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The extensive utilization of natural polymers in tissue engineering is attributed to their excellent biocompatibility, degradability, and resemblance to the natural extracellular matrix. These polymers have a wide range of applications such as delivering therapeutic medicine, detecting diseases, sensing biological substances, promoting tissue regeneration, and treating diseases. This is a brief review of current developments in the properties and uses of widely used biomedical polymers derived from nature. Additionally, it explores the correlation between the characteristics and functions of these materials in different biomedical applications and highlights the prospective direction for the advancement of natural polymer materials in tissue engineering. [ABSTRACT FROM AUTHOR]

A common malignant bone neoplasm in teenagers is Osteosarcoma. Chemotherapy, surgical therapy, and radiation therapy together comprise the usual clinical course of treatment for Osteosarcoma. While Osteosarcoma and other bone tumors are typically treated surgically, however, surgical resection frequently fails to completely eradicate tumors, and in turn becomes the primary reason for postoperative recurrence and metastasis, ultimately leading to a high rate of mortality. Patients still require radiation and/or chemotherapy after surgery to stop the spread of the tumor and its metastases, and both treatments have an adverse influence on the body's organ systems. In the postoperative management of osteosarcoma, bone scaffolds can load cargos (growth factors or drugs) and function as drug delivery systems (DDSs). This review describes the different kinds of bone scaffolds that are currently available and highlights key studies that use scaffolds as DDSs for the treatment of osteosarcomas. The discussion also includes difficulties and perspectives regarding the use of scaffold-based DDSs. The study may serve as a source for outlining efficient and secure postoperative osteosarcoma treatment plans. [ABSTRACT FROM AUTHOR]

Conventional oral vaccine delivery in poultry is challenging due to vaccine degradation in the gastrointestinal (GI) environment and the need for cold-chain storage. Microencapsulation offers a solution by protecting vaccines from GI degradation and improving stability. Natural polymers like alginate and cashew gum have mucoadhesive properties, making them promising candidates for oral vaccine delivery. This study developed cashew-alginate microbeads and a powdered dose form for oral vaccine delivery in chickens. The microbeads were created using ionotropic gelation, while the powdered form was obtained via freeze-drying. These formulations were characterized for size, shape, and stability using scanning electron microscopy (SEM), light microscopy, X-ray diffraction (XRD), and Energy Dispersive X-ray (EDX). Peak adhesion time (PAT) was determined using chicken intestinal and esophageal tissues, and antigenicity was assessed with in-vitro hemagglutination (HA) and hemagglutination inhibition (HI) assays. The microbeads exhibited a spherical shape with a porous structure, suggesting enhanced antigen accommodation. Hemagglutination Inhibition tests indicated that the experimental vaccine remained effective without cold-chain storage for three months. These findings suggest that cashew-alginate microbeads are promising for oral vaccine delivery in poultry. [ABSTRACT FROM AUTHOR]

Nowadays, plastic contamination worldwide is a concerning reality that can be addressed with appropriate society education as well as looking for innovative polymeric alternatives based on the reuse of waste and recycling with a circular economy point of view, thus taking into consideration that a future world without plastic is quite impossible to conceive. In this regard, in this review, we focus on sustainable polymeric materials, biodegradable and bio-based polymers, additives, and micro/nanoparticles to be used to obtain new environmentally friendly polymeric-based materials. Although biodegradable polymers possess poorer overall properties than traditional ones, they have gained a huge interest in many industrial sectors due to their inherent biodegradability in natural environments. Therefore, several strategies have been proposed to improve their properties and extend their industrial applications. Blending strategies, as well as the development of composites and nanocomposites, have shown promising perspectives for improving their performances, emphasizing biopolymeric blend formulations and bio-based micro and nanoparticles to produce fully sustainable polymeric-based materials. The Review also summarizes recent developments in polymeric blends, composites, and nanocomposite plasticization, with a particular focus on naturally derived plasticizers and their chemical modifications to increase their compatibility with the polymeric matrices. The current state of the art of the most important bio-based and biodegradable polymers is also reviewed, mainly focusing on their synthesis and processing methods scalable to the industrial sector, such as melt and solution blending approaches like melt-extrusion, injection molding, film forming as well as solution electrospinning, among others, without neglecting their degradation processes. [ABSTRACT FROM AUTHOR]

Introduction: Natural biopolymers are used for various purposes in healthcare, such as tissue engineering, drug delivery, and wound healing. Bacterial cellulose and chitosan were preferred in this study due to their non-cytotoxic, biodegradable, biocompatible, and non-inflammatory properties. The study reports the development of a magnetic bacterial cellulose-chitosan (BC-CS-Fe3O4) nanocomposite that can be used as a biocompatible scaffold for tissue engineering. Iron oxide nanoparticles were included in the composite to provide superparamagnetic properties that are useful in a variety of applications, including osteogenic differentiation, magnetic imaging, drug delivery, and thermal induction for cancer treatment. Methods: The magnetic nanocomposite was prepared by immersing Fe3O4 in a mixture of bacterial cellulose-chitosan scaffold and then freeze-drying it. The resulting nanocomposite was characterized using FE-SEM and FTIR techniques. The swelling ratio and mechanical strength of the scaffolds were evaluated experimentally. The biodegradability of the scaffolds was assessed using PBS for 8 weeks at 37°C. The cytotoxicity and osteogenic differentiation of the nanocomposite were studied using human adipose-derived mesenchymal stem cells (ADSCs) and alizarin red staining. One-way ANOVA with Tukey's multiple comparisons test was used for statistical analysis. Results: The FTIR spectra demonstrated the formation of bonds between functional groups of nanoparticles. FE-SEM images showed the integrity of the fibrillar network. The magnetic nanocomposite has the highest swelling ratio (2445% ± 23.34) and tensile strength (5.08 MPa). After 8 weeks, the biodegradation ratios of BC, BC-CS, and BC-CS-Fe3O4 scaffolds were 0.75% ± 0.35, 2.5% ± 0.1, and 9.5% ± 0.7, respectively. Magnetic nanocomposites have low toxicity (P < 0.0001) and higher osteogenic potential compared to other scaffolds. Conclusion: Based on its high tensile strength, low water absorption, suitable degradability, low cytotoxicity, and high ability to induce an increase in calcium deposits by stem cells, the magnetic BC-CS-Fe3O4 nanocomposite scaffold can be a suitable candidate as a biomaterial for osteogenic differentiation. [ABSTRACT FROM AUTHOR]

