Gelatin Nanofibers Research Articles

Strontium-doped gelatin scaffolds promote M2 macrophage switch and angiogenesis through modulating the polarization of neutrophils.

The immune system mediates inflammation, vascularization and the first response to injuries or implanted biomaterials. Although the function of neutrophils in tissue repair has been extensively studied, its complete role in the tissue regeneration of biomaterials, specifically the resolution of inflammation and promotion of angiogenesis, is unclear. Here, we fabricate nanofibrous gelatin scaffolds containing 10% (w/w) strontium-hydroxyapatite (SrHA) via phase-separation methods to investigate Sr-mediated regulation of neutrophil polarization and, subsequently, the effects on angiogenesis and macrophage polarization. Compared with neutrophils cultured on pure gelatin or HA-incorporated gelatin scaffolds, neutrophils on SrHA-incorporated gelatin scaffolds show more N2 polarization in vitro and in vivo and significantly greater production of immunomodulatory and angiogenic factors. The Sr-induced immunomodulatory and proangiogenic functions of neutrophils are mediated through NF-κB pathway downregulation and increased STAT3 phosphorylation. Thus, neutrophils play a vital role in tissue engineering, and Sr-incorporated scaffolds efficiently promote neutrophil polarization to the N2 phenotype, enhancing resolution of inflammation and ultimately promoting angiogenesis and tissue regeneration. Thus, incorporation of neutrophils in analyses of the immune characteristics of scaffolds and the development of immunomodulatory biomaterials that can regulate neutrophils are novel and promising strategies in tissue engineering.

Fabrication of Gelatin-ZnO Nanofibers for Antibacterial Applications.

In this study, GNF@ZnO composites (gelatin nanofibers (GNF) with zinc oxide (ZnO) nanoparticles (NPs)) as a novel antibacterial agent were obtained using a wet chemistry approach. The physicochemical characterization of ZnO nanoparticles (NPs) and GNF@ZnO composites, as well as the evaluation of their antibacterial activity toward Gram-positive (Staphyloccocus aureus and Bacillus pumilus) and Gram-negative (Escherichia coli and Pseudomonas fluorescens) bacteria were performed. ZnO NPs were synthesized using a facile sol-gel approach. Gelatin nanofibers (GNF) were obtained by an electrospinning technique. GNF@ZnO composites were obtained by adding previously produced GNF into a Zn2+ methanol solution during ZnO NPs synthesis. Crystal structure, phase, and elemental compositions, morphology, as well as photoluminescent properties of pristine ZnO NPs, pristine GNF, and GNF@ZnO composites were characterized using powder X-ray diffraction (XRD), FTIR analysis, transmission and scanning electron microscopies (TEM/SEM), and photoluminescence spectroscopy. SEM, EDX, as well as FTIR analyses, confirmed the adsorption of ZnO NPs on the GNF surface. The pristine ZnO NPs were highly crystalline and monodispersed with a size of approximately 7 nm and had a high surface area (83 m2/g). The thickness of the pristine gelatin nanofiber was around 1 µm. The antibacterial properties of GNF@ZnO composites were investigated by a disk diffusion assay on agar plates. Results show that both pristine ZnO NPs and their GNF-based composites have the strongest antibacterial properties against Pseudomonas fluorescence and Staphylococcus aureus, with the zone of inhibition above 10 mm. Right behind them is Escherichia coli with slightly less inhibition of bacterial growth. These properties of GNF@ZnO composites suggest their suitability for a range of antimicrobial uses, such as in the food industry or in biomedical applications.

