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Biomolecules ; 11(1)2021 01 15.
Artigo em Inglês | MEDLINE | ID: mdl-33467560

RESUMO

The use of 5-fluorouracil (5FU) is associated with multifaceted challenges and poor pharmacokinetics. Poly(lactic-co-glycolic acid)-lipid hybrid nanoparticles (PLNs)-based therapy has received attention as efficient carriers for a diversity of drugs. This study evaluated the in vivo chemotherapeutic and anti-proliferative efficacy of 5FU-loaded PLNs against 1,2-dimethylhydrazine (Di-MH) prompted colon dysplasia in mice compared to free 5FU. 5FU PLNs were prepared. Male Swiss albino mice were distributed to six experimental groups. Group 1: Saline group. All the other groups were injected weekly with Di-MH [20 mg/kg, s.c.]. Group 2: Di-MH induced colon dysplasia control group. Groups 3 and 4: Di-MH + free 5FU treated group [2.5 and 5 mg/kg]. Groups 5 and 6: Di-MH + 5FU-PLNs treated group [2.5 and 5 mg/kg]. Free 5FU and 5FU-PLNs doses were administered orally, twice weekly. Treatment with 5FU-PLNs induced a higher cytoprotective effect compared to free 5FU as indicated by lower mucosal histopathologic score and reduction in number of Ki-67 immunpositive proliferating nuclei. Additionally, there was significant upregulation of p53 and caspase 3 genes in colon specimens. Our results support the validity of utilizing the PLNs technique to improve the chemopreventive action of 5FU in treating colon cancer.


Assuntos
Quimioprevenção , Fluoruracila/farmacologia , Lecitinas/química , Nanopartículas/química , Copolímero de Ácido Poliláctico e Ácido Poliglicólico/química , Polímeros/química , Animais , Apoptose , Colo/efeitos dos fármacos , Colo/patologia , Modelos Animais de Doenças , Liberação Controlada de Fármacos , Antígeno Ki-67/metabolismo , Lipídeos/química , Masculino , Camundongos , Tamanho da Partícula , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Eletricidade Estática , Proteína Supressora de Tumor p53/genética , Proteína Supressora de Tumor p53/metabolismo
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