Inhibitory properties of an eco‐friendly composition based on gum arabic polysaccharide and citric acid salt–sodium citrate for corrosion prevention of low‐carbon steel in neutral environment was investigated. Corrosion resistance of low‐carbon steel in a 0.1% NaCl solution with and without composition after 3 and 24 h immersion was investigated by electrochemical and weight loss methods. The inhibitory composition with 0.5 g/L concentration was obtained by adding 0.25 g/L of gum arabic and 0.25 g/L of sodium citrate in 1L 0.1% NaCl solution. It was established that the inhibitory efficiency of the composition is enhanced with increasing concentration (0; 0.25; 0.50; 0.75; 1; 1.50; 2.0 g/L) and reaches a maximum at 2.0 g/L of each component. The protective effect of the composition is determined by the combination of two compounds of different natures, which have hydroxyl and carboxyl functional groups. The inhibitory ability of the composition is due to the dominant competitive adsorption between citrate anions with gum arabic and chloride ions on the steel surface. Adsorption of citrate and gum arabic on the steel surface corresponds to the Frumkin isotherm, and the Gibbs energy value was −12.25 kJ/mol, which indicates physical adsorption. The morphology and chemical content of the steel surface after immersion in a solution with an inhibitory composition were investigated by the scanning electron microscopy (SEM) and EDX analysis. The formation of a protective film based on gum arabic and citrate probably occurs by chelation, which effectively blocks the access of corrosively active Cl− ions. It was shown that the corrosion rate Km was 0.42·10−5 g/cm2·h and the inhibitory efficiency for protection of the steel was 80.4% after 24 h immersion in a 0.1% NaCl solution with composition. [ABSTRACT FROM AUTHOR]

Despite advancements in early detection and treatment in developed countries, colorectal cancer (CRC) remains the third most common malignancy and the second-leading cause of cancer-related deaths worldwide. Conventional chemotherapy, a key option for CRC treatment, has several drawbacks, including poor selectivity and the development of multiple drug resistance, which often lead to severe side effects. In recent years, the use of polysaccharides as drug delivery systems (DDSs) to enhance drug efficacy has gained significant attention. Among these polysaccharides, chitosan (CS), a linear, mucoadhesive polymer, has shown promise in cancer treatment. This review summarizes current research on the potential applications of CS-based hydrogels as DDSs for CRC treatment, with a particular focus on smart hydrogels. These smart CS-based hydrogel systems are categorized into two main types: stimuli-responsive injectable hydrogels that undergo sol-gel transitions in situ, and single-, dual-, and multi-stimuli-responsive CS-based hydrogels capable of releasing drugs in response to various triggers. The review also discusses the structural characteristics of CS, the methods for preparing CS-based hydrogels, and recent scientific advances in smart CS-based hydrogels for CRC treatment. [ABSTRACT FROM AUTHOR]

This study presents an innovative method for producing thermosensitive bioink from chitosan hydrogels saturated with carbon dioxide and agarose. It focuses on a detailed characterisation of their physicochemical properties and potential applications in biomedicine and tissue engineering. The ORO test approved the rapid regeneration of the three-dimensional structure of chitosan–agarose composites in a unidirectional bench press simulation test. The diffusion of dyes through the chitosan–agarose hydrogel membranes strongly depended on the share of both polymers in the composite and the molecular weight of the dyes. Glucose, as a nutrient marker, also diffused through all membranes regardless of composition. Biocompatibility assessment using MTT tests on 46BR.1N fibroblasts and HaCaT keratinocytes confirmed the safety of the bioink. The regenerative potential of the bioink was confirmed by efficient cell migration, especially HaCaT. Long-term viability studies showed that chitosan–agarose scaffolds, unlike the agarose ones, support cell proliferation and survival, especially 14 days after bioink extrusion. Experiments in a skin wound model in mice confirmed the biocompatibility of the tested dressing and the beneficial action of chitosan on healing. Studies on vessel formation in chicken embryos highlight the potential of the chitosan–agarose composition to enhance proangiogenic effects. This composition meets all entry criteria and possesses excellent biological properties. [ABSTRACT FROM AUTHOR]

