Advances in nanocarriers as drug delivery systems in Chagas disease
International Journal of Nanomedicine
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Advances in nanocarriers as drug delivery systems
in Chagas disease
This article was published in the following Dove Press journal:
International Journal of Nanomedicine
Christian Quijia Quezada 1,2
Clênia S Azevedo 1
Sébastien Charneau 3
Jaime M Santana 1
Marlus Chorilli 2
Marcella B Carneiro 4
Izabela Marques Dourado
Bastos 1
1
Pathogen-Host Interface Laboratory,
Department of Cell Biology, Institute of
Biology, University of Brasilia, Brasília,
Brazil; 2Department of Drugs and
Medicines, São Paulo State University
(UNESP), Araraquara, São Paulo, Brazil;
3
Laboratory of Protein Chemistry and
Biochemistry, Department of Cell
Biology, Institute of Biology, University of
Brasilia, Brasília, Brazil; 4Electron
Microscopy Laboratory, Department of
Cell Biology, Institute of Biology,
University of Brasilia, Brasília, Brazil
Abstract: Chagas disease is one of the most important public health problems in Latin
America due to its high mortality and morbidity levels. There is no effective treatment for
this disease since drugs are usually toxic with low bioavailability. Serious efforts to achieve
disease control and eventual eradication have been unsuccessful to date, emphasizing the
need for rapid diagnosis, drug development, and a reliable vaccine. Novel systems for drug
and vaccine administration based on nanocarriers represent a promising avenue for Chagas
disease treatment. Nanoparticulate systems can reduce toxicity, and increase the efficacy and
bioavailability of active compounds by prolonging release, and therefore improve the
therapeutic index. Moreover, nanoparticles are able to interact with the host’s immune
system, modulating the immune response to favour the elimination of pathogenic microorganisms. In addition, new advances in diagnostic assays, such as nanobiosensors, are
beneficial in that they enable precise identification of the pathogen. In this review, we
provide an overview of the strategies and nanocarrier-based delivery systems for antichagasic
agents, such as liposomes, micelles, nanoemulsions, polymeric and non-polymeric nanoparticles. We address recent progress, with a particular focus on the advances of nanovaccines
and nanodiagnostics, exploring new perspectives on Chagas disease treatment.
Keywords: delivery systems, nanobiosensors, nanodiagnostics, nanoparticle systems,
nanovaccine
Introduction
Correspondence: Izabela Marques
Dourado Bastos
Departamento de Biologia Celular,
Universidade de Brasilia, Brasília 70910900, DF, Brazil
Tel +55 613 107 3051
Email
Chagas disease, caused by the protozoan Trypanosoma cruzi, is endemic in Latin
America, where between five and eight million people are infected. The disease is
spreading to non-endemic countries, such as Australia, Canada, Japan, Spain and
United States of America (USA).1 It is mainly transmitted by faecal contamination
of Reduviidae insects through insect bites or another injury of the skin2 parasite can
also be spread by blood transfusion, organ transplantation, congenital contamination, and consumption of contaminated food and drinks.3 The T. cruzi biological
cycle is comprised of three fundamental forms: (1) infective trypomastigotes found
in mammalian blood and in the hindgut of triatomine bugs as metacyclic forms, (2)
epimastigotes, the proliferative form located in the bug’s midgut, and (3) amastigotes that multiply by binary fission inside mammalian host cells, causing disruption and the release of new trypomastigotes into the bloodstream capable of
invading any nucleated cell to begin a new reproductive cycle.4 Regarding clinical
symptoms, Chagas disease can manifest both an acute phase which is asymptomatic
in most cases and a chronic phase that is depicted by digestive and/or cardiac
lesions.5 Treatment is based on the nitroheterocyclic compounds benznidazole and
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http://doi.org/10.2147/IJN.S206109
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International Journal of Nanomedicine downloaded from https://www.dovepress.com/ by 88.198.20.149 on 01-Nov-2019
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Quijia Quezada et al
nifurtimox. However, in long-term therapy, both of the
aforementioned induce serious side effects and cross-resistance. To date, research into the production of Chagas
disease vaccines has been conducted. The main difficulties
have been finding a protective antigen and generating
attenuated parasites that will not trigger pathology in the
long-term.6 Therefore, in the absence of vaccines, control
measures for Chagas disease remain limited to diagnosis
and treatment.5
Nanocarriers has demonstrated important results in
terms of increasing the efficacy and decreasing the toxicity
of drugs, antigens, and adjuvants currently used against
some diseases. The use of nanocarriers against pathogens
provides a greater ability to overcome biological barriers,
maintenance of drug integrity in biological media, with
higher specificity to target cells and tissues together with
prolonged drug release in comparison to conventional
drugs.7 Moreover, nanodiagnostic systems have been
developed to improve the accuracy of sample preparation
and detection of infectious pathogens by means of a simple, quick, accurate and inexpensive technique.8
In this review, we provide an overview of synthetic
methods, physical characteristics and delivery systems
based on nanocarriers for various antitrypanosomal agents,
through liposomes, micelles, mesoporous silica nanoparticles, polymeric and non-polymeric nanoparticles (Figure 1).
In this context, we highlight new perspectives and innovative
Figure 1 Nanomaterials used against Chagas disease. Strategies and application of
nanocarrier-based drug delivery systems, such as liposomes, micelles, mesoporous
silica nanoparticles, polymeric and non-polymeric nanoparticles to optimize the
delivery of antitrypanosomal agents.
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strategies on the treatment of Chag (...truncated)