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

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 proposed 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 proposed solutions under varying temperature and humidity conditions. Quantitative protein recovery limits were determined at nine facilities. Compared with the conventional solution, the proposed 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.

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2024-09-20
DOI
https://doi.org/10.1038/s41598-024-72473-1
Primary Topic
Medical Device Sterilization and Disinfection
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Toshiaki Shimizu, Seiichi Kato, Yuki Nagahara, Atsushi Tanemura et al.
Scientific Reports
Medical Device Sterilization and Disinfection
article

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

Toshiaki Shimizu, Seiichi Kato, Yuki Nagahara, Atsushi Tanemura, Shinji Fujii, Satoshi Fujita, Yuko Nakano, Atsushi Saitô, Ryusuke Nakaoka, Eiichi Yamamoto, Masafumi Mori, Shinichi Matsumoto, Tomoko Naito, Takahide Mori, Tsuyoshi Kajiura, Takamasa Suzuki, Takayoshi Nakamura, Yuko Miyamoto, Hiroki Muramatsu, Toshiki Inoue, Junki Hosaka, Ayaka Itagaki, Masatake Shimizu, Miyuki Uematsu, Masaki Takashina, Hayato Kosaka
article en

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 proposed 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 proposed solutions under varying temperature and humidity conditions. Quantitative protein recovery limits were determined at nine facilities. Compared with the conventional solution, the proposed 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.

Scientific ReportsVol. 14(1)
University of Fukui (JP), Fujifilm (Japan) (JP), Osaka City General Hospital (JP), Ono Pharmaceutical (Japan) (JP), Sekisui Medical (Japan) (JP), National Institute of Health Sciences (JP), Osaka University Hospital (JP), Furukawa Electric (Japan) (JP), Ehime University (JP), Ebara (Japan) (JP), ShinEtsu Chemical (Japan) (JP)
Japan Agency for Medical Research and Development
Industry, innovation and infrastructure
Openalex Percentile: Top 85%
Medical Device Sterilization and Disinfection
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.