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Effects of Different Disinfection and Sterilization Methods on Tensile Strength of Materials Used for Single-Use Devices

机译:消毒和灭菌方法对一次性设备材料抗张强度的影响

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摘要

Driven by economic and time constraints, some medical centers and third parties are resterilizing single-use devices (SUDs) for reuse. The steam autoclave is quick, but most plastics used in SUDs cannot survive the temperature. Thus, a number of new methods of cleaning, disinfecting, and sterilizing these complex devices are being introduced on the market. The present study investigated the effects of a range of methods on the tensile strength of latex rubber, silicone elastomer, 2 different formulations of polyurethane, nylon, and high-density poly-ethylene (HDPE) specimens. The methods used were sodium hypochlorite bleach (Clorox™), peracetic acid + hydrogen peroxide (Steris™), formaldehyde gas (Chemiclave™), low-temperature peracetic acid and gas plasma (Plazlyte™), and low-temperature hydrogen peroxide gas plasma (Sterrad™). The results showed that silicone elastomer was minimally affected, whereas the strengths of nylon, polyethylene, and latex were reduced by some of the methods. Depending on the formulation, the strength of polyurethane either increased or decreased. The data demonstrated that disinfection and sterilization can affect the tensile strength of certain materials used in medical devices.
机译:在经济和时间限制的驱使下,一些医疗中心和第三方正在对一次性设备(SUD)进行再消毒以供重复使用。蒸汽高压釜很快,但是SUD中使用的大多数塑料都无法承受温度。因此,市场上正在引入许多清洁,消毒和灭菌这些复杂设备的新方法。本研究调查了一系列方法对乳胶,有机硅弹性体,聚氨酯,尼龙和高密度聚乙烯(HDPE)标本的两种不同配方的拉伸强度的影响。使用的方法是次氯酸钠漂白剂(Clorox ™),过氧乙酸+过氧化氢(Steris ™),甲醛气体(Chemiclave ™),低温过氧乙酸和气体等离子体(Plazlyte ™),以及低温过氧化氢气体等离子体(Sterrad ™)。结果表明,有机硅弹性体受到的影响最小,而尼龙,聚乙烯和胶乳的强度却因某些方法而降低。根据配方,聚氨酯的强度会增加或降低。数据表明消毒和灭菌会影响医疗设备中使用的某些材料的拉伸强度。

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  • 来源
    《Biomedical Instrumentation & Technology》 |2002年第1期|23-27|共5页
  • 作者单位

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

    From the Division of Mechanics and Materials Science, U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, Rockville, Md;

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