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Volume 4, Issue 8 (Suppl) J Infect Dis Ther 2016
ISSN: 2332-0877, JIDT an open access journal Infection Control 2016
November 28-29, 2016
Page 22
conferenceseries.com
November 28-29, 2016 Valencia, Spain
4th World Congress on
Infection Prevention and Control
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 it 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. In his civil career he works internationally as a 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 Netherlands and has extensive practical experience in cell biology, immuno-hematology, biodefense and
transfusion medicine.
Stef Stienstra
Dutch Armed Forces/Royal Dutch Navy, Netherlands
Stef Stienstra, J Infect Dis Ther 2016, 4:8 (Suppl)