Preparation and liver targeting of floxuridinyl dibutyrate solid lipid nanoparticles / 药学学报
Acta Pharmaceutica Sinica
; (12): 761-765, 2008.
Article
em Zh
| WPRIM
| ID: wpr-277799
Biblioteca responsável:
WPRO
ABSTRACT
This paper described the preparation and liver targeting traits of new solid lipid nanoparticles (SLN) containing floxuridinyl dibutyrate (FUDRB) modified with beta-D-galactosides (G2). FUDRB-SLN and FUDRB-G2SLN were prepared by thin layer ultrasonic technique. Transmission electron microscopy micrograph analysis demonstrated that the particle sizes of FUDRB-SLN and FUDRB-G2SLN were (137.5 +/- 11.1) nm and (95.0 +/- 10.7) nm. Drug loading were 9.64% and 8.56%, and entrapment efficiency were 99.81% and 96.23%, respectively. The concentrations of floxuridine (FUDR) in serum and some organs (liver, kidney and lung) were determined by RP-HPLC after iv administration of SLN. FUDR release was confirmed, and a significant enrichment of SLN modified with G2 was observed in liver with G2 complex (targeting rates of SLN-G2 was 8.28 for liver) in comparison with FUDR-sol (targeting rate was 2.56). FUDR could be detected in liver in mice at 480 min after iv administration of FUDRB-G2SLN. These results suggested that incorporation of G2 (4%-5%, g/g) into SLN enhanced the liver targeting-ability of FUDRB. SLN containing G2 could be a useful drug carrier system for liver targeting.
Texto completo:
1
Base de dados:
WPRIM
Assunto principal:
Tamanho da Partícula
/
Sangue
/
Portadores de Fármacos
/
Farmacocinética
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Distribuição Tecidual
/
Química
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Sistemas de Liberação de Medicamentos
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Floxuridina
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Área Sob a Curva
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Composição de Medicamentos
Tipo de estudo:
Prognostic_studies
Limite:
Animals
Idioma:
Zh
Revista:
Acta Pharmaceutica Sinica
Ano de publicação:
2008
Tipo de documento:
Article