ArticlePDF Available

Phytochemical, Pharmacological importance of Patchouli (Pogostemon cablin (Blanco) Benth) an aromatic medicinal plant

Authors:
  • Osmania University, Hyderabad, India

Abstract and Figures

Aromatic plants have been commercially used as spices, natural flavor, raw material for essential-oil industry and other medicinal purpose. The use of essential oils continues to rise, both as a separate commodity and indirectly through a large range of beautycare and aromatherapy products. Patchouli (Pogostemon cablin (Blanco) Benth; is a species from the genus Pogostemon and a bushy herb of the mint family. Patchouli leaves are the source for essential oils that constitutes more than 70 chemical compounds. The presence of these compounds imparts excellent therapeutic properties to Patchouli oils that cure various problems tormenting human beings. Production of patchouli oil in India is limited (10–15 tons/ annum). Global demand of Patchouli is 1600 tons of oil per annum with a value of 240 crores. It helps cultivators to meet the demand of the spices and pharmaceutical industry. The present communication constitutes a review on the study of phytochemistry, pharmacological activities, medicinal importance of an aromatic medicinal plant, Patchouli (Pogostemon cablin Blanco) Benth. A wide range of phytochemical constituents have been isolated from Patchouli (Pogostemon cablin (Blanco) Benth which possesses activities like antimicrobial, cytotoxic activity, antiemetic activity, analgesic, anti-mutagenic activity and anti-inflammatory activity and other important activities. Based upon the given significant information, Pogostemon cablin can be developed into novel natural medicine.
Content may be subject to copyright.
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
7
Chakrapani.P, Venkatesh.K, Chandra Sekhar Singh.B, Arun Jyothi.B, Prem Kumar, Amareshwari.P, A. Roja Rani*
*Department of Genetics and Biotechnology, Osmania University, Hyderabad, Andhra Pradesh, India.
*Corresponding author’s E-mail: anupalli_rr@yahoo.com
Accepted on: 29-04-2013; Finalized on: 31-07-2013.
ABSTRACT
Aromatic plants have been commercially used as spices, natural flavor, raw material for essential-oil industry and other medicinal
purpose. The use of essential oils continues to rise, both as a separate commodity and indirectly through a large range of beauty-
care and aromatherapy products. Patchouli (Pogostemon cablin (Blanco) Benth; is a species from the genus Pogostemon and a
bushy herb of the mint family. Patchouli leaves are the source for essential oils that constitutes more than 70 chemical compounds.
The presence of these compounds imparts excellent therapeutic properties to Patchouli oils that cure various problems tormenting
human beings. Production of patchouli oil in India is limited (10–15 tons/ annum). Global demand of Patchouli is 1600 tons of oil per
annum with a value of 240 crores. It helps cultivators to meet the demand of the spices and pharmaceutical industry. The present
communication constitutes a review on the study of phytochemistry, pharmacological activities, medicinal importance of an
aromatic medicinal plant, Patchouli (Pogostemon cablin Blanco) Benth. A wide range of phytochemical constituents have been
isolated from Patchouli (Pogostemon cablin (Blanco) Benth which possesses activities like antimicrobial, cytotoxic activity,
antiemetic activity, analgesic, anti-mutagenic activity and anti-inflammatory activity and other important activities. Based upon the
given significant information, Pogostemon cablin can be developed into novel natural medicine.
Keywords: aromatic plants, natural medicine, phytochemicals, Pogostemon cablin, therapeutic properties.
INTRODUCTION
edicinal plants have provided modern medicine
with numerous plant derived therapeutic
agents.1 Many parts of medicaments are based
on indigenous herbals and in recent years, the interest
towards the medicinal plants has increased in a great
deal. Apart from this, people from different places have
also taken this matter seriously by conducting various
researches on plant based medicines. In the commercial
market, medicinal herbs are used as raw drugs, extracts
or tinctures.2 Medicinal plants are used in aromatherapy,
a form of alternative medicine that uses volatile plant
materials, known as essential oils, and other aromatic
compounds for the purpose of altering a person's mind,
mood, cognitive function or health. Some essential oils
such as tea tree3 have demonstrated anti-microbial
effects, but there is still a lack of clinical evidence
demonstrating efficacy against bacterial, fungal, or viral
infections.4 However some evidence exists that essential
oils may have therapeutic potential.5
People are settling for remedies that are not just effective
but are harmless in the long run. Herbal oils are of various
types depending on herbs used to extract the oil. The
most important bioactive constituents of plants are
alkaloids, tannins, flavonoids, and phenolic compounds.6
Amongst popular oils, Patchouli oil extracted from
Pogostemon cablin is known not just for its health
benefits but also for its fragrance.7 Patchouli is a
perennial herb and a fragrant plant that basically grows in
the tropical region throughout the world. Though
patchouli oil is known for its perfumery uses and there
are other medicinal properties attached with patchouli
oil.8 Patchouli oil’s growing demand can be understood as
it can neither be replaced inorganically nor synthesized
because of its complex molecular structure.9 Hence, the
only alternative is to cultivate the plant extensively.10 The
aim of the present paper is to review the importance of
patchouli extractions in the treatment of diseases that
may be useful for the applications of this medicinal plant
in the treatment of diseases.
Pogostemon cablin
The plant patchouli belongs to the family Lamiaceae (mint
family). Traditionally it had been considered closely
related to Verbenaceae.11 The plants of this family are
frequently aromatic in all parts and widely used culinary
herbs such as basil, mint, rosemary, sage, savory,
marjoram, oregano, thyme, lavender and perilla.12-14 The
name Patchouli was derived from Tamil (patchai: green
and ellai: leaf).
Patchouli is a species from the genus Pogostemon and a
bushy herb of the mint family, with erect stems, two or
three feet (about 0.75 meters) in height and bearing small
pale pink-white flowers. The plant is native to tropical
regions of Asia and is now extensively cultivated in China,
India, Thailand, Indonesia, Malaysia, Mauritius,
Philippines, West Africa and Vietnam.15 Indian demand
for patchouli oil is around 220 tonnes valued at 33 crores,
while global demand is to the tune of 1600 tonnes of oil
per annum with a value of 240 crores.16 The scent of
patchouli is heavy, strong and used for centuries in
perfumes. Even though other species of Patchouli are
cultivated, Pogostemon cablin is considered as superior as
Phytochemical, Pharmacological importance of Patchouli (Pogostemon cablin (Blanco)
Benth) an aromatic medicinal plant
Review
Article
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
8
it grows well in warm to tropical climates.17 The seed-
bearing flowers are very fragrant and bloom in late fall.
