Biodegradable Polymeric Materials Research Articles

Some Aspects of Using Polymer Materials in Electrical Engineering

AbstractPolymer materials are an integral part of our life, and in recent decades they have found an increasing number of applications in electrical engineering. They are used not only as insulators, protective materials and flexible substrates, but also as electrically conductive materials for instance in batteries, capacitors, sensing systems and photovoltaics. These materials are light, low-cost, and easy to manufacture. Their properties can be tailored according to the demands of the particular application. The drawback of polymeric materials, especially petroleum-based plastics, is their impact on the environment due to difficult and/or costly recycling. A possible solution to this problem could be replacing conventional plastics with biodegradable polymer materials obtained from nature like proteins and polysaccharides or synthesised from biological products like poly(lactic acid) or from petroleum like poly(butyleneadipate-co terephthalate). This paper provides an overview of the most commonly used conventional polymeric materials and their potential biodegradable substitutes used in electrotechnical applications.

Enhancing the degradation properties of poly (trimethylene carbonate) by simple and effective copolymerization of trimethylene carbonate with p-dioxanone

Biodegradable polymeric materials play an important role in the field of clinical science. However, the advancement of non-toxic polymeric materials with excellent performance and controlled degradation properties remains a challenge. Herein, a series of biodegradable and bioresorbable poly (trimethylene carbonate-co-p-dioxanone) [P(TMC-co-PDO), PTD] copolymers were prepared as polymer materials through random copolymerization of trimethylene carbonate (TMC) and p-dioxanone (PDO). In vitro enzymatic degradation mediated by aspergillus oryzae lipase showed that PTD polymer materials exhibit a controllable degradation rate and well form-stability by regulating the PDO content in the composition. The relationship between the chemical structure and the final performance of the PTD copolymers at the molecular level was studied in detail. The results indicate that the introduction of PDO significantly enhances the form-stability of low molecular weight PTMC and significantly accelerates its degradation rate. This initiative provides a feasible strategy for the modification and extensive application of low molecular weight PTMC. It is envisioned that this PTD is a promising candidate for clinical polymer implantable drug delivery systems.

Bio-Based and Biodegradable Polymeric Materials for a Circular Economy.

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.

Targeted PHA Microsphere-Loaded Triple-Drug System with Sustained Drug Release for Synergistic Chemotherapy and Gene Therapy.

The combination of paclitaxel (PTX) with other chemotherapy drugs (e.g., gemcitabine, GEM) or genetic drugs (e.g., siRNA) has been shown to enhance therapeutic efficacy against tumors, reduce individual drug dosages, and prevent drug resistance associated with single-drug treatments. However, the varying solubility of chemotherapy drugs and genetic drugs presents a challenge in co-delivering these agents. In this study, nanoparticles loaded with PTX were prepared using the biodegradable polymer material poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx). These nanoparticles were surface-modified with target proteins (Affibody molecules) and RALA cationic peptides to create core-shell structured microspheres with targeted and cationic functionalization. A three-drug co-delivery system (PTX@PHBHHx-ARP/siRNAGEM) were developed by electrostatically adsorbing siRNA chains containing GEM onto the microsphere surface. The encapsulation efficiency of PTX in the nanodrug was found to be 81.02%, with a drug loading of 5.09%. The chemogene adsorption capacity of siRNAGEM was determined to be 97.3%. Morphological and size characterization of the nanodrug revealed that PTX@PHBHHx-ARP/siRNAGEM is a rough-surfaced microsphere with a particle size of approximately 150 nm. This nanodrug exhibited targeting capabilities toward BT474 cells with HER2 overexpression while showing limited targeting ability toward MCF-7 cells with low HER2 expression. Results from the MTT assay demonstrated that PTX@PHBHHx-ARP/siRNAGEM exhibits high cytotoxicity and excellent combination therapy efficacy compared to physically mixed PTX/GEM/siRNA. Additionally, Western blot analysis confirmed that siRNA-mediated reduction of Bcl-2 expression significantly enhanced cell apoptosis mediated by PTX or GEM in tumor cells, thereby increasing cell sensitivity to PTX and GEM. This study presents a novel targeted nanosystem for the co-delivery of chemotherapy drugs and genetic drugs.

