2014Zhongguo shiyan fangjixue zazhiRequires access

Study on Qualtaive Method of Salidroside of Artifical Cultivation Ultivation Rhodiola Rosea by HPLC-MS

Xiaolin Zhao

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Abstract

To determine the petals,stems,roots planted content Rhodiola different medicinal parts。 Method: Each 1 g sample is dissolved after 60% ethanol,ultrasonic cleaner cleaning 50 min,filtered,rotary evaporated,add 2 mL of methanol,microporous filter membrane( 0. 45 μm) filter using CAPCELL PAK C18 column(( 2. 0 mm × 150 mm,i. d.,3 μm),column temperature 30 ℃,wavelength 278 nm,sample temperature 10 ℃,injection volume of 10 μL. The mobile phase was methanol-1% acetic acid solution 45 ∶55, flow rate of 1 mL·min- 1for quantitative analysis. Result: The effective parts of salidroside content in the order of the petals( 35. 00 mg),root( 18. 89 mg),stems( 1. 59 mg). Conclusion: A detection of salidroside content in Rhodiola rosea was established by high performance liquid chromatography. It can be applied to the analysis on the salidroside in the different medicinal materials.

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What this paper is about

To determine the petals,stems,roots planted content Rhodiola different medicinal parts。 Method: Each 1 g sample is dissolved after 60% ethanol,ultrasonic cleaner cleaning 50 min,filtered,rotary evaporated,add 2 mL of methanol,microporous filter membrane( 0. 45 μm) filter using CAPCELL PAK C18 column(( 2. 0 mm × 150 mm,i. d.,3 μm),column temperature 30 ℃,wavelength 278 nm,sample temperature 10 ℃,injection volume of 10 μL. The mobile phase was methanol-1% acetic acid solution 45 ∶55, flow rate of 1 mL·min- 1for quantitative analysis. Result: The effective parts of salidroside content in the order of the petals( 35. 00 mg),root( 18. 89 mg),stems( 1. 59 mg). Conclusion: A detection of salidroside content in Rhodiola rosea was established by high performance liquid chromatography. It can be applied to the analysis on the salidroside in the different medicinal materials.

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Available abstract

To determine the petals,stems,roots planted content Rhodiola different medicinal parts。 Method: Each 1 g sample is dissolved after 60% ethanol,ultrasonic cleaner cleaning 50 min,filtered,rotary evaporated,add 2 mL of methanol,microporous filter membrane( 0. 45 μm) filter using CAPCELL PAK C18 column(( 2. 0 mm × 150 mm,i. d.,3 μm),column temperature 30 ℃,wavelength 278 nm,sample temperature 10 ℃,injection volume of 10 μL. The mobile phase was methanol-1% acetic acid solution 45 ∶55, flow rate of 1 mL·min- 1for quantitative analysis. Result: The effective parts of salidroside content in the order of the petals( 35. 00 mg),root( 18. 89 mg),stems( 1. 59 mg). Conclusion: A detection of salidroside content in Rhodiola rosea was established by high performance liquid chromatography. It can be applied to the analysis on the salidroside in the different medicinal materials.

Key concepts: Salidroside, Rhodiola rosea, Chromatography, Rhodiola, High-performance liquid chromatography, Chemistry, Methanol, Acetic acid

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