Figure 1: Pogostemon cablin. Benth
In absence of modern medicinal remedies people relied
on herbal remedies derived from herbs and spices. There
are many medicinal herbs and spices, which find place in
day-to-day uses, many of these are used as herbal
remedies.18 In patchouli fresh or dried leaves are used
apart from the essential oils.19 The flowers, leaves, and
seeds of the plant give off the signature patchouli scent
and even more when crushed.20
Scientific Classification21
Category : Dicot
Kingdom : Plantae
Subkingdom : Tracheobionta
Super division : Spermatophyta
Division : Magnoliophyta
Class : Magnoliopsida
Subclass : Asteridae
Order : Lamiales
Family : Lamiaceae
Genus : Pogostemon
Species : Cablin
Binomial name : Pogostemon cablin Benth
Synonyms : Patchouli, Patchouly, Pachouli.22
Sanskrit synonyms: Patra, Gandhaparta.23
Vernacular Names24-26
Malaysia : Dhalum Wangi, Tilam Wangi, Nilam
English : Patchouli
Indonesia : Nilam Wangi (General), Nilam (Acheh),
Singalon (Batak)
Thailand : Phimsen (Bangkok)
Vietnam : (Ho (aws) c h (uw) (ow) ng)
Philippines : Kabling (Tagalog); Katluen (Bisaya) Kadlum
(Bikol, Bisaya, Sulu)
China : Guang Huo Xiang
Korea : Hyangdulkkaephul
India : Pachi (Sanskrit); Pachauli (Hindi); Pachapat,
Patchouli (Bengali); Pachila, Kattam (Malayalam);
Pachetene (Kannada); Pacha, Sugandhi pandi (Gujarati);
Panch (Marathi)
French : Patchouli
Spanish : Pachuli
Commercial Cultivation of Patchouli
Commercial cultivation of the crop in India was first
attempted by Tata Oil Mills in 1942. After initial stray
attempts to grow the crop, its systematic cultivation
started in 1962 by Central Institute of Medicinal and
Aromatic Plants (CIMAP).27 Since there is no replacement
for patchouli oil; its unique market position in aroma
industry has further increased.9 Patchouli is commercially
cultivated in the Indian states of Karnataka, Maharashtra,
Kerala, Goa, Gujarat and Assam.28,29 At present, the global
requirement of patchouli is met mainly through the
production from Indonesia. However, due to adverse
conditions in Indonesia, the supply of oil is irregular.
India’s available infrastructure and environment can
provide an opportunity to gain a major part of the world
market.30
Essential Oils
Patchouli oil has a very earthy aroma that matures with
aging. Patchouli oil is extracted from the leaves of the
plant which are harvested in the wet season and then
dried for several days. Dewi Haryani extracted patchouli
oil using steam distillation.31,20 Sesquiterpene cyclase
patchoulol synthase was purified and characterized from
P.cablin.32 Molecular distillation studies were performed
for purification of patchouli oil from P.cablin.33 Ultrasonic
extraction method used to get higher yield of patchouli
oil. The ultrasound is used to penetrate into the leave
cells to extract the patchouli essential oil from the
leaves.34
The Traditional Uses of Patchouli Essential Oil
Patchouli oil can be attributed to its properties like anti-
depressant, antiphlogistic, antiseptic, aphrodisiac,
astringent, cicatrisant, cytophylactic, deodorant, diuretic,
febrifuge, fungicide, insecticide, sedative, tonic,
cicatrisant, cytophylactic, deodorant, stimulant, euphoric.
It has been used in India, China and Japan for various
medicinal purposes. Because of its primary antiseptic
properties, it is used to treat athlete's foot, dandruff,
wounds and scars. It gives relief from constipation and
acts as an antidote against insect bites temporarily.
Patchouli alcohol is a fragrance ingredient used in
decorative cosmetics, fine fragrances, shampoos, toilet
soaps, non-cosmetic products such as household cleaners
and detergents.35 97.5 percentile use level in formulae for
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
9
use in cosmetics in general has been reported to be
0.11%,36 which would result in a conservative calculated
maximum daily exposure on the skin of 0.0028 mg/kg for
high end users of these products. The volatile oil of P.
cablin and the Chinese crude drug Herba pogostemonis, is
widely used in the cosmetic and oral hygiene industries.
Patchoulic alcohol is commonly used as an indicator for
the quality assessment of dried P. cablin.37 It also used as
daily dosage along with other herbs for treatment of
asthma.38
Ayurvedic Properties
The P.cablin is used in treatment of ayurvedic Rasa, Guna
and Virya.23
Aromatherapy
In India this essential oil with the lyrical name of
patchapat has long been used to keep moths and other
insects out of linens, woolen shawls and rugs.39 It is the
characteristic scent found in Indian bedspreads and
cottons. Hand-woven silk and wool rugs from Persia,
India, and Turkey have dried patchouli leaves laid on
them before they were rolled for shipping. To some
people the scent of patchouli is exotic, sensual, and
luxurious, but to others it is repellent. The leaves must be
fermented and aged before being distilled, which can take
as long as 24 hours. Even then, the translucent yellow oil
smells harsh. As it ages, it develops patchouli’s distinctive
scent. It also has a reputation as an aphrodisiac, a notion
that probably originated in India. All attempts to make
synthetic patchouli have failed utterly.40
Table 1: Phytochemical constituents isolated from Pogostemon cablin (Micheal Tierra (1992); Daniel M (2006); Baby P et
al., (2007). http://www.globinmed.com/index).
