Wound-dressing Materials Research Articles

In-vitro and in-vivo studies of Tridax procumbens leaf extract incorporated bilayer polycaprolactone/polyvinyl alcohol-chitosan electrospun nanofiber for wound dressing application.

This study was an attempt to fabricate an antibacterial wound dressing, which was a bilayered polycaprolactone / polyvinyl alcohol-chitosan (PCL/PVA-CS) nanofibrous membrane. Entrapping ethanolic leaf extract of Tridax procumbens L. (PCL/PVA-CS/Tp). The membrane was prepared using the electrospinning technique to obtain beadless uniform nanofibers. The extract was then infused into the membrane by spraying and exposing to high temperature. in vitro antibacterial activity and cell viability of the membranes were performed. An optimized concentration of 800μg. mL-1 of Tp extract in PCL/PVA-CS/Tp evinced better antibacterial effect on E. coli than S. aureus and also showed rapid wound closure with a positive impact on the viability of L929 cell line. The tissue regeneration efficacy of PCL/PVA-CS/Tp was validated by the experiments on mice models with subcutaneous wounds created using biopsy punch and laser radiation causing burns. Furthermore, in vivo assessments illustrated that the biopsy punch wounds healed more rapidly than laser burn though healing was significant in both. The healing processes such as anti-inflammation and re-epithelialization were observed through histological study. The upregulation of proteins namely VEGF and CD31 along with a decrease in protein levels of Wnt and TGF-β indicated significant wound healing. In conclusion, the bilayered membrane infused with plant extract could be considered a potential material for wound dressing.

Development of gelatine and alginate based inks for 3D bioprinters and characterization.

Three-dimensional (3D) printing is a rapidly evolving technology. This study focuses on developing biopolymeric inks tailored for Three-dimensional (3D) printing applications, specifically to produce 3D-printed materials for wound dressing. Humic Acid (HA) was incorporated into the ink formulations due to its anti-inflammatory properties. Although alginate-gelatine-based inks are widely available, no existing systems include HA as an additional component, underscoring the originality of this work.This innovation addresses a key challenge in wound care by promoting healing while minimizing inflammatory responses. Alginate(Alg) used in this study was extracted from Cystoseira barbata, a brown algae species collected from Gideros Bay in Kastamonu, located along Turkey's western Black Sea coast. This is the first study to purify alginate from algae sourced from this regio. The extraction process was optimized. Four biopolymeric ink formulations were prepared in the study and were used to print 3D-biomaterials, which underwent characterization focusing on basic physicochemical properties. Biocompatibility was evaluated through cell viability tests (MTT assays), and Immune response analysis was evaluated through inflammatory markers; pro-inflammatory cytokines (IL-1β, TNFα), and the anti-inflammatory cytokine (IL-10). In conclusion, this study successfully purified and characterized alginate from algae collected in a previously unstudied region, Gideros Bay. A novel ink formulation, incorporating humic acid, was developed and 3D-printed for the first time. The results demonstrate that the printed materials in the study possess high potential for use as wound dressing materials, marking a significant contribution to the literature.

Evaluation of Carboxymethyl Cellulose/Gelatin Hydrogel-Based Dressing Containing Cefdinir for Wound Healing Promotion in Animal Model.

