Microdermabrasion is a popular technique used in the treatment of several skin problems, including acne, acne scarring, striae distensae, and photoaging. This article will review the relevant literature and use an evidence-based approach to evaluate the clinical efficacy of microdermabrasion in skin care. In summary, microdermabrasion appears to be a procedure that can produce changes in dermal matrix constituents and result in improvement in skin contour irregularities. It may also be beneficial in improving transepidermal delivery of certain medications. Its role in the treatment of dyschromias and acne vulgaris is limited.
In this study, a new sorbent based on the gold nanoparticle loaded in activated carbon (Au-NP-AC) was synthesized and modified by bis(4-methoxy salicylaldehyde)-1,2-phenylenediamine (BMSAPD). This sorbent, which is abbreviated as Au-NP-AC-BMSAPD, has been applied for the enrichment and preconcentration of trace amounts of Co(2+), Cu(2+), Ni(2+), Fe(2+), Pb(2+), and Zn(2+) ions in real samples. All metal ions under study were retained on the Au-NP-AC-BMSAPD sorbent by complexation of the ions with the BMSAPD ligand, providing an efficient preconcentration fashion. The retained metal ions were then eluted from the sorbent by HNO(3) and detected by flame atomic absorption spectrometry. The analytical parameters including pH, amount of ligand, and the nature of the eluent and solid phase were evaluated to obtain the optimum condition for the preconcentration factor. Following the optimum conditions, a preconcentration factor of 200 was obtained for all the metal ions under study with detection limits of 1.4-2.6 ng mL(-1). The method has been successfully applied for the extraction and determination of the ion content in the same real samples with recoveries in the range of 95-99.6% and a relative standard deviation lower than 4.0%.
In this work, a room temperature and short method (30min) for synthesis of nanosized rod-like metal organic polymer (MOP) has been described. Reaction of 1,4-phenylenedioxy diacetic acid with zinc salt leads to the formation of [Zn(CHO)(HO)] and subsequently was loaded on activated carbon following sonication and structurally characterized by FTIR, SEM, EDX and XRD analysis. The combination of this new composite with sonication was applied for rapid and efficient adsorption of Bromocresol Purple (BCP). Effects of initial BCP concentration, mass of adsorbent and sonication time on response were investigated and optimized by central composite design (CCD). Analysis of variation (ANOVA) was adapted to experimental data to find best optimum conditions which was set at 15.22mgL, 2.41min, 0.02g and 0.009mg for initial BCP concentration, sonication time and adsorbent mass, respectively. Conduction of similar experiments at specified condition permit achievement of 98.69% removal percentage. 1,4-phenylenedioxy diacetic acid and Zn(NO3).4HO which have applied for preparation of MOP are interesting antibacterial properties and accordingly MOP was screened in vitro for their antibacterial actively against Proteus vulgaris bacteria and experimental results reveal this MOP was able to inhibit growth of the tested bacteria. The experimental data were best fitted by pseudo-second order and Langmuir for kinetic model and the adsorption equilibrium isotherm, respectively.
In this work, MOF‐5 composited with Ag2O nanoparticles was prepared and characterized via X‐ray diffraction, field emission‐scanning electron microscopy, energy‐dispersive spectroscopy and FT‐IR analysis. This new material was subsequently employed for removing basic yellow dye [Auramine O (AO)] from aqueous solution under ultrasound irradiation. Several experiments were designed by central composite design in which operational parameters such as such as pH, MOF‐5‐Ag2O mass and initial concentration of AO involved in the process were optimized. The significance of individual parameters and their possible interactions were investigated using analysis of variance (anova). The optimum values of 6, 0.025 g and 6 mg l−1 were obtained for the pH, MOF‐5‐Ag2O‐NPs mass and the initial concentrations of AO, respectively, with desirability of 1.0. At such conditions, the efficiency for the removal of AO was found to be 89.45%. Various isotherm models for fitting the experimental equilibrium data were studied, and it was found that the Langmuir model has the highest efficiency for correlation of experimental equilibrium data, so that the monolayer adsorption capacity of MOF‐5‐Ag2O for successful removal of AO was 260.70 mg g−1 at optimal conditions.
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<em>meso</em>-Tetrakis(3-pyridyl)porphyrinatoiron(III) chloride encapsulated on NaY Zeolite [Fe(T-3-PyP)@NaY] was synthesized as a heterogeneous “ship-in-a-bottle” type catalyst and characterized by Fourier transform infrared (FT-IR), atomic absorption (AA), diffused reflectance UV-Vis (DR UV-Vis), X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis. The catalytic activity of Fe(T-3-PyP)@NaY was examined for the epoxidation of cyclohexene by PhI(OAc)<sub>2</sub> in CH<sub>3</sub>CN/H<sub>2</sub>O (5:1) and compared to that of Fe(T-3-PyP) as a homogenous catalyst. We found that the heterogeneous catalyst Fe(T-3-PyP)@NaY was stable and reusable for several times, and provided a mild condition and exhibited high activity and selectivity in the oxidation of alkenes to epoxides(16-94%). As representative examples for the use of Fe(T-3-PyP)@NaY/ PhI(OAc)<sub>2</sub> in organic oxidations, oxidation of 4-nitrobenzylalcohol to 4-nitrobenzaldehyde (97 %), oxidative dehydrogenation of diethyl 4-(2,6-dichlorophenyl)-2,6-dimethyl- 1,4-dihydro-3,5-pyridinedicarboxylate to the corresponding pyridine (100 %), diphenylacetic acid to benzophenone (64 %) was achieved.
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