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Impact of exogenous direct electric current on the expression of mRNA related to OPG, in SaOS-2 cells using quantitative reverse transcription polymerase chain reaction: A qualitative and quantitative analysis 外源直流电对SaOS-2细胞中OPG相关mRNA表达影响的定量逆转录聚合酶链反应:定性和定量分析
Q1 Medicine Pub Date : 2025-11-01 DOI: 10.1016/j.jobcr.2025.10.009
Aparajita Pandey , Ashish Agrawal , Parimal Das , Ritu Dixit , Prashant Ranjan , Sushit kumar sonu

Objective

To assess OPG gene expression in SaOS-2 cells after exposure to pulsed direct current (30 μA/10 s, square wave) using qRT-PCR at different time points (5, 7,12, and 24 h).

Materials and methods

The study investigated the effects of direct current (DC) electrical. stimulation on SaOS-2 cells by exposing experimental. groups to DC (30 μA, 10-s pulses) for 5, 7, 12, and 24 h, while control groups received no stimulation. Stainless steel electrodes were utilized, and both groups were cultured under identical. conditions. Qualitative assessments included cell morphology analysis through phase contrast microscopy, while quantitative evaluations involved MTT assays for cell viability and quantitative reverse transcription PCR (qRT-PCR) for osteoprotegerin (OPG) gene expression. RNA was isolated after stimulation, followed by complementary DNA (cDNA) synthesis for gene analysis. Data were analyzed to assess stimulation-induced cellular and genetic responses.

Results

Direct current stimulation induced time-dependent cytotoxicity in SaOS-2 cells, with cell death increasing from approximately 10 % at 5 h to about 52 % at 24 h qRT-PCR reveals significant downregulation of OPG expression, nearly eliminated between 12 and 24 h (p < 0.0001), indicating strong inhibitory effects on both cell viability and gene expression.

Conclusion

Direct electrical. stimulation downregulated OPG expression in SaOS-2 cells in a time-dependent manner, with a significant decrease observed as early as 5 h. The MTT assay reveals time-dependent cytotoxicity from DC stimulation. Reduced OPG expression suggests potential. enhancement of osteoclastic activity, indicating a possible role of DC stimulation in bone remodelling, which warrants further investigation.
目的应用qRT-PCR技术检测30 μA/10 s脉冲直流电刺激下SaOS-2细胞在不同时间点(5、7、12、24 h) OPG基因的表达。材料与方法研究了直流(DC)电流的影响。对SaOS-2细胞的刺激。30 μA, 10-s脉冲刺激5、7、12、24 h,对照组不刺激。采用不锈钢电极,两组在相同条件下培养。条件。定性评估包括通过相对比显微镜进行细胞形态分析,而定量评估包括细胞活力的MTT检测和骨保护素(OPG)基因表达的定量反转录PCR (qRT-PCR)。刺激后分离RNA,合成互补DNA (cDNA)进行基因分析。分析数据以评估刺激诱导的细胞和遗传反应。结果直流电刺激对SaOS-2细胞产生了时间依赖性的细胞毒性,细胞死亡率从5 h时的约10%增加到24 h时的约52%,qRT-PCR显示OPG表达显著下调,在12 - 24 h期间几乎消除(p < 0.0001),表明对细胞活力和基因表达都有很强的抑制作用。ConclusionDirect电。刺激以时间依赖性的方式下调了SaOS-2细胞中OPG的表达,早在5小时就观察到显著的下降。MTT试验揭示了DC刺激的时间依赖性细胞毒性。OPG表达减少提示有潜力。破骨细胞活性增强,表明DC刺激在骨重塑中的可能作用,值得进一步研究。
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引用次数: 0
Evaluation of clinical efficacy of Cention N and Tetric N-ceram in class I carious lesion in primary mandibular molars. 氮化钙与氮化钙治疗下颌磨牙I级龋齿的临床疗效评价。
Q1 Medicine Pub Date : 2025-11-01 Epub Date: 2025-08-09 DOI: 10.1016/j.jobcr.2025.08.006
Mayur Mhole, Sandeep Tandon, Shriya Gupta, Harshita Gosavi, A Rizwan Ali, Mineet Kaul

Background: Tetric N-Ceram, recently introduced as an alternative to bulk-fill flowable and traditional non-flowable composite. Cention N, recently introduced tooth-coloured filling material for bulk placement in retentive preparations.

Aim: The aim of the present study is to evaluate the performance of Tetric N Ceram and Cention N as restorative materials in Class 1 carious lesions in primary mandibular molars.

Design: A prospective double-blind, split-mouth, parallel-group, randomized study was conducted on 34 patients having bilateral Class I carious lesions on mandibular primary molars. 68 teeth were divided into 2 groups: Group 1 was treated with Cention N and Group 2 with Tetric N Ceram. All restorations were clinically evaluated at Baseline - 24hrs, 3, 6 and 9 months for marginal integrity (MI), secondary caries(SC) and gross fracture(GF) using the US Public Health Service criteria (modified Ryge criteria). For post-operative sensitivity(POS), Wong Bakers faces pain rating scale was used.

Results: Intragroup comparison of MI, SC and GF in Group 1 and group 2 showed non-significant difference at all-time intervals. Intergroup comparison showed non-significant difference for MI, SC, GF and POS at all-time intervals.

