Lower Biodegradation Rate Research Articles

Microbial Consortia in the Remediation of Single-Use Waste: The Case of Face Masks

This study presents the results of evaluating hydrocarbonoclastic consortia in the biodegradation of microplastics derived from single-use, triple-layered polypropylene face masks. The choice of this carbon source was driven by the need to address the increase in single-use waste generated during the recent SARS-CoV-2 pandemic, as the use of face masks was a mandatory protective measure. Two bubble column bioreactors were used, each containing hydrocarbonoclastic consortia sourced from the Port of Veracruz and the Gulf of Mexico. The biodegradation activity of these consortia was assessed by observing the physical appearance of microplastic samples under a stereoscope and a microscope, as well as by calculating the weight loss of polypropylene after 15 days. The results revealed that the consortium from the Gulf of Mexico, with a maturity of 1 year, showed a higher capacity for polypropylene biodegradation, achieving a 19.98% degradation rate. This consortium also demonstrated more stable kinetics during the experimentation period. In contrast, the younger consortium from the Port of Veracruz exhibited a lower biodegradation rate of 3.77% and variable growth kinetics. Hydrocarbonoclastic bacteria identified within the consortia included Pseudomonas aeruginosa, Enterococcus faecalis, and Vibrio parahaemolyticus, among others. The hydrocarbonoclastic consortia have the potential to biodegrade from various forms of plastic waste, including single-use face masks.

Maximizing diclofenac bioremoval efficiency using Chlorella vulgaris strain H1 and Chlorella sorokiniana strain H2: Unveiling the impact of acetic acid on microalgae

BackgroundDiclofenac (DFC) is a commonly detected pharmaceutical pollutant in wastewater, posing environmental risks. Microalgae have emerged as potential candidates for bioremediation due to their ability to degrade pollutants. This study focuses on investigating the biodegradation potential of two newly isolated microalgae strains, Chlorella vulgaris strain H1 and Chlorella sorokiniana strain H2, towards DFC removal. The optimization of pH is crucial for enhancing the efficiency of bioremediation processes. Therefore, in addition to assessing the biodegradation potential of microalgae, this study also investigates the impact of adjusting the pH of the culture medium using acetic acid as an additional carbon source on the biodegradation process. MethodsThrough genetic analysis using 18S rDNA sequencing, the microalgae strains were identified. Various parameters including growth dynamics, chlorophyll content, cell proliferation, photosynthetic activity, and DFC biodegradation efficiency were comprehensively assessed. Additionally, the impact of incorporating acetic acid as an additional carbon source in the culture medium on the biodegradation process was examined. Significant FindingsC. sorokiniana strain H2 demonstrated superior biodegradation rates compared to C. vulgaris strain H1 across varying DFC concentrations. Specifically, C. sorokiniana strain H2 exhibited remarkable biodegradation rates of 84 %, 83.72 %, and 29.57 % for DFC concentrations of 12.5 mg L−1, 25 mg L−1, and 100 mg L−1, respectively. In contrast, C. vulgaris strain H1 showed lower biodegradation rates of 66.64 %, 29.24 %, and 1.83 % for the corresponding DFC concentrations. The study highlights the potential of C. sorokiniana strain H2 as a promising candidate for the removal of pharmaceutical pollutants like DFC from wastewater. Furthermore, the use of acetic acid as a supplementary carbon source enhanced the biodegradation efficiency, suggesting a potential strategy for optimizing bioremediation processes.

Functionalised Sodium-Carboxymethylcellulose-Collagen Bioactive Bilayer as an Acellular Skin Substitute for Future Use in Diabetic Wound Management: The Evaluation of Physicochemical, Cell Viability, and Antibacterial Effects.

