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Journal <strong>of</strong> Current Pharmaceutical Research 2010; 3(1): 47-50<br />

been reported in this regard. In the present study, sincere effort has<br />

been attempted to establish the scientific validity <strong>of</strong> the antiinflammatory<br />

activity <strong>of</strong> the aerial part <strong>of</strong> plant.<br />

2. MATERIALS AND METHODS<br />

Plant material<br />

The fresh leaves <strong>of</strong> the plant Indig<strong>of</strong>era tinctoria Linn.<br />

were collected from Budhara, Porsa <strong>and</strong> campus <strong>of</strong> Shri R.N.S<br />

College <strong>of</strong> Pharmacy Gormi, Bhind (M.P.). It was further<br />

authenticated by taxonomist Dr. A. N. Rai, department <strong>of</strong> Botany,<br />

Dr. H.S. Gour University, Sagar,M.P. The leaves were cut into<br />

small pieces <strong>and</strong> shade dried at room temperature, dried leaves was<br />

subject to size reduction to a coarse powder by using a dry grinder.<br />

Chemicals<br />

Carrageenan was purchased from Himedia Laboratories<br />

Pvt. Ltd., Mumbai <strong>and</strong> Ibupr<strong>of</strong>en was obtained from Glenmark<br />

Pharmaceutical Ltd., Mumbai as a gift sample.<br />

Animal experiments<br />

Wister albino rats weighing 200±20 g were taken from<br />

Shri R.N.S College <strong>of</strong> Pharmacy, Gormi, Bhind (M.P.) <strong>and</strong><br />

maintained under constant condition (temperature: 20±2 o C,<br />

humidity: 40-60% , 12-h light/ 12-h dark cycle) for two weeks <strong>and</strong><br />

housed in stainless steel cages in a laboratory room. The animals<br />

were access to water ad libitum <strong>and</strong> st<strong>and</strong>ard rodent diet. All<br />

animal experiment conducted in accordance with Institutional<br />

Animal Ethical Committee (IAEC licence<br />

no1030/A/07/CPCSEA.).<br />

Table 1. Phytochemical <strong>screening</strong> <strong>of</strong> Petroleum ether & ethanolic<br />

extracts <strong>of</strong> Indig<strong>of</strong>era Tinctoria linn.<br />

Preparation <strong>of</strong> plant Extract<br />

The course powder plant material was extracted with<br />

petroleum ether (60-80 o C) for 72 hours <strong>and</strong> then using ethanol in<br />

soxhlet extractor for 48 hours (Harbosne et.al., 1984). Alcoholic<br />

extract was concentrated under the vacuum in rotary flash<br />

evaporator <strong>and</strong> successively in hot air oven till solid to semisolid<br />

mass. Extracts were stored in an airtight container in refrigerator<br />

below 10 o C.<br />

<strong>Preliminary</strong> <strong>phytochemical</strong> investigations:-<br />

The petroleum ether extract <strong>and</strong> ethanolic extract<br />

subjected to preliminary qualitative chemical analysis. St<strong>and</strong>ard<br />

method were used for preliminary <strong>phytochemical</strong> <strong>screening</strong> <strong>of</strong> the<br />

extract was performed to know the phytoconstituents in the extract<br />

.(Kokate. et.al., 2007, Kh<strong>and</strong>elwal et.al.,2004), <strong>and</strong> it was found<br />

that extract contains carbohydrate, glycosides, proteins, steroid,<br />

amino acids, tannins <strong>and</strong> flavoniods.<br />

Table 2. Physical contents <strong>of</strong> leaves <strong>of</strong> Indig<strong>of</strong>era Tinctoria linn.<br />

S. NO. PARAMETERS PERCENTAGE<br />

1. Total ash 12.5%<br />

2. Acid insoluble ash 3.5%<br />

3. Water soluble ash 9%<br />

4 Sulphated ash 20%<br />

5. Extractive value 14.2%<br />

6. Loss on drying 6.9%<br />

S.<br />

NO.<br />

PHOTOCHEMICAL<br />

CONSTITUENTS<br />

EXTRACT<br />

PETROLEUM<br />

ETHER<br />

1. Alkaloids - -<br />

2. Fats <strong>and</strong> oils + -<br />

3. Carbohydrates - +<br />

4. Glycosides + +<br />

5. Steroids + +<br />

6. proteins - +<br />

7. Amino acid - -<br />

8. Tannins - +<br />

9. Flavonoides - +<br />

ETHANOL<br />

Determination <strong>of</strong> physical constants:-<br />

Leaves analysis parameters like total ash, acid insoluble<br />

ash, water soluble ash, Sulphated ash, loss on drying were use for<br />

the determination <strong>of</strong> quality <strong>and</strong> purity <strong>of</strong> the crude drug <strong>and</strong><br />

extractive value were used for evaluation <strong>and</strong> study <strong>of</strong> antiinflammatory<br />

activity (Evans et .al., 2002) .<br />

Ethanolic extract <strong>of</strong> leaves <strong>of</strong> Indig<strong>of</strong>era tinctoria linn<br />

(250, 500 & 1000 mg/kg bwt, p.o.) were prepared in tween 80<br />

(1%w/v solution).<br />

Carrageenan induced paw oedema in rats<br />

Pedal inflammation in hind paw <strong>of</strong> Wister albino rats<br />

(200±20 g) was produced according the method described (by<br />

Winter,et.al., 1962). Oedema was induced by sub-planter injection<br />

(+) represent presence & (-) absence <strong>of</strong> respective components<br />

48

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