Conclusion: Tetric N Ceram and Cention N in terms of MI, SC, GF and POS provide similar results.

背景:n-陶瓷,最近被引入作为可流动和传统非流动复合材料的替代品。Cention N,最近推出了牙色填充材料,用于在固位制剂中大量放置。目的:评价氮化钛和氮化钛作为修复材料在初生下颌磨牙1级龋病中的应用效果。设计:对34例双侧下颌初级磨牙I类龋齿患者进行前瞻性双盲、裂口、平行组、随机研究。68颗牙分为2组:1组使用N型牙膜,2组使用N型牙膜。采用美国公共卫生服务标准(修订的Ryge标准),在基线- 24小时、3个月、6个月和9个月时对所有修复体进行边缘完整性(MI)、继发龋齿(SC)和总骨折(GF)的临床评估。术后敏感性(POS)采用Wong Bakers faces疼痛评定量表。结果:组内比较1、2组MI、SC、GF均无显著性差异。组间比较显示MI、SC、GF和POS在时间间隔上无显著差异。结论:在心肌梗死、SC、GF、POS等指标上,Tetric N Ceram与Cention N具有相似的结果。
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引用次数: 0
The effect of Lactobacillus rhamnosus administration against Porphyromonas gingivalis in vivo 鼠李糖乳杆菌在体内对牙龈卟啉单胞菌的作用
Q1 Medicine Pub Date : 2025-11-01 DOI: 10.1016/j.jobcr.2025.10.025
Syafrizal Aji Pamungkas , Chiquita Prahasanti , Sylvia Wardah , Devi Luciana Kusriawati , Maria Jessica Anggakusuma , Michael Ganda Wijaya , Michelle Suhartono , Wibi Riawan , Zulvikar Syambani Ulhaq

Background

Periodontitis is a chronic inflammatory disease initiated by polymicrobial infection, characterized by an imbalance between subgingival microbiota and host immune defense. This imbalance results in the destruction of tooth-supporting tissues, with Porphyromonas gingivalis identified as a key pathogen. Conventional periodontal therapies may not fully control destructive inflammation, highlighting the need for effective adjunctive strategies.

Objective

To evaluate the impact of the probiotic Lactobacillus rhamnosus on inflammatory responses and wound healing processes in an in vivo periodontitis model.

Methods

Gingival tissue samples from a P. gingivalis-induced periodontitis model were analyzed to determine the effects of L. rhamnosus supplementation on the levels of pro- and anti-inflammatory mediators and wound healing markers.

Results

In a rat model of periodontitis, probiotic supplementation suppressed inflammation by reducing TNF-α, IL-6, and IL-1β levels while increasing IL-10 expression in the gingival epithelium, thereby restoring the balance between pro- and anti-inflammatory mediators. Additionally, treatment accelerated wound healing, as indicated by upregulation of TGF-β1 and downregulation of MMP-8.

Conclusion

Our study shows that L. rhamnosus attenuates periodontitis primarily by modulating the host inflammatory response through downregulation of pro-inflammatory cytokines. These findings highlight its potential as an immunomodulatory probiotic and support future clinical trials as an adjunct to conventional periodontal therapy.
牙周炎是一种由多微生物感染引起的慢性炎症性疾病,其特征是龈下微生物群与宿主免疫防御之间的不平衡。这种不平衡导致牙齿支持组织的破坏,牙龈卟啉单胞菌被确定为关键病原体。传统的牙周治疗可能不能完全控制破坏性炎症,强调需要有效的辅助策略。目的探讨鼠李糖乳杆菌对体内牙周炎模型炎症反应和创面愈合过程的影响。方法对牙龈假单胞菌诱导的牙周炎模型的牙龈组织样本进行分析,观察鼠李糖添加对促炎介质和抗炎介质及创面愈合标志物水平的影响。结果在大鼠牙周炎模型中,补充益生菌可通过降低牙龈上皮中TNF-α、IL-6和IL-1β水平,增加IL-10表达来抑制炎症,从而恢复促炎介质和抗炎介质之间的平衡。此外,TGF-β1的上调和MMP-8的下调表明,治疗加速了伤口愈合。结论鼠李糖主要通过下调促炎细胞因子调节宿主炎症反应来减轻牙周炎。这些发现强调了其作为免疫调节益生菌的潜力,并支持未来的临床试验作为传统牙周治疗的辅助。
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引用次数: 0
Comparison of reproducibility and workability of single and adjacent implant placement protocol under dynamic real time navigation systems between operators: A clinical trial. 在操作者之间动态实时导航系统下单个和相邻种植体放置方案的可重复性和可操作性的比较:一项临床试验。
Q1 Medicine Pub Date : 2025-11-01 Epub Date: 2025-08-09 DOI: 10.1016/j.jobcr.2025.08.003
Vamshi Nizampuram, Sahana Selvaganesh, Thiyaneswaran Nesappan

Introduction: Dynamic navigation (DN), a computer-assisted technique integrating CBCT data and real-time video, has emerged as a promising approach to place implants in the recent years. This study aims to evaluate the consistency and ease of use of a dynamic navigation system for implant placement by comparing the accuracy in single and adjacent implant placements and workability achieved by three different operators.

