Impact of weathered and virgin polyethylene terephthalate (PET) micro- and nanoplastics on growth dynamics and the production of extracellular polymeric substances (EPS) of microalgae.

The ever-increasing plastic waste accumulation in the marine environment necessitates a deeper understanding of microalgae interactions with micro- and nanoplastics (MNP), and the role of extracellular polymeric substances (EPS). EPS, known for its adhesive properties and produced as an algal stress response, may facilitate aggregation of both algae and MNPs, thereby impacting ecological and hydrodynamic processes such as the trophic transfer or vertical transport of MNPs. Moreover, gaining a deeper understanding of the impact of weathering processes on the potential toxicological effects of plastic particles, and the comparative significance of plastic-specific effects relative to those of naturally occurring particles such as kaolin clay, is imperative. Therefore, this study investigated the impact of fragmented, polydisperse virgin polyethylene terephthalate (PET, Daverage = 910 nm) and weathered PET (Daverage = 1700 nm) on the growth and the production of EPS of Rhodomonas salina. Algae were exposed to a range of low MNP concentrations (10, 100 and 1000 and 10,000 MNPs ml-1) for 11 days. A natural particle control (kaolin, Daverage = 1600 nm) was deployed to differentiate particle effects from plastic effects. It was observed that exposure to both weathered PET and virgin PET resulted in initially increased growth rates (7.80 % and 7.28 % respectively), followed by significant decreases in algae cell density (-30.1 % and -11.2 % respectively). Furthermore, exposure to weathered PET caused a simultaneous elevation in cellular EPS production (76.51 %). The effects of plastics were significantly larger than the effect of kaolin. Also, the observed effects were amplified by the weathering of the plastics. These observations underscore the interactions between particle type, age and concentration, and their distinct impacts on algae density and growth inhibition. The observations indicate a role for EPS as an algal protection mechanism, potentially affecting the environmental fate of MNP - microalgae aggregates.

Low prevalence of microplastic contamination in the bottom sediments and deep-sea waters of the Bransfield strait, Antarctica.

Despite the remoteness of the Antarctic continent and Southern Ocean, microplastic (MPs) contamination has been evidenced in recent years. However, the deep-sea compartments of the Southern Ocean are yet to be investigated. In the present study, we conducted a baseline MP assessment of the deep-sea waters and bottom sediments of the Bransfield Strait, Antarctica. A low abundance of suspected MPs was found. The average MP abundances in bottom sediments and water samples were 0.09 MP/g (range of 0-0.2 MP/g) and 7.00 MP/L (range of 0-16 MP/L), respectively. The majority of the particles were fibers identified as cellulose, although polyethylene terephthalate (PET) and polyacrylonitrile (PAN) was also detected. These results suggest low MP contamination levels in the Southern Ocean's deepest environmental compartments. However, future studies must aim to investigate the smallest MP fractions and, if possible, nanoplastic (<1 µm) contamination in these remote compartments.

[Advances in the structure and function of MHETase].

Polyethylene terephthalate (PET) is one of the widely used plastics, but its waste pollution has become a global environmental issue. The discovery of polyethylene terephthalate hydrolase (PETase) has provided a green and environmentally friendly approach for PET degradation. However, PETase produces intermediate products that inhibit the enzyme's further activity, leading to a decrease in enzyme efficiency. Mono(2-hydroxyethyl) terephthalate hydrolase (MHETase) works synergistically with PETase to further degrade the intermediate product MHET into ethylene glycol (EG) and terephthalic acid (TPA). MHETase exhibits extremely high specificity for MHET and is crucial for the complete degradation of PET. This article comprehensively reviews MHETase from various perspectives, including its three-dimensional structure, substrate binding, and catalytic mechanism. It demonstrates the structural features and key residues associated with the enzyme's degrading activity and discusses the progress in enzyme engineering modifications. Additionally, the study envisions the development of a two-enzyme PET degradation system by combining MHETase with PETase, aiming to provide valuable references for designing and developing more efficient PET hydrolytic enzyme systems.

Biofilm formation of Streptococcus mutans, Streptococcus sanguinis, Staphylococcus epidermidis, Staphylococcus aureus, Lactobacillus casei, and Candida Albicans on 5 thermoform and 3D printed orthodontic clear aligner and retainer materials at 3 time points: an in vitro study.

