Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.
Department of Pharmaceutical Technology, University of Applied Sciences (BHT), Luxemburger Street 10, 13353, Berlin, Germany.
AAPS PharmSciTech. 2023 Jul 28;24(6):161. doi: 10.1208/s12249-023-02600-0.
Periodontitis is a chronic inflammatory disease of the gums caused by pathogenic microorganisms damaging and destroying periodontal tissues. Chlorhexidine digluconate (CHX) is a commonly used antimicrobial agent for the treatment of periodontitis. However, it has many drawbacks, such as toxicity due to the high dosage required, low prolonged release, and low adhesion in the periodontal pocket. The objective of this study was to develop and optimize CHX-encapsulated polymeric nanoparticles (NPs) loaded into in situ gel-forming (ISGF) using design of experiment (DoE) to improve the treatment of periodontitis and overcome these limitations. CHX-NPs were optimized from 0.046%w/v chitosan, 0.05%w/w gelatin, and 0.25%w/w CHX. After that, the optimized of CHX-NPs was loaded into a thermosensitive ISGF, which was a mixture of 15%w/v Poloxamer 407 and 1% hydroxypropyl methylcellulose (HPMC). The optimized CHX-NPs, loaded into ISGF, was evaluated by measuring gelling temperature and time, pH, viscosity, compatibility, in vitro drug release, antibacterial activity, cytotoxicity, and stability. The results showed that the size, PDI, and zeta potential of optimized CHX-NPs were 53.07±10.17 nm, 0.36±0.02, and 27.63±4.16 mV, respectively. Moreover, the optimized ISGF loading CHX-NPs showed a gelling temperature at 34.3±1.2°C within 120.00±17.32 s with a pH value of 4.06. The viscosity of the formulations at 4°C was 54.33±0.99 cP. The DSC and FTIR showed no interaction between ingredients. The optimal formulations showed a prolonged release of up to 7 days while providing potential antibacterial activity and were safe for normal gingival fibroblast cells. Moreover, the formulations had high stability at 4°C and 25°C for 3 months. In conclusion, the study achieved the successful development of ISGF loading CHX-NPs formulations for effectiveness use in periodontal treatment.
牙周炎是一种由致病微生物破坏和破坏牙周组织引起的慢性炎症性疾病。洗必泰葡萄糖酸(CHX)是一种常用于治疗牙周炎的抗菌药物。然而,由于需要高剂量,其具有许多缺点,例如毒性、低持续释放和在牙周袋中的低粘附性。本研究的目的是开发和优化 CHX 包封的聚合物纳米颗粒(NPs)负载到原位凝胶形成(ISGF)中,使用实验设计(DoE)来改善牙周炎的治疗并克服这些限制。CHX-NPs 是从 0.046%w/v 壳聚糖、0.05%w/w 明胶和 0.25%w/w CHX 中优化得到的。之后,将优化的 CHX-NPs 负载到热敏感的 ISGF 中,ISGF 是 15%w/v 泊洛沙姆 407 和 1%羟丙基甲基纤维素(HPMC)的混合物。通过测量胶凝温度和时间、pH 值、粘度、相容性、体外药物释放、抗菌活性、细胞毒性和稳定性来评估优化的 CHX-NPs 负载到 ISGF 中。结果表明,优化的 CHX-NPs 的粒径、PDI 和 Zeta 电位分别为 53.07±10.17nm、0.36±0.02 和 27.63±4.16mV。此外,优化的 ISGF 负载 CHX-NPs 表现出在 34.3±1.2°C 的胶凝温度,在 120.00±17.32s 内,pH 值为 4.06。制剂在 4°C 时的粘度为 54.33±0.99cP。DSC 和 FTIR 表明成分之间没有相互作用。最佳制剂显示出长达 7 天的延长释放,同时提供潜在的抗菌活性,对正常牙龈成纤维细胞安全。此外,制剂在 4°C 和 25°C 下 3 个月具有高稳定性。总之,本研究成功开发了用于牙周治疗的 ISGF 负载 CHX-NPs 制剂。