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Chemical and structural investigation of lipid nanoparticles: drug-lipid interaction and molecular distribution

机译:脂质纳米颗粒的化学和结构研究:药物-脂质相互作用和分子分布

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Lipid nanoparticles are a promising alternative to existing carriers in chemical or drug delivery systems. A key challenge is to determine how chemicals are incorporated and distributed inside nanoparticles, which assists in controlling chemical retention and release characteristics. This study reports the chemical and structural investigation of gamma-oryzanol loading inside a model lipid nanoparticle drug delivery system composed of cetyl palmitate as solid lipid and Miglyol 812 (R) as liquid lipid. The lipid nanoparticles were prepared by high pressure homogenization at varying liquid lipid content, in comparison with the gamma-oryzanol free systems. The size of the lipid nanoparticles, as measured by the photon correlation spectroscopy, was found to decrease with increased liquid lipid content from 200 to 160 nm. High-resolution proton nuclear magnetic resonance (H-1-NMR) measurements of the medium chain triglyceride of the liquid lipid has confirmed successful incorporation of the liquid lipid in the lipid nanoparticles. Differential scanning calorimetric and powder x-ray diffraction measurements provide complementary results to the H-1-NMR, whereby the crystallinity of the lipid nanoparticles diminishes with an increase in the liquid lipid content. For the distribution of gamma-oryzanol inside the lipid nanoparticles, the H-1-NMR revealed that the chemical shifts of the liquid lipid in gamma-oryzanol loaded systems were found at rather higher field than those in gamma-oryzanol free systems, suggesting incorporation of gamma-oryzanol in the liquid lipid. In addition, the phase-separated structure was observed by atomic force microscopy for lipid nanoparticles with 0% liquid lipid, but not for lipid nanoparticles with 5 and 10% liquid lipid. Raman spectroscopic and mapping measurements further revealed preferential incorporation of gamma-oryzanol in the liquid part rather than the solid part of in the lipid nanoparticles. Simple models representing the distribution of gamma-oryzanol and lipids (solid and liquid) inside the lipid nanoparticle systems are proposed.
机译:脂质纳米颗粒是化学或药物递送系统中现有载体的有希望的替代物。一个关键的挑战是确定化学物质如何结合并分布在纳米粒子内部,这有助于控制化学物质的保留和释放特性。这项研究报告了在模型脂质纳米颗粒药物传递系统中γ-谷维素负载量的化学和结构研究,该模型由棕榈酸十六烷基酯作为固体脂质和Miglyol 812(R)作为液体脂质组成。与无γ-谷杂醇的系统相比,通过在不同的液体脂质含量下高压均质化来制备脂质纳米颗粒。发现通过光子相关光谱法测量的脂质纳米颗粒的尺寸随着液体脂质含量从200nm增加至160nm而减小。液体脂质的中链甘油三酸酯的高分辨率质子核磁共振(H-1-NMR)测量已确认液体脂质成功地掺入了脂质纳米颗粒中。差示扫描量热法和粉末X射线衍射测量提供了与H-1-NMR互补的结果,由此脂质纳米颗粒的结晶度随着液体脂质含量的增加而降低。对于γ-谷维素在脂质纳米颗粒内部的分布,H-1-NMR揭示了在载有γ-谷维素的系统中液体脂质的化学位移比在无γ-谷维素的系统中更高。液体脂质中的γ-谷维素含量。另外,通过原子力显微镜观察到液体脂质为0%的脂质纳米颗粒的相分离结构,但液体脂质为5%和10%的脂质纳米颗粒却没有观察到。拉曼光谱和作图测量进一步揭示了在脂质纳米颗粒中液体部分而非固体部分中优先掺入了γ-谷维素。提出了代表脂质纳米颗粒系统内γ-谷维素和脂质(固体和液体)分布的简单模型。

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