Spectrophotometric determination of ciprofloxacin in serum using iron(III) ion as chromogenic agent

An analytical procedure for the determination of ciprofloxacin in serum without previous extraction has been developed. The determination was carried out using iron(III) nitrate as chromogenic agent, with the addition of sodium dodecylsulfate, at pH = 3.0. Absorbance was measured at 430 nn. The range of linearity was between 0.5 - 20.0 mu g/mL with a detection limit 0.2 mu g/mL

Raman spectroscopy as a new biochemical diagnostic tool

In this review, Raman spectroscopy is described as a new and potentially powerful diagnostic tool in comparison to routine biochemical tests. Advanced instrumentation and new Raman spectroscopy techniques enable rapid and simultaneous identification and/or determination of se veral biochemical parameters, such as glucose, acetone, creatinine, urea, lipid profile, uric acid, total protein, etc, with a very low limit of detection. Raman spectroscopy could also be applied in molecule and cell characterization, as well as diagnostics of atherosclerosis in its early stage. Raman spectroscopy is nondestructive and could be applied to all kinds of samples, which simplifies the diagnostics of numerous disea ses and pathologic states. Special attention is paid to literature data illustrating the application of Raman spectroscopy for transdermal glucose monitoring and cancer diagnostics

Determination of flavonoids and total polyphenol contents in commercial apple juices

© 2018 Czech Academy of Agricultural Sciences. All Rights Reserved. We propose a sensitive and selective spectrofluorimetric method for the determination of flavonoids as expressed in 'quercetin equivalent' in apple juices. The method is based on the strong emission of the aluminium(III)-quercetin complex at 480 nm with excitation at 420 nm, and it is successfully applied for the determination of flavonoids in commercial apple juices and compared with results obtained in reference spectrophotometric determination. The flavonoid content in commercial apple juices was found to range from 5.53 to 15.55 mg/l quercetin equivalent. The very good agreement between the two methods indicates the suitability of the proposed spectrofluorimetric method for the precise and accurate determination of flavonoids. In addition, the total polyphenol content was determined spectrophotometrically using the Folin-Ciocalteu (FC) method and the antioxidative activity of the tested juices was tested in a DPPH assay and these values were correlated with each other. The obtained profiles of compounds with antioxidative ability lead us to conclude that fruit juice labels based only on fruit % might sometimes misinform consumers

Zinc complex-based determination of rutin in dietary supplements

The aim of this study was to develop and validate a simple, rapid, sensitive and low-cost method for determination of rutin in tablets. The proposed spectrophotometric method is based on the formation of the Zn2+-rutin complex in methanol 70% (v/v) at pH 8.52, and detection at λmax= 410 nm. The concentration range over which the response was linear was 0.3-12.2 μg ml-1. The limit of detection (LOD) and the limit of quantification (LOQ) were 0.21 μg ml-1 and 0.63 μg ml-1, respectively. The proposed method was successfully applied to the determination of rutin in herbal dietary supplements. The reliability of the method was checked by comparison with results obtained by the established RP-HPLC/UV method. The proposed method fulfills all aimed requirements

Intermolecular and low-frequency intramolecular Raman scattering study of racemic ibuprofen

We report the low-temperature Raman scattering study of racemic ibuprofen. Detailed analysis of the racemic ibuprofen crystal symmetry, related to the vibrational properties of the system, has been presented. The first principle calculations of a single ibuprofen molecule dynamical properties are compered with experimental data. Nineteen, out of 26 modes expected for the spectral region below 200 cm(-1), have been observed

Development and validation of spectrofluorimetric and LC–MS/MS methods for the determination of hesperidin in human plasma and pharmaceutical forms

The spectrofluorometric method, based on fluorescence properties of aluminium (III)–hesperidin complex, for the determination of hesperidin in human plasma and pharmaceutical forms has been developed and validated. The complex shows strong emission in the presence of surfactant betain sulfonate SB 12 at 476 nm with excitation at 390 nm. Linearity range in pharmaceutical forms of hesperidin was 0.06 – 24.4 μg mL-1 with LOD 0.016 μg mL-1 and LOQ 0.049 μg mL-1. Recovery values in the range 99.3 – 99.7% indicate good accuracy of the method. A linear dependence of the intensity of fluorescence of the complex on the concentration of hesperidin in plasma was obtained in concentration range from 0.1 – 12.2 μg mL-1. The LOD was 0.032 μg mL-1 while LOQ was 0.096 μg mL-1. Recovery values were in the range 98.4 – 99.8%. The reliability of the method was checked by LC-MS/MS method for plasma samples and HPLC/UV method for tablets with direct determination of hesperidin after separation. Linearity range in determination of hesperidin in pharmaceutical forms was obtained in the range from 0.05 to 10.00 μg mL-1. The LOD was 0.01 μg mL-1 and LOQ was 0.03 μg mL-1. Linearity range in plasma determination of hesperidin was 0.02 – 10.00 μg mL-1 with LOD 0.005 μg mL-1 and LOQ 0.015 μg mL-1. Good agreement between two methods indicate the usability of the proposed spectroflurometric method for the simple, precise and accurate determination of hesperidin in clinical and quality control laboratories