Biodegradable Research Articles

Effect of Specific Surface Area and Hydrophobicity of Electrospun Nanofibers on the Sustained Release Performance of Diclofenac Sodium.

Nanofibers produced by electrospinning are suitable options for slow-release materials. Diclofenac sodium (DS) is a nonsteroidal anti-inflammatory medication with a brief half-life that can serve as an effective sustained-release agent. This paper presents a novel method for producing DS-sustained release nanofibers by electrostatic spinning processes. During the preparation, the slow-release capabilities of biodegradable materials poly(lactic acid) (PLA) and polycaprolactone (PCL) are investigated. A composite drug-carrying scaffold is prepared to enhance the sustained-release performance. The sustained release ability is affected by the specific surface area of the nanofibers and the hydrophobicity of the polymer. The findings indicate that the composite nanofiber with a PLA/PCL ratio of 1:1 demonstrates the most effective sustained-release performance. The release rate is mostly influenced by the hydrophobicity of the polymer at this point. Sustained-release kinetic simulations were performed and revealed that the release of nanofibers follows a first-order release paradigm. This work presents a straightforward approach for creating a sustained-release formulation of DS.

The influence of age on the biological response to biodegradable zinc arterial implants

Medical devices to treat arterial diseases of older humans are routinely designed and developed using young animals. This is the case despite the significant declines of tissue regeneration, cell proliferation, and inflammation in aged humans that are not reflected in young animals. The widespread use of age-mismatched animals is particularly a concern for the testing of interactive materials, such as biodegradable metals whose dynamic interfaces continuously impact local cell and tissue regenerative processes. In order to determine the importance and impact of age differences in biodegradable stent material biocompatibility, we implanted both inert (platinum) and biodegradable (zinc) metal wires into the arteries of 1 year old and 3-month-old rats for a period of 6 months and compared the biological responses. It was found that the older animals developed a significantly larger neointimal encapsulating tissue for zinc implants vs. a smaller tissue response for the platinum implants relative to the younger rats. The neointimas of older rats contained dramatically fewer macrophages for both implant metals. The presence of neointimal smooth muscle cells was also decreased in the older rats. Endothelial cell regeneration in the old arteries was not impacted by the different metal implants. These findings demonstrate that neointimal responses to metal implants in arterial tissue are strongly impacted by age-related changes. The findings also suggest that the reliance on young animal models to evaluate metal implants intended for the arteries of considerably older individuals may substantially over predict the biocompatibility.

Advances in Paper‐Based Photodetectors: Fabrications, Performances, and Applications

AbstractWith the development of wearable electronic technology, the flexible photodetectors have attracted widespread attention, and it is of great significance to develop flexible, eco‐friendly and low‐cost photodetectors. Cellulose paper, as a flexible, eco‐friendly, low‐cost, lightweight, customizable, biodegradable and renewable material, has received enthusiastic attention and rapid development in the field of photodetectors in recent years. In this review, it is focused on the research progress of paper‐based (PB) photodetectors. First, the fabrication methods of PB photodetectors are discussed, including electrode materials and optoelectronic functional materials. Then, this review systematically summarizes and analyzes the achievements of PB photodetectors on photoelectric performances (spectral response range, responsivity, detectivity, response/recovery times and on/off ratio) and flexibility characteristics (bending angle and bending cycle). In terms of key performance indicators, the PB photodetectors reported so far can detect multiple wavelengths of light from UV to near‐infrared with the maximum detectivity of 1013 Jones. In addition, the various applications of PB photodetectors is reviewed and discussed. Finally, it is look forward to the future development of PB photodetectors in terms of fabrication methods, photoelectric and flexible performances, and applications. With this review, it is hope that it will promoted the future development of PB photodetectors.

