Multifunctional PAMAM nanoparticles with sequential antimicrobial-remineralization therapy for dentin caries management

IF 6.1 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Mingxiao Liu, Jiahe Li, Ziyou Wang, Miao Chen, Jianru Yi, Zhihe Zhao and Kunneng Liang
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Abstract

Dentin caries is a multifactorial pathological process characterized by bacterial colonization and biofilm formation that result in concurrent acid-mediated demineralization and matrix metalloproteinase (MMP)-mediated degradation of the collagenous matrix. While remineralization therapies offer minimal invasiveness, their long-term efficacy is compromised by ongoing collagen degradation and persistent bacterial acid production that counteract remineralization efforts. To address these limitations, we designed PAMAM-G4@EG (PGE) nanoparticles (NPs) using polyamide amine (PAMAM) dendrimers as mineral deposition templates, with antimicrobial peptide G(IIKK)4I–NH2 (G4) grafted onto the external surface groups and epigallocatechin gallate (EG) encapsulated within the internal cavities to provide biofilm disintegration and collagen protection for comprehensive dentin caries intervention. First, the PGE NPs reach lesion surfaces and accelerate EG release under acidic conditions. EG loosens Streptococcus mutans (S. mutans) biofilms, followed by G4-mediated disruption of planktonic S. mutans cell membranes. In vitro antimicrobial assays demonstrated a bactericidal efficacy of 99.75% after PGE intervention. Upon deeper lesion penetration, PGE releases EG to inhibit MMP activity and preserve the collagen scaffold, achieving a 74% reduction in hydroxyproline (HYP) levels. Simultaneously, PAMAM promotes controlled hydroxyapatite (HA) deposition, facilitating dentin remineralization. Treatment with PGE in artificial saliva containing collagenase restored dentin hardness to 89.88% of intact values. In vivo validation using a rat caries model confirmed therapeutic efficacy through significant reductions in Keyes scores, decreased salivary S. mutans counts, and increased molar mineral density. These findings demonstrate the therapeutic efficacy of PGE in dentin caries prevention and treatment, supporting its potential for clinical application.

Abstract Image

多功能PAMAM纳米颗粒与顺序抗菌再矿化治疗的牙本质龋齿管理。
牙本质龋齿是一个多因素的病理过程,以细菌定植和生物膜形成为特征,导致酸介导的脱矿和基质金属蛋白酶(MMP)介导的胶原基质降解。虽然再矿化治疗具有最小的侵入性,但其长期疗效受到持续的胶原降解和持续的细菌产酸的影响,这些细菌产酸会抵消再矿化的努力。为了解决这些局限性,我们设计了PAMAM-G4@EG (PGE)纳米颗粒(NPs),以聚酰胺胺(PAMAM)树突为矿物沉积模板,抗菌肽G(IIKK)4I-NH2 (G4)移植到外表面基团上,表没食子儿茶素没食子酸酯(EG)包裹在内腔内,为全面的牙本质龋齿干预提供生物膜分解和胶原保护。首先,PGE NPs到达病变表面,并在酸性条件下加速EG的释放。EG使变形链球菌(S. mutans)生物膜松动,随后g4介导的浮游变形链球菌细胞膜破坏。体外抗菌试验表明,PGE干预后的杀菌效果为99.75%。在更深的病变穿透后,PGE释放EG以抑制MMP活性并保存胶原支架,实现羟基脯氨酸(HYP)水平降低74%。同时,PAMAM促进羟基磷灰石(HA)沉积,促进牙本质再矿化。在含胶原酶的人工唾液中应用PGE处理后,牙本质硬度恢复到完好值的89.88%。使用大鼠龋齿模型进行体内验证,通过显著降低Keyes评分、降低唾液变形链球菌计数和增加臼齿矿物质密度,证实了治疗效果。这些结果证明了PGE在预防和治疗牙本质龋齿方面的疗效,支持其临床应用的潜力。
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来源期刊
Journal of Materials Chemistry B
Journal of Materials Chemistry B MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.30%
发文量
866
期刊介绍: Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive: Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices
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