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利用 iRGD 靶向脂质体作为荧光探针,通过动态对比增强近红外荧光成像对炎症性关节炎小鼠的滑膜炎进行定量分析。

Synovitis in mice with inflammatory arthritis monitored with quantitative analysis of dynamic contrast-enhanced NIR fluorescence imaging using iRGD-targeted liposomes as fluorescence probes.

机构信息

Department of Ultrasonography, Guangdong Second Provincial General Hospital Affiliated to Southern Medical University, Guangzhou, China.

Department of Ultrasonography, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.

出版信息

Int J Nanomedicine. 2018 Mar 23;13:1841-1850. doi: 10.2147/IJN.S155475. eCollection 2018.

Abstract

BACKGROUND

Rheumatoid arthritis (RA) is a common inflammatory disorder characterized primarily by synovitis and pannus formation in multiple joints, causing joints destruction and irreversible disability in most cases. Early diagnosis and effective therapy monitoring of RA are of importance for achieving the favorable prognosis.

METHODS

We first prepared the targeted fluorescence probes, and then explored the feasibility of near-infrared (NIR) fluorescence molecular imaging to detect and evaluate the RA via the targeted fluorescence probes by quantitative analysis in this study.

RESULTS

The targeted fluorescence probes (indocyanine green-liposomes decorated with iRGD peptide [iLPs]) was successfully prepared. The quantitative analysis found that strong fluorescence signal was detected in inflamed paws and the fluorescence signal in iLPs group was 3.03-fold higher than that in non-targeted (indocyanine green-liposomes decorated without iRGD peptide [LPs]) group (<0.01) at 15 min after injection, whereas the fluorescence signal from iLPs signal can almost not be observed in the non-inflamed paws, showing the high sensitivity and accuracy for arthritis by the NIR fluorescence imaging based on iLPs.

CONCLUSION

The NIR fluorescence imaging by iLPs may facilitate improved arthritis diagnosis and early assessment of the disease progression by providing an in vivo characterization of angiogenesis in inflammatory joint diseases.

摘要

背景

类风湿关节炎(RA)是一种常见的炎症性疾病,主要表现为多个关节的滑膜炎和血管翳形成,导致大多数情况下关节破坏和不可逆残疾。早期诊断和有效的治疗监测对于实现良好的预后非常重要。

方法

我们首先制备了靶向荧光探针,然后通过定量分析探讨了通过靶向荧光探针进行近红外(NIR)荧光分子成像来检测和评估 RA 的可行性。

结果

成功制备了靶向荧光探针(iRGD 肽修饰的吲哚菁绿脂质体 [iLPs])。定量分析发现,在注射后 15 分钟,炎症性爪子中检测到强烈的荧光信号,而 iLPs 组的荧光信号比非靶向组(未修饰 iRGD 肽的吲哚菁绿脂质体 [LPs])高 3.03 倍(<0.01),而在非炎症性爪子中几乎观察不到 iLPs 的荧光信号,表明基于 iLPs 的 NIR 荧光成像对关节炎具有高灵敏度和准确性。

结论

iLPs 的 NIR 荧光成像可能通过提供炎症性关节疾病中血管生成的体内特征,有助于改善关节炎的诊断和疾病进展的早期评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/664c/5870656/50c40fd2b639/ijn-13-1841Fig1.jpg

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