Methods: This study included Forty-eight patients requiring dental implants, total of sixty implants were randomly assigned to 3 operators of varying experiences, the implants were planned and placed under DN. The accuracy of implant placement were measured in terms of mesio-distal, apico-coronal displacement and angulations using Evalunav application (Navident, Claronav, Canada). Secondary outcome variables are the number of errors encountered during the procedure and the time taken for the procedure by different practitioners. Kruskal Wallis Test followed by the Post hoc Mann Whitney U test. The level of significance was set at P < 0.05.

Results: There were no significant differences in the accuracy of single implants (P > 0.05). For adjacent implants (T1), the displacement in mesiodistal direction was significantly different (P = 0.003) and also for apico-coronal position of T1-abutment group when compared to controls with a P value of 0.026. Experienced surgeons had the highest error rates as well and longest time (18.27 ± 5.62 versus 15 min).

Conclusions: The operating surgeon do not determine the accuracy rather the navigation system comes with a steep learning curve that needs to be acquired prior to practicing the same.

动态导航(DN)是一种结合CBCT数据和实时视频的计算机辅助技术,近年来已成为一种很有前途的植入方法。本研究旨在通过比较三种不同操作人员在单个和相邻种植体放置时的准确性和可操作性,来评估动态导航系统在种植体放置时的一致性和易用性。方法:本研究纳入48例需要种植体的患者,共60颗种植体随机分配给3名不同经验的操作人员,计划种植体并放置在DN下。使用Evalunav应用程序(Navident, Claronav, Canada)测量种植体放置的准确性,包括中-远端,根尖-冠状位移和角度。次要的结果变量是在手术过程中遇到的错误数量和不同的医生在手术中所花费的时间。Kruskal Wallis测试然后是Post hoc Mann Whitney U测试。结果:单颗种植体的准确性无显著性差异(P < 0.05)。邻近种植体(T1)的中远端位移与对照组相比有显著差异(P = 0.003), T1基台组的顶冠位置与对照组相比也有显著差异(P值为0.026)。经验丰富的外科医生错误率最高,时间最长(18.27±5.62 vs 15 min)。结论:手术医生不能决定导航系统的准确性,而导航系统需要一个陡峭的学习曲线,需要在实践之前获得。
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引用次数: 0
Nano-particle coated or impregnated acrylic resins in dental applications: A systematic review of in Vivo Evidence on mechanical properties, biocompatibility and clinical performance. 纳米颗粒包覆或浸渍丙烯酸树脂在牙科中的应用:机械性能、生物相容性和临床性能的体内证据的系统综述。
Q1 Medicine Pub Date : 2025-11-01 Epub Date: 2025-08-07 DOI: 10.1016/j.jobcr.2025.07.018
Parthasarthy Natarajan, Seenivasan Madhan Kumar, Shanmuganathan Natarajan, Dr K S Sridharan, Dr S Narayana Kalkura

Background: Acrylic resins are extensively used in prosthodontics, orthodontics and maxillofacial prosthetics due to their ease of fabrication and cost-effectiveness. However, conventional acrylic materials are susceptible to microbial colonization, mechanical deterioration and esthetic compromise. To overcome these limitations, recent research has explored the incorporation of nanoparticles into polymethyl methacrylate (PMMA)-based resins to enhance their antimicrobial efficacy, mechanical strength, biocompatibility, and long-term durability.

Methods: This systematic review was conducted according to PRISMA guidelines. An extensive literature search was performed across PubMed/MEDLINE, Scopus, Web of Science, Cochrane Library and Embase for studies published up to January 18, 2025. Only in vivo studies conducted on humans or animals evaluating nanoparticle-coated or nanoparticle-impregnated acrylic resins were included. Standalone in vitro studies were excluded. Risk of bias was assessed using Cochrane's RoB 2.0 tool for randomized controlled trials (RCTs), ROBINS-I for non-randomized studies and the SYRCLE tool for animal studies.

Results: Out of 3154 records initially identified, six studies met the eligibility criteria. The nanoparticles incorporated included silver, titanium dioxide, nanocopper, nanogold and quaternary ammonium polyethyleneimine (QPEI). All included studies reported antimicrobial activity with nanogold, nanocopper and QPEI showing sustained microbial inhibition. Mechanical outcomes varied: silver and titanium dioxide nanoparticles were associated with reduced material strength, whereas nanocopper maintained mechanical performance. Esthetic outcomes indicated that silver-based modifications caused discoloration, while nanocopper and QPEI preserved color stability.

Conclusion: Nanoparticle-modified acrylic resins exhibit enhanced antimicrobial and biocompatibility profiles with certain formulations particularly those incorporating nanocopper, nanogold and QPEI showing greater clinical potential. However, mechanical durability and esthetic alterations remain challenges especially with silver and titanium-based additives. Further well-designed, long-term randomized controlled trials are warranted to validate the clinical applicability of these nano-enhanced acrylic materials.

