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用于光学/MR 双模式癌症成像的肿瘤靶向壳聚糖纳米颗粒。

Tumor targeting chitosan nanoparticles for dual-modality optical/MR cancer imaging.

机构信息

Department of Life and Nanopharmaceutical Science, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Korea.

出版信息

Bioconjug Chem. 2010 Apr 21;21(4):578-82. doi: 10.1021/bc900408z.

Abstract

We report tumor targeting nanoparticles for optical/MR dual imaging based on self-assembled glycol chitosan to be a potential multimodal imaging probe. To develop an optical/MR dual imaging probe, biocompatible and water-soluble glycol chitosan (M(w) = 50 kDa) were chemically modified with 5beta-cholanic acid (CA), resulting in amphiphilic glycol chitosan-5beta-cholanic acid conjugates (GC-CA). For optical imaging near-infrared fluorescence (NIRF) dye, Cy5.5, was conjugated to GC-CA resulting in Cy5-labeled GC-CA conjugates (Cy5.5-GC-CA). Moreover, in order to chelate gadolinium (Gd(III)) in the Cy5.5-GC-CA conjugates, 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) was directly conjugated in Cy5.5-GC-CA. Finally, the excess GdCl(3) was added to DOTA modified Cy5.5-GC-CA conjugates in distilled water (pH 5.5). The freshly prepared Gd(III) encapsulated Cy5.5-GC-CA conjugates were spontaneously self-assembled into stable Cy5.5 labeled and Gd(III) encapsulated chitosan nanoparticles (Cy5.5-CNP-Gd(III)). The Cy5.5-CNP-Gd(III) was spherical in shape and approximately 350 nm in size. From the cellular experiment, it was demonstrated that Cy5.5-CNP-Gd(III) were efficiently taken up and distributed in cytoplasm (NIRF filter; red). When the Cy5.5-GC-Gd(III) were systemically administrated into the tail vein of tumor-bearing mice, large amounts of nanoparticles were successfully localized within the tumor, which was confirmed by noninvasive near-infrared fluorescence and MR imaging system simultaneously. These results revealed that the dual-modal imaging probe of Cy5.5-CNP-Gd(III) has the potential to be used as an optical/MR dual imaging agent for cancer treatment.

摘要

我们报告了一种基于自组装的乙二醇壳聚糖的用于光学/MR 双重成像的肿瘤靶向纳米粒子,作为一种潜在的多模态成像探针。为了开发光学/MR 双重成像探针,将生物相容性和水溶性的乙二醇壳聚糖(M(w)= 50 kDa)用 5β-胆酸(CA)化学修饰,得到两亲性的乙二醇壳聚糖-5β-胆酸缀合物(GC-CA)。为了进行光学成像近红外荧光(NIRF)染料,将 Cy5.5 与 GC-CA 缀合,得到 Cy5 标记的 GC-CA 缀合物(Cy5.5-GC-CA)。此外,为了在 Cy5.5-GC-CA 缀合物中螯合钆(Gd(III)),1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸(DOTA)直接与 Cy5.5-GC-CA 缀合。最后,将过量的 GdCl3 添加到 DOTA 修饰的 Cy5.5-GC-CA 缀合物中蒸馏水(pH 5.5)。新鲜制备的 Gd(III)包封的 Cy5.5-GC-CA 缀合物自发地自组装成稳定的 Cy5.5 标记和 Gd(III)包封的壳聚糖纳米颗粒(Cy5.5-CNP-Gd(III))。Cy5.5-CNP-Gd(III)呈球形,大小约为 350nm。从细胞实验中可以证明,Cy5.5-CNP-Gd(III)被有效摄取并分布在细胞质中(NIRF 滤波器;红色)。当 Cy5.5-GC-Gd(III)经尾静脉系统给药于荷瘤小鼠时,大量的纳米颗粒成功地定位于肿瘤内,这一点通过非侵入性近红外荧光和磁共振成像系统同时得到证实。这些结果表明,Cy5.5-CNP-Gd(III)的双模态成像探针有可能成为癌症治疗的光学/MR 双模态成像剂。

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