Spray-dried cyclophosphamide-loaded polyhydroxyalkanoate microparticles: design and characterization

Background and purpose: Cyclophosphamide (CP) is a widely used antitumor and immunosuppressive drug, but it is highly cytotoxic and has carcinogenic and teratogenic potential. To reduce adverse effects of CP therapy and the frequency of its administration, the microencapsulation of CP into biodegradable polymeric matrices can be performed. However, according to the literature, only a few polymers were found suitable to encapsulate CP and achieve its’ sustained release. Experimental approach: In this research, spray-dried cyclophosphamide-loaded poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) microparticles were prepared and characterized in terms of their average hydrodynamic diameter, polydispersity index, surface morphology, zeta potential, encapsulation efficiency, drug loading, thermal properties and cytotoxicity against 3T3 cells. Key results: The obtained CP-loaded microparticles had a regular spherical shape, uniform size distribution with an average diameter of 4.21±0.04 μm and zeta potential of -34.2±0.2 mV. The encap­sulation of cyclophosphamide into the PHBV matrix led to a decrease in melting and degradation tempe­ratures and an increase in diameter, glass transition and cold crystallization temperatures compared to blank microparticles. Moreover, microencapsulation of cyclophosphamide lowered its cytotoxicity compared to the pure drug: the number of dead cells in the culture decreased by 28 %, while their metabolic activity increased by 20 %. The cumulative in vitro drug release studies showed a gradual release of CP up to 18 days, so the obtained microparticle formulation can be used as a sustained-release cyclophosphamide delivery system. Conclusion: In this research, a novel cyclophosphamide-loaded platform based on PHBV micro­particles was established and characterized. Overall, this study offers promising prospects for cancer therapy in the future.

Eco‐Friendly, Recyclable Supramolecular Inks Incorporating Multi‐Walled Carbon Nanotubes

AbstractIn contemporary society, with its emphasis on environmental stewardship, the development of “green” (eco‐friendly) inks is of paramount importance. These inks are utilized across a broad spectrum of applications, ranging from the printing of packaging material to the 3D printing of functional components. This study explores the synthesis of eco‐friendly, biodegradable supramolecular polymer materials predicated on ureido‐pyrimidinone (UPy). The subsequent formulation of these materials into functional inks is achieved by the incorporation of multi‐walled carbon nanotubes (MWCNTs). These resultant inks exhibit outstanding photothermal conversion properties, robust electrical conductivity, intrinsic self‐repair capabilities, and superior writability. Moreover, this research demonstrates the recyclability of MWCNTs within the ink matrix, exhibiting a recovery efficiency of ≈90%. Such a high recovery rate offers a novel perspective on the sustainable reuse of conductive fillers in polymer‐based inks.

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.

Screening and safety assessment of migrating substances released from biodegradable packaging materials into milk

Biodegradable polymeric packaging materials are being studied for their potential to replace traditional petroleum-based ones for food contact applications. However, potential safety concerns associated with the utilization of these biodegradable polymers have not been studied in detail. In this study, we conducted non-targeted screening and migration studies on two types of biodegradable milk packaging materials, which were composed of a mixture of polylactic acid (PLA), poly(butylene adipate-co-terephthalate) (PBAT), polybutylene succinate (PBS), and cellulose. In particular, we monitored the transfer of migrating substances from the packaging materials into a food simulant (50% ethanol) and into a real food (fat free and whole milk). A screening study identified seven compounds in the biodegradable packaging bags, including degradation products of antioxidants, lubricants, and plasticizers such as triethylene glycol, diethyl succinate, glycerin, 2,4-di-tert-butylphenol, and 13-docosenamide were identified. The migration studies indicated that the types and amounts of migrating substances transferred into the real food were appreciably lower than those transferred into the food simulant. Most of the detected migrating substances were below the levels established in the European Union regulations. However, the triethylene glycol levels (68-144 mg/kg) in the food simulant exceeded the limits (60 mg/kg) for one of the packaging materials tested. A safety assessment suggested that there is a low level of safety risk associated with one of the biodegradable packaging materials. This study provides important insights into the safety of biodegradable packaging materials that might be used in the food industry.

