Effects of benzalkonium chloride on innate immunity physiology of the human nasal mucosa in vivo

Citation
T. Storaas et al., Effects of benzalkonium chloride on innate immunity physiology of the human nasal mucosa in vivo, LARYNGOSCOP, 110(9), 2000, pp. 1543-1547
Citations number
28
Categorie Soggetti
Otolaryngology
Journal title
LARYNGOSCOPE
ISSN journal
0023852X → ACNP
Volume
110
Issue
9
Year of publication
2000
Pages
1543 - 1547
Database
ISI
SICI code
0023-852X(200009)110:9<1543:EOBCOI>2.0.ZU;2-L
Abstract
Objective: Benzalkonium chloride (BC) is a preservative commonly used in na sal decongestant sprays. It has been suggested that BC may be harmful to th e nasal mucosa. The present study, involving healthy volunteers, examines e ffects of BC on nasal mucosal end-organ functions. Methods: Isotonic saline and BC (0.1 mg/mL) were administered acutely to the nasal mucosa using a n asal pool device. Nasal symptoms were determined, Nasal lavage fluid levels of alpha(2)-macroglobulin and fucose were measured as indices of plasma ex udation and glandular secretion, respectively. In addition, BC (0.1 mg/mL) was given as single actuations of 100 mu L per nasal cavity three times dai ly for 10 days. The ability of histamine (0.4 mg/mL) to evoke nasal symptom s and plasma exudation responses was determined before and after the repeat ed BC administration series. Results: BC produced immediate nasal smart or pain (P < .05), but tolerance to this response developed by repeated admini strations. BC increased nasal mucosal output of fucose (P < .05), whereas n asal lavage fluid levels of alpha(2)-macroglobulin were unaffected. Histami ne produced significant symptoms and mucosal exudation of alpha(2)-macroglo bulin (P values < .01), equally before and after the 10 days of BC exposure . Conclusions: BC in dosages commonly used as preservative in nasal deconge stant sprays produced short-term glandular secretion and nasal smart or pai n. However, 10 days' frequent exposure to BC was not associated with untowa rd symptomatic effects, nor was a sensitive mucosal variable such as histam ine-induced exudative responsiveness affected by this repeated exposure to BC.