INTRODUCTION: Orthodontic clear aligners and retainers have numerous advantages that is making them ever increasingly popular. However, they might, similar to any other oral appliance, contribute to biofilm formation and finally dental caries or white spot lesions or gingival inflammations. The literature on biofilm formation on orthodontic clear appliances is very scarce and limited to a few microorganisms and materials. Therefore, this experimental study evaluated the biofilm formation on 5 thermoformed and 3D printed CAD/CAM orthodontic retainers in 3 intervals. METHODS: In this in vitro study, 345 specimens (270 test discs and 45 negative controls) were created from fabricated retainers. Retainers included a 3D printed CAD/CAM material (Detax) and four thermoformed retainers [Erkodent (polyethylene terephthalate glycol [PETG]); EasyVac (polyethylene); DB (polyester based on terephthalic acid); and Clear Tech]. They were all 1 mm thick, and all completely fabricated, i.e., heated or printed. The discs were placed in 96-well plates. Microorganisms were cultured on 270 discs for 24 h (90 discs), 72 h (90 other discs), and 5 days or 120 h (90 other discs). Biofilm formation of the strains and negative controls was measured using the microtiter plate assay by ELISA reading. The microbes' ability to produce biofilm was categorized based on the comparison of average optical density (OD) of tests versus a cut-off point OD (ODc) calculated as the average of the OD of corresponding negative controls plus 3× its standard deviation: non-biofilm former [OD ≤ ODc], weak biofilm former [ODc < OD ≤ (2 × ODc)], moderate biofilm former [(2 × ODc) < OD ≤ (4 × ODc)], and strong biofilm former [(4 × ODc) < OD]. These were also converted to ranked scores between zero (no biofilm) and 3. The difference between ODs with control ODs were calculated. These were analyzed using 3-way ANOVA, 2-way ANOVA, and Tukey tests (α = 0.05, α = 0.008). RESULTS: The 3-way ANOVA showed that the overall difference among the ΔODs of 5 retainers (all microorganisms and all intervals combined, n = 270) was not significant (F = 1.860, P = 0.119). Nevertheless, the difference among 3 intervals (F = 31.607, P = 0.0000) and the difference among the 6 microorganisms (F = 24.044, P = 0.0000) were significant. According to the Tukey test, the differences between the 1st interval with either of the other two intervals was significant (both P values = 0.000). There were significant differences between Candida albicans with all other organisms (all 5 P values = 0.0000). All other pairwise comparisons were insignificant (all 10 P values ≥ 0.1). After taking the averages of the 3 intervals, the order of the biofilm generation for different materials were as follows: Detax (average score: 1.56), Easyvac (1.67), Erkodent (1.78), Clear Tech (1.83), BD (2.28). CONCLUSIONS: As far as these 6 microorganisms are of concern, there might not be a significant overall difference among the clear retainer materials tested in this study. A significant overall increase was observed between the first and third days, which later did not significantly increase more until day 5. The Candida albicans biofilm was more intense than the tested 5 bacteria, which themselves showed rather similar growth patterns to each other.

Degradation of polyethylene terephthalate (PET) plastics by wastewater bacteria engineered via conjugation.

Wastewater treatment plants are one of the major pathways for microplastics to enter the environment. In general, microplastics are contaminants of global concern that pose risks to ecosystems and human health. Here, we present a proof-of-concept for reduction of microplastic pollution emitted from wastewater treatment plants: delivery of recombinant DNA to bacteria in wastewater to enable degradation of polyethylene terephthalate (PET). Using a broad-host-range conjugative plasmid, we enabled various bacterial species from a municipal wastewater sample to express FAST-PETase, which was released into the extracellular environment. We found that FAST-PETase purified from some transconjugant isolates could degrade about 40% of a 0.25 mm thick commercial PET film within 4 days at 50°C. We then demonstrated partial degradation of a post-consumer PET product over 5-7 days by exposure to conditioned media from isolates. These results have broad implications for addressing the global plastic pollution problem by enabling environmental bacteria to degrade PET.

Persistence of two coronaviruses and efficacy of steam vapor disinfection on two types of carpet.

