Fabrication of pectin-based nanoemulsions loaded with itraconazole for pharmaceutical application

被引:55
作者
Burapapadh, Kanokporn [1 ,2 ,3 ]
Kumpugdee-Vollrath, Mont [3 ]
Chantasart, Doungdaw [4 ]
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] Univ Appl Sci Berlin, Dept Pharmaceut Engn, D-13353 Berlin, Germany
[4] Mahidol Univ, Dept Pharm, Fac Pharm, Bangkok 10400, Thailand
关键词
Pectin; Nanoemulsions; Itraconazole; Simple homogenization; DRUG; EMULSION; DISSOLUTION; FORMULATION; ABSORPTION;
D O I
10.1016/j.carbpol.2010.04.071
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of this study was to prepare nanoemulsions containing itraconazole (ITZ), a poorly water-soluble drug, using pectin as a polymeric emulsifier. Nanoemulsions were prepared by simple homogenization to avoid high-pressure conditions. The influences of type of internal phase, type and concentration of pectin on the droplet size, morphology, and zeta potential of the pectin-based emulsions were also examined. Nanoemulsions were achieved when chloroform was used as an internal phase while using caprylic/capric triglyceride can produce only micron-sized emulsions. Pectin with high degree of esterification offered good emulsion properties because of its high amount of hydrophobic molecules. The droplet size of emulsions decreased with the increased pectin concentration. The addition of 117 to the emulsion formulation was essential to obtain the nano-sized emulsions, resulting from the molecular association between 117 and pectin. It appears that 3% (w/w) pectin provided the most stable emulsion with the highest percent creaming. The obtained nanoemulsions may be subsequently developed as a self-emulsifying drug delivery system. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:384 / 393
页数:10
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