Concentration Of Microspheres Research Articles

Establishment of fluorescence multi-flow cytometric immunoassay for the simultaneous quantitative detection of six allergen-sIgE antibodies

BackgroundThe in vitro specific IgE (sIgE) assays now commonly used in clinical laboratories are not only time-consuming and expensive but also require many serum samples. To address these limitations, a novel fluorescent microsphere-based multiplex flow cytometric immunoassay was developed. This innovative assay enables rapid and simultaneous quantitative detection of multiple allergen-sIgE antibodies. ObjectiveTo establish a new method for the simultaneous quantitative detection of 6 allergen-sIgE antibodies based on fluorescence multiplex flow cytometry. MethodsSix different encoded fluorescent microspheres were selected to covalently couple 6 allergens, and their antigen-coupling activities were verified. After optimizing the multiplexing procedure and reaction conditions, including the concentration of microspheres encapsulated by allergens, reaction temperature, and reaction time, standard curves were established to quantify the 6 allergen-sIgE, and their performance was evaluated according to clinical guidelines. ResultsThe chosen analytical mode was optimized for the detection of the 6 allergens-sIgE for 70 minutes. The established coefficients of variation for multiplex flow cytometry reproducibility and intermediate precision were less than 10%. Linear regression analysis showed a highly significant quantitative correlation between the results of the multiple analyses of Dermatophagoides pteronyssinus, Dermatophagoides farinae, Artemisia, and cat hair allergens and ImmunoCAP (Thermo Fisher Scientific): the r2 values ranged from 0.85 to 0.97 (P < .0001). In addition, there was a high correlation between the results of the multiplex analysis of dog hair allergens and the capture enzyme-linked immunosorbent assay (r2 = 0.92, P < .0001). ConclusionA high-throughput system called multiplex flow cytometry has been developed for the simultaneous detection of 6 inhalant allergens. The method has the advantage of being rapid and using less serum. Furthermore, it has the potential to be expanded to include other allergens and biologic agents.

Remarkable lubricity of CNTs microspheres as additives in oil lubricant for ceramic components

Severe wear was often caused by adhesive wear and tribo-chemical reaction for ceramic components. In view of this situation, potentials of carbon nanotubes (CNTs) used as oil additives were explored for lubrication of ceramic/steel tribo-components. Microscopic morphology and dispersion stability of the prepared CNTs were characterized. CNTs microspheres were formed and this might because of their aggregation that also lead to the weak dispersion stability. Additionally, nano-fluids containing various concentration of CNTs microspheres were prepared for exploring the optimum concentration, where their lubricating behavior for ceramic/steel tribo-components was investigated to determine the relation between CNTs microspheres and tribological properties. The results indicated that the optimum concentration was 0.2 wt%, where 53.1 % of friction reduction and 50.7 % of wear resistance were achieved at high contact stress of 1.35 GPa. The superior lubricity of CNTs microspheres might be attributed to their rolling movement and formation of protective film.

Comparison of Physicochemical Characteristics and Biostimulatory Functions in Two Calcium Hydroxyapatite-Based Dermal Fillers.

&nbsp; Dermal fillers containing calcium hydroxyapatite (CaHA) are categorized as biostimulatory. However, differences in CaHA biomaterial likely affect the resultant induction of collagen synthesis, and variability in microsphere shape and size likely influences a patient&rsquo;s immune response. This study compares 2 CaHA based fillers: one suspended in carboxymethylcellulose (denoted "CaHA/CMC"), and one crosslinked with 1,4-butanediol diglycidyl ether to hyaluronic acid (denoted "CaHA/HA"). To characterize CaHA/CMC and CaHA/HA fillers to stimulate in vitro collagen biosynthesis. Physicochemical evaluations included G&prime; and extrusion force. Scanning electron microscopy (SEM) was used to characterize isolated CaHA microspheres and freeze-dried formulations. Collagen I and III expression were evaluated using immunofluorescence. CaHA/CMC showed higher G&prime; (P&lt;0.001) and lower extrusion force (P=0.0003), with uniform polymeric-matrix interactions, compared with CaHA/HA. On SEM, isolated microspheres and freeze-dried CaHA/CMC showed round and smooth surfaced microspheres of similar size. Isolated microspheres and freeze-dried CaHA/HA showed nonhomogeneous, broken microspheres, of various sizes, with fragments embedded in the polymer matrix. Although both fillers induced collagen III expression, only CaHA/CMC induced longer-lasting collagen I expression, with increases of 123% (P=0.007) and 164% (P&lt;0.0001) at 2 and 5 mg/mL, respectively, compared with control. CaHA/CMC also increased collagen I expression at equivalent CaHA microsphere concentrations at 2 (P=0.0052) and 5 mg/mL (P&lt;0.0001), compared with CaHA/HA. The physicochemical characteristics selected for evaluation were more favorable for CaHA/CMC than CaHA/HA. When compared with CaHA/HA, the smooth, homogeneous microsphere composition of CaHA/CMC promoted significantly more collagen I biosynthesis, an essential process for tissue augmentation and long-lasting aesthetic improvement.&nbsp;Citation: Kunzler C, Hartmann C, Nowag B, et al. Comparison of physicochemical characteristics and biostimulatory functions in two calcium hydroxyapatite-based dermal fillers. J Drugs Dermatol. 2023;22(9):910-916. doi:10.36849/JDD.7684.

