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Page 31

Journal of Clinical and Experimental Toxicology | Volume: 03 | ISSN: 2630-4570

allied

academies

November 04-05, 2019 | Prague, Czech Republic

2

nd

World Congress on

TOXICOLOGY AND APPLIED PHARMACOLOGY

Notes:

Brazilian natural products as a promisingmedicine for the treatment of inflammatory

diseases and its nanoformulation

Luzia Kalyne Almeida Moreira Leal

Federal University of Ceará, Brazil

D

uring the development of new bioactive materials as

tools for therapeutic use, one of the key questions is

to understand how they interact with biological systems.

In this way, it is essential to describe the mechanism of

action aiming to understand how these materials induce

their pharmacological effects and if these actions may

cause health risks. New materials such as nanoparticles

have attracted the attention of academy and industry.

In particular, in Brazil we have researched several plant

extracts and free or nanoencapsulated molecules for the

treatment of inflammatory diseases using experimental

models

in vitro

and

in vivo

. We have investigated the anti-

inflammatory effect and toxicity of plant products, including

imidazole alkaloids (Epiisopiloturine (EPI) and epiisopilosine

(EPIIS) from Pilocarpus microphyllus Stapf), eugenol (a

free or nanoencapsulated terpene) and dry extract of

Amburana cearensis (microparticles). The EPI and EPIIS are

side products in the Brazilian pharmaceutical industry which

showed anti-inflammatory and antioxidant activities. Both

alkaloids inhibited the degranulation of activated human

neutrophils. This effect was accompanied by the reduction

of ROS, the prevention of the increase of intracellular Ca2+

and decrease of the density of cytosolic NF-kB, and inhibition

of TNF-α and IL-6 production. The EPI and EPIIS also inhibited

carrageenan-induced inflammatory hypernociception in

mice and reduced myeloperoxidase (MPO) levels. Eugenol

(EUG) is a terpene present in essential oils of plants which

has attracted attention due to its anti-inflammatory

properties, as well as antioxidant effect. Despite of these

pharmacological properties it presents irritant effect on skin

which limit its use in topic, suchas for treatment of dermatitis.

To overcome it, we developed eugenol- loaded polymeric

nanocapsules. The EUG, inhibited the ROS production in

human neutrophil, but it was toxic in human keratinocyte

and did not interfere with ear edema induced by TPA inmice.

However, the nanocapsules of EUG (NCEUG) prevented its

cytotoxicity in keratinocytes, and reduced ear thickness

of mice (experimental model of dermatitis) reducing the

MPO activity and the concentrations of IL-6 and KC (CXCL

1). Together, these results showed that NCEUG promoted

a reduction in cytotoxicity of EUG and improved its anti-

inflammatory effect. Parkinson’s and Alzheimer’s Disease are

neurodegenerative diseases which neuroinflammation has

an important role. Microglia is part of the innate immunity

of central nervous system, being it activation one of the main

mechanisms of inflammation responses. The standardized

dry extract of A. cearensis (actives markers: coumarin and

amburoside) reduced LPS-stimulated nitrite release on

microglial and reduced the expression of iNOS (Western

blot analysis). These findings suggest that molecules and/

or plant extract from Brazilian medicinal plants, and its

nanoencapsulation possess promising anti-inflammatory

potential acting through the modulation of inflammatory

response appear non-toxic.

Biography

Luzia Kalyne Almeida Moreira Leal is pharmacist and received her PhD

in Pharmacology from the Federal University of Ceará, Brazil in 2006.

She is Pharmacognosy professor at Federal University of Ceará since

1996. Her research interests are in Pharmacognosy and Pharmacology

of Natural Products for the development of new medicines to treat

inflammatory diseases. She is founder and coordinator of the Center of

Pharmaceutical and Cosmetics Studies.

e:

kalyneleal@gmail.com

Luzia Kalyne Almeida Moreira Leal, J Clin Exp Tox, Volume: 03

DOI: 10.35841/2630-4570-C2-009