TY - JOUR
T1 - The effects of different extraction solvents of varying polarities on polyphenols of Orthosiphon stamineus and evaluation of the free radical-scavenging activity
AU - Akowuah, G. A.
AU - Ismail, Z.
AU - Norhayati, I.
AU - Sadikun, A.
N1 - Funding Information:
This study was supported by Intensifying Research Priority Areas (IRPA) Grant from the Ministry of Science, Technology, and Environment, Malaysia.
PY - 2005/11
Y1 - 2005/11
N2 - Leaf powder of Orthosiphon stamineus was extracted with the following solvents; distilled water, 50% aqueous methanol, methanol, 70% aqueous acetone and chloroform, at 2, 4 and 8 h, respectively, on a water bath at 40°C. The extracts were subjected to qualitative and quantitative HPLC analyses of the polyphenols, the most dominant chemical constituents in the leaf. Chloroform extraction from 4 to 8 h at 40°C gave the highest amount of sinensetin and eupatorin. The extraction with 70% aqueous acetone extracts at 4 and 8 h gave a high yield of 3′-hydroxy-5,6,7,4′-tetramethoxyflavone. The yield of rosmarinic acid was high in 50% methanol extracts at 2, 4 and 8 h of extraction. The extracts were screened for free radical-scavenging potential, using a 1,1-diphenyl-2-picrylhydrazyl in vitro model system. The extracts exhibited significant radical-scavenging activity and the acetone extracts showed the highest activity.
AB - Leaf powder of Orthosiphon stamineus was extracted with the following solvents; distilled water, 50% aqueous methanol, methanol, 70% aqueous acetone and chloroform, at 2, 4 and 8 h, respectively, on a water bath at 40°C. The extracts were subjected to qualitative and quantitative HPLC analyses of the polyphenols, the most dominant chemical constituents in the leaf. Chloroform extraction from 4 to 8 h at 40°C gave the highest amount of sinensetin and eupatorin. The extraction with 70% aqueous acetone extracts at 4 and 8 h gave a high yield of 3′-hydroxy-5,6,7,4′-tetramethoxyflavone. The yield of rosmarinic acid was high in 50% methanol extracts at 2, 4 and 8 h of extraction. The extracts were screened for free radical-scavenging potential, using a 1,1-diphenyl-2-picrylhydrazyl in vitro model system. The extracts exhibited significant radical-scavenging activity and the acetone extracts showed the highest activity.
KW - HPLC
KW - Lipophilic flavones
KW - Orthosiphon stamineus
KW - Rosmarinic acid
UR - http://www.scopus.com/inward/record.url?scp=19444385005&partnerID=8YFLogxK
U2 - 10.1016/j.foodchem.2004.09.028
DO - 10.1016/j.foodchem.2004.09.028
M3 - Article
AN - SCOPUS:19444385005
SN - 0308-8146
VL - 93
SP - 311
EP - 317
JO - Food Chemistry
JF - Food Chemistry
IS - 2
ER -