ISOLASI SENYAWA PENGHAMBAT ENZIM TIROSINASE DARI KULIT BATANG KAYU MANIS (CINNAMOMUM BURMANNII (NEES & T. NEES) BLUME)
Hyperpigmentation is an increase in melanin production triggered by the tyrosinase enzyme as a catalyst for melanin formation. Previous studies showed that the phenolic compounds and essential oil content in cinnamon have tyrosinase inhibitory activity. This study aimed to determine the potential...
Saved in:
| Main Author: | |
|---|---|
| Format: | Final Project |
| Language: | Indonesia |
| Online Access: | https://digilib.itb.ac.id/gdl/view/66093 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Institution: | Institut Teknologi Bandung |
| Language: | Indonesia |
| Summary: | Hyperpigmentation is an increase in melanin production triggered by the tyrosinase enzyme as a catalyst
for melanin formation. Previous studies showed that the phenolic compounds and essential oil content in
cinnamon have tyrosinase inhibitory activity. This study aimed to determine the potential of ethanol extract
and cinnamon bark fraction (Cinnamomum burmannii (Nees & T. Nees) Blume) as inhibitors of the
tyrosinase enzyme and isolate the active compound. Simplicia powder was extracted by the maceration
method using 96% ethanol as solvent and monitored by thin-layer chromatography. Fractionation was
carried out by liquid-liquid extraction method using n-hexane, ethyl acetate, and ethanol-water as solvents.
Quantitative activity tests on extracts and fractions were carried out. The absorbance data processed into
the value of % inhibition at each concentration and IC50 was determined by linear regression between logs
concentration and % inhibition. The IC50 values of extract samples, n-hexane fraction, ethyl acetate fraction,
and water-ethanol fraction were 9.442,41 ± 61,37 ; 728,95 ± 27,09; 1.173, 42 ± 45,15; and >10.000 µg/mL.
Using bioautography thin layer chromatography method, white spots on a gray background indicated
enzyme inhibitory activity. Subfractionation was carried out by classical column chromatography, and
selected subfractions were purified using the preparative thin layer chromatography method. The purity
test was carried out using single expansion thin layer chromatography with three mobile phases and twodimensional thin layer chromatography. The purity test results obtained isolates W, isolates X, isolates Y,
and isolates Z. The isolates were then characterized using spesific spray reagent. The ethanolic extract of
cinnamon bark contains compounds with phenol, flavonoid, coumarin, and triterpenoid groups. The nhexane fraction gave more potent inhibitory activity to the tyrosinase enzyme than the ethanol extract,
ethyl acetate fraction, and ethanol-air fraction. From the n- hexane-fraction, isolates W, X, Y, and Z were
obtained, the result showed triterpenoid group compounds presence and qualitative inhibitory activity of
the tyrosinase enzyme.
|
|---|