High performance flexible green triboelectric nanogenerator with polyethylene oxide/mica tribo-positive composite material

Innovating novel, green, biodegradable, and recyclable polymers are critical for the development of environmentally sustainable solutions, eliminating concerns of pollution and microplastic accumulation. Herin, this study presents remarkably enhanced tribo-positive polyethylene oxide (PEO) polarity, by incorporating for the first time, a clay inorganic filler, creating a novel biodegradable composite triboelectric material. The low-cost composite comprised a biodegradable polymeric PEO matrix, an abundant naturally sourced muscovite mica micro-platelet filler, and integrated simple material fabrication methods. A 4 cm2 PEO/Mica film was paired with polytetrafluoroethylene (PTFE), generating a peak-to-peak voltage, current density, and transferred charge density of respectfully, 296 V, 24.2 mA m−2, and 110.3 µC m−2. Reducing the film thickness to 40 µm dramatically enhanced the electrical output, resulting in a peak-to-peak voltage and instantaneous power density of respectfully, 424 V and 12.1 W m−2. The addition of mica greatly improved the dielectric permittivity, promoting the outstanding triboelectric performance. The composite material's long-term stability and flexibility demonstrated significant advantages for self-powering small electronic systems. Furthermore, PEOs facile water solubility allowed mica separation, recovery, recyclability, and integration within new PEO/Mica films, resulted in preserved triboelectric outputs. The PEO/Mica composite delivers exceptional sustainable, recyclable, and tribo-positive attributes, serving as an excellent energy harvesting solution.

Maleic Anhydride-Derived Copolymers Conjugated with Beta-Lactam Antibiotics: Synthesis, Characterization, In Vitro Activity/Stability Tests with Antibacterial Studies

The synthesis and characterization of biocompatible three different maleic anhydride co-polymer conjugated with two different beta-lactam antibiotics at in vitro conditions were conducted. The polymer–drug conjugates were synthesized by coupling β-lactam antibiotics via amide bonds to the copolymer. In this work, six different drug-functionalized maleic anhydride copolymers (DFMACs) were synthesized by the chemical conjugation method. This method is based on the ring-opening reaction of the anhydride ring of the copolymer to form an amide bond linking the drug. The synthesized DFMACs were characterized by 1H NMR and FTIR/ATR spectroscopies and analyses were carried out by UV/VIS spectroscopy and Zeta-sizer instrument in detail with consecutive antibacterial tests. The existence of a newly formed amide covalent bond between the drug and the copolymer chains was confirmed by 1H NMR and FTIR/ATR studies. This is the first report on the application of the selected branched biodegradable polymeric matrices for the covalent conjugation of ampicillin and cefalexin. Optimum stability and activity conditions for the synthesized DFMACs were determined. Analyses were conducted under in vitro conditions including varying pH values and simulated body fluids as a function of time to obtain new drug delivery system candidates for the two different antibiotics.

Novel DNA-Binding Activity Exhibited by Poly(aspartic acid) Hydrolase-1 Inhibits Poly(aspartic acid) Hydrolase Activity.

Significant attention has been shifted toward the use and development of biodegradable polymeric materials to mitigate environmental accumulation and potential health impacts. One such material, poly(aspartic acid) (PAA), is a biodegradable alternative to superabsorbent poly(carboxylates), like poly(acrylate). Three enzymes are known to hydrolyze PAA: PahZ1KT-1 and PahZ2KT-1 from Sphingomonas sp. KT-1 and PahZ1KP-2 from Pedobacter sp. KP-2. We previously reported the X-ray crystal structure for PahZ1KT-1, which revealed a homodimer complex with a strongly cationic surface spanning one side of each monomer. Here, we report the first characterization of any polymer hydrolase binding to DNA, where modeling data predict binding of the polyanionic DNA near the cationic substrate binding surface. Our data reveal that PahZ1 homologues from Sphingomonas sp. KT-1 and Pedobacter sp. KP-2 bind ssDNA and dsDNA with nanomolar binding affinities. PahZ1KT-1 binds ssDNA and dsDNA with an apparent dissociation constant, KD,app = 81 ± 14 and 19 ± 1 nM, respectively, and these estimates are similar to the same behaviors exhibited by PahZ1KP-2. Gel permeation chromatography data reveal that dsDNA binding promotes inhibition of PahZ1-catalyzed PAA biodegradation for each homologue. We propose a working model wherein binding of PahZ1 to extracellular biofilm DNA aids in the localization of the hydrolase to the environment in which PAA would first be encountered, thereby providing a mechanism to degrade extracellular PAA and potentially harvest aspartic acid for nutritional uptake.

