Structure Of Polyesters Research Articles

Ring‐opening copolymerization of ε‐caprolactone and δ‐valerolactone to cyclic polyesters by a bimolecular system

AbstractBio‐based plastics have received much attraction because they are an alternative to petroleum‐based plastics in recent years. Among them, aliphatic polyesters have garnered the most attention due to their excellent properties. Polyester is primarily synthesized through ring opening polymerization of monomer, and the catalysts used are mostly synthesized through “click” reaction in the laboratory, which exhibits inferior activity and little commercial value. Herein, a facile approach was developed for the synthesis of high molecular‐weight cyclic aliphatic polyesters, specifically poly(valerolactone‐co‐caprolactone) with varying compositions. This involved the ring‐opening copolymerization of ε‐caprolactone (ε‐CL) and δ‐valerolactone (δ‐VL) in the absence of an initiator with commercial hydrogen bond donor triclorocarban and an organic base. The structure and properties of the prepared cyclic polyester were investigated using GPC, 13C NMR, 1H NMR, MALDI‐TOF mass spectrometry, TOF‐SIMS mass spectrometry, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and X‐ray diffraction (XRD) techniques. The results show that the molecular weight of cyclic polyester can rapidly exceed 40 kDa, with a PDI of approximately 1.10. In comparison to linear polyester, it has a higher melting point and superior thermodynamic properties, thus presenting greater application potential. Finally, based on nuclear magnetic resonance titration, the potential catalytic processes and mechanisms of bimolecular systems on monomers in different environments were discussed. This study not only offers new insights into the structure and properties of cyclic polyesters, but also presents novel bimolecular catalytic systems using commercial urea hydrogen bond donors for the synthesis of cyclic polymer polyesters.

Mucoadhesive poly(ethylene glycol)-based biodegradable polyesters with in-chain model drug

Mucoadhesive polymers have received significant interest in drug delivery due to the prolonged residence time on various mucus gel layers. Not only local effects but also the systemic uptake of active pharmaceutical ingredients can be enhanced by such mucoadhesive excipients. In this study, we design novel poly(ethylene glycol) based mucoadhesive polyesters bearing unsaturated or sulfhydryl functionalities and model drug fluorescein polymerized in the polymeric backbone. The structure of polyesters was confirmed via 1H NMR and FTIR, while their molar masses, determined by gel permeation chromatography, were found to be between 3.6 and 4.0 kDa. Enzymatic degradation studies showed the ability of lipase to degrade the polymeric chains. Because of the mucoadhesive groups, the viscosity of mucus mixtures with these polymers increased 1.8-fold for the double bond, while 4.3-fold for thiol functional polymers, compared to PEG. Prolonged residence time on porcine intestinal mucosa was detected, as 3 h after application, up to 69 % of the polymers were still on the mucosa, whereas PEG was completely removed within 30 mins. Highly pH and enzyme-dependent release of fluorescein was noticed; only pH > 6.8 caused significant drug release. According to the results of this study, PEG-based unsaturated and thiolated polyesters with in-chain model drugs are great mucoadhesive and biodegradable drug carriers with sustained release properties.

Correlation of Enzymatic Depolymerization Rates with the Structure of Polyethylene-Like Long-Chain Aliphatic Polyesters.

Long-chain aliphatic polyesters are emerging sustainable materials that exhibit polyethylene-like properties while being amenable to chemical recycling and biodegradation. However, varying polyester chemical structures results in markedly different degradation rates, which cannot be predicted from commonly correlated bulk polyester properties, such as polymer melting temperature. To elucidate these structure-degradability relationships, long-chain polyesters varying in their monomer composition and crystallinity were subjected to enzymatic hydrolysis, the rates of which were quantified via detection of formed monomers. Copolymers with poorly water-soluble, long-chain diol monomers (e.g., 1,18-octadecanediol) demonstrated strongly reduced depolymerization rates compared to copolymers with shorter chain length diol monomers. This was illustrated by, e.g., the 20× faster hydrolysis of PE-4,18, consisting of 1,4-butanediol and 1,18-octadecanedicarboxylic acid monomers, relative to PE-18,4. The insoluble long-chain diol monomer released upon hydrolysis was proposed to remain attached to the bulk polymer surface, decreasing the accessibility of the remaining ester bonds to enzymes for further hydrolysis. Tuning of polyester crystallinity via the introduction of branched monomers led to variable hydrolysis rates, which increased by an order of magnitude when crystallinity decreased from 72% to 45%. The results reported enables the informed design of polyester structures with balanced material properties and amenability to depolymerization.

