Articles Tập 67 Số CĐ13-HNKH Bệnh viện 19-8 09/09/2026

FORMULATION DEVELOPMENT OF A MOUTH RINSE CONTAINING BIDENS PILOSA L. AND CAMELLIA SINENSIS L. EXTRACTS FOR THE INHIBITION OF COMMON ORAL PATHOGENS

Le Minh Kha1,2, Pham Nguyen Tuong Van1,2, Le Thi Bich Tram1,2, Nguyen Bich Thuan1,2, Tran Hoang Thong1,2, Le Phuong Thao1,2
1 Faculty of Pharmacy, School of Medicine and Pharmacy, Tra Vinh University
2 Khoa Dược, Trường Y Dược, Đại học Trà Vinh
DOI: 10.52163/yhc.v67iCD13.6520
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Abstract

Background: Oral biofilm-associated diseases support the development of mouth rinses capable of controlling microorganisms and limiting plaque formation. Objective: To develop and screen mouth rinse formulations containing Bidens pilosa L. and Camellia sinensis L. extracts and to evaluate their antimicrobial and biofilm formation-inhibitory activities. Materials and methods: Ten formulations were prepared by varying the concentrations of B. pilosa extract (0.128–0.512 µg/mL), green tea extract (0.064–0.128 µg/mL), sorbitol (4–6%), and SLS (0.2–0.5%). The formulations were evaluated for organoleptic characteristics, pH, preliminary stability, and minimum inhibitory concentration (MIC) against Streptococcus mutans and Candida albicans using a resazurin-based broth microdilution assay. Biofilm formation inhibition by CT8, Listerine, and Ngoc Chau was quantified using crystal violet staining. Results: All formulations were clear, preliminarily stable, and had pH values of 6.80–7.18. CT8 and CT9 showed the best MIC values against S. mutans (<1.9 µL/mL) and C. albicans (15.6 µL/mL). CT8 reduced biofilm biomass by 74.02–92.59% over the concentration range of 1.9–500 µL/mL. At 3.9 µL/mL, CT8 reduced biofilm biomass by 84.05 ± 3.96% against S. mutans and 86.85 ± 1.77% against C. albicans, values that were significantly higher than those of the two commercial reference products under the present assay conditions (p < 0.001). Conclusion: CT8 was identified as a promising formulation based on its formulation properties, antimicrobial activity, and inhibition of biofilm formation

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