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      Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens

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          Abstract

          Advances in nanotechnology have demonstrated potential application of nanoparticles for effective and targeted drug delivery. Here, we investigated the antimicrobial and immunological properties and the feasibility of using nanoparticles to deliver antimicrobial agents to treat a cutaneous pathogen. Nanoparticles synthesized with chitosan and alginate demonstrated a direct antimicrobial activity in vitro against Propionibacterium acnes, the bacterium linked to the pathogenesis of acne. By electron microscopy imaging, chitosan-alginate nanoparticles were found to induce disruption of the P. acnes cell membrane, providing a mechanism for the bactericidal effect. The chitosan-alginate nanoparticles also exhibited anti-inflammatory properties as they inhibited P. acnes induced inflammatory cytokine production in human monocytes and keratinocytes. Furthermore, benzoyl peroxide, a commonly used anti-acne drug, was effectively encapsulated in the chitosan-alginate nanoparticles and demonstrated superior antimicrobial activity against P. acnes compared to benzoyl peroxide alone while demonstrating less toxicity to eukaryotic cells. Together, these data suggest the potential utility of topical delivery of chitosan-alginate nanoparticle encapsulated drug therapy for the treatment of dermatologic conditions with infectious and inflammatory components.

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          Most cited references46

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          Preparation and antibacterial activity of chitosan nanoparticles.

          Chitosan nanoparticles, such as those prepared in this study, may exhibit potential antibacterial activity as their unique character. The purpose of this study was to evaluate the in vitro antibacterial activity of chitosan nanoparticles and copper-loaded nanoparticles against various microorganisms. Chitosan nanoparticles were prepared based on the ionic gelation of chitosan with tripolyphosphate anions. Copper ions were adsorbed onto the chitosan nanoparticles mainly by ion-exchange resins and surface chelation to form copper-loaded nanoparticles. The physicochemical properties of the nanoparticles were determined by size and zeta potential analysis, atomic force microscopy (AFM), FTIR analysis, and XRD pattern. The antibacterial activity of chitosan nanoparticles and copper-loaded nanoparticles against E. coli, S. choleraesuis, S. typhimurium, and S. aureus was evaluated by calculation of minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). Results show that chitosan nanoparticles and copper-loaded nanoparticles could inhibit the growth of various bacteria tested. Their MIC values were less than 0.25 microg/mL, and the MBC values of nanoparticles reached 1 microg/mL. AFM revealed that the exposure of S. choleraesuis to the chitosan nanoparticles led to the disruption of cell membranes and the leakage of cytoplasm.
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            Nanomedicine.

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              Combating antimicrobial resistance: policy recommendations to save lives.

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                Author and article information

                Journal
                0426720
                4839
                J Invest Dermatol
                J. Invest. Dermatol.
                The Journal of investigative dermatology
                0022-202X
                1523-1747
                9 October 2012
                29 November 2012
                May 2013
                01 November 2013
                : 133
                : 5
                : 1231-1239
                Affiliations
                [1 ]Division of Dermatology, Department of Medicine, Albert Einstein College of Medicine, Bronx NY, 10467
                [2 ]Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx NY, 10467
                [3 ]Division of Dermatology, David Geffen School of Medicine at University of California, Los Angeles, CA 90095
                [4 ]Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at University of California, Los Angeles, CA 90095
                [5 ]Department of Microbiology, Immunology, and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, CA 90095
                [6 ]Department of Dermatology, West Los Angeles Veterans Administration Medical Center, Los Angeles, CA 90073
                Author notes
                Address correspondence to: Jenny Kim, M.D., Ph.D., Division of Dermatology, David Geffen School of Medicine at UCLA, 52-121 CHS, 10833 Le Conte Avenue, Los Angeles, CA 90095, Tel: (310) 825-5420, Fax: (310) 206-9878, jekim@ 123456mednet.ucla.edu
                Article
                NIHMS410935
                10.1038/jid.2012.399
                3631294
                23190896
                3d0e519a-bcdd-4198-b3a4-fa05da93cb03
                History
                Funding
                Funded by: National Institute of Arthritis and Musculoskeletal and Skin Diseases : NIAMS
                Award ID: R01 AR053542 || AR
                Funded by: National Institute of Allergy and Infectious Diseases Extramural Activities : NIAID
                Award ID: R01 AI059091 || AI
                Funded by: National Institute of Arthritis and Musculoskeletal and Skin Diseases : NIAMS
                Award ID: K08 AR048551 || AR
                Categories
                Article

                Dermatology
                acne,nanoparticle,chitosan,antimicrobial,inflammation,skin infection
                Dermatology
                acne, nanoparticle, chitosan, antimicrobial, inflammation, skin infection

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