Effect of polydopamine on bonding characteristics and color stability of blood contaminated Biodentine to composite.

IF 2.7 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Frontiers in dental medicine Pub Date : 2026-09-11 eCollection Date: 2026-01-01 DOI:10.3389/fdmed.2026.1945910
Ihtisam Alam, Aravind R Kudva, S Vidhyadhara Shetty, Jayprakash Kukkila
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Abstract

Introduction: Calcium silicate cements such as Biodentine are frequently placed in a blood-contaminated field during vital pulp therapy and must subsequently be bonded to an overlying resin composite. Polydopamine (PDA) improves the wettability and bond strength of mineral trioxide aggregate to resin composite, but its effect on blood-contaminated Biodentine is unknown.

Aim: To determine the effect of PDA pretreatment on the shear bond strength (SBS), failure mode and colour change (ΔE) of blood-contaminated and uncontaminated Biodentine bonded to resin composite.

Materials and methods: Seventy-six standardised Biodentine specimens (5 mm diameter × 3 mm) were prepared with blood contamination (present/absent) and PDA pretreatment (present/absent) as the two factors (n = 19 per cell). After adhesive application, bulk-fill composite build-up and 45 days of storage at 37 °C, SBS was measured, failure modes and ΔE was analysed.

Results: Blood contamination significantly reduced SBS [F(1,72) = 18.86, P < 0.001, partial η 2 = 0.21] and the contamination × PDA interaction was significant [F(1,72) = 7.39, P = 0.008, partial η 2 = 0.09], whereas the main effect of PDA was not [F(1,72) = 2.07, P = 0.155]. Simple-effect analysis showed that PDA increased SBS in contaminated specimens (6.44 → 7.77 MPa; mean difference 1.33 MPa, 95% CI 0.43-2.23; P = 0.004) but not in uncontaminated specimens (8.70 → 8.29 MPa; P = 0.368). Without PDA, contamination lowered SBS by 2.26 MPa (P < 0.001), whereas after PDA pretreatment the difference between contaminated and uncontaminated specimens was no longer significant (P = 0.254). Contamination significantly increased ΔE (P < 0.001) whereas PDA did not (P = 0.102); all groups exceeded the clinical acceptability threshold. Failure-mode distribution differed significantly among groups (Fisher-Freeman-Halton exact P = 0.021; Cramér's V = 0.30), cohesive failure within Biodentine predominating in the contaminated groups.

Conclusions: Within the limitations of this in vitro study, blood contamination occurring during setting reduced the shear bond strength of Biodentine to resin composite and increased its discolouration. PDA pretreatment significantly improved bond strength in contaminated specimens only, abolishing the statistically significant contamination penalty, and did so without aggravating colour change.

聚多巴胺对血污生物登汀与复合材料结合特性及颜色稳定性的影响。
在重要的牙髓治疗过程中,硅酸钙胶合剂(如Biodentine)经常被放置在血液污染的区域,随后必须与覆盖的树脂复合材料结合。聚多巴胺(PDA)提高了矿物三氧化物聚集体与树脂复合材料的润湿性和结合强度,但其对血液污染的生物登汀的影响尚不清楚。目的:探讨PDA预处理对血污染和未污染生物牙定与树脂复合材料的剪切结合强度(SBS)、破坏模式和颜色变化(ΔE)的影响。材料与方法:以血液污染(存在/不存在)和PDA预处理(存在/不存在)为2个因素(n = 19 /细胞)制备76份标准化的Biodentine标本(直径5 mm × 3 mm)。在涂胶、堆填复合材料堆积和在37°C下储存45天后,测量了SBS,分析了失效模式和ΔE。结果:血液污染可显著降低SBS [F(1,72) = 18.86, P η 2 = 0.21],且污染与PDA交互作用显著[F(1,72) = 7.39, P = 0.008,部分η 2 = 0.09],而PDA的主要作用不显著[F(1,72) = 2.07, P = 0.155]。单效应分析显示,PDA使污染标本SBS增加(6.44→7.77 MPa,平均差值1.33 MPa, 95% CI 0.43 ~ 2.23, P = 0.004),而对未污染标本SBS没有增加(8.70→8.29 MPa, P = 0.368)。无PDA时,污染使SBS降低2.26 MPa (P = 0.254)。污染显著增加ΔE (P P = 0.102);所有组均超过临床可接受阈值。失败模式在不同组间的分布差异显著(Fisher-Freeman-Halton精确P = 0.021; cramamer’s V = 0.30),污染组以百奥汀内聚失败为主。结论:在本体外研究的局限性内,凝固过程中发生的血液污染降低了生物奥登汀与树脂复合材料的剪切结合强度,并增加了其变色。PDA预处理仅显著提高了污染标本的粘结强度,消除了统计上显著的污染惩罚,并且没有加重颜色变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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