| Literature DB >> 30287370 |
Fiamma Gláucia-Silva1, Manoela Torres-Rêgo2, Karla Samara Rocha Soares3, Igor Zumba Damasceno4, Denise Vilarinho Tambourgi5, Arnóbio Antônio da Silva-Júnior6, Matheus de Freitas Fernandes-Pedrosa7.
Abstract
Snakebite envenoming is a tropical disease neglected worldwide. In Brazil, the Crotalus durissus cascavella (CDC) snake belongs to a genus with venom of highest lethality. A search for new immunoadjuvants aimed to expand the therapeutic alternatives to improve vaccines and antivenom. This approach proposed to produce small and narrow-sized cationic CDC venom-loaded chitosan nanoparticles (CHNP) able to induce antibody response against the CDC venom. The ionic gelation method induced the formation of stable and slightly smooth spherical nanoparticles (<160 nm) with protein loading efficiency superior to 90%. The interactions between venom proteins and CHNP assessed using FT-IR spectroscopy corroborated with the in vitro release behavior of proteins from nanoparticles. Finally, the immunization animal model using BALB/c mice demonstrated the higher effectiveness of CDC venom-loaded CHNP compared to aluminum hydroxide, a conventional immunoadjuvant. Thus, CHNPs loaded with CDC venom exhibited a promising biotechnological approach to immunotherapy.Entities:
Keywords: Antivenom; Chitosan nanoparticles; Crotalus durissus cascavella
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Year: 2018 PMID: 30287370 DOI: 10.1016/j.ijbiomac.2018.09.203
Source DB: PubMed Journal: Int J Biol Macromol ISSN: 0141-8130 Impact factor: 6.953