The skin serves as a critical barrier against external pathogens, and its wound healing is a complex biological process that requires careful management to ensure optimal tissue regeneration. Hydrogels, a class of hydrophilic polymers, have emerged as promising materials for wound dressings due to their biocompatibility, biodegradability, and ability to create a moist wound environment conducive to cell proliferation and migration. In this research, a hydrogel dressing containing cefdinir (Cef) was made from a combination of carboxymethyl cellulose (CMC) and gelatin (Gel) by a physical crosslinking method, and their physicochemical, mechanical, and biological properties were investigated. Results show that the addition of Cef does not cause a significant change in the morphology or the tensile strength of the wound dressing. The swelling and degradation rate of the hydrogel slightly increased in the presence of Cef. The presence of Cef enhanced antibacterial effects up to 2.5-fold against P. aeruginosa (35 mm), S. aureus (36 mm), and S. pyogenes (35 mm). The results of the cytotoxicity test showed the absence of cytotoxicity in both drug-containing and drug-free wound dressings, as well as a survival rate of over 75% in cells after 48 h. The drug-containing wound dressing accelerates the formation of the epidermis layer and the production of fibroblast cells, and as a result, accelerates the wound healing process. The percentage of wound healing on the ninth day of treatment for an untreated wound was 30%, while this percentage was 40% with a wound dressing without medicine and 60% with a wound dressing containing medicine, and on the fifteenth day of treatment, the wound treated with both wound dressings had more than 85% healing. As a result, it is possible to use CMC/Gel hydrogel polymeric wound dressing containing Cef as a wound dressing for wound healing, according to the desired physicochemical properties and biocompatibility.

Evaluative Analysis of Stimuli Responsive Nanohydrogel as Wound Dressing Material Impregnated with Zinc Oxide and Iron Oxide Nanoparticles

Evaluative Analysis of Stimuli Responsive Nanohydrogel as Wound Dressing Material Impregnated with Zinc Oxide and Iron Oxide Nanoparticles

Progress in Biomass-Based Electrospun Nanofibers in Bio-Medical Application

Traditional biomedical applications in wound dressing and tissue engineering materials frequently lack the appropriate balance of environmental friendliness, antibacterial effectiveness, and mechanical strength. A growing number of medical applications are focusing on electrospun nanofibers because of their special qualities, which include a high surface area-to-volume ratio, tailor-made mechanical strength and more eco-friendly. The goal of this review paper is to thoroughly examine the corpus of research that is currently available about electrospun, nanofibers especially made from aloe vera and pineapple leaf fibers for use in biomedical applications. This review's goals include optimizing electrospinning conditions, assessing biocompatibility, researching antibacterial activity, and its current challenge.

Design and Characterization of Stimuli Responsive Nanohydrogel as Wound Dressing Material Impregnated with Zinc Oxide and Iron Oxide Nanoparticles

Recent advances in wound care have been propelled by the integration of stimuli responsive materials and innovative technologies, enabling the development of responsive and adaptive solutions. This paper presents a Stimuli responsive Nanohydrogel as wound dressing material that leverages the unique properties of zinc oxide (ZnO) and iron oxide (Fe₂O₃) nanoparticles to enhance wound healing and provide real-time monitoring capabilities. Material is designed using a hydrogel matrix, which is embedded with tracking key wound parameters, such as pH, temperature, moisture levels, and glucose concentration. Zinc oxide(ZnO) and iron oxide (Fe₂O₃) nanoparticles provides the material with enhanced antimicrobial properties, promoting a sterile healing environment and reducing the risk of infections. Additionally, these nanoparticles support tissue regeneration and possess anti-inflammatory properties, contributing to accelerated wound healing. Stimuli-responsive nanohydrogel works as a control unit, allowing for dynamic adjustments in drug release and moisture retention to match the wound's specific needs. This responsive feedback mechanism minimizes the need for frequent dressing changes, thereby reducing patient discomfort and healthcare costs. The stimuli responsive dressing material offers a promising solution for improved clinical outcomes and patient quality of life.

Synthesis of Carboxylate-Dialdehyde Cellulose to Use as a Component in Composite Thin Films for an Antibacterial Material in Wound Dressing.

