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Sterilization of Human Amniotic Membrane Using an Ozone Hydrodynamic System.
Botelho, Túlia; Kawata, Bianca Akemi; Móbille Awoyama, Silvia; Laurindo Igreja Marrafa, Pedro Augusto; Carvalho, Henrique Cunha; de Lima, Carlos José; Barrinha Fernandes, Adriana.
Afiliación
  • Botelho T; Center for Innovation, Technology and Education - CITÉ, Parque de Inovação Tecnológica de São José dos Campos, São José dos Campos, SP, 12247-016, Brazil.
  • Kawata BA; Faculdade Santo Antônio - FSA, Caçapava, SP, Brazil.
  • Móbille Awoyama S; Center for Innovation, Technology and Education - CITÉ, Parque de Inovação Tecnológica de São José dos Campos, São José dos Campos, SP, 12247-016, Brazil. kawata.bianca@gmail.com.
  • Laurindo Igreja Marrafa PA; Universidade Anhembi Morumbi - UAM, Biomedical Engineering Institute, São Paulo, SP, 04546-001, Brazil. kawata.bianca@gmail.com.
  • Carvalho HC; Center for Innovation, Technology and Education - CITÉ, Parque de Inovação Tecnológica de São José dos Campos, São José dos Campos, SP, 12247-016, Brazil.
  • de Lima CJ; Centro Universitário FUNVIC - UNIFUNVIC, College of Pharmacy, Pindamonhangaba, SP, 12412-825, Brazil.
  • Barrinha Fernandes A; Center for Innovation, Technology and Education - CITÉ, Parque de Inovação Tecnológica de São José dos Campos, São José dos Campos, SP, 12247-016, Brazil.
Ann Biomed Eng ; 52(5): 1425-1434, 2024 May.
Article en En | MEDLINE | ID: mdl-38411861
ABSTRACT
Human amniotic membrane (hAM) is an important biomaterial for Tissue Engineering, due to its great regenerative properties and potential use as a scaffold. The most used procedure to sterilize biomaterials is gamma-irradiation, but this method can affect several properties, causing damage to the structure and reducing the growth factors. The present work evaluated the efficiency of a new method based on ozonated dynamic water for hAM sterilization. HAM fragments were experimentally contaminated with Staphylococcus aureus, Escherichia coli, Candida albicans, Staphylococcus epidermidis, and Clostridium sporogenes (106 CFU/mL) and submitted to sterilization process for 5, 10 and 15 min. The analyses did not reveal microbial activity after 10 min for S. aureus and C. sporogenes and after 15 min for E. coli and S. epidermidis. The microbial activity of C. albicans was reduced with the exposure time increase, but the evaluated time was insufficient for complete sterilization. The depyrogenation process was investigated for different ozonation times (15, 20, 25, 30, and 35 min) to evaluate the ozone sterilization potential and presented promising results after 35 min. The ozone effect on hAM structure was evaluated by histological analysis. A decrease in epithelium average thickness was observed with the exposure time increase. Furthermore, some damage in the epithelium was observed when hAM was exposed for 10 and 15 min. It can indicate that ozone, besides being effective in sterilization, could promote the hAM sample's de-epithelization, becoming a possible new method for removing the epithelial layer to use hAM as a scaffold.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ozono / Staphylococcus aureus Límite: Humans Idioma: En Revista: Ann Biomed Eng Año: 2024 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ozono / Staphylococcus aureus Límite: Humans Idioma: En Revista: Ann Biomed Eng Año: 2024 Tipo del documento: Article País de afiliación: Brasil