Determination of Citrinin in Red Yeast Rice by High Performance Liquid Chromatography with Immuno-Affinity Column

2014 ◽  
Vol 1073-1076 ◽  
pp. 353-356
Author(s):  
Wei Meng ◽  
Li Xin Zhu ◽  
Xue Mei Guo ◽  
Kai Hong Li ◽  
Ren Rong Liu

To prepare immune-affinity column (IAC) of citrinin, CNBr activated Sepharose 4FF was used as a carrier to couple with monoclonal antibody against citrinin. A reversed-phase high performance liquid chromatography (HPLC) with fluorescence detection method was used to determine the samples elution after the IAC cleaning up. The fluorescence excitation and emission maxima of citrinin were 331 and 500 nm, respectively. Citrinin is determined by HPLC with a retention time of 6.5 min (flow rate of 1 mL/min) with acetonitrile-H2O (45:55, v/v, pH 2.0). The linear range is 1-500 ng/mL. The column capacity is 0.35 μg when using 0.5 mL CNBr activated Sepharose 4FF and 500 μg monoclonal antibody against citrinin. Average recoveries of citrinin from red yeast rice spiked at levels of 0.1-0.6 mg/kg range from 74.2% to 87.12%. 16 samples of red yeast rice were determined by HPLC with immune-affinity column. The results show 12 samples contain citrinin, and concentrations of citrinin of red yeast rice are 100.6~443.6 μg/kg. The IAC method is found to be highly effective, sensitive and convenient for isolating the target analyte from samples.

2020 ◽  
Vol 20 (13) ◽  
pp. 1053-1059
Author(s):  
Mahmoud M. Sebaiy ◽  
Noha I. Ziedan

Background: Allergic diseases are considered as the major burden on public health with increased prevalence globally. Histamine H1-receptor antagonists are the foremost commonly used drugs in the treatment of allergic disorders. The target drug in this study, loratadine, belongs to this class of drugs and its biometabolite desloratadine which is also a non-sedating H1 receptor antagonist with anti-histaminic activity being 2.5 to 4 times greater than loratadine. This study aimed to develop and validate a novel isocratic Reversed-phase High-Performance Liquid Chromatography (RP-HPLC) method for rapid and simultaneous separation and determination of loratadine and its metabolite, desloratadine in human plasma. Methods: The drug extraction method from plasma was based on protein precipitation technique. The separation was carried out on a Thermo Scientific BDS Hypersil C18 column (5μm, 250 x 4.60 mm) in a mobile phase of MeOH: 0.025M KH2PO4 adjusted to pH 3.50 using orthophosphoric acid (85: 15, v/v) at an ambient temperature. The flow rate was maintained at 1 mL/min and maximum absorption was measured using the PDA detector at 248 nm. Results: The retention times of loratadine and desloratadine in plasma samples were recorded to be 4.10 and 5.08 minutes, respectively, indicating a short analysis time. Limits of detection were found to be 1.80 and 1.97 ng/mL for loratadine and desloratadine, respectively, showing a high degree of sensitivity of the method. The method was then validated according to FDA guidelines for the determination of the two analytes in human plasma. Conclusion: The results obtained indicate that the proposed method is rapid, sensitive in the nanogram range, accurate, selective, robust and reproducible compared to other reported methods.


1994 ◽  
Vol 59 (3) ◽  
pp. 569-574 ◽  
Author(s):  
Josef Královský ◽  
Marta Kalhousová ◽  
Petr Šlosar

The reversed-phase high-performance liquid chromatography of some selected, industrially important aromatic sulfones has been investigated. The chromatographic behaviour of three groups of aromatic sulfones has been studied. The optimum conditions of separation and UV spectra of the sulfones and some of their hydroxy and benzyloxy derivatives are presented. The dependences of capacity factors vs methanol content in mobile phase are mentioned. The results obtained have been applied to the quantitative analysis of different technical-grade samples and isomer mixtures. For all the separation methods mentioned the concentration ranges of linear calibration curves have been determined.


Sign in / Sign up

Export Citation Format

Share Document