharmacophore approach, which does not affect the interface. The study also shows that methods for protein binding interface predictions should perform above approximately F-score = 0.7 accuracy level to capture the biological function of a protein.

Synthesis of novel bioadhesive hydrogels via facile Thiol-Ene click chemistry for wound healing applications

Development of outstanding, cost-effective and elastic hydrogels as bioadhesive using Thiol-Ene click chemistry was verified. The visible light photocrosslinkable hydrogels composed of methacrylated chitosan/2,2′-(Ethylenedioxy) diethanethiol formed in presence of eosin-Y photoinitiator. Such hydrogels hold great promise for wound healing applications due to their tunable properties. Main components of hydrogels were extensively characterized using spectroscopic techniques for chemical analysis, thermal analysis, and topologic nanostructure. Various optimization conditions for best gelation time were investigated. Mechanical properties of tensile strength and elongation at break (%) were verified for best wound healing applications. Optimum hydrogel was subjected to for cytotoxicity and microbial suppression evaluation and in-vivo wound healing test for efficient wound healing evaluations. Our results demonstrate the potential use of injectable hydrogels as valuable bioadhesives in bioengineering and biomedical applications, particularly in wound closure and patches.

Laser-Induced Graphene-Based Fabry-Pérot Cavity Label-Free Immunosensors for the Quantification of Cortisol

There is a strong and growing need to monitor stress biomarkers in human beings and animals for real-time wellness assessment, which is a key indicator of health. Toward this, we report an optical fiber immunosensor based on laser-induced graphene (LIG) for the potential quantification and monitoring of cortisol hormone. The developed sensors were created using the Fabry-Pérot cavity principle. The cavities were filled with polyimide (PI) and, in some cases, PI mixed with gold nanoparticles. The interferometers were tested for temperature and refractive index, and an increase of two times in the sensitivity to the refractive index was observed due to the addition of the gold nanoparticles. In addition, the PI cavity was partially transformed into LIG using a CO2 20 kHz pulsed laser. The resulting LIG morphology was quite porous and presented a leafy texture. The presence of LIG creates a second cavity within the interferometer, and as a consequence, the spectral response of the interferometers resembled the Vernier effect. The refractive index behavior of the LIG-modified interferometers shows improvements in sensitivity up to 15.3 times due to the creation of the LIG cavity. The interferometers were then functionalized with anti-cortisol to promote an affinity for cortisol. Excellent sensitivities of up to -34.7±0.7 nm/log(ng/mL) were achieved within few ng/mL concentration ranges (within the 0.5 to 3 ng/mL). The results obtained show an increase of up to 50 times in sensitivity when compared with other cortisol sensors. The achieved limit of detection was 0.1 ng/mL for the proposed sensors. The sensors’ responses were also shown to be immune to the interference from substances such as glucose, sucrose, fructose, and ascorbic acid. This study lays the foundation for new cortisol biosensors demonstrating a great potential for detection in a simple and highly sensitive way, opening its path for relevant biomedical and environmental monitoring applications in real samples. As a future outline, selectivity studies employing the detection of cortisol in the presence of interfering agents, both using synthetic and real samples, will be accomplished in order to fully investigate the potential of these sensing tools in real-life scenarios.

Lipid-based Nanocarrier Drug Delivery Approach for Biomedical Application

Abstract: The development of nanosized drug-carrier systems has been investigated over the past few decades using various techniques. The two main categories of these systems are polymeric nanoparticles and lipid nanoparticles (LNPs). The toxicological risk associated with lipid nanoparticles is significantly lower than the danger associated with polymeric nanoparticles due to the materials' natural and biological origins. Lipid-based drug delivery systems like Nanostructured lipid carriers (NLCs) and Solid Lipid Nanoparticles (SLNs) are well-established nanotechnology systems for preparing all major pharmaceuticals. These delivery systems can be scaled up with easy manufacturing procedures and are biocompatible. NLCs are the second generation of lipid-based nanocarriers (SLNs), formed by combining solid and liquid biocompatible lipids to form an unstructured matrix that provides high entrapment efficiency of active constituents. LNPs can promote the distribution of active pharmaceutical ingredients to the target site. Increasing the active drug concentration to target organ LNPs enhances the therapeutic effectiveness and reduces the side effects. This paper reviews the structure of SLNs and different NLCs, various steps involved in manufacturing lipid nanoparticles, excipients used in the formulation, and applications for targeted drug delivery.

