scholarly journals New Liquid Chromatography Method with Ultraviolet Detection for Analysis of Anthocyanins and Anthocyanidins in Vaccinium myrtillus Fruit Dry Extracts and Commercial Preparations

2007 ◽  
Vol 90 (4) ◽  
pp. 911-919 ◽  
Author(s):  
Ciro Cassinese ◽  
Eric De Combarieu ◽  
Mario Falzoni ◽  
Nicola Fuzzati ◽  
Roberto Pace ◽  
...  

Abstract The Vaccinium myrtillus fruits (bilberry) are a well-known anthocyanins source, and their extracts are widely used in dietary botanicals and pharmaceutical products for the treatment of vascular and vision disorders. Different analytical methods used for standardization of the bilberry extracts and their preparations are available from pharmacopeias and from the literature. However, the methods reported in the literature do not allow the detection of free anthocyanidins, which are markers of poor product quality. A new liquid chromatography method was developed and validated for the identification and quantification of both anthocyanins and anthocyanidins present in bilberry extracts and products. The method shows a good reproducibility and, due to its high specificity, is suitable to identify unequivocally the botanical raw materials used for manufacturing and to evaluate the extract composition, thus ensuring a high degree of product consistency and quality. Forty typical bilberry preparations belonging to 24 different brands were purchased in the marketplace and evaluated for their quality by using the developed method. Results revealed marked differences among the brands despite a common origin and labeling.

Author(s):  
Adriane Lettnin Roll Feijó ◽  
Fernanda Macke Hellwig ◽  
Clésio Soldateli Paim ◽  
Marcelo Donadel Malesuik

This study aimed to develop and validate a stability-indicating liquid chromatography method for the determination of tirofiban hydrochloride and two synthetic impurities (impurity A and impurity C). The method utilizes a RP-18 column (250 mm × 4.6 mm; 5 μm) with the PDA detector for quantitation. A mixture of triethylamine 0.1% (acidified to pH 5.5 with phosphoric acid) and acetonitrile was used as the mobile phase at a flow rate of 1 mL min−1 with gradient elution. The method presented satisfactory linearity, precision, accuracy and robustness, as well as low limits of detection and quantification, which demonstrate sensitivity in the determination of tirofiban and impurities A and C. It was selective for the determination of the drug and impurities analysed, without interference of the degradation products generated under forced conditions, demonstrating the stability-indicating capacity of the proposed method. Tirofiban showed to be practically stable to oxidative (30% H2O2 for 24 h) and thermal (75 ºC for 24 h) conditions, but presented degradation to UVA light and acid hydrolysis, obeying the first order kinetics for both. In this way, it can be used as a stability-indicating method in the quality control of the raw material of tirofiban hydrochloride, as well as of the finished product. The obtained results demonstrate the importance of deepening the studies in this area, in order to guarantee the quality of commercialized pharmaceutical products.


Author(s):  
Benny Antony ◽  
Merina Benny ◽  
Binu T Kuruvilla ◽  
Nishant Kumar Gupta

Objective: The objective of this study was to develop a simple and sensitive ultra-performance liquid chromatography (UPLC) method for determination of nitrate and nitrite in plant extracts and biological samples.Methods: Nitrate was analyzed directly by injecting the filtered sample into UPLC and monitoring the chromatogram at 222 nm whereas, for nitrite analysis, the samples were derivatized using Griess reagent, and chromatogram was monitored at 520 nm. The method was validated for accuracy and precision.Results: The calibration curve was obtained in the range of 0.05–500 μg/ml for nitrate and 5–3200 ng/ml for nitrite which were extremely linear, where both correlation coefficients were >0.9990. Accuracy of the method was found as 99.87% and 100.24% for nitrate and nitrite, respectively. High degree of precision and repeatability was obtained since coefficient of variation values were <2.1%. Among the three commonly used anticoagulants, i.e., K2EDTA, Li-Heparin, and sodium citrate, Li-Heparin did not show any interference with nitrate or nitrite analysis.Conclusion: Results clearly indicate the sensitivity and suitability of the developed method for estimation of nitrate and nitrite in plant extracts and biological samples. Our findings also indicate that Li-Heparin does not interfere with analysis and thus can be used as anticoagulant while collecting blood.


2020 ◽  
Vol 12 (35) ◽  
pp. 4310-4318
Author(s):  
Mairique Waszczuk ◽  
Sara Elis Bianchi ◽  
Simony Martiny ◽  
Vanessa Pittol ◽  
Denise S. Lacerda ◽  
...  

Pterostilbene is a natural constituent present in blueberries and other fruits, with several preventive and therapeutic properties for human health.


2019 ◽  
Vol 57 (8) ◽  
pp. 724-729 ◽  
Author(s):  
Mahmoud M Sebaiy ◽  
Wafaa S Hassan ◽  
Mostafa E Elhennawy

Abstract A high performance liquid chromatography method had been developed and validated for rapid simultaneous separation and determination of three anti-helicobacter drugs, oxytetracycline (OXY), tinidazole (TIN) and esomeprazole (ESM) in human plasma within 6 minutes. Drugs extraction method from plasma was based on protein precipitation technique. Separation was carried out on a Equisil BDS C18 column (5 μm, 150 × 4.60 mm) using a mobile phase of acetonitrile: 0.025 M KH2PO4 (25: 75, v/v) adjusted to pH 3.50 with ortho-phosphoric acid at ambient temperature. The flow rate was 1 mL/min and maximum absorption was measured using Diode Array (DAD) detector at 285 nm. The retention times of OXY, TIN and ESM were recorded to be 2.68, 3.52 and 5.17 minutes, respectively, indicating a shorter analysis time. Limits of detection were also reported to be 0.10, 0.07 and 0.04 μg/mL for OXY, TIN and ESM, respectively, showing a high degree of the method sensitivity. The method was then validated according to FDA guidelines for the determination of the drugs clinically in human plasma specially regarding pharmacokinetic and bioequivalence studies.


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