Antimicrobial Effects of Novel Triple Antibiotic Paste-Mimic Scaffolds on Actinomyces naeslundii Biofilm.

Antimicrobial Effects of Novel Triple Antibiotic Paste-Mimic Scaffolds on Actinomyces naeslundii Biofilm.
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DOI:
10.1016/j.joen.2015.03.005
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发表时间:
2015-08
影响因子:
4.2
通讯作者:
Bottino MC
Bottino MC
中科院分区:
医学2区
文献类型:
--
作者:
Albuquerque MT;Ryan SJ;Münchow EA;Kamocka MM;Gregory RL;Valera MC;Bottino MC

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内氏放线菌已从诊断为坏死牙髓的外伤恒牙中回收。在这项工作中,提出了一种三重抗生素糊剂(TAP)模拟支架作为药物输送策略,以消除A。内氏牙本质生物膜将甲硝唑、环丙沙星和米诺环素加入到聚对二氧环己酮(PDS)聚合物溶液中,并纺成纤维支架。纤维形态,力学性能,和药物释放分别采用扫描电子显微镜,微拉伸测试,和高效液相色谱法进行了研究。将人牙本质标本(4 × 4 × 1 mm 3,n = 4/组)接种A. Naeslundii(ATCC 43146)培养7天以形成生物膜。将感染的牙本质标本暴露于TAP模拟支架、TAP溶液(阳性对照)和纯PDS(无药物支架)。牙本质感染(7天生物膜)的样本用于比较(阴性对照)。进行共聚焦激光扫描显微镜以确定细菌活力。支架显示亚微米平均纤维直径(PDS = 689 ± 312 nm和TAP模拟物= 718 ± 125 nm)。总体而言,TAP模拟支架的机械性能显著低于PDS(P ≤ 0.040)。在前24小时内,观察到所有药物的爆发释放。观察到甲硝唑和环丙沙星持续维持4周以上,但米诺环素没有。共聚焦激光扫描显微镜显示完全消除了所有暴露于TAP溶液的活菌。同时,与阴性对照和PDS相比,TAP模拟支架导致活菌百分比的显著(P <0.05)降低。我们的研究结果表明,TAP模拟支架在根除/消除细菌生物膜方面具有显着的潜力,这是再生牙髓学的关键步骤。
Actinomyces naeslundii has been recovered from traumatized permanent teeth diagnosed with necrotic pulps. In this work, a triple antibiotic paste (TAP)–mimic scaffold is proposed as a drug-delivery strategy to eliminate A. naeslundii dentin biofilm. Metronidazole, ciprofloxacin, and minocycline were added to a polydioxanone (PDS) polymer solution and spun into fibrous scaffolds. Fiber morphology, mechanical properties, and drug release were investigated by using scanning electron microscopy, microtensile testing, and high-performance liquid chromatography, respectively. Human dentin specimens (4 × 4 × 1 mm3, n = 4/group) were inoculated with A. naeslundii (ATCC 43146) for 7 days for biofilm formation. The infected dentin specimens were exposed to TAP-mimic scaffolds, TAP solution (positive control), and pure PDS (drug-free scaffold). Dentin infected (7-day biofilm) specimens were used for comparison (negative control). Confocal laser scanning microscopy was done to determine bacterial viability. Scaffolds displayed a submicron mean fiber diameter (PDS = 689 ± 312 nm and TAP-mimic = 718 ± 125 nm). Overall, TAP-mimic scaffolds showed significantly (P ≤ .040) lower mechanical properties than PDS. Within the first 24 hours, a burst release for all drugs was seen. A sustained maintenance of metronidazole and ciprofloxacin was observed over 4 weeks, but not for minocycline. Confocal laser scanning microscopy demonstrated complete elimination of all viable bacteria exposed to the TAP solution. Meanwhile, TAP-mimic scaffolds led to a significant (P < .05) reduction in the percentage of viable bacteria compared with the negative control and PDS. Our findings suggest that TAP-mimic scaffolds hold significant potential in the eradication/elimination of bacterial biofilm, a critical step in regenerative endodontics.