Targeting-specific Nanoprobes in the Second Near-infrared Window for Biomedical Applications

Targeting-specific Nanoprobes in the Second Near-infrared Window for Biomedical Applications

Recent Advances in Biomedical Nanotechnology Related to Natural Products.

Natural product processing via nanotechnology has opened the door to innovative and significant applications in medical fields. On one hand, plants-derived bioactive ingredients such as phenols, pentacyclic triterpenes and flavonoids exhibit significant pharmacological activities, on another hand, most of them are hydrophobic in nature, posing challenges to their use. To overcome this issue, nanoencapsulation technology is employed to encapsulate these lipophilic compounds and enhance their bioavailability. In this regard, various nano-sized vehicles, including degradable functional polymer organic compounds, mesoporous silicon or carbon materials, offer superior stability and retention for bioactive ingredients against decomposition and loss during delivery as well as sustained release. On the other hand, some naturally occurring polymers, lipids and even microorganisms, which constitute a significant portion of Earth's biomass, show promising potential for biomedical applications as well. Through nano-processing, these natural products can be developed into nano-delivery systems with desirable characteristics for encapsulation a wide range of bioactive components and therapeutic agents, facilitating in vivo drug transport. Beyond the presentation of the most recent nanoencapsulation and nano-processing advancements with formulations mainly based on natural products, this review emphasizes the importance of their physicochemical properties at the nanoscale and their potential in disease therapy.

Research Progress of Chitosan-based Multifunctional Nanoparticles in Cancer Targeted Therapy.

Conventional tumor therapeutic modalities, such as radiotherapy, chemotherapy, and surgery, involve low tumor inhibition efficiency, non-targeted drug delivery, and side effects. The development of novel and practical nano-drug delivery systems (DDSs) for targeted tumor therapy has become particularly important. Among various bioactive nanoparticles, chitosan is considered a suitable candidate for drug delivery due to its non-toxicity, good biocompatibility, and biodegradability. The amino and hydroxyl groups of chitosan endow it with the diverse function of chemical modification, thereby improving its physical and biological properties to meet the requirements of advanced biomedical applications. Therefore, it is necessary to review the property and applications of chitosan-based materials in biomedicine. In this review, the characteristics of chitosan related to its applications are first introduced, and then the preparation and modification of chitosan-based nanoparticles, including the function tailoring of chitosan-modified nanoparticles, are demonstrated and discussed. Finally, the opportunities and challenges of chitosan-based nanomaterials in this emerging field are proposed from the perspective of the rational and systematic design for the biomedicine field.

Barium titanate–silicon elastomer based body coupled antenna for wearable microwave head imaging applications

This paper presents a flexible monopole antenna fed by a coplanar waveguide (CPW) feeding line with a barium titanate (BaTiO3) silicon-elastomer impedance matching layer for microwave head imaging applications. The operating frequency bandwidth of the proposed antenna is 614 MHz which is from 0.475 GHz to 1.089 GHz. In biomedical microwave sensing and imaging applications, the major challenge is the high power loss due to reflection between the BaTiO3 and the antenna due to impedance mismatch. Therefore, the proposed BaTiO3 silicon-elastomer composite is designed to have dielectric property of 20 which acts as an impedance matching layer for the monopole antenna. The proposed antenna has dimensions of 70×30×6 mm. The flexibility of the antenna is provided by the use of the silicon elastomer. It has been shown that the power radiated into an artificial head phantom improved by almost 160% as compared to antenna without impedance matching layer. Moreover, the SAR level is 0.0286 W/kg when 1 mW of power is transmitted, which is well below the limit set by the regulation. This makes the antenna suitable for wearable biomedical applications due to its wideband characteristic and improved power penetration into human head.

