Pregled bibliografske jedinice broj: 674212
Do multi-use cellulosic textiles provide safe protection against contamination of sterilized items?
Do multi-use cellulosic textiles provide safe protection against contamination of sterilized items? // Cellulose, 21 (2014), 3; 2101-2109 doi:10.1007/s10570-014-0199-1 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 674212 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Do multi-use cellulosic textiles provide safe protection against contamination of sterilized items?
Autori
Rogina-Car, Beti ; Budimir, Ana ; Turčić, Vatka ; Katović, Drago
Izvornik
Cellulose (0969-0239) 21
(2014), 3;
2101-2109
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
cellulose; multiple use medical textiles; microbial barrier; sterilization; Geobacillus stearothermophilus; Bacillus atrophaeus
Sažetak
The aim of this study was to determine whether multiple use cellulosic medical textiles could provide protection against contamination after sterilization, regardless of the barrier system of only qualified materials, as per EN 868- 2, used in the process. New methods for testing permeability and durability of the microbial barrier cellulosic textiles were developed. The most resistant forms of microorganisms of apathogenic bacterial endospore of the Bacilllus genus: Geobacillus stearothermophilus and Bacillus atrophaeus were used. Testing was performed after 1, 10, 20, 30 and 50 cycles of washing and sterilization under real hospital conditions. The durability of the textile microbial barrier (one layer) was tested after 1, 2 and 3 months of storage under controlled conditions. Bacterial permeability occurs in cellulosic medical textiles when they are contaminated with an extremely high quantity of aerobe bacterial spores. During the testing of microbial barrier durability, the package remained uncontaminated after 1, 2 and 3 months of storage. Medical cellulose textiles used under real hospital conditions functioned properly as a microbial barrier system after 50 cycles of washing and sterilization and 3 months of storage, as the sterilized content was not contaminated at all ; they could be used a microbe barrier system for packing in sterilization, regardless of the fact that they do not meet the standard EN 868- 02:2009 Packaging materials for terminally sterilized medical devices. Part 2: Sterilization wrap - requirements and test methods or the International standard, for example EN ISO 11607- 1:2009 Packaging for terminally sterilized medical devices, Part 1: Requirements for materials, sterile barrier systems and packaging systems.
Izvorni jezik
Engleski
Znanstvena područja
Tekstilna tehnologija
POVEZANOST RADA
Projekti:
108-1080114-0017 - Genotipovi i činitelji virulencije uzročnika bolničkih infekcija (Budimir, Ana, MZOS ) ( CroRIS)
117-1171419-1407 - Alternativni ekološki povoljni procesi i metode kemijske modifikacije celuloze (Katović, Drago, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Tekstilno-tehnološki fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus