Formulation of Polyherbal and Evaluation for Anti Diabetic Effect

 

H.S. Chandel1, A. Pathak2 and M. Tailang2*

1Truba Institute of Pharmacy- Bhopal (M.P), India

2Department of Pharmacy, Barkatullah University- Bhopal(M.P), India

3Department of Drug Technology, Faculty of Medical Technology- Derna, Libya

 

INTRODUCTION:

Herbal medicines have played a vital role in the therapeutics when safe and efficient therapy is required. Herbs had been used by all cultures throughout history but India has one of the oldest, richest and most diverse cultural living traditions associated with the use of medicinal plants1. Presently the need for herbal drugs is growing because of the fact that these are biosafe with no side effects. Many analysis-based studies regarding pharmacological research in India2,3, have been conducted in the past. Pharmaceutical research across the world shows that, natural products are potential sources of novel molecules for drug development4 .

Diabetes is the world’s largest endocrine disease involving metabolic disorder of carbohydrate, fat and protein. According to the WHO projections, the prevalence of diabetes is likely to increase by 35%5. Statistical projections about India suggest that the number of diabetics will rise from 15 million in 1995 to 57 million in the year of 2025 making it the country with the highest number of diabetics in the world6. In this work a polyherbal formulation was developed and compared with that of a marketed formulation.

 

MATERIALS AND METHODS:

Different herbs based on exhaustive literature survey were selected and these were authenticated by the Head Department of Pharmacy Barkatullah University Bhopal. Purified water was used in the entire study.

 

Method of Preparation

1.      All the individual drugs were dried using hot air oven at 40şC for 24 hours.

2.      The individual drugs were then crushed using Willing grinder and passed through mesh no. 40.

3.      The individual drugs were then weighed as per the quantity required on digital precision balance (Accuracy: 0.1g, Jyoti Scientific, India).

4.      The drugs were mixed geometrically using double cone blender (Jyoti Scientific, India; TIP/PCS/DCB/01).

The mixed formulation was unloaded in a polythene bag, weighed, labeled and packed in glass bottles. The weight of the formulation was 100 grams. Two formulations with different herbs were prepared. Both the formulations were prepared with same method as reported. The constituents of both the formulations are as follows:

 

 


Table 1 Ingredients for Formulation 1

Sr. No.

Ingredient

Quantity taken

1.                  

Gudmar foil

15 gm

2.                  

Jamun seed

15 gm

3.                  

Karela seed

10 gm

4.                  

Kundroo root

10 gm

5.                  

Asgandg

10 gm

6.                  

Pure shilajeet

1 gm

7.                  

Neem Kauree

10 gm

8.                  

Gurhal pushp

5 gm

9.                  

Tulsi root

9 gm

10.                

Vijaysar wood

15 gm

 

Pharmacological Evaluation

The methanolic extracts of the formulations were utilized for the pharmacological screening of the formulations. One gram of methanolic extracts of in-house prepared formulations were separately triturated with polyvinyl pyrrolidone (PVP 0.2 g) and added water for injection in success amount to make up the final volume to 100 ml (0.2%w/v). Adult albino rats of either sex (100-200 Gms) were selected for the study and were divided in to groups of six in each group. Rats were acclimatized for a period of two-three days in the new environment and subsequently used for further study. Toxicological studies revealed that albino rats tolerated considerably high dose of methanolic extract (700 µg/kg body weight, orally) without any toxic manifestation. Therefore doses of 150 µg twice a day/kg-body weight, twice a day, of methanolic extracts were administered orally to the alloxan induced diabetic albino rats7. Animals were divided in four groups of six animals each. The diabetes was experimentally induced by i.v. administration of alloxan monohydrate 150 µg twice a day/kg of body weight. Alloxan is given by rapid intravenous injection, as its half-life in the body is only a few seconds. The diabetes is induced within 24 hours if the rats were fasted before the alloxan injection. Diabetes is checked by measuring blood glucose level using Glucometer8. Haemo gluco test 200-800R(HGT) method was utilized for the measurement of blood glucose level. Blood Sample collected by retro orbital puncture under light ether anesthesia. The blood glucose level was determined after fixed intervals of four days and the study was continued for a period of twenty-eight days.

 

Group-I: Control

Adult albino rats were fed with 0.1 ml poly vinyl pyrolidone (PVP) solution (0.2%w/v).

Group-II: Glibenclamide treated

Adult albino rats were orally administered with 50 µg twice a day/Kg of body weight of Glibenclamide.

Group-III: Formulation-1 extract treated

Adult albino rats were orally administered with 150 µg twice a day/kg of body weight of methanolic extract of Formulation-1.

Group-IV: Marketed formulation extract treated

Adult albino rats were orally administered with 150 µg twice a day/kg of body weight of methanolic extract of Madhushoonya (Meghdoot).

 


 

 

 

Table 2. Estimation of Blood glucose level in alloxan induced diabetic albino rats.

