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Page 76

Volume 4, Issue 2

American Journal of Ethnomedicine

ISSN 2348-9502

Natural Products Congress & World Pharma Congress 2017

October 16-18, 2017

3

rd

World Congress on

NATURAL PRODUCTS CHEMISTRY AND RESEARCH

&

12

th

WORLD PHARMA CONGRESS

October 16-18, 2017 Budapest, Hungary

Chemical study, antioxidant analysis and evaluation of the larvicidal potential against

Aedes Aegypti

Larvae

of essential oil of

Ocimum Basilicum Linn

Sheylla SMS Almeida

UNIFAP, Brasil

T

he purpose of this research was to accomplish chemical study, antioxidant analysis and evaluation of the larvicidal

potential against

Aedes aegypti larvae

of essential oil from the leaves of

O. basilicum Linn

. The research was carried out

in the Pharmacognosy and Phytochemistry Laboratory, Department of Biologicaland Health Sciences, Federal University

of Amapá (UNIFAP), between July 2013 and March 2014. Arthropoda Laboratory, Department of Biological and Health

Sciences, Federal University of Amapá (UNIFAP) between September 2013 and March 2014. The essential oil was obtained

by hydrodistillation; the identification and quantification of components was achieved with the use of GC-MS analysis. The

antioxidante activity was evaluated by the method of sequestration of DPPH. The essential oil was tested in the third larval

state of the development of the mosquito Aedes Aegypti. The third larval instar were exposed to different concentrations of the

oil (500, 400, 300, 200 and 130 ppm) in triplicates. Chromatographic analysis identified that the major constituents found in

essential oil of

O. basilicum

were limonene (13%), 1,8-cineole (15%), linalool (20%) and methyl chavicol (45%). In trials of free

radicals sequestration, the essential oil showed (AA%) 67.35±1.11 in the highest concentration and inhibitory concentration,

IC50 value of 61.517 mg/mL. The essential oil of

O. basilicum

showed larvicidal potential with CL50 of 67.22 ppm. A more

detailed study should be done to verify the larvicidal potential and biological mechanism of action, as several authors claimed

that the constituent of essential oils affect the nervous system of the mosquito Aedes Aegypti and the action mechanism is not

yet fully elucidated. New studies demand the development of tests using samples of lower concentrations to verify the degree

of toxicity in other animal species, including man, and preparation of formulations that may function as a natural alternative

to combat mosquito larvae.

sheyllasusan@yahoo.com.br

Piroxicam loaded solid lipid nanoparticles for topical delivery: Preparation, characterization and

in

vitro

permeation assessment

Soliman Mohammadi-Samani

1

, Shirin Zojaji

2

and

Elaheh Entezar-Almahdi

1

1

Shiraz University of Medical Sciences, Iran

2

International Branch of Shiraz University of Medical Sciences, Iran

D

uring the recent years, there has been rising attention to the development of topical delivery systems to facilitate drug

permeation through the skin.The drugs commonly used are those with debatable oral administration. Although piroxicam

is a valuable anti-inflammatory, antipyretic and analgesic drug, long term oral administration is limited due to the various GI

side effects. The main aim of this study was to prepare and assess a topical formulation of piroxicam based on Solid Lipid

Nanoparticles (SLNs), to improve its percutaneous permeation rate. Topical nano-lipidic gel of piroxicamwas formulated and its

pharmaceutical characteristics were evaluated. Piroxicam loaded SLNs were formulated by solvent emulsification evaporation

method. The SLNs were composed of stearic acid and cholesterol as lipid phase, Brij35 and Brij72 as a stabilizer and acetone was

used to dissolve the lipidic ingredients of the formulation. Particle size assessment, drug loading determination, entrapment

efficiency assessment, and

in vitro

release study and skin permeation of the piroxicam was determined to characterize the SLNs

and then these nanoparticles were formulated in gel as topical delivery system to assess percutaneous permeation of piroxicam.

The SLNs were prepared in different size ranges from 100-300 nm and drug release behavior from two different nano-sized

SLN suspensions was evaluated. Piroxicam nano-lipidic gel showed increased skin permeation of the drug over commercial

piroxicam gel formulation and also mean particle size of formulated SLNs had significant effect on permeation rates.

smsamani@sums.ac.ir

American Journal of Ethnomedicine, 4:2

DOI: 10.21767/2348-9502-C1-003