Chemical Composition, Cytotoxicity and Antioxidant Activity of Essential Oils of Acalypha hispida Flowers
Acalypha hispida (Burm.) F. flowers (Euphorbiaceae) were subjected to distillation using a hydro-distiller (all-glass Clavenger apparatus) to extract the essential oil present in the plant samples. GC and GC/MS analysis were carried out on the essential oil and was found to contain 44 compounds constituting 99.98% of the total oil composition. The compounds were identified by spectral comparison to be mainly alcohols, esters, ketones, terpenes and hydrocarbons. The principal constituents are 15, 16-Epoxylabda-13 (16), 14-dien-8α-ol (12.75%), 8, 14-Cedranoxide (12.19%), Curcumene (10.14%), 1-Hexandecene (8.37%) and Ethyl vanillin (6.87%) while others were present in trace amounts. Brine shrimp lethality assay was carried out using brine shrimps at 10, 100 and 1000 ppm to determine the toxicity of the oils to living organisms (shrimps). LC50 value (μg mL-1) of 4.3715 obtained showed that the essential oil of A. hispida flower is toxic. The antioxidant properties of essential oils of A. hispida flowers were investigated using the UV/Visible spectrophotometer. The oil exhibited weak activity as a radical scavenger in the experiment using 2, 2-diphenyl-1-picrylhydrazyl radical (DPPH), indicating that A. hispida oil has very weak ability to donate hydrogen when compared with the standard Butylatedhydroxylanisole (BHA). The absorption is stoichiometric with respect to the number of electron taken up. At 20 μg mL-1, the oil activity was 0.9360±0.037 (26.5% inhibition) which was less than that of BHA (70.2%).
October 15, 2010; Accepted: January 11, 2011;
Published: February 09, 2011
Antioxidant are agents that neutralizes harmful compounds called free radicals
which damage living cells, spoil food and degrade materials such as rubber,
gasoline and lubricating oils. Antioxidants can take the form of drugs e.g.,
enzymes in the body, vitamin supplements or industrial additives. They are routinely
added to metals, oils, foodstuffs and other materials to prevent free radical
damage. Free radicals also play very important roles in human health and are
beneficial in combating several diseases. However, excess formation is harmful
to the body organs. Any molecule can become a free radical by either losing
or gaining an electron. Once initiated these free radicals get involved in chain
reaction with stable types. The compounds thus formed have longer stability
in the body and increase the potential for cellular damage. Free radicals damage
the cell at the site of their operation causing serious health disorders. Antioxidants
therefore, work to control the level of free radicals before they do oxidative
damage to the body (Alan and Miller, 1996; Gill,
1992; Halliwell, 1999; Newman
et al., 2000).
Essential oils are employed as antioxidants due to their small molecular size
and their ability to easily penetrate the skin tissue. They are lipid soluble
and are capable of penetrating the membranes easily even in conditions where
oxygen deficiency leads to hardening of membranes. Studies reveal that essential
oils serve as powerful antioxidants that produce adverse environment for damaging
free radicals thus, preventing mutations and oxidants in cells. They therefore
function as scavengers for free radicals. Essential oils may be extracted from
plants, fruits, flowers, barks, roots and seeds with each possessing unique
characteristics (Potterat, 1997; Bray,
The plant Acalypha belongs to the sole genus subtribe Acalyphinae of
the family Euphorbiaceae which comprises about 570 species, a large portion
of which are weeds while others are ornamental plants. They are found in the
tropics of Africa, America and Asia. Some of the species are well known in folklore
medicine and a few have actually appeared in homeopathic pharmacopoeia. Acalypha
hispida also known as chenille plant or Philippine medusa appears as a small
shrub growing to a height of 1-3 m. In ethno-medical practices, the root and
flower decoction is used for kidney ailments and as a diuretic. Leaf poultice
is used as a cure for leprosy, the decoction of leaves and flowers are taken
internally as laxative and for treatment of gonorrhea. Bark is used as expectorant
and for asthma (Iwu et al., 1999;
Kafaru, 2000; Sofowora, 2008). Previous work done
on the leaves of A. hispida revealed the presence of phenolics, flavonoids,
glycosides, steroids, saponins, phlobatannins, and hydroxyanthraquinones (Iniagbe
et al., 2009; Okorondu et al., 2009).
The antifungal, antibacterial, anti-ulcer and anti-tumor properties of extracts
of leaves of A. hispida have been established (Ejechi
and Soucey, 1999; Adesina et al., 2000; Gutierrez-Lugo
et al., 2002). In this study we report the cytotoxicity and antioxidant
activities of essential oils of A. hispida flowers. The goal was achieved
by subjecting the essential oil of A. hispida to Brine shrimp lethality
assay for determination of the toxic level. In vitro antioxidant assay
determined by the effect on DPPH radical (2, 2-diphenyl-1-picrylhydrazyl) was
carried out. DPPH radical gives strong absorption at 517 nm (deep violet colour)
in visible spectroscopy. The absorption vanishes or is decolorized as the electron
becomes paired off in the presence of a free radical scavenger.