BACKGROUND: Coronaviruses, a group of highly transmissible and potentially pathogenic viruses, can be transmitted indirectly to humans via fomites. To date, no study has investigated their persistence on carpet fibers. Establishing persistence is essential before testing the efficacy of a disinfectant. METHODS: The persistence of BCoV and HCoV OC43 on polyethylene terephthalate (PET) and nylon carpet was first determined using infectivity and RT-qPCR assays. Then, the disinfectant efficacy of steam vapor was evaluated against both coronaviruses on nylon carpet. RESULTS: Immediately after inoculation of carpet coupons, 32.50% of BCoV and 3.87% of HCoV OC43 were recovered from PET carpet, compared to 34.86% of BCoV and 24.37% of HCoV OC43 recovered from nylon carpet. After incubation at room temperature for 1 h, BCoV and HCoV OC43 showed a 3.6 and > 2.8 log10 TCID50 reduction on PET carpet, and a 0.6 and 1.8 log10 TCID50 reduction on nylon carpet. Based on first-order decay kinetics, the whole gRNA of BCoV and HCoV OC43 were stable with k values of 1.19 and 0.67 h- 1 on PET carpet and 0.86 and 0.27 h- 1 on nylon carpet, respectively. A 15-s steam vapor treatment achieved a > 3.0 log10 TCID50 reduction of BCoV and > 3.2 log10 TCID50 reduction of HCoV OC43 on nylon carpet. CONCLUSION: BCoV was more resistant to desiccation on both carpet types than HCoV OC43. Both viruses lost infectivity quicker on PET carpet than on nylon carpet. Steam vapor inactivated both coronaviruses on nylon carpet within 15 s.

Microplastic Particles Contain Ice Nucleation Sites That Can Be Inhibited by Atmospheric Aging.

Recent research has shown that microplastics are widespread in the atmosphere. However, we know little about their ability to nucleate ice and their impact on ice formation in clouds. Ice nucleation by microplastics could also limit their long-range transport and global distribution. The present study explores the heterogeneous ice-nucleating ability of seven microplastic samples in immersion freezing mode. Two polypropylene samples and one polyethylene terephthalate sample froze heterogeneously with median freezing temperatures of -20.9, -23.2, and -21.9 °C, respectively. The number of ice nucleation sites per surface area, ns(T), ranged from 10-1 to 104 cm-2 in a temperature interval of -15 to -25 °C, which is comparable to that of volcanic ash and fungal spores. After exposure to ozone or a combination of UV light and ozone, simulating atmospheric aging, the ice nucleation activity decreased in some cases and remained unchanged in others. Our freezing data suggest that microplastics may promote ice formation in cloud droplets. In addition, based on a comparison of our freezing results and previous simulations using a global transport model, ice nucleation by microplastics will impact their long-range transport to faraway locations and global distribution.

Upcycling waste polyethylene terephthalate (PET) bottles into high-performance activated carbon for electrochemical desalination.

Upcycling waste polyethylene terephthalate (PET) bottles has attracted intensive research interests. This simultaneously alleviates plastic pollution and achieves a waste-to-resource strategy. Waste PET water bottles were used to fabricate value-added activated carbon (AC) electrodes for capacitive deionization (CDI). The KOH activation temperature (greater than 700 °C) prominently affected the physi-chemical properties and desalination performance of PET-derived activated carbons (PET-AC). Profiting from a large Brunauer-Emmet-Teller specific surface area (1448 m2 g-1) with a good mesoporous structure (the ratio of the mesopore volume to the total pore volume was 41.3%), PET-AC-1000 (activated at 1000 °C) possessed a huge specific capacitance of 108 F g-1 for capacitive ion storage. Moreover, when utilized as the electrode material in single-pass CDI, PET-AC-1000 exhibited a maximum electrosorption capacity of 10.82 ± 0.11 mg g-1 and a low level of energy consumption (0.07 kWh mol-1), associated with good electrochemical charging-discharging cyclic stability. The results provide a promising facile approach to tackle the challenge of plastic pollution and promote the advancement of electrode materials for economic affordable and energy-efficient electrochemical desalination process, which meets the United Nations (UN) sustainable development goals (SDGs).

Dual-porous ZIF-8 heterogeneous catalysts with increased reaction sites for efficient PET glycolysis.