Upcycling of industrial footwear waste into nonwoven fibrous structures with thermal and acoustic insulation properties

The footwear industry significantly impacts the environment, from raw material extraction to waste disposal. Transforming waste into new products is a viable option to mitigate the environmental consequences, reducing the reliance on virgin raw materials. This work aims to develop thermal and acoustic insulation materials using polyester waste from footwear industry. Two nonwoven and two compressed nonwoven structures, comprising 80% polyester waste and 20% commercial recycled polyester (matrix), were produced. The materials were created through needle-punching and compression molding techniques. The study included the production of sandwich and monolayer nonwoven structures, which were evaluated considering area weight, thickness, air permeability, mechanical properties, morphology using field emission scanning electron microscopy, and thermal and acoustic properties. The nonwoven samples presented high tensile strength (893 kPa and 629 kPa) and the highest strain (79.7% and 73.3%) and compressed nonwoven structures showed higher tensile strength (2700 kPa and 1291 kPa) but reduced strain (25.8% and 40.8%). Nonwoven samples showed thermal conductivity of 0.041 W/K.m and 0.037 W/K.m. Compressed nonwoven samples had higher values at 0.060 W/K.m and 0.070 W/K.m. While the sample with the highest conductivity exceeds typical insulation levels, other samples are suitable for thermal insulation. Nonwoven structures exhibited good absorption coefficients (0.640–0.644), suitable for acoustic insulation. Compressed nonwoven structures had lower values (0.291–0.536), unsuitable for this purpose. In summary, this study underscores the potential of 100% recycled polyester structures derived from footwear and textile industry waste, showcasing remarkable acoustic and thermal insulation properties ideal for the construction sector.

The GPAT4/6/8 clade functions in Arabidopsis root suberization nonredundantly with the GPAT5/7 clade required for suberin lamellae

Lipid polymers such as cutin and suberin strengthen the diffusion barrier properties of the cell wall in specific cell types and are essential for water relations, mineral nutrition, and stress protection in plants. Land plant-specific glycerol-3-phosphate acyltransferases (GPATs) of different clades are central players in cutin and suberin monomer biosynthesis. Here, we show that the GPAT4/6/8 clade in Arabidopsis thaliana, which is known to mediate cutin formation, is also required for developmentally regulated root suberization, in addition to the established roles of GPAT5/7 in suberization. The GPAT5/7 clade is mainly required for abscisic acid-regulated suberization. In addition, the GPAT5/7 clade is crucial for the formation of the typical lamellated suberin ultrastructure observed by transmission electron microscopy, as distinct amorphous globular polyester structures were deposited in the apoplast of the gpat5 gpat7 double mutant, in contrast to the thinner but still lamellated suberin deposition in the gpat4 gpat6 gpat8 triple mutant. Site-directed mutagenesis revealed that the intrinsic phosphatase activity of GPAT4, GPAT6, and GPAT8, which leads to monoacylglycerol biosynthesis, contributes to suberin formation. GPAT5/7 lack an active phosphatase domain and the amorphous globular polyester structure observed in the gpat5 gpat7 double mutant was partially reverted by treatment with a phosphatase inhibitor or the expression of phosphatase-dead variants of GPAT4/6/8. Thus, GPATs that lack an active phosphatase domain synthetize lysophosphatidic acids that might play a role in the formation of the lamellated structure of suberin. GPATs with active and nonactive phosphatase domains appear to have nonredundant functions and must cooperate to achieve the efficient biosynthesis of correctly structured suberin.