Fabrication of eugenol loaded gelatin nanofibers by electrospinning technique as active packaging material

The aim of this work was to develop a novel degradable bioactive film with poly (lactic acid), gelatin and eugenol, and electrospinning technology was used to develop an active internal layer for the active films to encapsulate eugenol. An annealing treatment was used to improve the adhesion of the active layer onto the poly (lactic acid) film. The results showed that eugenol could be efficiently encapsulated in nanofibers (92.72 g/100 g). The internal active layer containing it showed a uniform fiber morphology observed by scanning electron microscope. The diameter of nanofibers was enlarged and the hydrophobicity was enhanced, the antioxidant activity and antibacterial activity were improved as the addition of eugenol compared with pure gelatin nanofibers. In particular, nanofibers containing 4 μL/mL eugenol (G3) showed the highest antioxidant activity (32.99 mg DPPH/g dry weight), radical scavenging activity (43.80%), and significant microbial growth inhibition with CFU of about 3 log units (E. coli) and 2.5 log units (S. aureus) lower than the control. In conclusion, our results suggested that active layer could be an effective method to encapsulate eugenol, and the poly (lactic acid)/gelatin nanofibers bilayer film was a novel biodegradable packaging material with excellent antioxidant activity and antibacterial activity.

Alginate-magnetic short nanofibers 3D composite hydrogel enhances the encapsulated human olfactory mucosa stem cells bioactivity for potential nerve regeneration application

The design of 3D hydrogel constructs to elicit highly controlled cell response is a major field of interest in developing tissue engineering. The bioactivity of encapsulated cells inside pure alginate hydrogel is limited by its relatively inertness. Combining short nanofibers within a hydrogel serves as a promising method to develop a cell friendly environment mimicking the extracellular matrix. In this paper, we fabricated alginate hydrogels incorporating different magnetic short nanofibers (M.SNFs) content for olfactory ecto-mesenchymal stem cells (OE-MSCs) encapsulation. Wet-electrospun gelatin and superparamagnetic iron oxide nanoparticles (SPIONs) nanocomposite nanofibers were chopped using sonication under optimized conditions and subsequently embedded in alginate hydrogels. The storage modulus of hydrogel without M.SNFs as well as with 1 and 5 mg/mL of M.SNFs were in the range of nerve tissue. For cell encapsulation, OE-MSCs were used as a new hope for neuronal regeneration due to their neural crest origin. Resazurin analyses and LIVE/DEAD staining confirmed that the composite hydrogels containing M.SNFs can preserve the cell viability after 7 days. Moreover, the proliferation rate was enhanced in M.SNF/hydrogels compared to alginate hydrogel. The presence of SPIONs in the short nanofibers can accelerate neural-like differentiation of OE-MSCs rather than the sample without SPIONs.

Fabrication of New Hybrid Scaffolds for in vivo Perivascular Application to Treat Limb Ischemia.

Cell therapies are emerging as a new therapeutic frontier for the treatment of ischemic disease. However, femoral occlusions can be challenging environments for effective therapeutic cell delivery. In this study, cell-engineered hybrid scaffolds are implanted around the occluded femoral artery and the therapeutic benefit through the formation of new collateral arteries is investigated. First, it is reported the fabrication of different hybrid “hard-soft” 3D channel-shaped scaffolds comprising either poly(ε-caprolactone) (PCL) or polylactic-co-glycolic acid (PLGA) and electro-spun of gelatin (GL) nanofibers. Both PCL-GL and PLGA-GL scaffolds show anisotropic characteristics in mechanical tests and PLGA displays a greater rigidity and faster degradability in wet conditions. The resulting constructs are engineered using human adventitial pericytes (APCs) and both exhibit excellent biocompatibility. The 3D environment also induces expressional changes in APCs, conferring a more pronounced proangiogenic secretory profile. Bioprinting of alginate-pluronic gel (AG/PL), containing APCs and endothelial cells, completes the hybrid scaffold providing accurate spatial organization of the delivered cells. The scaffolds implantation around the mice occluded femoral artery shows that bioengineered PLGA hybrid scaffold outperforms the PCL counterpart accelerating limb blood flow recovery through the formation arterioles with diameters >50 μm, demonstrating the therapeutic potential in stimulating reparative angiogenesis.