Poly (ethylene terephthalate) (PET) has been widely used for drink bottles, food packing, films, and fibers, resulting in millions of tons of waste PET. Less than 10% of that waste is recycled, and the rest is discarded or incinerated. Waste PET upcycling employs chemical recycling and particularly glycolysis to create the bis(2-hydroxyethyl) terephthalate (BHET) monomer. Herein, we report a dual-porous zeolitic imidazolate framework-8 nanoparticle (DPZIF-8) heterogeneous catalyst for efficient PET glycolysis. The DPZIF-8 nanoparticles were prepared using a triethylamine modulator, which can control the nucleation and growth mechanisms of the ZIF-8 nanoparticles. The DPZIF-8 nanoparticles include both intrinsic micropores and particle-particle adhesion-induced mesopores that can provide a larger external surface area of the zinc sites in the ZIF-8 architecture. The PET glycolysis catalyzed by DPZIF-8 at 180 °C and 1 atm for 4 h shows a PET conversion of 91.7% and a BHET yield of 76.1%, the latter particularly being much higher than with a traditional heterogeneous ZIF-8 catalyst. This dual-porous structure rational design strategy can be versatile for other metal-organic frameworks (MOFs) to increase the interfacial catalytic reaction sites between the metal-organic framework and the polymer, enhancing the PET depolymerization performance and efficiency.

Functionalized Collagen I Membranes as a Bruch's Membrane Mimetic for Outer Retinal In Vitro Models.

Physiologically relevant in vitro models of the human outer retina are required to better elucidate the complex interplay of retinal tissue layers and investigate their role in retinal degenerative disorders. Materials currently used to mimic the function of Bruch's membrane fail to replicate a range of important structural, mechanical, and biochemical properties. Here, we detail the fabrication of a surface-functionalized, fibrous collagen I membrane. We demonstrate its ability to better replicate a range of important material properties akin to the function of human Bruch's membrane when compared with a commonly utilized synthetic polyethylene terephthalate alternative. We further reveal the ability of this membrane to support the culture of the ARPE-19 cell line, as well as human pluripotent stem cell-derived RPE-like cells and human umbilical vein endothelial cells. This material could provide greater physiological relevance to the native Bruch's membrane than current synthetic materials and further improve the outcomes of in vitro outer retinal models.

Enhanced activation of peroxymonosulfate by ZIF-67/g-C3N4 S-scheme photocatalyst under visible light assistance for degradation of polyethylene terephthalate.

Photocatalyst-activated peroxymonosulfate (PMS) degradation of pollutants is already widely used for wastewater treatment under visible light. Polyethylene terephthalate (PET) is widely used in daily life, but waste plastics have an irreversible negative impact on the environment. In this paper, the ZIF-67/g-C3N4 S-scheme heterojunction catalyst was synthesized as a photocatalyst to achieve a good effect on PET degradation in coordination with PMS. The results indicated that PET could be degraded up to 60.63 ± 2.12 % under the combined effect of catalyst, PMS, and light. In this experiment, the influence of catalyst-to-plastic ratio, PMS concentration, aqueous pH, and inorganic anions on plastic degradation by the photocatalytic synergistic PMS system was discussed, and the excellent performance of this system for degrading PET was highlighted through a comparative test. Electron spin resonance (ESR) and free radical quenching experiments demonstrated that SO4•- contributes the largest amount to the PET degradation performance. Furthermore, results from gas chromatography and liquid chromatography-mass spectrometry (LC-MS) indicated that the plastic degradation products include CO, CH4, and organic small-molecule liquid fuels. Finally, a possible mechanism for the light/PMS system to degrade PET in water was suggested. This paper provides a feasible solution to treat waste microplastics in water.

Binding between Cu2+/Zn2+ and aged polyethylene and polyethylene terephthalate microplastics in swine wastewaters: Adsorption behavior, and mechanism insights.

