Method to evaluate the dustiness of pharmaceutical powders

被引:41
作者
Boundy, Maryanne [1 ]
Leith, David
Polton, Thomas
机构
[1] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
[2] Pfizer Inc, New York, NY 10017 USA
关键词
dustiness measurement; pharmaceuticals; toxic powders;
D O I
10.1093/annhyg/mel004
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The trend among pharmaceutical companies to develop selective drugs of high potency has pushed the industry to consider the potential of each hazardous ingredient to become airborne. Dustiness issues are not unique to the pharmaceutical industry, but are relevant to any industry where powdered materials are mixed, transferred and handled. Interest in dustiness is also driven by concerns for worker health, the potential for plant explosions and the prevention of product loss. Unlike other industries, the pharmaceutical industry is limited by the milligram quantity of powdered material available for testing during product development. These needs have led to the development of a bench-top dustiness tester that requires only 10 mg of powder and fully contains the generated aerosol. The powder is dispersed within a 5.7 liter glass chamber that contains a respirable mass sampler and a closed-face sampler to quantify the respirable and total dust that are generated with a given energy input. The tester distinguished differences in dustiness levels of five different powders. Finer powders were dustier, and the respirable dust percentage was always less than that for total dust. Four testers have been built and evaluated using pharmaceutical grade lactose. Dustiness measurements determined using all four testers were comparable. The pharmaceutical industry uses surrogates such as lactose to represent active compounds in tests that estimate the dust concentration likely to occur in a new manufacturing operation. Differences between the dustiness of the active compound and its surrogate challenge the relevance of the surrogate tests to represent true exposures in the workplace. The tester can determine the dustiness of both the active compound and its surrogate, and the resultant ratio can help to interpret dust concentrations from surrogate tests. Further, dustiness information may allow the pharmaceutical researcher to select powder formulations that present low airborne concentrations in the workplace.
引用
收藏
页码:453 / 458
页数:6
相关论文
共 23 条
  • [1] OCCUPATIONAL EXPOSURE LIMITS FOR THERAPEUTIC SUBSTANCES
    AGIUS, R
    [J]. ANNALS OF OCCUPATIONAL HYGIENE, 1989, 33 (04) : 555 - 562
  • [2] [Anonymous], J POWDER BULK SOLIDS
  • [3] Occupational toxicology and the control of exposure to pharmaceutical agents at work
    Binks, SP
    [J]. OCCUPATIONAL MEDICINE-OXFORD, 2003, 53 (06): : 363 - 370
  • [4] *BRIT OCC HYG SOC, 1985, DUST EST METH DR 1 2
  • [5] Cawley B., 1993, APPL OCCUP ENVIRON H, P624, DOI DOI 10.1080/1047322X.1993.10388170
  • [6] AN APPARATUS AND METHODOLOGY FOR PREDICTING THE DUSTINESS OF MATERIALS
    COWHERD, C
    GRELINGER, MA
    ENGLEHART, PJ
    KENT, RF
    WONG, KF
    [J]. AMERICAN INDUSTRIAL HYGIENE ASSOCIATION JOURNAL, 1989, 50 (03): : 123 - 130
  • [7] Methods for characterizing the dustiness estimation of powders
    Hamelmann, F
    Schmidt, E
    [J]. CHEMICAL ENGINEERING & TECHNOLOGY, 2004, 27 (08) : 844 - 847
  • [8] Hamelmann F., 2003, KONA, V21, P7, DOI [10.14356/kona.2003006, DOI 10.14356/KONA.2003006]
  • [9] Heidel DS, 2001, DRUGS PHARM SCI, V108, P19
  • [10] Health effects of exposure to active pharmaceutical ingredients (APIs)
    Heron, RJL
    Pickering, FC
    [J]. OCCUPATIONAL MEDICINE-OXFORD, 2003, 53 (06): : 357 - 362