International Journal of Scientific & Engineering Research, Volume 4, Issue 4, April‐2013 238

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Evaluation of Anti Tumor Activity of Curcuma

Amda Roxb. Rhizome

Amit Upadhyay*1, Ravi Kant Sharma1, Gurdeep Singh1, A.K. Jain2

Abstract- Aqueous and alcoholic extracts of curcuma amda roxb. rhizomes have been evaluated for its anti tumour activity in Swiss albino mice. Alcoholic extract exhibited more potent anti tumour activity than aqueous extract. In-vitro cytotoxicity studies were confirmed by brine shrimp bioassay method. A significant increase in the life span and a decrease in the cancer cell number and tumour weight were noted in the tumour induced mice after treatment with both of the extracts in ehrlich ascites carcinoma (EAC) model. The hematological parameters were also corrected by aqueous and ethanolic extracts in tumour induced mice. These observations are suggestive of the anti tumour effect of aqueous and alcoholic extracts of Curcuma amda Roxb. rhizomes in ehrlich ascites carcinoma.

Keywords- anti tumour activity, brine shrimp bioassay, curcuma amda roxb., ehrlich ascites carcinoma.

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I. INTRODUCTION
Cancer is a major cause of concern for public health service in most developed as well as under developed countries. The present study is focused on the evaluation of anti cancer activity of aqueous and alcoholic extracts of curcuma amda roxb. Rhizomes on primary stages of cancer. Curcuma amda roxb. is a species belongs to India and has not been worked for its possible anti cancer activity. On the basis of above facts, the present study has been under taken on the plant to carry out a preliminary investigation for its possible anticancer activity by in-vitro cytotoxic activity in the brine shrimp lethality bioassay method. Further in-vivo anti tumour activity was confirmed in the ehrlich ascites carcinoma model.
II. MATERIALS AND METHODS
Whole plant of curcuma amda roxb. was collected in and around sheopur (M.P.) district and authenticated by Dr. R.A.S. Chauhan, H.O.D., department of Botany, Ambah post graduation college, Ambah, Morena, M.P.
For alcoholic extraction, the crude drug was shade dried for thirty days and than coarsely powdered. The coarse powder was loaded in thimble made of whatman filter no.1 and extracted
in the soxhlet extraction column with 1-2 L of 95% alcohol for 30-40 cycles for each batch. The extract so obtained was thick and syrupy with characteristic odour. The final extract was thick and was stored separately in vacuum.
For aqueous extraction, a dried coarse powdered crude drug was transferred to the round bottom flask and 1.5-2 L of distilled water was added to the round bottom flask and soaked for 24 hrs. this was then boiled for 4-5 hrs. the extract so For aqueous extraction, a dried coarse
powdered crude drug was transferred to the round bottom flask and 1.5-2 L of distilled water was added to the round bottom flask and soaked for 24 hrs. this was then boiled for 4-5 hrs. the extract so obtained was decanted in to beaker and then
concentrated to 1/6th of the total volume on water bath. This was preserved by adding few drops of
chloroform and kept in the refrigerator.

III. IN-VITRO CYTOTOXICITY STUDIES

Brine shrimp (artemia salina) eggs were collected from the fisheries research station Banglore and stored in an airtight opaque container at room temperature. Drug samples of the concentration 10,
100, 1000 mcg/ml were prepared and transferred to vials of 7 ml capacity. Three replicate were

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prepared for each dose level. Control vials were prepared by adding equal volumes of distilled water. Hatching of brine shrimp eggs was done by adding 2.5 L of artificial sea water to the special chamber. About 30 mg of the eggs were washed with water and then sprinkled in to the compartment which was darkened, aeration was provided in the compartments. After 48 hrs the photographic nauplli were collected by pipette from the lighted side and used for bioassay.
To carry out bioassay 48 hr. old nauplli were drawn in a pipette along with water and ten nauplli were transferred to each sample vial and artificial sea water was added to each vial and volume was made up to 5 ml. A drop of dry yeast suspension (3 mg in 5 ml sea water) was added to each vial as food for shrimps. The vials were maintained under illumination. After 24 hrs survivors were counted, by using 5X magnifying glass, and the percent deaths and Lc50 values were calculated by using provit method for aqueous and alcoholic extracts.

IV. ACUTE TOXICITY STUDY

Albino mice of either sex weighing 20-30 gm were selected. Drug samples were prepared by dissolving in water by heating and these were administered intraperitonialy. Three groups for each extract containing two animals in each group were used. Drugs were administered intraperitonialy after administration the animals were observed continuously for 1 hr, frequently for the next four hrs and then after 24 hrs.

