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Optimisation of ultrasound extraction for flavonoids from semen astragali complanati and its identification by HPLC‐DAD‐MS/MS

Identifieur interne : 000E35 ( Istex/Corpus ); précédent : 000E34; suivant : 000E36

Optimisation of ultrasound extraction for flavonoids from semen astragali complanati and its identification by HPLC‐DAD‐MS/MS

Auteurs : Qing-An Zhang ; Xue-Hui Fan ; Tao Li ; Zhi-Qi Zhang ; Ying-Kun Liu ; Xiao-Ping Li

Source :

RBID : ISTEX:9A3EAA17655CDB6AB9F1916381F504087434E8CC

Abstract

The optimisation of ultrasound extraction of semen astragali complanati flavonoids was studied by measuring characteristic absorbance at 266 nm as the response and using response surface methodology (four‐variable, three‐level Box–Behnken design, BBD) in this article. The optimal conditions were obtained as 52 °C, 34 min, 26:1 (mL:g) and 100 mesh (0.120–0.150 mm) for extraction temperature, extraction time, solvent‐to‐sample ratio as well as particle size, respectively. Under these conditions, validation experiments were carried out and the experimental value of A266 was 0.9907 ± 0.032 (n = 3), which corresponded to an experimental extraction yield of 7.08%. Compounds in the extracts obtained with the optimum extraction conditions were identified by high‐performance liquid chromatography coupled with diode array and mass spectrometry detectors (HPLC–DAD–MS). Among the 14 compounds that were tentatively identified in the extracts according to their ultraviolet‐visible spectroscopy, mass spectrometry and related literature reports, four were reported for the first time.

Url:
DOI: 10.1111/ijfs.12178

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ISTEX:9A3EAA17655CDB6AB9F1916381F504087434E8CC

