FORMULATION OF METHOTREXATE LOADED SOLID LIPID NANOPARTICLES BY MICRO EMULSION TECHNIQUE

Q3 Materials Science
Ayesha Siddiqua Gazi, A. Krishnasailaja
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引用次数: 2

Abstract

The aim of this study was to develop and characterize Methotrexate loadedsolid lipid nanoparticles by Micro emulsion technique. Methotrexate is a preferable anti metabolite drug. It is used in the treatment of certain cancers like breast cancer, skin and lung cancer. Clinical studies have revealed that the curative effect of MTX tablet regarding cancers was limited due to its toxic dose-related side effects to normal cells, nephrotoxicity, and bone marrow suppression, acute and chronic hepatotoxicity and also due to the drug resistance of the tumour cells. Hence, there is a need to develop methotrexate solid lipid nanoparticles in order to minimize the adverse effects associated with the MTX tablet dosage form. -The objective of the research work is to formulate, characterize and evaluate Methotrexate solid lipid nanoparticles by micro emulsification solidification technique. Solid lipid nanoparticles prepared by using lipids stearic acid and glycerol monostearate by varying the concentration of surfactant. Three formulations were prepared with each lipid. Micro emulsion technique was adopted for preparation of solid lipid nanoparticles. Each formulation was evaluated for drug content, entrapment efficiency, loading capacity& invitro drug release studies. Both the lipids were compared for the characterization and evaluation parameters. On comparison Glycerol monostearate was found to be a better lipid over Stearic acid for the preparation of Methotrexate solid lipid nanoparticles because of its smaller mean particle diameter (238.8 nm), higher stability (-56.5 mV) and greater entrapment efficiency. Methotrexate solid lipid nanoparticles were successfully prepared with higher stability and drug release rate.
微乳法制备甲氨蝶呤负载固体脂质纳米颗粒
本研究的目的是利用微乳液技术开发和表征甲氨蝶呤负载的固体脂质纳米颗粒。甲氨蝶呤是一种较好的抗代谢药物。它用于治疗某些癌症,如乳腺癌癌症、皮肤癌和癌症。临床研究表明,MTX片治疗癌症的疗效有限,原因是其对正常细胞的毒性剂量相关副作用、肾毒性和骨髓抑制、急性和慢性肝毒性以及肿瘤细胞的耐药性。因此,有必要开发甲氨蝶呤固体脂质纳米颗粒,以最大限度地减少与MTX片剂剂型相关的不良影响。研究工作的目的是通过微乳化固化技术制备、表征和评估甲氨蝶啶固体脂质纳米粒子。通过改变表面活性剂的浓度,用脂质硬脂酸和甘油单硬脂酸酯制备固体脂质纳米颗粒。用每种脂质制备三种制剂。采用微乳液技术制备固体脂质纳米粒子。对每种制剂的药物含量、包封率、载药量和体外释药研究进行了评估。比较两种脂质的特征和评价参数。相比之下,在制备甲氨蝶呤固体脂质纳米颗粒时,发现单硬脂酸甘油酯是比硬脂酸更好的脂质,因为它的平均粒径更小(238.8nm)、更高的稳定性(-56.5mV)和更高的包封效率。成功制备了具有较高稳定性和药物释放率的甲氨蝶呤固体脂质纳米粒子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Nanomaterials
Current Nanomaterials Materials Science-Materials Science (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
53
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