Polyacrylic acid polymers hydrogels intended to topical drug delivery: preparation and characterization

被引:103
作者
Calixto, Giovana [1 ]
Yoshii, Ana Carolina [1 ]
Rocha e Silva, Hilris [1 ]
Ferreira Cury, Beatriz Stringhetti [1 ]
Chorilli, Marlus [1 ]
机构
[1] Sao Paulo State Univ UNESP, Dept Drugs & Pharmaceut, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bioadhesion; hydrogel; metronidazole; polyacrylic acid polymers; topical drug delivery system; CROSS-LINKED HYDROGELS; VITRO RELEASE KINETICS; IN-VITRO; RHEOLOGICAL CHARACTERIZATION; ADHESIVE PROPERTIES; SYSTEMS; MUCOADHESIVE; GELS; FORMULATION; BEHAVIOR;
D O I
10.3109/10837450.2014.882941
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Context: Bioadhesiviness of polyacrylic acid polymers make them promising hydrogels to design topical drug delivery systems, allowing a close contact with biological substrate as well as an enhanced local concentration gradient, both factors that may improve the biological performance of the drugs. Aim: Texture and bioadhesive properties of hydrogels were assessed by using texture analyzer and they were correlated with their rheological behavior and performance as drug delivery systems. Methods: Aqueous dispersions of both polymers were prepared at 0.5%, 1.0% and 1.5% w/v. Hardness, compressibility, adhesiveness, cohesiveness, bioadhesion, continuous flow, oscillatory dynamic test and in vitro drug release were evaluated. Results: Rheological and texture parameters were dependent on polymer concentration and C974P polymer built the strongest structures. Both 1.5% hydrogels presented high bioadhesion values. About 50% of the metronidazole (MTZ) was sustained released from hydrogels within 2 h with an initial burst release at early stage. After, the release rates were decreased and 10% of the MTZ was released in the next 10 h. The drug release process was driven by Fickian diffusion and complex mechanism for PP and C974P hydrogels, respectively. Conclusion: The set of results demonstrated that these hydrogels are promising to be used as topical controlled drug delivery system.
引用
收藏
页码:490 / 496
页数:7
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