Patchouli (Pogostemon cablin Benth): Chemistry, Biology, and
Anti-inflammatory Activities: A Review
Khairan
1,2,3,4
, Syaifullah Muhammad
4,5
and Muhammad Diah
6
1
Departement of Pharmacy, Universitas Syiah Kuala, Banda Aceh, Indonesia
2
Pusat Riset Obat Herbal, Universitas Syiah Kuala, Banda Aceh, Indonesia
3
Pusat Riset Etnoscience, Universitas Syiah Kuala, Banda Aceh, Indonesia
4
PUI-Nilam Aceh-Atsiri Research Centre, Universitas Syiah Kuala, Banda Aceh, Indonesia
5
Department of Chemical Engineering, Universitas Syiah Kuala, Banda Aceh, Indonesia
6
Division of Cardiology, Department of Internal Medicine, Dr. Zainoel Abidin Hospital, Faculty of Medicine,
Universitas Syiah Kuala, Banda Aceh, Indonesia
Keywords: Pogostemon cablin Benth, Phytochemicals, Biology Activities, Anti-Inflammatory Activity.
Abstract: Patchouli (Pogostemon cablin Benth) is an essential oil and an aromatic medicinal plant, industrially valued
due to widely used in flavours, fragrance and pharmaceuticals. Recently, researchers are showing deep interest
towards patchouli alcohol. In Indonesia, patchouli is commonly known as ‘nilam’ which stand for Nederlands
Indische Land ook Acheh Maatscappij. Understanding the chemistry, biology, and anti-inflammatory
activities allows its utilization in medicine, toiletries, perfumery and insecticides. This review provides a
comprehensive information on chemical compositions of patchouli species and its extracts by gas
chromatography-mass spectroscopy (GC-MS) and gas chromatography-flame ionization detection (GC-FID).
The biological activities of patchouli towards microorganisms is also being reviewed. This review also
provides an additional information on anti-inflammatory activities of Pogostemon cablin Benth.
1 INTRODUCTION
Nowadays, the natural product from plants are widely
used as herbal medicines and health therapy to treat
various diseases. Some products including essential
oils, dyes, cosmetics, and drugs also derived from
natural products. Currently, several medicinal and
aromatic plants are widely cultivated by farmers and
industrial agricultural both large and small scale to
obtain plants metabolites that are indispensable for
industrial needs (Lubbe and Verpoorte, 2011). The
aromatic plants are capable to produce some
essentials oils that are useful for several therapeutics
such as pharmaceutical, perfume and food industries.
For example, perfumes, cosmetics, and other health
products used 90% of essential oils sourced from
plants.
In Indonesia, patchouli oil (Pogostemon cablin
Benth) is commonly known as ‘NILAM’ which stand
for Nederlands Indische Land ook Acheh
Maatscappij. P. cablin is an herbaceous plant, spread
in Southeast Asia, especially Vietnam, Malaysia,
Thailand, and Indonesia. P. cablin mainly contains of
patchouli alcohol, this compound is functioned as
long-lasting aroma or as fixative in perfumes
industries. This compound commonly used as
indicator to determine the quality of essential oils
from patchouli (Anonis, 2006). Patchouli alcohol,
commonly used in the perfume manufacturing
industry and some products such as soap, detergents,
body lotions, and cosmetics (Swamy and Sinniah,
2015), deodorants, and insecticides (Hasegawa et al.,
1992).
P. cablin is also known contain several
metabolites such as sesquiterpenes, hydrocarbons,
patchoulol, patchoulene, bulnesene, guaiene,
caryophyllene, elemene, and copaene. P. cablin also
contains others bioactive compounds such as
flavonoids and glycosides (Hasegawa et al., 1992). In
addition, patchouli oil is also widely used as
aromatherapy to increase sexual arousal
(aphrodisiac), to mitigate depression, and anxiety to
calm nerves. Several studies reported that patchouli
oil are potentials used for treatments of antimicrobial,
analgesic, antioxidant, antiplatelet, aphrodisiac,
antithrombotic, antidepressant, antimutagenic,
Khairan, ., Muhammad, S. and Diah, M.