Chemical constituents
Patchouli alcohol 3-octanone Benzaldehyde dimethylphenol octanoic-acid
Pogostol 4-methyl-pentanoic-acid b-elemene epiguaipyridine Ombuine
nor-patchoulinol a-bulnesene b-patchoulene epoxycaryophyllen
e
p-vinyl-phenol
Seychellene a-bulnesene oxide b-pinene Eugenol pachypodol
nor-patchoulinol a-bulnesone Bulnesol eugenol cinnamic
aldehyde patchouli-alcohol
patchoulipyridine a-guaiene Cadinene g-patchoulene Patchoulipyridine
Methylchavicol a-guaiene oxide Camphene guaiacol pentanoic-acid
Limonene a-patchoulene caryophyllene guaipyridine phenol
Pinene a-pinene caryophyllene-oxide heptanoic-acid pogostol
p-methoxycinnamaldehyde anethole cinnamaldehyde humulene pogostone
1,10-epoxy-alphabulnesene anisaldehyde cis-2-
pentylcyclopropylcarboxylic
-acid limonene rhamnetin
1-alpha,5-alpha-epoxy-
alpha-guaiene Apigenin cycloseychellene nonanoic-acid seychellene
1-beta,5-beta-epoxy-alpha-
guaiene apigenin-7-o-beta-d-(-6"-
p-coumaroyl)-glucoside d-patchoulene nordehydropatcho
ulol tannin
2-methyl-butyric-acid apigenin-7-o-beta-
glucoside;; benzaldehyde dehydracetic-acid norpatchoulenol trans-2-
pentylcyclopropylcar
boxylic-acid
2-methylhexanoic-acid azulene dhelwangin o-cresol
Table 2: Phytochemical constituents isolated from Pogostemon cablin (Guan Let al., 1994)
Compounds from Pogostemon cablin
Identification method
Reference
Patchouli alcohol 1H-NMR, IR, MS and UV Guan L et al., 1994
Pogostone 1H-NMR, IR, MS and UV Guan L et al., 1994
Friedelin
(Isolated first time)
1H-NMR, IR, MS and UV Guan L et al., 1994
Epifriedelinol (Isolated first time) 1H-NMR, IR, MS and UV Guan L et al., 1994
Retusine
(Isolated first time) 1H-NMR, IR, MS and UV Guan L et al., 1994
Oleanolic acid (Isolated first time) 1H-NMR, IR, MS and UV Guan L et al., 1994
Beta-sitosterol
(Isolated first time)
1H-NMR, IR, MS and UV Guan L et al., 1994
Daucosterol
(Isolated first time)
1H-NMR, IR, MS and UV Guan L et al., 1994
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
10
Table 3: Chemical constituents obtained from P. cablin (Supawan B et al., 2006)
Compound Kovat’s Index % Area
Sesquiterpenes
δ-elemene 1339 t
β-patchoulene 1380 t
β-elemene 1391 0.33
cis-thujopsene 1429 0.25
trans-caryophyllene 1418 2.24
α-guaiene 1439 7.22
γ-patchoulene 1441 3.89
α-humulene 1454 0.48
α-patchoulene 1456 2.27
Seychellene 1460 0.98
Valencene 1491 0.85
β-selinene 1485 t
α-selinene 1494 0.23
Viridiflorene 1493 1.91
Germacrene A 1503 11.73
α-bulnesene 1505 0.86
7-epi-α-selinene 1517 0.17
Oxygenated sesquiterpenes
Longipinanol 1566 t
Globulol 1583 4.62
Patchouli alcohol 1659
60.30
Others
1-octen-3-ol 0978 0.20
t = trace (less than 0.01)
Table 4: Phytochemical constituents
Sesquiterpene hydroperoxides 1-3 Acetone extract
Kiuchi Fet al., 2004)
Licochalcone A Cytotoxicity-guided fractionation Park EJet al., (1998)
Ombuin Cytotoxicity-guided fractionation Park EJet al.,1998
5, 7-dihydroxy-3',4'- dimethoxyflavanone Cytotoxicity-guided fractionation Park EJet al.,1998
Delta-guaiene, GC/MS technology Luo Jet al., 2002
Aciphyllene GC/MS technology Luo Jet al., 2002
Phytochemical Constituents of Patchouli
Literature survey established the fact that patchouli oil
has more than 70 chemical compounds. Patchouli alcohol,
pogostol, seychellene, nor-patchoulinol,
patchoulipyridine, methylchavicol, limonene, pinene, p-
methoxy cinnamaldehyde etc41, 42, 43 and others have
extracted phytochemical constituents from P.cablin
through distillation process.44-47
Chemical constituents
Three terpenoids Germacrene, Patchoulol or patchouli
alcohol, Norpatchoulenol found in patchouli oil are
responsible for the typical patchouli scent.48-50 TLC and
HPLC were used to identify the possible chemical markers
for evaluating the quality of the crude drug "Pogostemoni
herba" (aerial part of P. cablin), a component of Kampo
medicines. In addition to the reported patchouli alcohol
and 2-hydroxy-6-methyl-3-(4-methylpentanoyl)-4-pyrone,
three phenylethanoids (acteoside, isoacteoside, and
crenatoside) were isolated from this plant material for
the first time.51
RT-PCR strategy was developed to isolate and functionally
characterize the respective patchouli oil synthase genes.
Unexpectedly, only five terpene synthase cDNA genes
were isolated. Four of the cDNAs encode for synthases
catalyzing the biosynthesis of one major sesquiterpene,
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
11
including a gamma-curcumene synthase, two germacrene
D synthases, and a germacrene A synthase. The fifth
cDNA encodes for a patchoulol synthase, which catalyzes
the conversion of FPP to patchoulol plus at least 13
additional sesquiterpene products.48 The study on the
chemical constituents of an essential oil of P. cablin was
carried out by hydrodistillation of leaf explants and the oil
analyzed by GC/MS and identified twenty two
compounds. Among these eighteen were sesquiterpenes
and three oxygenated sesquiterpenes.52
Germacrene A Germacrene B Germacrene C Germacrene D Germacrene E
Figure 2: Five different germacrene compounds
PHARMACOLOGICAL STUDIES
Antimicrobial Activity
Kuntal Das et al.,53 evaluated the anti microbial property
of patchouli oil against several microorganisms viz.
Bacillus substilis, Staphylococcus aureus, Streptococcus
pyogenes, Enterobacter aerogenes, Pseudomonus
aeruginosa, Escherichia coli, Klebsiella pneumoniae and
Serratia marcescens by agar diffusion technique and
found that the dose of 300 mcg/ml patchouli oil gave
maximum zone of inhibition against Staphylococcus
(14.53±0.37) followed by 12.15 ± 0.35 against
Streptococcus. Patchouli alcohol, a major component in
patchouli oil, and the extract showed higher antibacterial
activity than the mixture of β-sitosterol and stigmasterol
and 7,3′,4-tri-O-methyleriodictyol.54 The essential oil of P.
cablin showed antibacterial activity against
periodontopathic bacteria, including Actinobacillus,
Capnocytophaga, Fusobacterium, Eikenella.55
Antiviral activity
The anti-influenza A (H2N2) virus activity of patchouli
alcohol was studied in vitro, in vivo and in silico. The CC
(50) of patchouli alcohol was above 20 µM. It could inhibit
influenza virus with an IC (50) of 4.03 ± 0.23 µM. In the
influenza mouse model, patchouli alcohol showed
obvious protection against the viral infection at a dose of
5 mg-1kg-1day.56 The methanol extract from the leaves of
P.cablin, showed potent in vitro antiviral activity (99.8%
inhibition at a concentration of 10 µgmL-1) against
influenza virus A/PR/8/34 (H1N1). Patchouli alcohol did
not show anti-influenza virus activity against
A/Guizhou/54/89 (H3N2).57
Anti fungal activity
P. cablin oil (100 micro g/ml) inhibited the mycelial
growth of Candida albicans58 as well as Aspergillus niger
and Aspergillus flavus with MICs (minimal inhibitory
concentrations) in the range of 0.78-12.5 mg mL-1.59
Other Activities
Patchouli oil main constituent, patchouli alcohol was
found to be toxic and repellent against Formosan
subterranean termites.60 The Stomoxys calcitrans (L.)
(Diptera: Muscidae) repellency of 21 essential oils (EOs)
alone or in combination with Calophyllum inophyllum L.
