Karstification plays a crucial role in forming magnificent scenery, and storing oil, natural gas, mineral resources, and water. Through the inspiration of karstification, a hierarchical layered double hydroxide (LDH) with funnel-like and cave-like structures (called Karst-LDH) is formed by the dissolution of acrylic acid/water solution. Meanwhile, the results of transmission electron microscopy (TEM) and scanning electron microscopy (SEM) show that Karst-LDH has complicated and interconnected internal pipe networks. The actual maximum phosphate adsorption capacity of Karst-LDH reaches 126.38 mg g-1 due to the unique structures, protonation, ligand exchange, ion exchange, and hydrogen bonding, which is over ten times that of general LDH with a regular hexagonal structure. The results of isotherms and thermodynamics also indicate that Karst-LDH conforms to more heterogeneous and multilayer adsorption with a higher entropy-driven process. Karst-LDH exhibits good selectivity for chloride and nitrate ions. The change in the frontier orbital interaction between phosphate and different LDHs is a significant reason for quick macropore transmission, mesopore interception, and finally, phosphate storage in Karst-LDH. This work provides an efficient way for the design and fabrication of high adsorption performance materials with unique karst-type structures, which can be used for multiple fields potentially.
Dietary intake can modify the impact of metals on human health, and is also closely related to glucose metabolism in human bodies. However, research on their interaction is limited. We used data based on 1738 adults aged ≥20 years from the National Health and Nutrition Examination Survey 2011-2016. We combined linear regression and restricted cubic splines with Bayesian kernel machine regression (BKMR) to identify metals associated with each glucose metabolism index (P < 0.05 and the posterior inclusion probabilities of BKMR >0.5) in eight non-essential heavy metals (barium, cadmium, antimony, tungsten, uranium, arsenic, lead, and thallium) and glucose metabolism indexes [fasting plasma glucose (FPG), blood hemoglobin A1c (HbA1c) and homeostatic model assessment of insulin resistance (HOMA-IR)]. We identified two pairs of metals associated with glucose metabolism indexes: cadmium and tungsten to HbA1c and barium and thallium to HOMA-IR. Then, the cross-validated kernel ensemble (CVEK) approach was applied to identify the specific nutrient group (nutrients) that interacted with the association. By using the CVEK model, we identified significant interactions between the energy-adjusted diet inflammatory index (E-DII) and cadmium, tungsten and barium (all P < 0.05); macro-nutrients and cadmium, tungsten and barium (all P < 0.05); minerals and cadmium, tungsten, barium and thallium (all P < 0.05); and A vitamins and thallium (P = 0.043). Furthermore, a lower E-DII, a lower intake of carbohydrates and phosphorus, and a higher consumption of magnesium seem to attenuate the positive association between metals and glucose metabolism indexes. Our finding identifying the nutrients that interact with non-essential heavy metals could provide a feasible nutritional guideline for the general population to protect against the adverse effects of non-essential heavy metals on glucose metabolism.
Cadmium , Metals, Heavy , Adult , Humans , Nutrition Surveys , Barium , Thallium , Tungsten , Glycated Hemoglobin , Bayes Theorem , Glucose
In precision dairy farming, computer vision-based approaches have been widely employed to monitor the cattle conditions (e.g., the physical, physiology, health and welfare). To this end, the accurate and effective identification of individual cow is a prerequisite. In this paper, a deep learning re-identification network model, Global and Part Network (GPN), is proposed to identify individual cow face. The GPN model, with ResNet50 as backbone network to generate a pooling of feature maps, builds three branch modules (Middle branch, Global branch and Part branch) to learn more discriminative and robust feature representation from the maps. Specifically, the Middle branch and the Global branch separately extract the global features of middle dimension and high dimension from the maps, and the Part branch extracts the local features in the unified block, all of which are integrated to act as the feature representation for cow face re-identification. By performing such strategies, the GPN model not only extracts the discriminative global and local features, but also learns the subtle differences among different cow faces. To further improve the performance of the proposed framework, a Global and Part Network with Spatial Transform (GPN-ST) model is also developed to incorporate an attention mechanism module in the Part branch. Additionally, to test the efficiency of the proposed approach, a large-scale cow face dataset is constructed, which contains 130,000 images with 3000 cows under different conditions (e.g., occlusion, change of viewpoints and illumination, blur, and background clutters). The results of various contrast experiments show that the GPN outperforms the representative re-identification methods, and the improved GPN-ST model has a higher accuracy rate (up by 2.8% and 2.2% respectively) in Rank-1 and mAP, compared with the GPN model. In conclusion, using the Global and Part feature deep network with attention mechanism can effectively ameliorate the efficiency of cow face re-identification.
