Research scholar, I.K. Gujral Punjab Technical University, Jalandhar, India.
Research and Development, I.K. Gujral Punjab Technical University, Jalandhar, India.
Drug Dev Ind Pharm. 2020 Feb;46(2):329-342. doi: 10.1080/03639045.2020.1721527. Epub 2020 Feb 5.
The purpose of present research was to develop and statistically optimize nitrendipine nanoemulsion gel for transdermal delivery using box-behnken statistical design. The nanoemulsion formulations bearing nitrendipine were prepared by application of ternary phase diagram and spontaneous emulsification method. Box-behnken design was employed for the optimization of nitrendipine loaded nanoemulsion. The independent variables were oil, surfactant and co-surfactant while globule size, drug content and zeta potential were dependent variables. The optimized nanoemulsion formulation was incorporated into gel and evaluated for release, permeation studies, confocal laser scanning microscopy, skin irritation and histopathological studies. The optimized formulation through box-behnken statistical design showed globule size of 20.43 ± 1.50 nm, drug content of 97.05 ± 1.77% and zeta potential of -15.45 ± 0.35 mV. The study confirmed the enhanced delivery of nitrendipine from nanoemulsion gel than compare to drug solution by virtue of better permeation and solubility. Nanoemulsion gel was proved significantly superior by confocal laser scanning microscopy for satisfactory permeation and distribution of gel, deep into the rat skin. The optimized gel was found with no allergic dermal effects and was proved safe by histopathological studies for transdermal application. Results reveals that developed nitrendipine nanoemulsion gel overcomes the limitation of low penetration and accentuate permeation through albino Wistar rat skin. It was concluded that nanoemulsion gel could be utilized as a potential carrier for transdermal delivery of nitrendipine.
本研究旨在开发并通过 Box-Behnken 统计设计对用于透皮给药的硝苯地平纳米乳凝胶进行统计学优化。载有硝苯地平的纳米乳制剂是通过应用三元相图和自发乳化法制备的。采用 Box-Behnken 设计对载有硝苯地平的纳米乳进行优化。独立变量为油、表面活性剂和共溶剂,而粒径、药物含量和 Zeta 电位为依赖变量。将优化的纳米乳制剂掺入凝胶中,并对其进行释放、渗透研究、共聚焦激光扫描显微镜、皮肤刺激性和组织病理学研究。通过 Box-Behnken 统计设计优化的配方显示粒径为 20.43 ± 1.50nm、药物含量为 97.05 ± 1.77%和 Zeta 电位为-15.45 ± 0.35mV。研究证实,纳米乳凝胶比药物溶液具有更好的渗透性和溶解性,从而增强了硝苯地平的传递。共聚焦激光扫描显微镜证实纳米乳凝胶具有更好的渗透性和分布性,能够深入到大鼠皮肤中,优于其他凝胶。优化的凝胶没有发现过敏的皮肤影响,并通过组织病理学研究证明其可安全用于透皮应用。结果表明,开发的硝苯地平纳米乳凝胶克服了低渗透性的限制,通过白化 Wistar 大鼠皮肤增强了渗透。可以得出结论,纳米乳凝胶可用作硝苯地平经皮给药的潜在载体。