Sheep Bone Ultrastructure Analyses Reveal Differences in Bone Maturation around Mg-Based and Ti Implants.

Magnesium alloys are some of the most convenient biodegradable materials for bone fracture treatment due to their tailorable degradation rate, biocompatibility, and mechanical properties resembling those of bone. Despite the fact that magnesium-based implants and ZX00 (Mg-0.45Zn-0.45Ca in wt.%), in particular, have been shown to have suitable degradation rates and good osseointegration, knowledge gaps remain in our understanding of the impact of their degradation properties on the bone's ultrastructure. Bone is a hierarchically structured material, where not only the microstructure but also the ultrastructure are important as properties like the local mechanical response are determined by it. This study presents the first comparative analysis of bone ultrastructure parameters with high spatial resolution around ZX00 and Ti implants after 6, 12, and 24 weeks of healing. The mineralization was investigated, revealing a significant decrease in the lattice spacing of the (002) Bragg's peak closer to the ZX00 implant in comparison to Ti, while no significant difference in the crystallite size was observed. The hydroxyapatite platelet thickness and osteon density demonstrated a decrease closer to the ZX00 implant interface. Correlative indentation and strain maps obtained by scanning X-ray diffraction measurements revealed a higher stiffness and faster mechanical adaptation of the bone surrounding Ti implants as compared to the ZX00 ones. Thus, the results suggest the incorporation of Mg2+ ions into the bone ultrastructure, as well as a lower degree of remodeling and stiffness of the bone in the presence of ZX00 implants than Ti.

Obtention and Characterization of Microcrystalline Cellulose from Industrial Melon Residues Following a Biorefinery Approach.

Residual melon by-products were explored for the first time as a bioresource of microcrystalline cellulose (MCC) obtention. Two alkaline extraction methods were employed, the traditional (4.5% NaOH, 2 h, 80 °C) and a thermo-alkaline in the autoclave (2% NaOH, 1 h, 100 °C), obtaining a yield of MCC ranging from 4.76 to 9.15% and 2.32 to 3.29%, respectively. The final MCCs were characterized for their chemical groups by Fourier-transform infrared spectroscopy (FTIR), crystallinity with X-ray diffraction, and morphology analyzed by scanning electron microscope (SEM). FTIR spectra showed that the traditional protocol allows for a more effective hemicellulose and lignin removal from the melon residues than the thermo-alkaline process. The degree of crystallinity of MCC ranged from 51.51 to 61.94% and 54.80 to 55.07% for the thermo-alkaline and traditional processes, respectively. The peaks detected in X-ray diffraction patterns indicated the presence of Type I cellulose. SEM analysis revealed microcrystals with rough surfaces and great porosity, which could remark their high-water absorption capacity and drug-carrier capacities. Thus, these findings could respond to the need to valorize industrial melon by-products as raw materials for MCC obtention with potential applications as biodegradable materials.

Morphological, thermal and mechanical properties of wheat‐straw reinforced copper nanocomposite