Smart materials for drug delivery are designed to offer a precise and controlled release of therapeutic agents. By responding to specific physiological stimuli, such as changes in temperature and pH, these materials improve treatment efficacy and minimize side effects, paving the way for personalized therapeutic solutions. In this study, we present the fabrication of dual-responsive alginate/poly(N-isopropylacrylamide) (PNIPAM) microspheres, having the ability to respond to both pH and temperature variations and embedding the lipophilic bioactive compound Ozoile. Ozoile® Stable Ozonides is obtained from extra virgin olive oil and acts as an inducer, interacting with major biological pathways by means of modulating the systemic redox balance. The dual-responsive microspheres are prepared by electrospray technique without the use of organic solvents. PNIPAM is synthesized by radical polymerization using the APS/TEMED redox initiators. The microspheres are further optimized with a chitosan coating to enhance their stability and modulate the degradation kinetics of the gel matrix. A comprehensive morphological analysis, Fourier transform infrared (FTIR) spectroscopy, and degradation assays are conducted to confirm the structural stability and pH-responsive behavior of the hydrogel microspheres. A study of the volume phase transition temperature (VPTT) by differential scanning calorimetry (DSC) is used to assess the microsphere thermal response. This research introduces a promising methodology for the development of targeted drug delivery systems, which are particularly useful in the context of oxidative stress modulation and inflammation management. [ABSTRACT FROM AUTHOR]

This study presents the development and characterization of pantoprazole-loaded microspheres utilizing the solvent evaporation technique, aimed at enhancing the delivery of this proton pump inhibitor. Pantoprazole, used to treat gastric ulcers and gastroesophageal reflux disease (GERD), suffers from stability and bioavailability issues in acidic environments. To overcome these challenges, microspheres were created to protect pantoprazole from degradation while ensuring controlled release in the gastrointestinal tract. The emulsion-solvent evaporation method incorporated enteric-coating polymers, specifically Eudragit S100 and hydroxypropyl methylcellulose phthalate (HPMCP), chosen for their protective barrier against acidity. Characterization involved assessments of morphology, particle size distribution, encapsulation efficiency, and drug release profiles. Scanning electron microscopy (SEM) revealed spherical microspheres with a smooth surface, ideal for oral delivery. High encapsulation efficiency indicated effective loading of pantoprazole. In vitro release studies showed significant protection of pantoprazole in acidic media, with sustained release under physiological conditions. Formulations F1 and F4 demonstrated superior performance in protecting and releasing pantoprazole. This study underscores the potential of pantoprazole-loaded microspheres as an effective delivery system, improving drug stability, bioavailability, and controlled release for better therapeutic outcomes in acid-related disorders. [ABSTRACT FROM AUTHOR]

ABSTRACT: Polymers can be produced naturally by organisms, such as chitosan, whey proteins, gums, pectins or gelatins; or in laboratories, synthetically, such as polyvinyl alcohol, polyethylene glycol and polylactic-co-glycolic acid. Polymers have a long history of use in the food industry, traditionally as gelling, thickening or stabilizing agents, used for the formation and modification of food matrixes. However, in recent years, polymers have been used as encapsulating materials for the incorporation of bioactives in foods. Incorporating into products such as breads, juices, or dairy products with the aim of fortifying, increasing stability or preventing degradation. The main encapsulation systems used in the food industry include liposomes, emulsions, nano- and microparticles, and their structure and formulation depend on the characteristics of the food, either as an encapsulating agent or as a bioactive component. In this work, the main natural and synthetic polymers used in food matrixes are reviewed, highlighting their applications as encapsulation systems and purposes of use.

The global demand for wound dressing material has increased, and conventional dressings are unable to meet needs due to various limitations. Researchers have recently turned to electrospinning, a versatile and straightforward method, to address these limitations. Due to its intrinsic qualities, which include a remarkable similarity to the extracellular matrix, researchers have focused their attention on electrospun nanofibrous dressings. Drug-infused electrospun nanofibers are emerging as a potential alternative for wound dressings. Also, substantial surface area in relation to volume, porosity, similarity to the skin's extracellular matrix, and a sequential electrospinning process that facilitates the continuous release of drugs are other points to consider. At the same time, natural carbohydrate polymers possess distinctive characteristics, such as compatibility with biological systems, biodegradability, engaging in cell communication through signaling mechanisms, easy chemical modifications, and wide accessibility, making them desirable polymers for tissue engineering. In the process of electrospinning, various natural carbohydrate polymers have been used extensively to produce nonwoven materials. However, future active electrospun nanofiber dressing can show wound management with wound color map, pH monitoring, infection detection, and drug release capability. This review depicts the current picture of some important carbohydrate polymers, marketed products used in electrospinning, and various applications in wound dressing. [ABSTRACT FROM AUTHOR]

Gene therapy is the technique of inserting foreign genetic elements into host cells to achieve a therapeutic effect. Although gene therapy was initially formulated as a potential remedy for specific genetic problems, it currently offers solutions for many diseases with varying inheritance patterns and acquired diseases. There are two major groups of vectors for gene therapy: viral vector gene therapy and non-viral vector gene therapy. This review examines the role of a macromolecule's chemical and physical architecture in non-viral gene delivery, including their design and synthesis. Polymers can boost circulation, improve delivery, and control cargo release through various methods. The prominent examples discussed include poly-L-lysine, polyethyleneimine, comb polymers, brush polymers, and star polymers, as well as hydrogels and natural polymers and their modifications. While significant progress has been made, challenges still exist in gene stabilization, targeting specificity, and cellular uptake. Overcoming cytotoxicity, improving delivery efficiency, and utilizing natural polymers and hybrid systems are vital factors for prospects. This comprehensive review provides an illuminating overview of the field, guiding the way toward innovative non-viral-based gene delivery solutions. [ABSTRACT FROM AUTHOR]