Preparation and structure investigation of polyethylene terephthalate polyester reinforced Ni0.5Zn0.5Fe2O4 nanoparticles for gamma ray shielding performance

Defects of high atomic materials gamma-ray shielding such as low chemical stability, low mechanical properties, and heaviness lead us to investigate other light and flexible materials such as polymers. Polymer-doped nanosized materials are the most frequently examined materials. In this study, polyethylene terephthalate [(C10H8O4)n] was doped with Ni0.5Zn0.5Fe2O4 nanoparticles up to 40 wt% (0.0, 10.0, 20.0, 40.0 wt%) prepared by Sol–Gel auto-combustion method with the help of Gelatin. The polyester/Nanofiller composite structures were identified using x-ray photoelectron spectroscopy, x-ray diffraction, Scanning, and Transmission electron microscope as well as density measurements. x-ray photoelectron spectroscopy confirmed the successful doping of nanofiller in the polyester structure as Zn signals appear in the atomic composition and Fe signals appear in the deconvolution of the peaks. x-ray diffraction, transmission, and scanning electron microscope display the same result. x-ray diffraction graph information with the Scherer equation offered the crystal size of the composite (26 nm). Polyester/nanofiller samples were scanned against gamma-ray and experimental shielding factors were computed using a narrow beam transmission technique with sodium iodide detector and two-point sources Cs-137 and Co-60. Experimental Linear and mass attenuation coefficient values swelled as percentages of nanofiller increased in the polyester structure. Experimental Mass attenuation values were compared with theoretical ones estimated from XCOM and Physics-X programs. The difference between them does not exceed 12% which is acceptable as the x-ray photoelectron spectroscopy atomic composition utilized in the theoretical data calculation does not reveal Ni signals. This may occur at the depth of the composite structure. Finally, the half-value layer, the Tenth value layer, and the Mean free path are determined experimentally, and their values are reduced as the nanofiller doping percentage rises in the structure. This result confirms the efficiency of nanofiller addition to the polyester structure to attenuate gamma-ray.

Phosphine-Capped Effects Enable Full-Color Clusteroluminescence in Nonconjugated Polyesters.

Full-color luminophores have advanced applications in materials and engineering, but constructing color-tunable clusteroluminescence (CL) from nonconjugated polymers based on through-space interactions remains a huge challenge. Herein, we develop phosphine-capped nonconjugated polyesters exhibiting blue-to-red CL (400-700 nm) based on phosphine-initiated copolymerization of epoxides and cyclic anhydrides, especially P1-0.5TPP, which exhibits red CL (610 nm) with a high quantum yield of 32%. Experiments and theoretical calculations disclose that the phosphine-capped effect in polyesters brings about conformational changes and induces phosphine-ester clusters by through-space (n,π*) interactions. Moreover, CL colors and efficiencies can be easily tailored by types of phosphines, compositions and structures of polyesters, and concentration. Significantly, the role of polymer motions (group, segmental, and chain motions) on CL originating from microregions inside polyesters is revealed. Further, phosphine-capped nonconjugated polyesters are demonstrated to be nonconjugated dyes and fluorescent fibers and are also used for multicolor light-emitting diodes including white light. This work not only provides an engineering strategy based on the end-group effect to prepare full-color clusteroluminogens but also broadens the prospects for material applications.

Influence of plastic shape on interim fragmentation of compostable materials during composting

