Without further sample preparation, the loaded filters are immediately analyzed via transmission infrared spectroscopy, and the mineral amount is quantified in real-time using a partial least squares regression algorithm. Due to the inherent molecular selectivity for crystalline as well as organic matrix components, infrared spectroscopy uniquely allows to precisely determine the particle composition even in complex samples such as dust from coal mines or clay-rich environments. For establishing a robust partial least squares regression model, a method was developed for generating calibration samples representative in size and composition for respirable mine dust via aerodynamic size separation. Combined with experimental design strategies, this allows tailoring the calibration set to the demands of air quality management in underground mining scenarios, i.e., the respirable particle size regime and the matrix of the target analyte.Oxidation reactions of alcohols have been of interest due to their broad applications in different fields. Oxoammonium cation (TEMPO+) of 2,2,6,6-tetramethyl piperidine-1-oxyl (TEMPO) is a high-potential oxidant for the selective oxidation of primary alcohols, with hydroxylamine (TEMPOH) as a side product. TEMPO or TEMPO+ has been widely applied for various reactions. However, the conversion mechanisms among TEMPO, TEMPO+, and TEMPOH are not well understood and remain controversial, due to complications in the direct observation of the reactions. In this work, two-dimensional correlation (2D-COS) UV-visible (UV-Vis) spectroscopy is applied to examine the correlations between the characteristic bands of each species, to obtain insights into the complete reaction mechanisms. Series of dynamic UV-Vis spectra of solutions under different external perturbations (as a function of reaction time) were recorded and used in the generation of 2D-COS synchronous and asynchronous maps. The key UV-Vis band assignments are as follows 250 nm and 400 nm for TEMPO, 290 nm and 480 nm for TEMPO+, and 200 nm and 315 nm for TEMPOH. The results indicate that the conversion between TEMPO and TEMPOH in acidic solution is a reversible process, which reaches an equilibrium state after two hours. However, the reaction becomes irreversible after three hours, due to a higher degree of irreversible protonation of TEMPOH to form TEMPOH-H+. Fast conversion from TEMPO to TEMPO+ is observed when sodium hypochlorite co-oxidant is added. The synproportionation-disproportionation also reaches an equilibrium. However, there is no evidence of the conversion from TEMPOH to TEMPO+ under the reaction conditions. At high reaction temperature, the formation of TEMPOH occurs first from TEMPO+ decomposition, followed by TEMPO decomposition. These detailed mechanisms are beneficial in designing the optimum process conditions for the oxidation of specific alcohols.Chronic kidney disease (CKD) affects more than 10% of the global population and is associated with significant morbidity and mortality. In most cases, this disease is developed silently, and it can progress to the end-stage renal failure. Therefore, early detection becomes critical for initiating effective interventions. Routine diagnosis of CKD requires both blood test and urinalyses in a clinical laboratory, which are time-consuming and have low sensitivity and specificity. Surface-enhanced Raman scattering (SERS) is an emerging method for rapidly assessing kidney function or injury. https://www.selleckchem.com/products/2-c-methylcytidine.html This study was designed to compare the differences between the SERS properties of the serum and urine for easy and simple detection of CKD. Enrolled for this study were 126 CKD patients (Stages 2-5) and 97 healthy individuals. SERS spectra of both the serum and urine samples were acquired using a Raman spectrometer (785 nm excitation). The correlation of chemical parameters of kidney function with the spectra was examined using44 for the eGFR (p  less then  0.001) and 0.6579 for the urine microalbumin (p  less then  0.001). In conclusion, the accuracy of associations between SERS findings of the serum and urine samples with clinical conclusions of CKD diagnosis in this limited number of patients is similar, suggesting that SERS may be used as a rapid and easy-to-use method for early screening of CKD, which however needs further evaluation in a large cohort study. This study aimed to evaluate polypharmacy, potentially inappropriate prescribing (PIP) and medication complexity in Turkish older patients in the community pharmacy setting and to determine the factors associated with PIP. This descriptive cross-sectional study was conducted in the community pharmacy setting in Istanbul. Older patients (≥65years old) who chronically used at least one medication and visited the community pharmacy for any reason in the past 4 months were invited in this study. PIP was determined by using the Ghent Older People's Prescriptions Community Pharmacy Screening (GheOP S)-tool. The Turkish version of the Medication Regimen Complexity Index (MRCI) was used to determine medication complexity. Polypharmacy (defined as the concurrent use of five or more medications) was found in 69.0% of 158 patients. A total of 398 PIPs were detected and 83.5% (n=132) of older patients had at least one PIP. The median (IQR) MRCI score was 12.5 (7.0-19.6). The factors associated with having ≥2 PIP were advanced age (≥75years old) (OR=2.87, 95% CI 1.41-5.81; <0.05), higher number of chronic diseases (when ≥3, OR=8.51, 95% CI 3.66-19.76; <0.05), receiving polypharmacy (OR=8.92, 95% CI 4.09-19.46; <0.05), and higher MRCI scores (when MRCI ≥12.5, OR=4.40, 95% CI 2.22-8.71; <0.05). More than half of the Turkish older patients had polypharmacy and the rate of PIP was high. A higher number of PIP was associated with advanced age, higher number of chronic diseases, polypharmacy, and more complex medication regimens. More than half of the Turkish older patients had polypharmacy and the rate of PIP was high. A higher number of PIP was associated with advanced age, higher number of chronic diseases, polypharmacy, and more complex medication regimens.