AKTIVITAS ANTIOKSIDAN, TOTAL FENOL, TOTAL FLAVONOID, TOTAL KAROTENOID DARI BERBAGAI EKSTRAK BUAH PARIA (MOMORDICA CHARANTIA L.) DAN ISOLASI SENYAWA ANTIOKSIDAN
Recently various degenerative diseases in people due to the oxidative damage in body’s cells which attacked by free radicals. Antioxidants are compound that can inhibit negative impact of free radicals in body. Antioxidant can inhibit the oxidation reaction by binding to free radicals. Bitter gou...
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Format: | Final Project |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/45488 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Recently various degenerative diseases in people due to the oxidative damage in body’s
cells which attacked by free radicals. Antioxidants are compound that can inhibit negative
impact of free radicals in body. Antioxidant can inhibit the oxidation reaction by binding to
free radicals. Bitter gourd (Momordica charantia L.) is a plant that can grow well in
Indonesia and is believed to have many benefits. Based on several studies, bitter gourd
fruit was known to have the effect of antioxidant. In addition, bitter gourd fruit have been
used by people for treating various diseases. This research aimed to determine IC50 DPPH
scavenging activity; determine total phenolic, total flavonoid, and total carotenoid of each
extracts; analyze correlation of total phenolic, total flavonoid, and total carotenoid with
IC50 DPPH scavenging activity; and isolation antioxidant compound of bitter gourd fruit
extract. Crude drug of bitter gourd fruit was extracted by reflux apparatus using three
solvents with increasing polarity, n-hexane, ethyl acetate and ethanol. Each extract was
monitored by TLC. IC50 DPPH scavenging activity, total phenolic, total flavonoid, and
total carotenoid of each extract was determined by ultraviolet-visible spectrophotometry
and their correlation with IC50 DPPH scavenging activity by Pearson’s method. Ethyl
acetate fruit extract was fractionated by vacuum liquid chromatography. Fraction 4 was
subfractionated by column chromatography. Subfraction 28 was purified by washing and
recrystallization method. Purity test was performed by TLC. Characterization of isolate
was performed by using specific spray reagent, ultraviolet-visible spectrophotometry, two
dimentional paper chromatography, and infrared spectrophotometry. Fruit crude drug of
bitter gourd (Momordica charantia L.) contained alkaloid, flavonoid, phenolic, terpenoid,
steroid/triterpenoid groups. Ethanol fruit extract of bitter gourd (density of its 1 % extract
0.75 g/mL) showed the highest antioxidant activities with the lowest value of IC50 DPPH
scavenging activity (1.01 µg/mL). The highest total phenolic content, total flavonoid
content, and total carotenoid content values were given by ethanol fruit extract (1.66 g
GAE/100 g), ethyl acetate fruit extract (3.41 g QE/100 g), and n-hexane fruit extract (0.88
g BE/100 g), respectively. An antioxidant compound H was obtained from ethyl acetate
fruit extract. Ethyl acetate and ethanol of bitter gourd fruit extracts were very strong
antioxidant. Total phenolic content of bitter gourd fruit extracts showed negative and high
correlation with IC50 DPPH scavenging activity (p<0.01). Phenolic compounds were the
major contributor in bitter gourd fruit extract using DPPH assay. Antioxidant compound H
was flavonol aglycone that had free -OH group in C-3 and expected had free -OH in ring A
and or ring B.
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