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A test method to assess the contribution of fluid shear stress to the cleaning of reusable device surfaces
Author(s) -
Hariharan Prasanna,
Paruchuri Sai Sameer,
Topoleski L. D. Timmie,
Rinaldi Jean E.,
Casamento Jon P.,
Myers Matthew R.,
Vesnovsky Oleg
Publication year - 2019
Publication title -
journal of biomedical materials research part b: applied biomaterials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.665
H-Index - 108
eISSN - 1552-4981
pISSN - 1552-4973
DOI - 10.1002/jbm.b.34206
Subject(s) - shear stress , materials science , shear (geology) , biomedical engineering , cleaning agent , composite material , chemistry , medicine , organic chemistry
Adequate cleaning of reusable medical devices is critical for preventing cross‐infection among patients. For reusable medical devices, cleaning using mechanical brushes and detergent may not be sufficient to completely remove the infectious contaminants from the surfaces. This study evaluates the role of fluid flow‐induced shear stress in the detachment and removal of contaminants from device surfaces. A stainless‐steel test coupon, acting as a surrogate for a device surface, was coated with artificial clot of varying mass. The test coupon was exposed to fluid shear stress both with and without an enzymatic detergent. The relationship between clot removal quantity and the applied shear stress was obtained for multiple clot masses. Our results showed that fluid shear increased the effectiveness of the cleaning process. In the absence of flow, soaking the clot surface in the enzymatic detergent removed 67%, 77%, and 95% of the clot for 16 mg, 6.8 mg, and 1 mg initial masses, respectively. In the presence of fluid shear (0.3 Pa for 5 min), approximately 85%, 97%, and 99% of the clot was removed from the surface. The clot mass removed followed a linear relationship ( R 2 = 0.98) versus the applied fluid shear stress. This study showed that different cleaning processes such as fluid shear and detergent action contribute to the soil removal process. This method could be used to evaluate cleaning protocols for minimizing contaminant residue after the reprocessing of medical devices. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 1132–1140, 2019.