Biodegradable Polymer Research Articles

Exploring the potential of insect gut symbionts for polyethylene biodegradation

The global issue of synthetic plastic pollution is escalating, necessitating innovative bioremediation approaches. Specific insect species have developed symbiotic associations with intestinal microorganisms that possess the ability to degrade resistant plant materials, such as lignocellulose. This is the first study to our knowledge to isolate, characterize, and compare microbial isolates (yeast and bacteria) extracted from the guts of wood-feeding termites (WFT) and lesser waxworms (LWW). The objective was to determine their efficacy in decomposing recalcitrant pollutants, such as low-density polyethylene (LDPE). The isolates belonged to numerous taxonomic groups, as determined by molecular identification; these groups included Bacillus, Citrobacter, Cellulosimicrobium, Rhodococcus, Pseudomonas, Candida, and others. A number of isolates had the potential to degrade LDPE. After 45 days of incubation, the polymer sheets lost 19.8 % of their weight for Bacillus cereus (LDPE-DB2) and 15.4 % of their weight for Candida guilliermondii (LDPE-DY6). Additionally, LDPE degraded by LDPE-DY6 showed a tensile strength loss of 50.3 % compared to that degraded by LDPE-DB2 (58.3 %). During this time, robust biofilm formation was observed on the surfaces of the polymers. Extracellular enzymes such as cutinases, aryl alcohol oxidases, and peroxidases, secreted by specific yeast and bacterial isolates, contribute to the degradation of plastic and recalcitrant biopolymers. Notably, the isolates from LWW demonstrated a greater advantage in this regard than those from WFT. Bacillus cereus, Pseudomonas aeruginosa, Candida guilliermondii, and Sterigmatomyces halophilus were found to have the highest activities in degrading LDPE among the studied WFT and LWW gut-derived symbionts. This study paves the way for a new opportunity to enhance polyethylene degradation by insect gut bacteria and yeasts that may facilitate biotechnological applications for plastic waste remediation.

3D Printed PLA Porous Scaffolds with Engineered Cell Size and Porosity Promote the Effectiveness of the Kelvin Model for Bone Tissue Engineering

AbstractIn this study, the aim is to investigate the effect of engineering the cell size and porosity of 3D‐printed poly lactic acid (PLA) porous scaffolds from the Kelvin model for bone tissue engineering applications. The Kelvin model is used as a bone tissue scaffold with different cell sizes and porosities. PLA, as a biodegradable and biocompatible polymer, is used to fabricate these scaffolds using the FDM technique. A compression test is used to evaluate the mechanical properties of scaffolds. The MTT assay has been used to investigate cell viability. For osteogenic differentiation studies, ALP activity and ARS assays are used. Increasing the porosity reduces the mechanical properties of the scaffold. While increasing the cell size at constant porosity increases the Young's modulus and yield stress in the samples, it is also observed that, in high porosities, the increase in cell size weakens the mechanical properties. Also, Kelvin model scaffolds help the proliferation and osteogenic differentiation of cells and have no toxic effect. It is demonstrated that this approach promotes the effectiveness of the Kelvin architecture for bone tissue engineering. As a result, designing the most suitable model based on cell size and porosity for the treatment process in the targeted area could be promising.

Development of Eco‐Friendly Chitosan‐Dextran Polyblend Electrolyte for Enhanced Performance in Primary Magnesium Batteries

The potential of next‐generation batteries lies in solid biodegradable polymer electrolytes. This research delves into a solid blend polymer electrolyte (SBPE) for magnesium conduction, utilizing a chitosan‐dextran blend matrix doped with magnesium perchlorate (Mg(ClO4)2) salt. The electrolyte films are prepared using a conventional solution casting technique. Through techniques like X‐ray diffraction and Fourier transform infrared spectroscopy, the successful incorporation of Mg(ClO4)2 into the blend matrix is confirmed. Notably, the SBPE containing 30 wt% of Mg(ClO4)2 demonstrates the highest ionic conductivity of 6.99 × 10−4 S cm−1 and a prominent ionic transference number of 0.84. Thermogravimetric analysis is carried out to study thermal stability. Differential scanning calorimetry analysis of the electrolyte systems gives insight into their thermal properties. Additionally, it showcases favorable electrochemical stability of 2.66 V. The oxidation and reduction peaks are observed in the cyclic voltammetry curve of the highest conducting sample. Furthermore, the discharge performance of Mg/(CS + DN + Mg(ClO4)2)/cathode cells is explored with varied cathode materials, illustrating the SBPE's potential for magnesium‐ion batteries. This study unveils a sustainable, biodegradable, and economical electrolyte solution for advanced energy storage systems.