Common experience with rotting wooden buildings demonstrates that fragmentation is a necessary natural process during biodegradation. In analogy, the loss of structural integrity of biodegradable plastics during biodegradation produces interim microplastic fragments. It is currently not known which parameters govern fragmentation kinetics: chemical structure, physical shape, and composite layers, or composting conditions may all be relevant. Here we investigated the influence of physical shape on the fragmentation of a polyester blend during laboratory tests simulating industrial composting. Methods previously validated on micronized granules as model shape were applied to shapes that better represent consumer products, such as micronized thin films and shredded plastic-coated paper cups. The peak interim number of detected fragments, which are between 3 and 2000 µm, ranked highest for micronized films, lower for micronized plastic granules, and even lower for coated paper cups. The layered structure of polyester on cellulose may thus have stabilized the biodegrading polyester compound against fragmentation. For thin films, fragment counts dissipated with halftime of 2.5 days, and less than 10–8% of the initially added polyester mass was detected in fragments between 3 and 25 µm at the last sampling time point. The physical shape and multilayer structure of the polymer-containing product were found to be decisive for fragmentation kinetics, indicating that tests on micronized polymer granules might not be representative of the release mechanism of fragments from consumer products containing plastic coatings.

Polyimide films with ultralow dielectric loss for 5G applications: Influence and mechanism of ester groups in molecular chains

Polyimides are ideal candidates for 5G high-frequency communications due to their good thermal stability, mechanical properties and processability. However, the exploration of how to reduce their high-frequency dissipation factor (Df) remains an urgent and alluring challenge. Inspired by the molecular structure of liquid crystal polyester, which is insensitive to high-frequency electric fields, here we design two series of polyimides derived from diamines with multiple ester groups (AXEB, X = 1, 2 or 3) and 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) or p-phenylene bis (trimellitate anhydride) (TA2EB). We investigated the effects of ester number on the aggregation structure, water absorption, dielectric properties, heat resistance and mechanical properties of the polyimides and find that the Df of the multiple ester-containing polyimides decreases rapidly with increasing frequency and number of ester groups. Wide-angle X-ray diffraction analysis, polarized optical microscopy observations and molecular dynamics simulations show that the unique properties of these polyimides benefit from the tight packing of the molecular chain and the strong intermolecular interaction force caused by the ester group, as well as the resulting prolonged dipole relaxation time and the greatly reduced water absorption. Therefore, the polyimide films show extremely low Df values of 0.0030 for AXEB-6FDA and 0.0013 for AXEB-TA2EB. Furthermore, AXEB-TA2EB also shows excellent thermal stability, mechanical properties, electrical properties and permittivity. More importantly, their ultralow moisture rate (<0.83 %) ensures that the high-frequency Df remains stable in different humid environments, even after soaking in water. This method can also be extended to other polymers, thus providing a new strategy for the design of low dielectric loss materials.

The competition between radical copolymerization and charge separation of cyclic ketene acetals and electron‐deficient olefins

AbstractCyclic ketene acetals (CKAs) possess unique features in two aspects. On one hand, after the addition of a radical on the alkene, CKAs can undergo ring‐opening via radical rearrangement, enabling polyester preparation based on chain‐growth polymerization. On the other hand, the alkene connected with two electron‐donating oxygens in a strained form exhibit unique reactivities, resulting in complex reactions in the presence of electron deficient compounds. In this investigation, fundamental studies on CKA radical ring‐opening polymerization and charge‐mediated reactions were performed. Alternating copolymers of CKA and maleimides, or maleates, were prepared and characterized. Quantum chemistry modeling from the perspectives of reaction kinetics and thermodynamics enabled an in‐depth mechanistic study on the side reactions between CKA and maleic anhydride or itaconic anhydride, inspiring the techniques to minimize those side reactions in competition with radical copolymerization. After purifying the anhydride monomers with sublimation, the copolymerization with CKA successfully occurred. The anhydride containing polyester structures with an alternating sequence were confirmed with comprehensive characterizations. Facile post‐functionalization with an alcohol was performed, resulting in carboxylate containing polyesters.

Hexagonal Phase Formation and Crystalline Structural Transition in Long-Spaced Aliphatic Polyesters with Side Groups.

Side substitution is an effective method for the chemical modification and functionalization of linear polyesters. The presence of side groups can have a profound effect on the crystalline structure and phase transition of semicrystalline polyesters. Herein, we synthesized the long-spaced polyesters with -OH and -CH3 side groups and various methylene segment lengths and studied the effects of the side groups on the crystal polymorph and phase transition of substituted polyesters. The substituted polyesters grow in the thermally stable phase (form I) at a higher temperature. However, the polyesters crystallize in a metastable hexagonal phase (form II) with trans chain conformation at a lower temperature. The metastable form II transforms into the more stable form I during long-time annealing or upon heating; this phase transition is accompanied by chain tilting and crystal lamellar thickening. This study has elucidated the critical role of side groups in the polymorphic crystallization and phase transition of linear polyesters.