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.

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.

Genetic Algorithms for Optimized Selection of Biodegradable Polymers in Sustainable Manufacturing Processes

Sustainable Manufacturing Practices (SMP), particularly in the selection of materials, have become essential due to environmental issues caused by the expansion of industry. Compared to conventional polymers, biodegradable Polymer Materials (BPM) are growing more commonly as an approach to reducing trash pollution. Suitable materials can be challenging due to numerous considerations, like ecological impact, expenditure, and material properties. When addressing sophisticated trade-offs, standard approaches drop. To compete with such challenges, employing Genetic Algorithms (GA) may be more successful, as they have their foundation in the basic concepts of biological development and the natural selection process. With a focus on BPM, this study provides a GA model for optimal packaging substance selection. Out of the four algorithms for computation used for practical testing—PSO, ACO, and SA—the GA model is the most effective. The findings demonstrate that GA can be used to enhance SMP and performs well in enormous search spaces that contain numerous different combinations of materials.

Application Analysis of Biodegradable Polymer Materials in Food Packaging

With the rapid development of biotechnology, the society pays more attention than in the past to the production and development of environmental protection. Choosing materials has always been a more important part of environmental protection work, among them, the degradable polymer materials are also professional research topics, it can be self-degradation under certain conditions, with far-reaching environmental protection value and social significance. Food packaging is a kind of carrier that plays a protective role in packaging, preservation and sales of food, the application of degradable polymer materials in food packaging can play a positive role in environmental protection, reducing environmental pollution and building an ecological society. In this paper, the active application of biodegradable polymer materials for food packaging is elaborated, hoping to provide theoretical reference.

Significantly enhanced crystallization of poly(L‐lactide) by incorporation of poly(D‐lactide) grafted cellulose nanocrystals

AbstractPoly(L‐lactic acid) (PLLA), as a green, biodegradable polymer material, has garnered considerable attention due to its ease of processing and exceptional properties. However, the inherent slow crystallization rate and brittleness of PLLA substantially restrict its extensive applications across various domains. In present work, PLLA and poly(D‐lactide) (PDLA)‐modified cellulose nanocrystals (CNCs), referred as CNC‐g‐L and CNC‐g‐D, are serving as nano‐fillers to enhance the crystallization rate of PLLA. Our findings demonstrate that both nano‐fillers could enhance the crystallization rate of PLLA, but the CNC‐g‐D shows a more efficient nucleation agent compared with its counterpart, CNC‐g‐L. Isothermal crystallization analysis indicates that CNC‐g‐D substantially increases nucleation density of PLLA, with pronounced crystallization at an elevated temperature of 155°C as confirmed by differential scanning calorimetry (DSC) and polarized optical microscopy (POM). Wide‐angle x‐ray diffraction (WAXD) analysis shows the preformation of stereocomplex crystals on the CNC‐g‐D surface may result in a fast crystallization rate. Meanwhile, after incorporation of different nano‐fillers, the toughness property of PLLA has also been significantly enhanced. Our result has shown the CNC‐g‐D could serve as an efficient nucleation agent toward PLLA and also facilitate to aiding in establishing comprehensive structure–property relationships of polymer materials.