背景:丙烯酸树脂因其易于制造和成本效益而广泛应用于口腔修复学,正畸学和颌面修复学。然而,传统的丙烯酸材料容易受到微生物定植,机械退化和美学妥协。为了克服这些限制,最近的研究探索了将纳米颗粒掺入聚甲基丙烯酸甲酯(PMMA)基树脂中,以提高其抗菌功效、机械强度、生物相容性和长期耐久性。方法:根据PRISMA指南进行系统评价。在PubMed/MEDLINE、Scopus、Web of Science、Cochrane Library和Embase上进行了广泛的文献检索,检索截止到2025年1月18日发表的研究。仅包括对人类或动物进行的体内研究,评估纳米颗粒涂层或纳米颗粒浸渍丙烯酸树脂。排除了独立的体外研究。随机对照试验(rct)采用Cochrane的RoB 2.0工具评估偏倚风险,非随机研究采用ROBINS-I工具评估偏倚风险,动物研究采用sycle工具评估偏倚风险。结果:在最初确定的3154条记录中,有6项研究符合资格标准。纳米颗粒包括银、二氧化钛、纳米铜、纳米金和季铵聚乙烯亚胺(QPEI)。所有纳入的研究报告了纳米金、纳米铜和QPEI的抗菌活性,显示出持续的微生物抑制作用。力学结果不同:银和二氧化钛纳米粒子与材料强度降低有关,而纳米铜则保持机械性能。美学结果表明,银基改性引起变色,而纳米铜和QPEI保持了颜色稳定性。结论:纳米颗粒改性丙烯酸树脂在某些配方中表现出增强的抗菌和生物相容性,特别是那些含有纳米铜、纳米金和QPEI的配方,显示出更大的临床潜力。然而,机械耐久性和美观的改变仍然是挑战,特别是银和钛基添加剂。需要进一步精心设计的长期随机对照试验来验证这些纳米增强丙烯酸材料的临床适用性。
{"title":"Nano-particle coated or impregnated acrylic resins in dental applications: A systematic review of in Vivo Evidence on mechanical properties, biocompatibility and clinical performance.","authors":"Parthasarthy Natarajan, Seenivasan Madhan Kumar, Shanmuganathan Natarajan, Dr K S Sridharan, Dr S Narayana Kalkura","doi":"10.1016/j.jobcr.2025.07.018","DOIUrl":"10.1016/j.jobcr.2025.07.018","url":null,"abstract":"<p><strong>Background: </strong>Acrylic resins are extensively used in prosthodontics, orthodontics and maxillofacial prosthetics due to their ease of fabrication and cost-effectiveness. However, conventional acrylic materials are susceptible to microbial colonization, mechanical deterioration and esthetic compromise. To overcome these limitations, recent research has explored the incorporation of nanoparticles into polymethyl methacrylate (PMMA)-based resins to enhance their antimicrobial efficacy, mechanical strength, biocompatibility, and long-term durability.</p><p><strong>Methods: </strong>This systematic review was conducted according to PRISMA guidelines. An extensive literature search was performed across PubMed/MEDLINE, Scopus, Web of Science, Cochrane Library and Embase for studies published up to January 18, 2025. Only in vivo studies conducted on humans or animals evaluating nanoparticle-coated or nanoparticle-impregnated acrylic resins were included. Standalone in vitro studies were excluded. Risk of bias was assessed using Cochrane's RoB 2.0 tool for randomized controlled trials (RCTs), ROBINS-I for non-randomized studies and the SYRCLE tool for animal studies.</p><p><strong>Results: </strong>Out of 3154 records initially identified, six studies met the eligibility criteria. The nanoparticles incorporated included silver, titanium dioxide, nanocopper, nanogold and quaternary ammonium polyethyleneimine (QPEI). All included studies reported antimicrobial activity with nanogold, nanocopper and QPEI showing sustained microbial inhibition. Mechanical outcomes varied: silver and titanium dioxide nanoparticles were associated with reduced material strength, whereas nanocopper maintained mechanical performance. Esthetic outcomes indicated that silver-based modifications caused discoloration, while nanocopper and QPEI preserved color stability.</p><p><strong>Conclusion: </strong>Nanoparticle-modified acrylic resins exhibit enhanced antimicrobial and biocompatibility profiles with certain formulations particularly those incorporating nanocopper, nanogold and QPEI showing greater clinical potential. However, mechanical durability and esthetic alterations remain challenges especially with silver and titanium-based additives. Further well-designed, long-term randomized controlled trials are warranted to validate the clinical applicability of these nano-enhanced acrylic materials.</p>","PeriodicalId":16609,"journal":{"name":"Journal of oral biology and craniofacial research","volume":"15 6","pages":"1190-1199"},"PeriodicalIF":0.0,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12355065/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144873671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparative evaluation of fluoride release from different modifications of glass ionomer dental restorative material in primary teeth at different time intervals: An ex vivo study. 不同改性玻璃离聚体牙齿修复材料在不同时间间隔内对乳牙中氟化物释放的比较评价:一项离体研究。
Q1 Medicine Pub Date : 2025-11-01 Epub Date: 2025-08-09 DOI: 10.1016/j.jobcr.2025.07.029
Vivek Mehta, Nikhil Srivastava, Saif Ali Chaudhry, Vivek Rana

Purpose: This ex vivo study aims to evaluate and compare the fluoride-releasing capabilities of different modifications of Glass ionomer cement, namely Giomer, Zirconomer, and Pediatric GIC (type IX) with Resin-modified Glass ionomer cement (RMGIC) in the primary dentition at first, fourteenth, and twenty-eighth days.