Highly Selective O-Phenylene Bisurea Catalysts for ROP: Stabilization of Oxyanion Transition State by a Semiflexible Hydrogen Bond Pocket.

Organocatalyzed ring-opening polymerization (ROP) is a versatile technique for synthesizing biodegradable polymers, including polyesters and polycarbonates. We introduce o-phenylene bisurea (OPBU) (di)anions as a novel class of organocatalysts that are fast, easily tunable, mildly basic, and exceptionally selective. These catalysts surpass previous generations, such as thiourea, urea, and TBD, in selectivity (kp/ktr) by 8 to 120 times. OPBU catalysts facilitate the ROP of various monomers, achieving high conversions (>95%) in seconds to minutes, producing polymers with precise molecular weights and very low dispersities (Đ ≈ 1.01). This performance nearly matches the ideal distribution expected from living polymerization (Poisson distribution). Density functional theory (DFT) calculations reveal that the catalysts stabilize the oxyanion transition state via a hydrogen bond pocket similar to the "oxyanion hole" in enzymatic catalysis. Both experimental and theoretical analyses highlight the critical role of the semirigid o-phenylene linker in creating a hydrogen bond pocket that is tight yet flexible enough to accommodate the oxyanion transition state effectively. These new insights have provided a new class of organic catalysts whose accessibility, moderate basicity, excellent solubility, and unparalleled selectivity and tunability open up new opportunities for controlled polymer synthesis.

Investigating the Effect of Carbon Nanomaterials Reinforcing Poly(ε-Caprolactone) Printed Scaffolds for Bone Repair Applications.

Scaffolds, three-dimensional (3D) substrates providing appropriate mechanical support and biological environments for new tissue formation, are the most common approaches in tissue engineering. To improve scaffold properties such as mechanical properties, surface characteristics, biocompatibility and biodegradability, different types of fillers have been used reinforcing biocompatible and biodegradable polymers. This paper investigates and compares the mechanical and biological behaviors of 3D printed poly(ε-caprolactone) scaffolds reinforced with graphene (G) and graphene oxide (GO) at different concentrations. Results show that contrary to G which improves mechanical properties and enhances cell attachment and proliferation, GO seems to show some cytotoxicity, particular at high contents.

Materials based on biodegradable polymers chitosan/gelatin: a review of potential applications.

Increased mass manufacturing and the pervasive use of plastics in many facets of daily life have had detrimental effects on the environment. As a result, these worries heighten the possibility of climate change due to the carbon dioxide emissions from burning conventional, non-biodegradable polymers. Accordingly, biodegradable gelatin and chitosan polymers are being created as a sustainable substitute for non-biodegradable polymeric materials in various applications. Chitosan is the only naturally occurring cationic alkaline polysaccharide, a well-known edible polymer derived from chitin. The biological activities of chitosan, such as its antioxidant, anticancer, and antimicrobial qualities, have recently piqued the interest of researchers. Similarly, gelatin is a naturally occurring polymer derived from the hydrolytic breakdown of collagen protein and offers various medicinal advantages owing to its unique amino acid composition. In this review, we present an overview of recent studies focusing on applying chitosan and gelatin polymers in various fields. These include using gelatin and chitosan as food packaging, antioxidants and antimicrobial properties, properties encapsulating biologically active substances, tissue engineering, microencapsulation technology, water treatment, and drug delivery. This review emphasizes the significance of investigating sustainable options for non-biodegradable plastics. It showcases the diverse uses of gelatin and chitosan polymers in tackling environmental issues and driving progress across different industries.