Interconnected porous nanofibrous gelatin scaffolds prepared via a combined thermally induced phase separation/particulate leaching method

To mimic the fibrous architecture of collagen, the nanofibrous gelatin scaffolds are fabricated employing a thermally induced phase separation (TIPS) technique. The influences of processing parameters, including polymer concentration and solvent mixture composition on the scaffold microstructure are investigated. However, using the TIPS technique, a limited pore size range is generally obtained. To yield the well-interconnected macroporous structures with equiaxed pores and nanofibrous architectures, the TIPS technique is combined with particulate leaching. The macroporous structure of produced scaffolds duplicates the predefined three-dimensional template structure. The homogenous macrostructure with well-interconnected equiaxed pores and no particular orientation is created. Modulating the size and shape of microspheres has precise control over porosity, pore size, and interconnection of the matrix. Because of the well-interconnected macroporous nanofibrous structure, the useful applications of these scaffolds in the tissue engineering field are expected.

Active packaging based on swim bladder gelatin/galangal root oil nanofibers: Preparation, properties and antibacterial application

In this work, swim bladder gelatin (SBG) nanofibers incorporating galangal root oil/β-cyclodextrin (GRO/β-CD) were fabricated by electrospinning for antibacterial packaging use. SBG exhibits desirable fiber-forming properties due to its unique amino acid composition. Specifically, β-CD played an essential role in preventing GRO volatilization by forming GRO/β-CD inclusion complex during electrospinning. FTIR and XRD results confirmed that GRO was successfully encapsulated in the β-CD cavity through the process assisted with ultrasound. Besides, the hydrogen bonding interactions were major forces both in inclusion complex and nanofibers, which enhanced the thermal stability. The release kinetic curve demonstrated that the release mechanism of GRO from nanofibers was subject to Fickian diffusion. In the application experiment, the prepared nanofiber mats showed efficient inhibitory effect against EHEC O157, and little influence on the sensory properties of beef. Our findings provided a feasible strategy to explore application potential of natural antibacterial substances in active food packaging.

Biomimetic Nanoengineered Scaffold for Enhanced Full-Thickness Cutaneous Wound Healing

Wound healing is a complex process which is based on the coordinated signaling molecules and dynamic interactions between the engineered scaffold and newly formed tissue. So far, most of the engineered scaffolds used for the healing of full-thickness skin wound do not mimic the natural extracellular matrix (ECM) complexity and therefore are not able to provide an appropriate niche for endogenous tissue regeneration. To address this gap and to accelerate the wound healing process, we present biomimetic bilayer scaffolds compositing of gelatin nanofibers (GFS) and photocrosslinkable composite hydrogels loaded with epidermal growth factors (EGF). The nanofibers operate as the dermis layer and EFG-loaded composite hydrogels acted as the epidermis matrix for the full-thickness wound healing application. The hydrogels are composed of gelatin metacryloyl (GelMA) modified with silicate nanoplatelets (Laponite). To overcome the challenges of transdermal delivery of EGF including short half-life and lack of efficient formulation precise, controlled delivery was attained by immobilization of EGF on Laponite. It is shown that the addition of 1wt% silicate nanoplatelet increases the compressive modulus of the hydrogels by 170%. In vitro wound closure analysis also demonstrated improved adhesion of the scaffolds to the native tissue by 3.5 folds. Moreover, the tunable hemostatic ability of the scaffolds due to the negatively charged nanoplatelets is shown. In an established excisional full-thickness wound model, an enhanced wound closure (up to 93.1 ± 1.54%) after 14 days relative to controls (GFS and saline-treated groups) is demonstrated. The engineered adhesive and hemostatic scaffolds with sustained release of the growth factors have the potential to stimulate complete skin regeneration for full-thickness wound healing.

