首页|首批1型单纯疱疹病毒溶瘤活性测定国家候选标准品的研制

首批1型单纯疱疹病毒溶瘤活性测定国家候选标准品的研制

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目的:研制首批1型单纯疱疹病毒(herpes simplex virus 1,HSV-1)溶瘤活性测定国家标准品.方法:按2020年版《中华人民共和国药典》三部相关要求,分别进行HSV-1溶瘤活性测定液体标准品和冻干标准品的制备和质量检测,并使用热加速试验进行稳定性考察,以U-2 OS细胞/CCK-8法分别在3家实验室对标准品的溶瘤活性进行协作标定.对比研究液体标准品和冻干标准品,选择其中更为适用的1种作为国家标准品.结果:制备的2种HSV-1溶瘤活性测定标准品的质量检测结果均符合要求,其中冻干标准品水分含量为1.09%,分装精度为0.15%.稳定性试验结果用阿伦尼乌斯公式计算,初步预测液体标准品溶瘤活性在-70℃下降低10%需7.7年;冻干标准品溶瘤活性在-70℃下降低10%需6.1 ×105年,其稳定性得到很大提高.3个实验室协作标定进行了共21次测定,液体标准品的溶瘤活性值几何均数为7.08 × 104 U·mL-1,冻干标准品的溶瘤活性值几何均数为1.82 × 104 U·支-1.HSV-1标准品原液在冻干后溶瘤活性由7.08 × 104 U·mL-1下降至3.03 × 104 U·mL-1,但因其溶瘤活性在预稀释100倍后仍然出现良好的S型量效关系曲线,并不影响它作为标准品使用的要求.将液体标准品作为样品,用冻干标准品作为标准品进行校准后,3家实验室结果的几何变异系数(GCV)由64.4%下降到29.2%,实验的精密度得到较大提高.结论:该批HSV-1溶瘤活性测定冻干标准品各项指标均符合相关要求,与液体标准品相比更适合作为国家标准品使用,其溶瘤活性赋值为1.82 × 104 U·支-1.
Preparation of the candidate first Chinese national standard for oncolytic activity assay of herpes simplex virus type 1
Objective:To establish the first national standard for oncolytic activity assay of herpes simplex virus type 1(HSV-1).Methods:According to the requirements in Chinese Pharmacopoeia(Volume Ⅲ,2020 edi-tion),the liquid and freeze-dried standard for oncolytic activity of HSV-1 were prepared and tested,of which the stability were evaluated by thermal acceleration test.The oncolytic activity of the standard was calibrated col-laboratively by U-2 OS cells/CCK-8 method in 3 laboratories.The liquid standard was compared with the freeze-dried standard,and the more suitable one was selected as the national standard.Results:The prepared standard substance was all qualified,among which the moisture content of the freeze-dried standard was 1.09%and the dispensing accuracy was 0.15%.The results of stability test were calculated by Arrhenius formula.It was preliminarily predicted that it would take 7.7 years for the oncolytic activity of liquid standard to decrease by 10%at-70 ℃,and it would take 6.1 × 105 years for the oncolytic activity of lyophilized standard to decrease by 10%at-70 ℃.Compared with liquid standard,the stability of lyophilized standard was greatly improved.Twenty-one times of collaborative calibration tests by 3 laboratories showed that the oncolytic activity liquid standard was 7.08 × 104 U·mL-1 and the oncolytic activity liquid standard was 1.82 × 104 U·vial-1.After lyophilized,the oncolytic activity of the bulk of HSV-1 standard decreased from 7.08 × 104 U·mL-1 to 3.03 × 104 U·mL-1.However,the good S-shaped dose-response curve still appeared after 100 times of pre-dilution,which did not affect the requirements of its use as a standard.When the liquid standard was used as the sample and the freeze-dried standard was used as the standard for calibration,the geometric coefficient of variation(GCV)of the results of the 3 laboratories decreased from 64.4%to 29.2%,and the precision of the experiment was greatly improved.Conclusion:The batch of freeze-dried HSV-1 standards for oncolytic activity assay meets the relavant require-ments,and is more suitable for use as a national standard than liquid standards.Its oncolytic activity is assigned a value of 1.82 × 104 U·vial-1.

herpes simplex virus type 1(HSV-1)U-2 OS cells/CCK-8 methodoncolytic activitystandard substancefreeze-dryingstability

秦玺、胡金盼、李永红、史新昌、丁有学、毕华、韩春梅、郑红梅、饶春明、梁成罡

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中国食品药品检定研究院,北京 100050

厦门大学公共卫生和生命科学学院,厦门 361005

1型单纯疱疹病毒(HSV-1) U-2 OS细胞/CCK-8法 溶瘤活性 标准品 冻干 稳定性

国家科技重大专项

2018ZX09733002-005

2024

药物分析杂志
中国药学会

药物分析杂志

CSTPCD北大核心
影响因子:1.039
ISSN:0254-1793
年,卷(期):2024.44(4)
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