Development of pectin nanoparticles through mechanical homogenization for dissolution enhancement of itraconazole

被引:48
作者
Burapapadh, Kanokporn [1 ,2 ,4 ]
Takeuchi, Hirofumi [3 ]
Sriamornsak, Pornsak [1 ,2 ]
机构
[1] Silpakorn Univ, Dept Pharmaceut Technol, Fac Pharm, Nakhon Pathom 73000, Thailand
[2] Silpakorn Univ, Pharmaceut Biopolymer Grp PBiG, Fac Pharm, Nakhon Pathom 73000, Thailand
[3] Gifu Pharmaceut Univ, Lab Pharmaceut Engn, 1-25-4 Daigaku Nishi, Gifu 5011196, Japan
[4] Rangsit Univ, Fac Pharm, Pathum Thani 12000, Thailand
关键词
Pectin; Poorly water-soluble drug; Itraconazole; Nanoparticles; Stability; CITRUS PECTIN; AMIDATION; GELATION; PH;
D O I
10.1016/j.ajps.2015.07.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A simple method to fabricate itraconazole (ITZ)-loaded pectin nanoparticles prepared from nanoemulsion templates is described in this study. Nanoemulsions containing ITZ were prepared by a mechanical homogenization using pectin as emulsifier. After freeze-drying, the morphology, crystallinity state, thermal properties, drug dissolution and stability of the obtained pectin nanoparticles were characterized. The results demonstrated that the morphology of freeze-dried products was different, depending on the type of internal phase; the nanoparticles prepared from chloroform-based nanoemulsions were completely dried and provided a fragile characteristic. The pectin nanoparticles also demonstrated good properties in terms of redispersibility, thermal properties, drug crystallinity and dissolution. The ITZ-loaded pectin nanoparticles showed high percentage of drug dissolved (about 60-80% within 2 h), and maintained their good dissolution properties even after 1-year storage. The results suggested that freeze-dried pectin nanoparticles prepared from nanoemulsions could be used as an effective carrier for enhancement of ITZ dissolution. (C) 2016 The Authors. Production and hosting by Elsevier B.V. on behalf of Shenyang Pharmaceutical University.
引用
收藏
页码:365 / 375
页数:11
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