In Vitro Antiplatelet Activity of Ocimum basilicum (Basil) Leaf Extract
Rusell Alen V. Fernandez
Discipline: biology (non-specific)
Abstract:
Platelets play a crucial function in hemostasis. Pathological conditions such
as thrombosis in cardiovascular and cerebrovascular events must be
adequately acknowledged, and the population should possess a more
profound comprehension of the disease. The development and ongoing
research of a novel natural-source anticoagulant is now emphasized. This
study examines the in vitro antiplatelet activity of Ocimum basilicum (basil)
employing two distinct methodologies: the Giemsa Microplate Assay and
the Spectrophotometric Assay. The extracts underwent Soxhlet extraction
with 95% ethanol, followed by rotary evaporation and subsequent
concentration using a centrifuge machine to yield a pure extract. In the
Giemsa Microplate Assay, Ocimum basilicum (basil) leaf extract was
categorized into three concentrations: 10 mg/mL, 30 mg/mL, and 50 mg/mL,
with each concentration undergoing analysis in a 96-well microplate. An
adequate quantity of platelets was utilized to assess the antiplatelet
activity of each concentration, supplemented with 2.0M Calcium chloride as
an aggregator, and thereafter incubated at 37?C for 5 minutes. Following
washing with distilled water, substantial antiplatelet activity was observed
at the lowest concentration of extract, while minimal platelet inhibition
occurred at the higher doses. The positive control and the leaf extract
demonstrate equivalent inhibitory effects on platelets at the lowest
concentration. In the Spectrophotometric Assay, three distinct
concentrations were generated: 1 mg/mL, 3 mg/mL, and 5 mg/mL. The
subsequent amounts were analyzed via spectrophotometric assay utilizing
Platelet-Rich Plasma (PRP). Two trials were conducted: first, the PRPs
including the extracts underwent a spectrophotometric test without an
aggregator; second, the PRPs containing the extracts were submitted to a
spectrophotometric assay with an aggregator. A notable disparity existed
in the antiplatelet activity across the various setups; hence, the 3 mg/mL
concentration, when not utilizing an aggregator, demonstrated potential
antiplatelet action among all concentrations. The incorporation of aspirin
solution (positive control) and normal saline solution (negative control)
was crucial in the various procedures.
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