The wound healing mechanism is dynamic and well-orchestrated; yet, it is a complicated process. The hallmark of wound healing is to promote wound regeneration in less time without invading skin pathogens at the injury site. This study developed a sodium-carboxymethylcellulose (Na-CMC) bilayer scaffold that was later integrated with silver nanoparticles/graphene quantum dot nanoparticles (AgNPs/GQDs) as an acellular skin substitute for future use in diabetic wounds. The bilayer scaffold was prepared by layering the Na-CMC gauze onto the ovine tendon collagen type 1 (OTC-1). The bilayer scaffold was post-crosslinked with 0.1% (w/v) genipin (GNP) as a natural crosslinking agent. The physical and chemical characteristics of the bilayer scaffold were evaluated. The results demonstrate that crosslinked (CL) groups exhibited a high-water absorption capacity (>1000%) and an ideal water vapour evaporation rate (2000 g/m2 h) with a lower biodegradation rate and good hydrophilicity, compression, resilience, and porosity than the non-crosslinked (NC) groups. The minimum inhibitory concentration (MIC) of AgNPs/GQDs presented some bactericidal effects against Gram-positive and Gram-negative bacteria. The cytotoxicity tests on bilayer scaffolds demonstrated good cell viability for human epidermal keratinocytes (HEKs) and human dermal fibroblasts (HDFs). Therefore, the Na-CMC bilayer scaffold could be a potential candidate for future diabetic wound care.

Biodegradation, Antibacterial Performance, and Cytocompatibility of a Novel ZK30-Cu-Mn Biomedical Alloy Produced by Selective Laser Melting.

In the present study, an antibacterial biomedical magnesium (Mg) alloy with a low biodegradation rate was designed, and ZK30-0.2Cu-xMn (x = 0, 0.4, 0.8, 1.2, and 1.6 wt%) was produced by selective laser melting, which is a widely applied laser powder bed fusion additive manufacturing technology. Alloying with Mn evidently influenced the grain size, hardness, and biodegradation behavior. On the other hand, increasing Mn content to 0.8 wt% resulted in a decrease of biodegradation rate which is attributed to the decreased grain size and relatively protective surface layer of manganese oxide. Higher Mn contents increased the biodegradation rate attributed to the presence of the Mn-rich particles. Taken together, ZK30-0.2Cu-0.8Mn exhibited the lowest biodegradation rate, strong antibacterial performance, and good cytocompatibility.

Sorption and attenuation of petroleum VOCs in five unsaturated soils: Microcosms and column experiments

The fate of volatile organic compounds (VOC) vapors in the unsaturated zone is the basis for evaluating the natural attenuation potential and vapor intrusion risk. Microcosm and column experiments were conducted to study the effects chemical speciation and soil types/properties on the fate of petroleum VOCs in unsaturated zone. The biodegradation and total attenuation rates of the seven VOCs obtained by microcosm experiments in black soil and yellow earth were also generally higher than those in floodplain soil, lateritic red earth, and quartz sand. The VOC vapors in floodplain soil, lateritic red earth, and quartz sand showed slow total attenuation rates (<0.3 d−1). N-pentane, methylcyclopentane, and methylcyclohexane showed lower biodegradation rates than octane and three monoaromatic hydrocarbons. Volatilization into the atmosphere and biodegradation are two important natural attenuation paths for VOCs in unsaturated soil columns. The volatilization loss fractions of different volatile hydrocarbons in all five unsaturated soils were generally in the order: n-pentane (93.5%–97.8%) > methylcyclopentane (77.2%–85.5%) > methylcyclohexane (53.5%–69.2%) > benzene (17.1%–73.3%) > toluene (0–45.7%) > octane (1.9%–34.2%) > m-xylene (0–5.7%). The fractions by volatilization into the atmosphere of all seven hydrocarbons in quartz sand, lateritic red earth, and floodplain soil were close and higher compared to the yellow earth and black soil. Overall, this study illustrated the important roles chemical speciation and soil properties in determining the vapor-phase transport and natural attenuation of VOCs in the unsaturated zone.

Biodegradation performance of ball burnished magnesium alloy in stimulated body fluids for bioresorbable implant applications