Wound infections can lead to life-threatening infection and death. Antibacterial materials from biopolymers in the form of films are a promising strategy for wound dressings. Carboxylate-dialdehyde cellulose (CDAC) is a proper candidate for use as an antibacterial material due to its biocompatibility, nontoxicity, and antibacterial property. Additionally, CDAC can be synthesized from cellulose through environmentally friendly and nontoxic methods. Thus, this study aims to synthesize CDAC from microcrystalline cellulose (MCC) PH102 and use it in composite films for an antibacterial application. The CDAC was synthesized using Fe2+/H2O2, followed by NaIO4 oxidation. The obtained CDAC was characterized in terms of carboxylate and aldehyde content as well as FTIR and XRD spectra. The CDAC was mixed with HPMC in different ratios to prepare films. To determine the optimal formulation for clindamycin HCl loading, the films were evaluated for morphology, mechanical properties, and swelling ratio. Finally, the films containing clindamycin HCl were evaluated for drug loading content, in vitro drug release, and antibacterial activity. This study found that CDAC contained 2.1 ± 0.2 carboxylate and 4.15 ± 0.2 mmol/g of aldehyde content. The FTIR spectra confirmed the successful synthesis. X-ray diffractograms indicated that CDAC was less crystalline than MCC. The film, consisting of CDAC and HPMC E50 in the ratio of 2:1 (D2H1), was identified as the most suitable for clindamycin HCl loading due to its superior appearance, mechanical strength, and swelling properties compared to other formulations. D2H1 exhibited a high drug loading capacity (91.49 ± 5.48%) and demonstrated faster drug release than the film composed only of HPMC because of the higher swelling ratio and lower mechanical strength. This formulation was effective against Staphylococcus aureus (MSSA), S. aureus (MRSA), and Pseudomonas aeruginosa. Furthermore, the D2H1 film containing clindamycin HCl showed a larger inhibition zone against these bacteria, likely due to a synergistic effect. This study found that CDAC has the potential to be applied as an antibacterial material for wound dressing.

Fabrication, Characterization and Release Profile of Aloe Vera Extracts/PVA Composite Electrospun Nanofiber

Aloe vera is a well-known remedy that carries many beneficial health effects such as painkiller, anti-inflammatory, promote skin growth and repair. The combination of bioactive natural product of aloe vera as a drug model and polyvinyl alcohol (PVA) as the base material or carrier in the electrospinning process were studied. Smooth straight and continues electrospun fibers were collected with the Field Effect Scanning Electron Microscope (FESEM) images show no formation of bead (defect signed) in the electrospun membrane when the concentration was set at 10% w/w of PVA nanofibre. The morphological structure of the electrospun membranes shows a smooth and longitudinal fiber when aloe vera is mixed with the PVA polymer with percentage ratio of aloe vera over PVA is less than 25%. The Fourier Transform Infrared Spectroscopy (FTIR) shows no reaction between PVA and aloe vera by not showing peaks other than the initial materials. The Differential Scanning Calorimetry (DSC) proves the presence of aloin indicating the presence of aloe vera in nanofiber. The release profile of the electrospun aloe vera in PVA shows a higher initial burst release at the 50% and 70% concentration levels indicating very little control of the release or none at all. These results show the potential of aloe vera – PVA electrospun nanofibers membrane as a promising material for wound dressing and topical drug delivery.

Injectable Hydrogel With Glycyrrhizic Acid and Asiaticoside-Loaded Liposomes for Wound Healing.

Open skin wounds increase the risk of infections and can compromise health. Therefore, applying medications to promote healing at the injury site is crucial. In practice, direct drug delivery is often difficult to maintain for a long time due to rapid absorption or wiping off, which reduces the efficiency of wound healing. Consequently, the development of bioactive materials with both antibacterial and wound-healing properties is highly desirable. This study synthesized liposomes loaded with glycyrrhizic acid (GA) and asiaticoside (AS) by film dispersion-ultrasonication method, which were then incorporated into a GelMA solution and cross-linked by ultraviolet light to form a bioactive composite hydrogel for wound dressings. This hydrogel is conducive to the transport of nutrients and gas exchange. Compared with GelMA hydrogel (swelling rate 69.8% ± 5.7%), the swelling rate of GelMA/Lip@GA@AS is lower, at 52.1% ± 1.0%. GelMA/Lip@GA@AS also has better compression and rheological properties, and the invitro biodegradability is not significantly different from that of the collagenase-treated group. In addition, the hydrogel polymer has a stable drug release rate, good biocompatibility, and an angiogenic promoting effect. Invitro experiments prove that, at concentrations of 0.5, 1, 2, and 3 mg/mL, GelMA/Lip@GA@AS can inhibit the growth of Staphylococcus aureus. We synthesized GelMA/Lip@GA@AS hydrogel and found it possesses advantageous mechanical properties, rheology, and biodegradability. Experimental results invitro showed that the bioactive hydrogel could efficiently release drugs, exhibit biocompatibility, and enhance angiogenesis and antimicrobial effects. These results suggest the promising application of GelMA/Lip@GA@AS hydrogel in wound-dressing materials.