Designing Biomimetic Triple-Layered Nanofibrous Vascular Grafts via Combinatorial Electrospinning Approach

Biomimetic vascular grafts with multi-layered nanostructures can mimic structure and function of native blood vessels, but it is often challenging. This study demonstrates the feasibility of using combinatorial electrospinning approach for designing triple-layered nanofibrous tubular scaffold with inner and outer layer made up of co-axial poly(lactic-co-glycolic acid) (PLGA)/gelatin nanofibers (PLGA-core/gelatin-shell) and the intermediate layer with PLGA nanofibers that mimics native vascular structure. The assessment of biomechanical and biological analysis showed enhanced mechanical strength, suture strength and biocompatibility when cultured with human umbilical vein endothelial cells (HUVECs). Altogether, the results suggest that the combinatorial electrospinning approach is potentially useful for the fabrication of biomimetic vascular grafts suitable for cardiovascular tissue engineering applications.

Effect of crosslinkable sugar molecules on the physico-chemical and antioxidant properties of fish gelatin nanofibers

In this study, gelatin nanofibers that were stable against hydrolytic degradation environment were prepared via electrospinning of aqueous fish gelatin, an eco-friendly sugar crosslinking agent, and a mild heat treatment crosslinking process. Next, the formation of the Maillard reacted products according to the sugar type and the physicochemical properties and antioxidant functions of the sugar-crosslinked gelatin nanofibers were investigated. The addition of sugar to the gelatin nanofibers increased the Maillard reactivity in the order of sucrose < glucose < fructose, thereby increasing the stability of the gelatin nanofibers against hydrolytic degradation. In addition, sugar crosslinking enhanced the mechanical properties, wetting and hygroscopic properties of the gelatin nanofibers. Moreover, due to the production of Maillard reactants, the sugar-modified nanofibers exhibited an excellent antioxidant effect compared with existing gelatin nanofibers.

A tailored polylactic acid/polycaprolactone biodegradable and bioactive 3D porous scaffold containing gelatin nanofibers and Taurine for bone regeneration

The focus of the current study was to develop a functional and bioactive scaffold through the combination of 3D polylactic acid (PLA)/polycaprolactone (PCL) with gelatin nanofibers (GNFs) and Taurine (Tau) for bone defect regeneration. GNFs were fabricated via electrospinning dispersed in PLA/PCL polymer solution, Tau with different concentrations was added, and the polymer solution converted into a 3D and porous scaffold via the thermally-induced phase separation technique. The characterization results showed that the scaffolds have interconnected pores with the porosity of up to 90%. Moreover, Tau increased the wettability and weight loss rate, while compromised the compressive strengths. The scaffolds were hemo- and cytocompatible and supported cell viability and proliferation. The in vivo studies showed that the defects treated with scaffolds filled with new bone. The computed tomography (CT) imaging and histopathological observation revealed that the PLA/PCL/Gel/Tau 10% provided the highest new bone formation, angiogenesis, and woven bone among the treatment groups. Our finding illustrated that the fabricated scaffold was able to regenerate bone within the defect and can be considered as the effective scaffold for bone tissue engineering application.

Fabrication of ultrathin artificial basement membrane for epithelial cell culture

Basement membranes are essential for epithelial and endothelial tissue organization. To mimic them, we developed a fabrication method to produce ultrathin membrane of collagen IV and laminin. A honeycomb microframe of thickness 50 μm and compartment-size 400 μm was firstly patterned in polyethylene glycol diacrylate (PEGDA) by using lithography and vacuum assisted UV curing techniques. Then, a monolayer of gelatin nanofibers was electrospun and crosslinked on the microframe to form a secondary structure, a fiber mesh with much smaller pore sizes, in each of the honeycomb compartments. Finally, a collagen IV-laminin gel layer was deposited and dehydrated, leading to the formation of ultrathin membrane over a large area with a nanofiber backbone. Such an artificial basement membrane is mechanically stable and fully bio-compatible. It is also semi-permeable which can slow down considerably the diffusion of large size molecules. More importantly, it can be used to improve the monolayer formation of epithelial cells. Thus, this culture device recapitulates the biological basement membrane, permits the epithelial tissue formation, and allows mimicking a sophisticated cellular microenvironment.