Direct ink writing is especially relevant to the biomedical field due to the customizable extrusion and the possibility of creating pre‐designed architectures. Abundant natural polymers are sustainable and biocompatible alternatives to synthetic and persistent polymers. The printing of pure nanocellulose suspensions proves difficult due to low solid loadings, high shrinkage, as well as non‐fitting rheology. Emulsion gels (emulgel) alternatives gain attention in the field owing to their favorable viscoelastic properties and the possibility of creating multiphase systems. The authors’ sulfur‐free cationic cellulose nanocrystals (CNC) of low degree of substitution enable straightforward deployment in Pickering emulsions. An emulgel ink co‐stabilized by cationic CNC and α‐cyclodextrin is introduced as an interfacial inclusion complex. All ink components are natural and biodegradable compounds. The produced emulgel inks allow for high fidelity printing and minimum shrinkage upon drying that relaxes the need for supports, even in complex overhanging structures. A low yield stress (230–270 Pa) facilitates the inclusion of cells for biomedical applications into the formulation. The emulgel can be tuned to the desired rheological properties and be equipped with both polar and apolar compounds due to the biphasic system, making it a promising platform for biocompatible additive manufacturing. [ABSTRACT FROM AUTHOR]

In this study, the appropriate polymer solutions were prepared to create chitosan/PVA blends. By altering the ratio of the ingredients, several chitosan/PVA mixtures were produced, as follows: 12% chitosan and 88% PVA, 40% chitosan and 60% PVA, and 15% chitosan and 85% PVA. To generate physically crosslinked hydrogels for the drug delivery of atenolol, several acid cross-linkers, such as fumaric acid and phthalic acid, were applied to the chitosan/PVA blends. The formulations included 15% chitosan and 85% PVA with 0.02% (0.0024, 0.0041, 0.02) mol of fumaric acid, as well as 15% chitosan and 85% PVA with 0.002, 0.003, and 0.0064 mol of phthalic acid. Using an ultraviolet-visible spectrophotometer, the chemical structures of the modified and unmodified chitosan (Chitosan/PVA) hydrogels were examined. Results regarding the formation of ionic cross-links between the protonated hydroxyl groups of the chitosan and the anionic functional groups of the cross-linking agent were established. The swelling ratio was determined for each hydrogel structure as a function of time in three distinct fluids with pH values of 2, 4, and 7.5, and at three distinct temperatures of 42°C and 44°C. The samples with the greatest swelling ratios were identified as PVA.PA0.002 (chitosan) and PVA.FA0.0024. [ABSTRACT FROM AUTHOR]

In recent years, the interest in medical monitoring for human health has been rapidly increasing due to widespread concern. Hydrogels are widely used in medical monitoring and other fields due to their excellent mechanical properties, electrical conductivity and adhesion. However, some of the non-degradable materials in hydrogels may cause some environmental damage and resource waste. Therefore, organic renewable natural polymers with excellent properties of biocompatibility, biodegradability, low cost and non-toxicity are expected to serve as an alternative to those non-degradable materials, and also provide a broad application prospect for the development of natural-polymer-based hydrogels as flexible electronic devices. This paper reviews the progress of research on many different types of natural-polymer-based hydrogels such as proteins and polysaccharides. The applications of natural-polymer-based hydrogels in body movement detection and biomedical monitoring are then discussed. Finally, the present challenges and future prospects of natural polymer-based hydrogels are summarized. [ABSTRACT FROM AUTHOR]

The issue of water and wind erosion of soil remains critically important. Polymeric materials offer a promising solution to this problem. In this study, we prepared and applied an interpolyelectrolyte complex (IPEC) composed of the biopolymers chitosan and sodium carboxymethyl cellulose (Na-CMC) for the structuring of forest sandy soils and the enhancement of the pre-sowing treatment of Scots pine (Pinus sylvestris L.) seeds. A nonstoichiometric IPEC [Chitosan]:[Na-CMC] = [3:7] was synthesized, and its composition was determined using gravimetry, turbidimetry, and rheoviscosimetry methods. Soil surface treatment with IPEC involved the sequential application of a chitosan polycation (0.006% w/w) and Na-CMC polyanion (0.02% w/w) relative to the air-dry soil weight. The prepared IPEC increased soil moisture by 77%, extended water retention time by sixfold, doubled the content of agronomically valuable soil fractions > 0.25 mm, enhanced soil resistance to water erosion by 64% and wind erosion by 81%, and improved the mechanical strength of the soil-polymer crust by 17.5 times. Additionally, IPEC application resulted in slight increases in the content of humus, mobile potassium, mobile phosphorus, ammonium nitrogen, and mineral salts in the soil while maintaining soil solution pH stability and significantly increasing nitrate nitrogen levels. The novel application technologies of biopolymers and IPEC led to a 16–25% improvement in Scots pine seed germination and seedling growth metrics. [ABSTRACT FROM AUTHOR]

The development of strategies allowing either the production of high value phenolics, or the isolation of properties‐enhanced materials from technical lignins represents a fundamental step in the industrial upcycling of technical lignins. Both aims are met by the strategy presented in the present work, relying on the coupling of solvent‐based fractionation with the oxidative action of a new type of alkaline‐stable genetically modified bacterial laccase. The described approach succeeded in the tandem, high‐yield and selective isolation of valuable lignin‐monomeric compounds (MCs) and high molecular weight and hydrophobicity‐tailored polymerised materials (PMs) from two technical lignins, namely softwood kraft lignin (SKL), and wheat straw organosolv lignin (WSL). With respect to MCs, higher yields as compared to similar studies (up to 17.2 mg/g) were achieved. PMs from SKL samples where characterised by an almost quadrupled Mw, while in the case of WSL the Mw was approximately doubled. Noteworthy, the reaction conditions were optimized in terms of reaction temperature, time, enzymatic loading, and alkalinity for the selective production of single MCs. Most interestingly, technical lignins as well as their fractions and the PMs deriving from their laccase‐catalysed oxidation showed increased hydrophobicity. [ABSTRACT FROM AUTHOR]

