Paper · 2024 · Сорбционные и хроматографические процессы

Determining flavonoids in the skin of Citrus reticulata

Vladimir F. Selemenev; Victor I. Deineka; Yaroslava Yu. Salasina; et al.

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claims
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verbatim quotes
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citations
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Open access · cc-by

Abstract

n this work we studied the flavonoid composition of tangerine skins using 10 kinds of tangerines from various producers. The tangerine skins were peeled from fruit purchased from the market in Belgorod and dried at room temperature outside direct sunlight. The compositions of “green” ethanol-based extraction solutions and the “weighed portion of plant material: volume of extraction solution” ratios were chosen for extraction to ensure a high yield of flavonoids. For separation, reverse-phase HPLC on the Kromasil 100-5C18 stationary phase was used in environmentally friendly mobile phase compositions that contained ethanol as an organic modifier. In gradient elution mode all mobile phases contained 0.2 vol. % orthophosphoric acid. To assign extract components, we used samples of a number of substances and parameters of electronic absorption spectra in comparison with published data. It was found that the chromatographic profiles of the extracts of the studied samples were noticeably different. A number of the least lipophilic compounds, derivatives of cinnamic acids, were found in all extracts. After that, we discovered two flavanone glycosides, the main of which was hesperidin (hesperitin-7-rutinoside) with a content of is 26.0-39.9 mg per 1 g of dried raw material, and naringin (naringenin-7-neohesperidiside) in significantly smaller quantities, from 0 to 1.15 mg per 1 g. But of greatest interest were polymethoxylated flavones, among which the main component was nobiletin (5,6,7,8,3′,4′-hexamethoxyflavone) with a content from 0.03 to almost 11 mg/g in dried peel and tangeretin (5,6,7,8,4′-pentamethoxyflavone), found in slightly smaller quantities, 0.1-5.4 mg/g. It was established that nobiletin and tangeretin were mostly accumulated in the skins of small tangerines. On the whole, tangerine skin is a great source of highly biologically active flavonoids, so its processing is an important task for the food industry.

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Claims 7

Observationobservedoriginal resultmeasured

Claim · model-written summary

Chromatographic profiles differed among tangerine samples.

Taxon
Citrus reticulataCitrus reticulatat0
Outcome
chromatographic profilese0
Direction
noticeably differente0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“chromatographic profiles of the extracts of the studied samples were noticeably different”

✓ located verbatim in the source · abstract, characters 917–1006 · show in text ↑
t0

“Citrus reticulata”

✓ located verbatim in the source · title, characters 38–55 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Cinnamic-acid derivatives were found in all extracts.

Taxon
Citrus reticulataCitrus reticulatat0
Outcome
derivatives of cinnamic acidse0
Qualifier
all extractse0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“derivatives of cinnamic acids, were found in all extracts”

✓ located verbatim in the source · abstract, characters 1052–1109 · show in text ↑
t0

“Citrus reticulata”

✓ located verbatim in the source · title, characters 38–55 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Hesperidin content was 26.0-39.9 mg per 1 g of dried material.

Taxon
Citrus reticulataCitrus reticulatat0
Outcome
hesperidin (hesperitin-7-rutinoside) with a contente0
Value
26.0-39.9 mg per 1 g of dried raw materiale0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“hesperidin (hesperitin-7-rutinoside) with a content of is 26.0-39.9 mg per 1 g of dried raw material”

✓ located verbatim in the source · abstract, characters 1185–1285 · show in text ↑
t0

“Citrus reticulata”

✓ located verbatim in the source · title, characters 38–55 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Naringin content ranged from 0 to 1.15 mg per 1 g.

Taxon
Citrus reticulataCitrus reticulatat0
Outcome
naringin (naringenin-7-neohesperidiside)e0
Direction
smallere0
Value
0 to 1.15 mg per 1 ge0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“naringin (naringenin-7-neohesperidiside) in significantly smaller quantities, from 0 to 1.15 mg per 1 g”

✓ located verbatim in the source · abstract, characters 1291–1394 · show in text ↑
t0

“Citrus reticulata”

✓ located verbatim in the source · title, characters 38–55 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Nobiletin content ranged from 0.03 to almost 11 mg/g in dried peel.

Taxon
Citrus reticulataCitrus reticulatat0
Organ / stage
dried peele0
Outcome
nobiletin (5,6,7,8,3′,4′-hexamethoxyflavone)e0
Value
0.03 to almost 11 mg/ge0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“nobiletin (5,6,7,8,3′,4′-hexamethoxyflavone) with a content from 0.03 to almost 11 mg/g in dried peel”

✓ located verbatim in the source · abstract, characters 1488–1589 · show in text ↑
t0

“Citrus reticulata”

✓ located verbatim in the source · title, characters 38–55 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Tangeretin content was 0.1-5.4 mg/g.

Taxon
Citrus reticulataCitrus reticulatat0
Outcome
tangeretin (5,6,7,8,4′-pentamethoxyflavone)e0
Direction
smallere0
Value
0.1-5.4 mg/ge0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“tangeretin (5,6,7,8,4′-pentamethoxyflavone), found in slightly smaller quantities, 0.1-5.4 mg/g”

✓ located verbatim in the source · abstract, characters 1594–1689 · show in text ↑
t0

“Citrus reticulata”

✓ located verbatim in the source · title, characters 38–55 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Nobiletin and tangeretin accumulated mostly in small tangerine skins.

Taxon
tangerinesCitrus reticulatae0
Organ / stage
skins of small tangerinese0
Outcome
nobiletin and tangeretine0
Direction
mostly accumulatede0

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Citrus reticulata
Citrus reticulata · TaxonJoe Ravi · CC BY-SA 3.0 · Wikimedia Commons ↗

Verbatim

e0

“nobiletin and tangeretin were mostly accumulated in the skins of small tangerines”

✓ located verbatim in the source · abstract, characters 1715–1796 · show in text ↑