Patchouli (Pogostemon cablin Benth): Chemistry, Biology, and Anti-inflammatory Activities: A Review.
DOI: 10.5220/0009956600670073
In Proceedings of the 2nd International Conference of Essential Oils (ICEO 2019), pages 67-73
ISBN: 978-989-758-456-5
Copyright
c
2020 by SCITEPRESS – Science and Technology Publications, Lda. All rights reserved
67
fibronolytic, antiemetic, and cytotoxic activity
(Swamy and Sinniah, 2015; Chakrapani et al., 2013;
Priya et al., 2014). In this review, we described some
chemicals compounds containing in P. cablin and the
biological activities on some bacteria, fungi and
others microorganisms. In this review, the anti-
inflammatory activities of P. cablin also
communicated.
2 CHEMICALS COMPOSITION
OF PATCHOULI OIL
(Pogostemon cablin benth)
Patchouli oil contains some secondary metabolites
and some volatile and in-volatile compounds. Some
of these compounds are described as shown below.
2.1 Phytochemicals
The phytochemicals screening results showed that P.
cablin contains several secondary metabolites
including monoterpenoids, triterpenoids,
sesquiterpenoids, phytosterols, flavonoids, organic
acids, lignins, glycosides, alcohols and aldehydes.
The main of phytochemicals from P. cablin were
patchouli alcohol, α-patchoulene, β-patchoulene, α-
bulnesene, seychellene, norpatchoulenol, pogostone,
eugenol and pogostol (Mallapa et al., 2016).
2.2 Volatile Chemical Composition of
Pogostemon cablin Benth
P. cablin generally contains volatile and non-volatile
compounds. The volatile compounds generally
derived from the leaves and stems such as
monoterpenes, sesquiterpenes, and alcohol. Ling
mentioned that P. cablin consisting of patchouli
alcohol (31.86%), seychellene (9.58%), α-guaiene
(8.82%), δ-guaiene (8.65%), δ-patchoulene (8.8%)
8.48%), ß-patchoulene (6.91%), and pogostone
(3.83%) (Ling et al., 1992). Zang also reported that
96% compounds containing in P. cablin were
generally in the form of volatile compounds (Zhnag
et al., 2003). Some volatile compounds such as
geranium ketone, 7-patchoulene, α-patchoulene, α-
bulnesene, 5-cedrol and eucalyptus oil ketene. Zhou
also reported that the aerial part of P. cablin contains
four compounds derived from patchoulene namely
8α, 9α-dihydroxypatchoulol; 3α, 8α-
dihydroxypatchoulol; 6α-hydroxypatchoulol and 2ß,
12-dihydroxypatchoulol (Zhou et al., 2011). Zhou
also successfully identified four sesquiterpenoid
compounds from the aerial part of P. cablin such as
(5R) -5-hydroxypathoulol, (9R) -9-
hydroxypatchoulol, (8S) -8-hydroxypatoulol and
(3R) -3-hydroxypathoulol (Zhou et al., 2011). The
main structure of terpenoids contained in volatile oil
from P. cablin can be seen in Figure 1.
Figure 1: The main structure of terpenoids contained in
volatile oil from P. cablin.
2.3 Non-volatile Chemical Composition of
Pogostemon cablin Benth
Besides volatile compounds, P. cablin also contains
several non-volatile compounds. Guan reported that
two flavones compounds such as retusine (1) and
pachypodol (2) also available in P. cablin. Guan also
reported that ethanolic extracts from leaves and stems
of P. cablin contain four non-volatile compounds
(flavonoids glycosides) such as isorhamnetin-3-O-ß-
D-galactoside (3), hyperoside (4), 3,5,8,3',4'-
pentahydroxy-7-methoxyflavone-3-O-β-D-
galactoside (5) and isisolidone-7-O-α-L-
rhamnopyranoside (6). Some researchers also
reported several other types of flavone compounds
such as 3α-hydroxypatchoulane-3-O-β-D-
glucopyranoside (7), 15-hydroxypatchoulol 15-O-β-
D-glucopyranoside (8) (Ding et al. (2009) Friedelin
(9), epifriedelinol (10), oleanolic acid (11), ß-
sitosterol (12), eugenol (13), cinnamaldehyde (14),
benzaldehyde (15), patchoulipyridine (16),
epiguaipyridine (17), and daucosterin (18) [Guan et
al., 1994; Itokawa et al., 1981; Treasure 2005).