Despite advancements in therapeutic techniques, restoring bone tissue after damage remains a challenging task. Tissue engineering or targeted drug delivery solutions aim to meet the pressing clinical demand for treatment alternatives by creating substitute materials that imitate the structural and biological characteristics of healthy tissue. Polymers derived from natural sources typically exhibit enhanced biological compatibility and bioactivity when compared to manufactured polymers. Chitosan is a unique polysaccharide derived from chitin through deacetylation, offering biodegradability, biocompatibility, and antibacterial activity. Its cationic charge sets it apart from other polymers, making it a valuable resource for various applications. Modifications such as thiolation, alkylation, acetylation, or hydrophilic group incorporation can enhance chitosan's swelling behavior, cross-linking, adhesion, permeation, controllable drug release, enzyme inhibition, and antioxidative properties. Chitosan scaffolds possess considerable potential for utilization in several biological applications. An intriguing application is its use in the areas of drug distribution and bone tissue engineering. Due to their excellent biocompatibility and lack of toxicity, they are an optimal material for this particular usage. This article provides a comprehensive analysis of osteoporosis, including its pathophysiology, current treatment options, the utilization of natural polymers in disease management, and the potential use of chitosan scaffolds for drug delivery systems aimed at treating the condition. [ABSTRACT FROM AUTHOR]

This study focuses on the development of adsorptive materials to retain degraded 5w40 motor oil. The materials were prepared using xanthan (XG) and XG esterified with acrylic acid (XGAC) as the polymeric matrix. LignoBoost lignin (LB), LB esterified with oleic (LBOL), stearic acid (LBST) and montmorillonite (CL) were added into XG and XGAC matrices to obtain the adsorbents. Adsorption experiments revealed that XG/CL/LBOL had the highest adsorption capacity at 46.80 g/g, followed by XGAC/CL at 45.73 g/g, and XG/CL at 37.58 g/g. The kinetic studies, employing the pseudo-second-order (PSO) model, indicated rapid sorption rates with a good correlation to experimental data. FTIR spectra analysis have evidenced the physical nature of adsorption process, involving interactions such as hydrogen bonding, van der Waals forces, and π–π interactions. Equilibrium data fitting to the Henry, Freundlich, and Temkin isotherm models showed that the adsorption occurs within materials diverse pore structures, enhancing oil retention. Structural parameters like density, porosity, and surface area were pivotal, with XG/CL/LBOL showing the most favorable properties for high oil adsorption. Additionally, it was found that the adsorption efficiency was influenced by the material's morphology and the presence of chemical modifications. This comprehensive evaluation highlights the potential of these novel adsorptive materials for environmental remediation applications, offering an efficient and sustainable approach to reducing degraded motor oil pollution. [ABSTRACT FROM AUTHOR]

Cardiovascular diseases remain a leading cause of mortality globally, with atherosclerosis representing a significant pathological means, often leading to myocardial infarction. Coronary artery bypass surgery, a common procedure used to treat coronary artery disease, presents challenges due to the limited autologous tissue availability or the shortcomings of synthetic grafts. Consequently, there is a growing interest in tissue engineering approaches to develop vascular substitutes. This review offers an updated picture of the state of the art in vascular tissue engineering, emphasising the design of scaffolds and dynamic culture conditions following a biomimetic approach. By emulating native vessel properties and, in particular, by mimicking the three-layer structure of the vascular wall, tissue-engineered grafts can improve long-term patency and clinical outcomes. Furthermore, ongoing research focuses on enhancing biomimicry through innovative scaffold materials, surface functionalisation strategies, and the use of bioreactors mimicking the physiological microenvironment. Through a multidisciplinary lens, this review provides insight into the latest advancements and future directions of vascular tissue engineering, with particular reference to employing biomimicry to create systems capable of reproducing the structure–function relationships present in the arterial wall. Despite the existence of a gap between benchtop innovation and clinical translation, it appears that the biomimetic technologies developed to date demonstrate promising results in preventing vascular occlusion due to blood clotting under laboratory conditions and in preclinical studies. Therefore, a multifaceted biomimetic approach could represent a winning strategy to ensure the translation of vascular tissue engineering into clinical practice. [ABSTRACT FROM AUTHOR]

This work focused on the preparation and investigation of polyurethane (SO-PU)-containing sunflower oil glycerides. By transesterification of sunflower oil with glycerol, we synthesized a glyceride mixture with an equilibrium composition, which was used as a new diol component in polyurethanes in addition to poly(ε-caprolactone)diol (PCLD2000). The structure of the glyceride mixture was characterized by physicochemical methods, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), nuclear magnetic resonance spectroscopy (NMR), and size exclusion chromatography (SEC) measurements. The synthesis of polyurethanes was performed in two steps: first the prepolymer with the isocyanate end was synthesized, followed by crosslinking with an additional amount of diisocyanate. For the synthesis of the prepolymer, 4,4′-methylene diphenyl diisocyanate (MDI) or 1,6-hexamethylene diisocyanate (HDI) were used as isocyanate components, while the crosslinking was carried out using an additional amount of MDI or HDI. The obtained SO-PU flexible polymer films were characterized by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The so-obtained flexible SO-PU films were proved to be suitable for the preparation of potentially biocompatible and/or biodegradable scaffolds. In addition, the stress versus strain curves for the SO-PU polymers were interpreted in terms of a mechanical model, taking into account the yield and the strain hardening. [ABSTRACT FROM AUTHOR]