The co-precipitation method is used to fabricate layered double hydroxide (LDH) nanohybrids with surface engineering of graphene oxide (GO) by radially grafting borate-LDH (BLDH) to BLDH@GO nanosheets, aiming at improving the surface characteristics and compatibility of LDH with the polymer matrix. The results prove the successful fabrication of BLDH@GO and LDH@GO nanosheets. The nanosheets are mixed into polypropylene (PP) by melt blending to study the structure and properties of the composites. The PP composites with BLDH@GO and BLDH have both exfoliation structures and aggregation structures, and the two nanosheets show enhanced interfacial interactions with the PP matrix compared with LDH and LDH@GO. The initial decomposition temperatures of the PP composites are lower than those of the neat PP, but the thermal degradation temperatures of the PP composites are higher. Compared with the other samples, BLDH@GO provides a higher nucleation density, reflected in a smaller spherulite size and a higher crystallization temperature confirmed by the differential scanning calorimetry (DSC) results. BLDH@GO shifts the crystallization temperature of PP to higher values (compared to the neat PP) due to the nucleation effect, which is in line with the increase in the nucleation density detected by polarized optical microscopy (POM).
The selective dispersion of neutral nanoplates (NNP) and the control of the interfacial structure of copolymers are challenging. In this work, we employ coarse-grained molecular dynamics (CGMD) to investigate the dispersion of NNP and the interfacial structure. The introduction of NNP significantly changes the interfacial structure and formation mechanism of diblock copolymers (DBCP), which is related to the matrix phase, distribution, composition, and length of two different chain segments (A and B) in AmBn-DBCP. The phase-weak groups that have a poor interaction with NNP will stack easily, whereas the stacking degree for the phase-rich groups that have a strong interaction with NNP decreases due to the addition of NNP. The interaction between two phases will be enhanced, which is favorable for the formation of a random network structure. Due to the strong interaction of the phase-rich groups with NNP, the NNP change the accumulation types of phase-weak groups and enhances the combination of two chain segments in favor of the formation of a cylindrical micelle-like structure. The transmission electron microscopy (TEM) images show that layered double hydroxide (LDH) orientationally distributes in the acrylic acid chain segments in ethylene acrylic acid (EAA) random copolymers, which is in agreement with the theoretical simulation results. This proves that the selective dispersion of LDH in copolymers affects their interfacial structure.
The enhanced toughness of flame-retardant polymer composites is still a big challenge due to the deterioration of their mechanical properties. In this work, polypropylene (PP)/nanohybrid expandable graphite (nEG) flame-retardant composites toughened by octene-ethylene copolymer (POE) were fabricated for obtaining good mechanical properties and flame retardancy. The structure, rheological and crystallization behaviors, morphology, flame retardancy, and mechanical property of PP/nEG/POE composites with different contents of POE were investigated. Results show that the elongation at break and impact strength of PP composites were significantly improved due to the incorporation of POE. The elongation at break and notched impact strength of toughened PP composites with only 20% POE were increased to 521.6% and 22.9 kJ m-2 from 16.1% and 9.3 kJ m-2 for untoughened PP composites, respectively. The scanning electron micrography (SEM) images showed that POE droplets were dispersed finely and uniformly in the PP matrix, exhibiting a typical two-phase structure. Additionally, the interfacial adhesion between the matrix and inorganic particles was enhanced due to the addition of POE. The rheological behaviors of PP composites showed improved elasticity and longer relaxation times, and a stress-yield behavior appeared with the addition of POE. The interfacial interaction in PP composites was enhanced and the formation of an interparticle network was further proved. Additionally, the toughened PP/nEG20 composites with different contents of POE exhibited excellent flame retardancy. Therefore, the toughened flame-retardant PP composites should possess a wider range of application potential.
