EVALUATION OF ANTIMICROBIAL PROPERTIES OF ETHYL ACETATE EXTRACT OF THE LEAVES OF NAPOLEONEAE IMPERIALISFAMILY
Abstract
A.F. Onyegbule1*, C.F. Anowi2, T.H. Gugu3and A.U.
EVALUATION OF ANTIMICROBIAL PROPERTIES OF ETHYL ACE
TATE
EXTRACT OF THE LEAVES OF
NAPOLEONEAE IMPERIALIS
FAMILY
LECYTHIACEAE
A.F. Onyegbule
1
*, C.F. Anowi
2
, T.H. Gugu
3
and A.U. Uto
-
Nedosa
4
1
* Dept of Pharmaceutical and Medicinal Chemistry, Faculty of Pharmaceutical Sciences,
Nnamdi Azikiwe University, Awka,
Nigeria
2
Dept of Pharmacognosy and Traditional Medicine, Facu
lty of Pharmaceutical sciences,
Nnamdi Azi
kiwe University, Awka, Nigeria
3
Dept of Pharmaceutical Microbiology and Bio
technology,
Facu
lty of Pharmaceutical
Sciences,
Nnamdi Az
ikiwe University, A
wka, Nigeria
4
Dept of Pharmacology and Toxicology, Facu
lty of Pharmaceutical Sciences,
Nnamdi Azikiwe University, Awka, Nigeria
ABSTRACT
N
apoleon
aea imperialis
is used to treat wounds
in Anambra State, Nigeria
. Against this background,
ethyl acetate extract of the leaves were screened against some microorganisms so as to ascert
ain this
claim and to recommend it for further investigation for possible inclusion into official compendium.
T
he
plant leaves were dried, po
wdered subjected to cold maceration with ethyl acetate for 24
hours.
Phytochemical screening was done for alkaloids, saponin, essential oil, phenolic group, steroidal nucleus,
simple sugar, starch, cyanogenic glycoside, proteins and flavonoid using standar
d procedures.
Antimicrobial screenings were done using agar diffusion technique. Antibacterial activity test was
conducted by screening against six
pathogens comprising both Gram
-
positive and Gram
-
negative bacteria
obtained from pharmaceutical
microbiology
laboratory stock. The extract was screened against 24
hour
broth culture of bacteria seeded in the nutrient agar at concentrations 400, 200, 100, 50, 25, 12.5, 6.25
and
3.125 mg/ml in DMSO and incubated at 37
o
C
, for 24 hours and measuring the inhibition z
one diameter
-
IZD.
T
he
phytochemical screening showed availability of alkaloid, saponins, tannins, glycosides and
proteins. Ethyl acetate extract exhibited activity against
E.
coli
,
B.subtilis
and
Pseudomonas aeruginosa
with minimal inhibitory
concentrati
on
of about 50
mg/ml for
E.
coli
, 100
mg/ml for
Pseudomonas
aeruginosa
and 200
mg/ml for
B.
subtilis
.
The
extract demonstrated activities against certain bacteria
confirming the use of the plant in ethno pharmacology and since the root extract are more oft
en used, it is
yet to be confirmed if it has more activity than the leaves against the test organisms. Taking the least IZD
of the standard (Ampicillin) as the breaking point, most of the extracts passed the breaking point.
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