Materials and methods: Fifty-six extracted human primary molars were allocated into four groups: Group 1, Resin-modified GIC; Group 2, Giomer; Group 3, Zirconomer; and Group 4, Pediatric GIC (type IX). The tooth samples (n = 14) were restored as per the manufacturer's instructions after making class II cavities in primary molars. Extracted tooth specimens were placed in deionized water, and the fluoride ions released were measured for 28 days. The tooth samples were evaluated for cumulative fluoride levels at the end of 24 h, 14th day, and 28th day under normal atmospheric conditions, using a fluoride ion-selective electrode (Orion STAR-A214 Ion analyzer). The data obtained was subjected to statistical analysis, and the results are discussed herein.

Results: Fluoride ions releasing capability was exhibited by primary teeth restored with all the above-mentioned materials. The primary teeth restored with Zirconomer exhibited significantly higher fluoride-releasing capability among the above-compared materials, and the primary teeth restored with Giomer exhibited the least fluoride ions release on 24 h, 14th day, and 28th day, and the difference of fluoride ions releasing ability between the four groups was statistically significant at each time interval (P < 0.001).

Conclusion: The primary teeth restored with Zirconomer exhibited superior fluoride-releasing ability compared to other restorative materials. Therefore, Zirconomer can be a promising restorative material for primary teeth due to its enhanced anti-caries effect.

目的:本体外研究旨在评估和比较不同改性玻璃离子水门钉(Giomer, Zirconomer, Pediatric GIC (type IX))与树脂改性玻璃离子水门钉(RMGIC)在初级牙列第1天、第14天和第28天的氟化物释放能力。材料与方法:56颗拔除的人乳牙分为4组:1组树脂改性GIC;第2组,聚物;第3族,锆共聚物;第4组为小儿GIC (IX型)。14个牙齿样本在制作出初级磨牙II级蛀牙后,按照制造商的说明进行修复。拔牙标本置于去离子水中,测定28天氟离子释放量。在正常大气条件下,使用氟离子选择电极(Orion STAR-A214离子分析仪)评估牙齿样品在24小时、14天和28天的累积氟化物水平。对所得数据进行了统计分析,并对结果进行了讨论。结果:采用上述材料修复的乳牙均表现出释放氟离子的能力。使用锆聚体修复的乳牙在上述材料中释放氟离子的能力明显高于其他材料,而使用聚聚体修复的乳牙在24 h、第14天、第28天释放氟离子的能力最小,且在各时间间隔内,四组间释放氟离子的能力差异均有统计学意义(P)。与其他修复材料相比,锆合金修复的乳牙具有更好的氟释放能力。因此,锆合金具有较好的抗龋效果,是一种很有前途的乳牙修复材料。
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引用次数: 0
Samarium-doped hydroxyapatite: An effective approach for enhancing biomineralization in dental caries management. 掺钐羟基磷灰石:龋治疗中加强生物矿化的有效方法。
Q1 Medicine Pub Date : 2025-11-01 Epub Date: 2025-08-08 DOI: 10.1016/j.jobcr.2025.07.026
C P Harini, Radha Gosala, Ramya Ramadoss

Background: Dental caries is a widespread non-communicable disease caused by interactions among acidogenic bacteria, fermentable carbohydrates, and host factors, leading to tooth demineralization. In dentin caries, this process exposes dentinal tubules, causing sensitivity and structural degradation. Despite available agents, effective dentin remineralization remains a challenge. Recent studies highlight samarium-doped hydroxyapatite (Sm-HAp) as a potential biomaterial for promoting remineralization.

Aim: To synthesize and characterize the samarium doped hydroxyapatite (Sm-HAp) as a potential agent in dentin remineralization.

Materials and methods: Sm-HAp was synthesized via wet-chemical precipitation. Characterization was performed using SEM for morphology, FTIR for functional groups, and XRD for crystalline features. MTT assay evaluated for biocompatibility and in vitro mineralization analyzed on human tooth samples.

Results: SEM showed flake-like, and needle-shaped crystals. XRD indicated the formation Sm doped hydroxyapatite without any additional phase, which further confirmed by FTIR. MTT assay showed >85 % cell viability, confirming high biocompatibility and also an efficient dentine mineralization was observed with Sm-HAp treatment.

Conclusion: Sm-HAp demonstrates favorable structural, chemical, and biological properties, supporting its potential as a dentin remineralizing agent in dental caries management.

背景:龋齿是一种广泛存在的非传染性疾病,由产酸细菌、可发酵碳水化合物和宿主因素相互作用引起,导致牙齿脱矿。在牙本质龋齿中,这个过程暴露了牙本质小管,导致敏感和结构退化。尽管有可用的药物,有效的牙本质再矿化仍然是一个挑战。最近的研究表明,钐掺杂羟基磷灰石(Sm-HAp)是一种潜在的促进再矿化的生物材料。目的:合成并表征钐掺杂羟基磷灰石(Sm-HAp)作为牙本质再矿化的潜在剂。材料与方法:采用湿化学沉淀法合成Sm-HAp。用SEM表征形貌,FTIR表征官能团,XRD表征晶体特征。MTT法评价了人类牙齿样品的生物相容性和体外矿化分析。结果:扫描电镜显示片状、针状晶体。XRD分析表明形成了Sm掺杂的羟基磷灰石,没有任何附加相,FTIR进一步证实了这一点。MTT实验显示细胞存活率为> 85%,证实了Sm-HAp处理的高生物相容性和有效的牙本质矿化。结论:Sm-HAp具有良好的结构、化学和生物学特性,支持其作为牙本质再矿化剂在龋齿治疗中的潜力。
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引用次数: 0
Possible applicability of flavonoid hesperetin for the treatment of dental biofilm-forming Candida glabrata 黄酮类橙皮苷治疗牙生物膜形成的光念珠菌的可能适用性
Q1 Medicine Pub Date : 2025-11-01 DOI: 10.1016/j.jobcr.2025.10.016
Bhavesh Sureendar , Vinothini Gunasekaran , Dhanraj Ganapathy, Palanivel Sathishkumar

Background

Biofilm formation is a key virulence factor for Candida glabrata because it forms an extracellular matrix that prevents antifungal passage, which resists antifungal agents and causes treatment failure. To overcome this, the present study aimed to investigate the therapeutic potential of phytocompounds as an alternative choice in eliminating dental biofilm-forming C. glabrata.

