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Electrophoretically Lodged Chitosan/Eudragit Elizabeth 100/AgNPs Blend Films in Titanium Substrate being a Sterling silver Relieve System.
coli, S. G150 aureus and S. epidermis). Negative visual read-out was observed for all tested non-specific bacteria except for MRSA. Assay takes an average of 5 min and presents a powerful point-of-care diagnostic platform for the detection of MRSA.The purpose of the research was to develop an improved solid phase microextraction (SPME)-based sampling protocol for the therapeutic drug monitoring of tranexamic acid (TXA) from plasma and urine of patients with chronic renal dysfunction (CRD) in order to correct the current dosing schedule to accommodate these patients. A 12-fold improvement in sampling efficiency (25 min for 96 samples -22 s per sample) was achieved with the use of hydrophilic-lipophilic balance (HLB)-coated SPME devices, thereby enabling high throughput profiling of TXA in the plasma and urine of 49 CRD patients undergoing cardiac surgery. A limit of quantification of 10 μg/mL and 25 μg/mL was obtained for plasma and urine respectively while a method accuracy of 103-105% and a precision of less than 8% was achieved. The results from this study were ultimately used by clinicians at the Toronto General Hospital to design a corrective pharmacokinetic dosing schedule for CRD patients. This green method further presents potential application in the clinical field for the fast high throughput monitoring of TXA not only in plasma but also in urine - a biological matrix seldom explored for the analysis of TXA - without the need for solvent-assisted extraction, extensive sample pre-treatment or clean-up, derivatization or excessive pH adjustment to improve amenability for analytical separation.Nonribosomal cyclopeptide cyclosporin A (CsA), produced by fungus Tolypocladium inflatum, is an extremely important immunosuppressive drug used in organ transplantations and for therapy of autoimmune diseases. Here we report for the first time production of CsA, along with related cyclosporins B and C, by Tolypocladium inflatum strains of marine origin (White Sea). Cyclosporins A-C contain an unusual amino acid, (4R)-4-((E)-2-butenyl)-4,N-dimethyl-l-threonine (MeBmt), and are prone to isomerization to non-active isocyclosporin by N→O acyl shift of valine connected to MeBmt in acidic conditions. CsA and isoCsA are not distinguishable in MS analysis of [M+H]+ ions due to rapid [CsA + H]+→[isoCsA + H]+ conversion. We found that the N→O acyl shift is completely suppressed in cyclosporine [M+2H]2+ ions, and their collision-induced dissociation (CID) can be used for rapid and unambiguous analysis of cyclosporins and isocylosporins. Fragmentation patterns of [CsA+2H]2+ and [isoCsA+2H]2+ ions were analyzed and explained. The developed approach could be useful for MS analysis of other peptides containing β-hydroxy-α-amino acids.Differential mobility spectrometry (DMS) analysis of electrosurgical smoke can be used to distinguish cancerous and healthy tissues. Mass spectrometry studies of surgical smoke have revealed phospholipids as the key compounds enabling this discrimination. Lecithin is a mixture of phospholipids encountered in tissues. We hypothesized that DMS is capable of detecting and quantifying lecithin from water solution in headspace chamber, paving way for analysis of surgical smoke. We measured different lecithin concentrations in a biologically relevant range considering healthy and cancerous tissues with DMS and trained regression models to predict the analyte concentration. The models were internally cross-validated and externally validated. The best cross-validation results were obtained with convolutional neural networks, with root mean square error (RMSE) = 0.38 mg/ml. This is the first demonstration of estimation of analyte concentration from DMS measurements with neural networks. The best external validation results were acquired with sparse linear regression methods, with RMSE varying from 0.40 mg/ml to 0.41 mg/ml. The results demonstrate that DMS is sufficiently sensitive to detect biologically relevant changes in phospholipid concentration, potentially explaining its ability to detect cancerous tissue. In the future, we aim to reproduce the results by using surgical smoke as the medium. In this scenario, the complex background of surgical smoke will be the main challenge to overcome. Predicting concentration with neural networks also lays the foundation for wider analytical usage of DMS.In the paper results of Laser-Induced Breakdown Spectroscopy (LIBS) measurements of Al and Si content in aqueous solutions are presented. Calibration curves exhibit good linearity and satisfying R2 coefficients of determination (over 0.99). The calibration procedures were next used for the determination of Al and Si concentration in biological material transferred into water solutions of unknown Al and Si content. Obtained data were verified by the AAS method (atomic absorption spectrometry). Measurement results showed good conformity. The LIBS spectra were also processed using Factorial Analysis (FA). It was found for Si samples that instead of a classic approach based on the selection of a particular spectral line for the calibration the FA makes possible the use of entire spectra to obtain quantitative information on the investigated material.A simple method for measuring water levels from 1 mg L-1 to 5000 mg L-1 in oils that uses no chemical reagents or matrix specific calibrations is described. The approach involves capturing the water from the oil on an infrared transparent membrane and then recording an IR spectrum in transmission mode through the membrane. A classic spectrum of liquid water is obtained for all oil types, as both dissolved water and emulsion-based water are extracted to form an adsorbed layer of water on the membrane surface. The method was tested with three types of oils that are identified as difficult in the ASTM method E2412, as these oils, exhibit distortions in the water bands due to interactions of the water with the oil, or have significant levels of scattering due to the presence of water droplets. In comparing water concentrations measured by Karl Fischer titration, a high level of linearity (R2 > 0.995) is obtained over the range of 1 mg L-1 to 5000 mg L-1 with slope values of 0.99 for power steering fluid, 0.98 for vegetable oils, and 0.
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