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摘要:
In this study, a new formulation of silica nanocomposite containing nifedipine (NI) loaded freeze-dried solid-lipid nanoparticles (NI-SLNs) and silica have been developed with improved flowability of powders, which can lead to the formulation of a widely acceptable oral dosage form. The stable NI-SLNs were prepared using two phospholipids, hydrogenated soybean phosphatidylcholine and dipalmitoylphosphatidylglycerol mixed with 2.5% w/v trehalose as a cryoprotectant followed by lyophilization. We employed various grades of two types of silica, such as fumed and precipitated. Silica improved the poor flow property of NI-SLNs to good category as per USP-29. In addition, most of the silica nanocomposites showed the satisfactory results in their physicochemical properties such as particle size, polydispersity index, zeta potential, and recovered potency by around 100 nm, 0.3, -50 mV, and 80%, respectively. Furthermore, it was found that NI-SLNs were easily released form nanocomposites within 30 min, therefore, suggesting an improvement of drug dissolutions. Among them, precipitated silica cooperated fairly in improving the powder characteristics as well as the physicochemical, morphological, and pharmaceutical properties.
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篇名 Improving Flow Property of Nifedipine Loaded Solid-Lipid Nanoparticles by Means of Silica for Oral Solid Dosage Form
来源期刊 药理与制药(英文) 学科 医学
关键词 SILICA Solid-Lipid Nanoparticle SOLID DOSAGE Form NIFEDIPINE FLOWABILITY
年,卷(期) 2014,(12) 所属期刊栏目
研究方向 页码范围 1119-1129
页数 11页 分类号 R73
字数 语种
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研究主题发展历程
节点文献
SILICA
Solid-Lipid
Nanoparticle
SOLID
DOSAGE
Form
NIFEDIPINE
FLOWABILITY
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研究分支
研究去脉
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期刊影响力
药理与制药(英文)
月刊
2157-9423
武汉市江夏区汤逊湖北路38号光谷总部空间
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444
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