Method

The antifungal potential of various phytocompounds against C. glabrata was evaluated through zone of inhibition (ZOI) and minimum inhibitory concentration (MIC) studies. The antibiofilm potential of phytocompounds was evaluated against C. glabrata and confirmed through CV staining, MTT assay and CLSM analysis. The biocompatibility of hesperetin was checked by hemocompatibility test on human RBCs.

Results

Quercetin, morin, rutin, naringin, and hesperetin exhibits antifungal activity towards C. glabrata. Hesperetin shows slightly higher antifungal activity (ZOI: 14.6 ± 0.57 mm and MIC: 0.3 ± 0.01 mM) for C. glabrata, compared to other tested phytocompounds. The 100 % deadness of C. glabrata cells in biofilm was observed at 2MIC (0.6 mM) of hesperetin. Interestingly, hesperetin demonstrates acceptable level hemolysis (5 %) on RBCs up to 10 mM.

Conclusions

These findings suggest that hesperetin is a novel natural antifungal agent capable of effectively inhibiting the biofilm-forming C. glabrata, with the potential for development into safe, phyto-based therapeutics for managing dental infections.
生物膜形成是秃念珠菌的关键毒力因素,因为它形成细胞外基质,阻止抗真菌药物通过,从而抵抗抗真菌药物并导致治疗失败。为了克服这一点,本研究旨在研究植物化合物作为消除牙齿生物膜形成的光牙锥体的替代选择的治疗潜力。方法通过抑菌区(ZOI)和最低抑菌浓度(MIC)研究,评价不同植物化合物对赤霉病的抑菌潜力。通过CV染色、MTT试验和CLSM分析,评价了植物化合物对光棘球蚴的抗菌潜力。采用人红细胞血液相容性试验检测橙皮苷的生物相容性。结果槲皮素、桑皮素、芦丁、柚皮素和橙皮素对光斑夜蛾具有抗真菌活性。橙皮苷对赤霉病菌的抑制活性(ZOI: 14.6±0.57 mm, MIC: 0.3±0.01 mm)略高于其他植物化合物。hesperetin浓度为2MIC (0.6 mM)时,生物膜中光斑锥体细胞的死亡率为100%。有趣的是,橙皮素对红细胞的溶血作用可达10毫米(5%)。结论这些发现表明橙皮素是一种新型的天然抗真菌剂,能够有效抑制形成生物膜的C. glabrata,具有发展成为安全的、基于植物的治疗牙齿感染的潜力。
{"title":"Possible applicability of flavonoid hesperetin for the treatment of dental biofilm-forming Candida glabrata","authors":"Bhavesh Sureendar ,&nbsp;Vinothini Gunasekaran ,&nbsp;Dhanraj Ganapathy,&nbsp;Palanivel Sathishkumar","doi":"10.1016/j.jobcr.2025.10.016","DOIUrl":"10.1016/j.jobcr.2025.10.016","url":null,"abstract":"<div><h3>Background</h3><div>Biofilm formation is a key virulence factor for <em>Candida glabrata</em> because it forms an extracellular matrix that prevents antifungal passage, which resists antifungal agents and causes treatment failure. To overcome this, the present study aimed to investigate the therapeutic potential of phytocompounds as an alternative choice in eliminating dental biofilm-forming <em>C. glabrata</em>.</div></div><div><h3>Method</h3><div>The antifungal potential of various phytocompounds against <em>C. glabrata</em> was evaluated through zone of inhibition (ZOI) and minimum inhibitory concentration (MIC) studies. The antibiofilm potential of phytocompounds was evaluated against <em>C. glabrata</em> and confirmed through CV staining, MTT assay and CLSM analysis. The biocompatibility of hesperetin was checked by hemocompatibility test on human RBCs.</div></div><div><h3>Results</h3><div>Quercetin, morin, rutin, naringin, and hesperetin exhibits antifungal activity towards <em>C. glabrata</em>. Hesperetin shows slightly higher antifungal activity (ZOI: 14.6 ± 0.57 mm and MIC: 0.3 ± 0.01 mM) for <em>C. glabrata</em>, compared to other tested phytocompounds. The 100 % deadness of <em>C. glabrata</em> cells in biofilm was observed at 2MIC (0.6 mM) of hesperetin. Interestingly, hesperetin demonstrates acceptable level hemolysis (5 %) on RBCs up to 10 mM.</div></div><div><h3>Conclusions</h3><div>These findings suggest that hesperetin is a novel natural antifungal agent capable of effectively inhibiting the biofilm-forming <em>C. glabrata</em>, with the potential for development into safe, phyto-based therapeutics for managing dental infections.</div></div>","PeriodicalId":16609,"journal":{"name":"Journal of oral biology and craniofacial research","volume":"15 6","pages":"Pages 1799-1805"},"PeriodicalIF":0.0,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145415752","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integrative nanoformulation of paclitaxel, ruthenium (II), and curcumin for enhanced oral cancer cell suppression 紫杉醇、钌(II)和姜黄素的整合纳米配方增强口腔癌细胞抑制
Q1 Medicine Pub Date : 2025-11-01 DOI: 10.1016/j.jobcr.2025.10.024
Rethinam Senthil , Deepak Angamuthu , P. Geetha Sravanthy , Pradeep Kumar R.