(Clusiaceae), nut oil (tamanu oil) examined using an
exposed human hand bioassay. Results were compared
with those of commonly used repellent N, N-diethyl-3-
methylbenzamide (DEET). In tests with six human male
volunteers at a dose of 0.5 mg/cm2, patchouli (protection
time (PT), 3.67 h) was the most effective EO but less
active than DEET (4.47h).61 The undiluted oil of P. cablin
showed most effective and provided 2h of complete
repellency against Culex quinquefasciatus and Anopheles
dirus when compare with other essential oils.62
Figure 3: Patchoulol Chemical structure
Figure 4: Norpatchoulenol Chemical structure
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
12
Evaluation of the toxicity
Patchouli oil was evaluated for toxicity against
Choristoneura rosaceana, LC (50) and LD (50) values
confirmed that patchouli oil was the most toxic to C.
rosaceana larvae, with LC (50) = 2.8 µL mL (-1) and LD (50)
= 8.0 µg insect (-1).63
Anti-mutagenic activity of flavonoids
Methanol extract from P. cablin showed a suppressive
effect on umu gene expression of SOS response in
Salmonella typhimurium TA1535/pSK1002 against the
mutagen 2-(2-furyl)-3-(5-nitro-2-furyl) acrylamide
(furylfuramide).64
Anti-emetic principles
n-hexane extract of patchouli alcohol, pogostol, stigmast-
4-en-3-one, retusin and pachypodol exhibited anti-emetic
effects.65
Cytotoxic activity of patchouli
Licochalcone A, ombuin, and 5, 7-dihydroxy- 3, 4
dimethoxyflavanone were isolated from the aerial parts
of Pogostemon cablin by cytotoxicity guided fractionation
and it showed in vitro cytotoxicity in the P388 cell line (ED
50 9.12 µg/ml) and Pl PLCλl inhibition activity.
Treatment of promyelocytic leukemia cells (HL 60) with
compound Licochalcone A induced terminal
differentiation with the generation of monocyte using
nonspecific acid esterase assay.45
Location and activation of smell brain centers
Marchwicka et al.,66 using MRI brain scans data
determined more smell brain centers in female and male
human’s brains using olfactory and trigeminal nerve-
mediated stimuli during stimulation by patchouli.
Studies conducted the effects of P.cablin essential oil
inhalation on the body weight, food efficiency rate and
serum leptin in SD (Sprague Dawley) rats.67
Recombinant Technology
Farnesyl diphosphate synthase (FPPS) of yeast has been
coupled to patchoulol synthase (PTS) of plant origin (P.
cablin). Expression of the fusion proteins in S. cerevisiae
increased the production of patchoulol, the main
sesquiterpene produced by PTS, up to 2-fold.68
Incubations of isotopically pure (2-(2) H (1)) (E, E)-farnesyl
diphosphate with recombinant patchoulol synthase (PTS)
from P. cablin afforded a 65:35 mixture of
monodeuterated and dideuterated patchoulols as well as
numerous sesquiterpene hydrocarbons. Extensive NMR
analyses of the labeled patchoulol mixture and
comparisons of the spectra with those of unlabeled
alcohol led to the conclusion that the deuterium label was
located at positions (patchoulol numbering system) C5
(both isotopomers, ca. 100%) and C12 (minor isotopomer,
30-35%), that is approximately 2:1 mixture of (5-(2)H(1))-
and (5,12-(2)H(2)-patchoulols.69
GC-MS Fingerprint Studies
The GC fingerprint performed by gas chromatography
with patchouli alcohol and pogostone as chemical
markers can be used for identification of patchouli oil.70
For controlling the quality, standard fingerprint of P.cablin
collected from different regions of China was developed
by using GC-MS. Nine compounds including beta-
patchoulene, caryophyllene, alpha-guaiene, seychellene,
beta-guaiene, delta-guaiene, pathulenol, patchouli
alcohol and pogostone were identified among 10 main
peaks in P. cablin.71
Several experiments were carried out to test different
habitats, collection periods, processing methods, the level
of spreading manure and using agricultural chemical with
the volatile oil assay of pharmacopoeia and GC-MS
method.72 A gas chromatography-tandem mass
spectrometry (GC/MS/MS) method has been successfully
developed for the determination of patchoulic alcohol
content in the samples of dried P. cablin and was found to
be convenient in particular to tackle the complicated
matrix problems always encountered in the herbs which
contain high level of essential oils.37 The chemical
constituents of the volatile oil of the stems and leaves of
P. cablin collected from Leizhou county have been
analyzed by GC-MS and found patchouli alcohol, delta-
guaiene, alpha-guaiene, seychellene, alpha-patchoulene,
aciphyllene, trans-caryophyllene as main constituents.73
Pharmacokinetics
The pharmacokinetic parameters demonstrated patchouli
alcohol was consistent with the two-compartment open
model and showed linear pharmacokinetics. The T1/2
beta, AUC and MRT of patchouli alcohol in patchouli oil
were all higher than that of patchouli alcohol. This
method is quick, precise and reliable.74
CONCLUSION
The literature survey revealed that Patchouli
(Pogostemon cablin (Blanco) Benth. has been widely
studied for its pharmacological activities and regarded as
one of the best panacea in Ayurvedic medicine. It is a
versatile plant having a wide spectrum of medicinal
activities. It can be concluded that P. cablin is an
important source of many pharmacologically and
medicinally important chemicals such as sesquiterpenes
and three oxygenated sesquiterpenes. There is not
sufficient scientifically valid evidence to state that
patchouli extract could be potentially harmful to human
beings. As the global scenario is now changing towards
the use of non toxic plant products,75 development of
modern drugs from P. cablin should be emphasized. It is
also clear that much needs to be discovered, both as to
the active ingredients and their biological effects.
Furthermore, the information summarized here is
intended to serve as a reference tool to researchers in the
field of phytochemical, pharmacological studies,
identification of medicinal properties of P. cablin. Detailed
research on the chemistry and pharmacology of products
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
13
of plant origin are much essential and this may eventually
lead to the discovery of medicine that can be used in the
treatment of several diseases.76 The development of
these traditional systems of medicines with the
perspectives of safety, efficacy and quality will help not
only to preserve this traditional heritage but also to
rationalize the use of natural products in the health care.
Acknowledgement: We are thankful to Department of
Genetics, Osmania University; Central Institute of
Medicinal and Aromatic Plants (CIMAP); for providing
valuable information on importance of plant; UGC-JRF in
Engineering and Technology Division for financial support,
UGC-CAS, DST, DBT-ISLARE, DST-PURSE for guidance in
literature survey. Special thanks to my colleagues for their
valuable suggestions in preparation of the manuscript.
REFERENCES
1. Malhotra S, Pal Singh A, A Review of Pharmacology of
Phytochemicals from Indian Medicinal Plants, The Internet
J Alternative Medicine, 5, 1, 2007.
2. Amrit Pal Singh, Phytochemicals: Their Role in the Modern
Era, The Science Advisory Board, 2002.
3. Carson CF, Hammer KA, Riley TV, "Melaleuca alternifolia
(Tea Tree) oil: a review of antimicrobial and other
medicinal properties", Clinical Microbiology Reviews, 19
(1), 2006, 50 – 62. DOI 10.1128/CMR.19.1.50-62.
4. Van der Watt G, Janca A, "Aromatherapy in nursing and
mental health care", Contemporary Nurse, 30 (1), 2008,
69–75 DOI 5555/conu.673.30.1.69.