BACKGROUND: Metals play an important role in type 2 diabetes mellitus (T2DM). This study aimed to explore the association of T2DM risk with single metal exposure and multi-metal co-exposure. METHODS: A case-control study with 223 T2DM patients and 302 controls was conducted. Serum concentrations of 19 metals were determined by inductively coupled plasma mass spectrometry (ICP-MS). Those metals with greater effects were screened out and co-exposure effects of metals were assessed by least absolute shrinkage and selection operator (LASSO) regression. RESULTS: Serum calcium (Ca), selenium (Se) and vanadium (V) were found with greater effects. Higher levels of Ca and Se were associated with increased T2DM risk (OR = 2.23, 95%CI: 1.38-3.62, Ptrend = 0.002; OR = 3.16, 95%CI: 1.82-5.50, Ptrend < 0.001), but higher V level was associated with decreased T2DM risk (OR = 0.58, 95%CI: 0.34-0.97, Ptrend < 0.001). Serum Ca and V concentrations were nonlinearly associated with T2DM risk (Poverall < 0.001, Pnonliearity < 0.001); however, Se concentration was linearly associated with T2DM risk (Poverall < 0.001, Pnonliearity = 0.389). High co-exposure score of serum Ca, Se and V was associated with increased T2DM risk (OR = 3.50, 95%CI: 2.08-5.89, Ptrend < 0.001) as a non-linear relationship (Poverall < 0.001, Pnonliearity = 0.003). CONCLUSIONS: This study suggest that higher levels of serum Ca and Se were associated with increased T2DM risk, but higher serum V level was associated with decreased T2DM risk. Moreover, co-exposure of serum Ca, Se and V was nonlinearly associated with T2DM risk, and high co-exposure score was positively associated with T2DM risk.
Calcium/toxicity , Diabetes Mellitus, Type 2/epidemiology , Environmental Exposure/statistics & numerical data , Environmental Pollutants/toxicity , Selenium/toxicity , Vanadium/toxicity , Adult , Asian People , Calcium/blood , Case-Control Studies , Diabetes Mellitus, Type 2/blood , Environmental Pollutants/blood , Female , Humans , Male , Middle Aged , Selenium/blood , Vanadium/blood
Highly effective photocatalysts for the hydrogen-evolution reaction were developed by conferring the linkers of NH2 -MIL-125(Ti), a metal-organic framework (MOF) constructed from TiOx clusters and 2-aminoterephthalic acid (linkers), with active copper centers. This design enables effective transfer of electrons from the linkers to the transient Cu2+ /Cu+ centers, leading to 7000-fold and 27-fold increase of carrier density and lifetime of photogenerated charges, respectively, as well as high-rate production of H2 under visible-light irradiation. This work provides a novel design of a photocatalyst for hydrogen evolution using non-noble Cu2+ /Cu+ as co-catalysts.
As an environmentally friendly and renewable energy source, hydrogen peroxide (H2O2) could be produced photocatalytically through selective two-electron reduction of O2 using effective photocatalysts. Metal organic frameworks (MOFs), as hybrid porous materials consisting of organic linkers and metal oxide clusters, have aroused great interest in the design of effective catalysts for photocatalysis under visible light irradiation due to their unique properties, such as large surface area, good chemical stability, and diverse and tunable chemical components. In this perspective, we highlight our recent progress in the application of various MOF-based nanomaterials for photocatalytic H2O2 production from the selective two-electron reduction of O2 in a single-phase system (acetonitrile) and two-phase system (water/benzyl alcohol). Photocatalytic H2O2 production in the single-phase system achieved a higher activity using NiO as a cocatalyst of the MOF rather than Pt. Photocatalytic H2O2 production in the two-phase system using various hydrophobic MOFs showed further improved activity compared to the single-phase system. It has been possible to design a hydrophobic MOF-based photocatalyst with high activity and stability under recycling conditions. These studies gathered in this perspective revealed the novel application of MOFs in the field of energy production.
