Pró-fármaco ativado por enzima, uma estratégia promissora na quimioterapia
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
---|---|
Data(s) |
27/05/2014
27/05/2014
01/11/2006
|
Resumo |
Strategies that promote selective activation of prodrugs by enzymes can be divided into two major classes: 1) deliver of a monoclonal antibody-enzyme immunoconjugate that can recognize a specific antigen and promote the prodrug to a citotoxic drug, with a high selectivity for the target cells, and 2) selective gene delivery encoding an enzyme that can promote the prodrug to a citotoxic drug for the target cells. In this article are discussed ADEPT (antibody-directed enzyme prodrug therapy), GDEPT (gene-directed enzyme prodrug therapy), VDEPT (virus-directed enzyme prodrug therapy), GPAT (genetic prodrug activation therapy) and PDEPT (polymer-directed enzyme prodrug therapy) approaches, their clinical trials, advantages, disadvantages and perspectives. |
Formato |
1307-1316 |
Identificador |
http://dx.doi.org/10.1590/S0100-40422006000600028 Quimica Nova, v. 29, n. 6, p. 1307-1316, 2006. 0100-4042 1678-7064 http://hdl.handle.net/11449/69198 10.1590/S0100-40422006000600028 S0100-40422006000600028 WOS:000242341600028 2-s2.0-33845716527 2-s2.0-33845716527.pdf |
Idioma(s) |
por |
Relação |
Química Nova |
Direitos |
openAccess |
Palavras-Chave | #Cancer #Enzymes #Prodrugs |
Tipo |
info:eu-repo/semantics/article |