Reactivity of N terminal histidine of peptides towards excipients/impurity of excipients: A case study of liraglutide excipient compatibility study

The selection of quality excipients is a crucial step in peptide formulation development. Apart from excipient incompatibility, process-related impurities or degradants of an excipient can interact with peptide-active pharmaceutical ingredients, forming the interaction products. The formaldehyde has been reported as an impurity of excipient in polyethylene glycol, glycerol, magnesium stearate, microcrystalline cellulose, mannitol, etc. The peptide contains various amino acids such as histidine, lysine, and arginine having free amine groups. These amine groups act as strong nucleophile and can increase the reactivity of peptides. PLGA is the most widely used biodegradable polymer in sustained-release formulations. The hydrolysis of PLGA generates glycolic acid and lactic acid impurities, which can form the interaction product with the amines of peptides. During the formulation development of Liraglutide, we have found few interaction products. The systematic characterization and mechanistic understanding of these interaction products lead us to imidazopyrimidine, glycolyl, and lactolyl moieties. These interaction products have been characterized thoroughly with the use of LC-HRMS, MS/MS, and hydrogen-deuterium exchange mass studies. The study revealed that the reactivity of N-terminal histidine must be considered for formulation development. Moreover, the quality of excipients with respect to presence of impurities must be considered as critical material attributes.

A Kinetic-Based Criterion for Polymer Biodegradability Applicable to Both Accelerated and Standard Long-Term Composting Biodegradation Tests

A Kinetic-Based Criterion for Polymer Biodegradability Applicable to Both Accelerated and Standard Long-Term Composting Biodegradation Tests

Experimental and numerical analysis of natural fillers loaded and E-glass reinforced epoxy sandwich composites

Natural fibers play a crucial role in sandwich composites due to their biodegradability, ease of manufacturing, and ability to reduce pollution. The research aims to develop new biodegradable polymer composites using pine tree leaves (PTL) fillers loaded with epoxy through hand layup technique with different wt. % of PTL fillers. The molded composites were characterized to analyze the crystal size and plane orientations, surface morphology, thermal resistance, and presence of elemental compositions in the PTL filler-loaded epoxy composites through X-ray diffraction (XRD), Field emission scanning electron microscope (FESEM), Energy dispersive analysis (EDX), Differential scanning calorimetry (DSC), and Thermogravimetric analysis (TGA). The 40 wt % of PTL epoxy composites showed a maximum tensile strength of 32 ± 0.5 MPa, a compressive strength of 15 ± 0.5 MPa, a flexural strength of 55 ± 0.5 MPa, and a Shore D hardness of 73 ± 0.5 SHN. The mechanical strength of 40 wt% PTL fillers loaded epoxy composite was enhanced by adding a single and double layer of E-glass fiber on the bottom and top of the PTL fillers loaded epoxy composite, achieving a maximum tensile strength of 76 ± 0.5 MPa. The 40 wt% PTL fillers loaded double E-glass fiber on the bottom and top of the PTL fillers loaded epoxy sandwich composite attained the maximum tensile strength of 156 ± 0.5 MPa, compressive strength of 29 ± 0.5 MPa, flexural strength of 220 ± 0.5 MPa, and Shore D hardness of 79 ± 0.5 SHN. The PTL fillers loaded and reinforced double E-glass fiber epoxy sandwich composite would be used in low-strength structural applications.

The effect of polylactic acid-based blend films modified with various biodegradable polymers on the preservation of strawberries

Polylactic acid (PLA) has garnered much attention in the field of fruit and vegetable packaging. Despite its poor flexibility and water resistance, PLA film faces challenges in being used for strawberry storage and freshness preservation due to its inability to maintain flavor quality. In this study, a series of PLA-based modified films was produced by melt blending and extrusion cast processing with PLA as the main component, along with flexible biodegradable polyesters or polycarbonate as the secondary component. First, five different biodegradable polymers were used to investigate the effect of the flexibility and barrier properties of different dispersed phases on the morphology, mechanical properties, and water vapor barrier of PLA-based blend films. Next, the impact on the freshness of strawberries was assessed through examination of fruit color and weight, as well as the levels of O2 and CO2 in the packaging bags. The results showed that the size of the dispersed phase and interfacial bonding with PLA were the key factors determining the mechanical and barrier properties of the blend films. The PLA-polycaprolactone (PCL) blend showed the best compatibility among them, with PCL having the smallest dispersion size (D=0.58 µm), higher toughness than the other four PLA blends, and greater enhancement of PLA. Additionally, it exhibited a similar rate of quality loss in strawberry preservation compared to commercial PE. As a result, the color and luster were more completely preserved. The results of this study may help the future development of degradable plastics, to reduce environmental pollution.