(Figure 2).
Ding reported that ethanolic and buthanolic
extracts from leaves and stems of P. cablin contains
several glycosides compunds such as apigenin 7- (O-
methylglucuronide), apigenin-7-galacturonide,
luteolin 7-O- (6-O-methyl-β-D-
glucuronopyranoside), quercetin-7-β-D-glucoside,
syringaresinol-β-D-glucoside, verbascoside,
orobanchoside and campneoside I (Ding et al., 2009).
ICEO 2019 - 2nd International Conference of Essential Oil Indonesia
68
Figure 2: Structure of some non-volatile compounds apart
from flavonoids in P. cablin.
However, the quality of essential oils from P.
cablin is highly depend on chemotypes and others
factor such as environmental conditions, ways of
adaptation, climate, gene quality, dryness of leaves,
geographical location (geographical index), and time
of harvest. The research conducted by Blank.
mentioned that P. cablin planted in different harvest
seasons would have different chemotypes both
qualitatively and quantitatively. Interestingly, the
main compound of patchouli alcohol (patchoulol)
was founded in all plants that planted in different
seasons
(Blank et al., 2011). (Table 1).
Besides the harvesting seasons, the chemical
content of the patchouli alcohol was also strongly
influenced by the geographical indication. Yunhui
reported that patchouli alcohol and pogostone from P.
cablin were differences in percentage of yield of 36
samples in three provinces in China (Guangdong,
Guangxi and Hunan Provinces)
(Yinhui et al.,2006).,
Figure 3.
Table 1: The percentage of main volatile compounds from
P. cablin Benth in different seasons of harvesting time
using gas chromatograph equipped with a flame ionization
detector (GC-FID) (Blank et al., 2011).
Note: 1
st
: harvest (May 2008); 2
nd
: harvest (August 2008);
3
th
: harvest (November 2008); and 4
th
: harvest (February
2009)
Figure 3: The percentages of patchouli alcohol and
pogostone from 36 samples of P. cablin in three provinces
in China (Yinhui et al.,2006).
Yunhui also mentioned that Guangdong Province
(S1-S23) had percentage of patchouli alcohol and
pogostone were 43.51 and 7.47%, respectively.
While, Guangxi Province (S24-S33) had percentage
of patchouli alcohol and pogostone were 40.81 and
9.65%, respectively. Interestingly, the samples from
Hunan Province (S34-S36) had the highest patchouli
Main volatile
compounds
Percentage of abundance
compounds (%) each harvest
time
1
st
2
nd
3
th
4
th
α-Pinene 0.00 0.00 0.00 0.00
ß-Pinene 0.00 0.00 0.00 0.00
Limonene 0.00 0.00 0.00 0.00
Acetophenone 0.00 0.00 0.00 0.00
ß-Patcoulene 2.30 2.81 2.62 2.02
ß-Elemene 0.72 0.39 1.06 0.45
ß-Caryophyllene 2.41 1.18 2.24 1.53
α-Guaiene 7.43 3.73 5.99 4.44
Seychellene 5.01 3.01 4.58 3.25
α-Humulene 0.63 0.30 0.33 0.32
α-Patcoulene 3.14 1.71 2.81 1.95
α-Bulnesene 10.32 5.82 8.37 6.48
(E)nerolidol 0.00 0.00 0.00 0.00
Caryophyllene
oxide
0.00 0.00 0.00 0.00
ß-Atlantol 0.00 0.54 1.01 1.17
Pogostol 4.18 5.04 4.30 5.06
Pathoulol 55.25 68.41 61.17 62.15
Patchouli (Pogostemon cablin Benth): Chemistry, Biology, and Anti-inflammatory Activities: A Review
69
alcohol content (51.70%) and the lowest pogostone
content (2.11%). These results indicate that plant
sources (cultivation sources), growth temperature
(climate) and time of growth (harvesting time) greatly
affect the chemical composition of essential oils of P.
cablin
(Yinhui et al.,2006).