5. Edris AE, Pharmaceutical and therapeutic potentials of
essential oils and their individual volatile constituents: a
review. Phytotherapy Research 21 (4), 2007, 308–23 DOI
10.1002/ptr.2072.
6. Hill AF, Economic Botany: A Textbook of Useful Plants and
Plant Products. 2nd Ed. Mc Graw-Hill Book Company, New
York, 1952, 151.
7. Mercoledi, Luglio, Ten reasons why Patchouli Oil is the
answer to your problem, Avatara. AyurvedicTherapies Blog,
2011.
8. By Patricia, Patchouli Oil Benefits: Soaps, Lotions, Perfumes
and Scents, 2009, April 14.
9. Farooqi AA, Vasundhara, Srinivasappa MKN, Patchouli
cultivation as an intercrop in plantations. In: National
Seminaron Transfer of Technology of Medicinal and
Aromatic Crops, held at Bangalore, 20-22 February, 2001,
182-188.
10. Kumara Swamy M, Anuradha M, Analysis of genetic
variability in patchouli cultivars (Pogostemon cablin Benth.)
by using RAPD Markers, Research in Biotechnology, 2(6),
2011, 64-71.
11. Raymond M. Harley, Sandy Atkins, Andrey L. Budantsev,
"Labiatae", 2004, 167-275.
12. Wink M, Evolution of secondary metabolites from an
ecological and molecular phylogenetic perspective,
Phytochemistry, 64, 2003, 3–19.
13. Celiktas OY, Kocabas EEH, Bedir E, Sukan FV, Ozek T, Baser
KHC, Antimicrobial activities of methanol extracts and
essential oils of Rosmarinus officinalis, depending on
location and seasonal variations, Food Chemistry, 100,
2007, 553-559.
14. Hussain AI, Anwar F, Sherazi STH, Przybylski R, Chemical
composition, Antioxidant and antimicrobial activities of
basil (Ocimum basilicum) essential oils depends on seasonal
variations, Food Chemistry 108, 2008, 986-995.
15. Christopher Mcmahon, Monograph-Patchouli (Pogostemon
cablin). Saturday, June 18,
http://www.whitelotusblog.com/monograph-patchouli-
pogostemon-cablin.html, 2011.
16. Vijaya kumar K, Patchouli and India-A great leaf forward. In:
National Seminar of Prospectus and Potentials of Medicinal
and Aromatic Crops, held at Bangalore, 18-19 June, 2004,
106-107.
17. Temperance M, Properties of Patchouli Oil, 2012,
http://temperancem.hubpages.com/hub/Properties-of-
Patchouli-Oil.
18. Herbsnspicesinfo, Medicinal plants, Spices, and Herbal
Remedies as Ayurveda in India.
http://www.herbsnspicesinfo.com/2001.
19. Ageless, Sallamander concepts 1998 – 2011. 28 Jan, 2011.
20. Temperance M, Hubpages Inc, 2011.
21. USDA-NRCS (2012) Plants Database. Plants Profile.
Pogostemon cablin (Blanco) Benth.
22. Dreamherbs, Herbal Products (Pogostemon cablin) Mar 22,
2011. http://dreamherbs.com/herbal-
products/pogostemon-cablin/.
23. Eby Abraham MD, Ayurvedic medicinal plants, 2008.
http://ayurvedicmedicinalplants.com/index
24. Oyen LPA, Nguyen Xuan Dung Prosea, The BACIS Archives.
PlantResources of South-east Asia. Prosea's "Essential-oil
plants", 1999.
25. Arief H, Hariana Tumbuhan Obat dan Khasiatnya 2 Penebar
Swadaya Jakarta. pp 145. © Copyright 2010-2011, All
Rights Reserved - Global Information Hub On Integrated
Medicine (Globinmed).
26. Peter Hanelt Mensfeld’s, Encyclopedia of Agricultural and
Horticultural Crops, 2 Springer-Verlag Berlin, 2002, 1967.
27. Kumar A, Gauniyal AK, Virmani OP, Cultivationof
Pogostemon cablin forits oil, Current research on
medicinal and aromatic plants, 8(2), 1986, 79-86.
28. Venugopal CK, Biotechnological approaches for production
and cultivation of patchouli. In: First Annual Report for
2003-04, submitted to Department of Biotechnology,
Government of India, New Delhi, 2001, 8.
29. Venugopal CK, Praveen J, Umesh RN, Anand NM, Potentials
and problems of patchouli cultivation in North Karnataka,
Paper presented in Second Global Submit on Medicinal and
Aromatic Plants, October 25-29, New Delhi, India, 2004.
30. Raghu C, Economics of Production and Marketing Of
Patchouli In North Karnataka (Thesis), Department of
Agricutlural ollege of Agriculture, Dharwad Univeristy of
Agricultural Sciences, Economics C, 2006.
31. Dewi S. Haryani, Extraction of patchouli oil using steam
distillation, A thesis submitted in Faculty of Chemical and
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
14
Natural Resources Engineering Universiti Malaysia Pahang,
14 May, 2008.
32. Munck SL, Croteau R, Purification and characterization of
the sesquiterpene cyclase patchoulol synthase from
Pogostemon cablin, Arch Biochem Biophys, 282(1), 1990,
58-64.
33. Hu HY, Peng JF, Huang SL, Study on purification technology
of patchouly oil with molecular distillation, Zhongguo
Zhong Yao Za Zhi, 29(4), 2004, 320-2, 379.
34. Mohd NB Nasharudin, Patchoili oil extraction using
ultrasonic extraction method. A thesis submitted in
fulfillment of the requirement for the award of the degree
of Bachelor of Chemical Engineering, Faculty of Chemical
Engineering and Natural Resources, University Malaysia
Pahang, 2008.
35. Bhatia SP, Letizia CS, Api AM, Fragrance material review on
patchouli alcohol, Food and Chemical Toxicology, 46, 2008,
255–S256.
36. IFRA (International Fragrance Association), Use Level
Survey, September, 2004.
37. Zhao Z, Lu J, Leung K, Chan CL, Jiang ZH, Determination of
patchoulic alcohol in Herba Pogostemonis by GC-MS-MS,
Chem Pharm Bull (Tokyo), 53(7), 2005, 856-60.
38. Fu JX, Measurement of MEFV in 66 cases of asthma in the
convalescent stage and after treatment with Chinese herbs,
Zhong Xi Yi Jie He Za Zhi, 9(11), 1989, 658-9, 644.
39. Aparup Mukherjee, Organic facts, RuralTech Services, 2011.
40. Kathi Keville, Discovery Communications, LLC. The number-
one nonfiction media company, 2011.
41. Micheal Tierra, Planetary Herbology, Lotus Press Twin
Lakes, 1992, 251.
42. Daniel M, Medicinal Plants Chemistry and Properties
Science, Publishers New Hampshire, 2006.
43. Baby P. Skaria, Joy PP, Samuel Mathew, Qracy, Aromatic
Plants:Horticulture Science Series, Laxmi Art Creations New
Delhi, 01, 2007.