A recyclable polyester library from reversible alternating copolymerization of aldehyde and cyclic anhydride

Our society is pursuing chemically recyclable polymers to accelerate the green revolution in plastics. Here, we develop a recyclable polyester library from the alternating copolymerization of aldehyde and cyclic anhydride. Although these two monomer sets have little or no thermodynamic driving force for homopolymerization, their copolymerization demonstrates the unexpected alternating characteristics. In addition to readily available monomers, the method is performed under mild conditions, uses common Lewis/Brønsted acids as catalysts, achieves the facile tuning of polyester structure using two distinct monomer sets, and yields 60 polyesters. Interestingly, the copolymerization exhibits the chemical reversibility attributed to its relatively low enthalpy, which makes the resulting polyesters perform closed-loop recycling to monomers at high temperatures. This study provides a modular, efficient, and facile synthesis of recyclable polyesters using sustainable monomers.

Design of Chitosan-Polyester Composites to Reduce Particulate Contamination of Washing Wastewater

In this research, the modification of different polyester structures (fabrics and knits) by the biopolymer chitosan was studied to evaluate the effects of the polyester structure and treatments on the particulate pollution of wastewater. The pristine polyester and the chitosan-polyester fabric and polyester knit composites were washed cyclically with standard ECE A detergent at 60 °C. The laser diffraction technique was used to characterize the particle size of the washing wastewaters from the 1–5, 6–10 and 1–10 wash cycles. In addition, the total solids (TS), total suspended solids (TSS), total dissolved solids (TDS), turbidity and chemical oxygen demand (COD) were also determined, according to standard procedures. The obtained results show the influence of the polyester fabrics and polyester knit structures and chitosan-polyester composites on the particle size distribution (PSD) in the washing wastewater. Differences in the values of the characteristic parameters, especially the span value and shape factor (k) of the individual curves, are visible, indicating the release of particles during the washing process. The experimental results show that the laser diffraction technique is suitable for characterizing the particle dimensions of the washing wastewater for different pristine polyester structures and chitosan-polyester composites. Modification with chitosan has been shown to provide potential protection against the release of microplastic particles into the environment.

The Stability of the Chitosan Coating on Polyester Fabric in the Washing Process

The sensitivity of chitosan to environmental conditions and processing conditions can stress its structure and cause degradation of this polymer on various application carriers. The stability of chitosan in a designed textile structure of standard polyester fabric with chitosan was analysed in a multiple washing process with a standard detergent by studying the properties before and after 10 washing cycles. The chitosan was coated on standard and alkali treated polyester fabrics. Washing was performed with an ECE A reference detergent at 60 °C according to the Standard protocol HRN EN ISO 6330 in 10 cycles. The washing stability of chitosan onto polyester fabrics was monitored by a staining test, zeta potential, breaking force, breaking elongation, pilling propensity, touch, whiteness, moisture transport, antimicrobial activity and morphological features. The staining test confirmed the wash stability of chitosan coated on alkali hydrolised polyester fabrics, while the chitosan coated on standard polyester fabric disappeared. Zeta potential proved to be the significant parameter for determining chitosan` stability. The tensile properties of fabric samples were harmonised with other characterisation parameters. Coating of polyester fabric with chitosan increased the elasticity of all samples. The antimicrobial activity of polyester fabrics coated with chitosan against Staphylococcus aureus was reduced by 20% after 10 washing cycles. All the characterisation parameters proved that polyester fabric as a chitosan carrier should be surface modified for designing a stable bioactive textile structure of chitosan and polyester.

Ring Opening Copolymerization of Boron-Containing Anhydride with Epoxides as a Controlled Platform to Functional Polyesters.

