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Bioadhesive Matrix Tablets Loaded with Lipophilic Nanoparticles as Vehicles for Drugs for Periodontitis Treatment: Development and Characterization

机译:载有亲脂性纳米颗粒的生物粘附基质片剂作为治疗牙周炎药物的载体:开发和表征

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摘要

Periodontitis treatment is usually focused on the reduction or eradication of periodontal pathogens using antibiotics against anaerobic bacteria, such as metronidazole (MTR). Moreover, recently the correlation between periodontal diseases and overexpression of reactive oxygen species (ROS) led to the introduction of antioxidant biomolecules in therapy. In this work, bioadhesive buccal tablets, consisting of a hydrophilic matrix loaded with metronidazole and lipophilic nanoparticles as a vehicle of curcumin, were developed. Curcumin (CUR)-loaded nanostructured lipid carriers (NLC) were prepared using glycyrrhetic acid, hexadecanol, isopropyl palmitate and Tween 80 as a surfactant. As method, homogenization followed by high-frequency sonication was used. After dialysis, CUR-NLC dispersion was evaluated in terms of drug loading (DL, 2.2% w/w) and drug recovery (DR, 88% w/w). NLC, characterized by dynamic light scattering and scanning electron microscopy (SEM), exhibited a spherical shape, an average particle size of 121.6 nm and PDI and PZ values considered optimal for a colloidal nanoparticle dispersion indicating good stability of the system. Subsequently, a hydrophilic sponge was obtained by lyophilization of a gel based on trehalose, Natrosol and PVP-K90, loaded with CUR-NLC and MTR. By compression of the sponge, matrix tablets were obtained and characterized in term of porosity, swelling index, mucoadhesion and drugs release. The ability of the matrix tablets to release CUR and MTR when applied on buccal mucosa and the aptitude of actives to penetrate and/or permeate the tissue were evaluated. The data demonstrate the ability of NLC to promote the penetration of CUR into the lipophilic domains of the mucosal membrane, while MTR can penetrate and permeate the mucosal tissue, where it can perform a loco-regional antibacterial activity. These results strongly support the possibility of using this novel matrix tablet for delivering MTR together with CUR for topical treatment of periodontal diseases.
机译:牙周炎的治疗通常集中在使用针对厌氧细菌的抗生素(例如甲硝唑(MTR))减少或根除牙周病原体。此外,最近牙周疾病与活性氧(ROS)过度表达之间的相关性导致在治疗中引入抗氧化剂生物分子。在这项工作中,开发了一种生物粘附的口腔片剂,该片剂由载有甲硝唑和亲脂性纳米颗粒的亲水性基质(作为姜黄素的载体)组成。载有姜黄素(CUR)的纳米结构脂质载体(NLC)是使用甘草次酸,十六烷醇,棕榈酸异丙酯和Tween 80作为表面活性剂制备的。作为方法,使用均质化然后高频超声处理。透析后,根据载药量(DL,2.2%w / w)和药物回收率(DR,88%w / w)评估CUR-NLC分散度。以动态光散射和扫描电子显微镜(SEM)为特征的NLC呈球形,平均粒径为121.6 nm,PDI和PZ值被认为是胶体纳米颗粒分散体的最佳选择,表明系统具有良好的稳定性。随后,通过冻干基于海藻糖,Natrosol和装载有CUR-NLC和MTR的PVP-K90的凝胶获得亲水海绵。通过压缩海绵,获得基质片剂,并在孔隙率,溶胀指数,粘膜粘附性和药物释放方面进行表征。评估了在口腔粘膜上施用时,基质片剂释放CUR和MTR的能力以及活性成分渗透和/或渗透组织的能力。数据证明了NLC能够促进CUR渗透进入粘膜的亲脂性区域,而MTR可以渗透并渗透到粘膜组织中,在粘膜组织中可以执行局部区域的抗菌活性。这些结果强烈支持使用这种新型基质片剂与CUR一起递送MTR进行牙周疾病局部治疗的可能性。

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