This study assessed bioplastics made from different mass proportions of commercial chitosan and banana plant pseudostem-derived hemicelluloses. The bioplastics were prepared by the casting method and characterized for moisture content, water solubility, opacity, water absorption, tensile strength, and thermogravimetric properties. The formulations with hemicelluloses addition showed higher moisture content and water solubility than the chitosan-only bioplastic, the maximum values of these properties (22.3 and 22.4%) were achieved when hemicelluloses were added at the proportion of 10 and 5%, respectively. A positive linear correlation (r = 0.86) was found between added hemicelluloses and opacity, with the highest opacity (1.95 mm−1) achieved in the formulation with the maximum hemicellulose incorporation. The bioplastics containing hemicelluloses exhibited lower swelling (water absorption) than that made only of chitosan, with the formulation featuring the highest hemicelluloses content showed the lowest swelling (229.2%). A negative linear correlation (r = 0.95) was observed between added hemicelluloses and swelling values. The formulation with the highest hemicelluloses content demonstrated statistically significant differences and exhibited the highest tensile strength (18.7 MPa) and Young's modulus (66.1 MPa). Thermogravimetric analysis revealed four stages of mass loss in the bioplastics. Hemicelluloses addition decreased the temperature at maximum mass loss, and the formulation with the lowest hemicelluloses content showed a higher degradation rate than the others. [ABSTRACT FROM AUTHOR]

Starch-based biodegradable films are a type of packaging material that can naturally decompose in the environment. Current challenges regarding starch-based film applications are their high solubility and low hydrophobicity. Prior studies have shown that plasma application improves the physical, chemical, and mechanical properties of these films. This work evaluates the plasma application strategy regarding the process stage in which plasma should be applied (starch granule, film-forming solution, or film). Three groups of films were produced: a film produced with the plasma-treated starch, a film produced by subjecting the film-forming solution to plasma treatment, and a plasma-treated film produced with the untreated starch. A 22 face-centered experimental design was applied to each group of films to attain the optimal film of each group. The design consisted of applying plasma at 100, 200, and 300 Hz for 0, 10, and 20 min to each group. The results showed significant differences regarding their physical-chemical and morphological properties. Most chemical changes occurred in the starch subjected to plasma prior to film formation, while the films produced with the untreated starch presented physical changes. Plasma-treated films presented reduced solubility and higher hydrophobicity. [ABSTRACT FROM AUTHOR]

Chitosan is one of the most promising natural polymers, its fundamental scientific research is growing uninterruptedly and has been applied in a wide and varied range of domains, including biomedical and water treatment applications. Therefore, the search and implementation of non-synthetic and non-toxic cross-linkers for chitosan-based hydrogels is crucial for the development of more sustainable and biocompatible materials. Herein, an alternative approach has been developed to explore and exploit methanolic and aqueous extracts from five red seaweed species as covalent cross-linkers for chitosan-based hydrogels. The formation of a gel could be denoted for all extracts, whereas the protein-rich methanolic extractions afforded instantaneous gel-forming ability and greater stiffness and stability. The obtained hydrogels present large porous system with high degrees of swelling up to ca. 3000 %, and were successfully applied as dye adsorbent to remove industrial dye methyl orange withing a circular process with adsorption capacities of 728.46 ± 66.17 mg/g. Furthermore, cytotoxicity and cell-adhesion studies revealed the biocompatibility of the hydrogels and their potential applicability for tissue-engineering. This work demonstrated that methanolic and aqueous extracts from different red seaweed species could replace toxic cross-linkers. Furthermore, the unexpected ability of some extracts could pave the way for the development of new formulations for additive manufacturing, in particular for 3D printing approaches.

The extensive utilization of natural polymers in tissue engineering is attributed to their excellent biocompatibility, degradability, and resemblance to the natural extracellular matrix. These polymers have a wide range of applications such as delivering therapeutic medicine, detecting diseases, sensing biological substances, promoting tissue regeneration, and treating diseases. This is a brief review of current developments in the properties and uses of widely used biomedical polymers derived from nature. Additionally, it explores the correlation between the characteristics and functions of these materials in different biomedical applications and highlights the prospective direction for the advancement of natural polymer materials in tissue engineering.

The mannose-rich exopolysaccharide EPS B3-15, produced by the thermophilic Bacillus licheniformis B3-15, was previously reported to possess promising potentialities as antiviral and immunomodulatory agent, and in preventing the adhesion of Pseudomonas aeruginosa and Staphylococcus aureus. In this study, EPS B3-15 was evaluated for its anti-inflammatory activity in LPS-induced macrophages and the ability to contrast the adhesion of Klebsiella pneumoniae and Streptococcus pneumoniae as pathogenic bacteria of the respiratory tract. Without affecting the macrophages viability, the EPS at low concentration (300 μg/mL) significantly downregulated the gene expression of iNOS and the consequent NO generation, and it also decreased the production of pro-inflammatory cytokines. Moreover, the EPS reduced the adhesion of Str. pneumoniae (47 %) more efficiently than K. pneumoniae (38 %), due to its ability to modify the abiotic surfaces properties and alter the charges of bacterial-cell surface of Gram-positive more than Gram-negative. As able to reduce the inflammatory responses in macrophage cells and simultaneously prevent biofilm-related to the respiratory tract infections, EPS B3-15 could have potential use as nasal spray with anti-inflammatory action and surface-coating agent for medical devices.

Sutures are essential for wound healing. Sutures cannot influence biological healing processes; hence their efficacy is still limited. Active healing sutures must be made. We created a biocompatible, biodegradable polymer suture material to reduce allergic reactions. Non-biocompatible materials that cause tissue rejection and inflammation impede wound healing. To improve wound healing, cellulose and chitosan (CS) were utilized to make a suture material. Dip coating with graphene oxide (GO) nanoparticles improved the suture material. The properties were assessed using FTIR, SEM, EDS, and other analytical methods. In an immersion investigation, coated suture material deterioration in simulated bodily fluid (SBF) was examined. When coated suture material inhibited bacterial growth, its antibacterial activity was tested. These properties suggest that GO nanoparticles, cellulose, and chitosan may be coupled for the first time to generate an aggressive mediator. Coated suture biocompatibility is assessed using in vitro cell survival and hemolysis tests. This paper reviews the latest suture material innovations and explores how natural polymers can advance this area.