Boron-functionalized polymers are used in opto-electronics, biology, and medicine. Methods to produce boron-functionalized and degradable polyesters remain exceedingly rare but relevant where (bio)dissipation is required, for example, in self-assembled nanostructures, dynamic polymer networks, and bio-imaging. Here, a boronic ester-phthalic anhydride and various epoxides (cyclohexene oxide, vinyl-cyclohexene oxide, propene oxide, allyl glycidyl ether) undergo controlled ring-opening copolymerization (ROCOP), catalyzed by organometallic complexes [Zn(II)Mg(II) or Al(III)K(I)] or a phosphazene organobase. The polymerizations are well controlled allowing for the modulation of the polyester structures (e.g., by epoxide selection, AB, or ABA blocks), molar masses (9.4 < Mn < 40 kg/mol), and uptake of boron functionalities (esters, acids, "ates", boroxines, and fluorescent groups) in the polymer. The boronic ester-functionalized polymers are amorphous, with high glass transition temperatures (81 < Tg < 224 °C) and good thermal stability (285 < Td < 322 °C). The boronic ester-polyesters are deprotected to yield boronic acid- and borate-polyesters; the ionic polymers are water soluble and degradable under alkaline conditions. Using a hydrophilic macro-initiator in alternating epoxide/anhydride ROCOP, and lactone ring opening polymerization, produces amphiphilic AB and ABC copolyesters. Alternatively, the boron-functionalities are subjected to Pd(II)-catalyzed cross-couplings to install fluorescent groups (BODIPY). The utility of this new monomer as a platform to construct specialized polyesters materials is exemplified here in the synthesis of fluorescent spherical nanoparticles that self-assemble in water (Dh = 40 nm). The selective copolymerization, variable structural composition, and adjustable boron loading represent a versatile technology for future explorations of degradable, well-defined, and functional polymers.

Microcrystalline cellulose grafted hyperbranched polyester with roll comb structure for synergistic toughening and strengthening of microbial PHBV/bio-based polyester elastomer composites

The brittle feature of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) is the major challenge that strongly restricts its application at present. Successfully synthesized bio-based engineering polyester elastomers (BEPE) were combined with PHBV to create entirely bio-composites with the intention of toughening PHBV. Herein, the 2,2-Bis(hydroxymethyl)-propionic acid (DMPA) was grafted onto microcrystalline cellulose (MCC) and then further transformed into hyperbranched polyester structure via polycondensation. The modified MCC, named MCHBP, had plenty of terminal hydroxyl groups, which get dispersed between PHBV and BEPE. Besides, a large number of terminal hydroxyl groups of MCHBP can interact with the carbonyl groups of PHBV or BEPE in a wide range of hydrogen bonds, and subsequently increase the adhesion and stress transfer between the PHBV and BEPE. The tensile toughness and the elongation at break of the PHBV/BEPE composites with 0.5phr MCHBP were improved by 559.7 % and 221.8 % in comparison to those of PHBV/BEPE composites. Results also showed that MCHBP can play a heterogeneous nucleation effect on the crystallization of PHBV. Therefore, this research can address the current issue of biopolymers' weak mechanical qualities and may have uses in food packaging.

Hydroxypropyl-β-cyclodextrin-based polyester TFC membrane for efficient antibiotic desalination

Preparation of membranes with loose structure is often required for excellent small organic molecules desalination, but remains a grand challenge. In this work, a loose thin film composite (TFC) membrane was fabricated via interfacial polymerization of hydroxypropyl-β-cyclodextrin (HP-β-CD) and trimesoyl chloride. Besides, tannic acid was added in the aqueous phase to boost the rejection rate of the membrane by reducing the “outer space” distance among HP-β-CD. The resulting membrane exhibited an optimal permeability of 82.9 L m−2h−1 bar−1 along with antibiotic desalination efficiency (94.8 % for tetracycline hydrochloride and 8.5% for NaCl). Moreover, experiment results demonstrate that the tannic acid incorporated HP-β-CD-based polyester (TIHP) membrane was also endowed with enhanced chlorine resistance and antifouling ability deriving from its rich hydroxyl and polyester structures, which makes the membrane promising for the purification of antibiotics in pharmaceutical fields.

