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首页> 外文期刊>Pharmaceutical research >Solid lipid nanoparticles (SLN) and oil-loaded SLN studied by spectrofluorometry and Raman spectroscopy.
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Solid lipid nanoparticles (SLN) and oil-loaded SLN studied by spectrofluorometry and Raman spectroscopy.

机译:通过荧光分光光度法和拉曼光谱研究了固体脂质纳米颗粒(SLN)和油载SLN。

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PURPOSE: Recently, colloidal dispersions made of mixtures from solid and liquid lipids have been described to overcome the poor drug loading capacity of solid lipid nanoparticles (SLN). It has been proposed that these nanostructured lipid carriers (NLC) are composed of oily droplets, which are embedded in a solid lipid matrix. High loading capacities and controlled release characteristics have been claimed. It is the objective of the present paper to investigate these new NLC particles in more detail to obtain insights into their structure. METHODS: Colloidal lipid dispersions were produced by high-pressure homogenization. Particle sizes were estimated by laser diffraction and photon correlation spectroscopy. The hydrophobic fluorescent marker nile red (NR) was used as model drug, and by fluorometric spectroscopy, the molecular environment (polarity) was elucidated because of solvatochromism of NR. The packaging of the lipid nanoparticles was investigated by Raman spectroscopy and by densimetry. The light propagation in lipid nanodispersions was examined by refractometry to obtain further insights into the nanostructural compositions of the carriers. RESULTS: Fluorometric spectroscopy clearly demonstrates that NLC nanoparticles offer two nanocompartments of different polarity to accommodate NR. Nevertheless, in both compartments, NR experiences less protection from the outer water phase than in a nanoemulsion. In conventional SLN, lipid crystallization leads to the expulsion of the lipophilic NR from the solid lipid. Measurements performed by densimetry and Raman spectroscopy confirm the idea of intact glyceryl behenate lattices in spite of oil loading. The lipid crystals are not disturbed in their structure as it could be suggested in case of oil incorporation. Refractometric data reveal the idea of light protection because of incorporation of sensitive drug molecules in NLC. CONCLUSION: Neither SLN nor NLC lipid nanoparticles did show any advantage with respect to incorporation rate compared to conventional nanoemulsions. The experimental data let us conclude that NLC lipid nanoparticles are not spherical solid lipid particles with embedded liquid droplets, but they are rather solid platelets with oil present between the solid platelet and the surfactant layer.
机译:用途:最近,已经描述了由固体和液体脂质的混合物制成的胶体分散体,以克服固体脂质纳米颗粒(SLN)较弱的药物负载能力。已经提出,这些纳米结构脂质载体(NLC)由油性小滴组成,其被包埋在固体脂质基质中。已要求高负载能力和控释特性。本文的目的是更详细地研究这些新的NLC颗粒,以获取对其结构的见解。方法:通过高压均质法制备胶体脂质分散体。通过激光衍射和光子相关光谱法估计粒径。疏水性荧光标记尼罗红(NR)被用作模型药物,并且通过荧光光谱法,由于NR的溶剂变色作用,阐明了分子环境(极性)。通过拉曼光谱法和密度法研究脂质纳米颗粒的包装。通过折光法检查了脂质纳米分散体中的光传播,以进一步了解载体的纳米结构组成。结果:荧光光谱清楚地表明,NLC纳米颗粒提供了两种极性不同的纳米隔室,以适应NR。然而,在两个隔室中,与纳米乳液相比,NR对外部水相的保护作用都较小。在常规SLN中,脂质结晶导致亲脂性NR从固体脂质中排出。通过密度测定法和拉曼光谱法进行的测量证实了尽管装载了油,但完整的山be酸甘油酯晶格的想法。脂质晶体的结构没有受到干扰,因为在掺入油的情况下可能会暗示。由于NLC中掺入了敏感的药物分子,折光仪数据揭示了光保护的想法。结论:与常规纳米乳剂相比,SLN和NLC脂质纳米颗粒均未显示出任何掺入率方面的优势。实验数据使我们得出结论,NLC脂质纳米颗粒不是带有嵌入液滴的球形固体脂质颗粒,而是相当固体的血小板,在固体血小板和表面活性剂层之间存在油。

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