Background

Oral squamous cell carcinoma (OSCC) often responds poorly to conventional chemotherapy. This study aimed to enhance the efficacy of paclitaxel (PTX) by co-encapsulating it with a ruthenium (II) complex (Ru-II) and curcumin nanoparticles (C-NP).

Methods

C-NPs were prepared via wet milling, and Ru-II was synthesized through ligand coordination and reduction. The conjugate (CoENC-PTX) was obtained by combining PTX, Ru-II, and C-NP, followed by ultrafiltration. Characterization was performed using UV–Vis, FTIR, XRD, and HRSEM. In vitro evaluations included drug release, cytotoxicity assays on OSCC cells, live/dead cell labeling, and quantitative PCR (qPCR) analysis.

Results

CoENC-PTX showed efficient encapsulation with distinct spectral, crystalline, and morphological features. Drug release exhibited a biphasic profile, with 94.8 % release in 48 h. Cytotoxicity assays indicated dose-dependent reduction in OSCC cell viability, with maximum effect at 100 μg/mL. Live/dead staining confirmed apoptosis, while qPCR revealed p53 and c-Myc overexpression, indicating apoptosis activation and cell cycle regulation.

Conclusion

The PTX–Ru-II–C-NP formulation significantly improved the anticancer activity against OSCC, offering a promising synergistic approach for oral cancer therapy.
背景:口腔鳞状细胞癌(OSCC)通常对常规化疗反应不佳。本研究旨在通过钌(II)配合物(Ru-II)和姜黄素纳米颗粒(C-NP)共包封紫杉醇(PTX)来提高其疗效。方法湿磨法制备sc - nps,配位还原法制备Ru-II。将PTX、Ru-II和C-NP结合得到共轭物(coencc -PTX),并进行超滤。采用UV-Vis, FTIR, XRD和HRSEM进行表征。体外评价包括药物释放、细胞毒性测定、活/死细胞标记和定量PCR (qPCR)分析。结果scencc - ptx包封效果良好,具有清晰的光谱、晶体和形态特征。药物释放呈双相分布,48 h内释放率为94.8%。细胞毒性试验显示,剂量依赖性地降低了OSCC细胞活力,在100 μg/mL时效果最大。活/死染色证实细胞凋亡,qPCR显示p53和c-Myc过表达,提示细胞凋亡活化和细胞周期调控。结论PTX-Ru-II-C-NP制剂可显著提高对OSCC的抗癌活性,为口腔癌的协同治疗提供了一条有前景的途径。
{"title":"Integrative nanoformulation of paclitaxel, ruthenium (II), and curcumin for enhanced oral cancer cell suppression","authors":"Rethinam Senthil ,&nbsp;Deepak Angamuthu ,&nbsp;P. Geetha Sravanthy ,&nbsp;Pradeep Kumar R.","doi":"10.1016/j.jobcr.2025.10.024","DOIUrl":"10.1016/j.jobcr.2025.10.024","url":null,"abstract":"<div><h3>Background</h3><div>Oral squamous cell carcinoma (OSCC) often responds poorly to conventional chemotherapy. This study aimed to enhance the efficacy of paclitaxel (PTX) by co-encapsulating it with a ruthenium (II) complex (Ru-II) and curcumin nanoparticles (C-NP).</div></div><div><h3>Methods</h3><div>C-NPs were prepared via wet milling, and Ru-II was synthesized through ligand coordination and reduction. The conjugate (CoENC-PTX) was obtained by combining PTX, Ru-II, and C-NP, followed by ultrafiltration. Characterization was performed using UV–Vis, FTIR, XRD, and HRSEM. In vitro evaluations included drug release, cytotoxicity assays on OSCC cells, live/dead cell labeling, and quantitative PCR (qPCR) analysis.</div></div><div><h3>Results</h3><div>CoENC-PTX showed efficient encapsulation with distinct spectral, crystalline, and morphological features. Drug release exhibited a biphasic profile, with 94.8 % release in 48 h. Cytotoxicity assays indicated dose-dependent reduction in OSCC cell viability, with maximum effect at 100 μg/mL. Live/dead staining confirmed apoptosis, while qPCR revealed p53 and c-Myc overexpression, indicating apoptosis activation and cell cycle regulation.</div></div><div><h3>Conclusion</h3><div>The PTX–Ru-II–C-NP formulation significantly improved the anticancer activity against OSCC, offering a promising synergistic approach for oral cancer therapy.</div></div>","PeriodicalId":16609,"journal":{"name":"Journal of oral biology and craniofacial research","volume":"15 6","pages":"Pages 1824-1830"},"PeriodicalIF":0.0,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145473776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Artificial Intelligence–driven spatial transcriptomics in OSCC: Mapping the tumor microenvironment and personalizing therapy 人工智能驱动的OSCC空间转录组学:绘制肿瘤微环境和个性化治疗
Q1 Medicine Pub Date : 2025-11-01 DOI: 10.1016/j.jobcr.2025.10.015
Soundharya Manogaran , Ramya Ramadoss , Suganya Panneer Selvam , Sandhya Sundar , Nitya Krishnasamy , Hemashree , Karunya Krishnakumar , Preethi Shankar
