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Isolation,characterization and antioxidant capacity assessment of the bioactive compounds derived from Hypoxis rooperi corm extract (African potato)
Authors:Olga Laporta  Laura Pérez-FonsRicardo Mallavia  Nuria CaturlaVicente Micol
Affiliation:Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Edificio Torregaitán, Avenida de la Universidad s/n, 03202-Elche, Alicante, Spain
Abstract:The rhizome of the plant Hypoxis rooperi (“African potato”) is known for its traditional and ethnomedical uses in the treatment of benign prostatic hyperplasia and other diseases. We have characterized an extract derived from H. rooperi, isolated its major bioactive compound, hypoxoside, and obtained its aglycone, rooperol, by enzymatic digestion. Absorption, fluorescence emission and bidimensional NMR complete spectral data of these compounds were obtained. The antioxidant capacity of both compounds was fully analyzed through the thiobarbituric acid reactive substances (TBARS) and Trolox equivalent antioxidant capacity (TEAC) assays, and it was compared to catechins and olive biophenolics. Both compounds showed a strong antioxidant capacity, although rooperol exhibited a higher antioxidant activity against lipid peroxidation which correlated to its strong affinity for phospholipid membranes as derived from its extremely high lipid/water partition coefficient (Kp = 3.4 × 104). The study of the lipophilic (EtOH) and hydrophilic (water) TEAC values revealed that more hydrophobic compounds, had greater lipophilic TEAC values than hydrophilic ones, probably indicating that lipophilic TEAC assay may be more reliable for these compounds. The H. rooperi extract also showed higher antioxidant efficacy compared to other strong antioxidant herbal extracts, such as olive leaf or green tea. Moreover, neither evidence of acute oral toxicity nor adverse effects were observed when the H. rooperi commercial extract containing 45% hypoxoside was used at a dosage of 2000 mg/kg. The results obtained in this work may contribute to understanding the biological activity described for these dicatechols and the African potato extract for food and cosmetic applications.
Keywords:AAPH  2  2&prime  -Azobis (2-methyl-propionamine) dihydrochloride  ABTS  2  2&prime  -azinobis (3-ethylbenzothiazoline-6-sulfonate)  AUC  area under the fluorescein decay curve  BHT  butylated hydroxytoluene (2  [6]-di-tert-butyl-p-cresol)  C  (+)-catechin  DMPC  1  2-dimyristoyl-sn-glycero-3-phosphocholine  EC  (&minus  )-epicatechin  ECG  (&minus  )-epicatechin gallate  EGCG  (&minus  )-epigallocatechin gallate  EYPC  egg yolk phosphatidylcholine  FL  disodium fluorescein (3  6-dihydroxy-spiro[isobenzofuran-1[3H]  9[9H]-xanthen]-3-one)  HPLC  high performance liquid chromatography  HSQC  heteronuclear single quantum coherence  LD50  lethal dose 50%  LUV  large unilamellar vesicles  MDA  malondialdehyde  MLV  multilamellar vesicles  NMR  nuclear magnetic resonance  ORAC  oxygen radical absorbance capacity  SUV  small unilamellar vesicles  TBARS  thiobarbituric acid reactive substances  TEAC  Trolox equivalent antioxidant capacity  TEP  1  1  3  3-tetraethoxypropane  UV&ndash  vis  ultraviolet&ndash  visible light
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