Fabrication of microspheres and characterization of antimicrobial and anti-inflammatory activity isolated fraction from total alcoholic extract of Cassia Fistula (Linn.) in carrageenan-Type-IV induced inflammatory rats

The Cassia fistula Linn is known as the golden shower tree. It’s also referred to as a "disease killer" in Ayurvedic medicine. The current study investigates the effect and estimate of antimicrobial and Anti-inflammatory activity guided fraction isolated from alcoholic extract of Cassia fistula (Linn.) root on carrageenan-Type IV induced Inflammatory rats for using Column fraction of alcoholic extract of root of Cassia fistula (Linn.) An in vivo carrageenan-induced paw edoema model was used to confirm further the anti-inflammatory effect of the fraction aloe-emodin and physcion-loaded microspheres. This study was designed first time for the isolation of alcoholic fraction of aloe emodin and Physcion by root extract and screening of pharmacological activities of Cassia fistula. Aloe-emodin and Physcion fraction demonstrated antibacterial and antifungal effectiveness against the studied pathogens in a dose-dependent manner, according to anti-microbial activity. 50 mg/ml concentration of Physcion-containing microspheres and aloe emodin's antibacterial efficacy against tested pathogens. The anti-inflammatory activity of Aloe emodin and Physcion was found in an equal manner. Both Microsphere samples were found capable of controlling the inflammation till 6 hours. According to the findings of this research, the chosen plant extracts have an immediate anti-inflammatory effect. There are three stages during which carrageenan-induced inflammation mediators are released.

Injectable antibacterial Ag-HA/ GelMA hydrogel for bone tissue engineering.

Background: Fracture or bone defect caused by accidental trauma or disease is a growing medical problem that threats to human health.Currently, most orthopedic implant materials must be removed via follow-up surgery, which requires a lengthy recovery period and may result in bacterial infection. Building bone tissue engineering scaffolds with hydrogel as a an efficient therapeutic strategy has outstanding bionic efficiency.By combining some bionic inorganic particles and hydrogels to imitate the organic-inorganic characteristics of natural bone extracellular matrix, developing injectable multifunctional hydrogels with bone tissue repair effects and also displaying excellent antibacterial activity possesses attractive advantages in the field of minimally invasive therapy in clinical. Methods: In the present work, a multifunctional injectable hydrogel formed by photocrosslinking was developed by introducing hydroxyapatite (HA) microspheres to Gelatin Methacryloyl (GelMA) hydrogel. Results: The composite hydrogels exhibited good adhesion and bending resistance properties due to the existence of HA. In addition, when the concentration of GelMA is 10% and the concentration of HA microspheres is 3%, HA/GelMA hydrogel system displayed increased microstructure stability, lower swelling rate, increased viscosity, and improved mechanical properties. Furthermore, the Ag-HA/GelMA demonstrated good antibacterial activity against Staphylococcus aureus and Escherichia coli, which could signifificantly lower the risk of bacterial infection following implantation. According to cell experiment, the Ag-HA/GelMA hydrogel is capable of cytocompatibility and has low toxicity to MC3T3 cell. Conclusion: Therefore, the new photothermal injectable antibacterial hydrogel materials proposed in this study will provide a promising clinical bone repair strategy and is expected to as a minimally invasive treatment biomaterial in bone repair fields.

