Abstract:
Background: Dialium ovoideum (Thwaites) is an endemic medicinal plant widely used in
indigenous medicine in Sri Lanka. However, its potential anticoagulant effect on human blood
remains unexplored. Investigating its influence on blood coagulation pathways may provide
preliminary evidence for its therapeutic application as a natural anticoagulant source.
Objective: To evaluate the in vitro anticoagulant activity of the methanolic extract of D. ovoideum
bark and screen its phytochemical constituents.
Method: This preliminary laboratory-based experimental study used fresh, healthy bark of D.
ovoideum, authenticated at the Department of Plant and Molecular Biology at the University of
Kelaniya. The bark was shade-dried, powdered, and extracted with methanol using a Soxhlet
apparatus (40 g powder: 250 mL methanol; 1:6.25). The solvent was evaporated and reconstituted
with Tris buffer (pH 7.4) to prepare four concentrations. Preliminary phytochemical screening was
conducted using standard qualitative tests. Venous blood samples were collected from six healthy
volunteers in sodium-citrated tubes and pooled plasma was separated by centrifugation at 3000
rpm for 15 minutes. Anticoagulant activity was assessed by Prothrombin time (PT) assay using a
HumaClot Duo Plus coagulometer. Positive and negative controls were included. All tests were
performed in triplicate. Statistical analysis was performed using one-way ANOVA in SPSS (p ≤
0.05).
Results: The methanolic bark extract yielded 13.82% (w/w). Phytochemical screening revealed
phenolics, tannins, flavonoids, alkaloids, saponins, and glycosides. The extract prolonged PT in a
concentration-dependent manner to 7.00 ± 0.12, 13.07 ± 0.29, 24.57 ± 0.40, and 25.73 ± 0.12
seconds at 156.25, 312.5, 625, and 1250 μg/mL, respectively. All concentrations showed a
significantly increased PT compared to the control (15.8 seconds) (p < 0.05).
Conclusion: These findings provide preliminary evidence that D.ovoideum bark extract exhibits
concentration-dependent in vitro anticoagulant activity on pooled human plasma.
