Comparison of Propofol Microbial Contamination Following Treatment With Drug Disposal Devices.

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Ransome van der Hoeven, Alan L Myers
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引用次数: 0

Abstract

Background: Pharmaceutical waste represents a major burden to the health care system and environment. Proper drug waste disposal devices are vitally needed, especially for propofol solutions that inherently carry a high risk of microbial contamination. Objectives: The aims of this study were to compare the capabilities of 2 drug disposal systems for decontamination of propofol solutions inoculated with medical pathogens and assess chemical degradation of propofol after treatment with Fenton reagents. Methods: Standard microbiological assays were used to assess survival and growth of Escherichia coli and Candida albicans inoculated into propofol solutions. Both a prototype instrument and a commercially marketed disposal device were tested for their ability to kill microbial growth. Furthermore, a propofol bioanalytical assay utilizing high-performance liquid chromatography (HPLC) was developed to measure propofol concentrations before and after treatment with a Fenton reagent cocktail (iron and hydrogen peroxide). Results: Propofol emulsion and diluted solutions lack antimicrobial properties and support the growth of microbes. The prototype instrument effectively killed E. coli and C. albicans inoculated into propofol solutions, while the commercial product did not kill or inhibit the growth of the microorganisms. Finally, propofol was chemically degraded to undetectable quantities (< 0.13 ppm) upon exposure to Fenton reagents in a prototype instrument. Conclusions: We show for the first time that propofol solutions inoculated with microbes are decontaminated upon exposure to Fenton reagents. Treatment with Fenton reagents also chemically destroys the propofol molecule. These results will support the development of novel drug disposal devices for real-time application in the pharmacy setting.

异丙酚药物处置装置处理后微生物污染的比较。
背景:医药废物是卫生保健系统和环境的主要负担。适当的药物废物处理装置是至关重要的,特别是对于具有微生物污染高风险的异丙酚溶液。目的:比较两种药物处理系统对接种医用病原体的异丙酚溶液的去污能力,并评估Fenton试剂处理后异丙酚的化学降解情况。方法:采用标准微生物学方法对接种于异丙酚溶液中的大肠杆菌和白色念珠菌进行存活和生长评价。测试了一种原型设备和一种商业销售的处理设备,以测试它们杀死微生物生长的能力。此外,利用高效液相色谱法(HPLC)开发了一种异丙酚生物分析方法,用于测量Fenton试剂混合物(铁和过氧化氢)处理前后异丙酚浓度。结果:异丙酚乳剂和稀释液缺乏抗菌性能,不利于微生物的生长。该原型仪器能有效杀灭接种于异丙酚溶液中的大肠杆菌和白色念珠菌,而商用产品不能杀灭或抑制微生物的生长。最后,在原型仪器中,暴露于Fenton试剂后,异丙酚被化学降解到不可检测的数量(< 0.13 ppm)。结论:我们首次证明接种微生物的异丙酚溶液在暴露于Fenton试剂后被去污。用芬顿试剂处理也会在化学上破坏异丙酚分子。这些结果将支持在药房设置实时应用的新型药物处置装置的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pharmacy Technology
Journal of Pharmacy Technology PHARMACOLOGY & PHARMACY-
CiteScore
1.50
自引率
0.00%
发文量
49
期刊介绍: For both pharmacists and technicians, jPT provides valuable information for those interested in the entire body of pharmacy practice. jPT covers new drugs, products, and equipment; therapeutic trends; organizational, legal, and educational activities; drug distribution and administration; and includes continuing education articles.
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