EFFECT OF ETHANOL EXTRACT OF BAECKEA FRUTESCENSL. LEAVES AND OCIMUM BASILICUM SEEDS ON MELANOGENESIS OF B16F10 MELANOMA CELLS AND HYPERPIGMENTATION-INDUCED GUINEA PIGS
Hyperpigmentation is the darkening area of skin caused by increasing melanin expression that can be caused by excessive exposure to the UV radiation. The UV radiation can increase tyrosinase production which plays an important role in melanin synthesis. Jungrahab (B. frutescens) leaves and basil...
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Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/52931 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Hyperpigmentation is the darkening area of skin caused by increasing melanin
expression that can be caused by excessive exposure to the UV radiation. The UV
radiation can increase tyrosinase production which plays an important role in
melanin synthesis. Jungrahab (B. frutescens) leaves and basil (O. basilicum) seeds
are two plants part that have potential to inhibit tyrosinase activity so that melanin
synthesis will be reduced. This research’s aim is to study the
antihyperpigmentation effect of the ethanol extract of jungrahab leaves and basil
seeds. Other objective of this research is to develop hyperpigmentation animal
model. The active compounds in basil seeds and jungrahab leaves were extracted
in 95% ethanol by maceration method. The effect of the extracts on
melanogenesis was tested on B16F10 melanoma cells and the expression of the
proteins involved in melanogenesis were determined using Western Blot analysis.
Hyperpigmentation was induced on the backs of brownish guinea pigs by daily
UVB radiation for 12 days, the UVB intensity was 3.6 mW/cm
2
. Jungrahab leaves
and basil seeds extracts and arbutin as a standard were formulated into cream
dosage form. Those creams were applied topically on hyperpigmented area for 14
days. The skin melanin level of each site of application was determined using
Mexameter. The four creams stabilty were evaluated through organoleptic, pH,
and viscosity examination. Its safety were evaluated through skin and eye
irritation test in rabbit. Results showed that the ethanol extracts of jungrahab
leaves and basil seeds could inhibit melanogenesis with percentage of inhibition
increased by the increase of extracts’s concentration. The extracts also reduced
the expression of Tyr, TRP-1, and TRP-2 proteins involved in melanogenesis. The
hyperpigmentation animal model was developed in this research showed by the
significantly (p<0.05) increased of melanin levels after 12 days of UVB radiation.
The creams containing 5 and 10 % of ethanol extracts of jungrahab leaves or basil
seeds significantly (p<0.05) decreased skin melanin content after 14 days of
application. During 28 days of storage the extracts creams showed stable pH and
good organoleptic profile. All three extract creams also showed stable viscosity
for 28 days of storage, but test the cream containing 10% of jungrahab showed
decreased viscosity. Those creams showed slight irritation potency indicated by
its primary cutaneous index irritation <0.5; on eye irritation test the cream
containing 10% of jungrahab has irritation effect on rabbit’s eye.
Hyperpigmentation animal model can be induced on brownish guinea pig using
UVB radiation (3.6 mW/cm
2
for 10 minutes). The ethanol extracts of jungrahab
iv
leaves and basil seeds are potential to inhibit melanin synthesis and had effect in
reducing hyperpigmentation at a minimum concentration of 5%.
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