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Letter to the Editors
Author(s) -
Baer Paul N.
Publication year - 1977
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.1977.48.7.427
Subject(s) - citation , center (category theory) , library science , computer science , crystallography , chemistry
I read with interest the article by Turnbull et al. in Applied Biosafety (Volume 13, Number 3, 2008). The use of ultraviolet light, specifically 254 nm radiation (UVC), has been considered by many in the biosafety community to be a high-risk, low-value disinfecting agent. Their paper is a clear reminder of both the utility and the limits of using UV to disinfect solid materials against biological organisms, including spores. However, in reading the paper, one reference needs clarification. The paper cites an anonymous ABSA position paper which, the authors conclude, indicates that ABSA recommends “...that UV lights within a biological safety cabinet are neither recommended nor required.” This document, which has also circulated on the ABSA Biosafety web server, is not an official ABSA document. It is one of two papers published in Applied Biosafety arguing for and against such a position. The “anonymous” article was actually written by Jyl Burgener. Christina Wilson and I authored the paper opposing such a move. ABSA has, to date, recognized the wisdom of allowing organizations and institutions to use their best judgment in determining when and where UV can be used and whether it is, as part of their risk assessment, a useful adjunct to disinfect items, including biosafety cabinets. As for NSF49 adopting such language, it should be noted that all major BSC manufacturers still provide UV lamps as an option. Most now have implemented the recommendations that Ms. Wilson and I made in 2006 by interlocking the UV source and the sash and allowing the UV lamp to be regulated by a timer. The change in language in NSF49 has also eliminated the routine evaluation of UV fluence during annual recertification. That loss will make it less likely that the UV sources in BSCs will maintain their efficacy without additional work by the end-users. It is my opinion that such a change has not been in the best interest of the biosafety community and the researchers we serve. Laboratories that continue to use UV sources will need to insist that their recertifiers continue to check their UV sources, as visual inspection of the source is not a sufficient check on 254 nm output. Thank you for allowing this clarification to be distributed.