The objective of the study was to formulate ketorolac tromethamine, a non-steroidal anti-inflammatory drug, into a sustained-release tablet. Using the wet granulation method, tamarind gum, tapioca starch, and chitosan, as well as their individual and combined polymers, were used to create sustain-release matrix tablets containing ketorolac tromethamine. UV spectroscopy was used for the identification of drugs, and FTIR and DSC were used for compatibility studies. Pre- and post-compression parameters were performed as part of the evaluation process. The dissolution aperture was used for the in-vitro drug release investigations. Kinetic analysis was performed on the optimized formulation's in-vitro drug release data. A stability analysis of the KT12 optimized formulation was conducted. The formulation KT12, which combines chitosan and tamarind gum, demonstrated the highest drug release (99.89%) after 24 hours. It was evident from the release statistics and swelling properties that the formulation KT12 had the best sustaining capabilities. According to stability studies, formulation KT12 exhibits physical stability. Thus, it was determined that a mixture of polymers (chitosan and tamarind gum) was effective in producing ketorolac tromethamine sustain-release matrix tablets, which delay drug release for up to 24 hours. [ABSTRACT FROM AUTHOR]

Synthesis of mono- and diketones as carbonyl group derivatives in biomacromolecular chemistry is very essential task for industrial biotechnology applications. However, there are various techniques to synthesize such carbonyl groups, the most common and efficient methods are the chemical oxidation of alcoholic biological macromolecule by suitable oxidizing agents. Therefore, diversified oxidants have emerged for such purpose, particularly for the derivatives of polysaccharides as natural polymeric carbohydrates in either acidic or alkaline solutions, however, the permanganate ion was found to be the most competitive oxidizing agent for clean and efficient synthesis of such carbonyl derivatives in alkaline media due to easy removal of formed Mn (IV) by complexation with fluoride ions, giving rise to the insoluble MnF4, which can be separated by filtration. Despite the extensive studies on the oxidation of organic compounds by alkaline permanganate. Little of knowledge regarding the type of electron transfer and transition states involved in the rate-determining processes during the oxidation of alcoholic macromolecules by this oxidant. In addition, the literature survey still remains suffering from a lack of information about the reaction kinetics, mechanistic in terms of the nature of electron-transfer and transition states in the rate determining steps of in such oxidation–reduction systems. All of the above arguments encouraged us to present the current review concerning the synthesis of either mono- or diketo derivatives of such homo (non-sulfated) or hetero (sulfated) polysaccharides using alkaline permanganate, aiming to compensate for the lack of information with respect to the nature of electron transfer pathway routes through pertinent interpretations and discussions, as well as to develop innovative methodologies for the synthesis of carbonyl derivatives of biological macromolecules with high potential applications in pharmaceutics and medicine as well as industrial biotechnology. [ABSTRACT FROM AUTHOR]

In clinical practice, tissue adhesives have emerged as an alternative tool for wound treatments due to their advantages in ease of use, rapid application, less pain, and minimal tissue damage. Since most tissue adhesives are designed for internal use or wound treatments, the biodegradation of adhesives is important. To endow tissue adhesives with biodegradability, in the past few decades, various biodegradable polymers, either natural polymers (such as chitosan, hyaluronic acid, gelatin, chondroitin sulfate, starch, sodium alginate, glucans, pectin, functional proteins, and peptides) or synthetic polymers (such as poly(lactic acid), polyurethanes, polycaprolactone, and poly(lactic-co-glycolic acid)), have been utilized to develop novel biodegradable tissue adhesives. Incorporated biodegradable polymers are degraded in vivo with time under specific conditions, leading to the destruction of the structure and the further degradation of tissue adhesives. In this review, we first summarize the strategies of utilizing biodegradable polymers to develop tissue adhesives. Furthermore, we provide a symmetric overview of the biodegradable polymers used for tissue adhesives, with a specific focus on the degradability and applications of these tissue adhesives. Additionally, the challenges and perspectives of biodegradable polymer-based tissue adhesives are discussed. We expect that this review can provide new inspirations for the design of novel biodegradable tissue adhesives for biomedical applications. [ABSTRACT FROM AUTHOR]

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Biocompatible and bioactive composite scaffolds are essential in bone tissue regeneration because of their bioactivity and multilevel porous assemblies. There is a high demand for three-dimensional (3D) scaffolds to treat bone regeneration defects, trauma, and congenital skeletal abnormalities in the current scenario. The main objective of this review is to collect all the possible information concerning synthetic and natural polymer-Bioglass (BG)-based scaffold materials and systematically present them to summarize the importance and need for these materials. The importance of the bone tissue engineering field has been highlighted. Given the current challenges, a comprehensive description of materials fabrication and patterns in scaffold structures is required. This review also includes the most crucial aspect of this study: why are polymeric materials mixed with BG materials? Individually, both BG and polymeric materials lack specific essential characteristics to enhance the scope of these materials. However, preparing the composites of both ensures the researchers that composites of polymers and BG have improved properties that make them versatile materials for bone tissue engineering applications. This study deals with the individual drawbacks of the inorganic BGs, synthetic polymers, and the deficiencies of natural polymers. This study has also included a brief description of various scaffold fabricating techniques. Finally, this study revealed that by manufacturing and developing novel composite materials-scaffolds bearing the capability to repair, heal, and regenerate accidentally damaged or badly injured bones, many occasional problems can be solved in vivo and in vitro. Moreover, this review demonstrated that natural polymeric materials present many advantages over synthetic bone grafts. Yet, synthetic biomaterials have one additional attractive feature, as they have the flexibility to be designed according to the desired demands. These features make them the best choice for a wide range of bone tissue engineering projects for orthopedic surgeons. [ABSTRACT FROM AUTHOR]

