A secondary metabolic product chromatography and mass spectrum of naked flowers and purple beads of naked flowers and purple roads
A technology of secondary metabolites, purple pearl authenticity, applied in the field of characterization of secondary metabolites chromatography and mass spectrometry fingerprints, can solve the confusion in the application of nude flower purple pearl base sources, the same thing with different names, the same name and different things, and authentic Problems such as inability to characterize medicinal materials, achieve good reproducibility and stability, large peak capacity, and simple operation
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Embodiment 1
[0038] Take a sample of Nasturtium purpurea (the origin of Baisha, harvest time in February 2017), pulverize, pass through a 40-mesh sieve, accurately weigh about 0.5 g of the sample powder, place it in a conical flask with a stopper, and add 25 mL of 50% methanol aqueous solution , weighed, sonicated for 30min, let cool, supplemented the weight loss with 50% methanol, shaken well, passed through a 0.22μm microporous membrane, and took the continuous filtrate as the test solution.
[0039] UPLC in Ultra Performance Liquid Chromatography (UPLC) Waters ACQUITY ARC TM Ultra-high performance liquid chromatograph; EclipsePlusC 18 RRHD chromatographic column, its specification is outer diameter 2.1mm×column length 150mm, packing diameter 1.8μm. The mobile phase is (A) 0.1% phosphoric acid aqueous solution and (B) acetonitrile, gradient elution, changing the gradient, optimizing the conditions for the fingerprint of violet bead, and selecting the spectrum with better results, 1-6 d...
Embodiment 2
[0054] Take a sample of Nasturtium purpurea (the place of origin, Baisha, harvested on October 15, 2016), pulverize, pass through a 40-mesh sieve, accurately weigh about 0.5 g of the sample powder, place it in a stoppered conical flask, add 50% methanol Aqueous solution 25mL, weighed, sonicated for 30min, let cool, supplemented the weight loss with 50% methanol, shaken well, passed through a 0.22μm microporous membrane, and took the subsequent filtrate as the test solution.
[0055] UPLC in Ultra Performance Liquid Chromatography (UPLC) Waters ACQUITY ARC TM Ultra-performance liquid chromatograph; phenomenex kintex XB-C 18 100A chromatographic column, its specification is outer diameter 2.1mm×column length 150mm, packing diameter 1.7μm. The mobile phase is (A) 0.1% phosphoric acid aqueous solution and (B) acetonitrile, gradient elution, changing the gradient, and optimizing the conditions for the fingerprint of violet bead. 1-7 different gradient elution as follows:
[005...
Embodiment 3
[0073] Take a sample of Nasturtium purpurea (the place of origin, Baisha, harvested on October 15, 2016), pulverize, pass through a 40-mesh sieve, accurately weigh about 0.5 g of the sample powder, place it in a stoppered conical flask, add 80% methanol Aqueous solution 25mL, weighed, sonicated for 45min, allowed to cool, supplemented with 80% methanol for weight loss, shaken well, passed through a 0.22μm microporous membrane, and took the subsequent filtrate as the test solution.
[0074] Using Ultra Performance Liquid Chromatography (UPLC) Waters ACQUITY ARC TM type ultra-performance liquid chromatograph; Phenomenex kintex XB-C 18 The chromatographic column has a specification of an outer diameter of 2.1 mm × a column length of 150 mm, and a packing diameter of 1.7 μm. The mobile phases were (A) 0.1% phosphoric acid in water and (B) acetonitrile, and the gradient elution was as follows:
[0075] time Mobile phase (v / v%) B time Mobile phase (v / v%) B 0mi...
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