Soybean oil is beneficial to improve the compatibility between polylactide (PLA) and succinylated lignin (SAL), which leads to the preparation of a host of biobased composites containing PLA, SAL, and epoxidized soybean oil (ESO). The introduction of SAL and ESO enables the relatively homogeneous morphology and slightly better miscibility obtained from triply PLA/SAL/ESO composites after dynamic vulcanization compared with unmodified PLA. The rigidity of the composites is found to decline gradually due to the addition of flexible molecular chains. According to the reaction between SAL and ESO, the Tg of PLA/SAL/ESO composites is susceptible to the movement of flexible molecular chains. The rheological behaviors of PLA/SAL/ESO under different conditions, i.e., temperature and frequency, exhibit a competition between viscidity and elasticity. The thermal stability of the composites displays a slight decrease due to the degradation of SAL and then the deterioration of ESO. The elongation at break and notched impact strength of the composites with augmentation of ESO increase by 12% and 0.5 kJ/m2, respectively. The triply biobased PLA/SAL/ESO composite is thus deemed as a bio-renewable and environmentally friendly product that may find vast applications.
Poly(D-lactic acid) (PDLA) with different polyethylene glycol (PEG) segment synthesized PDLA-PEG-PDLA triblock copolymer through the ring-opening reaction of D-LA and PEG will be used as a toughening modifier. The microstructure, crystal structures and crystallization behaviors of this triblock copolymer were investigated by Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and polarized optical microscopy (POM). The triblock copolymer is synthesized from the appearance of CH2 stretching vibration peak at 2910 cm-1 and C-O stretching vibration peak at 1200 cm-1 from PEG in FTIR spectra. Moreover, the chemical shift that is about 3.6 ppm in 1H NMR and 68.8ppm in 13C NMR proves this matter. The results of XRD and DSC reveal that PDLA and PEG are crystallized separately, and are not fully compatible, and microphase separation has occurred in this triblock copolymer. PEG can induce the triblock copolymer to accelerate the rate of crystallization, allowing it to crystallize more completely in the same amount of time. When the molecular weight of PEG is 6000 or the ratio of D-LA/PEG is 1/1, the crystallizability of PDLA-PEG-PDLA triblock copolymer is the best.
BACKGROUND: Uncoupling protein 1 (UCP1) has been reported to be associated with type 2 diabetes mellitus (T2DM) in different populations, however, little is reported in Chinese population. The present study aimed to explore the association between some polymorphisms of UCP1 with T2DM and the interactions between UCP1 and physical activity/sedentary behavior (PA/SB) lifestyle in Chinese population. METHODS: Three polymorphisms (rs1472268, rs3811790 and rs3811791) were genotyped in 929 T2DM patients and 1044 nondiabetic controls. The data of PA and SB were acquired. Logistic regression and linear regression were conducted to assess the association of UCP1 and T2DM and related traits. RESULTS: The CC genotype of rs3811791 was significantly associated with an increased risk of T2DM [odds ratio (OR) = 1.42, P = 0.042] and a higher level of triglyceride (TG) (ß = 0.048, P = 0.034). This association still existed in the group of SB ≥ 3 h/d (OR = 1.66, P = 0.009) and the group of PA ≥ 150 min/week and SB ≥ 3 h/d (OR = 1.60, P = 0.034). In the group of PA < 150 min/week and SB < 3h/d, CC genotype was associated with a higher level of homeostatic model assessment of insulin resistance (HOMA-IR) index, and in the group of PA < 150 min/week and SB ≥ 3 h/d, CC genotype was associated with increased level of TG and decreased high-density lipoprotein cholesterol (HDL-C). CONCLUSION: This study suggests that rs3811791 of UCP1 may be associated with T2DM and TG. Moreover, we demonstrate that SB interacted with rs3811791 of UCP1 was associated with T2DM, and PA interacted with rs3811791 of UCP1 was associated with the level of HOMA-IR, HDL-C, and TG.
Diabetes Mellitus, Type 2/genetics , Lipid Metabolism/genetics , Polymorphism, Genetic/genetics , Uncoupling Protein 1/genetics , Adult , Aged , Alleles , Case-Control Studies , China , Cholesterol, HDL/analysis , Exercise , Female , Genotype , Humans , Insulin Resistance/genetics , Male , Middle Aged , Odds Ratio , Sedentary Behavior , Triglycerides/analysis
In this work, the poly(d-lactic acid)-polyethylene glycol-poly(d-lactic acid) (PDLA-PEG-PDLA) triblock copolymer as a novel modification agent was incorporated into poly(l-lactic acid) (PLLA) to improve the thermal and mechanical properties of PLLA. The influences of molecular weight of PEG in the triblock copolymer on the structure, crystallization behaviors, heat resistance and tensile properties of PDLA-PEG-PDLA/PLLA blends were investigated by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC), polarized optical microscopy (POM), thermogravimetric analysis (TGA) and tensile testing. The results from FTIR, XRD and DSC confirm the formation of a polylactide stereocomplex in the PLLA blends. The structure and properties of the stereocomplex crystals are different from those of pure PLLA. The melting temperature (T m) of the stereocrystal is near 200 °C, which is significantly higher than that of the homogeneous crystal of PLLA. The effect of molecular weight of PEG on the crystal morphology of PLLA blends is also obvious. The improvement of tensile properties for PLLA blends is attributed to the crystal morphological features, which will potentially enhance the utility of the PLLA based polymer.