44. Guan L, Quan LH, Xu LZ, Cong PZ, Chemical constituents of
Pogostemon cablin (Blanco) Benth, Zhongguo Zhong Yao Za
Zhi, 19(6), 1994, 355-6, 383.
45. Park E J, Hae Ran Park, Ji Suk Lee, Jinwoong Kim,
Licochalcone A an inducer of Cell Differentiation and
Cytotoxic agent from Pogostemon cablin, Planta Med, 64,
1998.
46. Luo J, Guo X, Feng Y, Constituents analysis on volatile oil of
Pogostemon cablin from different collection time cultivated
in Hainan, Zhong Yao Cai, 25(1), 2002, 21-3.
47. Kiuchi F, Matsuo K, Ito M, Qui TK, Honda G, New
sesquiterpene hydroperoxides with trypanocidal activity
from Pogostemon cablin, Chem Pharm Bull (Tokyo), 52(12),
2004, 1495-6.
48. Deguerry F, Pastore L, Wu S, Clark A, Chappell J, Schalk M,
"The diverse sesquiterpene profile of patchouli,
Pogostemon cablin, is correlated with a limited number of
sesquiterpene synthases", Archives of Biochemistry and
Biophysics, 454 (2), 2006, 123–136.
49. Rivero Cruz B, Rivero Cruz I, Rodriguez JM, Cerda Garcia
Rojas CM, Mata R, Qualitative and quantitative analysis of
the active components of the essential oil from Brickellia
veronicaefolia by nuclear magnetic resonance
spectroscopy, J Nat Prod, 69(8), 2006, 1172-6.
50. Adewale MA, Germacrenes A–E and related compounds:
thermal, photochemical and acid induced transannular
cyclizations, Tetrahedron 65 (8), 2009, 1533–1552.
51. Amakura Y, Yoshimura M, Mouri C, Convenient TLC-based
Identification Test for the Crude Drug "Pogostemoni
herba", Yakugaku Zasshi, 128(12), 2008, 1833-7.
52. Supawan B, George BL, Thanapat S, Nijsiri R, Chemical
Constituents from Leaves and Cell Cultures of Pogostemon
cablin and Use of Precursor Feeding to Improve Patchouli
Alcohol Level, Science Asia, 32, 2006, 293-296.
53. Kuntal Das, Nilesh K. Gupta, Vijayabhaskar S, Manjunath
UM, Antimicrobial Potential of Patchouli Oil Cultivated
Under Acidic Soil Zone Of South India, Indian Journal of
Novel Drug delivery, 3(2), 2011, 104-111.
54. Ngampong K, Pornpat S, Boonsong K, Yupa P, Maliwan T,
Pareeya U, Development of Patchouli Extraction with
Quality Control and Isolation of Active Compounds with
Antibacterial Activity, Kasetsart J. (Nat. Sci.), 43, 2009, 519 -
525.
55. Osawa K, Matsumoto T, Maruyama T, Takiguchi T, Okuda K,
Takazoe I, Studies of the antibacterial activity of plant
extracts and their constituents against periodontopathic
bacteria, Bull Tokyo Dent Coll, 31(1), 1990, 17-21.
56. Wu H, Li B, Wang X, Jin M, Wang G, Inhibitory Effect and
Possible Mechanism of Action of Patchouli Alcohol against
Influenza A (H2N2) Virus. Molecules 16(8), 2011, 6489-501.
57. Kiyohara H, Ichino C, Kawamura Y, Nagai T, Sato N, Yamada
H, Patchouli alcohol: in vitro direct anti-influenza virus
sesquiterpene in Pogostemon cablin Benth, J Nat Med, 14,
2011.
58. Abe S, Sato Y, Inoue S, Anti-Candida albicans activity of
essential oils including Lemongrass (Cymbopogon citratus)
oil and its component citral, Nihon Ishinkin Gakkai Zasshi
44 (4), 2003, 285-91.
59. Seungwon Shin, Anti-Aspergillus Activities of Plant Essential
Oils and Their Combination Effects with Ketoconazole or
Amphotericin B, Arch Pharm Res, 26, 5, 2003, 389-393.
60. Zhu BC, Henderson G, Yu Y, Laine RA, Toxicity and
repellency of patchouli oil and patchouli alcohol against
Formosan subterranean termites Coptotermes formosanus
Shiraki (Isoptera: Rhinotermitidae), J Agric Food Chem,
30:51(16), 2003, 4585-4588.
61. Hieu TT, Kim SI, Lee SG, Ahn YJ, Repellency to Stomoxys
calcitrans (Diptera: Muscidae) of plant essential oils alone
or in combination with Calophyllum inophyllum nut oil, J
Med Entomol, 47(4), 2010, 575-80.
62. Trongtokit Y, Yupha Rongsriyam, Narumon Komalamisra,
Chamnarn Apiwathnasorn, Comparative Repellency of 38
Essential Oils against Mosquito Bites, Phytother Res, 19,
2005, 303– 309 DOI 10.1002/ptr.1637.
63. Machial CM, Shikano I, Smirle M, Bradbury R, Isman MB,
Evaluation of the toxicity of 17 essential oils against
Choristoneura rosaceana (Lepidoptera: Tortricidae) and
Int. J. Pharm. Sci. Rev. Res., 21(2), Jul – Aug 2013; n02, 7-15 ISSN 0976 – 044X
International
Journal of Pharmaceutical Sciences Review and Research
Available online at
www.globalresearchonline.net
15
Trichoplusia ni (Lepidoptera: Noctuidae), Pest Manag Sci
66(10), 2010, 1116-1121.
64. Miyazawa M, Okuno Y, Nakamura S, Kosaka H,
Antimutagenic activity of flavonoids from Pogostemon
cablin, J Agric Food Chem, 48(3), 2000, 642-647.
65. YangY, Kinoshita K, KoyamaK, Takahashi, Anti-
emetic principles of Pogostemon cablin (Blanco)
Benth, Phytomedicine, 6(2), 1999, 89-93.
66. Marchwicka WM, Stefańczyk L, Góraj B, The application of
functional magnetic resonance imaging for the assessment
of localisation and activation of cortex smell centers
depending on stimulus used in normal volunteers,
Otolaryngol Po,l 58(5), 2004, 881-886.
67. Hur MH, Kim C, Kim CH, Ahn HC, Ahn HY, The effects of
inhalation of essential oils on the body weight, food
efficiency rate and serum leptin of growing SD rats, Taehan
Kanho Hakhoe Chi, 36(2), 2006, 236-243.
68. Albertsen L, Chen Y, Bach LS, Diversion of flux toward
sesquiterpene production in Saccharomyces cerevisiae by
fusion of host and heterologous enzymes, Appl Environ
Microbiol, 77(3), 2011, 1033-1040.
69. Faraldos JA, Wu S, Chappell J, Coates RM, Doubly
deuterium-labeled patchouli alcohol from cyclization of
singly labeled [2-(2)H(1)] farnesyl diphosphate catalyzed by
recombinant patchoulol synthase, J Am Chem Soc
10:132(9), 2010, 2998-3008.
