2.3 Antibacterial Activity of
V. unguiculata (L.) Walp Leaves
The concentration of methanolic extract of V.
unguiculata (L.) Walp leaves was varied to be 5, 15
and 25 wt.% in DMSO. Mueller Hinton Agar
(MHA) medium was poured into petri dish in the
temperature of 45-50
o
C and the bacterium
suspension was spread in the medium. The
antibacterial was determined using dish paper
method. The incubation of treated medium was kept
at 35
o
C for 18-24 h. S. aureus and E. coli were
chosen as tested bacterial.
2.4 Antioxidant Activity of
V. unguiculata (L.) Walp Leaves
The antioxidant activity of methanolic extract of V.
unguiculata (L.) Walp leaves was determined using
spectrophotometer UV-Vis as an impact of colour
changed due to the reaction between of DPPH and
the extract. w milligram of DPPH was dissolved in
methanol until its volume 450 mL with the final
concentration of DPPH was 50 µM. The
concentration was varied to be 5, 10, 15 dan 20 ppm.
One millilitre of DPPH 50 µM was mixed with
2 mL of methanolic extract of methanolic extract of
V. unguiculata (L.) Walp leaves. The mixture was
homogenized, and it was left dark condition for 30
minutes. The absorbance of extract was measured at
516 nm. The inhibition percentage was determined
from the equation below:
%
100% (1)
3 RESULT AND DISCUSSION
3.1 Antibacterial Activity
The antibacterial properties of methanolic extract of
V. unguiculata (L.) Walp leaves was evaluated
against S. aureus and E. coli. The diameter of
inhibition zone was appeared as a clear zone around
the paper dish that used in antibacterial evaluation.
The inhibition zone result was showed in Table 1.
Table 1: The antibacterial activity of methanolic extract
of V. unguiculata (L.) Walp leaves
No Concentration (%)
Diameter of
inhibition zone (mm)
S. aureus E. coli
1 5 14 -
2 15 15,5 -
3 25 15 -
Based on that result, the methanolic extract of
methanolic extract of V. unguiculata (L.) Walp
leaves has a moderate potency to inhibit S. aureus
but diameter of inhibition was not found in E. coli.
The moderate potency of the extract had an
inhibition zone diameter was 15.5 mm.
The different result between the both bacterial
can be caused there was no active compound that
can be found presence of active compound that can
inhibit E. coli. Also, this assumption can be caused
by the different of cell walls structure in the Gram
and Positive negative. Bacterium Gram positive has
single laye with low lipid content (1-4%) and the
Gram negative bacterium has higher lipid content
(11-12%) and the outer membrane has three
component that constructed by liposaccharide,
lipoprotein, and phospholipid (Fardiaz, 1992).
3.2 Antioxidant Activity
The antioxidant activity determination of methanolic
extract of V. unguiculata (L.) Walp leaves was
carried out using DPPH method and the absorbance
was measured using spectrophotometer UV-VIS at
516 nm of wavelength. The following result in Table
2 was the absorbance of methanolic extract at
various concentration.
Table 2: Absorbance of methanolic extract of V.
unguiculata (L.) Walp leaves
No Concentration (ppm) Absorbance
1 Blank 0,963
2 5 0,864
3 10 0,843
4 15 0,832
5 20 0,810
The radical scavenging activity of this
methanolic extract were determined as %inhibition.
Minami et al (1998) The %inhibition of antioxidant
was categorized according to IC50 value. The
antioxidant molecules were categorized as very
strong antioxidant activity when the IC50 ≤ 10,
strong antioxidant activity when the IC50 between
10 and 100, and the poor antioxidant activity when