Development and validation of a gas chromatographic method for analysis of fosfomycin in chicken muscle samples

Summary A gas chromatographic method for the determination of residues of Fosfomycin in chicken muscle samples has been developed. Muscle samples were homogenised with TRIS buffer, containing phenylphosphonic acid (as internal standard) and Fosfomycin using a tissue homogenizer. Afterwards, the samples were ultrafiltered and the ultrafiltrate was evaporated to dryness. A silylation reagent for derivatization was used in order to reconstitute the residue. The linear concentration range of application was 10–150 μgg⁻¹, with a detection and quantitation limit of 3.11 and 10 μgg⁻¹, respectively. The method was efficient with a mean recovery of 87.83% from spiked muscle. The results obtained show that gas chromatography is a useful method for the determination of Fosfomycin residues in chicken muscle samples.     

Optimization and validation of a micellar electrokinetic chromatographic method for the analysis of several angiotensin-II-receptor antagonists

We have optimized a micellar electrokinetic capillary chromatographic method for the separation of six angiotensin-II-receptor antagonists (ARA-IIs): candesartan, eprosartan mesylate, irbesartan, losartan potassium, telmisartan, and valsartan. A face-centred central composite design was applied to study the effect of the pH, the molarity of the running buffer, and the concentration of the micelle-forming agent on the separation properties. A combination of the studied parameters permitted the separation of the six ARA-IIs, which was best carried out using a 55-mM sodium phosphate buffer solution (pH 6.5) containing 15 mM of sodium dodecyl sulfate. The same system can also be applied for the quantitative determination of these compounds, but only for the more stable ARA-IIs (candesartan, eprosartan mesylate, losartan potassium, and valsartan). Some system parameters (linearity, precision, and accuracy) were validated.     

Optimization and validation of chiral high-performance liquid chromatographic method for analysis of a fibrinogen (gpIIb/IIIa) receptor antagonist.

A chiral HPLC separation on an alpha 1-acid glycoprotein (AGP) column was developed for the separation of roxifiban, a fibrinogen receptor antagonist, from its related chiral impurities. The proposed method was optimized for mobile phase buffer concentration, organic modifier, and temperature using experimental design. The method was then validated for use in release testing of the roxifiban drug substance.     

Simple gas chromatographic method for furfural analysis

A new, simple, gas chromatographic method was developed for the direct analysis of 5-hydroxymethylfurfural (5-HMF), 2-furfural (2-F) and 5-methylfurfural (5-MF) in liquid and water soluble foods, using direct immersion SPME coupled to GC-FID and/or GC-TOF-MS. The fiber (DVB/CAR/PDMS) conditions were optimized: pH effect, temperature, adsorption and desorption times. The method is simple and accurate (RSD<8%), showed good recoveries (77-107%) and good limits of detection (GC-FID: 1.37 microgL(-1) for 2-F, 8.96 microgL(-1) for 5-MF, 6.52 microgL(-1) for 5-HMF; GC-TOF-MS: 0.3, 1.2 and 0.9 ngmL(-1) for 2-F, 5-MF and 5-HMF, respectively). It was applied to different commercial food matrices: honey, white, demerara, brown and yellow table sugars, and white and red balsamic vinegars. This one-step, sensitive and direct method for the analysis of furfurals will contribute to characterise and quantify their presence in the human diet.     

气相色谱毛细管柱操作参数最优化探索

本文对气相色谱毛细管柱如何选择合适的柱温与载气线速进行了探讨,提出了一种在最短时间内使一种难分离物质达到预期分离的最优化方法,本法数学模型简单.实验工作量小,最优操作参数范围的估计较可靠,改变了凭经验与直觉选择分析件的传统方法,可适用于现代具有微机控制的色谱仪。     

Dissociation Kinetics of Aqua[(1SR, 4RS, 7RS, 8SR, 11RS, 14RS)-5,5,7,12,12,14-Hexamethyl-1,4,8,11-Tetraazacyclotetradecane]Copper(II) (Red) Cation in Strongly Acidic,Aqueous Media

In order to investigate the effect of structure variation upon complex dissociation rate constants, the kinetics of the dissociation of (C·rac·5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane)copper(II) (red) cation has been examined spectrophotometrically at 25.0°C in 0.1–5.0 M HNO₃. The cleavage of the second copper-nitrogen bond is proposed as the rate-determining step for this reaction. The possible pathways for the cleavages of the copper-nitrogen bonds, the factors influencing the dissociation rates, and the factors affecting the relative importance of each of these possible pathways are considered.     

Evaluation of a capillary gas chromatographic impurity test procedure for 4-hexylaniline

A capillary gas chromatographic test procedure for the detection and quantitation of impurities in the bulk intermediate, 4-hexylaniline, is evaluated and found to be accurate and precise. 4-Hexylaniline is dissolved in methanol and chromatographed isothermally at a temperature of 195 degrees C on a 60-m x 0.32-mm 85% polyethylene glycol-15% dimethylsilicone blend (DX-4) film column. A flame ionization detector is used, and the impurities in the parent compound are estimated from peak areas on a percent basis compared with the area of the parent peak in the chromatogram. Response factors are determined for the known impurities. Validation of this test method includes a recovery study of known impurity spiked samples fortified in the range of 0.1-1% (w/w). A repeatability study is performed, consisting of the analysis of two different synthetic batch lots of 4-hexylaniline analyzed over three experimental run days using two chromatographic columns of different manufacturing lots. These data and other aspects of this test procedure are discussed.     

(1SR,2SR,3SR,4RS,5RS,6RS,7SR,8RS)‐7,8‐Dichloro­bicyclo­[4.2.0]octa‐2,3,4,5‐tetrayl tetra­acetate

In the title compound, C₁₆H₂₀Cl₂O₈, the bicyclic system contains a central non‐planar cyclo­hexane ring which is fused to a cyclo­butane moiety. The cyclo­hexane ring has a chair conformation and the whole system adopts a syn conformation. The structure provides information on the stereochemical course of the chlorination, photo‐oxidation and hydrox­ylation steps of the reaction.