Microplastics (MPs) have aroused growing environmental concerns due to their biotoxicity and vital roles in accelerating the spread of toxic elements. Illuminating the interactions between MPs and heavy metals (HMs) is crucial for understanding the transport and fate of HM-loaded MPs in specific environmentally relevant scenarios. Herein, the adsorption of copper (Cu2+) and zinc (Zn2+) ions over polyethylene (PE) and polyethylene terephthalate (PET) particulates before and after heat persulfate oxidation (HPO) treatment was comprehensively evaluated in simulated and real swine wastewaters. The effects of intrinsic properties (i.e., degree of weathering, size, type) of MPs and environmental factors (i.e., pH, ionic strength, and co-occurring species) on adsorption were investigated thoroughly. It was observed that HPO treatment expedites the fragmentation of pristine MPs, and renders MPs with a variety of oxygen-rich functional groups, which are likely to act as new active sites for binding both HMs. The adsorption of both HMs is pH- and ionic strength-dependent at a pH of 4-6. Co-occurring species such as humic acid (HA) and tetracycline (TC) appear to enhance the affinity of both aged MPs for Cu2+ and Zn2+ ions via bridging complexation. However, co-occurring nutrient species (e.g., phosphate and ammonia) demonstrate different impacts on the adsorption, improving uptake of Cu2+ by precipitation while lowering affinity for Zn2+ owing to the formation of soluble zinc-ammonia complex. Spectroscopic analysis indicates that the dominant adsorption mechanism mainly involves electrostatic interactions and surface complexation. These findings provided fundamental insights into the interactions between aged MPs and HMs in swine wastewaters and might be extended to other nutrient-rich wastewaters.

Polyethylene terephthalate nanoparticles induce oxidative damage in Chlorella vulgaris.

Polyethylene Terephthalate (PET) is a type of plastic largely used for packing food and beverages. Unfortunately, it includes a major portion of the plastic distributed through aquatic systems wherever systematic collection and recycling are lacking. Although PET is known to be non-toxic, it is not obvious whether the nanoparticles (NPs) formed due to their degradation have any direct/indirect effect on aquatic organisms. In order to study the effects on aquatic environment, fresh water algae Chlorella vulgaris was subjected to incremental concentrations of the NPs. We observed a concentration and duration of exposure dependent decrease in algal growth rate along with reduced total chlorophyll content. Scanning electron microscopy revealed deformities in cell shape and the uptake of Propidium Iodide suggested membrane damage in response to NP exposure. Intracellular Reactive Oxygen Species level was also found significantly higher, evidenced by Dichlorodihydrofluorescein diacetate staining. Activity of antioxidant enzymes Superoxide dismutase (SOD), Peroxidase (POD) and Catalase (CAT) were significantly higher in the NP exposed groups suggesting the cellular response to regain homeostasis. Further, expression levels of the genes psaB, psbC, and rbcL associated with photosynthesis increased above two fold with respect to the control inferring the possibility of damage to photosynthesis and the initial molecular responses to circumvent the situation. In short, our studies provide evidence for oxidative stress mediated cellular damages in Chlorella vulgaris exposed to NPs of PET.

Assessing the adsorption of a diverse range of pharmaceuticals to virgin and aged poly (ethylene terephthalate) microplastics in different environmental matrices.

In this study, the adsorption of a mixture of high-consumed drugs onto virgin and aged PET microplastics has been studied for the time ever. The target mixture comprised two anti-inflammatory drugs, diclofenac and ketoprofen, one anti-hypertensive, valsartan, and four common antibiotics, indomethacin, trimethoprim, isoniazid, and metronidazole. Two types of PET MPs (virgin and UV-aged) were used in the experimental procedure. Kinetic studies were conducted, and adsorption isotherms were obtained revealing the possible interactions that take place between adsorbents and adsorbates. Among the studied pharmaceuticals, diclofenac presents the highest uptake due to its hydrophobic nature, while aging appears to induce the adsorption of the drugs in MPs. Factors like pH or the environmental matrix were also evaluated. The results revealed that sorption is pH-dependent, while more complicated matrices like wastewater or seawater exhibit lower uptake than distilled water due to the natural organic matter present or the increased salinity, respectively. Finally, desorption studies were also conducted in three different aqueous solutions examining the pH effect. The desorption of the compounds was higher for diclofenac, followed by valsartan, and ketoprofen. The desorption percentages of antibiotics were quite low.

Bacterial surface display of PETase mutants and MHETase for an efficient dual-enzyme cascade catalysis.

Biological degradation of PET plastic holds great potential for plastic recycling. However, the high costs associated with preparing free enzymes for degrading PET make it unfeasible for industrial applications. Hence, we developed various cell catalysts by surface-displaying PETase mutants and MHETase using autotransporters in E. coli and P. putida. The efficiency of surface display was enhanced through modifying the host, co-expressing molecular chaperones, and evoluting the autotransporter. In strain EC9F, PET degradation rate was boosted to 3.85 mM/d, 51-fold and 23-fold increase compared to free enzyme and initial strain ED1, respectively. The reusability of cell catalyst EC9F was demonstrated with over 38 % and 30 % of its initial activity retained after 22 cycles of BHET degradation and 3 cycles of PET degradation. The highest reported PET degradation rate of 4.95 mM/d was achieved by the dual-enzyme cascade catalytic system EC9F+EM2+R, a mixture of cell catalyst EC9F and EM2 with surfactant rhamnolipid.

