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Prosiding Seminar Nasional Kimia Unesa 2012 – ISBN : 978-979-028-550-7

Surabaya, 25 Pebruari 2012

Curcuminoid Contents, Antioxidant and Anti-Inflammatory Activities of


Curcuma xanthorrhiza RoxB. and Curcuma domestica Val. Promising Lines
From Sukabumi of Indonesia

Waras Nurcholis1, 2), Laksmi Ambarsari1, 2), Ni Luh Putu Eka Kartika Sari2,
Latifah K Darusman1, 3)
1)
Biopharmaca Research Center, Bogor Agricultural University, Indonesia
2)
Department of Biochemistry, Bogor Agricultural University, Indonesia
3)
Department of Chemistry, Bogor Agricultural University, Indonesia

E-mail: wnurcholis@gmail.com or bfarmaka@gmail.com

ABSTRACT
The main bioactive substances in the rhizomes of Curcuma xanthorrhiza and
Curcuma domestica that have eficacy as antioxidant and anti-inflamatory
activities are curcuminoids. In this study, ethanol extracts of C. xanthorrhiza and
C. domestica promising lines from Sukabumi of Indonesia were investigated for
the presence of curcuminoids, antioxidant and anti-inflamatory activities. HPLC
method was used to determined curcuminoids content. The antioxidant (radical
scavenging) potential of the samples was evaluated using 2,2-diphenyl-1-
picrylhydrazyl (DPPH) free radical method. While for the anti-inflamatory
activity, the in vitro cyclooxygenase 2 (COX2) inhibition method was used. The
curcuminoid content of C. xanthorrhiza and C. domestica were 31.27 and 66.32
mg/ g, respectively. IC50 values for DPPH radical scavenging activity were 81.99
and 73.31 µg/ mL, with C. domestica having lowest value and most potent than C.
xanthorrhiza. Percent inhibition values for COX2 inhibitor activity were 74.84
and 67.96 %, with C. domestica having the highest value. In this study, the
ethanol extracts of C. domestica promosing line from Sukabumi of Indonesia
exhibited most in curcuminoids content, antioxidants properties and anti-
inflamatory activity than C. xanthorrhiza promosing line.

Keywords: Curcuminoid, Antioxidant, Anti-Inflamatory, Curcuma xanthorrhiza,


Curcuma domestica, Promosing line

INTRODUCTION diarrhea, dysentery, children’s


Curcuma xanthorrhiza Roxb., fevers, hemorrhoids, and skin
eruptions (Hwang et al., 2000).
also know as “temulawak” in
Indonesia, and Curcuma domestica Pharmacologically is has been
Val., known in Indonesia as reported that C. xanthorrhiza has the
antimicrobial (Hwang et al., 2000),
“kunyit”, are a medicinal plant from
the family Zingeberaceae distributed anti-metastatic (Choi et al., 2004),
anti-cancer (Huang et al., 1998), anti-
in Indonesia. Traditionally, C.
xanthorrhiza rhizomes have been candidal (Rukayadi et al., 2006),
anti-oxidant (Masuda et al., 1992)
used to treat stomach diseases, liver
disorders, constipation, bloody and hypolipidemic activities (Yasni
et al., 1993). The rhizomes of C.

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Prosiding Seminar Nasional Kimia Unesa 2012 – ISBN : 978-979-028-550-7
Surabaya, 25 Pebruari 2012

domestica are commonly used as a MATERIALS AND METHODS


flavoring, coloring agent and
Materials
preservative (Thaikert &
Paisooksantivatana, 2009). The The rhizomes of C.
traditional Indian medicine claims xanthorrhiza and C. domestica
the use of C. domestica powder promising lines were collected
against biliary disorders, anorexia, during July 2011 from the area of
coryza, cough, diabetic wounds, Sukabumi, West Java, Indonesia.
hepatic disorder, rheumatism and The authentic chemical standards of
sinusitis (Ammon et al., 1992). curcuminoid (curcumin,
Pharmacolological research has demethoxycurcumin, and
demonstrated that C. domestica bisdemethoxycurcumin) and 2,2-
possesses anti-inflammatory diphenyl-1-picrylhydrazyl were
(Mukophadhyay et al. 1982; Arora et obtained from Sigma-Aldrich, USA.
al., 1971; Chandra and Gupta, 1972), The bioassay kit COX was purchased
antioxidant (Unnikrishnan and Rao, from Cayman Chemicals. All the
1995; Pulla Reddy & Lokesh, 1992), chemicals and solvents used were
anti-protozoal (Rasmussen et al., analytical grade.
2000), nematocidal (Kiuchi et al.,
1993), anti-bacterial (Chopra et al.,
1941; Bhavani Shankar & Murthy, Extraction of plans
1979), antivenom (Ferreira et al., Fresh rhizomes of plant
1992), anti-HIV (Mazumber et al., materials were washed with water,
1995; Eigner and Scholz 1999), and cut into small pieces and dried for 5
anti-tumor activities (Huang et al., days in the sun (the moisture: <
1988). 10%). They were then ground in a
The main yellow bioactive grinder to be obtained in a powder
substances in the rhizomes of C. form (the size: 100 mesh). One kilo
xanthorrhiza and C. domestica are grams of the powder of plants were
curcuminoid (Duke, 2002; Chainani- macerated using 1 x 10 L ethanol
Wu, 2003). The pharmacological 70% in a tightly closed round bottom
effect of curcuminoids has been flask at room temperature for a
investigated, such as radical period of 24 h and filtered with
scavenging (Sreejayan & Rao, 1996), Whatman filter paper (type 4). The
the inhibition of nitric oxide (NO) whole process was repeated one
(Pan et al., 2000; Onoda et al., 2000), times and the filtrate was
anti-inflammation (Banerjee et al., concentrated under reduced pressure
2003), anti-tumor (Khar et al., 1999), on rotavapor (BUCHI, R-250,
anti-allergy (Ram et al., 2003) and Switzerland) at 50 °C temperature.
anti-dementia (Lim et al., 2001). This The concentrated extracts were then
study was undertaken to verify the used for the experiments.
variation C. xanthorrhiza and C.
domestica promising lines from
Sukabumi of Indonesia for their total Determination of curcuminoid
curcuminoid, antioxidant and anti- content
inflamatory activities. The curcuminoid content of
ethanol extract of C. xanthorrhiza
and C. domestica promising lines

