[钇铝硅酸盐玻璃微球:用于肝癌经济有效治疗的 "TheraSphere "生物类似配方。

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Cancer Biotherapy and Radiopharmaceuticals Pub Date : 2024-02-01 Epub Date: 2024-01-23 DOI:10.1089/cbr.2023.0118
K V Vimalnath, Ardhi Rajeswari, Anupam Dixit, Rubel Chakravarty, Haldhar D Sarma, Suyash Kulkarni, Ashish Jha, Ameya Puranik, Venkatesh Rangarajan, Madhumita Goswami, Sudipta Chakraborty
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引用次数: 0

摘要

背景:使用合适的β发射放射性核素进行选择性内放射治疗(SIRT)是一种治疗不可切除肝癌的有效方法。钇-90[T1/2 = 64.2 h,Eβ(max) = 2.28 MeV,未检测到γ-光子]因其良好的衰变特性而成为选择性内放射治疗的首选放射性同位素。研究目的本研究描述了本地开发和评估的本征放射性标记[90Y]钇铝硅酸盐([90Y]YAS)玻璃微球,一种与 "TheraSphere"(市售,美国 FDA 批准的制剂)类似的制剂,用于对人类患者中无法切除的肝癌进行 SIRT。研究方法合成了YAS玻璃微球,其成分为40Y2O3-20Al2O3-40SiO2(重量比),直径在20至36微米之间,转化效率几乎达到100%,球形度大于99%。在研究反应堆中对冷YAS玻璃微球进行热中子辐照,制备出了本征标记的[90Y]YAS玻璃微球。在对健康 Wistar 大鼠进行体外评估和体内研究后,对人类患者施用了定制剂量的[90Y]YAS 玻璃微球。研究结果生产出的[90Y]YAS 玻璃微球的比活度为 137.7 ± 8.6 MBq/mg YAS 玻璃(每微球 ∼ 6800 Bq),辐照结束时的放射性核素纯度为 99.94% ± 0.02%。该制剂在人血清中表现出良好的体外稳定性,在健康 Wistar 大鼠体内进行的生物分布研究显示,该制剂在肝脏中的保留率在给药后 7 天内>97%。在人类患者体内注射定制剂量的[90Y]YAS 玻璃微球后的不同时间点记录的钇-90 正电子发射断层扫描显示,该制剂在注射部位的保留率接近定量。结论:该研究证实了自主制备的[90Y]YAS玻璃微球适用于治疗不可切除肝细胞癌的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[90Y]Yttria Alumino Silicate Glass Microspheres: A Biosimilar Formulation to "TheraSphere" for Cost-Effective Treatment of Liver Cancer.

Background: Selective internal radiation therapy (SIRT) using a suitable β--emitting radionuclide is a promising treatment modality for unresectable liver carcinoma. Yttrium-90 (90Y) [T1/2 = 64.2 h, Eβ(max) = 2.28 MeV, no detectable γ-photon] is the most preferred radioisotope for SIRT owing to its favorable decay characteristics. Objective: The present study describes indigenous development and evaluation of intrinsically radiolabeled [90Y]yttria alumino silicate ([90Y]YAS) glass microsphere, a formulation biosimilar to "TheraSphere" (commercially available, U.S. FDA-approved formulation), for SIRT of unresectable liver carcinoma in human patients. Methods: YAS glass microspheres of composition 40Y2O3-20Al2O3-40SiO2 (w/w) and diameter ranging between 20 and 36 μm were synthesized with almost 100% conversion efficiency and >99% sphericity. Intrinsically labeled [90Y]YAS glass microspheres were produced by thermal neutron irradiation of cold YAS glass microspheres in a research reactor. Subsequent to in vitro evaluations and in vivo studies in healthy Wistar rats, customized doses of [90Y]YAS glass microspheres were administered in human patients. Results: [90Y]YAS glass microspheres were produced with 137.7 ± 8.6 MBq/mg YAS glass (∼6800 Bq per microsphere) specific activity and 99.94% ± 0.02% radionuclidic purity at the end of irradiation. The formulation exhibited excellent in vitro stability in human serum and showed >97% retention in the liver up to 7 d post-administration when biodistribution studies were carried out in healthy Wistar rats. Yttrium-90 positron emission tomography scans recorded at different time points post-administration of customized dose of [90Y]YAS glass microspheres in human patients showed near-quantitative retention of the formulation in the injected lobe. Conclusions: The study confirmed the suitability of indigenously prepared [90Y]YAS glass microspheres for clinical use in the treatment of unresectable hepatocellular carcinoma.

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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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