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Electrohydrodynamic Sprayable Amphiphilic Polysaccharide-Clasped Nanoscale Self-Assembly for In Vivo Imaging

机译:用于体内成像的电液动力学可喷涂两亲多糖 - 扣纳米级自动组装

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摘要

The work presented in this report demonstrates that amphiphilic polysaccharide-clasped self-assembly (Amp-SA) with nanometer size, encapsulating hydrophobic nanoparticles (NPs) can be generated via electrohydrodynamic spraying. It is observed that the formation of hydrophobic NP-encapsulated Amp-SA is dependent on the surface chemistry of NPs. The citrate-coated magnetic NPs (MNPs-Cit) were also prepared and compared. The hydrophobic magnetic NP-encapsulated Amp-SA (Amp-SA-M) exhibited around 2.7-2.8-fold higher values in r(2) relaxivity than that of MNPs-Cit. In addition, the resulting Amp-SA-M achieved similar to 17.2-fold higher values in r(2)/r(1) ratios than MNPs-Cit. The enhanced performances in magnetic transverse (r(2)) relaxivity and r(2)/r(1) ratio as well as the in vivo behavior of Amp-SA-M suggest the potential of Amp-SA-M as a promising MRI nanoprobe. This approach based on the nature-originated amphiphilic biopolymers may provide a novel insight into electrohydrodynamic techniques that have the ability to create various nanostructures, encapsulating high-quality hydrophobic nanomaterials for applications in diverse biotechnology.
机译:本报告中提出的作品表明,通过电液动力喷雾,可以产生具有纳米尺寸的两亲多糖 - 被克拉的自组装(AMP-SA),封装疏水性纳米颗粒(NPS)产生。观察到疏水性NP包封的AMP-SA的形成取决于NPS的表面化学。还制备并比较了柠檬酸盐涂覆的磁NPS(MNPS-CIT)。疏水性磁性NP-包封的AMP-SA(AMP-SA-M)在R(2)放松率高于MNPS-CIT的率高约2.7-2.8倍。此外,所得的AMP-SA-M类似于R(2)/ R(1)比的17.2倍较高的值比MNPS-CIT。磁横向(R(2))松弛率和R(2)/ R(1)比的增强性能以及AMP-SA-M的体内行为表明AMP-SA-M作为有前途的MRI的潜力Nanoprobe。该方法基于自然源自的两亲性生物聚合物可以提供一种新颖的洞察电学动力学技术,该技术具有产生各种纳米结构的能力,将高品质的疏水性纳米材料包封在不同的生物技术中的应用。

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