Study on pH dependent ON/OFF fluorescent switching behaviour of hydrothermally synthesised vanadium disulphide quantum dots (VS2-QDs)

It is fascinating to design and develop an inorganic quantum dot (QDs) which exhibit luminescence features with ion concentration, temperature, and pH sensitivity dependence. Vanadium disulphide (VS2) belongs to the family of transition metal dichalcogenides (TMDs), and is extensively studied owing to its layered characteristics features in sensing and filtrations technology, however, its fluorescence features have not been well studied so far. The current work describes a widely adopted eco-friendly hydrothermal approach for the synthesis of VS2-QDs. The average size of particles was determined to be ∼10 nm by transmission electron microscopy (TEM) and Zetasizer analysis. The synthetic approach adopted here facilitates in situ functionalization of QDs, which results in their high stability in aqueous medium and enhanced sensitivity towards their surroundings. As most of the QDs show the sensitivity towards pH, a thorough investigation of VS2 QDs for their pH dependent photoluminescence has been carried out. The VS2-QDs were discovered to exhibit a remarkable luminescence intensity that was found to be about 11 times higher in basic conditions (pH ∼ 13, QY = ∼4.80%) as compared to that in acidic conditions (pH ∼ 1, QY = ∼1.10%). The root cause of this ON/OFF florescence flipping may be related to the functional groups (such as −SO42−, −NH2, OH−, etc.) attached over the surface of QDs, acid etching, and protonation–deprotonation process. This paper highlights the pH dependent switching behaviour of VS2-QDs that could offer valuable information for designing a futuristic pH-based device for biomedical applications.

The effects of 3D printing parameters, structural design and post-processing on the mechanical properties and corrosion resistance of SLMed ZK60 porous scaffolds

High-quality porous Mg alloy scaffolds show promise in repairing large segmental bone defects. In this study, the authors prepared porous ZK60 scaffolds using the selective laser melting (SLM) method with three different model structures: Gyroid (G), Diamond (D), and Dodecahedral (Do). The researchers investigated the structural refinement, mechanical properties, and corrosive properties of SLM-ed ZK60 by adjusting the 3D printing parameters, specifically the scanning speed and laser power. The results show that, with optimized process parameters of a scanning speed of 400mm/s and a laser power of 110W, the relative density of the prepared samples was higher than 97%. After post-processing with electrolytic polishing, the G model scaffolds showed a smooth structural transition and the largest surface area compared to the other two models. The electrolytic polishing treatment also improved the structural refinement of the 70% designed porosity, with an error of only 4.3%. Additionally, the Do model scaffolds exhibited the best mechanical properties, with a yield strength of up to 24MPa and an elastic modulus of up to 425MPa. Furthermore, after coating treatment, the corrosion rate decreased from 5.67mm/year to 1.34mm/year after 48hours. These results demonstrate the potential of SLM-ed porous scaffolds for biomedical applications.

Formulation analysis and follow-up study of multi-turn configuration for performance enhancement of MEMS piezoresistive pressure sensor utilized for low-pressure measurement applications

Purpose The purpose of this research is to study the performance of piezoresistive pressure sensors using polysilicon as the piezoresistive material, which is typically used to measure pressure in high-temperature environments. Design/methodology/approach The performance of this sensor is enhanced by studying the influence of multi-turn configuration at which the piezoresistors are arranged. Different configurations are studied and compared by laying down their analytical solution. Findings The validation of analytical results is accomplished through finite element analysis using the software COMSOL Multiphysics. The best configuration, which uses a partial triple-turn configuration, was able to achieve a sensitivity of 116.00 mV/V/MPa over a simulated pressure range of 0 to 500 KPa. Originality/value The literature shows the study of single-turn and double-turn meander-shaped configuration of micro-electromechanical systems piezoresistive pressure sensor but multi-turn meander-shaped configuration using a square silicon diaphragm has not been reported. Its study has reflected promising results than its counterparts based on key performance parameters such as sensitivity and linearity and are more effective to be used for automotive, aviation, biomedical and consumer electronics applications.

