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Drug delivery system based on poly(ether-block-amide) and acrylic acid for controlled release of vancomycin
被引:6
作者:
Ortega, Alejandra
[1
]
Ivan Melendez-Ortiz, H.
[2
]
Garcia-Uriostegui, Lorena
[3
]
Avila-Soria, Griselda
[4
]
机构:
[1] Univ Nacl Autonoma Mexico, Inst Ciencias Nucl, Circuito Exterior S-N,Ciudad Univ, Mexico City 04510, DF, Mexico
[2] CONACyT, Ctr Invest Quim Aplicada, Blvd Enrique Reyna Hermosillo 140, Saltillo 25294, Coahuila, Mexico
[3] Univ Guadalajara, CONACyT, DMCyP, Zapopan 45020, Jalisco, Mexico
[4] Univ Nacl Autonoma Mexico, Inst Marine Sci & Limnol ICML, Reef Syst Unit, Lab Ecol Evolutionary Dev Biol, Puerto Morelos 77580, Quintana Roo, Mexico
关键词:
biomedical applications;
drug delivery systems;
grafting;
polyamides;
ELECTRON-BEAM IRRADIATION;
BIOMEDICAL APPLICATIONS;
THERMOPLASTIC ELASTOMERS;
PH;
SURFACES;
BEHAVIOR;
FILMS;
D O I:
10.1002/app.45745
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Poly(ether-block-amide) (PEBA) films were grafted with acrylic acid (AAc) by gamma radiation, using the oxidative pre-irradiation technique. The effect of dose, monomer concentration, temperature, and reaction time on the graft percentage of AAc onto PEBA was studied. The modified material PEBA-g-AAc was characterized by Fourier infrared spectroscopy (FTIR), scanning electron microscopy, and water contact angle. It was found that PEBA films did not suffer degradation at low doses (<30kGy) during the grafting process. Additionally, PEBA-g-AAc was proved as drug delivery system using vancomycin as drug model. The PEBA-g-AAc with 39 and 98% of AAc loaded 63 and 98 mgg(-1), respectively. The release profiles showed a sustained delivery by 48 h with a partial retention of drug, which depends of grafting percentage. The microbiological tests showed that PEBA-g-AAc was able to inhibit the growing of Staphylococcus aureus in three consecutive challenges. (c) 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 45745.
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页数:8
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