Evaluation of
Anti-Ulcer Activity of Chloroform and Alcoholic Extracts of Leaves of Mimusops
elengi
Sona verma1*,
Manish Mukati1, Nadeem Shaikh2, Rakesh Punasiya1
1.Yogeshwar College of
pharmacy Piplaj, Dist. Barwani Madhya Pradesh India 451551
2. Ali-Allana College of
Pharmacy Akkalkuwa, Dist. Nandurbar Maharashtra India 425415
*Correspondence: vermasona2015@gmail.com
DOI: https://doi.org/10.71431/IJRPAS.2026.5107
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Article
Information
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Abstract
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Research Article
Received: 19/01/2026
Revised :
29/01/2026
Accepted: 29/01/2026
Published:31/01/2026
Keywords
Anti-ulcer activity,
Gastric ulcer,
Herbal extract,
Ulcer index,
Gastroprotection
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Peptic ulcer disease is a chronic
gastrointestinal disorder resulting from an imbalance between aggressive
factors such as gastric acid, pepsin, reactive oxygen species and defensive
mechanisms including mucus secretion and mucosal integrity. Despite the availability
of several synthetic anti-ulcer drugs, their prolonged use is associated with
adverse effects and recurrence of ulcers. Hence, there is a growing interest
in herbal medicines as safer alternatives. The present study was designed to
evaluate the anti-ulcer activity of chloroform and alcoholic extracts using
experimentally induced gastric ulcer models in albino rats. Ulcers were
induced by standard ulcerogenic procedures as described in the thesis
protocol. The severity of gastric lesions was assessed by determining ulcer
index and percentage inhibition. Both extracts showed significant reduction
in ulcer index compared to the control group. The alcoholic extract exhibited
comparatively higher gastroprotective activity than the chloroform extract. The
results of the study confirm the potential anti-ulcer activity of the
extracts and support their traditional therapeutic use.
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INTRODUCTION
Peptic ulcer disease remains a major
gastrointestinal disorder affecting a large population worldwide. It is
characterized by mucosal damage occurring in the stomach or duodenum due to
excessive secretion of gastric acid and pepsin, oxidative stress, Helicobacter
pylori infection, stress, alcohol consumption and prolonged use of
non-steroidal anti-inflammatory drugs. The pathogenesis of ulcer involves an
imbalance between aggressive factors and protective mechanisms of the gastric mucosa.
[1-6]
Currently available anti-ulcer drugs such as
proton pump inhibitors, H₂-receptor blockers and antacids provide symptomatic
relief but are associated with adverse effects such as tolerance, rebound
acidity and relapse. Therefore, the search for safer and effective alternatives
from natural sources has gained significant attention. Herbal drugs are
considered safer, economical and more acceptable due to their minimal side
effects. In this context, the present study was undertaken to scientifically
evaluate the anti-ulcer activity of chloroform and alcoholic extracts using
experimental animal models. [7]
Fig. 1 Morphology of plant
Plant Profile
Name: - Mimusops elengi
Family: - Sapataceae
MATERIALS AND METHODS
Ø Experimental Animals
Healthy adult albino rats of either sex was selected for the
study. The animals were housed under standard laboratory conditions with
controlled temperature, humidity and 12-hour light–dark cycle. They were
provided with standard pellet diet and water ad libitum. All experimental
procedures were carried out as per institutional ethical guidelines. [8,9]
Ø Preparation of Extracts
The plant material was dried under shade, powdered and
subjected to extraction using chloroform and alcohol as solvents. The extracts
were filtered, concentrated under reduced pressure and stored in airtight
containers for further use. [10]
Ø Acute Toxicity Studies
Acute oral toxicity studies were performed to determine the
safe dose of extracts. Based on toxicity results, suitable doses were selected
for anti-ulcer evaluation. [11]
Ø Experimental Design
Animals were divided into different groups including control,
standard and test groups. The control group received vehicle only, the standard
group received a known anti-ulcer drug, while the test groups received
chloroform and alcoholic extracts at selected doses. [12]
Ø Induction of Gastric Ulcer
Gastric ulcers were induced using standard ulcerogenic
methods described in the thesis. After ulcer induction, animals were sacrificed
and stomachs were removed for macroscopic examination. [13]
Ø Evaluation Parameters
Ulcer index
Number and severity of gastric lesions
Percentage inhibition of ulcer formation [14]
Table 1. List of materials
used
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Sr. No.
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Name of the Material
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Manufacturer /Supplier
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1.
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Chloroform
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Kasliwal brothers Indore M.P.
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2.
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Ranitidine
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Ipca laboratory pvt. Ltd Indore
M.P.
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3.
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Aspirin
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Ipca laboratory
pvt. Ltd Indore M.P.
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4.