Skin injuries pose significant health challenges, with conditions like burns and diabetic, venous, and pressure ulcers presenting complex wound management scenarios. Effective wound care strategies for these injuries encompass a range of interventions, from simple wound dressings to bioactive materials and surgical procedures involving skin substitutes and skin grafting. This review explores the potential of natural polymers, including silk, collagen, gelatin, elastin, cellulose, chitosan, alginate, and hyaluronic acid, in wound management. Natural polymers offer several advantages, including abundance, biodegradability, and compatibility with traditional and modern material fabrication techniques, and have demonstrated safety and efficacy in clinical applications, modulating various facets of the wound healing process. Highlighting preclinical and clinical studies, along with commercial products, this review showcases the versatility and utility of natural polymers in wound management and provides insights into emerging developments, such as 3D bioprinting and stimuli‐responsive materials, which hold promise for personalized wound treatments. Additionally, we discuss the importance of the material format and morphology in engineering the next generation of wound dressings and skin substitutes, offering a pathway to optimize natural polymers for enhanced wound healing outcomes. [ABSTRACT FROM AUTHOR]

Hydraulic fracturing is vital in recovering hydrocarbons from oil and gas reservoirs. It involves injecting a fluid under high pressure into reservoir rock. A significant part of fracturing fluids is the addition of polymers that become gels or gel-like under reservoir conditions. Polymers are employed as viscosifiers and friction reducers to provide proppants in fracturing fluids as a transport medium. There are numerous systems for fracturing fluids based on macromolecules. The employment of natural and man-made linear polymers, and also, to a lesser extent, synthetic hyperbranched polymers, as additives in fracturing fluids in the past one to two decades has shown great promise in enhancing the stability of fracturing fluids under various challenging reservoir conditions. Modern innovations demonstrate the importance of developing chemical structures and properties to improve performance. Key challenges include maintaining viscosity under reservoir conditions and achieving suitable shear-thinning behavior. The physical architecture of macromolecules and novel crosslinking processes are essential in addressing these issues. The effect of macromolecule interactions on reservoir conditions is very critical in regard to efficient fluid qualities and successful fracturing operations. In future, there is the potential for ongoing studies to produce specialized macromolecular solutions for increased efficiency and sustainability in oil and gas applications. [ABSTRACT FROM AUTHOR]

More sustainable agricultural practices are critical to meeting humanity's food needs while minimizing adverse environmental impacts. Engineered nanomaterials used as nanocarriers promise to reduce the volume of agrochemicals required for crop production but concerns about nanocontamination of agricultural products necessitate the discovery of naturally occurring alternatives. Here, plant‐derived cellulose nanocrystals (CNC) as a "green" alternative to man‐made nanomaterials for the economical delivery of agrochemicals to plants are suggested. Using confocal microscopy and fluorescently labeled CNC, it is demonstrated that CNC can successfully penetrate the plant cell wall and enter cells without causing any negative effects on the overall plant phenotype, genome, and metabolome. The efficiency of CNC to deliver chemicals is demonstrated through in vitro tests involving CNC covalently conjugated with 2,4‐dichlorophenoxyacetic acid (2,4‐D). Plant cell culture experiments confirmed that CNC can be used as a 2,4‐D nanocarrier and reduces the volume of plant growth regulators needed to cultivate plant cells. This work creates a new platform for cyclical agricultural practices where CNC extracted from agricultural waste can be used for the direct delivery of agrochemicals to crops, thereby reducing the environmental burden created by both agricultural waste and excess herbicides. [ABSTRACT FROM AUTHOR]

The technique of encapsulating different materials into matrices that can both protect and release their contents under specific circumstances is known as encapsulation. It serves the primary function of shielding delicate components from outside influences, including heat, light, and humidity. This can be accomplished by a variety of procedures that, depending on the method and materials selected, result in the creation of particles with various structures. The materials used for encapsulation in food applications must be of high quality, acceptable for human consumption, and stable during processing and storage. The most suitable natural polymers for food applications are carbohydrates, proteins, or mixtures thereof. Volatile oils are end products of plant metabolism, accumulated and stored in various plant organs, cells, or secretory tissues. These are natural and are characterized by the scent of the aromatic plants they come from. Because of their antibacterial and antioxidant qualities, they are being utilized more and more in the food and pharmaceutical industries. Since volatile oils are highly sensitive to environmental changes, they must be stored under specific conditions after being extracted from a variety of plant sources. A promising method for increasing the applicability of volatile oils is their encapsulation into colloidal particles by natural polymers such as carbohydrates and proteins. Encapsulation hides the unfavorable taste of nutrients while shielding delicate dietary ingredients from the effects of heat, moisture, oxygen, and pH. This technique results in improved stability for volatile oils that are often sensitive to environmental factors and offers the possibility of using them in an aqueous system even if they are insoluble in water. This paper aims to provide an overview of the current advances in volatile oil encapsulation technologies and presents a variety of natural polymers used in the food industry for encapsulation. Also, a distinct section is created to highlight the current advances in dairy products enriched with encapsulated volatile oils. [ABSTRACT FROM AUTHOR]