Thermal Transport Phenomena in PEGDA-Based Nanocomposite Hydrogels Using Atomistic and Experimental Techniques.

Poly(ethylene glycol) diacrylate (PEGDA) hydrogel is a very peculiar, fascinating material with good chemical stability and biocompatibility. However, the poor thermal transport phenomenon in PEGDA, limits its performance in cartilage replacement and developing therapies for treating burns. In this article, a combined experimental and atomistic approach was adopted to investigate the thermal transport phenomena in PEGDA hydrogel with different weight concentrations of boron nitride nanoplatelets as a function of water content. The incorporation of boron nitride nanofillers helps in enhancing the thermal conductivity of PEGDA hydrogels, and the reinforcement effect was more dominating at lower water content. Experimental investigation was complemented with molecular dynamics-based studies to capture the effect of defective (bicrystalline) boron nitride nanosheets on the interfacial thermal conductance in PEGDA hydrogels. It can be concluded from the simulations that defective nanosheets are superior reinforcement for enhancing the thermal transport in PEGDA hydrogels, and this is independent of the water content. These biocompatible boron nitride nanoparticle (BNNP)-incorporated PEGDA hydrogels with enhanced thermal conductivity are promising materials in addressing locally overheating tissues such as cartilage replacement. They may have comprehensive utility for biomedical applications such as tissue engineering, drug delivery, biosensors, and burn therapy.

Photostability and photodynamic antimicrobial profile of dye extracts from four (4) plants: prospects for eco-friendly low-cost food disinfection and topical biomedical applications.

In this study, photostability and photodynamic antimicrobial performance of dye extracts from Hibiscus sabdariffa (HS) calyces, Sorghum bicolor (SB) leaf sheaths, Lawsonia inermis (LI) leaves and Curcuma longa (CL) roots were investigated in Acetate-HCl (AH) Buffer (pH 4.6), Tris Base-HCl (TBH) Buffer (pH 8.6), distilled water (dH2O), and Phosphate Buffer Saline (PBS, pH 7.2) using Bacillus subtilis as model for gram positive bacteria, Escherichia coli as model for gram negative bacteria, phage MS2 as model for non-envelope viruses and phage phi6 as model for envelope viruses including SARS CoV-2 which is the causative agent of COVID-19. Our results showed that the photostability of the dye extracts is in the decreasing order of LI > CL > SB > HS. The dye extract-HS is photostable in dH2O but bleaches in buffers-AH, TBH and PBS. The rate of bleaching is higher in AH compared to in TBH and PBS. The bleaching and buffers affected the photodynamic and non-photodynamic antimicrobial activity of the dye extracts. The photodynamic antibacterial activity of the dye extracts is in the decreasing order of CL > HS > LI > SB while the non-photodynamic antibacterial activity is in the decreasing order of LI > CL > HS > SB. The non-photodynamic antiviral activity pattern observed is the same as that of non-photodynamic antibacterial activity observed. However, the photodynamic antiviral activity of the dye extracts is in the decreasing order of CL > LI > HS > SB. Given their performance, the dye extracts maybe mostly suitable for environmental applications including fresh produce and food disinfection, sanitation of hands and contact surfaces where water can serve as diluent for the extracts and the microenvironment is free of salts.

Effect of Peptide-Polymer Host-Guest Electrostatic Interactions on Self-Assembling Peptide Hydrogels Structural and Mechanical Properties and Polymer Diffusivity.