Diffusion of curcumin in PLGA-based carriers for drug delivery: a molecular dynamics study

Context:The rapid growth and diversification of drug delivery systems have been significantly supported by advancements in micro- and nano-technologies, alongside the adoption of biodegradable polymeric materials like poly(lactic-co-glycolic acid) (PLGA) as microcarriers. These developments aim to reduce toxicity and enhance target specificity in drug delivery. The use of in silico methods, particularly molecular dynamics (MD) simulations, has emerged as a pivotal tool for predicting the dynamics of species within these systems. This approach aids in investigating drug delivery mechanisms, thereby reducing the costs associated with design and prototyping. In this study, we focus on elucidating the diffusion mechanisms in curcumin-loaded PLGA particles, which are critical for optimizing drug release and efficacy in therapeutic applications.Methods:We utilized MD to explore the diffusion behavior of curcumin in PLGA drug delivery systems. The simulations, executed with GROMACS, modeled curcumin molecules in a representative volume element of PLGA chains and water, referencing molecular structures from the Protein Data Bank and employing the CHARMM force field. We generated PLGA chains of varying lengths using the Polymer Modeler tool and arranged them in a bulk-like environment with Packmol. The simulation protocol included steps for energy minimization, T and p equilibration, and calculation of the isotropic diffusion coefficient from the mean square displacement. The Taguchi method was applied to assess the effects of hydration level, PLGA chain length, and density on diffusion.Results:Our results provide insight into the influence of PLGA chain length, hydration level, and polymer density on the diffusion coefficient of curcumin, offering a mechanistic understanding for the design of efficient drug delivery systems. The sensitivity analysis obtained through the Taguchi method identified hydration level and PLGA density as the most significant input parameters affecting curcumin diffusion, while the effect of PLGA chain length was negligible within the simulated range. We provided a regression equation capable to accurately fit MD results. The regression equation suggests that increases in hydration level and PLGA density result in a decrease in the diffusion coefficient.

Preparation and performance exploration of 2,5‐furandicarboxylic acid‐based copolyester bioplastics: Controlling thermal properties, tensile properties, and surface hydrophilicity through composition

AbstractTo improve the comprehensive properties of polybutylene furandicarboxylate (PBF), 2,5‐furandicarboxylic acid (2,5‐FDCA), and aliphatic chain diol 1,8‐octanediol and 1,4‐butanediol were used as monomers to synthesize a series of bio‐based polybutylene glycol‐octanediol 2,5‐furandicarboxylate (PBOF). The results showed that the chemical composition of PBOF could be controlled through the molar ratio of monomers. Compared with PBF, as the proportion of octanediol segments gradually increased, PBOF could gradually transform from semi‐crystalline thermoplastic to amorphous form, and the glass transition temperature (Tg) gradually decreased. The crystallization ability reduced but a part of the crystal area was still retained. The copolyesters still has a decomposition temperature above 370°C, indicating excellent thermal stability. The introduction of the octanediol segment significantly improved the tensile mechanical properties and flexibility of the POBF copolyester. These meet the requirements for the preparation of bio‐based engineering plastics. The water absorption rate of PBOF showed that it may have certain degradable potential. PBOF copolyesters have potential application prospects in bio‐based medical plastics and biodegradable packaging polymer materials after copolymerization modification.

Pea-like inspired design: Lignin nanospheres-mediated PVA film with high strength, low water evaporation permeability, strong UV resistance and anti-oxidation properties for extending food freshness

