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用于肿瘤磁共振成像的叶酸受体靶向双峰脂质体

Folate receptor targeted bimodal liposomes for tumor magnetic resonance imaging.

作者信息

Kamaly Nazila, Kalber Tammy, Thanou Maya, Bell Jimmy D, Miller Andrew D

机构信息

Imperial College Genetic Therapies Centre, Department of Chemistry, Imperial College London, UK.

出版信息

Bioconjug Chem. 2009 Apr;20(4):648-55. doi: 10.1021/bc8002259.

Abstract

Folate-targeted bimodal paramagnetic and fluorescent liposomes were developed and showed enhanced accumulation in a folate receptor expressing tumor model. These bimodal liposomes were composed of both a paramagnetic and a fluorescent lipid, and utilized a PEG-lipid amphiphile for prolonged in vivo circulation. The particles were formulated to ensure a size distribution of approximately 100 nm with a low polydispersity index. IGROV-1 cells were used to induce tumors in nude Balb/c mice, and the folate-targeted liposomes were injected intravenously. Rapid accumulation of the folate-targeted liposomes within the tumor tissue compared to nontargeted liposomes was observed. Furthermore, folate-labeled liposomes showed a 4-fold increase in tumor T(1) signal intensity at just 2 h postinjection with similar results being obtained for the nontargeted liposomes only 24 h postinjection. In addition, the folate-targeted liposomes were injected at half the nontargeted liposome dose, further demonstrating their effectiveness. Histological analysis of sectioned tumor slices revealed distinct fluorescence patterns between the targeted and nontargeted systems, with a more localized and hyperintense fluorescence signal observed from tumor sections post-folate-targeted liposome injections. These results demonstrate the effectiveness of folate targeting for dynamic real-time solid tumor MRI and provide insight into kinetics of targeted and nontargeted nanoparticles to solid tumors.

摘要

开发了叶酸靶向的双模态顺磁性和荧光脂质体,并在表达叶酸受体的肿瘤模型中显示出增强的蓄积。这些双模态脂质体由顺磁性脂质和荧光脂质组成,并利用聚乙二醇脂质两亲物实现体内循环时间延长。将颗粒制剂化以确保粒径分布约为100nm且多分散指数较低。使用IGROV-1细胞在裸Balb/c小鼠中诱导肿瘤,并静脉注射叶酸靶向脂质体。与非靶向脂质体相比,观察到叶酸靶向脂质体在肿瘤组织中迅速蓄积。此外,叶酸标记的脂质体在注射后仅2小时肿瘤T(1)信号强度就增加了4倍,而非靶向脂质体在注射后24小时才获得类似结果。此外,叶酸靶向脂质体的注射剂量是非靶向脂质体的一半,这进一步证明了它们的有效性。对切片肿瘤切片的组织学分析显示,靶向和非靶向系统之间有明显的荧光模式,在注射叶酸靶向脂质体后的肿瘤切片中观察到更局部化和高强度的荧光信号。这些结果证明了叶酸靶向用于动态实时实体瘤MRI的有效性,并提供了关于靶向和非靶向纳米颗粒在实体瘤中的动力学的见解。

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