Lenghty reverse poly(butylene oxide)-poly(ethylene oxide)-poly (butylene oxide) polymeric micelles and gels for sustained release of antifungal drugs

被引:19
作者
Figueroa-Ochoa, Edgar. B. [1 ]
Villar-Alvarez, Eva M. [2 ]
Cambon, Adriana [2 ]
Mistry, Dharmista [3 ]
Llovo, Jose [4 ]
Attwood, David [5 ]
Barbosa, Silvia [2 ]
Soltero, J. F. Armando [1 ]
Taboada, Pablo [2 ]
机构
[1] Univ Guadalajara, CUCEI, Dept Ingn Quim, Lab Reol, Blv M Garcia Barragan 1421, Guadalajara, Jalisco, Mexico
[2] Univ Santiago de Compostela, Dept Fis Mat Condensada, Grp Fis Coloides & Polimeros, Santiago De Compostela 15782, Spain
[3] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England
[4] Serv Microbiol & Parasitol, Complejo Hosp Santiago De Compostela, Santiago De Compostela 15782, Spain
[5] Univ Manchester, Sch Pharm & Pharmaceut Sci, Manchester M13 9PL, Lancs, England
关键词
Reverse block copolymers; Polymeric micelle; Gelling network; Controlled release; Antifungal activity; LENGTHY HYDROPHILIC BLOCKS; SELF-ASSOCIATION PROPERTIES; PHENYL GLYCIDYL ETHER; ETHYLENE-OXIDE; 1,2-BUTYLENE OXIDE; AQUEOUS-SOLUTION; DIBLOCK COPOLYMERS; TRIBLOCK COPOLYMER; IN-VITRO; CANCER-THERAPY;
D O I
10.1016/j.ijpharm.2016.06.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this work, we present a detailed study of the potential application of polymeric micelles and gels of four different reverse triblock poly(butylene oxide)-poly(ethylene oxide)-poly(butylene oxide) copolymers (BOnEOmBOn, where n denotes the respective block lengths), specifically BO8EO90BO8, BO14EO378BO14, BO20EO411BO20 and BO21EO385BO21, as effective drug transport nanocarriers. In particular, we tested the use of this kind of polymeric nanostructures as reservoirs for the sustained delivery of the antifungals griseofulvin and fluconazole for oral and topical administration. Polymeric micelles and gels formed by these copolymers were shown to solubilize important amounts of these two drugs and to have a good stability in physiologically relevant conditions for oral or topical administration. These polymeric micellar nanocarriers were able to release drugs in a sustained manner, being the release rate slower as the copolymer chain hydrophobicity increased. Different sustained drug release profiles were observed depending on the medium conditions. Gel nanocarriers were shown to display longer sustained release rates than micellar formulations, with the existence of a pulsatile-like release mode under certain solution conditions as a result of their inner network structure. Certain bioadhesive properties were observed for the polymeric physical gels, being moderately tuned by the length and hydrophobicity of the polymeric chains. Furthermore, polymeric gels and micelles showed activity against the yeast Candida albicans and the mould demartophytes (Trichophyton rubrum and Microsporum canis) and, thus, may be useful for the treatment of different cutaneous fungal infections. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 29
页数:13
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