Quantitative Determination of Alkaloids from Roots of Hydrastis canadensis L. and Dietary Supplements Using Ultra-Performance Liquid Chromatography with UV Detection

2012 ◽  
Vol 95 (5) ◽  
pp. 1398-1405 ◽  
Author(s):  
Bharathi Avula ◽  
Yan-Hong Wang ◽  
Ikhlas A Khan

Abstract Ultra-performance liquid chromatography (UPLC) with UV detection was used for the quantification of alkaloids from roots of Hydrastis canadensis L. (goldenseal) and dietary supplements claiming to contain goldenseal. The analysis was performed on a Waters Acquity UPLC system with an Acquity UPLC BEH Shield RP18 column using gradient elution with ammonium formate and acetonitrile containing formic acid. The chromatographic run time was less than 6 min. The detection wavelength used for β-hydrastine and canadine was 290 nm; for hydrastinine, coptisine, jatrorrhizine, palmatine, and berberine, it was 344 nm. A total of five different extraction solvents, including 100% methanol, 90% methanol, 90% methanol + 1% acetic acid, 90% acetonitrile + 0.1% phosphoric acid, and 100% acetonitrile, were tested for recovery of the major compounds. The samples extracted with the 90% methanol + 1% acetic acid displayed the best recovery (>97%). The analytical method was validated for linearity, repeatability, LOD, and LOQ. The RSDs for intraday and interday experiments were less than 3.5%, and the recovery was 98–103%. UPLC/MS with a quadrupole mass analyzer and electrospray ionization source was used to confirm the identity of seven alkaloids. The analytical method was successfully applied to confirm the identification of seven alkaloids from the roots of H. canadensis, dietary supplements that claimed to contain goldenseal, and possible adulterant species.

Author(s):  
João Roberto Fortes Mazzei ◽  
Estevão Freire ◽  
Eduardo Gonçalves Serra ◽  
José Ronaldo de Macedo ◽  
Angélica Castanheira de Oliveira ◽  
...  

In this work, an analytical method for the determination of residues for the pesticides-focus was optimized: Azoxystrobin, Boscalide, Carbendazim, Chloranthranilprole, Clothianidin, Diafentiuron, Difenoconazole, Dimetomorfe, Espinetoram, Espinosade A, Espinosade D, Fenurox, Metalaxyl M, Methoxyfenozide, Tiametoxan in soil derived from tomato planting, in order to compare the levels of contamination of these compounds in soil samples. The modified QuEChERS extraction method and Ultra Performance Liquid Chromatography coupled with Sequential Mass Spectrometry were used, with ionization source by Electronebulization in ESI mode (+/-). The method consisted of extracting 15.0 g of soil with 15 ml of saturated calcium hydroxide solution pH 12.3 and 15 ml of acetonitrile, with a consequent partition in the “salting out” effect through 6.0 g of sulfate of anhydrous magnesium and 1.5 g of sodium chloride. The phases were separated by centrifugation at 3700 rpm for 7 min. The extracts were diluted with MeOH licrossolv® grade and injected in a chromatograph. The method was validated based on the parameters of linearity, LOD, LOQ, precision and accuracy. Linearity between 0.2 and 20.0 µg L-1, determination coefficients greater than 0.99. The LOQ values ​​for the method were 13 µg kg-1 for Spinosad and 7.0 µg kg-1 for the other pesticides. The method showed good precision, with RSD values ​​<20%, and accuracy, with recoveries between 70 and 120% for the vast majority of the analyzed compounds. The analytical curves were prepared with reference white soil extracts, in order to minimize the Matrix Effect. The method was considered adequate for the analysis of pesticide residues in soil, since it satisfies the validation parameters of chromatographic methods (European Commission, 2018). After validation, the method was used to analyze the residues of these pesticides in soil samples from conventional, organic and sustainable tomato plantations. Making it possible to compare the levels of environmental impacts generated. In addition to validating the analytical method for the pesticides-focus of the study, it was also possible to validate 240 more compounds, between authorized and unauthorized for use in tomato planting.


2019 ◽  
Vol 15 (5) ◽  
pp. 505-510
Author(s):  
Yanjuan Zheng ◽  
Qiushi Peng ◽  
Rui Dong ◽  
Tingyu Chen ◽  
Yi Bao ◽  
...  

Introduction: A rapid, and accurate Ultra Performance Liquid Chromatography (UPLC) method was developed to simultaneously analyze Methocarbamol, Paracetamol and the related substances Materials and Methods: Waters ACQUITY UPLC® BEH Phenyl C18 column was used in conjunction with UV detection at 225nm. Gradient elution with 0.05M, pH 6 phosphate buffer and acetonitrile flow at 0.3mL /min rate were used to separate the substances. The retention times for 4-Aminopheno, Paracetamol, Guaifenesin, Methocarbamol, and 4-Chloroacetanilide were 1.319 minute, 2.224 minute, 4.467 minute, 4.769 minute and 5.433 minute respectively. The concentration was linear in the range of 2-100 µg/ml for Methocarbamol, and 1-100 µg/mL for Paracetamol. The percentage recoveries were between 99.28±1.23% to 100.57±0.99% for Methocarbamol, and between 99.08±1.23% to 101.23±1.39% for Paracetamol. Results and Discussion: The validated optimal protocol is robust and accurate for simultaneous analysis of Methocarbamol, Paracetamol and the related substances, applicable for bulk powder as well as pharmaceutical formulation. Conclusion: In this paper, a highly sensitive, accurate, and precise UPLC method with UV-Vis detection was developed and validated for quality control of MET and PAR in bulk as well as in pharmaceutical preparations.


Author(s):  
Kishorkumar L. Mule

Objective: To develop and validate new, simple and rapid assay method for Prochlorperazine edisylate drug substance by UPLC as per ICH guidelines.Methods: Ultra performance liquid chromatographic method was developed, optimized and validated on Acquity UPLC by using Acquity BDH300 C4 (100 x 2.1 mm) 1.7µ column. 3.85g ammonium acetate in 1000 ml of water add 0.5 ml trifluoroacetic acid and 1 ml triethylamine (Mobile phase A): 0.5 ml trifluoroacetic acid in 1000 ml acetonitrile mobile phase (Mobile phase B) with gradient program. Detector wavelength 254 nm and column temperature 30 °C.Results: Linearity study was carried out for prochlorperazine edisylate, linearity was calculated from 80 % level to 120% with respect to specification level. The correlation coefficient (r) = 0.999 was proved that the method is robust. The resolution between known impurities and Prochlorperazine edisylate found more than 2.5, it was evident from specificity test that Prochlorperazine edisylate peak are well separated from its related impurities, hence the method is specific. Prochlorperazine edisylate sample solution and mobile phase were found to be stable for at least 3 d.Conclusion: A new, simple and rapid method has been developed and validated for assay determination of prochlorperazine edisylate in drug substance by Ultra Performance Liquid Chromatography (UPLC). The analytical method was developed and validated as per ICH guidelines. The developed method can be used for the fast assay determination of prochlorperazine edisylate drug substances in research laboratories and in the pharmaceutical industry. 


2014 ◽  
Vol 6 (13) ◽  
pp. 4610-4616 ◽  
Author(s):  
Chiguru Vishnuvardhan ◽  
R. Srinivas ◽  
N. Satheeshkumar

An isocratic reversed phase ultra performance liquid chromatography (RP-UPLC) method was developed for screening counterfeit medicines with UV detection at 210 nm.


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