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Deoxycholic acid-grafted PEGylated chitosan micelles for the delivery of mitomycin C.
Zhang, Xiu-Rong; Shi, Nian-Qiu; Zhao, Yang; Zhu, He-Yun; Guan, Jiao; Jin, Ying.
Afiliación
  • Zhang XR; Department of Pharmaceutics, School of Pharmacy, Jilin Medical College , Jilin City , PR China.
Drug Dev Ind Pharm ; 41(6): 916-26, 2015 Jun.
Article en En | MEDLINE | ID: mdl-24785368
Mitomycin C (MTC) was incorporated to a micelle system preparing from a polymer named deoxycholic acid chitosan-grafted poly(ethylene glycol) methyl ether (mPEG-CS-DA). mPEG-CS-DA was synthesized and characterized by (1)H nuclear magnetic resonance ((1)H-NMR) and Fourier transform infrared spectroscopy. mPEG-CS-DA formed a core-shell micellar structure with a critical micelle concentration of 6.57 µg/mL. The mPEG-CS-DA micelles were spherical with a hydrodynamic diameter of about 231 nm. After poly(ethylene glycol)ylation of deoxycholic acid chitosan (CS-DA), the encapsulation efficiency and drug loading efficiency increased from 50.62% to 56.42% and from 20.51% to 24.13%, respectively. The mPEG-CS-DA micelles possessed a higher drug release rate than the CS-DA micelles. For pharmacokinetics, the area under the curve (AUC) of the mPEG-CS-DA micelles was 1.5 times higher than that of MTC injection, and these micelles can enhance the bioavailability of MTC. mPEG-CS-DA micelles reduced the distribution of MTC in almost all normal tissues and had the potential to improve the kidney toxicity caused by MTC injection.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Portadores de Fármacos / Mitomicina / Sistemas de Liberación de Medicamentos / Antibióticos Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Drug Dev Ind Pharm Año: 2015 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Portadores de Fármacos / Mitomicina / Sistemas de Liberación de Medicamentos / Antibióticos Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Drug Dev Ind Pharm Año: 2015 Tipo del documento: Article Pais de publicación: Reino Unido