70. Cheng X, Zhang H, Yang L, Lin Z, Zou Z, Yu C, Identification
method with significant specificity of volatile oil of
Pogostemon cablin, Zhongguo Zhong Yao Za Zhi, 35(17),
2010, 2270-2272.
71. Hu LF, Li SP, Cao H, GC-MS fingerprint of Pogostemon cablin
in China, J Pharm Biomed Anal, 18:42(2), 2006, 200-206.
72. Li W, Wei G, Pan CM, Liu XX, Huang S, Xiu HH, Investigation
on the influential factors of the volatile oil and main
constituent content in Pogostemon cablin, Zhongguo Zhong
Yao Za Zhi, 29(1), 2004, 28-31.
73. Luo J, Feng Y, Guo X, Li X, GC-MS analysis of volatile oil of
herba Pogostemonis collected from Gaoyao county, Zhong
Yao Cai, 22 (1), 1999, 25-28.
74. Yang FC, Xu LZ, Zou ZM, Yang SL, Pharmacokinetics of
patchouli alcohol and patchouli alcohol in patchouli oil
after iv administrated to rats, Yao Xue Xue Bao 39(9), 2004,
726-729.
75. Sandeep D, Ramanjeet K, Ruhil S, Balhara M, Seema
Dhankhar, Chhillar AK, A review on Justicia adhatoda: A
potential source of natural medicine, African Journal of
Plant Science, 5(11), 2011, 620-627, 6.
76. Dev S, Current Sci, 73, 1997, 909.
Source of Support: Nil, Conflict of Interest: None.
... The presence of all these compounds in the plants, they are responsible for different medicinal properties such as antioxidant, antimicrobial, antiinflamatory and anticancer activities etc. Earlier studies have revealed that the most important bioactive compounds of medicinal plants are alkaloids, flavonoids, tannins, and phenolic compounds [12]. ...
Article
Full-text available
Objective: To explore the anti-nociceptive effect of patchouli alcohol (PA), the essential oil isolated from Pogostemon cablin (Blanco) Bent, and determine the mechanism in molecular levels. Methods: The acetic acid-induced writhing test and formalin-induced plantar injection test in mice were employed to confifirm the effect in vivo. Intracellular calcium ion was imaged to verify PA on mu-opioid receptor (MOR). Cyclooxygenase 2 (COX2) and MOR of mouse brain were expressed for determination of PA's target. Cellular experiments were carried out to find out COX2 and MOR expression induced by PA. Results: PA significantly reduced latency period of visceral pain and writhing induced by acetic acid saline solution (P<0.01) and allodynia after intra-plantar formalin (P<0.01) in mice. PA also up-regulated COX2 mRNA and protein (P<0.05) with a down-regulation of MOR (P<0.05) both in in vivo and in vitro experiments, which devote to the analgesic effect of PA. A decrease in the intracellular calcium level (P<0.05) induced by PA may play an important role in its anti-nociceptive effect. PA showed the characters of enhancing the MOR expression and reducing the intracellular calcium ion similar to opioid effect. Conclusions: Both COX2 and MOR are involved in the mechanism of PA's anti-nociceptive effect, and the up-regulation of the receptor expression and the inhibition of intracellular calcium are a new perspective to PA's effect on MOR.
Article
Full-text available
Essential oil glandular trichomes are the specialized anatomical and structural characteristic of plants amassing significant quantities of commercially and pharmaceutically valuable essential oil terpenoids. Developmental dynamics of these structures together with the oil secretory process and mechanisms have a direct bearing with the secondary metabolite production, sequestration and holding potential of the producer systems. Therefore, in this study, essential-oil gland trichomes of menthol mint leaf have been stereologically analysed to discern their anatomical archetype vis-à-vis volatile oil secretion and sequestration as integrated in the overall ontogeny of leaf. Cuticular 'dehiscence' or decapping, leading to collapsing of the peltate trichomes was found to be a notable characteristic of the menthol mint oil glands. Ecophysiological, evolutionary, phytopharming and biotechnological connotations of the novel phenomenon have been hypothesized.
Article
Full-text available
Patchouli (Pogostemon cablin), is a shrub with fragrant-smelling leaves from which patchouli oil is extracted. The oil has properties suitable for aromatherapy, relief of stress and anti-inflammatory activity. Water-steam distillation is the best method for extraction of patchouli oil. Fresh patchouli leaves gave much lower yield than dried leaves. Dried leaves fermented for 77 days at room temperature produced the highest yield (2.48% dry wt), which was much higher than from drying in an oven at 50°C for 40 h (0.30% dry wt). Soxhlet extraction of dried patchouli leaves with hexane for 15 h provided crude hexane extract (4.97% dry wt). The hexane extract was further separated and purified to obtain patchouli alcohol (0.05% dry wt), a mixture of β-sitosterol and stigmasterol (0.09% dry wt) and 7,3 ',4- tri-O-methyleriodictyol (0.04% dry wt). Antibacterial activity assay showed that patchouli oil could inhibit Staphylococcus aureus and Bacillus subtilis better than the hexane extract. Patchouli alcohol, a major component in patchouli oil, and the extract showed higher antibacterial activity than the mixture of β-sitosterol and stigmasterol and 7,3',4-tri-O-methyleriodictyol. Therefore, patchouli alcohol could be used as a marker for quality control of patchouli oils and the extracts. Quantitative determination of patchouli alcohol in the patchoulil oils and the hexane extract was performed by GC-MS using the new optimum conditions. The results showed that patchouli oil contained more patchouli alcohol than the hexane extract. Time of leaf harvesting (3 months, 6 months and 9 months) was also important. Three-month harvesting of patchouli leaves gave the highest amount of patchouli oil and patchouli alcohol.
