Patil Sandip, Powar Gauri Suresh, Harale Swapnil, Galatage Sunil T, Liu Sixi, Lopes Bruno Silvester, Sharma Devender Kumar, Patil Abhinandan Ravsaheb, Wen Feiqiu
Department of Haematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Sant Gajanan Maharaj College of Pharmacy, Mahagaon, Chinchewadi, India.
Infect Drug Resist. 2025 Aug 7;18:3933-3946. doi: 10.2147/IDR.S537534. eCollection 2025.
is a key pathogen in dental caries, and the development of novel antimicrobial formulations is crucial to combat its resistance. This study aimed to evaluate a licorice-resveratrol medicated lollipop formulation (LRML) for its antimicrobial and anti-biofilm activity against .
The LRML was developed using a heating and congealing method, incorporating licorice extract (5% w/w) and resveratrol (2% w/w) in a sucrose-based matrix. The physicochemical properties of the formulation, including hardness, drug content uniformity, moisture content, and dissolution profile, were evaluated. The antimicrobial activity was assessed through Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC), and time-kill assays. Anti-biofilm activity was evaluated using a crystal violet assay. The stability of the formulation was determined under accelerated conditions.
The LRML formulation showed efficient drug release, with formulation number LRML-7 demonstrating 96.87% release within 45 minutes. The antimicrobial tests revealed significant bactericidal effects against at concentrations above 0.2 µg/mL, with a notable reduction in bacterial growth in time-kill assays. The formulation also demonstrated substantial inhibition of biofilm formation at both MIC and Minimum Bactericidal Concentration (MBC) levels. Stability studies confirmed that the formulation retained its physicochemical properties over three months.
The LRML exhibited promising antimicrobial and anti-biofilm activities against , suggesting its potential as a novel therapeutic option for managing dental infections. Further clinical studies are required to optimize the formulation's efficacy and clinical applicability.
是龋齿的关键病原体,开发新型抗菌制剂对于对抗其耐药性至关重要。本研究旨在评估甘草-白藜芦醇含药棒棒糖制剂(LRML)对其抗菌和抗生物膜活性。
采用加热凝固法制备LRML,在蔗糖基质中加入甘草提取物(5%w/w)和白藜芦醇(2%w/w)。评估了制剂的物理化学性质,包括硬度、药物含量均匀性、水分含量和溶出曲线。通过最低抑菌浓度(MIC)、最低杀菌浓度(MBC)和时间杀菌试验评估抗菌活性。使用结晶紫试验评估抗生物膜活性。在加速条件下测定制剂的稳定性。
LRML制剂显示出高效的药物释放,制剂编号LRML-7在45分钟内释放率达96.87%。抗菌试验表明,浓度高于0.2µg/mL时对有显著杀菌作用,时间杀菌试验中细菌生长明显减少。该制剂在MIC和最低杀菌浓度(MBC)水平均显示出对生物膜形成的显著抑制作用。稳定性研究证实,该制剂在三个月内保持其物理化学性质。
LRML对显示出有前景的抗菌和抗生物膜活性,表明其作为治疗牙齿感染的新型治疗选择的潜力。需要进一步的临床研究来优化该制剂的疗效和临床适用性。