An efficient and convenient Fiber -2- based latex agglutination test for the detection of antibodies against fowl adenovirus serotype 4 in clinical samples

To detect the antibody against fowl adenovirus serotype 4 (FAdV-4) in clinical practice, the latex agglutination test (LAT) was developed by using the Fiber-2 protein of FAdV-4 as an antigen bound to sensitized latex microspheres. The concentration, time, and temperature of sensitization latex microspheres by the Fiber-2 protein were studied and optimized; the specificity, sensitivity, and repeatability of LAT were tested; and the method developed in the study was applied. The results showed that the optimum sensitization concentration of Fiber-2 protein was 0.8 mg/mL, the time was 120 min, and the temperature was 37 ℃. Except for antiserum against FAdV-4 and FAdV-10, LAT developed in the study could not agglutinate antisera against FAdV-1, FAdV-2, FAdV-3, FAdV-4, FAdV-5, FAdV-6, FAdV-8a, FAdV-8b, FAdV-11, Newcastle disease virus, infectious bronchitis virus, egg drop syndrome virus and Clostridium perfringens. Compared with the commercial FAdV-4 ELISA Kit, the titers in 21 clinical samples were low when tested by the developed LAT method, but there was no significant difference. The coefficients of variation among different batches and the same batch of latex-sensitized particles were between 0 % and 13.3 % and 0–8.7 %, respectively. The critical value of immune protective antibody against FAdV-4 was 25, and the titers in 40.9 % of clinical samples were higher than the immune critical point. The results showed that the Fiber-2-based LAT developed in the study has the characteristics of high specificity, sensitivity and repeatability, has the advantages of free equipment, long shelf life, and fast and easy operation, and is an effective and convenient method for serological diagnosis of FAdV-4 infection and evaluating the efficacy of vaccines.

Fabrication of a translational photoacoustic needle sensing probe for interstitial photoacoustic spectral analysis

In our previous study, we demonstrated the feasibility of using an all-optical interstitial photoacoustic (PA) needle sensing probe for quantitative study of tissue architectures with PA spectral analysis (PASA). In this work, we integrated the optical components into an 18 G steel needle sheath for clinical translation. The dimensions of the needle probe are identical to those of a core biopsy probe and are fully compatible with standard procedures such as prostate biopsy. To our knowledge, this is the first interstitial PA probe that can acquire signals with sufficient temporal length for statistics-based PASA. We treated the inner surface of the steel needle sheath and successfully suppressed the vibrational PA signals generated at the surface. Purposed at boosting the measurement sensitivity and extending sensing volume, we upgraded the Fabry-Pérot hydrophone with a plano-concave structure. The performance of the translational needle PA sensing probe was examined with phantoms containing microspheres. The trend of the linear spectral slopes shows negatively correlated to the microsphere dimensions while the midband-fits are positively correlated to microsphere diameters and concentrations. The PASA quantifications show the ability to differentiate microspheres with varied dimensions.

Plasmon-driven catalytic reactions in optoplasmonic sandwich hybrid structure.

As an interesting phenomenon in the field of surface enhanced Raman spectroscopy (SERS), the plasmon-driven catalytic reaction (PDSC) induced by plasmonic hot electrons has great value in the research of novel properties of surface plasmons and accuracy of SERS applications. In this work, an optoplasmonic sandwich hybrid structure is proposed for studying PDSC of p-aminothiophenol (PATP) molecules, which is composed of Au film, metal organic frameworks (MOFs) nanoparticles, zeolithic imidazolate (ZIF-8), and single S i O 2 microsphere (Au f i l m@M O F s@S i O 2). In order to analyze the novel, to the best of our knowledge, phenomenon of the PDSC in this micro-nano structure, the hot electron generation in the MOF without the plasmonic core is carried out by combining the plasmonic enhancement of gold film with the light concentration of microspheres. Experimental data show that the PDSC reactions is dependent on the size of the MOFs nanoparticle and the size of the S i O 2 microsphere, which is confirmed by the electromagnetic field simulation of the finite-difference time-domain method (FDTD). Our work not only strengthens the understanding of surface plasmon in optoplasmonic hybrid structures but also has broad application prospects in the SERS and plasmon-driven catalytic fields.

Synthesis and properties of SiO2/SiO2@Ag two-phase STFs.

