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载三磷酸腺苷的脂质体与等离子体纳米粒子用于基于表面增强拉曼散射的免疫分析。

Adenosine Triphosphate-Encapsulated Liposomes with Plasmonic Nanoparticles for Surface Enhanced Raman Scattering-Based Immunoassays.

机构信息

Department of Bioscience and Biotechnology, Konkuk University, Seoul 143-701, Korea.

School of Chemical and Biological Engineering, Seoul National University, Seoul 151-742, Korea.

出版信息

Sensors (Basel). 2017 Jun 23;17(7):1480. doi: 10.3390/s17071480.

Abstract

In this study, we prepared adenosine triphosphate (ATP) encapsulated liposomes, and assessed their applicability for the surface enhanced Raman scattering (SERS)-based assays with gold-silver alloy (Au@Ag)-assembled silica nanoparticles (NPs; SiO₂@Au@Ag). The liposomes were prepared by the thin film hydration method from a mixture of l-α-phosphatidylcholine, cholesterol, and PE-PEG2000 in chloroform; evaporating the solvent, followed by hydration of the resulting thin film with ATP in phosphate-buffered saline (PBS). Upon lysis of the liposome, the SERS intensity of the SiO₂@Au@Ag NPs increased with the logarithm of number of ATP-encapsulated liposomes after lysis in the range of 8 × 10⁶ to 8 × 10. The detection limit of liposome was calculated to be 1.3 × 10 mol. The successful application of ATP-encapsulated liposomes to SiO₂@Au@Ag NPs based SERS analysis has opened a new avenue for Raman label chemical (RCL)-encapsulated liposome-enhanced SERS-based immunoassays.

摘要

在这项研究中,我们制备了三磷酸腺苷(ATP)包封的脂质体,并评估了其在基于金-银合金(Au@Ag)组装的硅纳米颗粒(NPs;SiO₂@Au@Ag)的表面增强拉曼散射(SERS)测定中的适用性。脂质体通过薄膜水化法从氯仿中的 l-α-磷脂酰胆碱、胆固醇和 PE-PEG2000 的混合物中制备;蒸发溶剂,然后用 PBS 中的 ATP 水化所得薄膜。在脂质体裂解后,SiO₂@Au@Ag NPs 的 SERS 强度随着裂解后包裹的 ATP 脂质体数量的对数增加,范围为 8×10⁶ 至 8×10。脂质体的检测限计算为 1.3×10 mol。ATP 包封脂质体在基于 SiO₂@Au@Ag NPs 的 SERS 分析中的成功应用为拉曼标记化学(RCL)包封脂质体增强的基于 SERS 的免疫分析开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e547/5539552/3655b1d8fbb7/sensors-17-01480-sch001.jpg

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