Advanced alginate-based nanofiber aerogels: A synthetic matrix for high-efficiency lysozyme adsorption and controlled release

The development of materials with high lysozyme adsorption is critical for drug delivery and skin wound applications, as it enhances antibacterial properties, stability, and controlled release of therapeutic agents, thereby improving treatment efficacy and safety. Alginate-based nanofiber scaffolds, featuring high surface area and multiple adsorption sites, can efficiently absorb lysozyme and regulate its release through tunable pore channels, offering a promising approach to chronic wound management. In this study, we fabricated poly (vinyl alcohol-co-ethylene) (EVOH) nanofiber-based sodium alginate (ENSA) aerogels using a simple two-step crosslinking procedure. The resulting aerogels, with controllable porosity formed via high-pressure spraying techniques (aerogel film) and molding (aerogel sponge), were evaluated for their high-loading capacity and controllable release of lysozyme. The aerogel film exhibited a remarkable lysozyme adsorption capacity of 1965 ± 36 mg/g, while the aerogel sponge sustained lysozyme release over 14 days. Analysis of the drug-release mechanism through four kinetic models revealed two distinct processes: cation exchange and matrix diffusion. The aerogel's pore structure influenced the diffusion processes, enabling tailored drug release profiles. Additionally, the ENSA aerogels demonstrated good mechanical properties, non-cytotoxicity, and potent antibacterial activity, positioning them as promising materials for skin wound dressings.

Injectable Salecan/hyaluronic acid-based hydrogels with antibacterial, rapid self-healing, pH-responsive and controllable drug release capability for infected wound repair

Designing materials for wound dressings with superior therapeutic benefits, self-healing and injectable characteristics is important in clinical practice. Herein, a new self-healing injectable hydrogel was prepared via thermal treatment and dynamic Schiff base reaction by mixing oxidized hyaluronic acid (OHA) and hydrazided Salecan (Sal-ADH). The versatility of the wound dressing was confirmed by studying the inherent rheological properties, high swelling rate, sustained-release behavior of the drug, pH/hyaluronidase-dependent biodegradation, in vitro antimicrobial as well as in vivo wound healing performance. The presence of the antimicrobial drug polyhexamethylene biguanide (PHMB) conferred good antimicrobial properties to the Sal-ADH/OHA/PHMB (SOP) hydrogel, which could effectively prevent wound infection (the width of the inhibition circle of SOP-0.20 hydrogel was 4.97 mm, 5.93 mm for Staphylococcus aureus and Escherichia coli, respectively). The findings suggested that SOP hydrogel exhibited remarkable self-healing and injectability properties, as well as excellent hemostasis and biocompatibility. In vivo experiments indicated that the application of SOP hydrogels would obviously accelerate wound healing and attenuate the inflammatory response while increasing collagen deposition and angiogenesis. Altogether, antibacterial SOP hydrogels with moderate mechanical properties, pH-responsive release, excellent injectability, exceptional self-healing ability and anti-inflammatory effects could expand potential applications of injectable hydrogels in the biomedical field.