MATERIALS AND METHODS
Plant materials: Fresh samples of the A. hispida flowers were collected in September, 2009 at the Botanical Gardens, University of Ibadan. Specimens were identified at the Botany and Microbiology Department, University of Ibadan, Oyo State, Nigeria. The volatile oil was immediately collected from the fresh plant material by hydrodistillation.
Reagents: Hexane and methanol (BDH chemicals), Butylated Hydroxyanisole (BHA) and 2, 2-diphenyl-1-picrylhydrazyl radical (DPPH) were obtained from were obtained from Sigma Chemical Co. (Germany).
Major equipment used: UV-Visible Spectrophotometer (Unico1200 and Perkin Elmer lambda 25 models), GC-Mass spectrophotometer (Agilent Technologies), Hydro distiller-Clavenger apparatus.
Isolation of essential oils: The oil was obtained by hydro distillation
on a Clavenger type apparatus for 4 h in accordance with the British pharmacopoeia
specifications (1980). The essential oil was collected and stored at 4°C
until analysis. The oil yield was calculated relative to the dry matter.
Analysis of the essential oils
Gas chromatography: GC-MS analyses of the essential oil was analyzed
on an Agilent Technologies 7890A GC system coupled to a 5975C VLMSD mass spectrometer
with an injector 7683B series device. An Agilent (9091)-413:325°C HP-5 column
(30 mx320 μmx0.25 μm) was used with helium as carrier gas at a flow
rate of 3.3245 mL min-1. The GC oven temperature was initially programmed
at 50°C (hold for 1min) and finally at 300°C (hold for 5 min) at a rate
of 80°C min-1 while the trial temperature was 37.25°C. The
column heater was set at 250°C and was a split less mode while the pressure
was 10.153 psi with an average velocity of 66.45 cm sec-1 and a hold-up
time of 0.75245 min was recorded. Mass spectrometry was run in the Electron
Impact mode (EI) at 70 eV. The percentage compositions were obtained from electronic
integration measurements using Flame Ionization Detector (FID), set at 250°C.
The peak numbers and relative percentages of the characterized components are
given in Table 1.
Gas chromatography-mass spectrometry: The essential oils were analysed by GC-MS using an Agilent Technologies 7890A GC system coupled to a 5975C VLMSD mass spectrometer with an injector 7683B series device. An Agilent (9091)-413:325°C HP-5 column (30 m x 320 μm x 0.25 μm) was used with helium as carrier gas at a flow rate of 3.3245 mL min-1. GC oven temperature and conditions were as described above. The injector temperature was at 250°C. Mass spectra were recorded at 70 eV. Mass range was from m/z 30 to 500.
Identification of components: The individual constituents of the oil
were identified on the basis of their retention indices determined with a reference
to a homologous series of n-alkanes and by comparison of their mass spectral
fragmentation patterns (NIST 08.L database/chemstation data system) with data
previously reported in literature by Adams (2001), Joulain
and Konig, (1998), Mclafferty and Stauffer (1989).
Brine shrimp lethality test: The Brine Shrimp Lethality Test (BST) was
used to predict the presence in the oils, of cytotoxic activity (Meyer
et al., 1982). The shrimps eggs were hatched in sea water for
48 h at room temperature. The nauplii (harvested shrimps) were attracted to
one side of the vials with a light source. Solutions of the extracts were made
in DMSO, at varying concentrations (1000, 100, and 10 μg mL-1)
and incubated in triplicate vials with the brine shrimp larvae. Ten brine shrimp
larvae were placed in each of the triplicate vials. Control brine shrimp larvae
were placed in a mixture of sea water and DMSO only.
||Chemical composition of the essential oil from the flowers
of A. hispida by GC and GC/ MS analysis*
After 24 h the vials were examined against a lighted background and the average
number of larvae that survived in each vial was determined. The concentration
at fifty percent mortality of the larvae (LC50) was determined using
the Finney computer programme.
Scavenging effect on DPPH: A 0.5 mM of the radical source 2, 2-diphenyl-1-picrylhydrazyl
radical (DPPH) solution in methanol was prepared, and 3 mL of this solution
was mixed with 1 mL of the oil sample in methanol (Koleva
et al., 2002; Oloyede and Farombi, 2010).
The decrease in absorption at 517 nm of DPPH was measured after 10 min of incubation.
The actual decrease in absorption was measured against that of the control and
the percentage inhibition was also calculated. The same experiment was carried
out on butylatedhydroxylanisole (BHA) a known antioxidant. All test and analysis
were run in triplicates and the result obtained was averaged. The activities
were determined as a function of their %Inhibition which was calculated using
RESULTS AND DISCUSSION
The yield of the A. hispida flower oil was 0.40% (w/w) from 300 g of
the fresh flowers used. The colourless essential oils with characteristic smell
were analyzed both by GC and GC/MS systems using a polar column, resulting in
the identification of only 44 constituents in the hydrodistilled sample, representing
99.98% of the total essential oil. The oil yield of A. hispida is low
considering the fact that flowers are known to be rich in essential oils. Overall,
alcohols, esters, terpenes and hydrocarbons were found in the sample as the
dominating group of compounds (Table 1) for the hydro distilled
samples. Many chemical compounds of medicinal importance are been reported from
A. hispida (Iniagbe et al., 2009; Okorondu
et al., 2009). The nor-labdane-type diterpene 15, 16-Epoxylabda-13
(16), 14-dien-8α-ol reported in this plant has also been isolated from
another specie of Acalypha (Gina et al., 2006).
