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Volume 4, Issue 4(Suppl)

J Infect Dis Ther 2016

ISSN: 2332-0877, JIDT an open access journal

Infectious Diseases 2016

August 24-26, 2016

Page 29

conference

series

.com

August 24-26, 2016 Philadelphia, USA

&

Infectious Diseases

Joint Event on

2

nd

World Congress on

Pediatric Care & Pediatric Infectious Diseases

International Conference on

Stef Stienstra, J Infect Dis Ther 2016, 4:4(Suppl)

http://dx.doi.org/10.4172/2332-0877.C1.007

Stef Stienstra

Dutch Armed Forces/Royal Dutch Navy, Netherlands

Drug delivery by tattooing to treat cutaneous leishmaniasis

Background:

Leishmaniasis is a vector borne disease that is caused by obligate intra macrophage protozoa of the

Leishmania

species. Leishmaniasis can cause different clinical syndromes including cutaneous leishmaniasis (CL), in which the patient

generally presents with one or several ulcers or nodules on the skin, resulting from the infection of phagocytic cells located

in the dermis. It often results into severe scar tissue in the skin. Most of the twelve million people infected with

Leishmania

worldwide are CL cases and 1.5 million new cases occur annually.

Objective:

WHO has a program to develop new treatments for cutaneous leishmaniasis. This study establishes a proof of

concept that a tattoo device can target intra dermal drug delivery against cutaneous leishmaniasis (CL).

Methods:

The selected drug is oleylphosphocholine (OlPC) formulated as liposomes, particles known to be prone to

macrophage ingestion. First is shown that treatment of cultured

Leishmania

infected macrophages with OlPC liposomes

results in a direct dose dependent killing of intracellular parasites. Based on this,

in vivo

efficacy is demonstrated using a 10

day tattooing mediated treatment in mice infected with

L. major

and

L. mexicana

. In both models this regimen results in rapid

clinical recovery with complete regression of skin lesions by Day 28. Parasite counts and histopathology examination confirm

high treatment efficacy at the parasitic level. Low amount of drug required for tattooing combined with fast clinical recovery

may have a positive impact on CL patient management.

Results:

This first example of tattoomediated drug delivery could open to new therapeutic interventions in the treatment of skin

diseases. This study demonstrates that the use of a tattoo instrument for drug delivery is possible in the treatment of cutaneous

leishmaniasis and that this method can successfully eliminate intracellular parasites at the site of infection. After showing that

the selected drug oleylphosphocholine (OlPC) formulated as liposomes could efficiently reach intracellular parasites when in

contact with infected macrophages, the activity of the drug was compared

in vivo

in mouse models of Old (

L. major

) and New

World (

L. mexicana

) leishmaniasis. Three routes of administrations of the same drug formulation were investigated: systemic

(IP) administration, topical administration as a drop and administration via the tattoo instrument. Evaluation parameters

included clinical (lesion sizes) and parasitological parameters (burdens) using quantitative and qualitative methods. In all

experiments, the tattooing delivery procedure was the most efficacious at both the clinical and parasitological levels.

Limitations:

The used tattoo device, used routinely for permanent makeup procedures is not yet optimal for quantitative drug

delivery.

Biography

Stef Stienstra is a strategic and creative Consultant in Biomedical Science with a parallel career as a Commander of the reserve of the Royal Dutch Navy. For the

Dutch Armed Forces he has responsibility for the counter measures in CBNRe threats and (Medical) consequence management both in a military and a civilian

(terrorism) setting. He is a strategic functional specialist for “Health & Environment” of the 1-Civil-Military-Interaction Command (1-CMI) of the Dutch Armed Forces

and for 2015 also in the NATO Response Force (NRF), which is in 2015 the responsibility of the 1-German-Netherlands-Corps (1-GNC). In his civil career he works

internationally as Consultant or as Scientific Supervisory Board Member for several medical and biotech companies, merely involved in biodefense. He is also a

Visiting Professor for Punjab University in Pakistan and Rhein-Waal University in Germany. He has completed his studies in Medicine and in Biochemistry at the

University of Groningen in The Netherlands and has extensive practical experience in cell biology, immuno-hematology, biodefense and transfusion medicine.

Stienstra@t-online.de Stef.Stienstra@inter.nl.net