首页> 美国卫生研究院文献>Nanoscale Research Letters >Labeling the oily core of nanocapsules and lipid-core nanocapsules with a triglyceride conjugated to a fluorescent dye as a strategy to particle tracking in biological studies
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Labeling the oily core of nanocapsules and lipid-core nanocapsules with a triglyceride conjugated to a fluorescent dye as a strategy to particle tracking in biological studies

机译:用与荧光染料结合的甘油三酸酯标记纳米胶囊和脂质核心纳米胶囊的油性核心作为生物学研究中粒子追踪的策略

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摘要

The synthesis of novel fluorescent materials represents a very important step to obtain labeled nanoformulations in order to evaluate their biological behavior. The strategy of conjugating a fluorescent dye with triacylglycerol allows that either particles differing regarding supramolecular structure, i.e., nanoemulsions, nanocapsules, lipid-core nanocapsules, or surface charge, i.e., cationic nanocapsules and anionic nanocapsules, can be tracked using the same labeled material. In this way, a rhodamine B-conjugated triglyceride was obtained to prepare fluorescent polymeric nanocapsules. Different formulations were obtained, nanocapsules (NC) or lipid-core nanocapsules (LNC), using the labeled oil and Eudragit RS100, Eudragit S100, or poly(caprolactone) (PCL), respectively. The rhodamine B was coupled with the ricinolein by activating the carboxylic function using a carbodiimide derivative. Thin layer chromatography, proton nuclear magnetic resonance (1H-NMR), Fourier transform infrared spectroscopy (FTIR), UV-vis, and fluorescence spectroscopy were used to identify the new product. Fluorescent nanocapsule aqueous suspensions were prepared by the solvent displacement method. Their pH values were 4.6 (NC-RS100), 3.5 (NC-S100), and 5.0 (LNC-PCL). The volume-weighted mean diameter (D4.3) and polydispersity values were 150 nm and 1.05 (NC-RS100), 350 nm and 2.28 (NC-S100), and 270 nm and 1.67 (LNC-PCL). The mean diameters determined by photon correlation spectroscopy (PCS) (z-average) were around 200 nm. The zeta potential values were +5.85 mV (NC-RS100), -21.12 mV (NC-S100), and -19.25 mV (LNC-PCL). The wavelengths of maximum fluorescence emission were 567 nm (NC-RS100 and LNC-PCL) and 574 nm (NC-S100). Fluorescence microscopy was used to evaluate the cell uptake (human macrophage cell line) of the fluorescent nanocapsules in order to show the applicability of the approach. When the cells were treated with the fluorescent nanocapsules, red emission was detected around the cell nucleus. We demonstrated that the rhodamine B-conjugated triglyceride is a promising new material to obtain versatile dye-labeled nanocarriers presenting different chemical nature in their surfaces.
机译:新型荧光材料的合成代表了获得标记的纳米制剂以评估其生物学行为的非常重要的一步。将荧光染料与三酰基甘油缀合的策略允许使用相同的标记材料追踪在超分子结构即纳米乳剂,纳米胶囊,脂质核心纳米胶囊或表面电荷即阳离子纳米胶囊和阴离子纳米胶囊方面不同的任何颗粒。以这种方式,获得了若丹明B-缀合的甘油三酸酯,以制备荧光聚合物纳米胶囊。分别使用标记的油和Eudragit RS100,Eudragit S100或聚己内酯(PCL)获得了不同的制剂,纳米胶囊(NC)或脂质核心纳米胶囊(LNC)。罗丹明B通过使用碳二亚胺衍生物激活羧基官能团与蓖麻油精偶联。薄层色谱,质子核磁共振( 1 H-NMR),傅立叶变换红外光谱(FTIR),紫外可见光谱和荧光光谱被用于鉴定新产品。荧光纳米胶囊水悬浮液通过溶剂置换法制备。它们的pH值分别为4.6(NC-RS100),3.5(NC-S100)和5.0(LNC-PCL)。体积加权平均直径(D4.3)和多分散性值分别为150 nm和1.05(NC-RS100),350 nm和2.28(NC-S100),270 nm和1.67(LNC-PCL)。通过光子相关光谱法(PCS)(z平均)测定的平均直径约为200 nm。 zeta电位值为+5.85 mV(NC-RS100),-21.12 mV(NC-S100)和-19.25 mV(LNC-PCL)。最大荧光发射波长为567 nm(NC-RS100和LNC-PCL)和574 nm(NC-S100)。为了表明该方法的适用性,使用了荧光显微镜来评估荧光纳米胶囊的细胞摄取(人巨噬细胞系)。当用荧光纳米胶囊处理细胞时,在细胞核周围检测到红色发射。我们证明,若丹明B共轭甘油三酸酯是一种有前途的新材料,可用于获得多功能染料标记的纳米载体,这些载体在其表面呈现不同的化学性质。

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