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脂质体在正电子发射断层扫描中的应用和重要性。

The use and importance of liposomes in positron emission tomography.

机构信息

Department of Radiopharmacy, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey.

出版信息

Drug Deliv. 2012 Jan;19(1):68-80. doi: 10.3109/10717544.2011.635721.

Abstract

Among different imaging modalities, Positron Emission Tomography (PET) gained importance in routine hospital practice depending on ability to diagnose diseases in early stages and tracing of therapy by obtaining metabolic information. The combination of PET with Computed Tomography (CT) forms hybrid imaging modality that gives chance to obtain better images having higher resolution by fusing both functional and anatomical images in the same imaging modality at the same time. Therefore, better contrast agents are essentially needed. The advance in research about developing drug delivery systems as specific nanosized targeted systems gained an additional importance for obtaining better diagnosis and therapy of different diseases. Liposomes appear to be more attractive drug delivery systems in delivering either drugs or imaging ligands to target tissue or organ of diseases with higher accumulation by producing in nano-scale, long circulating by stealth effect and specific targeting by modifying with specific ligands or markers. The combination of positron emitting radionuclides with liposomes are commonly in research level nowadays and there is no commercially available liposome formulation for PET imaging. However by conjugating positron emitter radionuclide with liposomes can form promising diagnostic agents for improved diagnosis and following up treatments by increasing image signal/contrast in the target tissue in lower concentrations by specific targeting as the most important advantage of liposomes. More accurate and earlier diagnosis of several diseases can be obtained even in molecular level with the use of stable and effectively radiolabeled molecular target specific nano sized liposomes with longer half-lived positron emitting radionuclides.

摘要

在各种成像方式中,正电子发射断层扫描(PET)由于能够在早期诊断疾病并通过获得代谢信息来追踪治疗而在常规医院实践中变得重要。PET 与计算机断层扫描(CT)的结合形成了混合成像方式,通过在同一成像方式中同时融合功能和解剖图像,有机会获得具有更高分辨率的更好图像。因此,需要更好的对比剂。在开发药物输送系统作为特定的纳米靶向系统方面的研究进展获得了额外的重要性,以便更好地诊断和治疗不同的疾病。脂质体作为药物或成像配体的递送系统似乎更具吸引力,通过产生纳米级的大小、通过隐形效应实现长循环、通过与特定配体或标记物的修饰实现特异性靶向,可以将药物或成像配体递送到疾病的靶组织或器官,从而实现更高的积累。目前,正电子发射放射性核素与脂质体的结合通常处于研究水平,并且没有用于 PET 成像的商业上可获得的脂质体制剂。然而,通过将正电子发射放射性核素与脂质体缀合,可以形成有前途的诊断剂,通过特异性靶向,以更低的浓度在靶组织中增加图像信号/对比度,从而提高诊断和后续治疗的效果,这是脂质体的最重要优势。通过使用稳定且有效的放射性标记的分子靶向性纳米级脂质体与具有更长半衰期的正电子发射放射性核素,可以在分子水平上更准确、更早地诊断多种疾病。

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