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Prosiding Seminar Nasional Kimia Unesa 2012 – ISBN : 978-979-028-550-7
Surabaya, 25 Pebruari 2012

from Sukabumi was carried out (Ac − Acb) − (As − Asb)


according to the principle and = x 100
(Ac − Acb)
protocol previously described by
Jayaprakasha et al., (2002) using where Ac is the absorbance of
high performance liquid water plus DPPH (in ethanol), Acb is
chromatography (HPLC), with the absorbance of the blank (water
modification. The systems condition plus ethanol without DPPH), As is
of HPLC are C18 column, UV-Vis the absorbance of the sample plus
detector, 10 µL volum injection, and DPPH (in ethanol) and Asb is the
48 °C temperature column. It’s used absorbance of the sample plus
methanol as an additional mobile ethanol without DPPH. Different
phase, , which included solvents A: sample concentrations were used in
methanol; B: 2% acetic acid; and C: order to obtain calibration curves and
acetonitrile. to calculate the IC50 values (IC50:
concentration required to obtain a
50% radical scavenging activity). All
Antioxidant activity through test samples were conducted in
measurement of free radical triplicate (n = 3).
scavenging capacity by DPPH
assay
Determination of anti-
Free radical scavenging inflammatory activity
capacity was investigated on the
basis of the scavenging activity of The ethanol extracts of C.
DPPH by measuring the reduction of xanthorrhiza and C. domestica
absorbance at 517 nm. The method promising lines from Sukabumi was
was carried out as described by evaluated as anti-inflammatory with
Udenigwe et al., (2009) with a cyclooxygenase 2 (COX2) inhibitory
modification. The different activities. COX2 inhibition activity
concentrations of the plant extracts was measured using the Cayman
(12.5–200 µg/ml; total volume of 40 Chemical Colorimetric COX (ovine)
µL) in 96-well plates were mixed Inhibitor Screening Assay Kit. All
with 160 µL of 100 mM DPPH in procedures were performed as
ethanol and then incubated in the indicated in the assay kit instructions.
dark for 30 min at room temperature The ethanol extracts were dissolved
prior to reading the absorbance at in DMSO and added to the enzyme
517 nm in a micro plate reader. A reaction mixture.
negative control, containing water
instead of the sample and blank
RESULTS AND DISCUSSION
samples, using the same volume of
ethanol only in place of the DPPH Curcuminoids content
solution in ethanol, were all Curcuminoids compound are
evaluated at the same time per micro commonly in Curcuma species and
titre plate. have been reported to have several
The percentage of radical biological activities including
scavenging was calculated as antioxidant and anti-inflammatory
follows; properties (Itokawa et al., 2008). The
results of curcuminoids content on
% radical scavenging

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Prosiding Seminar Nasional Kimia Unesa 2012 – ISBN : 978-979-028-550-7
Surabaya, 25 Pebruari 2012

the ethanol extract of C. xanthorrhiza different successive extracts of C.