Peptide-based supramolecular hydrogels are an attractive class of soft materials for biomedical applications when biocompatibility is a key requirement as they exploit the physical self-assembly of short self-assembling peptides avoiding the need for chemical cross-linking. Based on the knowledge developed through our previous work, we designed two novel peptides, E(FKFE)2 and K(FEFK)2, that form transparent hydrogels at pH 7. We characterized the phase behavior of these peptides and showed the clear link that exists between the charge carried by the peptides and the physical state of the samples. We subsequently demonstrate the cytocompatibility of the hydrogel and its suitability for 3D cell culture using 3T3 fibroblasts and human mesenchymal stem cells. We then loaded the hydrogels with two polymers, poly-l-lysine and dextran. When polymer and peptide fibers carry opposite charges, the size of the elemental fibril formed decreases, while the overall level of fiber aggregation and fiber bundle formation increases. This overall network topology change, and increase in cross-link stability and density, leads to an overall increase in the hydrogel mechanical properties and stability, i.e., resistance to swelling when placed in excess media. Finally, we investigate the diffusion of the polymers out of the hydrogels and show how electrostatic interactions can be used to control the release of large molecules. The work clearly shows how polymers can be used to tailor the properties of peptide hydrogels through guided intermolecular interactions and demonstrates the potential of these new soft hydrogels for use in the biomedical field in particular for delivery or large molecular payloads and cells as well as scaffolds for 3D cell culture.

Surface modification of biomedical titanium alloy for hard tissue repair and reconstruction

In biomedical applications, various materials are used, including metals and their alloys, polymers and ceramics. Among them, titanium (Ti) and titanium alloys are widely utilised in implant materials due to their excellent corrosion resistance and high mechanical strength. However, despite these advantages, titanium is biologically inert and does not integrate well with human cells. Therefore, surface modification of titanium implants plays a crucial role in determining the rate of osseointegration and the overall success of the implants. The primary objective of this review is to provide a detailed introduction to surface modification technologies for titanium alloy implants. The aim is to enhance the biological activity, wear resistance, corrosion resistance and antibacterial properties and reduce the release of ions from the implants. By modifying the surface of titanium implants, it is possible to create a more favourable environment for cell adhesion, proliferation and differentiation. Various techniques, such as physical methods (e.g. sandblasting, acid etching) and chemical methods (e.g. surface oxidation, plasma treatment) can be employed to modify the surface properties of titanium implants. These surface modification techniques can enhance the interaction between the implant and the surrounding biological environment, promoting osseointegration and improving the long-term stability of the implant. Additionally, surface modifications can help reduce the release of potentially harmful ions from the implant, minimise bacterial adhesion and improve the overall biocompatibility of the implant. In conclusion, surface modification of titanium alloy implants is a critical aspect of biomedical engineering. By improving the biocompatibility of titanium implants, these modifications contribute to the success and longevity of implants used in hard tissue repair and reconstruction.

A Review Exploring the Wound-Healing Activity of Self-Healing Hydrogels: Fabrication, Characterization, Mechanism, and Biomedical Applications

AbstractThe natural physiological response to skin injury is wound healing. However, to restore skin continuity, wound healing is a complicated process that involves the collaboration of a variety of cell types and other mediators. This process ultimately results in tissue regeneration and the restoration of skin barrier function. Hydrogels are appealing dosage forms for biomedical regenerative medicine since they are composed of 3D networks with high water content and flexible rheological features. Hydrogels that can self-heal are particularly interesting for wound treatment because they can autonomously restore their original functionalities and repair structural damage. Recently, the use of self-healing hydrogels as biomedical materials has attracted increased interest. In this review, the self-healing systems used in tissue regeneration, especially wound healing, will be explored. A focus on the fabrication methods, characterization tests, and mechanism of self-healing will be introduced, along with the biomedical applications of self-healing hydrogels loaded with conventional and therapeutic biomaterials. In addition, the differences between hydrogels and self-healing hydrogels will be discussed. Graphical Abstract

Cellular Impact and Biodegradability of S‐ and N‐Doped Graphene Quantum Dots on Human Monocytes and Macrophages