3 BIOLOGY ACTIVITIES
3.1 Antibacterial Activities
Luo reported that aqueous P. cablin extract possess
antibacterial activity against Staphylococcus aureus,
Bacillus subtilis, Pseudomonas aeruginosa, Enteritis
coccus and Aerobacter aerogenes. Interestingly, this
extract has antibacterial activity against
Staphylococcus aureus significantly, but does not
show activity against Escherichia coli (Luo, 2005).
Pattnaik mentioned that patchouli oil was effective in
inhibiting on 20 bacterial strains and 12 fungal
strains. He also mentioned that the patchouli oil
derived from several countries with geographical
differences such as China, India, and Indonesia
showed antifungal activity against 17 of pathogenic
fungi, and effective against 16 commensal bacteria
from the skin, mucous membranes, nails, feet and
armpits (Pattnaik et al., 1996). Hammer also
mentioned that P. cablin extract were effective in
inhibiting Acenitobacter baumanii, Aeromonas
veronii, Candida albicans, Enterococcus faecalis,
Escherichia coli, Klebsiella pneumonia,
Pseudomonas aeruginosa, Salmonella enteric and
Staphyllococcus aureus. The organics leave extracts
of P. cablin were reported have significant activity
against Escherichia coli, Escherichia aerogenes,
Bacillus substilis, and Staphylococcus aureus.
Among all the compounds contained in patchouli oil,
pogostone and (-) - patchoulol have the greatest
therapeutic effect on bacteria (Hammer et al., 1999).
3.2 Antifungal Activities
The research conducted by Kocevski showed that
patchouli oil has antifungal activity against 11 fungal
types. However, it has no activity against Aspergillus
flavus, Aspergillus niger and Escherichia coli, but
showed antifungal activity against several
Aspergillus species at concentration of 44.52%
(Kocevski et al., 2013). Yang reported that patchouli
alcohol, α-bulnesene and patchoulene isolated from
P. cablin from China have activity on 12 types of
dermatophytes (dermatophytes) with MIC
50
values
were around 50-400 μg / L (Yang et al., 2000). In
addition, the combination of patchouli oil and sodium
artesunate has a synergistic effect on Plasmodium
berghei (Liu et al., 2000). Yu also reported that
pogostone from P. cablin had antifungal activity
against clinical isolate of Candida albicans at
concentrations of 50-400 µg / ml both in vitro and in
vivo (Yu et al., 2012). Lie showed that pogostone
from P. cablin is also effective as candidiasis
especially against Vulvovaginal candidiasis (Lie et
al., 1994).
3.3 Antiviral Activities
P. cablin extracts were reported have anti-influenza
activity against the FMI virus in vivo to the mouse
model by evaluating the pulmonary index, while the
methanolic extract of P. cablin leaves was known
have antiviral activity against influenza viruses
(Kiyohara et al., 2012). Gao reported that patchouli
alcohol in volatile oils obtained from isolation using
HPLC showed antiviral activity against H1N1 with an
IC
50
value of 2,635 µM. In addition, Gao also
reported that the methanol and ethyl acetate extracts
of P. cablin had an excellent antiviral effect against
the coxsackie B virus, with IC50 values of 26.92 and
13.84 µg / ml, respectively (Gao et al., 2009). P.
cablin was also known to have effects on Herpes
simplex types I and II in people with HIV-AIDS
(Buckle, 2002). However, until now it has not been
known exactly how the mechanism of action of P.
cablin as an antivirus.
