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用于药物负载与控释的多孔γ-Fe2O3@mWO3多功能纳米粒子的制备

Preparation of Porous γ-Fe2O3@mWO3 Multifunctional Nanoparticles for Drug Loading and Controlled Release.

作者信息

Peng Hongxia, Huang Qin, Wu Tengyan, Wen Jin, He Hengping

机构信息

Hunan Provincial Key Laboratory of Fine Ceramics and Powder Materials, School of Material and Environmental Engineering, Hunan University of Humanities, Science and Technology, 487 Di xing Road, Lou'di, 417000, Hunan Province, China.

National Electronic Ceramics Quality Supervision and Inspection Center, China.

出版信息

Curr Drug Deliv. 2018 Feb 14;15(2):278-285. doi: 10.2174/1567201814666170224144217.

Abstract

BACKGROUND

The use of chemotherapy drug is hindered by relatively low selectivity toward cancer cells and severe side effects from uptake by noncancerous cells and tissue. Thus, targeted drug delivery systems are preferred to increase the efficiency of drug delivery to specific tissues as well as to decrease its side effects. The aims of this paper are develop microwave-triggered controlled-release drug delivery systems using porous γ-Fe2O3@mWO3 multifunctional core-shell nanoparticles. We also studied its magnetic- microwave to heat responsive properties and large specific surface area. We chose ibuprofen (IBU) as a model drug to evaluate the loading and release function of the γ- Fe2O3@mWO3 nanoparticles.

METHODS

We used a direct precipitation method and thermal decomposition of CTAB template method to synthesize core-shell structured γ-Fe2O3@mWO3 nanoparticles. The specific surface areas were calculated by the Brunauer-Emmett-Teller (BET) method. The load drug and controlled release of the γ-Fe2O3@mWO3 triggered by microwave was determined with ultraviolet-visible spectroscopic analysis.

RESULTS

The γ-Fe2O3@mWO3 nanoparticles possesses high surface area of 100.09 m2/g, provides large accessible pore diameter of 6.0 nm for adsorption of drug molecules, high magnetization saturation value of 43.6 emu/g for drug targeting under foreign magnetic fields, quickly convert electromagnetic energy into thermal energy for controlled release by microwave-triggered which was caused by mWO3 shell. The IBU release of over 78% under microwave discontinuous irradiation out classes the 0.15% within 20s only stirring release. This multifunctional material shows good performance for targeting delivery and mWO3 microwave controlled release of anticancer drugs based on all the properties they possess.

CONCLUSION

The porous shell and the introduction of absorbing material not only increased the drug loading efficiency of the nanoparticles but also realized the microwave-stimulated anticancer drug controlled release. The nanoparticles would be very promising for microwave-induced controlled drug release, targeted drug delivery and hyperthermia therapy using microwave.

摘要

背景

化疗药物对癌细胞的选择性相对较低,且被非癌细胞和组织摄取会产生严重副作用,这阻碍了其应用。因此,靶向给药系统更受青睐,以提高药物向特定组织的递送效率并降低其副作用。本文旨在开发使用多孔γ-Fe2O3@mWO3多功能核壳纳米粒子的微波触发控释给药系统。我们还研究了其磁-微波热响应特性和大比表面积。我们选择布洛芬(IBU)作为模型药物来评估γ-Fe2O3@mWO3纳米粒子的负载和释放功能。

方法

我们采用直接沉淀法和CTAB模板热分解法合成核壳结构的γ-Fe2O3@mWO3纳米粒子。通过Brunauer-Emmett-Teller(BET)法计算比表面积。用紫外可见光谱分析测定微波触发的γ-Fe2O3@mWO3的载药和控释情况。

结果

γ-Fe2O3@mWO3纳米粒子具有100.09 m2/g的高比表面积,为药物分子吸附提供了6.0 nm的大孔径,在外部磁场下具有43.6 emu/g的高磁化饱和度值用于药物靶向,能快速将电磁能转化为热能以通过由mWO3壳引起的微波触发实现控释。在微波间断照射下布洛芬的释放率超过78%,远超仅搅拌释放20秒内的0.15%。基于其所有特性,这种多功能材料在抗癌药物的靶向递送和mWO3微波控释方面表现出良好性能。

结论

多孔壳层和吸收材料的引入不仅提高了纳米粒子的载药效率,还实现了微波刺激的抗癌药物控释。这些纳米粒子在微波诱导的控释、靶向给药和微波热疗方面具有很大潜力。

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