AbstractGraphene quantum dots (GQDs), small graphene domains with lateral dimensions lower than 10 nm, are increasingly used in electronics, composites, and biomedicine. Chemical doping of GQDs allows tuning their optical properties. Immune cells are among the first cells exposed to nanomaterials entering a living body, rapidly triggering a downstream immune response. However, the assessment of the impact of chemically‐doped GQDs on the immune system remains rather limited if not absent. In this context, the effects and the biodegradability of sulfur‐doped and nitrogen‐doped GQDs (S‐GQDs and N‐GQDs) on human monocytes and macrophages are evaluated. The metabolic activity, membrane integrity, apoptosis, and intracellular reactive oxygen species (ROS) generation are studied. In parallel, the degradation of GQDs using human myeloperoxidase and a peroxynitrite‐mediated system is investigated in test tube. Their degradation in macrophages is also pursued. High‐resolution transmission electron microscopy (HRTEM), fluorescence spectroscopy, Raman, and flow cytometry are used to confirm the degradation. Overall, both GQDs exert little activation on monocytes and macrophages although they decrease the metabolic viability in a dose‐dependent manner. The loss of native GQD structure and crystal lattice provide evidence of their biodegradability. Both the safety and biodegradability of S‐GQDs and N‐GQDs ensure their potential in biomedical applications.

Unveiling the versatility of gelatin methacryloyl hydrogels: a comprehensive journey into biomedical applications.

Gelatin methacryloyl (GelMA) hydrogels have gained significant recognition as versatile biomaterials in the biomedical domain. GelMA hydrogels emulate vital characteristics of the innate extracellular matrix (ECM) by integrating cell-adhering and matrix metalloproteinase-responsive peptide motifs. These features enable cellular proliferation and spreading within GelMA-based hydrogel scaffolds. Moreover, GelMA displays flexibility in processing, as it experiences crosslinking when exposed to light irradiation, supporting the development of hydrogels with adjustable mechanical characteristics. The drug delivery landscape has been reshaped by GelMA hydrogels, offering a favorable platform for the controlled and sustained release of therapeutic actives. The tunable physicochemical characteristics of GelMA enable precise modulation of the kinetics of drug release, ensuring optimal therapeutic effectiveness. In tissue engineering, GelMA hydrogels perform an essential role in the design of the scaffold, providing a biomimetic environment conducive to cell adhesion, proliferation, and differentiation. Incorporating GelMA in three-dimensional printing further improves its applicability in drug delivery and developing complicated tissue constructs with spatial precision. Wound healing applications showcase GelMA hydrogels as bioactive dressings, fostering a conducive microenvironment for tissue regeneration. The inherent biocompatibility and tunable mechanical characteristics of GelMA provide its efficiency in the closure of wounds and tissue repair.
GelMA hydrogels stand at the forefront of biomedical innovation, offering a versatile platform for addressing diverse challenges in drug delivery, tissue engineering, and wound healing. This review provides a comprehensive overview, fostering an in-depth understanding of GelMA hydrogel's potential impact on progressing biomedical sciences.&#xD.

Unlocking the Potential of CO2 Capture: A Synergistic Hybridization Strategy for Polymeric Hydrogels with Tunable Physicochemical Properties.

Unlocking CO2 capture potential remains a complex and challenging endeavor. Here, a blueprint is crafted for optimizing materials through CO2 capture and developing a synergistic hybridization strategy that involves synthesizing CO2-responsive hydrogels by integrating polymeric networks interpenetrated with polyethyleneimine (PEI) chains and inorganic CaCl2. Diverging from conventional CO2 absorbents, which typically serve a singular function in CO2 capture, these hybrid PEAC hydrogels additionally harness its presence to tune their optical and mechanical properties once interacting with CO2. Such synergistic functions entail two significant steps: (i) rapid CO2-fixing through PEI chains to generate abundant carbamic acid and carbamate species and (ii) mineralization via CaCl2 to induce the formation of CaCO3 micro-crystals within the hydrogel matrix. Due to the reversible bonding, the PEAC hydrogels enable the decoupling of CO2 through an acid fumigation treatment or a heating process, achieving dynamic CO2 capture-release cycles up to 8 times. Furthermore, the polyethyleneimine-acrylamide-calcium chloride (PEAC) hydrogel exhibits varying antibacterial attributes and high interfacial adhesive strength, which can be modulated by fine-tuning the compositions of PEI and CaCl2. This versatility underscores the promising potential of PEAC hydrogels, which not only unlocks CO2 capture capabilities but also offers opportunities in diverse biological and biomedical applications.