Magnesium alloys are found to be potential bioresorbable materials. However, the application range of these alloys as bioresorbable materials has been limited due to rapid degradation in physiological fluids. The current study deals with the enhancement of degradation behavior of Mg Ze41A alloy in SBF solution by ball burnishing. Further, the influence of burnishing parameters on biodegradation rate has been investigated by Tafel plots, polarization resistance, electrochemical impedance spectroscopy and surface morphology analysis of degraded samples. Additionally, the biodegradation rate has been estimated by ANFIS modeling. The biodegradation rate of Mg Ze41A has been reduced from 1.106 mm/yr to 0.367 mm/yr with an improvement of 68.82% at optimum burnishing condition of burnishing force 50 N, burnishing speed 1400 RPM, burnishing feed 125 mm/min and 2 passes. ANOVA analysis has revealed that burnishing force and feed have contributed the most for the enhancement. The shift in degradation potential towards noble direction and reduction in degradation current density in potentiodynamic polarization curves and the highest charge transfer resistance in electrochemical impedance spectroscopy of the burnished samples are observed for burnished samples. The results reveal that ball burnishing process is a potential surface modification method in reducing the biodegradation rate of Mg Ze41A alloy. The ball burnishing has resulted in lowest biodegradation rate at a degradation current density of 5.743 μA/cm2 and degradation potential of −1.513 V. The ANFIS model developed with 81 fuzzy rules and triangular membership function estimated the biodegradation rate with an accuracy of 95.03%. The decrease in biodegradation rate of ball burnished magnesium substrate in SBF is essentially due to cumulative effect of compressive residual stress, microhardness, surface finish, work hardening and grain refinement.

Effect of the anode material, applied current and reactor configuration on the atenolol toxicity during an electrooxidation process

Atenolol (ATL) is a beta-blocker pharmaceutical product which is excreted mainly unchanged and may represent a long-term risk for organisms present in the sea and in fresh water. Due to its low biodegradation rate, electrochemical advanced oxidation processes (EAOPs) can be used to remove this compound. In this work, ATL ecotoxicity was analyzed in the presence of sodium sulfate (Na2SO4), which is widely used as supporting electrolyte in EAOPs. Ecotoxicity values were expressed as the pollutant concentration that leads to a 50% inhibition of the root elongation of Lactuca sativa seeds in relation to the control (EC50(5 days)). The obtained values for ATL showed an EC50(5 days) of 1377 mg L−1 towards Lactuca sativa. When Na2SO4 was added, the toxicity of the sample increased but no synergy was detected between both compounds. With 2 g L−1 Na2SO4, ATL showed an EC50(5 days) of 972 mg L−1; and with 4 g L−1 Na2SO4 and higher concentrations, EC50 value for ATL was 0 mg L−1. Statistical tools were used to obtain the zones of the [ATL]-[Na2SO4] plane which are toxic towards Lactuca sativa.Solutions containing ATL and Na2SO4 were treated by electrooxidation. Two anode materials (a boron-doped diamond electrode and a microporous Sb-doped SnO2 ceramic one); three operation currents (0.4, 0.6 and 1 A); and two reactor configurations (one-compartment reactor and two-compartment reactor separated by a cation exchange membrane) were used. Lactuca sativa seeds and Vibrio fischeri bacterium tests were employed to evaluate the toxicity of the solutions before and after applying the electrooxidation process. In all the tests, the ecotoxicity of the treated sample increased. This fact is owing to the persulfate presence in the solution due to the sulfate electrochemical oxidation. Nevertheless, none of the final samples were toxic towards Vibrio fischeri because ecotoxicity values were lower than 10 TU; and, in the case of the one-compartment reactor, practically all of them were also non-toxic towards Lactuca sativa. The toxicity of the treated samples increased when using the two-compartment reactor in the presence of the BDD anode, and when the operation current was increased. This is attributed to the highest formation of persulfates. Amongst all the tests performed in this work, the lowest toxicity value (i.e., 3 TU) together with the complete mineralization and degradation degrees was achieved with the two-compartment reactor using the BDD anode and operating at 0.6 A.

Dielectric barrier discharge combined with Fe(III)-NTA activated persulfate for efficient degradation of enrofloxacin in water

ABSTRACT Enrofloxacin (ENR) is widely used in aquaculture due to its broad-spectrum activity against a large number of pathogenic bacteria. However, ENR exhibits strong adsorption and a low biodegradation rate in the environment. This study proposes a new method for degrading ENR, which combines dielectric barrier discharge (DBD) with advanced oxidation of peroxymonosulfate (PMS, HSO5 −) and the use of nitrilotriacetic acid (NTA) combined with Fe(III) activator to improve reaction efficiency. The effects on the degradation efficiency were experimentally investigated by adjusting the internal process parameters and adding coexisting substances. The ESR and free radical scavenging experiments showed that both hydroxyl and sulfate radicals contributed to the degradation of the pollutant ENR. Based on the identified intermediates, and three possible degradation pathways were suggested. And the intermediates were less harmful. In conclusion, the Fe(III)-NTA/PMS/DBD system may be an efficient, environmentally friendly and new technology with development potential.