3.4 Insecticidal Activities
P. cablin leaf extract at a concentration of 1% (w / w)
was known to be effective as a repellent against
Stegobium paniceum (Kardian, 1997). Chun reported
that patchouli oil was effective against Lasioderma
serricorne, Sitophilus zeamais, Tribolium confusum,
Falsogastrallus sauteri, and Coptotermes
formosanus Shiraki (Chun et al., 2000). Patchouli oil
is also effective as a repellent for mosquitoes Ades
aegypti, Anopheles stephensi and Culex
quinquefasciatus (Trongtokit et al., 2005;
Albuquerque et al., 2013; Gokulakrishnan et al.,
2013). Petroleum ether extract of P. cablin leaves was
also reported to be effective against
Dermatophagoides farina (Wu et al., 2010).
Progostone compounds from P. cablin were also
reported effective as larvicidal, antifeedant, pupicidal
activities against Spodoptera litura and Spodoptera
exigua (Huang et al., 2014).
ICEO 2019 - 2nd International Conference of Essential Oil Indonesia
70
3.5 Nematicidal Activities
Wiratno reported that patchouli oil from P. cablin has
nematicidal activity against root-knot nematode of
Meloidogyne incognita with a mortality rate of
around 4 ± 5.6% with IC
20
, IC
50
, and IC
90
values was
more than 19.2 mg / ml (Wiratno et al., 2009). Patidar
also reported that P. cablin extract at a concentration
of 500 ppm had nematicidal effect on second stage
juveniles (J2) Meloidogyne incognita with a percent
mortality of 28.25% after 48 hours of incubation of
time (Patidar et al., 2016).
4 ANTIOXIDANT EFFECTS
Hussin reported that patchouli oil had antioxidant
activity and radical scavenging by DPPH assay. The
results of the antioxidant effect test also showed that
patchouli oil from P. cablin had a higher activity than
mannitol. Polysaccharide compounds from P. cablin
are reported to be able to remove hydroxyl radicals
(•OH) and superoxide radicals (O
2
•) (Hussin et al.,
2012). Other results also show that P. cablin is very
effective in protecting A172 cells (human
neuroglioma cell line) from necrosis and apoptosis
induced by hydrogen peroxide (H
2
O
2
), which is
indicated by the ability of P. cablin act as reactive
oxygen (ROS)-scavenger (Kim et al., 2010). In
addition, patchouli alcohol reported able to reduce the
level of ROS and Ca
2+
ions to cells induced by Aß25-
35. P. cablin is also reported to be able to protect the
intestinal barrier function by protecting membrane’s
fluidity of epithelial cells through regulation of NO
and TNF-α in serum. The volatile oil from P. cablin
has also been reported to have an antitussive and
expectorant effect on ammonia-induced mice (Xie
and Tang, 2009).
5 ANTI-INFLAMMANTORY
ACTIVITIES
It has been reported that methanolic extract of P.
cablin possess anti-inflammatory activity by reduced
the level of malondialdehyde in paw endema on mice
by increasing the antioxidant activity of enzymes in
the liver (Lu et al., 2011). Lu also mentioned that this
extract was able to reduce the level of superoxide
dismutase activity, glutathione peroxidase,
gluthathione reductase, COX-2 and TNF-α in paw
endema of mice. The extract of P. cablin also reported
have strongest anti-inflammatory response by
regulation of interleukin-1β (IL-1β) and
prostaglandin E (2). Yu also reported that patchouli
alcohol from Pogostemonis plant mice was able to
inhibit ear edema and paw edema in xylene and
carrageenan-induced mice at concentration of 10-40
mg / kg body weight of mice. The patchouli alcohol
was also able to reduce the production of TNF-α, IL-
1ß, iNOS, and COX-2 in hind paw to carrageenan-
induced mice (Yu et al., 2011). In addition, Jin also
reported that patchouli alcohol has anti-inflammatory
activity against RAW264.7 and HT-29 cell lines
through suppressing ERK mediated by the NF-κB
pathway (Jin et al., 2013). Li mentioned that
pogostone has an anti-inflammatory effect and could
be potential developed as septic shock therapy (Li et
al., 2014). Besides that, Park reported that aqueous P.
cablin extract was be able to suppressed colon
inflammation by suppressing the expression of pro-
inflammatory cytokines (Park et al., 2014).
