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作为磁共振成像造影剂的钆(III)卟啉共轭壳聚糖纳米颗粒的研制

Development of Gd(III) porphyrin-conjugated chitosan nanoparticles as contrast agents for magnetic resonance imaging.

作者信息

Jahanbin Tania, Sauriat-Dorizon Hélène, Spearman Peter, Benderbous Soraya, Korri-Youssoufi Hafsa

机构信息

Université Paul Sabatier, Toulouse III, INSERM U825, CHU Purpan, 31059 Toulouse Cedex 9, France.

Institut de Chimie Moléculaire et des Matériaux d'Orsay, UMR CNRS 8182, ECBB, Université Paris-Sud, 91405 Orsay, France.

出版信息

Mater Sci Eng C Mater Biol Appl. 2015;52:325-32. doi: 10.1016/j.msec.2015.03.007. Epub 2015 Apr 10.

Abstract

A novel magnetic resonance imaging (MRI) contrast agent based on gadolinium meso-tetrakis(4-pyridyl)porphyrin [Gd(TPyP)] conjugated with chitosan nanoparticles has been developed. The chitosan nanoparticles were synthesized following an ionic gelation method and the conditions optimized to generate small nanoparticles (CNs) with a narrow size distribution of 35-65 nm. The gadolinium meso-tetrakis(4-pyridyl)porphyrin [Gd(TPyP)] was loaded into chitosan nanoparticles by passive adsorption. The interaction of chitosan with Gd(TPyP) has been examined by UV-visible, Fourier transform infrared spectroscopies (FT-IR) and inductively coupled plasma mass spectrometry (ICP-MS), which indicate the successful association of Gd(TPyP) without any structural distortion throughout the chitosan nanoparticles. The potential of Gd(TPyP)-CNs as MRI contrast agent has been investigated by magnetic resonance imaging (MRI) in-vitro. Relaxivities of Gd(TPyP)-CNs obtained from T1-weighted images, increased with Gd concentration and attained an optimum r1 of 38.35 mM(-1) s(-1), which is 12-fold higher compared to commercial Gd-DOTA (~4 mM(-1) s(-1) at 3T). The combination of such strong MRI contrast with the known properties of porphyrins in photodynamic therapy and biocompatibility of chitosan, presents a new perspective in using these compounds in cancer theranostics.

摘要

一种基于钆中-四(4-吡啶基)卟啉[Gd(TPyP)]与壳聚糖纳米颗粒结合的新型磁共振成像(MRI)造影剂已被研发出来。壳聚糖纳米颗粒采用离子凝胶法合成,并对条件进行了优化,以生成尺寸分布窄、大小为35-65 nm的小纳米颗粒(CNs)。钆中-四(4-吡啶基)卟啉[Gd(TPyP)]通过被动吸附加载到壳聚糖纳米颗粒中。通过紫外可见光谱、傅里叶变换红外光谱(FT-IR)和电感耦合等离子体质谱(ICP-MS)研究了壳聚糖与Gd(TPyP)的相互作用,结果表明Gd(TPyP)在整个壳聚糖纳米颗粒中成功缔合,且无任何结构扭曲。通过体外磁共振成像(MRI)研究了Gd(TPyP)-CNs作为MRI造影剂的潜力。从T1加权图像得到的Gd(TPyP)-CNs的弛豫率随钆浓度增加而增加,最佳r1达到38.35 mM(-1) s(-1),比市售的钆-二乙三胺五乙酸(Gd-DOTA,在3T场强下约为4 mM(-1) s(-1))高12倍。这种强大的MRI造影效果与卟啉在光动力疗法中的已知特性以及壳聚糖的生物相容性相结合,为在癌症诊疗中使用这些化合物提供了新的视角。

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