ZnO and Cu/ZnO-modified Magnesium orthopedic implant with improved osteoblast cellular activity: An in-vitro study

Mg-based biomaterials, due to their desirable mechanical integrity, natural bioabsorbability, and osteopromotive characteristics, are promising candidates for both orthopedic applications, such as the surgical fixation of injured musculoskeletal tissues, and cardiovascular applications like coronary artery stents. In the present study, nano- and micro-sized ZnO and Cu/ZnO bioactive particles were used to fabricate Mg-based biocomposites using friction stir processing (FSP). FSP resulted in significant microstructural modification in terms of grain refinement, uniform redistribution of secondary phase particles and homogenous dispersion of bioactive particles. Long-term biodegradation results through H2 evolution method illustrated that biodegradation rate of the bioabsorbable WE43 alloy was significantly reduced by addition of bioactive particles. In addition, fabricated biocomposites with addition of nano-sized particles resulted in lower biodegradation rate in comparison to those with micro-sized particles. Furthermore, uniform dispersion of bioactive particles resulted in superior in-vitro biocompatibility in contact with MC3T3-E1 mouse osteoblast cells. Mg–ZnO–N and Mg–Cu/ZnO–N biocomposites showed improved cell adhesion with elongated and spread morphology of MC3T3-E1 osteoblast cells. Live/dead staining and MTT assay indicated that number of healthy cells and cell viability after 24 h of incubation increased by uniform distribution of bioactive particles. Moreover, fabricated biocomposites with homogenous distribution of Zn2+ and Cu2+ ions showed higher ALP activity. Our findings propose that Mg–ZnO and Mg–Cu/ZnO biocomposites with homogenous dispersion of bioactive particles can be promising candidates for bone tissue regeneration applications.

Remote Outcomes with Poly-ε-Caprolactone Aortic Grafts in Rats.

Poly-ε-caprolactone ((1,7)-polyoxepan-2-one; PCL) is a biodegradable polymer widely used in various fields of bioengineering, but its behavior in long-term studies appears to depend on many conditions, such as application specificity, chemical structure, in vivo test systems, and even environmental conditions in which the construction is exploited in. In this study, we offer an observation of the remote outcomes of PCL tubular grafts for abdominal aorta replacement in an in vivo experiment on a rat model. Adult Wistar rats were implanted with PCL vascular matrices and observed for 180 days. The results of ultrasound diagnostics and X-ray tomography (CBCT) show that the grafts maintained patency for the entire follow-up period without thrombosis, leakage, or interruptions, but different types of tissue reactions were found at this time point. By the day of examination, all the implants revealed a confluent endothelial monolayer covering layers of hyperplastic neointima formed on the luminal surface of the grafts. Foreign body reactions were found in several explants including those without signs of stenosis. Most of the scaffolds showed a pronounced infiltration with fibroblastic cells. All the samples revealed subintimal calcium phosphate deposits. A correlation between chondroid metaplasia in profound cells of neointima and the process of mineralization was supported by immunohistochemical (IHC) staining for S100 proteins and EDS mapping. Microscopy showed that the scaffolds with an intensive inflammatory response or formed fibrotic capsules retain their fibrillar structure even on day 180 after implantation, but matrices infiltrated with viable cells partially save the original fibrillary network. This research highlights the advantages of PCL vascular scaffolds, such as graft permeability, revitalization, and good surgical outcomes. The disadvantages are low biodegradation rates and exceptionally high risks of mineralization and intimal hyperplasia.

