IMPROVEMENT ACTIVITY OF ANTIOXIDANT, TYROSINASE INHIBITION, AND ANTI-INFLAMMATORY OF PHALERIA MACROCARPA (SCHEFF.) BOERL) SEED EXTRACTS IN NANOEMULSION DOSAGE FORM: IN VITRO & IN VIVO STUDIES
Mahkota Dewa seed (Phaleria macrocarpa) has various phytochemical compounds and low pharmacological activities including antioxidants, tyrosinase enzyme inhibition, and antiinflammatory. The production of nanoemulsion preparations is expected to improve the activity of the extract of mahkota dewa...
Saved in:
Main Author: | |
---|---|
Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/61928 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Mahkota Dewa seed (Phaleria macrocarpa) has various phytochemical compounds and low
pharmacological activities including antioxidants, tyrosinase enzyme inhibition, and antiinflammatory. The production of nanoemulsion preparations is expected to improve the activity of the
extract of mahkota dewa seed with ethyl acetate. This study aims to test the mahkota dewa seed
nanoemulsion (NE-BMD) against antioxidant activity using the DPPH method, tyrosinase inhibition,
and anti-inflammatory using the protein denaturation method with BSA (Bovine Serum Albumin) in
vitro. This research is followed by in vivo testing using Wistar white male rats induced by 1%
carrageenan for anti-inflammatory activity in selected samples of NE-BMD. The preparation of the
NE-BMD was accomplished using the sonication method and followed by selecting two formulation.
The formulation contains 3% extract, 1% oleic acid, 12% Cremophor® RH40, and 2% PEG 400. The
results of characterization and evaluation of NE-BMD preparations showed that the particle size and
polydispersity index were 26.83±1.27 nm (IP: 0.36±0.03) for the F7 formulation and 30.73±1.50 nm
(IP: 0.32±0.06) for the F8 formulation. The result of the TEM evaluation showed a spherical globule
morphology of the NE-BMD. The antioxidant activity test showed the IC50 value of the BMD extract
was 207.01±23.02 ?g/mL, and the NE-BMD F7 and F8 were 15.62±1.40 ?g/mL and 28.39±4.69
?g/mL, respectively. The testing of tyrosinase enzyme inhibitory activity showed the IC50 values of
BMD extract was 938.91±43.98 ?g/mL, NE-BMD preparations F7 and F8 were 587.17±25.36 ?g/mL
and 692.79±30.63 ?g/mL, respectively. The protein denaturation testing showed the IC50 values of
BMD extract was 401.46±1.01 ?g/mL and NE-BMD preparations F7 and F8 were 94.39±1.24 ?g/mL
and 196.63±1.61 ?g/mL. Meanwhile, in vivo anti-inflammatory testing with doses 1 g/kgBW for BMD
extract and NE-BMD F7 preparations showed that significantly (p<0.05) improved anti-inflammatory
activity compared to single extracts BMD, based on the value of percent protein denaturation inhibition
and in vivo test. The results showed that NE-BMD preparations improve several pharmacological
activities.
|
---|