Soft body armor with a strain-sensing function using conductive shear thickening fluids (STFs) has gradually gained research interest. In this study, conductive SiO2@Ag core-shell microspheres were synthesized and the influence of process parameters on their properties was evaluated. Subsequently, SiO2 and SiO2@Ag were used as dispersed phases to prepare two-phase STFs, the effect of the core-shell microspheres' proportion on the rheological properties of the STFs was investigated, and its mechanism was discussed. The results indicated that SiO2@Ag core-shell microspheres were coated with elemental silver and when the concentration of sodium hydroxide and glucose were 0.07 and 0.09 mol L-1, respectively, the coating surface was the most uniform and compact, and the conductivity reached the minimum value of 0.56 Ω cm. The two-phase STFs exhibited good and reversible shear thickening behaviors and the critical shear rate decreased with increasing core-shell microsphere concentration. Additionally, when the mass fraction of SiO2 and SiO2@Ag core-shell microspheres was 45% and 20%, respectively, the thickening rate was 325%, and the resistance of two-phase STFs decreased simultaneously with the emergence of shear thickening that reached the lowest value of 795.16 kΩ. This study provides a novel strategy for synthesizing conductive STFs for strain-sensing flexible stab-resistant composites.

Calcium hydroxylapatite microspheres activate fibroblasts through direct contact to stimulate neocollagenesis

Calcium hydroxylapatite (CaHA; Radiesse, Merz North America) restores volume and stimulates collagen production. The aim of this research was to explore the role of dilution and diffusion in microsphere distribution and the effect of CaHA concentration on activation of fibroblasts to produce collagen. Ex vivo: Tissue dispersion of CaHA was assessed in abdominal tissue segments obtained from patients which were subsequently injected with CaHA diluted to 1:1 and hyperdiluted to 1:2. In vitro: Collagen type III (COLIII) and type I (COLI) expression of fibroblasts was evaluated after 24 and 72 h of incubation with CaHA concentrations of 1.5 (high dilution), 3.0, and 4.5mg/ml (low dilution). Ex vivo: The 1:2 CaHA hyperdilution increased dispersion and decreased concentration of CaHA microspheres compared with the 1:1 dilution. In vitro: CaHA incubation resulted in an increased mean COLIII expression of 123% at 24 h. COLI synthesis did not change after 24 h but increased up to 124% at 72 h. Only fibroblasts in direct contact with CaHA increased COLIII expression. COLIII high-expressing cells were fully activated by CaHA and resulted in the same level of COLIII expression per cell independent of the CaHA dilution. A 1:2 hyperdilution of CaHA increased tissue dispersion of CaHA microspheres. Direct contact of CaHA with fibroblasts was a key factor for inducing neocollagenesis. COLIII high-expressing cells were fully activated by CaHA and resulted in the same expression level of COLIII per cell independent of the CaHA amount in each dilution. This indicates that increased collagen expression was due to the activation of more fibroblasts.

Mapping in vivo microclimate pH distribution in exenatide-encapsulated PLGA microspheres.

The pH inside the aqueous pores of poly(lactic-co-glycolic acid) (PLGA) microspheres, often termed microclimate pH (μpH), has been widely evaluated in vitro and shown to commonly be deleterious to pH-labile encapsulated drug molecules. However, whether the in vitro μpH is representative of the actual in vivo values has long been remained a largely unresolved issue. Herein we quantitatively mapped, for the first time, the in vivo μpH distribution kinetics inside degrading PLGA microspheres by combining two previously validated techniques, a cage implant system and confocal laser scanning microscopy. PLGA (50/50, Mw=24-38kDa, acid-end capped and ester-capped) microsphere formulations with and without encapsulating exenatide, a pH-labile peptide that is known to be unstable when pH>4.5, were administered to rats subcutaneously via cage implants for up to 6weeks. The results were compared with two different in vitro conditions. Strikingly, the in vivo μpH developed similarly to the low microsphere concentration in vitro condition with 1-μm nylon bags but very different from conventional high microsphere concentration sample-and-separate conditions. Improved maintenance of stable external pH in the release media for the former condition may have been one important factor. Stability of exenatide remaining inside microspheres was evaluated by mass spectrometry and found that it was steadily degraded primarily via pH-dependent acylation with a trend that slightly paralleled the changes in μpH. This methodology may be useful to elucidate pH-triggered instability of PLGA encapsulated drugs in vivo and for improving in vivo-predictive in vitro conditions for assessing general PLGA microsphere performance.

