Development of Alginate-Based Biodegradable Radioactive Microspheres Labeled with Positron Emitter through Click Chemistry Reaction: Stability and PET Imaging Study.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Pharmaceutics Pub Date : 2024-10-07 Epub Date: 2024-08-22 DOI:10.1021/acs.molpharmaceut.4c00412
Arun Gupta, Ji Yong Park, Hyunjun Choi, Tae Hyeon Choi, Yujin Chung, Dong-Hyun Kim, Yun-Sang Lee
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Abstract

Biodegradable radioactive microspheres labeled with positron emitters hold significant promise for diagnostic and therapeutic applications in cancers and other diseases, including arthritis. The alginate-based polymeric microspheres offer advantages such as biocompatibility, biodegradability, and improved stability, making them suitable for clinical applications. In this study, we developed novel positron emission tomography (PET) microspheres using alginate biopolymer radiolabeled with gallium-68 (68Ga) through a straightforward conjugation reaction. Polyethylenimine (PEI)-decorated calcium alginate microspheres (PEI-CAMSs) were fabricated and further modified using azadibenzocyclooctyne-N-hydroxysuccinimide ester (ADIBO-NHS). Subsequently, azide-functionalized NOTA chelator (N3-NOTA) was labeled with [68Ga]Ga to obtain [68Ga]Ga-NOTA-N3, which was then reacted with the surface-modified PEI-CAMSs using strain-promoted alkyne-azide cycloaddition (SPAAC) reaction to develop [68Ga]Ga-NOTA-PEI-CAMSs, a novel PET microsphere. The radiolabeling efficiency and radiochemical stability of [68Ga]Ga-NOTA-PEI-CAMSs were determined using the radio-instant thin-layer chromatography-silica gel (radio-ITLC-SG) method. The in vivo PET images were also acquired to study the in vivo stability of the radiolabeled microspheres in normal mice. The radiolabeling efficiency of [68Ga]Ga-NOTA-PEI-CAMSs was over 99%, and the microspheres exhibited high stability (92%) in human blood serum. PET images demonstrated the stability and biodistribution of the microspheres in mice for up to 2 h post injection. This study highlights the potential of biodegradable PET microspheres for preoperative imaging and targeted radionuclide therapy. Overall, the straightforward synthesis method and efficient radiolabeling technique provide a promising platform for the development of theranostic microspheres using other radionuclides such as 90Y, 177Lu, 188Re, and 64Cu.

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通过点击化学反应开发标记有正电子发射器的藻酸盐基生物可降解放射性微球:稳定性和 PET 成像研究。
用正电子发射器标记的可生物降解放射性微球在癌症和其他疾病(包括关节炎)的诊断和治疗应用中大有可为。藻酸盐基聚合物微球具有生物相容性、生物可降解性和更高的稳定性等优点,适合临床应用。在这项研究中,我们利用藻酸盐生物聚合物,通过简单的共轭反应开发出了新型正电子发射断层扫描(PET)微球,并用镓-68(68Ga)进行了放射性标记。制备了聚乙烯亚胺(PEI)装饰的海藻酸钙微球(PEI-CAMSs),并使用叠氮苯并环辛炔-N-羟基琥珀酰亚胺酯(ADIBO-NHS)对其进行了进一步改性。随后,用[68Ga]Ga标记叠氮功能化的NOTA螯合剂(N3-NOTA),得到[68Ga]Ga-NOTA-N3,再用应变促进炔吖环化反应(SPAAC)将其与表面修饰的PEI-CAMS反应,得到[68Ga]Ga-NOTA-PEI-CAMS,这是一种新型的PET微球。利用放射瞬时薄层色谱-硅胶(radio-ITLC-SG)法测定了[68Ga]Ga-NOTA-PEI-CAMSs的放射性标记效率和放射化学稳定性。为了研究放射性标记微球在正常小鼠体内的稳定性,还采集了体内 PET 图像。[68Ga]Ga-NOTA-PEI-CAMS的放射性标记效率超过99%,微球在人血清中表现出较高的稳定性(92%)。PET 图像显示了微球在小鼠体内注射后长达 2 小时的稳定性和生物分布。这项研究凸显了生物可降解 PET 微球在术前成像和放射性核素靶向治疗方面的潜力。总之,简单的合成方法和高效的放射性标记技术为使用其他放射性核素(如 90Y、177Lu、188Re 和 64Cu)开发治疗微球提供了一个前景广阔的平台。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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