AbstractThe work summarizes an innovative nanocomposite including synthesized copper nanoparticle (CuNP) impregnated wheat straw (WS) (the agronomic waste from an wheat plant) reinforced unsaturated polyester resin has been established. The addition of nanoparticles (NPs) increased the antifungal properties (~11%), durability (~9%), and strength (~39%) of the composites. Therefore, these nanoparticles have been synthesized from a copper chloride dihydrate precursor and they have been impregnated into wheat straw via cationization. This copper‐impregnated wheat straw (CuIWS) was formulated and employed to create a strong and long‐lasting nanocomposite with unsaturated polyester resin. Their morphological, mechanical, chemical, biodegradability (BD), and thermal properties were estimated and relationships were explicated systematically. Particularly, the tensile strength of polyester resin, crude and treated WS (cationized and copper‐impregnated) composites were 11.70, 14.20, 20.92, and 22.34 N/mm2 respectively. Therefore the reinforcement capability for crude, cationized and copper‐impregnated WS composites increased by ~22%, 75%, and 92% respectively. The residual ash was just about 16.23%, 12.04% and 6.56% for copper impregnated wheat straw composite (CuIWSC), Cationized wheat straw composite (CWSC) and untreated wheat straw composite (UTWSC) respectively point to the existence of ~4.1% Cu incorporated into the wheat straw which holds up the energy dispersive x‐ray (EDX) spectra of ~4.2% copper content. Thermogravimetric analysis (TGA) indicates that the nanocomposites are stable up to 325°C. These nanocomposites also show superlative crystallinity compared to other ones. Water uptake capacity followed typical Fickian diffusion law. The developed nanocomposites might be suitable for automobile and aircraft parts, furniture, and other indoor to outdoor applications.Highlights TS of the composites increased by increasing the WS filling up to 15%. The crystallinity increased after the addition of nanoparticles. The typical water uptake properties followed the Fickian diffusion rule. Incorporation of nanoparticles increased 11% antifungal properties. The developed nanocomposites are used for inside and outside applications.

High-performance biodegradable poly(vinyl alcohol)/starch composites via alkaline-regulated crystalline engineering

The increasing demand for environmentally-friendly products has led to a growing focus on the development of high-performance biodegradable materials. However, achieving a balance between mechanical strength, water resistance, and biodegradability remains a challenge. Herein, the successful preparation of exceptional biodegradable poly(vinyl alcohol) (PVA)/starch (ST) composites using alkaline-regulated crystalline engineering is reported. The findings demonstrate that the alkali promotes ST gelatinization while inhibiting its recrystallization, resulting in improved compatibility and good dispersion in the PVA matrix. In contrast, the alkali enhances the crystallization of PVA, thereby improving the composites' water resistance. The composites exhibit outstanding mechanical properties, with a strain at break of approximately 400 % and a toughness of 54 MJ/m3, surpassing most reported works. Even in high humidity and water environments, the composites maintain their mechanical strength, with a strength of 13 MPa after soaking in water for 1 d, significantly higher than films without the addition of alkali. Moreover, the composites exhibit excellent biodegradability, with a degradation rate exceeding 40 % after a 60-d natural soil burial test. The flame retardancy is also greatly enhanced, with a limiting oxygen index (LOI) of 30 %. This study offers a promising avenue for the development of high-performance biodegradable materials such as dip-coating fabric, fire retardant coating, and industrial packaging.

Current paradigms and future challenges in harnessing gut bacterial symbionts of insects for biodegradation of plastic wastes.

The ubiquitous incorporation of plastics into daily life, coupled with inefficient recycling practices, has resulted in the accumulation of millions of metric tons of plastic waste, that poses a serious threat to the Earth's sustainability. Plastic pollution, a global problem, disrupts the ecological balance and endangers various life forms. Efforts to combat plastic pollution are underway, with a promising avenue being biological degradation facilitated by certain insects and their symbiotic gut microorganisms, particularly bacteria. This review consolidates existing knowledge on plastic degradation by insects and their influence on gut microbiota. Additionally, it delves into the potential mechanisms employed by insects in symbiosis with gut bacteria, exploring the bioconversion of waste plastics into value-added biodegradable polymers through mineralization. These insights hold significant promise for the bio-upcycling of plastic waste, opening new horizons for future biomanufacturing of high-value chemicals from plastic-derived compounds. Finally, we weigh the pros and cons of future research endeavors related to the bioprospection of plastic-degrading bacteria from underexplored insect species. We also underscore the importance of bioengineering depolymerases with novel characteristics, aiming for their application in the remediation and valorization of waste plastics.