Group

AIBGL

Mg/dL

First

Day

(mg/dl)

Forth

Day

(mg/dl)

Eighth

Day

(mg/dl)

Twelfth

Day

(mg/dl)

Sixteenth

Day

(mg/dl)

Twentieth

Day

(mg/dl)

Twenty- Forth Day (mg/dl)

Twenty- Eighth Day

(mg/dl)

GP-I

2% PVP w/v 0.1 ml

368.67

± 5.13

365.05

± 6.15

365.33 ±10.36

362.66 ±9.15

358.01

± 5.19

356.67 ±15.3

353.33

± 6.33

352.33

± 11.55

249.67

± 6.89

GP-II

Glibenclamide

50 µg twice a day/Kg

304.17

± 9.60

266.49 ± 6.11

210.33 ± 8.11

188.32

±12.11

165.33 ±11.52

154.33 ±5.56

134.5  ±5.89

121.14 ±13.23

101.33  ±5.33

GP-III

Formulation-1

150 µg twice a day/Kg

384.65

±8.36

365.87

±11.45

317.69

±8.56

268.47

±11.76

222.47

±9.21

186.23

±12.45

142.87

±10.58

119.46

±12.47

102.56

±10.56

GP-IV

Marketed Formulation 150 µg twice a day/Kg

356.78

±7.63

348.43

±8.43

310.67

±13.71

264.95

±14.42

218.46

±12.25

184.21

±11.43

142.38

±12.46

122.54

±12.42

105.78

±8.36

Values reported are Mean ± S.D. and n=6; AIBGL: Alloxan induced blood glucose level

 

Table 3. Percentage reduction of Blood glucose level in alloxan induced diabetic albino rats.

Group

First

Day

(mg/dl)

Forth

Day

(mg/dl)

Eighth

Day

(mg/dl)

Twelfth

Day

(mg/dl)

Sixteenth

Day

(mg/dl)

Twentieth

Day

(mg/dl)

Twenty- Forth

Day (mg/dl)

Twenty-Eighth Day

(mg/dl)

GP-I

2% PVP w/v 0.1 ml

0.98

0.97

1.63

2.71

3.25

4.16

4.43

5.15

GP-II

Glibenclamide

50 µg twice a day/Kg

12.38

30.85

38.08

45.64

49.26

55.78

60.17

66.68

GP-III

Formulation-1

150 µg twice a day/Kg

4.88

17.41

30.20

42.16

51.58

62.86

68.94

73.34

GP-IV

Marketed Formulation

150 µg twice a day/Kg

2.34

12.92

25.74

38.77

48.37

60.09

65.65

70.35


RESULTS AND DISCUSSION:

In the present work, we evaluated the hypoglycemic activity of the methanolic extracts of the marketed and prepared in-house formulations in alloxan induced diabetic rats. As shown in the table the methanolic extracts significantly reduced the blood glucose level in alloxan induced diabetic rats. The extracts were administered through oral routs in a dose of 150 mg twice a day/kg of body weight/twice a day with 0.2 % polyvinyl pyrrolidone solution. The hypoglycemic activity of methanolic extract of Formulaion-1 showed 73.34% antidiabetic activity whereas marketed formulation -2 showed 70.35% activity. The formulation showed potential for its use in anti diabetic therapy in the sense that the in house prepared formulation possesses a comparable activity when compared to that of the marketed formulation.

 

ACKNOWLEDGEMENTS:

Authors acknowledge Curator, Medicinal garden, Truba Institute of Pharmacy, Bhopal for providing all the herbs and Head Department of Pharmacy Barkatullah University for providing necessary facilities for completion of the present work.

 

REFERENCES

1.       Bhatt N, Ayurvedic drug industry - challenges of today and tomorrow, Proceeding of the first national symposium of Ayurvedic drug industry, organized by ADMA, New Delhi, 1998 Aug.

2.       Dandiya PC, Bapna JS. Pharmacological research in India, Ann Rev Pharmacol 1974; 14:115-126.

3.       Adithan C. Pharmacological research in India, 1972-1995 - An analysis based on IPS conferences. Indian J Pharmacol 1996; 28:125-128.

4.       Marles, R.J. and Farnsworth, N.R. Plant to patients: an ethnomedical approach. Phytomedicine 1995; 2: 137.

5.       King H., Aubert R.E., Herman W.H., Diabetes Care, Vol.21, 1998, 1414-1431.

6.       Grover J.K., Vats V, Rathi S.S., Dawar R., J.Ethnopharmacol, Vol. 76, 2001, 233-238.

7.       Obatomi D.K, Bikomo E.O, “Anti-Diabetic Properties of the African Mistletoe in Streptozotocin Induced Diabetic Rats” Journal of Ethnopharmacol. Vol.43 (1), 1994, 7-13.

8.       Pandey M, Khan A, “Hypoglycemic Effect of Defatted Seeds and Water Soluble Fibers of Syzygium cumuni in Alloxan Diabetic Rats”, Indian Journal of experimental biology, Vol.40, 2002, 1178.

 

Received on 24.02.2011

Accepted on 27.02.2011     

© A&V Publication all right reserved

Research Journal of Pharmacognosy and Phytochemistry. 3(3): May- June 2011, 134-136