Landfill leachate is generally transferred to in situ facilities for advanced treatment by using a pipe system. Because of its harmful and complex compounds, leachate may react with pipe materials, leading to corrosion and scaling. This experimental study uses typical PVC pipe material and investigates its anti-corrosion performance by placing the material samples into different aged leachates. By evaluating the changes in different experimental parameters, including calcium, magnesium, and chloride ion concentration, oxidation-reduction potential, dissolved oxygen, and pH, combined with a characterization of the material properties, we infer the main causes of pipe scaling-corrosion. Results show that the scaling is more intense in the younger leachate, and the concentration of calcium ions is the dominant influencing factor. The scaling might be resulted from joint actions of chemical precipitation and microbial metabolic activities. It is expected the study to provide useful insights into taking effective actions on anti-clogging, and enhance pipes design by selection of appropriate materials for future modification.
Polyvinyl Chloride/chemistry , Water Pollutants, Chemical/chemistry , Chemical Precipitation , Corrosion , Oxygen , Soil Microbiology
Graphitic carbon nitride (g-C3N4) fundamental photophysical processes exhibit a high frequency of charge trapping due to physicochemical defects. In this study, a copper phosphide (Cu3P) and g-C3N4 hybrid was synthesized via a facile phosphorization method. Cu3P, as an electron acceptor, efficiently captures the photogenerated electrons and drastically improved the charge separation rate to cause a significantly enhanced photocatalytic performance. Moreover, the robust and intimate chemical interactions between Cu3P and g-C3N4 offers a rectified charge-transfer channel that can lead to a higher H2 evolution rate (HRE, 277.2 µmol h-1 g-1) for this hybrid that is up to 370 times greater than that achieved from using bare g-C3N4 (HRE, 0.75 µmol h-1 g-1) with a quantum efficiency of 3.74% under visible light irradiation (λ = 420 nm). To better determine the photophysical characteristics of the Cu3P-induced charge antitrapping behavior, ultrafast time-resolved spectroscopy measurements were used to investigate the charge carriers' dynamics from femtosecond to nanosecond time domains. The experimental results clearly revealed that Cu3P can effectively enhance charge transfer and suppress photoelectron-hole recombination.
Lignin, a natural amorphous three-dimensional aromatic polymer, is investigated as an appropriate filler for biocomposites. The chemical modification of firsthand lignin is an effective pathway to accomplish acetoacetate functional groups replacing polar hydroxyl (-OH) groups, which capacitates lignin to possess better miscibility with poly(lactic acid) (PLA), compared with acidified lignin (Ac-lignin) and butyric lignin (By-lignin), for the sake of blending with poly(lactic acid) (PLA) to constitute a new biopolymer based composites. Generally speaking, the characterization of all PLA composites has been performed taking advantage of Fourier transform infrared (FTIR), scanning electron microscopy (SEM), dynamic Mechanical analysis (DMA), differential scanning calorimeter (DSC), thermogravimetric analysis (TGA), rheological analysis, and tensile test. Visibly, it is significant to highlight that the existence of acetoacetate functional groups enhances the miscibility, interfacial compatibility, and interface interaction between acetoacetate lignin (At-lignin) and PLA. Identical conclusions were obtained in this study where PLA/At-lignin biocomposites furthest maintain the tensile strength of pure PLA.