The cytotoxicity result of the essential oil showed an average death of 10 (10000
ppm), 16 (1000 ppm) and 22 (100 ppm). An LC50 value of 4.3715 μg
mL-1 with lower and upper confidence limits of 253.7717 and 426221.1000
μg mL-1, respectively showed that the essential oil of A.
hispida flower is toxic and therefore, its use at higher concentrations
should be monitored. The LC50 (μg mL-1) results is
further corroborated by the presence in the oil of hydrocarbon molecules which
accounts for the high toxicity of the oil. The free radical scavenging activity
was evaluated by the decrease in absorption of the stable hydroxyl radical 2,2-diphenylpicryl
hydrazyl radical (DPPH) at 517 nm. A. hispida essential oil decolorized
DPPH due to its hydrogen donating ability. The activity of the essential oil
of A. hispida flower on the stable radical DPPH decreased with decrease
in concentration. The free radical scavenging activity was compared with the
activities of a known antioxidant Butylated hydroxyanisole (BHA). At 20 μg
mL-1, the oil activity was 0.9360±0.037 (26.5% inhibition)
which was less than BHA (70.2%), at 40 μg mL-1 it was 0.7781±0.023
(21.3%) which was also less than BHA (65%) and at 60 μg mL-1
the activity was 0.6421±0.010 (5.26%) which was also less than BHA (62.5%).
Hence the oil of this plant has low antioxidant activity. The absorption is
stoichiometric with respect to the number of electron taken up. The percentage
inhibition is concentration dependent. DPPH is known to be a stable free radical
and accepts an electron or hydrogen radical to become a stable diamagnetic molecule
(Soares et al., 1997). The toxic nature of essential
oil from A. hispida flower shows that it has medicinal importance as
it has been established by other workers that secondary metabolites from plants
which are active medicinally are most times toxic to Brine shrimp larvae Artermia
silina nauplii which is a living organism with no advance nervous system
(Aiyelaagbe et al., 2009; Oloyede
et al., 2010). The results obtained from free radical scavenging
activities of the plant by using scavenging effect on 2,2-diphenylpicryl hydrazyl
radical (DPPH) and hydrogen peroxide method has shown that A hispida
is effective as an antioxidant; this result is also in agreement with results
obtained by other workers in screening medicinal plants for antioxidant activities
(Soares et al., 1997; Alma
et al., 2003; Mutes et al., 2010).
The essential oil composition of A. hispida flower investigated revealed
the presences of 44 compounds as determined by GC and GC/MS analysis constituting
99.98% of the total oil composition. The compounds were identified by spectral
comparison to be mainly alcohols, esters, ketones, terpenes and hydrocarbons.
The principal constituents are 15,16-Epoxylabda-13(16),14-dien-8α-ol (12.75%),
8,14-Cedranoxide (12.19%), Curcumene (10.14%), 1-Hexandecene (8.37%) and Ethyl
vanillin (6.87%) Brine shrimp lethality assay showed that the essential oil
of A. hispida flower is toxic (LC50 value (μg mL-1)
of 4.3715). The antioxidant properties of essential oils of A. hispida flowers
revealed weak activity as a radical scavenger in the experiment using 2, 2-diphenyl-1-picrylhydrazyl
radical (DPPH) indicating that A. hispida oil has very weak ability to
donate hydrogen when compared with a standard Butylatedhydroxylanisole (BHA).
The absorption is stoichiometric with respect to the number of electron taken
up. At 20 μg mL-1, the oil activity was 26.5% which was less
than that of BHA (70.2%). Thus the ability to scavenge free radicals is an important
property in order to minimize oxidative damage to living cells. Synthetic free
radicals available e.g., BHA and BHT have been found to be toxic, responsible
for liver damage, promoters of carcinogenesis and general consumer rejection
of synthetic food additives hence the need for their replacement with natural
antioxidants (Gulcin et al., 2002) that will
be supplied to human and animal organisms as food supplements or as specific
pharmaceutics (Azuma et al., 1995). This plant
may be found useful as antitumour, anticancer or antimicrobial agents due to
its high toxicity but its use must be monitored at high dosage level. Also the
nor-labdane-type diterpene 15, 16-Epoxylabda-13 (16), 14-dien-8α-ol is
a potential source of anti tumour agent. This compound has also been isolated
from another specie of Acalypha (Gina et al.,
2006). Cedranoxide found in the plant is a good source of insect pheromone
employed as sex attractant. The bisabolane sesquiterpenes curcumene is used
as insecticides, repellents, and insect feeding deterrents.
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