Periosteal expansion osteogenesis using a tubular dynamic frame device: An experimental study in rats.

Periosteal expansion osteogenesis (PEO) is a technique for augmenting bone by creating a gradual separation between the bone and periosteum. This study assessed PEO-induced bone formation around the femurs of rats using a dynamic frame device (DFD), consisting of a shape memory membrane made of polyethylene terephthalate (PET) formed into a tubular shape. The DFDs, consisting of a PET membrane coated with hydroxyapatite (HA)/gelatin on the bone-contact surface, were inserted between the periosteum and bone of the femurs of rats. In the experimental group, DFDs were suture-fixed to the femur with 4-0 Vicryl Rapid; in the control group, 4-0 silk thread was used for fixation. Five rats per group were euthanized at intervals of 3, 5, and 8 weeks postoperatively. Bone formation was evaluated via micro-CT imaging, histomorphometry, and histological analysis. Morphological analysis revealed new bone between the femur and the periosteum, expanded by the DFD, in all groups. The mean values of new bone were 0.30 mm2 proximally, 0.18 mm2 centrally, and 0.82 mm2 distally in the control group, compared to 1.05 mm2 proximally, 0.27 mm2 centrally, and 0.84 mm2 distally in the experimental group. A significant difference in new bone was observed in the proximal region of the experimental group. Histological examination showed that a single layer of newly formed neoplastic bone was noted on the cortical bone surface across all sites. The proximal portion displayed a bone marrow cavity at the center, encircled by a thick bone cortex with a layered structure. New bone formation was notable between existing cortical bone and the periosteum, particularly at both ends of the DFD. The use of PET in PEO was a viable option for achieving ideal bone morphology.

Negligible additive effect of environmental concentrations of fragmented polyethylene terephthalate microplastics on the growth and reproductive performance of Java medaka exposed to 17ß-estradiol and bisphenol A.

To investigate whether environmental concentrations of fragmented polyethylene terephthalate (PET) microplastics (MPs) have additional or combined effects on endocrine-disrupting activity, Java medaka (Oryzias javanicus) were exposed to 17ß-estradiol (E2; 5, 10, 50, and 100 ng L-1), bisphenol A (BPA; 5, 10, 50, and 100 µg L-1), and E2 and BPA combined with PET MPs (1 and 100 particles L-1) for 200 days. The growth parameters, such as body length and weight, were significantly decreased by the highest concentrations of E2 and BPA. A significant reduction in egg production was observed in female fish exposed to BPA, with an additive toxic effect of PET MPs. A female-biased sex ratio was observed in fish exposed to both chemicals. Exposure to E2 significantly increased the hepatosomatic index (HSI) in both sexes, while no significant effect was observed in the gonadosomatic index (GSI). Exposure to BPA significantly increased the HSI in female fish and decreased the GSI in both sexes of fish. An additive effect of PET MPs was observed on the GSI value of female exposed to BPA. Significant elevations in vitellogenin (VTG) levels were observed in both sexes due to exposure to E2 and BPA. Additive effects of PET MPs were observed on VTG levels in males exposed to E2 and BPA. Taken together, even long-term treatment with PET MPs induced only a negligible additive effect on the endocrine-disrupting activity in Java medaka at environmentally relevant concentrations.

Variable stiffness performance analysis of layer jamming actuator based on bionic adhesive flaps.

Soft actuators made of soft materials cannot generate precisely efficient output forces compared to rigid actuators. It is a promising strategy to equip soft actuators with variable stiffness modules of layer jamming mechanism, which could increase their stiffness as needed. Inspired by the gecko's the array of setae, bionic adhesive flaps with inclined micropillars are applied in layer jamming mechanism. In this paper, after the manufacturing process of the layer jamming actuator based on the bionic adhesive flaps is described, the equivalent stiffness models of the whole actuator are established in the unjammed and jammed states. And the shear adhesive force of a single micropillar is calculated based on the Kendall viscoelastic band model. The finite element simulation results of two bionic adhesive flaps show that the interlaminar shear stress and stiffness increase with the increase of pressure. The measurement of shear adhesive force show that the critical shear adhesive force of the bionic adhesive material is 3.2 times that of polyethylene terephthalate (PET) material, and exhibit the ability of anisotropic adhesion behavior. The variable stiffness performance of the layer jamming actuator based on bionic adhesive flaps is evaluated by three test methods, and the max stiffness reaches 8.027 N mm-1, which is 1.5 times higher than the stiffness of the layer jamming actuator based on the PET flaps. All results of simulation and experiment effectively verify the validity and superiority of applying the bionic adhesive flaps to the layer jamming mechanism to enhance the stiffness.