Article
Full-text available
The genetic relationships among patchouli cultivars were determined by using Random Amplified Polymorphic DNA (RAPD) technology. Among 45 decamer random primers used for PCR reactions, 10 primers showed reproducible results. Out of 98 amplification products recorded, 16.7 per cent were monomorphic and 83.3 per cent were polymorphic. The highest dissimilarity (7.35) was detected between KSM 4 and 5 and the least 3.61 between KSM 2 and 3. Dendrogram constructed by cluster analysis of RAPD markers using Unweighted Pair Group Method of Arithmetic Averages (UPGMA) produced two major clusters Overall, RAPD analysis revealed the existence of considerable genetic variations in patchouli cultivars. This information regarding genetic variability at the molecular level could be used to identify and develop genetically unique germplasm that complements existing cultivars. Patchouli (Pogostemon cablin Benth.) belonging to the family Lamiaceae, is an aromatic herb cultivated on a commercial scale in India, Indonesia, Malaysia, China and Singapore. The commercial oil from patchouli is extensively used in perfumes and cosmetics (Hasegawa et al., 1992, Maheswari et al., 1993). The oil is widely used in the manufacture of soaps, scents, body lotions and detergents. It is been used to treat dysentery, diarrhea, colds without fevers, vomiting and nausea. The essential oil may be used to treat acne, dry skin, fungal infections, dermatitis, dandruff and eczema (Kalra et al., 2006). The fresh leaves can help in healing burns. In aromatherapy, it is used to calm nerves, control appetite, relieves depression, stress and lack of sexual interest (Bowel et al., 2002). It also possesses insecticidal, antibacterial and antifungal properties (Kukreja et al., 1990, Yang, 1996, Pattnaik et al., 1996). Fibrinolytic and anti thrombotic activity of this essential oil is also been reported (Sumi, 2003, Eunkyung et al., 2002). Indian demand for patchouli oil is around 220 tonnes valued at 33 crores while global demand is to the tune of 1600 tonnes of oil per annum with a value of 240 crores (Vijaya Kumar, 2004). India is importing annually about 20 tonnes of pure patchouli oil and 100 tonnes of formulated oil which is
Article
Full-text available
Trees, shrubs, subshrubs or perennial or annual herbs, rarely climbers, aromatic or not. Roots rarely tuberous. Stems often quadrangular, erect to prostrate, somtimes forming usually present, of glandular, rarely scale-like, usually multicellular-uniseriate, simple, branched, dendroid or stellate, sometimes gland-tipped, large-headed subsessile glands rarely absent.
Article
Full-text available
The study on the chemical constituents of an essential oil of Pogostemon cablin was carried out by hydrodistillation of leaf explants and the oil analysed by Gas Chromatography Mass Spectrometry (GC/MS). The oil yield was found to be 0.30 % (v/w) of fresh weight. Twenty two compounds were identified by GC/ MS as eighteen sesquiterpenes and three oxygenated sesquiterpenes. Among these, patchouli alcohol (60.30 %) was the major component, followed by germacrene A (11.73 %). In order to study the chemical constituents of the essential oil of plant cell cultures, leaves were surface sterilised and callus cultures initiated on MS media containing naphthaleneacetic acid (0.5 mg/l), and benzyladenine (1 mg/l), followed by incubation in suitable culture conditions. Cell suspension cultures were initiated by subculturing callus cultures into new liquid media and maintained in the same conditions. Chemical constituents of the essential oils produced by both callus and cell suspension cultures were extracted with dichloromethane and analysed by GC and GC/ MS. The results showed that essential oil obtained from these cultures contained the same major constituents, namely patchouli alcohol, as in the intact plant, but the level was low, and also contained a small amount of minor constituents. Feeding cis-farnesol, the precursor of patchouli alcohol, to cell suspension cultures resulted in the patchouli alcohol being increased from 19.5 mg/l to 25.5 mg/l.
Article
Full-text available
In the present study, the anti-influenza A (H2N2) virus activity of patchouli alcohol was studied in vitro, in vivo and in silico. The CC₅₀ of patchouli alcohol was above 20 µM. Patchouli alcohol could inhibit influenza virus with an IC₅₀ of 4.03 ± 0.23 µM. MTT assay showed that the inhibition by patchouli alcohol appears strongly after penetration of the virus into the cell. In the influenza mouse model, patchouli alcohol showed obvious protection against the viral infection at a dose of 5 mg/kg/day. Flexible docking and molecular dynamic simulations indicated that patchouli alcohol was bound to the neuraminidase protein of influenza virus, with an interaction energy of -40.38 kcal mol⁻¹. The invariant key active-site residues Asp151, Arg152, Glu119, Glu276 and Tyr406 played important roles during the binding process. Based on spatial and energetic criteria, patchouli alcohol interfered with the NA functions. Results presented here suggest that patchouli alcohol possesses anti-influenza A (H2N2) virus properties, and therefore is a potential source of anti-influenza agents for the pharmaceutical industry.
Book
The selection of plants studied in this treatise is based on its significance, and its representation of members of different taxonomic families as well as of different classes (and subclasses) of compounds. All the available data on the chemical compounds and the pharmacological studies on these plants/compounds have been incorporated. The plants are arranged by the type and nature of chemical compounds they contain. Secondary metabolites have been included in this volume due to their great therapeutic role.
Article
Figure optionsView in workspaceDownload full-size imageDownload as PowerPoint slide
Article
Chemical composition, antioxidant and antimicrobial activities of the essential oils from aerial parts of basil (Ocimum basilicum L.) as affected by four seasonal, namely summer, autumn, winter and spring growing variation were investigated. The hydro-distilled essential oils content ranged from 0.5% to 0.8%, the maximum amounts were observed in winter while minimum in summer. The essential oils consisted of linalool as the most abundant component (56.7-60.6%), followed by epi-α-cadinol (8.6-11.4%), α-bergamotene (7.4-9.2%) and γ-cadinene (3.2-5.4%). Samples collected in winter were found to be richer in oxygenated monoterpenes (68.9%), while those of summer were higher in sesquiterpene hydrocarbons (24.3%). The contents of most of the chemical constituents varied significantly (p<0.05) with different seasons. The essential oils investigated, exhibited good antioxidant activity as measurements by DPPH free radical-scavenging ability, bleaching β-carotene in linoleic acid system and inhibition of linoleic acid oxidation. Evaluation of antimicrobial activity of the essential oils and linalool, the most abundant component, against bacterial strains: Staphylococcus aureus, Escherichia coli, Bacillus subtilis, Pasteurella multocida and pathogenic fungi Aspergillus niger, Mucor mucedo, Fusarium solani, Botryodiplodia theobromae, Rhizopus solani was assessed by disc diffusion method and measurement of determination of minimum inhibitory concentration. The results of antimicrobial assays indicated that all the tested microorganisms were affected. Both the antioxidant and antimicrobial activities of the oils varied significantly (p<0.05), as seasons changed. Copyright © 2007 Elsevier Ltd. All rights reserved.
Article
Rosmarinus officinalis is widely found in the lands of Aegean and Mediterranean regions of Turkey. The goal of this work was to test the antimicrobial activity of the essential oils and methanolic extracts of R. officinalis collected from three different regions at four different time intervals of the year against Staphylococcus aureus, Proteus vulgaris, Pseudomonas aeruginosa, Klebsiella pneumonia, Enterococcus feacalis, Escherichia coli, Staphylococcus epidermidis, Bacillus subtilis and Candida albicans. Essential oils were obtained from the aerial parts of the plant by using a Clevenger apparatus, for 4 h. After distillation, the distillates were filtered, air-dried and then extracted by using a Soxhlet apparatus for 9 h to obtain the methanolic extracts. The antimicrobial activities of the methanolic extracts were tested by the disc diffusion technique. The antimicrobial activities of the essential oils obtained from R. officinalis were determined by minimum inhibitory concentration (MIC).The results indicated that the tested bacteria were sensitive to the essential oils and partially to the methanolic extracts. The antimicrobial activities of the essential oils against the tested bacteria differed, depending on location and seasonal variations.
Article
A toxicologic and dermatologic review of patchouli alcohol when used as a fragrance ingredient is presented.