Literature DB >> 24620861

Nanoparticles as multifunctional devices for the topical treatment of cutaneous leishmaniasis.

Esther Moreno1, Juana Schwartz, Celia Fernández, Carmen Sanmartín, Paul Nguewa, Juan Manuel Irache, Socorro Espuelas.   

Abstract

INTRODUCTION: Cutaneous and mucocutaneous leishmaniasis are major tropical skin diseases. Topical treatment is currently limited to the least severe forms of cutaneous leishmaniasis (CL) without risk of dissemination. It is also recommended in combination with systemic therapy for more severe forms. Progresses in this modality of treatment are hindered by the heterogeneity of the disease and shortcomings in the clinical trials. AREAS COVERED: This review overlooks three major modalities of topical therapies in use or under investigation against CL: chemotherapy, photodynamic therapy and immunotherapy; either with older compounds such as paramomycin or more recent nitric oxide donors, antimicrobial peptides or silver derivatives. The advantages and limitations of their administration with newer formulation strategies such as nanoparticles (NPs) are discussed. EXPERT OPINION: The efficacy of a topical treatment against CL depends not only on the intrinsic antileishmanial activity of the drug but also on the amount of drug available in the dermis. NPs as sustained release systems and permeation enhancers could favour the creation of a drug reservoir in the dermis. Additionally, certain NPs have immunomodulatory properties or wound healing capabilities of benefit in CL treatment. Pending task is the selective delivery of active compounds to intracellular amastigotes, because even small NPs are unable to penetrate deeply into the skin to encounter infected macrophages (except in ulcerative lesions).

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Year:  2014        PMID: 24620861     DOI: 10.1517/17425247.2014.885500

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  11 in total

1.  Identification of Synthetic and Natural Host Defense Peptides with Leishmanicidal Activity.

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2.  Immunomodulatory nanoparticles ameliorate disease in the Leishmania (Viannia) panamensis mouse model.

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4.  The application of antimicrobial photodynamic therapy (aPDT) in dentistry: a critical review.

Authors:  E T Carrera; H B Dias; S C T Corbi; R A C Marcantonio; A C A Bernardi; V S Bagnato; M R Hamblin; A N S Rastelli
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5.  Aminophthalocyanine-Mediated Photodynamic Inactivation of Leishmania tropica.

Authors:  Ahmed Al-Qahtani; Saad Alkahtani; Bala Kolli; Pankaj Tripathi; Sujoy Dutta; Abdullah A Al-Kahtane; Xiong-Jie Jiang; Dennis K P Ng; Kwang Poo Chang
Journal:  Antimicrob Agents Chemother       Date:  2016-03-25       Impact factor: 5.191

6.  Pathogen- and Host-Directed Antileishmanial Effects Mediated by Polyhexanide (PHMB).

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Journal:  PLoS Negl Trop Dis       Date:  2015-10-02

7.  Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani.

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Journal:  Int J Parasitol Drugs Drug Resist       Date:  2016-02-12       Impact factor: 4.077

9.  Evaluation of Skin Permeation and Retention of Topical Dapsone in Murine Cutaneous Leishmaniasis Lesions.

Authors:  Esther Moreno; Alba Calvo; Juana Schwartz; Iñigo Navarro-Blasco; Elena González-Peñas; Carmen Sanmartín; Juan Manuel Irache; Socorro Espuelas
Journal:  Pharmaceutics       Date:  2019-11-13       Impact factor: 6.321

10.  Supplementation of host response by targeting nitric oxide to the macrophage cytosol is efficacious in the hamster model of visceral leishmaniasis and adds to efficacy of amphotericin B.

Authors:  Sanketkumar Pandya; Rahul Kumar Verma; Prashant Khare; Brajendra Tiwari; Dadi A Srinivasarao; Anuradha Dube; Neena Goyal; Amit Misra
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2016-01-14       Impact factor: 4.077

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