Assessment of microstructure, biocompatibility and in-vitro biodegradation of a biomedical Mg-Hydroxyapatite composite for bone tissue engineering

In the present study, an Mg-based biomedical composite is fabricated by addition of Hydroxyapatite bioactive nanoparticles into a substrate of bioabsorbable WE43 Mg alloy using multi pass friction stir processing (FSP). The findings indicate that applying 6 passes of FSP leads to a decrease of grain size by over 93%, crushing and redistribution of secondary phase particles within the Mg matrix, improved homogeneity of Hydroxyapatite bioactive particles and a reduction in their agglomeration. In vitro Biodegradation tests prove that as the number of FSP passes increases, the weight loss of fabricated bio-composites and biodegradation rate in simulated body fluid (SBF) decrease. Bioactivity of Mg-based bio-composites is assessed by in vitro immersion in SBF for 28 days. Biomineralization process shows that all fabricated Mg-Hydroxyapatite bio-composites exhibit bone-like apatite forming ability, and cauliflower-shaped Hydroxyapatite crystals form on their surface. Moreover, increasing the uniformity of Hydroxyapatite particles stimulates formation of cauliflower-shaped Hydroxyapatite denser crystals, which improves biocompatibility of bio-composites. Biocompatibility of fabricated bio-composites is also evaluated by MTT assay and DAPI staining. Mg-HA-6P demonstrates the highest number of healthy flattened spindle shaped L-929 fibroblast cells with 83.36% cell viability after 5 days of incubation compared to other samples. Increasing number of FSP passes causes high bioactivity, low biodegradation rate and homogeneous distribution of Hydroxyapatite particles, which in turn improve the viability of L-929 fibroblast cells. Furthermore, with the addition of Hydroxyapatite particles and an increase in the number of FSP passes, the yield strength values of the samples increase, reaching 212 MPa and 226 MPa for the Mg–6P and Mg–6P-HA samples, respectively.

Enhanced in-vitro biodegradation, bioactivity, and mechanical properties of Mg-based biocomposite via addition of calcium-silicate-based bioceramic through friction stir processing as resorbable temporary bone implant

Bioabsorbable Mg and alloys have been used as metallic biomaterials for orthopedic implant applications due to their similar mechanical properties to human natural bone. High biodegradation rate is the main reason for limiting clinical applications of Mg and alloys in biological media. In order to achieve long-lasting bio applications of bioabsorbable WE43 Mg alloy, it is necessary to improve strength and bioactivity and control biodegradation rate of this material. In this study, Mg-based biocomposites are produced using friction stir processing (FSP) by addition of wollastonite (CaSiO3) calcium-silicate-based bioactive reinforcing particle into Mg matrix. The results showed that applied severe plastic deformation during FSP caused formation of ultra-fine grain structure with homogenous distribution of secondary phase particles, which resulted in a remarkable improvement of ductility, strength and load bearing capacity of FSPed Mg matrix. Also, biodegradation behavior of resulting biocomposite was evaluated using electrochemical methods and in-vitro immersion test in simulated body fluid (SBF) and phosphate-buffered saline (PBS) at 37.5 °C. The results revealed that processed bioabsorbable Mg alloy showed a lower biodegradation rate compared to monolithic Mg alloy. Furthermore, the presence of wollastonite bioceramic particles significantly enhanced strength and reduced biodegradation of the Mg-based biocomposite. Moreover, the addition of wollastonite bioceramic particles positively affected the bioactivity of Mg matrix by forming a cauliflower shaped bone-like hydroxyapatite layer on the surface after 28 days of immersion in SBF and stimulate bone tissue regeneration.

Human metabolism and excretion kinetics of the surfactant 2,4,7,9-tetramethyl-5-decyne-4,7-diol (TMDD) after oral and dermal administration.