6 CONCLUSIONS AND
RECOMMENDATIONS
This review tries to summarize the latest research
related to the phytochemical content, biological
activity and anti-inflammatory effect of P. cablin.
The chemical constituents of P. cablin were strongly
influence by several factors including environmental
conditions, adaptation methods, climate, gene
quality, dryness of leaves, harvest time, and its
geographical location. However, further research
needed to develop patchouli oil as drug candidate
particularly for anti-inflammatory drugs.
ACKNOWLEDGEMENTS
The authors thank to Atsiri Research Center (ARC)
and Herbal Medicine Research Center (ProHerbal) of
Universitas Syiah Kuala for their support of this
study.
CONFLICT OF INTEREST
The authors declare that there are no conflicts of
interest.
REFERENCES
Albuquerque, E, L., Lima, J, K., Souza, F, H., Silva, I, M.,
Santos, A, A., Araujo, A, P., Blank, A, F., Lima, R, N.,
Alves, P, B., Bacci, L., 2013. Insecticidal and
Patchouli (Pogostemon cablin Benth): Chemistry, Biology, and Anti-inflammatory Activities: A Review
71
Repellence Activity of the Essential Oil of Pogostemon
Cablin Against Urban Ants Species. Acta Trop, 127(3)
181–186.
Anonis, D, P., 2006. Woody Notes in Perfumery, Patchouli
Oil, Absolute and Aroma Chemicals. Part I. Perfum.
Flavor, 31, 36–39.
Blank., Fitzgerald, A., Sant’ana., Pergentino, T, C., Santos.,
Santana, P., Blank, A., Fatima, M., do Nascimento, A,
P., Jesus., Ramos, H, C., Alves., Barreto P., 2011.
Chemical Characterization of the Essential Oil from
Patchouli Accessions Harvested Over Four Seasons,
Industrial Crops and Products, 34(1), 831– 837.
Buckle, J., 2002. Clinical Aromatherapy and AIDS, J.
Assoc. Nurses Aids Care, 13(3), 81–99.
Chakrapani, P., Venkatesh, K., Singh, B, C, S., Jyothi, B,
A., Kumar, P., Amareshwari, P., Roja, A, R., 2013.
Phytochemical, Pharmacological Importance of
Patchouli (Pagostemon cablin (Blanco) Benth) an
Aromatic Medicinal Plant, Int. J. Pharm. Sci. Rev. Res,
21(2), 7–15.
Chun, W., DeJun, Y., ShiLin, H., Qun, T., 2000.
Determination of Toxicity of Plant Essential Oils to
Museum Insect Pests, J. Southwest Agric. Univ, 22(6),
494–495.
Ding W, Liu M, Wei X 2009 J. Trop. Subtropical Bot., 17
610-616.
Gao X, Xiong S, Wang Y 2009 J Chin Med Mater. 32 761-
764.
Gokulakrishnan, J., Kuppusamy, E., Shanmugam, D.,
Appavu, A., Kaliyamoorthi, K., 2013. Pupicidal and
Repellent Activities of Pogostemon cablin Essential Oil
Chemical Compounds Againts Medically Important
Human Vector Mosquitoes Asian Pac. J. Trop. Dis,
3(1), 26–31.
Guan L, Quan L, Xu L 1994 China J Chin. Mater Med. 19
355-360.
Hammer, K, A., Carson, C, F., Riley, T, V., 1998. In-Vitro
Activity of Essential Oils, in Particular Melaleuca
alternifolia (Tea Tree) Oil and Tea Tree Oil Products,
Against Candida spp. Journal of Antimicrobial
Chemotherapy, 42, 591–595.
