N-methyl-N-((1-methyl-5-(3-(1-(2-methylbenzyl)piperidin-4-yl)propoxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine, a new cholinesterase and monoamine oxidase dual inhibitor

On the basis of N-((5-(3-(1-benzylpiperidin-4-yl)propoxy)-1-methyl-1H-indol-2-yl)methyl)-N-methylprop-2-yn-1-amine (II, ASS234) and QSAR predictions, in this work we have designed, synthesized, and evaluated a number of new indole derivatives from which we have identified N-methyl-N-((1-methyl-5-(3-(1-(2-methylbenzyl)piperidin-4-yl)propoxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine (2, MBA236) as a new cholinesterase and monoamine oxidase dual inhibitor.PostprintPostprintPeer reviewe

Validation of a Thin-Layer Chromatography for the Determination of Hydrocortisone Acetate and Lidocaine in a Pharmaceutical Preparation

A new specific, precise, accurate, and robust TLC-densitometry has been developed for the simultaneous determination of hydrocortisone acetate and lidocaine hydrochloride in combined pharmaceutical formulation. The chromatographic analysis was carried out using a mobile phase consisting of chloroform + acetone + ammonia (25%) in volume composition 8 : 2 : 0.1 and silica gel 60F 254 plates. Densitometric detection was performed in UV at wavelengths 200 nm and 250 nm, respectively, for lidocaine hydrochloride and hydrocortisone acetate. The validation of the proposed method was performed in terms of specificity, linearity, limit of detection (LOD), limit of quantification (LOQ), precision, accuracy, and robustness. The applied TLC procedure is linear in hydrocortisone acetate concentration range of 3.75 ÷ 12.50 g⋅spot −1 , and from 1.00 ÷ 2.50 g⋅spot −1 for lidocaine hydrochloride. The developed method was found to be accurate (the value of the coefficient of variation CV [%] is less than 3%), precise (CV [%] is less than 2%), specific, and robust. LOQ of hydrocortisone acetate is 0.198 g⋅spot −1 and LOD is 0.066 g⋅spot −1 . LOQ and LOD values for lidocaine hydrochloride are 0.270 and 0.090 g⋅spot −1 , respectively. The assay value of both bioactive substances is consistent with the limits recommended by Pharmacopoeia

The 42nd Symposium Chromatographic Methods of Investigating Organic Compounds : Book of abstracts

The 42nd Symposium Chromatographic Methods of Investigating Organic Compounds : Book of abstracts. June 4-7, 2019, Szczyrk, Polan

High-performance liquid chromatographic assay of 8-hydroxyquinoline sulfate and its stability in immunobiological preparations

Because of the ability of g-hydroxyquinoline sulfate (8-HQS) to irreversibly bind metals from rubber stoppers, the stability of 8-HQS in tuberculin solutions was investigated, For the determination of 8-HQS, a simple and sensitive reversed-phase HPLC method with detection at 240 nm was developed and validated. Rapid decreases in concentrations of 8-HQS were found in samples stored in original vials which were exposed to different temperatures and vial positions. (C) 1998 Elsevier Science B.V

Influence of UV/H2O2 processes on C- and N-disinfection by-products formation in different water matrices

The aim of this study was to investigate the influence of UV/H2O2 advanced oxidation process on the natural organic matter content and disinfection by-products formation potential of different water matrices. Three water matrices (two natural waters and a synthetic humic acid solution) with different natural organic matter characteristics and concentrations were analysed. The carbonaceous disinfection by-products: trihalomethanes, haloacetic acids and haloketones, as well as nitrogenous disinfection by-products: haloacetonitriles and chloropicrin were investigated after chlorination. The UV/H2O2 treatment resulted in significant trihalomethane and haloacetic acids precursors removal (up to 53% and 30%, respectively) in humic acid solution in conditions ≥ 1.0 mg H2O2/mg DOC, in combination with a dose of UV irradiation ≥ 3000 mJ/cm2. Under the same reaction conditions, in natural groundwater rich in hydrophobic natural organic matter, the advanced process was less effective in DBP precursors removal. On the other hand, the advanced process was very effective in trihalomethaneprecursors removal (up to 76%) in groundwater with hydrophyilic natural organic matter. Haloketones were formed after treatment in very low concentrations. Nitrogenous disinfection by-products were only formed in the natural water containing hydrophilic organic matter, during the advanced process at 3.0 mg H2O2/mg DOC. The UV/H2O2 process resulted in negligible organic matter mineralization, but increased the brominated disinfection by-products formation in waters with low to medium bromide contents. It was concluded that under the same advanced oxidation process reaction conditions different natural organic matter structures showed different reactivities with chlorine toward the formation of the investigated disinfection by-products