Microplastic contamination in the agri-food chain: The case of honeybees and beehive products

Microplastics, MPs, plastic fragments with a dimension lower than 5 mm, and microfibers, MFs, synthetic and natural/artificial fibrous fragments with a diameter lower than 50 μm, are ubiquitous pollutants identified in different environmental compartments. In this work the occurrence of MPs and MFs on honeybees, Apis mellifera, and beehive products was evaluated, using Fourier transform infrared microspectroscopy, confirming that MPs and MFs are widely present as air contaminants in all the apiary's areas (high and low urbanized areas) in Southern Italy.Results indicated that independently from the site, both honeybees and honey samples, are contaminated by MFs with non-natural color. The majority of MFs were of natural origin followed by artificial MFs and synthetic MFs. Moreover, the chemical composition of MFs isolated from honeybees reflect that used in synthetic fabrics, leading to the hypothesis that they are released from textile to air where are captured by bees. Results highlight that MFs represent a class of ubiquitous airborne anthropogenic pollutants. The identification of polytetrafluoroethylene, PTFE, MPs in honeybees confirm the recent findings that PTFE MPs are diffuse soil and air contaminants while the identification of polyethylene, PE, based MPs in honey samples, from low density urban sites, could be correlated to the large use of PE in agriculture. In the honey samples, also polycaprolactone, PCL, MPs were identified, mainly in high density urban sites, confirming that biodegradable materials could be further pollutants in the environments. The results indicate that honeybees are contaminated by MPs and MFs during their flights or picking up from the hive components, flowers, from other nest mates, from the clothes of the beekeeper, among others and some of them could be transferred to honey samples that could be also affected by soil contamination.

Polyvinyl alcohol-silk fibroin composite stents: A comprehensive investigation into biocompatibility and mechanical performance

Bioresorbable stents (BRS) are manufactured using biodegradable materials. As an alternative to those commonly used in commercial stents, this study explored the development of BRS using polyvinyl alcohol (PVA) and silk fibroin (SF). PVA is a promising material for the fabrication of BRS due to its biocompatibility and mechanical attributes, closely resembling those of aortic vessels. However, its application presents challenges in terms of cell adhesion and proliferation. SF has been extensively studied for its potential to enhance cell adhesion and proliferation, making it a promising biomaterial in the field of medical devices. SF was introduced by dissolving it in a PVA solution or by coating the hydrogel surface with a layer of SF. Initial tests revealed that overnight incubation of fetal bovine serum significantly increased cell viability in hydrogels. Viability assays confirmed that SF substantially improved cell viability compared to PVA alone. The method was extended to fabricate SF-coated stents, which demonstrated robust cell proliferation and improved performance compared to electrospun polycaprolactone scaffolds. In addition, the SF-coated stents displayed an increase in compressive strength, demonstrating improved biocompatibility and mechanical performance. Dynamic mechanical analysis evaluated the positive impact of SF on stent properties at physiological temperatures. The study revealed that PVA-SF stents offer a compromise between biocompatibility, mechanical strength, and elastic recovery, positioning them as a valuable alternative for cardiovascular stent applications. The dual benefits of enhanced biocompatibility and improved mechanical performance make SF-coated stents promising candidates for bioresorbable stent design.  

Application of Natural Functional Additives for Improving Bioactivity and Structure of Biopolymer-Based Films for Food Packaging: A Review.

The global trend towards conscious consumption plays an important role in consumer preferences regarding both the composition and quality of food and packaging materials, including sustainable ones. The development of biodegradable active packaging materials could reduce both the negative impact on the environment due to a decrease in the use of oil-based plastics and the amount of synthetic preservatives. This review discusses relevant functional additives for improving the bioactivity of biopolymer-based films. Addition of plant, microbial, animal and organic nanoparticles into bio-based films is discussed. Changes in mechanical, transparency, water and oxygen barrier properties are reviewed. Since microbial and oxidative deterioration are the main causes of food spoilage, antimicrobial and antioxidant properties of natural additives are discussed, including perspective ones for the development of biodegradable active packaging.

Characterization of cellulose nanocrystals from Zhombwe (Neorautanenia brachypus (harms) CA Sm.) bagasse.