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<note>Figure S1. The typical scanning curve for extracts from 190 to 550 nm (a), and absorbance curve at 266 nm for different ethanol solution extracts (b).Figure S2. The surface plots of A266 for the flavonoids extracted from semen astragali complanati as affected by ultrasonic extraction temperature, extraction time, solvent‐to‐sample ratio and particle size.Figure S3. Chromatograms for semen astragali complanati flavonoids at 260 and 330 nm, obtained by HPLC–DAD–MS/MS.Table S1. Box–Behnken design and observed responses*Table S2. Estimated regression coefficients for the quadratic polynomial model and the analysis of variance (ANOVA) for the experimental results.Table S3. Identified compounds in semen Astragali complanati extracts.</note>
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<keyword xml:id="ijfs12178-kwd-0001">Flavonoids</keyword>
<keyword xml:id="ijfs12178-kwd-0002">identification</keyword>
<keyword xml:id="ijfs12178-kwd-0003">optimisation</keyword>
<keyword xml:id="ijfs12178-kwd-0004">semen astragali complanati</keyword>
<keyword xml:id="ijfs12178-kwd-0005">ultrasound extraction</keyword>
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<fundingAgency>National Natural Science Foundation of China</fundingAgency>
<fundingNumber>31101324</fundingNumber>
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<fundingAgency>Natural Science Foundation of Shaanxi Province, China</fundingAgency>
<fundingNumber>2011JQ2003</fundingNumber>
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<fundingAgency>Fundamental Research Funds for the Central Universities of China</fundingAgency>
<fundingNumber>GK201002014</fundingNumber>
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<caption>
<b>Figure S1.</b>
The typical scanning curve for extracts from 190 to 550 nm (a), and absorbance curve at 266 nm for different ethanol solution extracts (b).</caption>
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<caption>
<b>Figure S2.</b>
The surface plots of A266 for the flavonoids extracted from semen astragali complanati as affected by ultrasonic extraction temperature, extraction time, solvent‐to‐sample ratio and particle size.</caption>
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<b>Figure S3.</b>
Chromatograms for semen astragali complanati flavonoids at 260 and 330 nm, obtained by HPLC–DAD–MS/MS.</caption>
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<b>Table S1.</b>
Box–Behnken design and observed responses*</caption>
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<b>Table S2.</b>
Estimated regression coefficients for the quadratic polynomial model and the analysis of variance (ANOVA) for the experimental results.</caption>
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<b>Table S3.</b>
Identified compounds in semen Astragali complanati extracts.</caption>
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<title type="main">Summary</title>
<p>The optimisation of ultrasound extraction of semen astragali complanati flavonoids was studied by measuring characteristic absorbance at 266 nm as the response and using response surface methodology (four‐variable, three‐level Box–Behnken design, BBD) in this article. The optimal conditions were obtained as 52 °C, 34 min, 26:1 (mL:g) and 100 mesh (0.120–0.150 mm) for extraction temperature, extraction time, solvent‐to‐sample ratio as well as particle size, respectively. Under these conditions, validation experiments were carried out and the experimental value of A
<sub>266</sub>
was 0.9907 ± 0.032 (
<i></i>
=
<i> </i>
3), which corresponded to an experimental extraction yield of 7.08%. Compounds in the extracts obtained with the optimum extraction conditions were identified by high‐performance liquid chromatography coupled with diode array and mass spectrometry detectors (HPLC–DAD–MS). Among the 14 compounds that were tentatively identified in the extracts according to their ultraviolet‐visible spectroscopy, mass spectrometry and related literature reports, four were reported for the first time.</p>
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<title>Optimisation of ultrasound extraction for flavonoids from semen astragali complanati and its identification by HPLC‐DAD‐MS/MS</title>
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<namePart type="given">Qing‐An</namePart>
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<affiliation>School of Food Engineering and Nutrition Science, Shaanxi Normal University, 710062, Xi'an, China</affiliation>
<description>Correspondence: Correspondent: E‐mail: </description>
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<namePart type="given">Xue‐Hui</namePart>
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<abstract>The optimisation of ultrasound extraction of semen astragali complanati flavonoids was studied by measuring characteristic absorbance at 266 nm as the response and using response surface methodology (four‐variable, three‐level Box–Behnken design, BBD) in this article. The optimal conditions were obtained as 52 °C, 34 min, 26:1 (mL:g) and 100 mesh (0.120–0.150 mm) for extraction temperature, extraction time, solvent‐to‐sample ratio as well as particle size, respectively. Under these conditions, validation experiments were carried out and the experimental value of A266 was 0.9907 ± 0.032 (n = 3), which corresponded to an experimental extraction yield of 7.08%. Compounds in the extracts obtained with the optimum extraction conditions were identified by high‐performance liquid chromatography coupled with diode array and mass spectrometry detectors (HPLC–DAD–MS). Among the 14 compounds that were tentatively identified in the extracts according to their ultraviolet‐visible spectroscopy, mass spectrometry and related literature reports, four were reported for the first time.</abstract>
<note type="additional physical form">Figure S1. The typical scanning curve for extracts from 190 to 550 nm (a), and absorbance curve at 266 nm for different ethanol solution extracts (b).Figure S2. The surface plots of A266 for the flavonoids extracted from semen astragali complanati as affected by ultrasonic extraction temperature, extraction time, solvent‐to‐sample ratio and particle size.Figure S3. Chromatograms for semen astragali complanati flavonoids at 260 and 330 nm, obtained by HPLC–DAD–MS/MS.Table S1. Box–Behnken design and observed responses*Table S2. Estimated regression coefficients for the quadratic polynomial model and the analysis of variance (ANOVA) for the experimental results.Table S3. Identified compounds in semen Astragali complanati extracts.</note>
<note type="funding">National Natural Science Foundation of China - No. 31101324; </note>
<note type="funding">Natural Science Foundation of Shaanxi Province, China - No. 2011JQ2003; </note>
<note type="funding">Fundamental Research Funds for the Central Universities of China - No. GK201002014; </note>
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<genre>keywords</genre>
<topic>Flavonoids</topic>
<topic>identification</topic>
<topic>optimisation</topic>
<topic>semen astragali complanati</topic>
<topic>ultrasound extraction</topic>
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<title>International Journal of Food Science & Technology</title>
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<topic>Original Article</topic>
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<identifier type="ISSN">0950-5423</identifier>
<identifier type="eISSN">1365-2621</identifier>
<identifier type="DOI">10.1111/(ISSN)1365-2621</identifier>
<identifier type="PublisherID">IJFS</identifier>
<part>
<date>2013</date>
<detail type="volume">
<caption>vol.</caption>
<number>48</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>9</number>
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<extent unit="pages">
<start>1970</start>
<end>1976</end>
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<accessCondition type="use and reproduction" contentType="copyright">International Journal of Food Science and Technology © 2013 Institute of Food Science and Technology© 2013 The Authors. International Journal of Food Science and Technology © 2013 Institute of Food Science and Technology</accessCondition>
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