Optimizing Polyhydroxyalkanoate production using a novel Bacillus paranthracis isolate: A response surface methodology approach

Microorganisms have emerged as promising resources for producing economical and sustainable bioproducts like Polyhydroxyalkanoate (PHA), a biodegradable polymer that can replace synthetic plastics. In this study, we screened a novel isolate, Bacillus paranthracis RSKS-3 strain, to produce PHA from sewage water, identifying it using Whole Genome Sequence. This study represents the first report on optimizing PHA production using B. paranthracis RSKS-3, employing Design Expert 12.0 software. Our findings reveal that four factors (temperature, inoculum size, potassium dihydrogen phosphate, and magnesium sulfate) significantly affect PHA production in the Plackett-Burman design experiment. Through Response Surface Methodology, we optimized PHA production to 0.647 g/L with specific values for potassium dihydrogen phosphate (0.55 %), inoculum size (3 %), magnesium sulfate (0.055 %), and a temperature of 35 °C, in agreement with the predicted value of 0.630 g/L. This optimization resulted in a substantial 13.29-fold increase in PHA production from 0.34 g/L to 4.52 g/L, underscoring the promising role of B. paranthracis RSKS-3 in eco-friendly PHA production and advancing sustainable bioproduct development.

Experimental and Computational Study of Modified Biopolymer Xanthan Gum with Synthetic Vinyl Monomers for Enhanced Oil Recovery

AbstractUtilizing xanthan gum, a biodegradable polymer, in enhanced oil recovery (EOR) is imperative wherever there is a need for innovation in oil production that is both cost-effective and environmentally friendly. Xanthan, chosen for its natural sourcing, availability, controllability, eco-friendliness, and biodegradability, proves resilient against harsh reservoir conditions owing to its rigid structure and elongated polysaccharide chains. This study investigates two modified xanthan gum composites, achieved by grafting with synthetic vinyl monomers through emulsified polymerization. Spectroscopic characterization using FTIR and 1H-NMR, along with surface morphology analysis via atomic force microscopy (AFM) and thermal behavior screening through TGA analysis, elucidates the properties of these modified composites. Rheological behavior under reservoir conditions, including stress scanning and viscosity/shear rate dependency, was evaluated. Material modeling with the Materials Studio program simulated the equilibrium adsorption of xanthan and modified biopolymer chains on SiO2-quartz crystal to assess wettability alteration. Simulation results indicate that XG-g-AM, MMA&TEVS exhibit greater stability and surface coverage with more negative electrostatic energies compared to XG and XG-g-AM&MMA. The laboratory runs on a sandstone-packed model to identify the disclosed XG-g-AM&MMA and XG-g-AM, MMA&TEVS biopolymers as promising EOR candidates and wettability modifiers in challenging sandstone reservoirs, as per experimental outcomes.

Small Particles, Big Potential: Polymeric Nanoparticles for Drug Delivery in Parkinson's Disease.

Despite the availability of a number of efficacious treatments for Parkinson's disease, their limitations and drawbacks, particularly related to low brain bioavailability and associated side effects, emphasize the need for alternative and more effective therapeutic approaches. Nanomedicine, the application of nanotechnology in medicine, has received considerable interest in recent years as a method of effectively delivering potentially therapeutic molecules to the brain. In particular, polymeric nanoparticles, constructed from biodegradable polymer, have shown great promise in enhancing therapeutic efficacy, reducing toxicity, and ensuring targeted delivery. However, their clinical translation remains a considerable challenge. This article reviews recent in vitro and in vivo studies using polymeric nanoparticles as drug and gene delivery systems for Parkinson's disease with their challenges and future directions. We are also particularly interested in the technical properties, mechanism, drugs release patterns, and delivery strategies to overcome the blood-brain barrier. © 2024 International Parkinson and Movement Disorder Society.