Hasegawa, Y., Tajima, K., Toi, N., 1992. An Additional
Constituent Occuring in the Oil From a Patchouli
Cultivar, Flavour Fragrance. J, 7, 333-335.
Huang, G, J., Deng, J, S., Chen, C, C., Huang, C, J., Sung,
P, J., Huang, S, S., Kuo, Y, H., 2014. Methanol Extract
of Antrodia Camphorata Protects Against
Lipopolysaccharide-Induced Acute Lung Injury by
Suppressing NF-κB and MAPK Pathways in Mice,
J.Agric.Food. Chem, 62(23), 5321–5329.
Hussin, N., Mondello, L., Costa, R., 2012. Quantitative and
Physical Evaluation of Patchouli Essential Oils
Obtained from Different Sources of Pogostemon
Cablin, Nat. Prod. Commun. 7 927.
Itokawa H, Suto K, Takeya K 1981 Chem Pharm. 29 254-
260.
Jeong, J, B., Shin, Y, K., Lee, S, H., 2013. Anti-
Inflammatory Activity of Patchouli Alcohol in
RAW264.7 and HT-29 cells, Food and Chemical
Toxicology, 55, 229–233.
Kardinan, A., Wikardi, E, A., 1997. The Prospect of
Botanical Insecticides on Stored Food Insects
Management, Biotrop. Spec. Publ, 59, 199–208.
Kim, H, W., Cho, S, J., Kim, B, Y., Cho, S, I., Kim, Y, K.,
2010. Pogostemon cablin as ROS Scavenger in
Oxidant-Induced Cell Death of Human Neuroglioma
Cells, Evid Based Complement Alternat Med. 7 239-47.
Kiyohara, H., Ichino, C., Kawamura, Y., Nagai, T., Sato,
N., Yamada, H., 2012. Patchouli Alcohol: In Vitro
Direct Anti-Influenza Virus Sesquiterpene in
Pogostemon Cablin Benth, J. Nat. Med, 66(1), 55-61.
Kocevski, D., Du, M., Kan, J., Jing, C., Lacanin, I.,
Pavlovic, H., 2013. Antifungal Effect of Allium
tuberosum, Cinnamomum cassia, and Pogostemon
cablin Essential Oils and Their Components Against
Population of Aspergillus species, J. Food Sci, 78,
M731–M737.
Li, Y, C., Xian Y F, Su Z R, Ip S P, Xie J H, Liao J B, Wu
D W, Li C W, Chen J N, Lin Z X, Lai X P 2014 J.
Ethnopharmacol. 157 212–221.
Lie, Quan L, Xu L 1994 China J Chin. Mater Med 19 355-
6.
Ling G, Lihui Q, Puzhu C 1992 Nat. Prod. Res. Dev. 2 5
Liu A, Yu Z, Lu L 2000 Chin. J. Parasitol Parasitic Dis.,
18 76.
Lu T C, Liao J C, Huang T H 2011 Evid. Based Complement
Alternat Med. 671-41.
Lubbe, A., Verpoorte, R., 2011. Cultivation of Medicinal
and Aromatic Plants for Specialty Industrial Materials,
Ind. Crop Prod. 34, 785–801.
Luo C 2005 J Chin Med Mater 28:700-710.
Mallappa, K, S., Uma, R, S., 2016. Patchouli (Pogostemon
cablin Benth.): Botany, Agrotechnology and
Biotechnological Aspects, Industrial Crops and
Products, 87, 161–176.
Park, S, Y., Neupane, G, P., Lee, S, O., Lee, J, S., Kim, M,
Y., Kim, S, Y., Park, B, C., Park, Y, J., Kim, J, A.,
2014. Protective Effects of Pogostemon cablin
Bentham Water Extract on Inflammatory Cytokine
Expression in TNBS-Induced Colitis in Rats, Arch.
Pharmacal. Res, 37, 253–262.