Computational Study of the Microsphere Concentration in Blood during Radioembolization

Computational fluid dynamics techniques are increasingly used to computer simulate radioembolization, a transcatheter intraarterial treatment for patients with inoperable tumors, and analyze the influence of treatment parameters on the microsphere distribution. Ongoing clinical research studies are exploring the influence of the microsphere density in tumors on the treatment outcome. In this preliminary study, we computationally analyzed the influence of the microsphere concentration in the vial on the microsphere concentration in the blood. A patient-specific case was used to simulate the blood flow and the microsphere transport during three radioembolization procedures in which the only parameter varied was the concentration of microspheres in the vial and the span of injection, resulting in three simulations with the same number of microspheres injected. Results showed that a time-varying microsphere concentration in the blood at the outlets of the computational domain can be analyzed using CFD, and also showed that there was a direct relationship between the variation of microsphere concentration in the vial and the variation of microsphere concentration in the blood. Future research will focus on elucidating the relationship between the microsphere concentration in the vial, the microsphere concentration in the blood, and the final microsphere distribution in the tissue.

Scalable Preparation of Sub-Millimeter Double-Shelled Al2O3 Hollow Spheres and Their Rapid Separation from Wastewater after Adsorption of Congo Red.

Porous double-shelled ceramic hollow spheres (PDSs) have attracted extensive attention due to their high specific surface areas and multifunctional designs. When used in wastewater treatment, millimeter or sub-millimeter spheres can be quickly separated from water by commercial sieves. However, the simple, scalable, and low-cost preparation of sub-millimeter PDSs in the solid phase remains a challenge. Herein, porous PDSs were facilely fabricated via a spheronization process utilizing pseudoboehmite powders and wet gelatin spheres as templates, which broke through the difficulty of preparing PDSs by one-step solid-state synthesis. Treating pseudoboehmite powder with nitric acid can improve the compressive strength of the PDSs. By controlling the rolling time and gelatin concentration of gelatin microspheres, the integrity, shell thickness, and double-shelled spacing of the gelatin microspheres were tuned. When the rolling time was 8–12 min, and the gelatin concentration in gelatin spheres was 250 g/L, and PDSs with a complete double-shelled structure, good mechanical property, and high specific surface area (327.5–509.6 m2/g) were obtained at 600 °C. The adsorption capacities of the PDSs for 100 mg/L Congo red solution (70.7 mg/g) were larger than those of single-shelled hollow spheres (49 mg/g), and larger diameters (608–862 μm) of the PDSs allow them to be rapidly separated from solution by a commercial sieve. This paper provides a facile and scalable method for the preparation of sub-millimeter PDSs and demonstrates their excellent adsorption capacity for Congo red solution.

Water-in-Oil Pickering Emulsions Stabilized by Hydrophobized Protein Microspheres.

Water-in-oil (w/o) Pickering emulsions have gained considerable attention in colloid science and daily applications. However, for the formation of w/o emulsions, especially those with high internal water content, the particulate stabilizers are required to be sufficiently hydrophobic, and synthetic or chemically modified particles have been mostly reported until now, which are not biocompatible and sustainable. We present a zein protein-based microsphere derived from the Pickering emulsion template, in which protein microspheres are feasibly in situ hydrophobized by silica nanoparticles, enabling the stabilization of w/o Pickering emulsions. The effects of microsphere concentration, water/oil volume ratio, oil types, and pH on the stabilization of prepared w/o emulsions are systematically studied, revealing prominent characteristics of the controllable size, high water fraction, universal adaptation of oils, as well as broad pH stability. As a demonstration, the Pickering emulsion effectively encapsulates vitamin C and shows high stability for long storage duration against ultraviolet radiation/heat. Therefore, this novel proteinaceous particle-stabilized w/o Pickering emulsion has great potential in the delivery and protection of water-soluble bioactive substrates.