Spatial transcriptomics (ST) represents a transformative approach in cancer research, offering high-resolution insights into the spatial organization of gene expression within tissues, particularly relevant for the complex tumor microenvironment (TME) of oral squamous cell carcinoma (OSCC). Unlike conventional bulk RNA sequencing, which masks spatial heterogeneity, ST retains the architectural context of tumors, enabling the mapping of molecular gradients, tumor–stroma interactions, and immune cell localization. Various ST platforms—such as 10x Genomics Visium, Slide-seqV2, MERFISH, NanoString GeoMx DSP, CosMx SMI, and BGI.
Stereo-seq—each offers unique advantages in resolution, sample compatibility, and transcriptome depth. Their application in OSCC has led to the identification of spatially distinct gene signatures, aiding in the stratification of tumor subtypes and uncovering novel prognostic markers. Furthermore, the integration of ST with artificial intelligence (AI) and machine learning has enhanced its analytical capabilities, enabling automated feature extraction, spatial clustering, and predictive modeling of disease progression. Despite these advancements, limitations such as high computational demands, limited access to fresh-frozen tissues, and platform-specific biases persist. Nonetheless, the synergy between ST and AI heralds a new era in precision pathology, with the potential to revolutionize diagnosis, risk assessment, and personalized therapeutic strategies for OSCC.
空间转录组学(ST)代表了癌症研究的一种变革方法,为组织内基因表达的空间组织提供了高分辨率的见解,特别是与口腔鳞状细胞癌(OSCC)的复杂肿瘤微环境(TME)相关。与传统的大体积RNA测序不同,它掩盖了空间异质性,ST保留了肿瘤的结构背景,能够绘制分子梯度、肿瘤-基质相互作用和免疫细胞定位。各种ST平台,如10x Genomics Visium, Slide-seqV2, MERFISH, NanoString GeoMx DSP, CosMx SMI和华大基因。Stereo-seq-each在分辨率,样品兼容性和转录组深度方面提供独特的优势。它们在OSCC中的应用导致了空间上不同基因特征的识别,有助于肿瘤亚型的分层和发现新的预后标志物。此外,ST与人工智能(AI)和机器学习的集成增强了其分析能力,实现了自动特征提取、空间聚类和疾病进展的预测建模。尽管取得了这些进步,但诸如高计算需求、获取新鲜冷冻组织的限制以及平台特定偏差等限制仍然存在。尽管如此,ST和AI之间的协同作用预示着精确病理学的新时代,有可能彻底改变OSCC的诊断、风险评估和个性化治疗策略。
{"title":"Artificial Intelligence–driven spatial transcriptomics in OSCC: Mapping the tumor microenvironment and personalizing therapy","authors":"Soundharya Manogaran ,&nbsp;Ramya Ramadoss ,&nbsp;Suganya Panneer Selvam ,&nbsp;Sandhya Sundar ,&nbsp;Nitya Krishnasamy ,&nbsp;Hemashree ,&nbsp;Karunya Krishnakumar ,&nbsp;Preethi Shankar","doi":"10.1016/j.jobcr.2025.10.015","DOIUrl":"10.1016/j.jobcr.2025.10.015","url":null,"abstract":"<div><div>Spatial transcriptomics (ST) represents a transformative approach in cancer research, offering high-resolution insights into the spatial organization of gene expression within tissues, particularly relevant for the complex tumor microenvironment (TME) of oral squamous cell carcinoma (OSCC). Unlike conventional bulk RNA sequencing, which masks spatial heterogeneity, ST retains the architectural context of tumors, enabling the mapping of molecular gradients, tumor–stroma interactions, and immune cell localization. Various ST platforms—such as 10x Genomics Visium, Slide-seqV2, MERFISH, NanoString GeoMx DSP, CosMx SMI, and BGI.</div><div>Stereo-seq—each offers unique advantages in resolution, sample compatibility, and transcriptome depth. Their application in OSCC has led to the identification of spatially distinct gene signatures, aiding in the stratification of tumor subtypes and uncovering novel prognostic markers. Furthermore, the integration of ST with artificial intelligence (AI) and machine learning has enhanced its analytical capabilities, enabling automated feature extraction, spatial clustering, and predictive modeling of disease progression. Despite these advancements, limitations such as high computational demands, limited access to fresh-frozen tissues, and platform-specific biases persist. Nonetheless, the synergy between ST and AI heralds a new era in precision pathology, with the potential to revolutionize diagnosis, risk assessment, and personalized therapeutic strategies for OSCC.</div></div>","PeriodicalId":16609,"journal":{"name":"Journal of oral biology and craniofacial research","volume":"15 6","pages":"Pages 1862-1873"},"PeriodicalIF":0.0,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145473779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Journal of oral biology and craniofacial research
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