The performances and microstructure of long glass fibre-reinforced polyamide 10T (PA10T/LGF) composites that experienced different ageing temperatures (160 and 200°C) with increasing ageing time are characterized by differential scanning calorimetry (DSC), mechanical analysis, thermogravimetric analysis (TGA) and scanning electron microscopy to probe the correlation between properties of the composites and thermo-oxidative ageing. The DSC results show that PA10T/LGF composites occur on degradation, the fracture of molecular chains and the destruction of crystallization structure, which leads to the crystallization and melting peaks of PA10T/LGF composites to shift to high temperature. On the basis of dynamic mechanical analysis data, the reduction of the interfacial bonding between the glass fibre and PA10T matrix and the motion of molecular chain segments result in the thermo-oxidative ageing of composites. According to the calculation of activation energy (E), thermo-oxidative temperature and ageing time can bring about the decline of the E value, proving the deterioration in performance of PA10T/LGF composites. In view of TGA, the increase in the thermo-oxidative temperature and ageing time promotes the degradation of PA10T/LGF composites. The tensile, flexural and notched impact strengths of PA10T/LGF composites decline with prolonging the ageing temperature and time. The surface of materials produces some microcracks and the cross-section surface of PA10T/LGF composites becomes rougher.
In this work, the ethylene-propylene-diene monomer/polypropylene (EPDM/PP) thermoplastic elastomer filled with intumescent flame retardants (IFR) is fabricated by melting blend. The IFR are constituted with melamine phosphate-pentaerythritol (MP/PER) by compounding and reactive extruding, respectively. The effects of two kinds of MP/PER with different contents on the thermal stability, flame retardancy, and mechanical properties of materials are investigated by Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), limiting oxygen index (LOI), UL-94, cone calorimeter test (CCT), and scanning electron microscopy (SEM). FTIR results show that the reactive extruded MP/PER partly generates melamine pyrophosphate (MPP) compared with compound masterbatches. TGA data indicate that the best thermal stability is achieved when the molar ratio of MP/PER reaches 1.8. All the reactive samples show a higher flame retardancy than compound ones. The CCT results also exhibit the same trend as above in heat release and smoke production rate. The EPDM/PP composites filled with 30 and 35% reactive MP/PER exhibit the improved flame retardancy but become stiffer and more brittle. SEM photos display that better dispersion and smaller particle size are obtained for reactive samples.
Constructing a porous conductive framework represents a promising strategy for designing high-performance anodes for Li-ion batteries. Here, porous CuO nanotubes/graphene with hierarchical architectures were fabricated by simple annealing of copper nanowires/graphene hybrids synthesized by a microwave-assisted process. In these nanoarchitectures, the embedded porous CuO nanotubes can prevent restacking of the graphene sheets, whereas graphene can increase the electrical conductivity of CuO. Moreover, these two components constitute a sandwich-like interlaced framework that favors ion diffusion, as well as promoting better electron transport. As a result, the as-prepared nanohybrid exhibits a high specific capacity of 725 mA h g-1 and a capacity retention of â¼81% after 250 cycles, as well as outstanding rate performance in comparison to those of bare CuO or a CuO-CNT (carbon nanotubes) hybrid.
This study developed an adhesive and transferable free-standing (FS) film with dual function of osteoinductivity and antibacterial activity, which was obtained by sequentially assembling vancomycin immobilized oxidized sodium alginate and dexamethasone encapsulated chitosan coated BSA nanoparticles on a poly-dopamine layer. The FS films enabled the dual release of vancomycin and dexamethasone. The FS films had excellent osteoinductivity and antibacterial activity by cell culture and antibacterial assay. The FS film was detached from substrates and transferred to non-fouling surfaces by a wet transfer method, which demonstrated that the adhesive FS film is potential to modify biopolymers with non-fouling surfaces in mild and biocompatible conditions for biomedical applications.
Adhesives/chemical synthesis , Alginates/chemistry , Anti-Bacterial Agents/chemistry , Dexamethasone/chemistry , Nanoparticles/chemistry , Serum Albumin, Bovine/chemistry , Vancomycin/chemistry , Adhesives/chemistry , Anti-Bacterial Agents/pharmacology , Biofouling/prevention & control , Cells, Cultured , Chitosan/chemistry , Dexamethasone/pharmacology , Dose-Response Relationship, Drug , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Humans , Indoles/chemistry , Microbial Sensitivity Tests , Molecular Structure , Oxidation-Reduction , Particle Size , Polymers/chemistry , Staphylococcus epidermidis/drug effects , Structure-Activity Relationship , Surface Properties , Vancomycin/pharmacology
