Translational nanoconstructs for targeted tissue accumulation and guided surgery in cancer

用于癌症靶向组织积累和引导手术的转化纳米结构

• 批准号: EP/X01374X/1
• 负责人: Carl Redshaw
• 金额: $ 72.96万
• 依托单位: University of Hull
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2023
• 资助国家: 英国
• 起止时间: 2023 至 无数据
• 项目状态: 未结题
• 来源: https://gtr.ukri.org/projects?ref=EP%2FX01374X%2F1
• 关键词: Translational; nanoconstructs; targeted; tissue; accumulation

This project aims to deliver transformative advances in the development of nanoparticle constructs for use in precision surgery and beyond (e.g. therapeutic drug delivery). This will be achieved by bringing together experts with complimentary expertise in calixarene chemistry, nanochemistry, PET (positron emission tomography) imaging and surgical imaging. By developing the chemistry of calixarenes, we will optimize the galectin receptor binding affinity and demonstrate selective cancer cell targeting. Our preliminary studies reveal that radiolabelled (18F) 'Clicked' calixarenes are readily accessible, with improved HPLC purification (achieved via guest incorporation), which enables in vivo bio-distribution, highlighting ideal (renal) clearance. A major benefit of employing a calixarene-based scaffold is the ability for further functionalization. With this in mind, using standard protocols (Click chemistry), the calixarene will be further modified with the addition of a NOTA motif. The incorporation of such a strongly binding motif will allow us to develop the radiolabelling of this new platform technology, with maximum flexibility i.e. with both 18F and 68Ga radionuclides. The functionalized calixarene scaffold will be immobilized on luminescent conjugated polymer nanoparticles to enhance the imaging capabilities. The biodistribution and tumour uptake of the delivery platform will then be accessed (PET imaging), and results will be fed back into the synthetic programme to allow us to optimize the results. Following successful in vitro studies, in vivo tumour uptake will be assessed; tumour and organ uptake will be quantified to assess biodistribution and tumour targeting. The final phase of the project will explore opportunities for using this technology for the collection of spectra in vivo, by combining with a customizable dual camera head. To evaluate depth sensitivity and multimodal guidance an endoscopic gamma probe will be used for multi-functional probe identification. Such a combined approach will be suitable for pre-clinical imaging with a focus on high resolution and signal quality.

该项目旨在为用于精密手术及其他领域（例如治疗药物输送）的纳米颗粒结构的开发提供变革性进展。这将通过汇集在杯芳烃化学，纳米化学，PET（正电子发射断层扫描）成像和外科成像方面具有互补专业知识的专家来实现。通过开发杯芳烃的化学，我们将优化半乳糖凝集素受体结合亲和力，并展示选择性癌细胞靶向。我们的初步研究表明，放射性标记的（18F）“点击”杯芳烃是容易获得的，具有改进的HPLC纯化（通过客体掺入实现），这使得能够在体内生物分布，突出了理想的（肾）清除。采用基于杯芳烃的支架的主要益处是进一步官能化的能力。考虑到这一点，使用标准方案（点击化学），杯芳烃将通过添加NOTA基序进一步修饰。这种强结合基序的掺入将使我们能够开发这种新平台技术的放射性标记，具有最大的灵活性，即使用18F和68 Ga放射性核素。将功能化的杯芳烃支架固定在发光共轭聚合物纳米颗粒上以增强成像能力。然后将访问递送平台的生物分布和肿瘤摄取（PET成像），结果将反馈到合成程序中，以使我们能够优化结果。体外研究成功后，将评估体内肿瘤摄取;将量化肿瘤和器官摄取，以评估生物分布和肿瘤靶向。该项目的最后阶段将探索通过结合可定制的双摄像头，将该技术用于体内光谱收集的机会。为了评价深度灵敏度和多模式引导，将使用内窥镜伽马探头进行多功能探头识别。这种组合方法将适合于临床前成像，重点是高分辨率和信号质量。