2,4,7,9-Tetramethyl-5-decyne-4,7-diol (TMDD) is a non-ionic surfactant with a wide range of applications. TMDD is considered a high-production chemical and, due to its low biodegradation rate, possesses a potentially high prevalence in the environment. However, despite its widespread use, toxicokinetic data and data on internal exposure to TMDD in the general population are completely lacking. Hence, we developed a human biomonitoring (HBM) method for TMDD. Our approach included a metabolism study with four subjects, who were administered an oral dose of 75µg TMDD/kg body weight and a dermal dose of 750µg/kg body weight. Terminal methyl-hydroxylated TMDD (1-OH-TMDD) was previously identified as the main urinary metabolite in our lab. The results of the oral and dermal applications were used to determine the toxicokinetic parameters of 1-OH-TMDD as a biomarker of exposure. Finally, the method was applied to 50 urine samples from non-occupationally exposed volunteers. Results show that TMDD was rapidly metabolized, with an average tmax of 1.7h and a rapid and almost complete (96%) excretion of 1-OH-TMDD until 12h after oral dosage. Elimination was bi-phasic, with half-lives of 0.75-1.6h and 3.4-3.6h for phases 1 and 2, respectively. The dermal application resulted in a delayed urinary excretion of this metabolite with a tmax of 12h and complete excretion after about 48h. The excreted amounts of 1-OH-TMDD represented 18% of the orally administered TMDD dose. The data of the metabolism study demonstrated a fast oral as well as substantial dermal resorption of TMDD. Moreover, the results indicated an effective metabolism of 1-OH-TMDD, which is excreted rapidly and completely via urine. Application of the method to 50 urine samples revealed a quantification rate of 90%, with an average concentration of 0.19ng/mL (0.97nmol/g creatinine). With the urinary excretion factor (Fue) derived from the metabolism study, we estimated an average daily intake of 1.65µg TMDD from environmental and dietary sources. In conclusion, 1-OH-TMDD in urine is a suitable biomarker of exposure to TMDD and can be applied for biomonitoring of the general population.

Fabrication of osteogenesis induced WE43 Mg-Hydroxyapatite composites with low biodegradability and increased biocompatibility for orthopedic implant applications

Good biocompatibility, low biodegradation rate and excellent mechanical properties are essential for desirable performance of metallic biomaterials during osseointegration process. In the present study, bioabsorbable WE43 Mg alloy was used for fabrication of bio-composites with addition of nanosized hydroxyapatite (HA) particles by means of multi pass friction stir processing (FSP) for orthopedic implant applications. Microstructure, in vitro biodegradation and biocompatibility, wettability, and microhardness of resultant bio-composites were characterized. Results showed that applying severe plastic deformation through FSP caused significant grain refinement of Mg matrix and homogenous dispersion of fragmented secondary phase particles. Moreover, applying higher number of FSP passes increased uniformity of distribution of HA nanoparticles throughout Mg matrix. Compared to coarse grain samples, grain refined samples showed lower Mg2+ concentration and H2 evolution in simulated body fluid (SBF). Moreover, addition of HA into Mg matrix, reduced Mg2+ release and H2 evolution. The bio-composites illustrated uniformly and flatly corroded surface compared to samples without HA nanoparticles. During immersion of the bio-composites in SBF solution, a cauliflower structure of Ca–P compounds deposited on the surface of bio-composites which confirmed acceptable biomineralization. Contact angle measurement demonstrated that wettability of fabricated bio-composites increased by increasing number of FSP passes. Mouse osteoblast MC3T3 cell culture indicated that the fabricated bio-composites with uniform distribution of HA nanoparticles showed excellent in vitro biocompatibility, cell viability, and cell proliferation. Eventually, it was found that applying further FSP and presence of HA nanoparticles resulted in increased microhardness which is an indication of higher load-bearing capability of the fabricated bone implants.

A New Colorimetric Test for Accurate Determination of Plastic Biodegradation.

As plastic waste is accumulating in both controlled waste management settings and natural settings, much research is devoted to search for solutions, also in the field of biodegradation. However, determining the biodegradability of plastics in natural environments remains a big challenge due to the often very low biodegradation rates. Many standardised test methods for biodegradation in natural environments exist. These are often based on mineralisation rates in controlled conditions and are thus indirect measurements of biodegradation. It is of interest for both researchers and companies to have tests that are more rapid, easier, and more reliable to screen different ecosystems and/or niches for their plastic biodegradation potential. In this study, the goal is to validate a colorimetric test, based on carbon nanodots, to screen biodegradation of different types of plastics in natural environments. After introducing carbon nanodots into the matrix of the target plastic, a fluorescent signal is released upon plastic biodegradation. The in-house-made carbon nanodots were first confirmed regarding their biocompatibility and chemical and photostability. Subsequently, the effectivity of the developed method was evaluated positively by an enzymatic degradation test with polycaprolactone with Candida antarctica lipase B. Finally, validation experiments were performed with enriched microorganisms and real environmental samples (freshwater and seawater), of which the results were compared with parallel, frequently used biodegradation measures such as O2 and CO2, dissolved organic carbon, growth and pH, to assess the reliability of the test. Our results indicate that this colorimetric test is a good alternative to other methods, but a combination of different methods gives the most information. In conclusion, this colorimetric test is a good fit to screen, in high throughput, the depolymerisation of plastics in natural environments and under different conditions in the lab.

