Zafar Farjad, Sheraz Muhammad Ali, Ali Syed Abid, Riaz Maryam, Ahmed Sofia, Anwar Zubair
Baqai Dental College, Baqai Medical University, Karachi-75340, Pakistan.
Baqai Institute of Pharmaceutical Sciences, Baqai Medical University, Karachi-75340, Pakistan.
Curr Drug Deliv. 2025 Mar 26. doi: 10.2174/0115672018377472250326061736.
The primary aim of this study was to develop an effective treatment strategy for periodontal diseases that maximizes therapeutic effects while minimizing systemic adverse effects. Specifically, the study focused on creating a xerogel-based localized drug delivery system for the slow release of doxycycline hyclate (DH) to treat periodontal disease.
Xerogels were prepared using the solvent casting method, with the solvent being evaporated slowly at ambient conditions. The prepared DH xerogels underwent comprehensive characterization to assess their in-silico compatibility, pharmacokinetics, and physicochemical properties. The properties studied included drying time and rate, thickness, moisture content, swelling index, organoleptic properties, scanning electron microscopy, FTIR spectroscopy, differential scanning calorimetry, drug release and kinetics, and antibacterial activity.
In-silico studies demonstrated compatibility between the ingredients, indicating minimal adverse effects on the body. The analysis revealed hydrogen bonding between the drug and polymers, changing the drug's crystallization characteristics to an amorphous form. The release profiles of DH from the xerogels indicated a slow release, ranging from 29.42% to 66.30% over 10 hours, following the Hopfenberg model.
The findings of this study suggest that the formulated xerogels are well-suited for periodontal applications. The slow-release profile of DH from the xerogels offers a promising approach for localized treatment of periodontal disease, reducing the risk of systemic adverse effects. This data is valuable for dental practitioners and pharmaceutical formulators, providing a new avenue for enhancing periodontal disease treatment.
本研究的主要目的是制定一种有效的牙周疾病治疗策略,在使全身不良反应最小化的同时最大化治疗效果。具体而言,该研究专注于创建一种基于干凝胶的局部给药系统,用于缓慢释放盐酸多西环素(DH)以治疗牙周疾病。
采用溶剂浇铸法制备干凝胶,溶剂在环境条件下缓慢蒸发。对制备的DH干凝胶进行全面表征,以评估其计算机模拟兼容性、药代动力学和物理化学性质。研究的性质包括干燥时间和速率、厚度、水分含量、溶胀指数、感官性质、扫描电子显微镜、傅里叶变换红外光谱、差示扫描量热法、药物释放和动力学以及抗菌活性。
计算机模拟研究表明成分之间具有兼容性,表明对身体的不良反应最小。分析揭示了药物与聚合物之间的氢键,将药物的结晶特性转变为无定形形式。DH从干凝胶中的释放曲线表明其为缓慢释放,在10小时内释放范围为29.42%至66.30%,符合霍普芬伯格模型。
本研究结果表明,所制备的干凝胶非常适合用于牙周应用。DH从干凝胶中的缓慢释放特性为牙周疾病的局部治疗提供了一种有前景的方法,降低了全身不良反应的风险。这些数据对牙科从业者和药物配方师具有重要价值,为加强牙周疾病治疗提供了一条新途径。