Glyceryl monostearate based nanoparticles of mefenamic acid: Fabrication and in vitro characterization

Rabee Kumar , Mohd Yasir , Shubhini A. Saraf , Praveen K. Gaur , Yatendra Kumar , Alok Pratap Singh
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引用次数: 22

Abstract

Objective

The aim of present research work was to fabricate and evaluate the Mefenamic acid (MF) loaded Solid lipid nanoparticles (SLNs) using Glyceryl monostearate as lipid and tween 80 as surfactant.

Method

MF loaded SLNs were prepared by Solvent Emulsification diffusion technique. Various batches were prepared by hit and trial method varying drug to lipid ratio and surfactant concentration and evaluated for particle size & distribution, particle morphology, zeta potential, percent drug loading and percent drug entrapment efficiency.

Result

Among various lipids like Glyceryl monostearate, Stearic acid and Palmitic acid, GMS was selected for the fabrication of SLNs it was due to the highest solubility of MF in GMS as compared to other above mentioned lipids. Particle size, polydispersity index (PDI), zeta potential, percent drug loading and percent drug entrapment efficiency were found to be 109.7 nm, 0.34, −20.3 mV, 43.00 and 75.45 respectively. Morphologically the SLNs were found to be spherical with rough surfaces. The optimized formulation exhibited 93.28% cumulative drug release after 24 h, while the release mechanism was found to be Fickian diffusion type.

Conclusion

It is concluded that Solvent Emulsification diffusion technique is suitable for fabrication of MF loaded SLNs. All evaluating parameters of optimized SLNs were found to be in acceptable range.

Abstract Image

单硬脂酸甘油基甲氧胺酸纳米颗粒:制备和体外表征
目的以单硬脂酸甘油酯为脂质,吐温80为表面活性剂,制备载甲氧胺酸固体脂质纳米颗粒(SLNs),并对其性能进行评价。方法采用溶剂乳化扩散法制备负载mf的sln。不同药脂比和表面活性剂浓度制备了不同批次的样品,并对其粒径进行了评价;分布、颗粒形态、zeta电位、载药量百分比和载药量百分比。结果在单硬脂酸甘油酯、硬脂酸和棕榈酸等多种脂质中,由于MF在GMS中的溶解度高于其他脂质,因此选择GMS作为制备sln的原料。粒径为109.7 nm, PDI为0.34,zeta电位为- 20.3 mV,载药率为43.00,包封率为75.45。形貌上发现sln为球形,表面粗糙。优化后的制剂在24 h后的累积释药量为93.28%,释药机制为菲克扩散型。结论溶剂乳化扩散技术适用于制备负载MF的sln。优化后的sln的评价参数均在可接受范围内。
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