Patidar, R, K., Debashish, S., Pathak, M., Shakywar, R, C.,
Rajesh K, P., 2016. Effect of Essential Oils on
Mortality, Hatching and Multiplication of Root-Knot
Nematode, Meloidogyne incognita and Its Impact on
Plant Growth Parameters. International Journal of
Agriculture, Environment and Biotechnology, 9(5),
887-895.
Pattnaik, S., Subramanyam, V, R., Kole, C., 1996.
Antibacterial Antifungal Activity of Ten Essential Oils
In Vitro, Microbios, 86, 237–246.
Priya, D., Swati, D., Vilasrao, D, K., 2014. A Review on
Pogostemon patchouli, Res. J. Pharmacogn.
Phytochem, 691, 41–47.
Swamy, M, K., Sinniah, U, R., 2015. A Comprehensive
Review on the Phytochemical Constituents and
Pharmacological Activities of Pogostemon cablin
Benth.: An Aromatic Medicinal Plant of Industrial
Importance, Molecules, 20(5), 8521–8547.
ICEO 2019 - 2nd International Conference of Essential Oil Indonesia
72
Treasure, J., 2005. Herbal Medicine and Cancer: An
Introductory Overview, 21(3), 177-83.
Trongtokit Y, Rongsriyam Y, Komalamisra N,
Apiwathnasorn C 2005 Phytother. Res. 19 303–
309.Zhang M G, Yuan M, Yuan P 2003 Chin. Tradit.
Herbal Drugs 34 749-751.
Wiratno, D., Taniwiryono, H., den Berg, V., Riksen, J, A,
G., Rietjens, I, M, C, M., Djiwanti, S,R., Kammenga,
J, E., Murk, A, J., 2009. Nematicidal Activity of Plant
Extracts Against the Root-Knot Nematode,
Meloidogyne incognite, The Open Natural Products
Journal, 2, 77-85.
Wu, H, Q., Li, J., He, Z, D., Liu, Z, G., 2010. Acaricidal
Activities of Traditional Chinese Medicine Against the
House Dust Mite, Dermatophagoides Farinae,
Parasitology, 137(6), 975–983.
Xie, Y, C., Tang, F., 2009. Protective Effect Pogostemon
cablin on Membrane Fluidity of Intestinal Epithelia
Cell in Ischemia/Reperfusion Rats After
Ischemia/Reperfusion, Chin. J. Integr. Tradit. West
Med, 29, 639-641.
Yang, D, P., Chaumont, J, P., Millet, J., 2000. Antifungal
Activity of the Essential Oils from Agastache rugosa
and Pogostemon cablin Against Dermatophytes and
Opportunistic Fungi, Chin. Pharm. J, 35, 9-11.
Yang, Y., Kong, W., Feng, H., Dou, X., Zhao, L., Xiao, Q.,
Yang, M., 2006. Quantitative and Fingerprinting
Analysis of Pogostemon cablin Based on GC-FID
Combined with Chemometrics, Journal of
Pharmaceutical and Biomedical Analysis, 121, 84–90.
Yu-Cui Li, Hai-Chun Lianga, Hai-Ming Chen, Li-Rong
Tan, Yu-Yang Yia, Zhen Qin, Wei-Min Zhang, Dian-
Wei Wu, Chu-Wen Li, Rong-Feng Lin, Zi-Ren Su,
Xiao-Ping La 2012 Phytomedicine 20 77– 83.
CuiLi, Y., FangXian, Y., Polp, S., RenSu, Z., YanSu, J.,
JinHe, J., FengXie, Q., PingLai, X., XiuLin, Z., 2011.
Anti-Inflammatory Activity of Patchouli Alcohol
Isolated from Pogostemonis Herba in Animal Models,
Fitoterapia, 82, 1295–1301.
Zhou, L., Xu, M., Yang, C, R., Wang, Y, F., Zhang, Y, J.,
2011. New Patchoulol-Type Sesquiterpenoids From
Pogostemon cablin. Helv. Chim. Acta, 94, 218-23.
Patchouli (Pogostemon cablin Benth): Chemistry, Biology, and Anti-inflammatory Activities: A Review
73