Physical properties and biological impact of 90Y microspheres prepared by sol-gel method for liver radioembolization

Microspheres for liver radioembolization for human use have high requirements in terms of their toxicity and biocompatibility on the one hand, but also typical properties such as physical and chemical durability or specific activity on the other hand. Developed manufacturing process based on the sol-gel method allowed to obtain spherical, yttrium trioxide grains of fully polycrystalline structure with diameters between 20 μm and 100 μm. The work is focused on a further investigation concerning the Y2O3 microspheres including physical, radiometric, dosimetric, and biological experiments. Neutron activation analysis confirmed a high concentration of radioactive 90Y in the sample. The developed procedure for determining the specific activity of a single microsphere showed that at the time of administration, the activity can be specified at the level of 2600–3200 Bq per microsphere. FLUKA Monte Carlo code was used to prepare model for the calculation of dose distributions at the microscopic level, indicating that locally occurring heterogeneities can lead to cold spots during radioembolization. The data obtained from the simulation enabled analysis of the absorbed dose delivered by gel 90Y2O3 microspheres as a function of radioactivity concentration, initial specific activity, or microsphere concentration in the sample. The reduction in colorectal cancer cell proliferation in vitro confirms the significant influence of beta ray radiation from yttrium-90 trioxide microspheres. Histopathological examination of the distribution of microspheres in the porcine model confirmed the proper location of yttrium trioxide microspheres inside blood vessels in a porcine model. Gel Y2O3 microspheres manufactured using the sol-gel method showed relevant properties, indicating the possible use of microspheres for further biological and preclinical studies.

(Digital Presentation) Synthesis of Multisize Layered Silica Inverse Opal Photonic Crystals

Today, human beings have found an increasing need for energy. The ever-increasing effort to shrink information systems at higher speeds has led to the common idea that photons are used as carriers of information instead of electrons. Photonic crystals have a structure whose dielectric constants and refractive indices change alternately in one, two, or three dimensions, which are called one-dimensional, two-dimensional, and three-dimensional photon crystals. Periodicity in the refractive index of the crystal structure causes a photonic bandgap that includes a range of frequencies in which light with a frequency of this range is not allowed to pass the crystal structure and is reflected or absorbed.In this work, Poly(methyl methacrylate) (PMMA) microspheres of different sizes were first synthesized using the suspension polymerization method. Concentrations of used materials including initializer, monomer, reaction temperature, reaction time, and rotation speed play important roles in determining the final diameter of PMMA microspheres. Then, the vertical deposition method is used for the growth of multi-layered opals of different sizes, one on top of another. On the other hand, inverse opals have porous and organized structures that are made using opals as the template. The method used in this study to make multisize layered inverse opal made of silica is as follows: 1- Fabrication of a uniform layer of polymer microspheres on a glass substrate with a specified size as a colloidal crystal template 2- Infiltration of void space between the microspheres of the opal template 3- Creating the next layer with different size on the first layer 4- Reinjection of the silica precursor. 5- Repeating the coating layer and injection of the precursor. 6- Finally, selective removal of the opal template by calcination or etching with an organic solvent to create the porous structure of the multisize layered Silica inverse opal photonic crystals. The silica precursor contains a mixture of ethanol, TEOS tetraethyl orthosilicate, and hydrochloric acid.The results show that the fabricated inverse opals are organized, crack-free, and uniform. It is possible to make the desired number of layers by changing the concentration of the PMMA microspheres' colloidal suspension. By changing the characteristics of photonic crystals, such as their constituent materials and refractive indices, lattice constants, and the number of layers, it is possible to control their photonic properties which are beneficial for different applications.

Precision dosimetry in yttrium-90 radioembolization through CT imaging of radiopaque microspheres in a rabbit liver model

PurposeTo perform precision dosimetry in yttrium-90 radioembolization through CT imaging of radiopaque microspheres in a rabbit liver model and to compare extracted dose metrics to those produced from conventional PET-based dosimetry.Materials and methodsA CT calibration phantom was designed containing posts with nominal microsphere concentrations of 0.5 mg/mL, 5.0 mg/mL, and 25.0 mg/mL. The mean Hounsfield unit was extracted from the post volumes to generate a calibration curve to relate Hounsfield units to microsphere concentration. A nominal bolus of 40 mg of microspheres was administered to the livers of eight rabbits, followed by PET/CT imaging. A CT-based activity distribution was calculated through the application of the calibration curve to the CT liver volume. Post-treatment dosimetry was performed through the convolution of yttrium-90 dose-voxel kernels and the PET- and CT-based cumulated activity distributions. The mean dose to the liver in PET- and CT-based dose distributions was compared through linear regression, ANOVA, and Bland–Altman analysis.ResultsA linear least-squares fit to the average Hounsfield unit and microsphere concentration data from the calibration phantom confirmed a strong correlation (r2 > 0.999) with a slope of 14.13 HU/mg/mL. A poor correlation was found between the mean dose derived from CT and PET (r2 = 0.374), while the ANOVA analysis revealed statistically significant differences (p < 10−12) between the MIRD-derived mean dose and the PET- and CT-derived mean dose. Bland–Altman analysis predicted an offset of 15.0 Gy between the mean dose in CT and PET. The dose within the liver was shown to be more heterogeneous in CT than in PET with an average coefficient of variation equal to 1.99 and 1.02, respectively.ConclusionThe benefits of a CT-based approach to post-treatment dosimetry in yttrium-90 radioembolization include improved visualization of the dose distribution, reduced partial volume effects, a better representation of dose heterogeneity, and the mitigation of respiratory motion effects. Post-treatment CT imaging of radiopaque microspheres in yttrium-90 radioembolization provides the means to perform precision dosimetry and extract accurate dose metrics used to refine the understanding of the dose–response relationship, which could ultimately improve future patient outcomes.