Effect of tannic acid on properties of electrospun gelatin nanofibres

Gelatin/tannic acid nanofibres have been prepared and the effects of production parameters, including high voltage, feeding rate and distance between tip of the needle and collector on the morphology of nanofibres are investigated. The results show that the average nanofibre diameter increases with raising the high voltage values, due to less branching of liquid jet. Increasing the feeding rate leads to an increase in the nanofibre diameter, up to a certain value (0.6-0.8 mL/h). Further increase in the feeding rate value causes the formation of a ribbon-like structure. The increment in the content of tannic acid as a crosslinker increases the viscosity of the spinning solution and the average nanofibre diameters. Also, the tensile strength of crosslinked nanofibres increases as compared to that of the gelatin nanofibres. Moreover, the addition of tannic acid to gelatin nanofibres significantly enhances the antibacterial property of nanofibres.

Alveolar mimics with periodic strain and its effect on the cell layer formation.

We report on the development of a new model of alveolar air-tissue interface on a chip. The model consists of an array of suspended hexagonal monolayers of gelatin nanofibers supported by microframes and a microfluidic device for the patch integration. The suspended monolayers are deformed to a central displacement of 40-80 µm at the air-liquid interface by application of air pressure in the range of 200-1,000 Pa. With respect to the diameter of the monolayers, that is, 500 µm, this displacement corresponds to a linear strain of 2-10% in agreement with the physiological strain range in the lung alveoli. The culture of A549 cells on the monolayers for an incubation time of 1-3 days showed viability in the model. We exerted a periodic strain of 5% at a frequency of 0.2 Hz for 1 hr to the cells. We found that the cells were strongly coupled to the nanofibers, but the strain reduced the coupling and induced remodeling of the actin cytoskeleton, which led to a better tissue formation. Our model can serve as a versatile tool in lung investigations such as in inhalation toxicology and therapy.

Multi-layer dressing made of laminated electrospun nanowebs and cellulose-based adhesive for comprehensive wound care

In this work, multi-layer wound dressing was made of laminated layers of electrospun fibers supported by adhesive sheet. Graft copolymerization of methyl methacrylate (MMA) and 2-Ethyl-1-hexyl acrylate (EHA) onto carboxymethyl cellulose (CMC) was conducted to obtain an adhesive sheet with 1.52 (N/cm2) loop tack, 1.7 (N/cm) peel strength and 25 s shear strength. Diclofenac sodium, anti-inflammatory drug, was loaded to the adhesive sheet with encapsulation efficiency 73%.The contact layer to wound was made of synthesized anti-bleeding agents, chitosan iodoacetamide (CI) loaded into electrospun polyvinyl alcohol (PVA) fibers. It was fabricated from fiber diameter 300 nm by electrospinning of 5% wt/v of CI (D.S. 18.7%) mixed with 10% wt/v PVA, at 20 kV and 17 cm airgap. The second, pain-relief layer was fabricated by encapsulating up to 50% wt/wt of capsaicin into gelatin nanofibers (197 nm) crosslinked by glyoxal. The third, antimicrobial layer was fabricated from PVA electrospun fibers loaded with 2% wt/wt gentamicin. Biocompatibility test showed insignificant adverse effects of the fabricated layers on fibroblast cells. Animal test on rat showed accelerated wound healing from 21 to 7 days for the multi-layer dressing. Histopathological findings corroborated the intactness of the epidermis layer of the treated samples.

