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含ε-聚-L-赖氨酸、富美肽和度米芬的漱口水在减轻口臭和龈上菌斑方面的疗效:一项随机临床试验。

Efficacy of a mouthwash containing ε-poly-L-lysine, funme peptides and domiphen in reducing halitosis and supragingival plaque: a randomized clinical trial.

作者信息

Shen Song, Liu Xu, Huang Jun, Sun Yi, Liu Bin, Song Wenzhu, Meng Lei, Du Mi, Feng Qiang

机构信息

Department of Human Microbiome & Implantology, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, Shandong University, Jinan, China.

Shandong University-BOP Joint Oral Microbiome Laboratory, Shandong University, Jinan, 250012, China.

出版信息

BMC Oral Health. 2024 May 3;24(1):525. doi: 10.1186/s12903-024-04255-0.

Abstract

OBJECTIVE

To evaluate the antibacterial effectiveness of a combination of ε-poly-L-lysine (ε-PL), funme peptide (FP) as well as domiphen against oral pathogens, and assess the efficacy of a BOP® mouthwash supplemented with this combination in reducing halitosis and supragingival plaque in a clinical trial.

MATERIALS AND METHODS

The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of the compound against Fusobacterium nucleatum, Porphyromonas gingivalis, Streptococcus mutans, and Aggregatibacter actinomycetemcomitans were determined by the gradient dilution method. Subsequently, the CCK-8 assay was used to detect the toxicity of mouthwash on human gingival fibroblastst, and the effectiveness in reducing halitosis and supragingival plaque of the mouthwash supplemented with the combination was analyzed by a randomized, double-blind, parallel-controlled clinical trial.

RESULTS

The combination exhibited significant inhibitory effects on tested oral pathogens with the MIC < 1.56% (v/v) and the MBC < 3.13% (v/v), and the mouthwash containing this combination did not inhibit the viability of human gingival fibroblasts at the test concentrations. The clinical trial showed that the test group displayed notably lower volatile sulfur compounds (VSCs) at 0, 10, 24 h, and 7 d post-mouthwash (P < 0.05), compared with the baseline. After 7 days, the VSC levels of the and control groups were reduced by 50.27% and 32.12%, respectively, and notably cutting severe halitosis by 57.03% in the test group. Additionally, the Plaque Index (PLI) of the test and control group decreased by 54.55% and 8.38%, respectively, and there was a significant difference in PLI between the two groups after 7 days (P < 0.01).

CONCLUSIONS

The combination of ε-PL, FP and domiphen demonstrated potent inhibitory and bactericidal effects against the tested oral pathogens, and the newly formulated mouthwash added with the combination exhibited anti-dental plaque and anti-halitosis properties in a clinical trial and was safe.

TRIAL REGISTRATION

The randomized controlled clinical trial was registered on Chinese Clinical Trial Registry (No. ChiCTR2300073816, Date: 21/07/2023).

摘要

目的

评估ε-聚-L-赖氨酸(ε-PL)、富美肽(FP)以及度米芬联合使用对口腔病原体的抗菌效果,并在一项临床试验中评估添加该联合制剂的BOP®漱口水在减轻口臭和龈上菌斑方面的疗效。

材料与方法

采用梯度稀释法测定该化合物对具核梭杆菌、牙龈卟啉单胞菌、变形链球菌和伴放线聚集杆菌的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。随后,采用CCK-8法检测漱口水对人牙龈成纤维细胞的毒性,并通过随机、双盲、平行对照临床试验分析添加该联合制剂的漱口水在减轻口臭和龈上菌斑方面的有效性。

结果

该联合制剂对受试口腔病原体表现出显著的抑制作用,MIC<1.56%(v/v),MBC<3.13%(v/v),且含该联合制剂的漱口水在试验浓度下未抑制人牙龈成纤维细胞的活力。临床试验表明,与基线相比,试验组在漱口水使用后0、10、24小时和7天时的挥发性硫化物(VSCs)显著降低(P<0.05)。7天后,试验组和对照组的VSC水平分别降低了50.27%和32.12%,试验组显著减轻重度口臭达57.03%。此外,试验组和对照组的菌斑指数(PLI)分别下降了54.55%和8.38%,7天后两组间PLI存在显著差异(P<0.01)。

结论

ε-PL、FP和度米芬联合使用对受试口腔病原体表现出强大的抑制和杀菌作用,新配制的添加该联合制剂的漱口水在临床试验中表现出抗牙菌斑和抗口臭特性且安全。

试验注册

该随机对照临床试验已在中国临床试验注册中心注册(注册号:ChiCTR2300073816,日期:2023年7月21日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77d/11069150/9ea6c07880e6/12903_2024_4255_Figa_HTML.jpg

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