Increased awareness of environmental pollution has changed focus to the use of biodegradable materials because they lack persistence in the environment. This article focused on the production of cellulose nanocrystals from Zhombwe, Neorautanenia brachypus (Harms) CA Sm. bagasse using steam explosion, alkaline treatment, bleaching, purification, and acid hydrolysis. The chemical composition after the treatments was determined using TAPPI standards. Further characterization was done using x-ray Diffraction (XRD), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The nanoscale dimensions and morphology of the extracted nanocrystals was determined through field emission scanning electron microscopy (FE-SEM). FTIR spectroscopy and DSC confirmed the removal of noncellulosic compounds. XRD revealed that N. brachypus bagasse contained cellulose type I, which partly endured morphological change to polymorph II after purification and hydrolysis. FE-SEM revealed elliptical to rod-shaped structures after acid hydrolysis, which had a mean length and width of 1103 nm and 597 nm respectively. TAPPI tests revealed that successive chemical treatments increased crystallinity by 29.7%, enriched cellulose content by 74.2%, reduced lignin content by 21.7%, and reduced hemicellulose to less than 1%. The semicrystalline nature of the material produced in our work is a promising candidate for swelling hydrogel applications in areas such as wound dressing, heavy metal removal, controlled drug delivery, agriculture, and sanitary products. Future studies may focus on surface modification of nanocrystals to improve their thermal stability and therefore expand their range for potential industrial applications.

A preliminary study of the temperature-responsive selective extraction performance of hydrogel derived from sulfobetaine methacrylate

BackgroundThe limited extraction selectivity caused by the single extraction selection mechanism of solid phase extraction (SPE) technology is one of the bottlenecks restricting its development. The development of environmentally sensitive materials provides a new opportunity to solve this problem. Based on this, we developed the sulfobetaine methacrylate hydrogel with abundant pore structure, a large number of adsorption sites and especially temperature responsiveness, and used as adsorbent for the extraction of pesticide residues in lychees. ResultsThe new hydrogel adsorbent was prepared by free radical copolymerization with sulfobetaine methacrylate as monomer, and used for the extraction of benzoylurea insecticides from lychees. Interestingly, the hydrogel showed an almost opposite temperature-selective extraction trend for different benzoylurea insecticides with similar structure and polarity, and opposite hydrophilicity, which may be caused by the temperature-sensitive and the special action site of the hydrogel, and the change of the diffusion of aqueous solution. In addition, the analysis method of three hydrophilic benzoylurea insecticides by sulfobetaine methacrylate hydrogel-SPE-HPLC was established. Under optimal conditions, the low limits of detection (0.030 μg L−1) and quantification (0.10 μg L−1), and the wide linear ranges (0.10–50.0 μg L−1) were achieved. Its application in lychee samples were also tested, and the satisfactory results were obtained, with the spiked recoveries from 80.79 % to 108.31 %. SignificanceThis was a great breakthrough in the selective extraction of similar targets. These properties, combined with low-cost, biodegradable raw materials and convenient, green synthesis method make the sulfobetaine methacrylate hydrogel a very promising solid phase adsorbent. Temperature-responsive selective mode can greatly enrich the selective extraction mechanism and promote its development and application in complex actual samples.

Research on the deformation behavior of pure zinc fabricated by forward extrusion and composite extrusion

Zinc and its alloys are biomedical biodegradable materials with broad application prospects. In this paper, commercially pure zinc bars were subjected to two different types of extrusion treatments, forward extrusion (FE) and composite extrusion (CE), at 120°C to study the changes in microstructure and mechanical properties. Compared to the virgin annealed state of pure zinc, the yield strength of CE decreased significantly from 73.67 MPa to 40.87 MPa, while the elongation of FE increased markedly from 9.23 % to 59 %. The anomalous phenomenon of decreasing strength and increasing ductility of extruded pure zinc is significantly different from that of extruded zinc and magnesium alloys. To investigate the reason for this anomaly, a detailed study of the microstructure evolution of pure zinc under three processing states was carried out using EBSD. Grain growth and texture weakening lead to a loss of strength, whereas the increase in ductility after extrusion is attributed to the activation of more slip systems.

