Suppr超能文献

用于光声成像的基于多功能光敏剂的造影剂。

Multifunctional photosensitizer-based contrast agents for photoacoustic imaging.

作者信息

Ho Chris Jun Hui, Balasundaram Ghayathri, Driessen Wouter, McLaren Ross, Wong Chi Lok, Dinish U S, Attia Amalina Binte Ebrahim, Ntziachristos Vasilis, Olivo Malini

机构信息

Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.

1] Institute for Biological and Medical Imaging, Helmholtz Center Munich, Germany [2] iThera Medical, GmbH, Germany.

出版信息

Sci Rep. 2014 Jun 18;4:5342. doi: 10.1038/srep05342.

Abstract

Photoacoustic imaging is a novel hybrid imaging modality combining the high spatial resolution of optical imaging with the high penetration depth of ultrasound imaging. Here, for the first time, we evaluate the efficacy of various photosensitizers that are widely used as photodynamic therapeutic (PDT) agents as photoacoustic contrast agents. Photoacoustic imaging of photosensitizers exhibits advantages over fluorescence imaging, which is prone to photobleaching and autofluorescence interference. In this work, we examined the photoacoustic activity of 5 photosensitizers: zinc phthalocyanine, protoporphyrin IX, 2,4-bis [4-(N,N-dibenzylamino)-2,6-dihydroxyphenyl] squaraine, chlorin e6 and methylene blue in phantoms, among which zinc phthalocyanine showed the highest photoacoustic activity. Subsequently, we evaluated its tumor localization efficiency and biodistribution at multiple time points in a murine model using photoacoustic imaging. We observed that the probe localized at the tumor within 10 minutes post injection, reaching peak accumulation around 1 hour and was cleared within 24 hours, thus, demonstrating the potential of photosensitizers as photoacoustic imaging contrast agents in vivo. This means that the known advantages of photosensitizers such as preferential tumor uptake and PDT efficacy can be combined with photoacoustic imaging capabilities to achieve longitudinal monitoring of cancer progression and therapy in vivo.

摘要

光声成像是一种新型的混合成像模式,它将光学成像的高空间分辨率与超声成像的高穿透深度结合在一起。在此,我们首次评估了各种广泛用作光动力治疗(PDT)剂的光敏剂作为光声造影剂的效果。光敏剂的光声成像比荧光成像具有优势,荧光成像容易出现光漂白和自发荧光干扰。在这项工作中,我们检测了5种光敏剂在体模中的光声活性:酞菁锌、原卟啉IX、2,4-双[4-(N,N-二苄基氨基)-2,6-二羟基苯基]方酸菁、氯e6和亚甲蓝,其中酞菁锌显示出最高的光声活性。随后,我们使用光声成像在小鼠模型的多个时间点评估了其肿瘤定位效率和生物分布。我们观察到,该探针在注射后10分钟内定位于肿瘤,在1小时左右达到积累峰值,并在24小时内清除,因此,证明了光敏剂作为体内光声成像造影剂的潜力。这意味着光敏剂的已知优势,如优先肿瘤摄取和PDT疗效,可以与光声成像能力相结合,以实现体内癌症进展和治疗的纵向监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad25/4061552/a303a2de9aa1/srep05342-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验