Bio-based additive manufacturing materials: An in-depth structure-property relationship study of UV-curing polyesters from itaconic acid

A series of bio-based polyester derived from itaconic acid was synthesized as alternative binder resin to polyester acrylates in UV-curing additive manufacturing processes. Different diols and dicarboxylic acids from both petrochemical and renewable resources were combined to create polyester structures that have not been previously described. Employing these monomers allowed for the synthesis of novel polyester resins with a bio-based content from 56 to 100%. The influence of the different chemical structures (double bond density, flexibility, aromatic content, etc.) of these itaconic acid-based materials on the physicochemical properties was thoroughly investigated for the first time. Subsequently, formulations derived from these polyesters were prepared and processed on a digital light processing (DLP)-machine to obtain test specimen. Mechanical and thermal characterization of cured parts revealed a dependency of the properties on both choice of monomers and crosslink density. Cyclic structures in the polyester resin resulted in very rigid materials with glass transition temperatures up to 97 °C and tensile modulus of 2400 MPa. The incorporation of longer aliphatic chains on the other hand gave rise to flexible materials with an elongation at break up to 50%. Hence, the materials described herein allow for additive manufacturing materials with tunable properties and an overall bio-based content up to 85%.

Трансформации спектров фотолюминесценции наноразмерных апконвертирующих фосфоров фантомами биологических тканей

Phantoms are often used to imitate biological tissues in laboratory conditions. Phantoms are usually made on the basis of natural and synthetic materials, as well as hydrogels and various bioactive compositions. Today to visualize biological tissues and study the processes occurring to them in in vitro and in vivo researches in real time, upconversion nanophosphors (UCNPs) are actively used. They have a whole set of unique photoluminescent properties and are promising components of modern tools for non-invasive optical diagnostics of the human and animals body. We have carried out the synthesis and complex characterization of β-NaYF4:Yb3+:Er3+/NaYF4 nanoparticles, which effectively convert radiation from the near-IR range into the visible region of the spectrum. The process has been developed to encapsulate them into the structure of aliphatic polyesters and to form bioresorbable polylactoglycolide scaffolds by anti-solvent 3D printing. We formed two types of tissue phantoms based on agarose, ultra-pasteurized cow's milk and melanin. Characterization and analysis of their optical properties were carried out. We studied the transformations of the photoluminescence spectrum of the synthesized UCNPs during the passage of their radiation through these phantoms, and performed the visualization of the photoluminescent polyester matrices placed in them.

Harnessing the power of polyol-based polyesters for biomedical innovations: synthesis, properties, and biodegradation.

Polyesters based on polyols have emerged as promising biomaterials for various biomedical applications, such as tissue engineering, drug delivery systems, and regenerative medicine, due to their biocompatibility, biodegradability, and versatile physicochemical properties. This review article provides an overview of the synthesis methods, performance, and biodegradation mechanisms of polyol-based polyesters, highlighting their potential for use in a wide range of biomedical applications. The synthesis techniques, such as simple polycondensation and enzymatic polymerization, allow for the fine-tuning of polyester structure and molecular weight, thereby enabling the tailoring of material properties to specific application requirements. The physicochemical properties of polyol-based polyesters, such as hydrophilicity, crystallinity, and mechanical properties, can be altered by incorporating different polyols. The article highlights the influence of various factors, such as molecular weight, crosslinking density, and degradation medium, on the biodegradation behavior of these materials, and the importance of understanding these factors for controlling degradation rates. Future research directions include the development of novel polyesters with improved properties, optimization of degradation rates, and exploration of advanced processing techniques for fabricating scaffolds and drug delivery systems. Overall, polyol-based polyesters hold significant potential in the field of biomedical applications, paving the way for groundbreaking advancements and innovative solutions that could revolutionize patient care and treatment outcomes.