Brain targeting efficiency of antimigrain drug loaded mucoadhesive intranasal nanoemulsion

被引:93
作者
Abdou, Ebtsam M. [1 ]
Kandil, Soha M. [2 ]
El Miniawy, Hala M. F. [3 ]
机构
[1] Natl Org Drug Control & Res NODCAR, Dept Pharmaceut, Cairo, Egypt
[2] Modern Univ Technol & Informat MTI, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo, Egypt
[3] Cairo Univ, Fac Vet Med, Dept Pathol, Giza, Egypt
关键词
Bioavailability; Brain targeting; Chitosan; Nanoemulsion; Nasal; Zolmitriptan; IN-VITRO; DELIVERY SYSTEM; DIRECT NOSE; NASAL; MICROEMULSION; ZOLMITRIPTAN; FORMULATIONS; CHITOSAN; BIOAVAILABILITY; SUMATRIPTAN;
D O I
10.1016/j.ijpharm.2017.07.030
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Zolmitriptan (ZT) is a well-tolerated drug in migraine treatment suffering from low bioavailability due to low amount of the drug that reaches the brain after oral and nasal delivery. Development of new nasal mucoadhesive nanoemulsion formulation for zolmitriptan may success in delivering the drug directly from the nose to the brain to achieve rapid onset of action and high drug concentration in the brain which is required for treatment of acute migraine. ZT mucoadhesive nanoemulsion were prepared and characterized for drug content, zeta potential, particle size, morphology, residence time and permeation through the nasal mucosa. The selected formula was tested in-vivo in mice for its pharmacokinetics in comparison with intravenous and nasal solution of zolmitriptan. Results showed that addition of chitosan as mucoadhesive agent in 0.3% concentration to the nanoemulsion enhanced its residence time and zetapotential with no significant effect on the globule size. All tested formulations showed higher permeability coefficients than the zolmitriptan solution through the nasal mucosa. In-vivo studies showed that the mucoadhesive nanoemulsion formulation of zolmitriptan has higher AUC(0-8) and shorter T-max in the brain than the intravenous or the nasal solution. This was related to the small globule size and higher permeability of the formulation. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:667 / 677
页数:11
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