Nanovenoms synthesis for its potential use in antisera production against rattlesnake venom (Crotalus durissus terrificus)
Fecha
2019Autor
Baudou, Federico Gastón
Giorgi, Exequiel David
Diaz, María Eugenia
Fusco, Luciano Sebastián
Municoy, Sofía
Desimone, Martín Federico
Leiva, Laura Cristina Ana
De Marzi, Mauricio Cesar
Metadatos
Mostrar el registro completo del ítemResumen
Snake antivenoms (AV) production involves successive
inoculations of venom (V) in increasing form together with the
addition of adjuvants (ADJ) that improve the immune response of
animals destined for immunizations. On the other hand,
nanoparticles (NP) are being studied with multiple purposes due to
their potential therapeutic and immunomodulatory use, and for
their ability to transport antigens and induce a specific response
against it. Therefore, it is of interest to associate V to NP in order to
replacing conventional ADJ in AV production. In this work,
nanovenoms (NV) were synthesized by adsorption of Crotalus
durissus terrificus (C.d.t.) V proteins with silica NP (NPsi) of 400 nm
size (positive/negative charge, +/-). The NPsi (-) were synthesized
according to the Stöber method, while a fraction was modified with
APTES (NPsi +), and its load and size was verified by potential Z and
DLS (dynamic light scattering) respectively. Then, 10 mg of NPsi +/-
were incubated with 1 mg / ml of whole V in PBS for 3 h under
stirring to favor proteins adsorption to the NPs surface. NV were
photographed under MET and also a FTIR (Fourier Transform
Infrared) was performed. Crotoxin presence, the main toxic
component of C.d.t. venom, was analyzed by hemolysis radial test
both in NV and supernatant. NV proteins desorbed by heat
treatment were analyzed by SDS-PAGE and immunoblotting. NV
FTIR spectra showed intermediate values between those that
exhibited C.d.t. V and the NPsi separately. SDS-PAGE and
immunoblotting tests confirmed the presence of proteins in NPsi
particles and hemolytic halos demonstrated that NPsi +/- were
capable of binding crotoxin molecules on their surface. The results
reveal the presence of V in both types of NPsi, preserving its activity
and therefore its native structure, evidences that allow progress in
an upcoming study such as the evaluation of immunogenic activity
in experimental animals.
Colecciones
- Documentos de conferencia [1098]