V. In‐vivo anticancer studies on mouse ehrlich

ascites carcinoma

:
Swiss albino mice from an inbred colony maintained under controlled conditions of light (12:12 hrs light:dark), temperature (25±20c) and humidity were used. Six to eight weeks old female
mice weighing 25±5 gm were used. All the animals were divided in to four groups (N=6), group 1 (tumour control), group 2(cisplatin), group
3(alcoholic extract of curcuma amda roxb.) and
group four (aqueous extract of curcuma amda roxb.). The doses selected for the extracts were about 1/10th of the safe dose found in acute toxicity
100mg/kg for group 3rd and 4th respectively. Both of the extracts were administered once a day, in the volume of 0.1 ml/10gm mouse through intraperitonial route. EAC was maintained and propagated intraperitonialy by serial transplantation in adult female swiss albino mice. The ascetic carcinoma bearing mice (donor) was taken 15 days after tumour transplantation.the ascetic fluid was drawn by using a 18 gauge needle in to sterile syringe and tumour viability was determined by trypan blue exclusion test and cells were counted using haemocytometer the ascetic fluid was suitably diluted in normal saline to get a concentration of 10cells/ml of tumour cells suspension. This was injected intraperitonialy to obtain ascetic tumour. The mice were weighed on the day of tumour inoculation and then for each
three days. Treatment was started from 10th day of tumour inoculation. Cisplatin (one dose) was injected on 10th day intraperitonialy. Extracts were
administered from 10th day for five days intra peritonialy. Parameters monitored during the study were percentage increase in weight as compared to day 0 weights, median survival time(MST) and
percentage increase in life span (% ILS), mean survival time(MEST), cell viability test (% survivors of malignant cells in ascetic fluid) and haematological parameters (total W.B.C. and
differential leukocyte counts, total R.B.C. and IV. haemoglobin content). All experimental protocols were approved by institutional animal ethics committee, S.R.C.P. Banmore and statistical analysis result were analysed by oneway ANOVA by ORIGIN 60 computer package.

Results and discussion:

Both the extract showed considerable cytotoxic activity in the brine shrimp lethality bioassay. The alcoholic extract of curcuma amda roxb. Was found to be very potent. In in-vivo cancer model (ehrlich ascites carcinoma model). The plant extract significantly reversed the tumour induced changes in the parameter monitored.

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Ta ble: summa ry of in vivo a ntica ncer a nt ica ncer studies on mouse ebrlicb ascites ca rcinoma


P3r3meters Groups 1" 2"" 3.-d 4"'

%increase in wl as compared to day 0

DayO

3.445±2.11

3.22±1 . 14

2. 36±66

2.27±1.31

SUrvival timeintumour

Day6

Day9

Day 12

Day 15

Median survival

MST

6.544±245

15.712±22

16. 33±211

19.65±217

16

10.66±0.21

18.66±0.34

16.68±23

0.412±266

22

12. 2±2.66

22. 91±3.3

18. 66±278

12. 11±2. 86

17

11.60±1.77

16. 16±213

0.06±1.2

0.03±0.11

19.6

induced mice

time (days)

%TIC 1 40 110.2 120.24

Mean survival

%ILS

MST

16. 10±1.4

46

22.77±0.8

II

19.71:1:213

19. 98

17. 91:1:0. 55

time(days)

%TIC

I SO

123

1 1 2

%ILS

48

24

17. 67

Tumour living

cell

No. ofTumour

19. 38±0. 17

8.66±0. 64

11 . 52±1. 10

10. 75±0. 62

no. in ascitic fluid of

tumour inducedmice living cell(millioo

cellslcm3) (mean±SE)

%decrease in 56.44 42. 75 45. 56 tumour cells

(compared to

control)

Total and differential Total no. ofWBC 31066±1190 10512±1066 201100±1128 25177±2019 countofWBC in tumour

bearing mice

celllmm3

Differential count Lymphocytes 40.4±1.16 72.1 . 66 52.4±7. 2 67.2±0.55

Neutrophils 56±1.12 20.3±0.72 42. 1:1:0.11 28. 1±0.11

Monocytes 1 .2±0.22 1.62±0.42 1.66±0.12 1.57±0.28

Total no. ofRBC Total no. (million 2.18±0.22 3.1 1 ±0. 56 2.98±0. 23 2. 63±36

I

Haemoglobin (gm"/o) Haemoglobin 9.6±0.4 12.2±0.65 10.12±0.87 11. 3±0.11 (gm%)

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