Subacute Pulmonary Toxicity of Glutaraldehyde Aerosols in a Human In Vitro Airway Tissue Model

• Published in: International journal of molecular sciences 2022-10, Vol.23 (20), p.12118
• Main Authors: Wang, Yiying, Wu, Qiangen, Ren, Baiping, Muskhelishvili, Levan, Davis, Kelly, Wynne, Rebecca, Rua, Diego, Cao, Xuefei
• Format: Article
• Language: English
• Subjects: Aerosols; Biocompatibility; Chronic obstructive pulmonary disease; Cytokines; Cytotoxicity; Disinfectants; Disinfection & disinfectants; Exposure; Glutaraldehyde; Goblet cells; Hazard identification; Health care facilities; Homeostasis; Inhalation; Irritation; Matrix metalloproteinase; Matrix metalloproteinases; Medical equipment; Metalloproteinase; Oxidative stress; Protein expression; Proteins; Respiration; Respiratory system; Respiratory tract; Statistical significance; Structure-function relationships; Toxicity
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms232012118

Glutaraldehyde (GA) has been cleared by the Center for Devices and Radiological Health (CDRH) of the Food and Drug Administration (FDA) as a high-level disinfectant for disinfecting heat-sensitive medical equipment in hospitals and healthcare facilities. Inhalation exposure to GA is known to cause respiratory irritation and sensitization in animals and humans. To reproduce some of the known in vivo effects elicited by GA, we used a liquid aerosol exposure system and evaluated the tissue responses in a human in vitro airway epithelial tissue model. The cultures were treated at the air interface with various concentrations of GA aerosols on five consecutive days and changes in tissue function and structure were evaluated at select timepoints during the treatment phase and after a 7-day recovery period. Exposure to GA aerosols caused oxidative stress, inhibition of ciliary beating frequency, aberrant mucin production, and disturbance of cytokine and matrix metalloproteinase secretion, as well as morphological transformation. Some effects, such as those on goblet cells and ciliated cells, persisted following the 7-day recovery period. Of note, the functional and structural disturbances observed in GA-treated cultures resemble those found in ortho-phthaldehyde (OPA)-treated cultures. Furthermore, our in vitro findings on GA toxicity partially and qualitatively mimicked those reported in the animal and human survey studies. Taken together, observations from this study demonstrate that the human air-liquid-interface (ALI) airway tissue model, integrated with an in vitro exposure system that simulates human inhalation exposure, could be used for in vitro-based human hazard identification and the risk characterization of aerosolized chemicals.