Key Points of Design and Risk Analysis in Production for Biodegradable Heart Occluder

Biodegradable heart occluder uses a biodegradable medical polymer material to replace or completely replace the metal material. After completing the repair function of the heart defect, the device is gradually degraded and safely absorbed by the human tissue. So it may minimize the risk of long-term complications that traditional metal heart occluder causing in the body after implantation. Based on the quality management concept of the entire lifecycle of medical device, this article briefly introduces design and development, as well as the product realization of biodegradable heart occluder. It analyzes the main risk points in design and production, and corresponding suggestions have been put forward. These suggestions are combined with the medical device good manufacturing practice and the appendix of implantable medical equipment to provide a reference for regulators and industry professionals.

Electrohydrodynamic Printing of Biodegradable PLGA Micro‐Patterns on 3D Polymer Structures

AbstractBiodegradable polymers such as polylactic‐co‐glycolic acids (PLGA) are used for various implantable devices such as tissue scaffolds, drug delivery devices, and biosensors in different forms. However, high‐resolution patterning of biodegradable polymers on implantable devices has not been explored much yet. While electrohydrodynamic printing (EHD) can achieve high‐resolution printing compared to other printing methods, EHD printing of PLGA solutions is rarely attempted due to unstable printing. Such printing instability originates from the volatile nature of PLGA inks, and it causes nozzle clogging or change of ink conditions during printing. Here, PLGA ink formulation and a voltage input profile are studied for stable and high‐resolution EHD printing. Addition of glycerol at an optimal ratio as well as the control of voltage pulse shape strongly influenced both the stability and resolution of EHD printing of PLGA patterns. With the optimized inks and voltage inputs, stable printing of PLGA micropatterns down to 5 µm is achieved on both conductive and insulating surfaces for controlled drug release. Furthermore, use of a ring type electrode allows for EHD printing of PLGA micropatterns on 3D surfaces of PLLA tubes and stent struts.

Biodegradable magnesium and zinc composite microspheres with synergistic osteogenic effect for enhanced bone regeneration

Biodegradable polymer microspheres in bone tissue engineering have become appealing as their non-invasive advantages in irregular damage bone repair. However, current microspheres used in BTE still lack sufficient osteogenic capacity to induce effective bone regeneration. In this study, we developed osteogenic composite microspheres concurrently loaded with magnesium oxide (MgO) and zinc oxide (ZnO), both of which are osteogenic active substances, using a facile and scalable emulsification method. The osteogenic composite microspheres exhibited a sequential yet complementary release profile characterized by a rapid release of Mg2+ and a gradual release of Zn2+ in a physiological environment, thereby maintaining the concentration of bioactive ions at a sustained high level. As a result, the combination of Mg2+ and Zn2+ in the composite microspheres led to a synergistic enhancement in biomimetic mineralization and the upregulation in the expression of osteogenic-related genes and proteins at the cellular level. Through a critical-sized calvarial rate defect model, the osteogenic composite microspheres were demonstrated to have strong osteogenic ability to promote new bone formation via ultrasonic imaging, histological and immunohistochemical evaluations. In sum, these osteogenic composite microspheres as microcarriers of Mg2+ and Zn2+ have great potential in the delivery of therapeutic ions for treating bone defects.

Comparative study of N-vinyl pyrrolidone and cyclic ketene acetal copolymer degradation under alkaline, enzymatic, or wastewater conditions

The (bio)degradability of cyclic ketene acetal (CKA)-containing polymers is dependent on the polymer structure and degradation conditions. Copolymers of N-vinyl pyrrolidone (NVP), with different CKA comonomers and architectures, were subjected to (bio)degradation under alkaline, enzymatic and wastewater conditions. Grafting CKA-co-NVP moieties onto a poly(ethylene oxide) (PEO) backbone promoted the enzymatic hydrolysis of CKA esters and improved the overall polymer biodegradability. Limited biodegradation was observed for poly(CKA-co-NVP) in the presence of wastewater sludge during an industrial biodegradability test under OECD 301F guidelines. Under less stringent test conditions poly(CKA-co-NVP) achieves small, yet non-negligible biodegradation. Structural analysis of the degradation products shed light into the degradation mechanisms, revealing CKA ester hydrolysis in all cases, while in presence of wastewater sludge, additional CKA end-group oxidation was clearly observed. However, effective amide hydrolysis or pyrrolidone unit biodegradation was not detected, with pyrrolidone-containing segments persisting through the biodegradation test.

