Design and validation of a method for evaluating medical device cleanliness by recovering and quantifying residual proteins on stainless plates

Author:

Uematsu Miyuki1,Miyamoto Yuko1,Shimizu Masatake2,Kajiura Takeshi2,Saito Atsushi3,Takashina Masaki3,Fujita Satoshi4,Nakano Yuko4,Shimizu Toshiaki5,Nagahara Yuki5,Kosaka Hayato5,Muramatsu Hiroki6,Mori Masafumi6,Suzuki Takamasa6,Nakamura Takayoshi7,Tanemura Atsushi7,Hosaka Junki8,Mori Takahide8,Kato Seiichi9,Itagaki Ayaka9,Inoue Toshiki9,Matsumoto Shinichi10,Naito Tomoko11,Fujii Shinji11,Nakaoka Ryusuke1,Yamamoto Eiichi1

Affiliation:

1. National Institute of Health Sciences

2. Inui Medics Co. Ltd.

3. Osaka University Hospital

4. Clean Chemical Co. Ltd.

5. Sakura Seiki Co. Ltd.

6. Suzuyo & Co. Ltd.

7. Nicca Chemical Co. Ltd.

8. FUJIFILM Wako Pure Chemical Corp.

9. Hogy Medical Co. Ltd.

10. Muranaka Medical Instruments Co. Ltd.

11. Miura Co., Ltd.

Abstract

Abstract We recently reported a method for recovering and quantifying residual proteins bound to surfaces of various medical instruments via thermal coagulation under neutral pH and room temperature. The method effectively recovered and solubilised coagulated proteins at high temperatures in dry and humid conditions, with a protein recovery rate of > 90%. This study validated the previous method by comparing residual protein recovery from test samples using a conventional extraction solution (1% SDS, [pH 11.0]) and novel solution (1% SDS, 10 mM TCEP, and 10 mM HEPES [pH 7.0]). To mimic soiled medical equipment, pseudo-blood-contaminated stainless steel plates were prepared. Residual protein was recovered using conventional and novel solutions under varying temperature and humidity conditions. Quantitative protein recovery limits were determined at nine facilities. Compared with the conventional solution, the novel solution recovered proteins more effectively from samples processed at temperatures > 60°C. However, low recovery rates were observed for samples processed at 95°C, possibly owing to differences in protein adhesion due to sample and plate-surface properties. Our findings present a method for quantifying residual proteins on medical instruments exposed to high temperatures during use or disinfection. Further studies should standardise test soiling conditions, materials, and solutions to evaluate cleaning methods.

Publisher

Research Square Platform LLC

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