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Rational design of rabies vaccine formulation for enhanced stability
Author(s) -
Veysel Kayser,
Alain Françon,
Hervé Pinton,
Jean-François Saluzzo,
Bernhardt L. Trout
Publication year - 2017
Publication title -
turkish journal of medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.277
H-Index - 27
eISSN - 1303-6165
pISSN - 1300-0144
DOI - 10.3906/sag-1610-82
Subject(s) - rabies , rabies virus , virology , medicine , potency , rabies vaccine , capsid , virus , clinical efficacy , in vitro , biology , biochemistry
Vaccines are often lyophilized in order to retain their stability and efficacy for a longer period of time. However, the same lyophilization process may also cause a major degradation of the vaccine, especially during early phases of manufacturing, leading to a loss of potency of the product. Many viral diseases, such as rabies, are acute and fatal unless the vaccine is administered prior to exposure or the onset of symptoms in the case of postexposure treatment.

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