scholarly journals Simultaneous analysis of sugars and organic acids in wine and grape juices by HPLC: Method validation and characterization of products from northeast Brazil

2018 ◽  
Vol 66 ◽  
pp. 160-167 ◽  
Author(s):  
Emanuela Monteiro Coelho ◽  
Carla Valéria da Silva Padilha ◽  
Gabriela Aquino Miskinis ◽  
Antônio Gomes Barroso de Sá ◽  
Giuliano Elias Pereira ◽  
...  
2019 ◽  
Vol 56 (10) ◽  
pp. 4575-4584 ◽  
Author(s):  
Marcos dos Santos Lima ◽  
Polyana Campos Nunes ◽  
Bernadete de Lourdes de Araújo Silva ◽  
Carla Valéria da Silva Padilha ◽  
Thaís Helena Figueiredo do Bonfim ◽  
...  

2013 ◽  
Vol 110 ◽  
pp. 665-674 ◽  
Author(s):  
Mariana Mirelle Pereira Natividade ◽  
Luiz Claudio Corrêa ◽  
Scheilla Vitorino Carvalho de Souza ◽  
Giuliano Elias Pereira ◽  
Luiz Carlos de Oliveira Lima

2012 ◽  
Vol 7 (9) ◽  
pp. 1934578X1200700 ◽  
Author(s):  
Somendu K. Roy ◽  
Amit Srivastava ◽  
Sanjay M. Jachak

The roots of Caesalpinia digyna have been reported to contain gallic acid derivatives and minor homoisoflavonoids, but HPLC-ESI-MS and HPLC analyses of the homoisoflavonoids were challenging due to their low concentration in the roots. Separation and identification was accomplished by HPLC-ESI-MS and further elaborated for quantification using a C18 column with detection at 330 nm. A gradient mobile phase consisting of methanol and water (0.1% acetic acid) was used. The developed HPLC method showed good linearity (r2≥0.998), high precision (RSD<5%) and a good recovery (99.3-104.5%) of the compounds. The lowest detection limit was 0.75 ng and the method was found to be robust. All the validation parameters were found to be within the permissible limits and, therefore, the developed method is accurate and reliable for the quality control of C. digyna and other Caesalpinia species. This is the first report of sample preparation on Diaion HP-20 resin and characterization of homoisoflavonoids by HPLC-ESI-MS, extended by extensive quantitative HPLC analysis of homoisoflavonoids in C. digyna roots and method validation.


2017 ◽  
Vol 228 ◽  
pp. 106-115 ◽  
Author(s):  
Carla Valéria da Silva Padilha ◽  
Gabriela Aquino Miskinis ◽  
Marcelo Eduardo Alves Olinda de Souza ◽  
Giuliano Elias Pereira ◽  
Débora de Oliveira ◽  
...  

2015 ◽  
Vol 10 (11) ◽  
pp. 1934578X1501001
Author(s):  
Miroslava Bittová ◽  
Dita Hladůvková ◽  
Vendula Roblová ◽  
Stanislav Kráčmar ◽  
Petr Kubáň ◽  
...  

Organic acids, deacetyl asperulosidic acid (DAA) and polyphenolic compounds in various noni ( Morinda citrifolia L.) products (4 juices, 4 dry fruit powders and 2 capsules with dry fruit powder) were analyzed. Reversed-phase high-performance liquid chromatography (RP-HPLC) coupled with a variable wavelength detector (VWD) and electrospray ionization time-of-flight mass spectrometer (ESI-TOF MS) was applied for simultaneous analysis of organic acids (malic, lactic, citric and succinic acid) and DAA. An RP-HPLC method with diode-array detector (DAD) was developed for the analysis of polyphenolic compound content (rutin, catechin, quercitrin, kaempferol, gallic acid, caffeic acid and p-coumaric acid). The developed methods can contribute to better characterization of available noni products that is required from the consumers. In our study, we discovered significant dissimilarities in the content of DAA, citric acid and several phenolic compounds in some samples.


2020 ◽  
Vol 16 (8) ◽  
pp. 1130-1139
Author(s):  
Singaram Sathiyanarayanan ◽  
Chidambaram Subramanian Venkatesan ◽  
Senthamaraikannan Kabilan

Background: Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator and commonly used as a pharmacologic cardiac stressing agents. Methods: HPLC method was used for the analysis of related substances. The degraded impurities during the process were isolated and characterized by IR, Mass and NMR spectral analysis. Results: Forced degradation study of regadenoson under conditions of hydrolysis (neutral, acidic and alkaline) and oxidations suggested in the ICH Q1A(R2) was accomplished. The drug showed significant degradation under all the above conditions. On the whole, five novel degradation products were found under diverse conditions along with process related impurities which were not reported earlier. Conclusion: All the degradation products were well characterized by using advanced spectroscopic techniques like IR, 1H NMR, 13C NMR and Mass spectra. The identification of these impurities will be productive for the quality control during the production and stability behavior of the regadenoson drug substance.


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