Article Summary
李永红 毕华 陈伟 饶春明.动态光散射法测定病毒载体基因治疗产品的平均粒径及粒径分布[J].现代生物医学进展英文版,2014,14(34):6611-6613.
动态光散射法测定病毒载体基因治疗产品的平均粒径及粒径分布
Measurement of Particle Size and Distribution of Viral Vector Gene TherapyProducts Using Dynamic Light Scattering (DLS)
  
DOI:
中文关键词: 动态光散射  粒径  粒径分布  病毒载体基因治疗产品  质量控制
英文关键词: Dynamic light scattering  Size  Size distribution  Viral vector gene therapy products  Quality control
基金项目:国家高技术研究发展(863)计划(2012AA020805);国家科技重大专项(2012ZX09304010)
Author NameAffiliation
LI Yong-hong, BI Hua, CHEN Wei, RAO Chun-ming 中国食品药品检定研究院卫生部生物技术产品检定方法及其标准化重点实验室 
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中文摘要:
      目的:建立病毒载体基因产品的粒径及分布的测定方法。方法:采用马尔文Zetasizer Nano ZS 型纳米粒度仪,以氯化钠注 射液作为稀释剂对样品进行适当稀释后,用手动测量方式进行测定。结果:测定的60 nm标准纳米粒子平均粒径为61.24± 0.68 nm,多分散指数(polydispersity index, PDI)为0.020± 0.012 nm。重组人新型P53 腺病毒注射液测定6 次,平均粒径为122.42± 1.80 nm,相对标准偏差(RSD)为1.4%;PDI值为0.056± 0.014 nm,RSD 为25.1%。重组人新型P53 腺病毒注射液于37℃存放时, 平均粒径和PDI值随时间延长有显著增加。至28 天时,平均粒径增加到130.50,PDI值增加到0.265。结论:动态光散射法快速、简 便、准确,可用于病毒载体基因治疗产品的粒径及分布的检测。
英文摘要:
      Objective:To establish the method to measure particle size and distribution of viral vector gene therapy products.Methods:The size and distribution were measured by Nano Particle Analyzer (Malvern Zetasizer Nano ZS) using sodium chloride injection as diluting agent, and manual operation mode was adopted.Results:The measurement result of the 60nm nanosphere size standard showed that the z-average diameter was 61.24± 0.68 nm, and the polydispersity index (PDI) was 0.020± 0.012. After measured by 6 times the z-average diameter result of the new type of recombinant human P53-adenovirus (new P53-Adv) injection was 122.42± 1.80 nm, and relative standard derivation (RSD) was 1.4%. The PDI value of the new P53-Adv injection was 0.056± 0.014, and relative standard derivation (RSD) was 25.1%. When the new P53-Adv injections were stored at 37℃ , the z-average diameter and PDI value increased with the incubation time. After incubation of 28 days the z-average diameter increased to130.50 nm, and the PDI increased to 0.265.Conclusion:The dynamic light scattering method which is fast, simple and accurate, can be used to measure the particle size and distribution of viral vector gene therapy products.
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