Cuproptosis-Inducible Chemotherapeutic/Cascade Catalytic Reactor System for Combating with Breast Cancer.

Cascade hydroxyl radical generating hydrogel reactor structures including a chemotherapeutic agent are invented for multiple treatment of breast cancer. Glucose oxidase (GOx) and cupric sulfate (Cu) are introduced for transforming accumulated glucose (in cancer cells) to hydroxyl radicals for starvation/chemodynamic therapy. Cu may also suppress cancer cell growth via cuproptosis-mediated cell death. Berberine hydrochloride (BER) is engaged as a chemotherapeutic agent in the hydrogel reactor for combining with starvation/chemodynamic/cuproptosis therapeutic modalities. Moreover, Cu is participated as a gel crosslinker by coordinating with catechol groups in hyaluronic acid-dopamine (HD) polymer. Controlling viscoelasticity of hydrogel reactor can extend the retention time following local injection and provide sustained drug release patterns. Low biodegradation rate of designed HD/BER/GOx/Cu hydrogel can reduce dosing frequency in local cancer therapy and avoid invasiveness-related inconveniences. Especially, it is anticipated that HD/BER/GOx/Cu hydrogel system can be applied for reducing size of breast cancer prior to surgery as well as tumor growth suppression in clinical application.

Extrusion-based 3D printing of biodegradable, osteogenic, paramagnetic, and porous FeMn-akermanite bone substitutes.

The development of biodegradable Fe-based bone implants has rapidly progressed in recent years. Most of the challenges encountered in developing such implants have been tackled individually or in combination using additive manufacturing technologies. Yet not all the challenges have been overcome. Herein, we present porous FeMn-akermanite composite scaffolds fabricated by extrusion-based 3D printing to address the unmet clinical needs associated with Fe-based biomaterials for bone regeneration, including low biodegradation rate, MRI-incompatibility, mechanical properties, and limited bioactivity. In this research, we developed inks containing Fe, 35 wt% Mn, and 20 or 30 vol% akermanite powder mixtures. 3D printing was optimized together with the debinding and sintering steps to obtain scaffolds with interconnected porosity of 69%. The Fe-matrix in the composites contained the γ-FeMn phase as well as nesosilicate phases. The former made the composites paramagnetic and, thus, MRI-friendly. The in vitro biodegradation rates of the composites with 20 and 30 vol% akermanite were respectively 0.24 and 0.27mm/y, falling within the ideal range of biodegradation rates for bone substitution. The yield strengths of the porous composites stayed within the range of the values of the trabecular bone, despite in vitro biodegradation for 28 d. All the composite scaffolds favored the adhesion, proliferation, and osteogenic differentiation of preosteoblasts, as revealed by Runx2 assay. Moreover, osteopontin was detected in the extracellular matrix of cells on the scaffolds. Altogether, these results demonstrate the remarkable potential of these composites in fulfilling the requirements of porous biodegradable bone substitutes, motivating future in vivo research. STATEMENT OF SIGNIFICANCE: We developed FeMn-akermanite composite scaffolds by taking advantage of the multi-material capacity of extrusion-based 3D printing. Our results demonstrated that the FeMn-akermanite scaffolds showed an exceptional performance in fulfilling all the requirements for bone substitution in vitro, i.e., a sufficient biodegradation rate, having mechanical properties in the range of trabecular bone even after 4 weeks biodegradation, paramagnetic, cytocompatible and most importantly osteogenic. Our results encourage further research on Fe-based bone implants in in vivo.

