Use of the next generation pharmaceutical impactor for particle size distribution measurements of live viral aerosol vaccines

被引:9
作者
Leung, K
Louca, E
Gray, M
Tipples, G
Coates, AL
机构
[1] Univ Toronto, Div Resp Med, Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[2] Hlth Canada, Natl Microbiol Lab, Winnipeg, MB, Canada
来源
JOURNAL OF AEROSOL MEDICINE-DEPOSITION CLEARANCE AND EFFECTS IN THE LUNG | 2005年 / 18卷 / 04期
关键词
next generation pharmaceutical impactor (NGI); particle size distribution measurement techniques; laser diffraction; measles vaccine virus;
D O I
10.1089/jam.2005.18.414
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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 mu m) and the NGI (2.93 +/- 0.22 mu m) and the IPI (4.26 +/- 0.1-7 and 4.26 +/- 0.24 mu m, respectively). For the measles vaccine assayed for plaque forming units, there were significant differences between the NGI MMD (6.14 +/- 0.39 mu m) compared to laser diffraction (4.95 +/- 0.16 mu m) 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.
引用
收藏
页码:414 / 426
页数:13
相关论文
共 22 条
[1]   An in vitro analysis of the output of budesonide from different nebulizers [J].
Barry, PW ;
O'Callaghan, C .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 104 (06) :1168-1173
[2]  
Bennett JV, 2002, B WORLD HEALTH ORGAN, V80, P806
[3]  
Brain J., 1985, AEROSOLS MED PRINCIP, P123
[4]   THE USE OF LASER DIFFRACTION FOR THE EVALUATION OF THE AEROSOL CLOUDS GENERATED BY MEDICAL NEBULIZERS [J].
CLARK, AR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 115 (01) :69-78
[5]   Alternative routes of measles immunization: a review [J].
Cutts, FT ;
Clements, CJ ;
Bennett, JV .
BIOLOGICALS, 1997, 25 (03) :323-338
[6]   Response to different measles vaccine strains given by aerosol and subcutaneous routes to schoolchildren: a randomised trial [J].
Dilraj, A ;
Cutts, FT ;
de Castro, JF ;
Wheeler, JG ;
Brown, D ;
Roth, C ;
Coovadia, HM ;
Bennett, JV .
LANCET, 2000, 355 (9206) :798-803
[7]  
Doyle C. C., 2003, AAPS PHARMSCITECH, V4, P1
[8]   Aerosolization of cationic lipid:pDNA complexes -: In vitro optimization of nebulizer parameters for human clinical studies [J].
Eastman, SJ ;
Tousignant, JD ;
Lukason, MJ ;
Chu, QM ;
Cheng, SH ;
Scheule, RK .
HUMAN GENE THERAPY, 1998, 9 (01) :43-52
[9]   Optimization of formulations and conditions for the aerosol delivery of functional cationic lipid:DNA complexes [J].
Eastman, SJ ;
Tousignant, JD ;
Lukason, MJ ;
Murray, H ;
Siegel, CS ;
Constantino, P ;
Harris, DJ ;
Cheng, SH ;
Scheule, RK .
HUMAN GENE THERAPY, 1997, 8 (03) :313-322
[10]   Parameters for plaque formation in the potency assay of Japanese measles vaccines [J].
Fukuda, A ;
Sengun, F ;
Sarpay, HE ;
Konobe, T ;
Saito, S ;
Umino, Y ;
Kohama, T .
JOURNAL OF VIROLOGICAL METHODS, 1996, 61 (1-2) :1-6