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Treatment of early caries lesions using biomimetic self-assembling peptides – a clinical safety trial
Objective We previously reported that a rationally designed biomimetic self-assembling peptide, P(11)−4, nucleated hydroxyapatite de novo and was apparently capable of in situ enamel regeneration following infiltration into caries-like lesions. Our present aim was to determine the safety and potenti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
British Dental Journal
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813405/ https://www.ncbi.nlm.nih.gov/pubmed/23969679 http://dx.doi.org/10.1038/sj.bdj.2013.741 |
Sumario: | Objective We previously reported that a rationally designed biomimetic self-assembling peptide, P(11)−4, nucleated hydroxyapatite de novo and was apparently capable of in situ enamel regeneration following infiltration into caries-like lesions. Our present aim was to determine the safety and potential clinical efficacy of a single application of P(11)−4 on early enamel lesions. Materials and methods Fifteen healthy adults with Class V 'white spot' lesions received a single application of P(11)−4. Adverse events and lesion appearances were recorded over 180 days. Results Patients treated with P(11)−4 experienced a total of 11 adverse events during the study, of which two were possibly related to the protocol. Efficacy evaluation suggested that treatment with P(11)−4 significantly decreased lesion size (p = 0.02) after 30 days and shifted the apparent progression of the lesions from 'arrested/progressing' to 'remineralising' (p <0.001). A highly significant improvement in the global impression of change was recorded at day 30 compared with baseline (p <0.001). Conclusions The results suggest that treatment of early caries lesions with P(11)−4 is safe, and that a single application is associated with significant enamel regeneration, presumably by promoting mineral deposition within the subsurface tissue. |
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