The effectiveness of enzymic irrigation in removing a nutrient‐stressed endodontic multispecies biofilm. (9th January 2014)

• Record Type: Journal Article
• Authors: Niazi, S. A.; Clark, D.; Do, T.; Gilbert, S. C.; Foschi, F.; Mannocci, F.; Beighton, D.
• Is Part Of: International endontic journal. Volume 47:Number 8(2014:Aug.)
• Page Start: 756
• Page End: 768
• Publication Date: 2014-01-09
• Subjects: Endodontics -- Periodicals; 617.6342
• DOI: 10.1111/iej.12214
• Languages: English
• ISSNs: 0143-2885

Abstract

<abstract abstract-type="main" id="iej12214-abs-0001"> <title>Abstract</title> <sec id="iej12214-sec-0001" sec-type="section"> <title>Aim</title> <p>To establish a nutrient‐stressed multispecies model biofilm and investigate the dynamics of biofilm killing and disruption by 1% trypsin and 1% proteinase K with or without ultrasonic activation.</p> </sec> <sec id="iej12214-sec-0002" sec-type="section"> <title>Methodology</title> <p>Nutrient‐stressed biofilms (<italic>Propionibacterium acnes</italic>, <italic> Staphylococcus epidermidis, Actinomyces radicidentis, Streptococcus mitis</italic> and <italic>Enterococcus faecalis </italic>OMGS 3202) were grown on hydroxyapatite discs and in prepared root canals of single‐rooted teeth in modified fluid universal medium. The treatment groups included trypsin, proteinase K, 0.2% chlorhexidine gluconate and 1% sodium hypochlorite (NaOCl) (with and without ultrasonics). NaOCl and chlorhexidine were the positive controls and untreated group, and sterile saline was the negative control. The biofilms were investigated using confocal laser scanning microscopy (CLSM) with live/dead staining and quantitative microbial culture.</p> </sec> <sec id="iej12214-sec-0003" sec-type="section"> <title>Results</title> <p>Nutrient stress in the multispecies biofilm was apparent as the medium pH became alkaline, glucose was absent, and serum proteins were degraded in the supernatant. The CLSM showed the percentage reduction in viable bacteria at the biofilm surface level due to nutrient starvation. On the disc model, trypsin and proteinase K were effective in killing bacteria; their aerobic viable counts were significantly lower (<italic>P</italic> < 0.01) than the negative control and chlorhexidine. NaOCl was the most effective agent (<italic>P</italic> < 0.001). In the tooth model, when compared to saline, trypsin with ultrasonics caused significant killing both aerobically and anaerobically (<italic>P</italic> < 0.05). Chlorhexidine (1.46 ± 0.42), trypsin (3.56 ± 1.18) and proteinase K (4.2 ± 1.01) with ultrasonics were significantly effective (<italic>P</italic> < 0.05) in reducing the substratum coverage as compared to saline with ultrasonics (12% <bold>± </bold>4.9).</p> </sec> <sec id="iej12214-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Trypsin with ultrasonic activation has a biofilm killing and disrupting potential.</p> </sec> </abstract>