4.5 Article

Ca2+ release and buffering effects of synthetic hydroxyapatite following bacterial acid challenge

期刊

BMC ORAL HEALTH
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12903-020-01080-z

关键词

Biofilm; Streptococcus mutans; Synthetic hydroxyapatite; Oral care; Dental caries

资金

  1. Dr. Kurt Wolff GmbH & Co. KG (Bielefeld, Germany)
  2. Medical Faculty of the University of Regensburg within the ReForM B program

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Background Synthetic particulate hydroxyapatite (HAP; Ca-5(PO4)(3)(OH)) is used as ingredient in oral care products but its effects on cariogenic biofilms are not clear yet. The primary mode of action of HAP may be acting as a calcium phosphate reservoir when deposited in oral biofilms and release Ca2+ and (hydrogen) phosphate ions upon bacterial acid challenge. The aim of this in vitro study was to test this hypothesis by investigating release of Ca2+ ions and potential buffering effects from HAP upon bacterial acid challenge in planktonic cultures and biofilms of Streptococcus mutans. Methods Planktonic cultures of S. mutans were grown in BHI broth with 1% sucrose or with additional 5% HAP or 5% silica for up to 48 h. Separately, biofilms of S. mutans were grown in BHI for 72 h in total. After 24 h of this biofilm culture, either BHI alone or BHI with additional 0.5% HAP or 0.5% silica was added. After 48 h, BHI with 1% sucrose was added to allow bacterial acid formation. Ca2+ release was determined colorimetrically and pH measurements were performed using a pH electrode. For statistical analysis, non-parametrical procedures were applied (n >= 10; Mann-Whitney U test; alpha = 0.05). Results Relevant release of Ca2+ was only evident in planktonic cultures or biofilms with HAP but not in both other groups (p <= 0.001). In suspended biofilms with HAP, median pH was 4.77 after 72 h and about 0.5 pH units higher as compared to both other groups (4.28 or 4.32, respectively; p <= 0.001). Conclusions Under the tested conditions, synthetic HAP releases Ca2+ ions upon bacterial acid challenge and may also show some buffering capacity but further studies are needed to investigate whether the concentrations tested here can also be reached clinically in dental biofilms.

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