Gelatin–chitosan–cellulose nanocrystals as an acellular scaffold for wound healing application: fabrication, characterisation and cytocompatibility towards primary human skin cells

Biopolymers that mimic the extracellular matrix are favourable in tissue engineering. However, the rapid degradation and the lack of mechanical and enzymatic stabilities of these biopolymers prompt researchers to composite different biopolymers. In this study, we aim to develop an acellular gelatin-chitosan-cellulose nanocrystal (GCCNC) scaffold as a potential wound dressing. The GCCNC mixture was homogenised via ultrasonication and the genipin crosslinking was performed by magnetic stirring. The mixture was then frozen at − 80 °C for 6 h and freeze-dried. The effects of different ratios of gelatin and chitosan with cellulose nanocrystals on the physiochemical properties, mechanical properties, and cellular biocompatibility were studied. Our results herein showed that G3C7CNC demonstrated a homogenous interconnected porous structure with a good porosity (67.37 ± 9.09%) and pore size (148.46 ± 48.68 µm), acceptable swelling ratio (1071.11 ± 140.26%), adequate water vapour transmission rate (315.59 ± 25.27 g/m2/day), low contact angle (70.21 ± 6.79°), and sufficient mechanical strength (modulus of 64.67 ± 12.42 MPa). The lower biodegradation rate in the G3C7CNC (0.06 ± 0.01 mg/hr) compared to G10CNC (0.48 ± 0.07 mg/hr) together with the absence of glass transition phenomenon indicated an increase in both enzymatic and thermal stabilities. Furthermore, G3C7CNC was non-cytotoxic and biocompatible with human epidermal keratinocytes (HEKs) and human dermal fibroblasts (HDFs). The presence of collagen type I and α-smooth muscle actin expression in HDFs, together with the expression of cytokeratin-14 in HEKs, demonstrated our scaffold’s ability to maintain normal skin physiological functions. Therefore, this study proposes that the fabricated GCCNC scaffold could serve as a potential acellular skin substitute in managing chronic wounds.

Understanding the mechanism of enhanced anaerobic biodegradation of biodegradable plastics after alkaline pretreatment

Biodegradable plastics (BPs) tend to replace conventional plastics, which increases the amount of BP waste entering the environment. The anaerobic environment exists extensively in nature, and anaerobic digestion has become a widely used technique for organic waste treatment. Many kinds of BPs have low biodegradability (BD) and biodegradation rates under anaerobic condition due to the limitation of hydrolysis, so they still have harmful environmental consequences in anaerobic environment. There is an urgent need to find an intervention method to improve the biodegradation of BPs. Therefore, this study aimed to investigate the effectiveness of alkaline pretreatment in accelerating the thermophilic anaerobic degradation of ten widely used BPs, such as poly (lactic acid) (PLA), poly (butylene adipate-co-terephthalate) (PBAT), thermoplastic starch (TPS), poly (butylene succinate-co-butylene adipate) (PBSA), cellulose diacetate (CDA), etc. The results showed that NaOH pretreatment significantly improved the solubility of PBSA, PLA, poly (propylene carbonate) (PPC), and TPS. Except for PBAT, pretreatment with an appropriate NaOH concentration could improve the BD and degradation rate. The pretreatment also reduced the lag phase in the anaerobic degradation of BPs such as PLA, PPC, and TPS. Specifically, for CDA and PBSA, the BD increased from 4.6 % and 30.5 % to 85.2 % and 88.7 %, with increments of 1752.2 % and 190.8 %, respectively. Microbial analysis indicated that NaOH pretreatment promoted the dissolution and hydrolysis of PBSA and PLA and the deacetylation of CDA, which contributed to rapid and complete degradation. This work not only provides a promising method for improving the degradation of BP waste but also lays the foundation for its large-scale application and safe disposal.

A Biodegradable, Bio-Based Polymer for the Production of Tools for Aquaculture: Processing, Properties and Biodegradation in Sea Water.

Bio-based, biodegradable polymers can dramatically reduce the carbon dioxide released into the environment by substituting fossil-derived polymers in some applications. In this work, prototypes of trays for aquaculture applications were produced via injection molding by using a biodegradable polymer, Mater-Bi®. A characterization carried out via calorimetric, rheological and mechanical tests revealed that the polymer employed shows properties suitable for the production of tools to be used in aquaculture applications. Moreover, the samples were subjected to a biodegradation test in conditions that simulate the marine environment. The as-treated samples were characterized from gravimetrical, morphological and calorimetric point of views. The obtained data showed a relatively low biodegradation rate of the thick molded samples. This behavior is of crucial importance since it implies a long life in marine water for these manufacts before their disappearing.