Programmable release of 2-O-d-glucopyranosyl-l-ascorbic acid and heparin from PCL-based nanofiber scaffold for reduction of inflammation and thrombosis

Reduction of inflammation and thrombosis caused by implanted devices is critical for clinical success. To this end, the strategy based on programmable release of anti-inflammatory and anti-thrombotic agents from the widely-used polycaprolactone (PCL)/gelatin nanofiber scaffold is developed. The release of 2-O-d-Glucopyranosyl-l-ascorbic Acid (AA-2G) and heparin are controlled by reactive oxygen species (ROS)-responsive poly(ethylene glycol)-based β-thioether ester copolymer (PEGDA-EDT) and mesoporous silica nanoparticles (MSN) in the nanofiber, respectively. The in vitro assay demonstrate that the scaffolds are hemocompatible with the resistance of platelet adhesion; the control release of AA-2G prevents initial inflammation and oxidation of the blood cells, and the subsequent release of heparin entitles nanofibers with long-term anti-thrombotic capability. In addition, rapid endothelialization is obtained on the surface of nanofiber scaffolds for the further enhancement of the hemocompatibility. In vivo implant evaluation convinces that the nanofiber scaffolds possess high biocompatibility with the substantial resistance for inflammation and thrombosis. Hence, our work paves a new way to develop the anti-inflammatory and anti-thrombotic tissue-engineering substrates through programmable delivery of two or multiple drugs.

Bioinspired Nanofiber Scaffold for Differentiating Bone Marrow-Derived Neural Stem Cells to Oligodendrocyte-Like Cells: Design, Fabrication, and Characterization.

BackgroundResearchers are trying to study the mechanism of neural stem cells (NSCs) differentiation to oligodendrocyte-like cells (OLCs) as well as to enhance the selective differentiation of NSCs to oligodendrocytes. However, the limitation in nerve tissue accessibility to isolate the NSCs as well as their differentiation toward oligodendrocytes is still challenging.PurposeIn the present study, a hybrid polycaprolactone (PCL)-gelatin nanofiber scaffold mimicking the native extracellular matrix and axon morphology to direct the differentiation of bone marrow-derived NSCs to OLCs was introduced.Materials and MethodsIn order to achieve a sustained release of T3, this factor was encapsulated within chitosan nanoparticles and chitosan-loaded T3 was incorporated within PCL nanofibers. Polyaniline graphene (PAG) nanocomposite was incorporated within gelatin nanofibers to endow the scaffold with conductive properties, which resemble the conductive behavior of axons. Biodegradation, water contact angle measurements, and scanning electron microscopy (SEM) observations as well as conductivity tests were used to evaluate the properties of the prepared scaffold. The concentration of PAG and T3-loaded chitosan NPs in nanofibers were optimized by examining the proliferation of cultured bone marrow-derived mesenchymal stem cells (BMSCs) on the scaffolds. The differentiation of BMSCs-derived NSCs cultured on the fabricated scaffolds into OLCs was analyzed by evaluating the expression of oligodendrocyte markers using immunofluorescence (ICC), RT-PCR and flowcytometric assays.ResultsIncorporating 2% PAG proved to have superior cell support and proliferation while guaranteeing electrical conductivity of 10.8 × 10−5 S/cm. Moreover, the scaffold containing 2% of T3-loaded chitosan NPs was considered to be the most biocompatible samples. Result of ICC, RT-PCR and flow cytometry showed high expression of O4, Olig2, platelet-derived growth factor receptor-alpha (PDGFR-α), O1, myelin/oligodendrocyte glycoprotein (MOG) and myelin basic protein (MBP) high expressed but low expression of glial fibrillary acidic protein (GFAP). ConclusionConsidering surface topography, biocompatibility, electrical conductivity and gene expression, the hybrid PCL/gelatin scaffold with the controlled release of T3 may be considered as a promising candidate to be used as an in vitro model to study patient-derived oligodendrocytes by isolating patient’s BMSCs in pathological conditions such as diseases or injuries. Moreover, the resulted oligodendrocytes can be used as a desirable source for transplanting in patients.

Feasibility of Using Vitamin E-Loaded Poly(ε-caprolactone)/Gelatin Nanofibrous Mat to Prevent Oxidative Stress in Skin.