Investigation of physical properties of microalgae‐pectin‐based bio‐composite with addition of pine needle for environmental application

AbstractPolymers and biopolymers have gained significance due to their applicability and use in industry reducing the negative impact of polymers based on petroleum. A possible solution for the conventional polymer's biodegradability is bio‐composites, which contain natural fibers or aggregates such as microalgae. Hence, microalgae biomass has a promising application to address the biodegradability issue of conventional polymers. In this study, Chlorella vulgaris biomass was mixed with pectin for control samples with glycerol as plasticizer. The mixture microalgae‐pectin‐glycerol, and the addition of pine needles was used to evaluate the tensile strength and compression of the bio‐composite. This bio‐composite showed a higher Young's modulus of 95.66 MPa for blend C2 and a higher strength with 20% of pectin concentration in the mixture. Additionally, the pine needle addition did not have a low effect between the compression results. On the other hand, analysis on elasticity showed that the full recovery of the bio‐composite happened after 10 min in all the blends. Also, the bio‐composite showed a slow release of nitrogen and phosphorous after 5 days of water addition, indicating an effective slow release for blend B for both nutrients. Water uptake capacity and loss of soluble material was studied using pullulan, chitosan, and cetyltrimethylammonium bromide additives. These cationic surfactants demonstrated their potential for reduction of water solubility of the bio‐composite.

Digital Light Processing Resins with Programmable Shape Memory for Biomedical Applications.

The creation of biodegradable and biocompatible shape memory polymers amenable to biofabrication techniques remains a challenge. The ability to create shape-changing biodegradable objects that are triggered at body temperature opens up possibilities in tissue engineering, minimally invasive surgery, and actuating bioimplants. Merging Digital Light Processing (DLP) printing with shape memory polymers brings us closer to new smart biomedical outcomes. Previously, we developed a poly(caprolactone-co-trimethylenecarbonate) urethane acrylate resin for the DLP fabrication of biodegradable 3D objects. In further studies, we observed that some of these resins possessed shape memory properties, triggered by body temperature (37 °C). In this subsequent study, we explored the shape memory properties and tunability of this resin family via changes in copolymer composition, molecular weight, and identity of the acrylate end-capping unit. We found that we could create a library of shape memory resins, amenable to DLP printing, which allowed the creation of shape-actuating structures with some tunability over the speed of shape memory and mechanical properties. We observed that increased mole fraction of caprolactone in the copolymer and increased molecular weight of the polymer led to a decrease in speed of the shape memory switch. Furthermore, we observed a trade-off between the composition and the end-capping moiety on the mechanical properties of the polymers. These polymeric resins were able to be processed into shapes that were able to perform work, including the release of cargo and grabbing/lifting of an object. This platform now provides a way to tune the speed and mechanical properties of a shape memory DLP object created from common and scalable polymerization techniques. This work ultimately provides a new platform to develop customizable and biodegradable devices capable of actuating and delivery devices for numerous biomedical applications.

New degradable PCL/thiazole composite for biological applications; characterization and spectroscopic studies

Polycaprolactone (PCL) is a biodegradable polymer widely used for medical implants and devices due to its biocompatibility, processability, and tunable degradation behavior. This study explores the incorporation of a thiazole-based antimicrobial compound into PCL at varying concentrations to develop new composite materials with both biodegradability and antibacterial function. Samples were solution cast and characterized using techniques like X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, UV–vis spectroscopy, antibacterial assays, and computational density functional theory (DFT) modeling. XRD showed up to 54 % crystallinity at the highest 0.03 g dye loading, indicating the thiazole impacted ordering and lamellar packing. FTIR and DFT calculations demonstrated multiple possible intermolecular bonding modes between the compounds. UV–vis spectra revealed the superimposed absorptions of the PCL matrix and emergent thiazole chromophore. Antibacterial tests exhibited marked growth inhibition of both gram-positive and gram-negative bacteria proportional to the thiazole concentration. The customizable PCL-thiazole blends offer biocompatible materials with functional antibacterial behavior for specialized applications in biomedicine.