Leung Kitty, Louca Emily, Gray Michael, Tipples Graham, Coates Allan L
Division of Respiratory Medicine, Hospital for Sick Children, University of Toronto, Ontario, Canada.
J Aerosol Med. 2005 Winter;18(4):414-26. doi: 10.1089/jam.2005.18.414.
Aerosol administration of live measles vaccine virus has proven to be extremely efficacious in field trials using an industrial compressor coupled to a disposable nebulizer (IPI). To develop a new system for administration, it is necessary to characterize the operating characteristics of the old system. There are no standardized techniques for measuring particle size of live biological agents. This study evaluated the Next Generation Pharmaceutical Impactor's (NGI) ability to particle size wet aerosols in an effort to measure the particle size distribution of live measles vaccine from the IPI nebulizer. As a control albuterol was aerosolized using a Pari LC Star, since the soluble albuterol is evenly distributed throughout the droplets and laser diffraction measurements should agree with those from the NGI, as long as the NGI is cooled to prevent heat transfer to the aerosol. Albuterol was also used as a control for the IPI using quantitative ultraviolet spectrophotometry. There was close agreement in MMD (mean +/- 95% CI) for the LC Star, measured by laser diffraction (3.24 +/- 0.06 microm) and the NGI (2.93 +/- 0.22 microm) and the IPI (4.26 +/- 0.17 and 4.26 +/- 0.24 microm, respectively). For the measles vaccine assayed for plaque forming units, there were significant differences between the NGI MMD (6.14 +/- 0.39 microm) compared to laser diffraction (4.95 +/- 0.16 microm) indicating that the vaccine is not evenly distributed among the droplets of various sizes. This is likely clumping of the virus due to gelatin in the formulation. These data indicate that the NGI is capable of particle sizing live biological agents.
在使用与一次性雾化器(IPI)相连的工业压缩机进行的现场试验中,雾化接种活麻疹疫苗病毒已被证明极其有效。为开发一种新的接种系统,有必要对旧系统的运行特性进行表征。目前尚无测量活生物制剂粒径的标准化技术。本研究评估了下一代药物撞击器(NGI)对湿气溶胶进行粒径分析的能力,以测量来自IPI雾化器的活麻疹疫苗的粒径分布。作为对照,使用Pari LC Star雾化沙丁胺醇,由于可溶性沙丁胺醇均匀分布在整个液滴中,只要将NGI冷却以防止热量传递给气溶胶,激光衍射测量结果应与NGI的测量结果一致。沙丁胺醇还被用作IPI的对照,采用定量紫外分光光度法。通过激光衍射测量的LC Star的质量中值直径(MMD,平均值±95%置信区间)为(3.24±0.06微米),与NGI的(2.93±0.22微米)以及IPI的(分别为4.26±0.17微米和4.26±0.24微米)结果非常一致。对于测定蚀斑形成单位的麻疹疫苗,NGI的MMD(6.14±0.39微米)与激光衍射结果(4.95±0.16微米)之间存在显著差异,这表明疫苗在不同大小的液滴中分布不均。这可能是由于制剂中的明胶导致病毒聚集。这些数据表明NGI能够对活生物制剂进行粒径分析。