Efficiency of Coagulation/Flocculation for the Removal of Complex Mixture of Textile Fibers from Water

Synthetic fibers enter wastewater treatment plants together with natural fibers, which may affect treatment efficiency, a fact not considered in previous studies. Therefore, the aim of the present study was to evaluate the efficiency of the coagulation/flocculation process for the removal of a mixture of textile fibers from different water matrices. Natural and synthetic fibers (100 mg/L; cotton, polyacrylonitrile, and polyamide) were added to a synthetic matrix, surface water and laundry wastewater and subjected to coagulation/flocculation experiments with ferric chloride (FeCl3) and polyaluminum chloride (PACl) under laboratory conditions. In the synthetic matrix, both coagulants were found to be effective, with FeCl3 having a lesser advantage, removing textile fibers almost completely from the water (up to 99% at a concentration of 3.94 mM). In surface water, all dosages had approximately similar high values, with the coagulant resulting in complete removal. In laundry effluent, the presence of surfactants is thought to affect coagulation efficiency. PACl was found to be effective in removing textile fibers from laundry wastewater, with the lowest removal efficiency being 89% and all dosages having similar removal efficiencies. Natural organic matter and bicarbonates showed a positive effect on the efficiency of FeCl3 in removing textile fibers from surface water. PACl showed better performance in coagulating laundry wastewater while surfactants had a negative effect on FeCl3 coagulation efficiency

The influence of different matrices on the nature and content of haloacetic acids precursors in ozonized water

This paper investigates the influence of different matrices (groundwater a realistic natural matrix and commercial humic acid solution a synthetic matrix) on the nature and content of haloacetic acid (HAA) precursors in ozonized water (0.4 to 3.0 mg O3/mg DOC; pH 6). Natural organic matter (NOM) characterization of the natural matrix showed it was largely of hydrophobic character (65% fulvic and 14% humic acids), with the hydrophilic fractions HPIA and HPI-NA at 12% and 9%, respectively. At approximately the same dissolved organic carbon (DOC) content of the investigated matrices (~10 mg /L), a greater degree of hydrophobicity was seen in the humic acid solution than in the natural matrix, resulting in a higher content of HAA precursors (559 ± 21 μg/L in the synthetic matrix compared to 309 ± 15 μg/L in the natural matrix). By applying different ozone doses (0.4 to 3.0 mg O3/mg DOC), the DOC content of the studied matrices was reduced by 6-22%, with a maximum process efficacy being achieved with 3.0 mg O3/mg DOC. Ozonation also lead to changes in the NOM structure, i.e. complete oxidation of the humic acid fractions in both investigated matrices. After oxidation, hydrophilic structures dominate the natural water matrix (65%), whereas the synthetic matrix has an equal distribution of hydrophobic and hydrophilic fractions (~50%). Changes in the content and structure of NOM during ozonation resulted in the reduction of the total HAA precursors content (63-85%, using 3.0 mg O3/mg DOC). Detailed analysis of the reactivity of the residual HAA precursor materials shows that ozonation using 3.0 mg O3/mg DOC reduced the reactivity of the NOM fractions in comparison to the raw water. By contrast, HAA precursor material present in the commercial HA solution was transformed after ozonation into other reactive compounds, i.e. precursors which originated from the fulvic acid and hydrophilic fractions. The results of the laboratory testing indicate that the application of ozonation can reduce the content of haloacetic acid precursors to some degree. However, in real applications of oxidative treatment in the preparation of drinking water, as well as the efficacy in reducing the total organic matter content, the nature of the residual NOM must also be taken into account, as it can include toxic reactive precursors to disinfection byproducts