and C. domestica promising lines xanthorrhiza and C. domestica. This
from Sukabumi are shown in Figure activity was increased by increasing
1A. The curcuminoids content of C. the concentration of sample extracts.
domestica (value, 66.32 mg/ g) most DPPH antioxidant assay is based on
highest than C. xanthorrhiza with the ability of DPPH, a stable free
value 31.27 mg/ g. The rhizomes of radical, to decolorize in the presence
C. xanthorrhiza and C. domestica of antioxidants. The DPPH radical
show different profiles in the three contains an odd electron, which is
major curcuminoids. The responsible for the absorbance at 517
curcuminoids in C. domestica are nm and also for a visible deep purple
mainly curcumin, demethoxy- color. When DPPH accepts an
curcumin, and bisdemethoxy- electron donated by an antioxidant
curcumin (Figure 1B) (Lechtenberg compound, the DPPH is decolorized,
et al., 2004; Thaikert & which can be quantitatively
Paisooksantivatana, 2009). While for measured from the changes in
the curcuminoids in C. xanthorrhiza absorbance. Thus, the DPPH radicals
are curcumin and demethoxy- were widely used to investigate the
curcumin (Figure 1C) (Lechtenberg scavenging activity of some natural
et al., 2004). compounds. DPPH is widely used to
evaluate the antioxidant activity of
natural compounds (Udenigwe et al.,
Antioxidant activity 2009). However, DPPH’s scavenging
The measures of antioxidant activity indicates the ability of the
activity were obtained using DPPH antioxidant compound to donate
(2,2-diphenyl-1-picrylhydrazyl) electrons or hydrogen, thereby
method. Figure 2 shows the DPPH converting the radical to a more
radical scavenging activity of the stable species (Bougatef et al., 2009).

A
C
70.
Curcumin
Curcuminoids content (mg/ g)

60.

50. B
66.32
40.

30.

20. 31.27
Demethoxycurcumin
10.

0.
Curcuma xanthorrhiza Curcuma domestica
Promising lines from Sukabumi
Bisdemethoxycurcumin

Figure 1. (A). Curcuminoids content of C. xanthorrhiza and C. domestica


promising lines from Sukabumi, West Java, Indonesia. (B). the curcuminoids
component of C. domestica: curcumin, demethoxycurcumin, and
bisdemethoxycurcumin. (C). the curcuminoids component of C. xanthorrhiza:
curcumin and demethoxycurcumin.

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Prosiding Seminar Nasional Kimia Unesa 2012 – ISBN : 978-979-028-550-7
Surabaya, 25 Pebruari 2012

0.8

Absorbance measured at 517 nm


0.7 C. xanthorrhiza
0.6 C. domestica
0.5

0.4

0.3

0.2

0.1

0.0
12.5 25 50 100 200
Concentration (µg/ mL)

Figure 2. Scavenging effect of C. xanthorrhiza and C. domestica promising lines


from Sukabumi, West Java, Indonesia on DPPH (2,2-diphenyl-1-picrylhydrazyl),
as measured by changes in absorbance at 517 nm.

Antioxidant activity using The results showed that the ethanol


DPPH radical scavenging assay extracts of C. xanthorrhiza and C.
reported with IC50 value is show in domestica have highest of
Figure 3. The lower the IC50 is the antioxidant activity (with IC50 value
higher the antioxidant activity of the < 200 µg/ mL, Blois, 1958). IC50
Curcuma promising lines. values for DPPH radical scavenging
activity were 81.99 and 73.31 µg/
mL, with C. domestica having lowest
90.00 81.99 value and most potent than C.
Antioxidant activity, IC50 value (µg/mL)

73.31
80.00 xanthorrhiza. Curcuminoids
compound are the major C.
70.00
xanthorrhiza and C. domestica
60.00 compounds with antioxidant activity
50.00 (Jayaprakasha et al., 2006; Masuda et
al., 1992). This study, we used
40.00
ethanol crude extract of C.
30.00 xanthorrhiza and C. domestica, so
20.00 it’s possible has pure compound
most stronger as DPPH free radical
10.00 scavenging activity than that
0.00 extracts.
C. domestica C. xanthorrhiza
Promising lines from Sukabumi
Anti-inflammatory activity
Figure 3. DPPH free radical Anti-inflammatory activity of C.
scavenging activity of C. xanthorrhiza and C. domestica
xanthorrhiza and C. domestica promising lines from Sukabumi was
promising lines from Sukabumi, evaluated through the percentages of
West Java, Indonesia.

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cyclooxygenase 2 (COX2) inhibition. curcuminoids content compared to


Results are given in Figure 4. Percent Curcuma xanthorrhiza, whic are also
inhibition values for COX2 inhibitor known to have antioxidant and anti-
activity of C. domestica and C. inflammatory activities.
xanthorrhiza were 74.84 and 67.96
%, with C. domestica having the
highest value. Curcuminoids ACKNOWLEDGEMENTS
compound are the major C. We express our gratitude to Dr.
xanthorrhiza and C. domestica Min Rahminiwati, dr. Lina Sulimin,
compounds with anti-inflammatory and Dr. Eka Intan Kumala Putri for
properties (Chainani-Wu, 2003; excellence technical support. This
Tohda et al., 2006; Ozaki, 1990). research was supported by grants
This study, we used ethanol crude from the Directorate General of
extract of C. xanthorrhiza and C. Higher Education, Ministry of
domestica, so it’s possible has pure Education and Culture Republic of
compound most stronger as anti- Indonesia (Hibah Kompetitif
inflammatory activity than that Penelitian Strategis Unggulan
extracts. Nasional Nomor: 476/SP2H/PL/
Dit.Litabmas/V/2011).

76 74.84
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