Fabrication and development of biogenic selenium nanoparticles incorporated alginate hydrogel wound care material: a pre-clinical study

ABSTRACT In this study, we attempted to make a nanocomposite wound dressing that was both interactive and bioactive. In order to characterize the biogenic selenium nanoparticles, characterization techniques such as SEM, EDX, DLS, Zetasizer, FTIR, and XRD were utilized. The XRD results showed that the peaks located at around 2θ = 23.9°, 30.1°, 41.6°, 44.1°, and 52.9° that are corresponded to the (100), (101), (110), (102), and (201) reflections of the pure hexagonal phase of selenium crystals. The results of zeta potential measurement showed that the biosynthesized SeNPs have a zeta potential of around −27.5 mV. Studies conducted on animals using a full-thickness wound model of the rat’s skin showed that the wound dressing was able to speed up the natural process of wound healing. Based on the findings, it was determined that the wound dressing has the potential to serve as an effective wound dressing and healing material.

Fabrication of MIL-101(Fe)-embedded biopolymeric films and their biomedical applications

The development of wound-dressing materials with superior therapeutic effects, controlled bioactive agent release, and optimal mechanical properties is crucial in healthcare. This study introduces innovative hydrogel films designed for the sustained release of the local anesthetic drug Procaine (PC), triggered by pH changes. These films are composed of MIL-101(Fe) particles and pectin polymers. MIL-101(Fe) was chosen for its high surface area, stability in aqueous environments, and biocompatibility, ensuring low toxicity to normal cells. MIL-101(Fe)-embedded-pectin hydrogels were synthesized and characterized using Fourier-transformed infrared (FTIR) spectroscopy, thermal gravimetric analysis (TGA), scanning electron microscopy (SEM), X-ray diffraction (XRD), inductively coupled plasma (ICP) spectrometry, particle size analysis, and goniometry. Rheological analysis assessed the hydrogels’ viscoelastic behavior, and UV-spectrophotometry was utilized for drug loading and release studies. The hydrogels exhibited shear-thinning properties, enhancing shape adaptability and recovery, crucial for wound-dressing applications. Controlled drug release was achieved by maintaining the PC solution’s pH between 8.2 and 9.8 during the drug-loading step. The hydrogel film’s impact on wound healing was evaluated through an in vitro wound healing assay, and cytotoxicity was assessed using a WST-1 cell proliferation assay with human dermal fibroblast cells. Results demonstrated that pectin composites enhance cell viability and support fibroblast cell migration without adverse effects, indicating their potential for effective wound healing applications. This study highlights the potential of MIL-101(Fe)-embedded-pectin hydrogels in advancing wound care technology.Graphical MIL-101(Fe)-embedded pectin film as wound dressing

Barnacle-inspired and polyphenol-assisted modification of bacterial cellulose-based wound dressings for promoting infectious wound healing

Bacterial cellulose (BC) is an ideal candidate for wound dressings due to its natural origin, exceptional water-holding capacity, pliability, biocompatibility, and high absorption capability. However, the lack of essential antimicrobial activity limits its biomedical applications. This study reported BC-based wound dressings containing silk fibroin protein (SF), offering the potential for biomimetic properties, and (−)-epigallocatechin-3-gallate (EGCG) for polyphenol-assisted surface modification to promote infectious wound healing. Glycerol was used as the carbon source to promote the formation of an adhesive layer by facilitating the β-sheet folding of SF, and different concentrations of EGCG were employed to interact with SF through strong hydrogen bonding facilitated by the polyphenolic groups. The functionalized membrane exhibited outstanding water-holding capacity, swelling ratio, and degradation properties, along with enhanced hydrophilicity, adhesiveness, and a remarkable free radical scavenging ability. Both in vitro and in vivo experiments confirmed its potent bacteriostatic activity. The composite membrane displayed excellent biocompatibility, including cellular and hemocompatibility. Importantly, it effectively promoted wound healing in murine back infections. These findings suggest the significant feasibility of the innovative modification approach, and that functionalized membranes have great potential as wound-dressing materials for infection management in future clinical applications.

