Compact microfluidic PET probe concentrator for preclinical and in vitro imaging

用于临床前和体外成像的紧凑型微流控 PET 探针浓缩器

• 批准号: 8737815
• 负责人: Robert Michael van Dam
• 金额: $ 22.74万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-19 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8737815
• 关键词: Address; Affect; Animal Model; Animals; Antineoplastic Agents; Area; Automation; Automobile Driving; Biochemical Pathway; Biological Process; Buffers; Cancer Biology; Cell physiology; Cells; Characteristics; Clinic; Collection; Computer software; Cytosine; DNA biosynthesis; Deoxyglucose; Development; Devices; Diagnostic; Dimensions; Disease; Drug Formulations; Drug Targeting; Ensure; Equipment; Gamma Rays; Gene Expression; Geometry; Glucose; Goals; Heating; High Pressure Liquid Chromatography; Human; Human Resources; Image; Imaging Device; In Vitro; Incentives; Intervention; Left; Liquid substance; Measures; Medical; Membrane; Metabolism; Microfluidic Microchips; Microfluidics; Miniaturization; Monitor; Mus; Normal Cell; Organic solvent product; Pathway interactions; Performance; Phase; Physiology; Positron-Emission Tomography; Procedures; Process; Production; Radiation; Radio; Radioactive; Radiolabeled; Recovery; Reporting; Research; Research Infrastructure; Research Personnel; Sampling; Solid; Solutions; Solvents; Speed; Staging; Surface; System; Techniques; Technology; Temperature; Tissues; Tracer; Translations; Water; anticancer research; aqueous; attenuation; base; cost; design; disease mechanisms study; drug development; enzyme activity; evaporation; flexibility; glucose metabolism; imaging modality; in vivo; in vivo imaging; miniaturize; molecular imaging; novel; novel diagnostics; novel therapeutics; operation; pre-clinical; pre-clinical research; pressure; prevent; prototype; public health relevance; radiotracer; research study; response; sample collection; sensor; tool; user-friendly

DESCRIPTION (provided by applicant): Positron emission tomography (PET) is a molecular imaging modality that utilizes radiolabeled probe molecules to target, image and quantify biological processes in vivo. PET probes can be used to study disease mechanisms, to develop novel diagnostics and therapeutics, detect early stage disease, and monitor response to therapy. Due to the high cost of equipment, infrastructure, and personnel currently required to produce PET probes, the availability and diversity of probes is severely limited (especially for research purposes), hindering both research that depends on this imaging tool and the translation of novel PET probes into medical practice. This challenge is being addressed by efforts to develop miniaturized PET probe production technology based on microfluidics with the eventual goal of an affordable, automated, user-friendly system with built-in radiation shielding that operates on a bench top instead of in a "hot cell". Such a system would enable on-demand production of diverse probes at affordable cost. Current miniaturization efforts have focused primarily on the synthesis itself, and not on downstream processes such as purification and formulation. Most PET tracers require a concentration process during formulation to reduce the volume after HPLC purification so that a sufficient amount of probe is contained in the limited volume that can be injected into small animal models such as mice without adversely affecting their physiology. Concentration is currently achieved by rotary evaporation, using bulky equipment occupying valuable real estate inside the hot cell. To prevent the concentrator from becoming the size-limiting factor in miniaturized radio synthesis, there is a need for development of miniature concentration technologies. In preliminary studies, a compact proof-of-concept microfluidic device to evaporatively concentrate aqueous solutions was developed, and successful concentration of the PET probe 1-(2'-deoxy-2'-[18F]fluoro- arabinofuranosyl) cytosine ([18F]FAC) dissolved in 1:99 EtOH : 10mM NH4H2PO4 (HPLC mobile phase) was demonstrated. This proof-of-concept chip will be further developed in this application into a robust, automated, compact system for routinely concentrating diverse probes. Aim 1 focuses on the development of a microfluidic chip with performance increased to at least match that typically achieved by rotary evaporation. In Aim 2, the chip parameters and operating conditions will be characterized to enable further performance optimization. The concentrated sample collection process will be optimized in Aim 3. In Aim 4, an upstream module will be developed to enable concentration of non-aqueous solutions, thereby extending this technology to all PET probes. A fully automated system (sample loading, concentration, and recovery) will be developed in Aim 5. This application will result in the development of a prototype microfluidic concentrator that will be a critical part of emerging benchtop production platforms for diverse PET probes that will accelerate preclinical research and translation of diagnostics and therapies to the clinic by increasing access to molecular imaging with PET.

描述（由申请人提供）：正电子发射断层扫描（PET）是一种分子成像模式，其利用放射性标记的探针分子来靶向、成像和量化体内生物过程。PET探针可用于研究疾病机制，开发新的诊断和治疗方法，检测早期疾病，并监测对治疗的反应。由于目前生产PET探头所需的设备、基础设施和人员成本高，探头的可用性和多样性受到严重限制（特别是用于研究目的），阻碍了依赖于这种成像工具的研究和新型PET探头向医疗实践的转化。这一挑战正在通过努力开发基于微流体的小型化PET探针生产技术来解决，最终目标是一个负担得起的，自动化的，用户友好的系统，具有内置的辐射屏蔽，在工作台上而不是在“热室”中操作。这样的系统将使得能够以可承受的成本按需生产不同的探针。 目前的小型化努力主要集中在合成本身，而不是下游过程，如纯化和配制。大多数PET示踪剂在配制过程中需要浓缩过程，以减少HPLC纯化后的体积，使得在有限的体积中包含足够量的探针，其可以注射到小动物模型如小鼠中，而不会对其生理产生不利影响。目前通过旋转蒸发实现浓缩，使用占据热室内部有价值的真实的资产的庞大设备。为了防止集中器成为小型化无线电合成中的尺寸限制因素，需要开发小型集中技术。 在初步研究中，开发了用于蒸发浓缩水溶液的紧凑的概念验证微流体装置，并且证明了溶解在1：99 EtOH：10 mM NH 4 H2 PO 4（HPLC移动的相）中的PET探针1-（2 '-脱氧-2'-[18 F]氟-阿拉伯呋喃糖基）胞嘧啶（[18 F]FAC）的成功浓缩。这种概念验证芯片将在本申请中进一步开发成一种强大的、自动化的、紧凑的系统，用于常规浓缩不同的探针。目标1专注于开发一种微流控芯片，其性能提高到至少与通常通过旋转蒸发实现的性能相匹配。在目标2中，将表征芯片参数和操作条件，以实现进一步的性能优化。将在目标3中优化浓缩样品收集过程。在目标4中，将开发一个上游模块，以实现非水溶液的浓缩，从而将该技术扩展到所有PET探头。将在目标5中开发一个全自动系统（样品加载、浓缩和回收）。 该应用将导致原型微流体浓缩器的开发，该原型微流体浓缩器将成为用于各种PET探针的新兴台式生产平台的关键部分，该平台将通过增加使用PET进行分子成像的机会来加速临床前研究以及诊断和治疗向临床的转化。