5.
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Saline Sodium chloride Injection
I.P.
Fresh leaves of Mimusops elengi
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Inven Pharmaceutical pvt. ltd Dhar
M.P.
Village Jodalli Taluka-kalghatagi
District of Dharwad (Karnataka)
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Table 2. Extractive values of different solvents for leaves
of Mimusops elengi
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Plant name
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Part
used
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Method
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Chloroform
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Alcohol
95
%
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Plant name
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Mimusops Elengi
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Leaves
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Hot percolation Process
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13.3%
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18.8%
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Mimusops Elengi
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Animals: - Albino Rats (200-250g) (72 No.)
At:- GRY Institute of Pharmacy, Borawan, Madhya Pradesh
CPCSEA registration Number: 1151/PO/Re/S/2008/CPCSEA
Models Used in Evaluations of antiulcer activity: Pylorus-ligated model
spiring induced
model [15]
RESULT
AND DISCUSSION
The results of the study demonstrated
that animals treated with chloroform and alcoholic extracts showed a marked
reduction in gastric lesions compared to the control group. The ulcer index was
significantly reduced in extract-treated groups. The alcoholic extract showed
higher percentage inhibition of ulcer formation compared to the chloroform
extract. The standard drug produced maximum protection, confirming the validity
of the experimental model.
The
significant reduction in ulcer index observed in extract-treated groups
indicates a protective effect on the gastric mucosa. The anti-ulcer activity
may be attributed to enhancement of mucosal defense mechanisms, reduction in
gastric acid secretion and antioxidant properties of phytoconstituents present
in the extracts. The superior activity of the alcoholic extract may be due to
better solubility and higher concentration of active compounds. These findings
are consistent with earlier reports highlighting the efficacy of alcoholic
extracts in ulcer management.
Table. No 3. Result
of chloroform and alcoholic extract
of Mimusops elengi on gastric
secretion, acidity, pH, ulcer index and percentage of ulcer inhibition of pylorus
ligated test.
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Groups
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Volume of gastric
secretion (ml/100)
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Free acidity
(mEq/l/100g)
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Total acidity
(mEq/l/100g)
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pH
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Ulcer index
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% ulcer
inhibition
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Control
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5.08±0.23
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81.83
±3.16
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175.00
±17.07
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2.70
± 0.12
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4.58
±0.436
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---------
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Ranitidine (50mg/kg)
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1.83±
0.38***
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31.66 ±4.01***
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65.00 ± 6.191***
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4.4 ± 0.17
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0.83±
0.460***
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81.82
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M.E. Alcoholic (200mg/kg)
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3.33±0.33**
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56.66
±8.02**
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91.66
±3.07**
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3.2
±0.1
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1.80±0.436**
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60.00
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M.E. Alcoholic (400mg/kg)
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2.66±0.55***
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48.33 ±7.49***
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71.66 ±6.00***
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3.61 ± 0.20
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1.16±
0.441***
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74.53
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M.E. chloroform (200mg/kg)
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4.66±0.66**
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75.0
±4.28**
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138.33
±8.72**
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2.77
± 0.13
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3.16 ± 0.333**
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30.89
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M.E. chloroform (400mg/kg)
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4.00±0.57**
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68.33 ±3.07**
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103.30 ±5.57**
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3.61 ± 0.20
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1.16±
0.441***
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74.53
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Table. No 4 Effect of chloroform and alcoholic
extract Mimusops elengi aspirin induced ulcer
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GROUPS
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ULCER INDEX
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% ULCER
INHIBITION
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Aspirin (100mg/kg)
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8.16 ± 0.47
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--
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Ranitidine (50mg/kg)
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0.91 ±
0.23***
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88.77
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M.E. Alcoholic (200mg/kg)
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3.08 ± 0.45**
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62.25
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M.E. Alcoholic (400mg/kg)
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1.75 ± 0.42***
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78.57
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M.E. chloroform (200mg/kg)
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6.33 ± 0.33**
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34.70
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M.E. chloroform (400mg/kg)
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3.16 ± 0.0.33**
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55.09
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Fig. 2 Effect of M.E extract
on Ulcer Index
Fig. 3 Effects of M.E extract
on % Gastric inhibition
CONCLUSION
The present study concludes that both chloroform and
alcoholic extracts exhibit significant anti-ulcer activity in experimental
animal models. Among the two, the alcoholic extract showed superior
gastroprotective effect. The findings provide scientific validation for the
traditional use of herbal remedies in ulcer treatment. Future studies should
focus on isolation of active constituents, mechanism of action and clinical
evaluation to establish therapeutic potential.
CONFLICT
OF INTEREST
This
manuscript is original and free from plagiarism. The authors agree that the
article may be checked using Turnitin plagiarism detection software.
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