Some occupational skin exposures lead to the formation of reactive oxygen species (ROS). The occupational exposure of workers to ROS has been found to be associated with an increased risk of developing skin injuries; therefore, it is essential to protect skin against ROS formation. Recently, some studies have been conducted on introducing better alternatives for skin protection. Nanofibers are good candidates for this purpose. The current study was carried out to assess vitamin E-loaded hybrid Poly(ε-caprolactone) (PCL)/gelatin (Gt) nanofibres mats as protective layers of skin exposed to occupational exposures. Vitamin E (VE) was successfully incorporated into PCL/Gt nanofibers while they were formed by electrospinning method. Nanofibers mats were characterized using scanning electron microscopy (SEM) and fourier transform infrared spectroscopy (FTIR). Their degradation behavior, in vitro release, biocompatibility, and antioxidant activity were studied. The diameters of the PCL/Gt/VE nanofibers decreased with the addition of vitamin E. The degradation rate of nanofibers was equal to 42.98 and 50.69% during 7 and 14 days, respectively. Nanofibers containing vitamin E showed an initial burst followed by a sustained release. The PCL/Gt/VE nanofibers exhibited good free radical scavenging activities despite being exposed to a high electrical potential during electrospinning. PCL/Gt/VE nanofibers supported a higher level of viability compared to PCL/Gt ones and significantly assisted human skin cells against tert-Butyl hydroperoxide (t-BHP) induced oxidative stress. Overall, PCL/Gt/VE nanofibers can potentially be used to protect skin against oxidative stress as a novel approach for worker's healthcare.

Fabrication of cellulose-based adhesive composite as an active packaging material to extend the shelf life of cheese

Traditional solutions of food packing are limited for antimicrobial packaging materials that interact with the product to inhibit the growth of microorganisms. In this work, adhesive composite was developed as an active packaging material using allyl isothiocyanate (AIC) in vapor phase. Such adhesive composite was made of gelatin electrospun fibers loaded by AIC and supportive adhesive sheet. Gelatin electrospun fibers loaded by AIC (2–10% v/v) into 24% wt/v gelatin solutions was produced using electrospinning apparatus at 15 kV, 15 cm air gap and 0.2 mL/h flow rate. This mat was supported by pressure-sensitive adhesive (PSA) made of hydroxyethyl cellulose backbone grafted by acrylic acid and methylbutyl acrylate [HEC-g-poly(AA-MBA)]. PSA was characterized in means of spectral, physicochemical and rheological analysis. Final product with AIC (2% v/v) showed significant antimicrobial activities against two food born bacteria including Staphylococcus aureus ATCC 25923 and Escherichia coli O157:H7. Antimicrobial activities on cheese showed that gelatin nanofibers loaded by AIC (10% v/v), applied in the headspace, extended the shelf life of cheese from 4 weeks to 8 weeks.

Prolonged-release of menthol through a superhydrophilic multilayered structure of balangu (Lallemantia royleana)-gelatin nanofibers.

This study aimed to develop a sandwich structure based on electrospun mats derived from gelatin (central layer) and Balangu seed gum (outer layers) and to compare its capability for prolonging the menthol release in the oral phase compared to the gelatin monolayer mat. The mesh-like structure and the smooth and uniform surface of the electrospun mats designed in this study were authenticated by Atomic Force Microscopy (AFM). By designing the sandwich structure, the dissolution time and contact angle of the mats were increased and their bioadhesive strength decreased. The swelling degree of the gelatin mat (453.25±32.56%) was significantly higher than that of the sandwich mat (297.71±22.68%) (p<0.05). Successful entrapment and the thermal stability of the produced mats were proved by X-ray diffraction (XRD), differential scanning calorimetry (DSC), and Fourier-transform infrared spectroscopy (FTIR) tests. The release kinetics in the human simulated saliva showed that the burst release of menthol from the structure of electrospun gelatin mats, due to its fast-dissolving nature, was well prolonged by the designed sandwich system. The Fickian Case-I release was the main mechanism in the menthol release and the Peppas-Sahlin was the most suitable model governing the release of menthol from these structures.