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Nimesulide, cetirizine, and pseudoephedrine hydrochloride separation was done by using acetonitrile/phosphate buffer/triethyl amine as the mobile phase (Jain et al. [2012]).
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This paper describes the use of the Box Behnken experimental design to optimise the factors affecting the separation of ethambutol hydrochloride (EB), its impurity 2-amino-1-butanol and the internal standard (phenylephrine hydrochloride) in a CE method for a pharmaceutical tablet assay.
The separation of naratriptan hydrochloride and its related products (impurities and degradation products) was obtained by developing a gradient high-performance liquid chromatography method with diode-array detector (HPLC-DAD).
Figure 2 Chromatogram for separation of pheniramine maleate and naphazoline hydrochloride in pharmaceutical formulations.
Cytosine β-D-arabinofuranoside hydrochloride (Sigma) (10 μM), a selective inhibitor of DNA strand separation which does not inhibit RNA synthesis was used 1 h before the test substance was added.
The separation of carbinoxamine enantiomers and internal standard (IS, pargeverine hydrochloride) was achieved on an amylose tris 5-chloro-2-methylphenylcarbamate) column witris 5-chloro-2-methylphenylcarbamateanol/etris 5-chloro-2-methylphenylcarbamatev/v/v/v) atris 5-chloro-2-methylphenylcarbamate
A Snovel method for the simultaneous separation and determination of two antiglaucoma drugs namely, dorzolamide hydrochloride (DOR) and timolol maleate (TIM) in aqueous humor samples (AH) was developed by using salting-out assisted liquid liquid microextraction (SALLME) combined with HPLC UV method.
Resolution of binary mixtures of paracetamol, phenylephrine hydrochloride and chlorpheniramine maleate with minimum sample pre-treatment and without analyte separation has been successfully achieved by methods of partial least squares algorithm with one dependent variable, principal component regression and hybrid linear analysis.
The azeotrope behavior is not happen for the binary system of acetone + AOME, which can provide the basis data to design the separation process, and promote the development of new technology to produce O-methylhydroxyamine hydrochloride effectively and economically.
The authors show that all Nup98 FG-domains tested undergo phase-separation in vitro at relatively low concentrations when diluted out of guanidinium hydrochloride.
100% separation between samples of the same taste class (e.g. caffeine and quinine hydrochloride of the bitter class) was also demonstrated, as well as a detection and classification of samples of the same substance with different concentrations.
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