Physical, antibacterial, blood coagulation, and healing promotion evaluations of chitosan derivative-based composite films

Chitosan is a potentially suitable material for wound dressing, but is undesirably water-insoluble. Although chitosan can be modified to produce water-soluble derivatives, the best chitosan derivative for wound dressings remains unclear. The present study introduced three water-soluble chitosan derivatives, namely, carboxymethyl chitosan, quaternized chitosan (QCS), and carboxymethyl quaternized chitosan, and explored the physical properties, biochemical properties, and wound care effectiveness of films of these derivatives. The QCS-based film exhibited higher absorption ability, mechanical properties, water-vapor permeability, electroconductivity, and antioxidant capacity than the other films. Most importantly, the cationic quaternary ammonium groups facilitated the antibacterial activity (>95 %) and blood coagulant capacity of the QCS-based film. As this film also promoted wound healing, it presented as an ideal candidate for wound dressings.

Electrospun Gelatin Scaffolds with Incorporated Antibiotics for Skin Wound Healing.

Recent advances in regenerative medicine provide encouraging strategies to produce artificial skin substitutes. Gelatin scaffolds are successfully used as wound-dressing materials due to their superior properties, such as biocompatibility and the ability to mimic the extracellular matrix of the surrounding environment. In this study, five gelatin combination solutions were prepared and successfully electrospun using an electrospinning technique. After careful screening, the optimal concentration of the most promising combination was selected for further investigation. The obtained scaffolds were crosslinked with 25% glutaraldehyde vapor and characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier-transform infrared spectroscopy. The incorporation of antibiotic agents such as ciprofloxacin hydrochloride and gentamicin sulfate into gelatin membranes improved the already existing antibacterial properties of antibiotic-free gelatin scaffolds against Pseudomonas aeruginosa and Staphylococcus aureus. Also, the outcomes from the in vivo model study revealed that skin regeneration was significantly accelerated with gelatin/ciprofloxacin scaffold treatment. Moreover, the gelatin nanofibers were found to strongly promote the neoangiogenic process in the in vivo chick embryo chorioallantoic membrane assay. Finally, the combination of gelatin's extracellular matrix and antibacterial agents in the scaffold suggests its potential for effective wound-healing treatments, emphasizing the importance of gelatin scaffolds in tissue engineering.

In situ alkali‐free growth of octahedral Ag2O nanoparticles by bacterial cellulose for efficient antibacterial application

AbstractUniform octahedral Ag2O nanoparticles were in situ synthesized within natural bacterial cellulose (BC) films without any inorganic alkali. The morphological transformation of Ag2O from nanoparticles and small nanoplates to an octahedral structure was well controlled by varying the UV exposure time. To reduce and anchor Ag2O nanoparticles, abundant hydroxyl groups on the surface of natural BC fibers ensured an ideal environment for the mild redox reaction between Ag+ and –OH groups. The structural features and structure–activity relationship of Ag2O/BC films were confirmed through TEM, energy dispersive spectroscopy assisted SEM analysis, Fourier transform IR, X‐ray photoelectron spectroscopy, TGA and XRD. The structure–antibacterial activity relationship of the Ag2O/BC films was proved against both Gram‐positive (Staphylococcus aureus) and Gram‐negative (Escherichia coli) bacteria. They also showed excellent performance in the photocatalytic degradation of organic dyes. Ag2O/BC films have potential bactericidal applications in the field of pharmacy, specifically for wound dressing and flexible wearable materials. © 2024 Society of Chemical Industry.

Stimulated Full-Thickness Cutaneous Wound Healing with Bioactive Dressings of Zinc and Cobalt Ion-Doped Bioactive Glass-Coated Eggshell Membranes in a Diabetic Rabbit Model.

