Characterization of a lab-scale process to produce whole IgG antivenom covering scorpion stings by genus tityus and centruroides of Colombia

ABSTRACT: Scorpion stings are a public health event in Colombia lacking official epidemiological data, and are considered a medical emergency. Despite the two local producers of antivenoms, neither of them is currently manufacturing scorpion antivenoms. We present the characterization of a lab-scale...

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Autores:
Estrada Gómez, Sebastián
Núñez Rangel, Vitelbina
Preciado Rojo, Lina María
Vargas Muñoz, Leidy Johana
Madrid Bracamonte, Carlos A.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/41073
Acceso en línea:
https://hdl.handle.net/10495/41073
Palabra clave:
Escorpiones
Scorpions
Ponzoñas
Venoms
Dosificación Letal Mediana
Lethal Dose 50
Antivenenos
Antivenins
Inmunoglobulina G
Immunoglobulin G
Colombia
https://id.nlm.nih.gov/mesh/D012605
https://id.nlm.nih.gov/mesh/D014688
https://id.nlm.nih.gov/mesh/D007928
https://id.nlm.nih.gov/mesh/D000997
https://id.nlm.nih.gov/mesh/D007074
https://id.nlm.nih.gov/mesh/D003105
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABSTRACT: Scorpion stings are a public health event in Colombia lacking official epidemiological data, and are considered a medical emergency. Despite the two local producers of antivenoms, neither of them is currently manufacturing scorpion antivenoms. We present the characterization of a lab-scale process to produce the first specific scorpion antivenom for Colombia, formulated to cover scorpion stings produced by Tityus pachyurus, Tityus asthenes, Tityus fuhrmanii, Centruroides spp. To do so, rabbits were immunized by subcutaneous injection with each venom using an immunization program of 3 months. After each rabbit reached the required IgG concentration, rabbits were bled, and plasma was separated by decantation under refrigeration. Immunoglobulins were purified from each hyperimmune plasma using a methodology including precipitation with ammonium sulfate, thermocoagulation, and purification through an ultrafiltration process using a ready-to-use and reusable laboratory crossflow tangential cassette with a polyethersulfone membrane. Each hyperimmune plasma was processed by being separated and freeze-dried at the end of the process. Rabbits were able to produce specific IgG antibodies recognizing the respective immunization venom; even an in vitro interspecies cross-recognition was detected. The separation and purification processes allowed us to obtain IgG products without considerable contaminants (except for albumin). The process was characterized, and critical stages were identified.