Characterization of polymethylmethacrylate microspheres loaded with silver and doxycycline for dental materials applications

ObjectivesThe manufacturing of polymethylmethacrylate(PMMA) microspheres loaded with doxycycline(DOX) and/or silver sulfate(Ag2SO4) to be incorporated into glass ionomer cement(GIC). MethodsPMMA microspheres were manufactured with Ag2SO4(1–5%) and/or DOX(5–15%). Particle size, encapsulation efficiency and drug release were measured by light microscope, ICP, and HPLC. Microspheres were added to a dental GIC(20%w/w). Drug release and DTS were investigated. Minimum inhibitory concentration and antibacterial effects of PMMA microspheres into GIC materials were tested. ResultsThe median diameter of 50 µm was obtained for microspheres. DOX was encapsulated at an efficiency of 8.3% using a theoretical loading of 15%DOX + 5%Ag2SO4. The Ag2SO4 encapsulation efficiency was 0.63% using a theoretical loading of 5%AgSO4. All groups showed burst release within the first day and continued released up to 15 days, with 60–83% of DOX and approximately 30% of silver. For GIC, approximately 15% of DOX and 0.18% of silver were released in a 7-day period. Microbiological results showed an antimicrobial effect against S. mutans when the lead formulation of microspheres was added. The DTS was reduced by the inclusion of microspheres. SignificancePMMA microspheres containing DOX and Ag2SO4 offer a sustained antimicrobial activity for dental applications and promising potential for the biomedical field.

Ingestion of polyethylene microspheres occur only in presence of prey in the jellyfish Aurelia aurita

Microplastic ingestion was studied in A. aurita, a bloom-forming, circumglobal medusa. Here, we determined whether factors such as the concentration of polyethylene microspheres (75–90 μm) or the absence/presence of prey affect the ingestion, duration of microspheres in the gastrovascular cavity (time of presence), and retention time. The presence of polyethylene microspheres' was determined by exposing medusae during 480 min to three different treatments (5000, 10,000, 20,000 particles L−1), and was checked every 10 min to ascertain whether they had incorporated any. Preliminary results show that microsphere ingestion occurred only in the presence of prey (⁓294 Artemia nauplii L−1). The time of presence of microbeads in A. aurita increased (103, 177, and 227 min), with increasing microplastic concentration, and the microbeads were egested within 150 min.This study initiates the understanding of the potential implications that arise of the encounter between jellyfish and microplastic agglomerates, and with perspectives for future research.

Laser Activated and Electroless Metalized Polyurethane Coatings Containing Copper(II) L-Tyrosine and Glass Microspheres.

Polyurethane coatings containing copper(II) L-tyrosine and glass microspheres were laser irradiated and underwent electroless metallization. Various sizes of glass microspheres were incorporated into the polyurethane coating matrix in order to examine their effects on surface activation and electroless metallization. The surface of the coatings was activated by using ArF excimer laser emitting ultraviolet radiation (λ = 193 nm) using different number of laser pulses and their fluence. The effects of surface activation and metallization were evaluated mainly based on optical and scanning electron microcopies (SEM), energy-dispersive X-ray spectroscopy (EDX) and photoelectron spectroscopy (XPS). It was found that the presence of glass microspheres enabled the reduction in copper complex content, intensified the ablation process (higher cone-like structures created) and resulted in higher content of copper metallic seeds. On the other hand, the glass microspheres concentration, which was higher for lower size microspheres, was advantageous for obtaining a fully metallized layer.