Eggshell membrane-based biomedical applications have recently received great attention for their wound-healing properties. However, there are limited studies on diabetic wound healing. In this regard, we devised four types of composite eggshell membrane mats with nanoscale coatings of bioactive glass/Zn/Co-doped bioactive glass (ESM + BAG, ESM + ZnBAG, ESM + CoBAG, and ESM + ZnCoBAG) as wound-dressing materials for chronic nonhealing diabetic wounds. A detailed study of the physicochemical properties of the mats was conducted. In vitro studies demonstrated cytocompatibility and viability of human dermal fibroblasts on all four types of mats. The cells also attached finely on the mats with the help of cellular extensions, as evident from scanning electron microscopy (SEM) and rhodamine-phalloidin and Hoechst 33342 staining of cellular components. Endowed with bioactive properties, these mats influenced all aspects of full-thickness skin wound healing in diabetic animal model studies. All of the mats, especially the ESM + ZnCoBAG mat, showed the earliest wound closure, effective renewal, and restructuring of the extracellular matrix in terms of an accurate and timely accumulation of collagen, elastin, and reticulin fibers. Hydroxyproline and sulfated glycosaminoglycans were significantly (p < 0.01, p < 0.05) higher in ESM-ZnCoBAG-treated wounds in comparison to ESM-BAG-treated wounds, which suggests that these newly developed mats have potential as an affordable diabetic wound care solution in biomedical research.

Enrichment of creatine-gelatin cryogel with Zataria multiflora essential oil and titanium dioxide nanoparticles as a potential wound dressing

The prevalence of microbial infections in wounds, particularly burn wounds, presents a significant medical concern due to the inherent vulnerability of compromised skin to pathogen colonization and invasion. This study focused on the synthesis and evaluation of a creatine-gelatin cryogel, enriched with Zataria multiflora essential oil and titanium dioxide nanoparticles for potential wound dressing applications. The chemical and physical characteristics of the formulation were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, atomic force microscopy, and mechanical tests. Further studies such as wound fluid absorptivity, water vapor transmission rate, solubility, moisture content, porosity, and release properties were investigated. The release test demonstrated an encapsulation efficiency of 98.8 % and a loading capacity of 16.45 %, signifying a suitable cryogel matrix. The disk diffusion assay demonstrated that the synthesized cryogel had excellent antimicrobial efficacy against Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, and Candida species. Additionally, the cryogel exhibited great cytocompatibility and hemocompatibility (∼100 %). Our findings suggest that the creatine-gelatin cryogel blend enriched with Zataria multiflora essential oil and titanium dioxide nanoparticles possesses structural integrity, a cell-friendly nature, moisture-retaining capabilities, and biocompatible characteristics. These properties collectively render it an exceptionally suitable material for advanced wound dressings. Moreover, the demonstrated functional properties of the cryogel, including its ability to prevent infection, exhibit antioxidant activity, and retain moisture, underscore its potential for effective burn wound management.

Designing of tragacanth gum-poly(2-(methacryloyloxy) ethyl] dimethyl-(3-sulfopropyl) ammonium hydroxide) and poly(acrylamide) based hydrogels for drug delivery and wound dressing applications

Bioactive tragacanth gum (TG) was functionalized by covalent crosslinking of poly[2-(methacryloyloxy) ethyl] dimethyl-(3-sulfopropyl) ammonium hydroxide (PMEDSAH) to design network structure in form of hydrogel wound dressings (HWD). These copolymers were encapsulated with antibiotic drug vancomycin to enhance wound healing potential of the dressings. The copolymers were characterized by SEM, AFM, FTIR, 13C NMR, XRD, and TGA-DSC analysis. SEM demonstrated uneven heterogeneous morphology and AFM revealed rough surface of copolymer. Inclusion of synthetic component into HD was confirmed by FTIR and 13C NMR. Hydrogel dressings absorbed 8.49 ​± ​1.03 ​g/g simulated wound fluid and exhibited non-hemolytic (3.7 ​± ​0.02 % hemolytic potential) and antioxidant (37.42 ​± ​1.54 ​% free radical scavenging in DPPH assay) properties. Polymers required 35.0 ​± ​5.0 ​mN detachment force to get it detach from the mucosal surface during mucoadhesive test. Tensile strength was found to be 1.88 ​± ​0.13 ​N/mm2 during mechanical stability test. Hydrogel dressings were permeable to O2/H2O and impermeable to microbes. Release of drug vancomycin occurred through non-Fickian diffusion mechanism and release profile was best described by Korsmeyer-Peppas kinetic model. Overall, these results revealed that these hydrogels could be explored as materials for hydrogel wound dressings.