Aligners: review of their chemical components, recycling, mechanical properties and therapeutic needs - Part 1 / Aligneurs : mise en perspective de la composition chimique, du recyclage, des propriétés mécaniques et des besoins thérapeutiques ­ Partie 1.

Introduction: The aligner is a thermoformed plastic device composed of various chemical components: polyurethane, polyethylene terephthalate glycol, polypropylene… All these plastics must be sufficiently resistant to abrasion and translucent for aesthetic purposes, but their solubility to salivary enzymes, insertion-disinsertion fatigue and recyclability vary according to material. From an orthodontic point of view, they must facilitate tooth movement. However, their behavior differs from that of orthodontic archwires: their Young's modulus, resilience and unloading curve are distinct, resulting in mechanical properties that fall significantly below the orthodontic requirements of multi-bracket systems. Objective: The aim of this article was to review the chemical composition, recycling and mechanical properties of aligners, and to put them into perspective with therapeutic indications. Materials and Methods: Literature data were approximated to orthodontic needs. Results: Neither plastic nor direct printing can match the mechanical properties of our archwires or the procedures of a reliable vestibular multi-attachment appliance. Discussion: Aligners remain an interesting tool in targeted indications.

Introduction: L'aligneur est un dispositif en plastique thermoformé dont la composition chimique est diverse : polyuréthane, polyéthylène téréphtalate glycol, polypropylène… Tous ces plastiques doivent être suffisamment résistants à l'abrasion et translucides pour être esthétiques mais ils présentent une solubilité aux enzymes salivaires, une fatigue liée à l'insertion-désinsertion et une recyclabilité qui sont variables selon le matériau. D'un point de vue orthodontique, ils doivent permettre de déplacer les dents. Mais leur comportement ne ressemble pas à celui des arcs orthodontiques : leur module de Young, leur résilience et leur courbe de décharge en sont éloignés et confèrent des propriétés mécaniques très inférieures aux exigences orthodontiques des appareils multi-attaches. Objectif: L'objectif de l'article était de faire le point sur la composition chimique, le recyclage, les propriétés mécaniques des aligneurs et de les mettre en perspective avec les indications thérapeutiques. Matériel et méthode: Les données de la littérature sont approchées des besoins orthodontiques. Résultats: Ni le plastique, ni l'impression directe ne sont en capacité de rivaliser avec les propriétés mécaniques de nos arcs ou avec les procédures d'un appareil multi-attache vestibulaire fiables. Discussion: Les aligneurs restent un outil intéressant dans des indications ciblées.

Polyester Microfibers Exposure Modulates Mytilus galloprovincialis Hemolymph Microbiome.

Microplastic (MP) contamination in the aquatic environment is a cause of concern worldwide since MP can be taken up by different organisms, altering different biological functions. In particular, evidence is accumulating that MP can affect the relationship between the host and its associated microbial communities (the microbiome), with potentially negative health consequences. Synthetic microfibers (MFs) represent one of the main MPs in the marine environment, which can be accumulated by filter-feeding invertebrates, such as bivalves, with consequent negative effects and transfer through the food chain. In the mussel Mytilus galloprovincialis, polyethylene terephthalate (PET) MFs, with a size distribution resembling that of an MF released from textile washing, have been previously shown to induce multiple stress responses. In this work, in the same experimental conditions, the effects of exposure to PET-MF (96 h, 10, and 100 µg/L) on mussel hemolymph microbiome were evaluated by 16S rRNA gene amplification and sequencing. The results show that PET-MF affects the composition of bacterial communities at the phylum, family and genus level, with stronger effects at the lowest concentration tested. The relationship between MF-induced changes in hemolymph microbial communities and responses observed at the whole organism level are discussed.