Immobilization of EPS-modified sodium alginate microcapsule by co-polymerization for methylene blue dye adsorption and kinetics

Exopolysaccharide (EPS) was extracted from Bacillus sp. and purified by ethanol precipitation method. This work mainly examines the dye removal efficiency of biopolymer beads (sodium alginate microcapsules) encapsulated with EPS extracted from Bacillus sp. Encapsulation of EPS-modified sodium alginate microcapsule was done by co-polymerization method. Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) confirmed the co-polymerization of sodium alginate and EPS in the microcapsule. The adsorption capacity of the microcapsule was found to be 0.58682 mg/mL which can be attributed to the larger surface area and increased surface sites in the microcapsule adsorbent. Increased dye removal efficiency of 83% was observed for the microcapsule with 50 mg/mL of EPS. The results of the methylene blue dye adsorption experiment show that the adsorption fitted into the Freundlich isotherm and followed pseudo-second-order reaction with correlation coefficients of 0.939 and 0.9673, respectively. The prepared sodium alginate biopolymer is biodegradable, and numerous studies have documented its biodegradability. Overall, these results evidenced that dye adsorption from textile effluent can be easily managed using the biodegradable polymer materials. Hence, this immobilization approach can be effectively used in textile dye removal process.

Peach Gum Polysaccharide as an Additive for Thermoplastic Starch to Produce Water-Soluble Films

Thermoplastic starch (TPS) has gained considerable attention during the last few years in developing starch-based biodegradable food packaging materials or edible coatings due to its high availability and low cost. TPS is manufactured from starch plasticized with food-grade plasticizers, making it suitable for food contact applications. In addition, TPS is bio-based and biodegradable, which, from an environmental perspective, closes the circle of the circular economy. However, the industrial application of TPS is somewhat limited due to its poor mechanical performance and low water resistance. However, the low water resistance could increase the water sensitivity of TPS, which could be advantageous for coating application or food encapsulation. The present work aims to tailor the water sensitivity of TPS by adding peach gum polysaccharide to obtain water-soluble films. With this aim, peach gum polysaccharide (PGP) was extracted from peach gum (PG) using the thermal hydrolysis method. Films of TPS-PG and TPS-PGP were prepared and characterized by their water sensitivity and mechanical, microstructural, and thermal properties. The results show that PGP allows the obtaining of films with water sensitivities higher than 70% but also improves TPS elongation at break, making the material more suitable for application as film.

Biodegradable Ferroelectric Molecular Plastic Crystal HOCH2(CF2)7CH2OH Structurally Inspired by Polyvinylidene Fluoride.

Ferroelectric materials, traditionally comprising inorganic ceramics and polymers, are commonly used in medical implantable devices. However, their nondegradable nature often necessitates secondary surgeries for removal. In contrast, ferroelectric molecular crystals have the advantages of easy solution processing, lightweight, and good biocompatibility, which are promising candidates for transient (short-term) implantable devices. Despite these benefits, the discovered biodegradable ferroelectric materials remain limited due to the absence of efficient design strategies. Here, inspired by the polar structure of polyvinylidene fluoride (PVDF), a ferroelectric molecular crystal 1H,1H,9H,9H-perfluoro-1,9-nonanediol (PFND), which undergoes a cubic-to-monoclinic ferroelectric plastic phase transition at 339 K, is discovered. This transition is facilitated by a 2D hydrogen bond network formed through O-H···O interactions among the oriented PFND molecules, which is crucial for the manifestation of ferroelectric properties. In this sense, by reducing the number of -CF2- groups from ≈5000 in PVDF to seven in PFND, it is demonstrated that this ferroelectric compound only needs simple solution processing while maintaining excellent biosafety, biocompatibility, and biodegradability. This work illuminates the path toward the development of new biodegradable ferroelectric molecular crystals, offering promising avenues for biomedical applications.