The excessive utilization of petroleum-based plastic products has inflicted significant harm upon the ecological and health problems, compelling individuals to continually seek renewable and biodegradable polymer materials as alternatives. Drawing inspiration from the structure of a natural pea pod, a unique interlocking packaging material based on a pea-like structure is obtained via green electrospinning and mild glutaraldehyde (GA) cross-linking method. Herein, polyvinyl alcohol (PVA) serves as a green protective layer encompassing the active lignin nanospheres (LNP) pod, forming a packaging film that prevents LNP migration. The LNP within the fibers can effectively shorten the fiber spacing, and when exposed to the GA vapor, they promote the bonding between neighboring fibers to form a tight interlock structure. Benefiting from the interlocking pea-like structure, the film exhibits excellent tensile strength (3.53 ± 0.02 MPa), wetting strength (1.92 ± 0.05 MPa), and outstanding water vapor barrier properties (3.27 ± 0.3 10−10 gm−1 s−1 Pa−1). Furthermore, the inclusion of LNP endows exceptional water resistance, UV-blocking capabilities, antibacterial and antioxidant properties, which can effectively prolong the storage life of perishable fruits. This eco-logical sustainable design holds tremendous potential in mitigating the burden on the environment, thus making a novel avenue for exploring alternatives to petroleum-derived plastics.

3D printing of PBAT-based composites filled with agro-wastes via selective laser sintering

Nowadays, biodegradable polymeric materials can play a key role in many fields, including food packaging and biomedical. In the present work, composite powders based on PBAT matrix were prepared by mixing spherical particles obtained by emulsion solvent process with two different biofillers coming from food agro-wastes: a corn by-product and a filler derived from wine production. Sustainable PBAT-based composites were then successfully realized for the first time by means of selective laser sintering (SLS). This paper combines the use of natural fillers within a biodegradable matrix and 3D printing process. Fillers and composite powders were completely characterized as well as the PBAT-based composites obtained by SLS. The effect of biofillers within the PBAT matrix was investigated, by means of TGA, DSC, SEM, and DMA analyses. The bio-based composites obtained by SLS showed increased complex structures. Regarding the processability the printed samples are characterized by a good level of dimensional accuracy and porosity. Thus, biomedical field could benefit from the use of these kinds of fully biodegradable PBAT-based composites.

Facile Green Synthesis of Zingerone Based Tissue‐Like Biodegradable Polyester with Shape‐Memory Features for Regenerative Medicine

AbstractThe abundance of plants as a renewable bioresource has captured the significant attention of researchers, driving them to explore new biodegradable polymeric materials. However, there are still many biobased materials with untapped potential, offering opportunities to synthesize novel biodegradable polymers with multifunctional properties. This work provides a unique solvent and catalyst‐free melt polycondensation process to prepare a series of polyesters using zingerol (Zing‐OH), a reduced form of zingerone, as a primary component for the first time. Briefly, Zing‐OH (a ginger‐based component) is employed in conjunction with a variety of renewable resources, such as citric acid (CA), sebacic acid (SA), and xylitol (Xy), to synthesize multifunctional soft tissue‐like ZCSX polyesters. Fourier‐transform infrared (FTIR) and 1H‐nuclear magnetic resonance (NMR) spectroscopy are used to validate the synthesis of the polyesters, while thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and universal testing machine (UTM) are employed to investigate their physicochemical properties. Moreover, the synthesized polyester's thermal, mechanical, and biodegradation properties can be fine‐tuned by simply varying the Zing‐OH feed ratio. The mechanical properties of the synthesized polymer resemble various human tissues, including the liver, uterus, bladder, breast, and temporal and nasal cartilage. This suggests that the synthesized polyesters can potentially be useful in tissue engineering applications. Furthermore, the polyester demonstrated exceptional recovery responses and good shape memory behavior at ambient body temperature. Additionally, as observed from Alamar blue, live/dead assays, and time‐dependent in vitro wound images, the synthesized polyester demonstrated antibacterial activity, good in vitro cytocompatibility, cell proliferation, and wound healing capabilities against mouse fibroblast cells (NIH/3T3). The developed biocompatible polyester also exhibits excellent hemocompatibility for human blood, indicating its potential use in the field of regenerative medicine.

Biodegradable Polymer Materials Based on Polyvinyl Alcohol, Starch, and Cellulose Derivatives

Biodegradable Polymer Materials Based on Polyvinyl Alcohol, Starch, and Cellulose Derivatives