68Ga-PSMA-11注射液的制备和质量控制回顾及建议

Review and Suggestions for the Preparation and Quality Control of 68Ga-PSMA-11 Injection

  • 摘要: 本研究制定了规范的68Ga-PSMA-11注射液制备流程,并参考国内外药典要求拟定了适用于本机构的68Ga-PSMA-11注射液质量控制标准。回顾2020—2022年度本机构316批次的68Ga-PSMA-11注射液的制备和质量控制结果,发现所有批次均成功制备得到68Ga-PSMA-11注射液,质量控制结果均符合拟定的标准。68Ga-PSMA-11的标记率为(85.3±11.4)%,受68Ge/68Ga发生器淋洗总体积的显著影响,随着淋洗总体积的增加而降低,而淋洗间隔时间对标记率影响很小。本研究有望指导核医学从业人员规范进行68Ga-PSMA-11注射液的制备和质量控制,从而提升该药物的质量与安全,并为其相关行业标准的制定提供参考。

     

    Abstract: In this study, a standardized preparation process for 68Ga-PSMA-11 injection was developed by optimizing the labeling conditions, and the quality control standards of 68Ga-PSMA-11 injection applicable to our institution were formulated by combining domestic and international pharmacopoeias. Reviewing the preparation and quality control results of a total of 316 batches of 68Ga-PSMA-11 injections from 2020—2022, it was found that all batches were successfully prepared to obtain 68Ga-PSMA-11 injections, and the quality control results were in full compliance with the proposed standards. The labeling rate of 68Ga-PSMA-11 was (85.3±11.4)%, and it was decreased significantly with increasing total elution volume of 68Ge/68Ga generator, while the elution interval time had little effect on the labeling rate. This study is expected to guide nuclear medicine practitioners to standardize the preparation and quality control process of 68Ga-PSMA-11 injection, thus improving the quality and safety of the drug, and providing a reference for related industry standards.

     

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