Towards medical imaging of drug photoactivation: Development of light responsive magnetic resonance imaging and chemical exchange saturation transfer contrast agents

Ilse M. Welleman, Carlijn L. F. van Beek, Ioana Belcin, A. Schulte, Rudi A J O Dierckx, B. L. Feringa, H. Boersma, W. Szymański
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Abstract

In recent years, the use of light to selectively and precisely activate drugs has been developed along the fundamental concepts of photopharmacology. One of the key methods in this field relies on transiently silencing the drug activity with photocleavable protecting groups (PPGs). To effectively utilize light‐activated drugs in future medical applications, physicians will require a reliable method to assess whether light penetrates deep enough into the tissues to activate the photoresponsive theragnostic agents. Here, we describe the development and evaluation of magnetic resonance (MR) imaging agents that allow for the detection of light penetration and drug activation in the tissues using non‐invasive whole‐body magnetic resonance imaging (MRI) and chemical exchange saturation transfer (CEST)‐MRI modalities. The approach relies on the use of PPG‐protected MR contrast agents, which upon irradiation with light change their imaging signal. A Gadolinium(III)‐based MRI contrast agent is presented that undergoes a significant change in relaxivity (25%) upon uncaging, providing a reliable indicator of light‐induced cargo release. Additionally, we introduce the first light‐responsive CEST‐MRI imaging agent, enabling positive signal enhancement (off‐to‐on) upon light activation, offering a novel approach to visualize the activation of photoactive agents in living tissues. This research provides a proof‐of‐principle for the non‐invasive, whole‐body imaging of light penetration and drug activation with high temporal resolution characteristic of MR methods.
实现药物光激活的医学成像:光响应磁共振成像和化学交换饱和转移造影剂的开发
近年来,根据光药理学的基本概念,利用光来选择性地、精确地激活药物的方法得到了发展。该领域的关键方法之一是利用光可裂解保护基团(PPG)瞬时抑制药物活性。为了在未来的医疗应用中有效利用光激活药物,医生需要一种可靠的方法来评估光是否能深入组织激活光致活性热敏剂。在此,我们介绍了磁共振成像(MR)制剂的开发和评估,该制剂可利用无创全身磁共振成像(MRI)和化学交换饱和转移(CEST)-MRI 模式检测光在组织中的穿透和药物激活情况。这种方法依赖于使用受 PPG 保护的磁共振造影剂,这些造影剂在光照射下会改变其成像信号。本文介绍了一种基于钆(III)的磁共振成像造影剂,这种造影剂在开笼后弛豫度会发生显著变化(25%),为光诱导的货物释放提供了可靠的指标。此外,我们还介绍了第一种光响应 CEST-MRI 成像剂,它能在光激活时实现正信号增强(从关到开),为活体组织中光活性剂的激活提供了一种新的可视化方法。这项研究为以磁共振方法特有的高时间分辨率对光穿透和药物激活进行无创全身成像提供了原理验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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