Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, College of Pharmacy, Yanbian University, Yanji 133002, Jilin Province, China; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, College of Pharmacy, Yanbian University, Yanji 133002, Jilin Province, China.
Int J Pharm. 2022 Aug 25;624:122056. doi: 10.1016/j.ijpharm.2022.122056. Epub 2022 Jul 26.
Mucoadhesive buccal films (MBFs) become the most promising buccal mucosal delivery system duo to its advantageous properties, including simple preparation technique and better patient compliance. The mechanical properties and mucoadhesion of MBFs are crucial in their successful performance as well as manufacturing and administration. In this study, we prepared hollow mesoporous silica nanoparticles-loaded ion-crosslinked bilayer films (CCS-PVA-TPP-FSM@HMSNs) using carboxymethyl chitosan (CCS) and polyvinyl alcohol (PVA) for buccal delivery of furosemide (FSM). The FSM-loaded hollow mesoporous silica nanoparticles (FSM@HMSNs) were firstly characterized by SEM, TEM, and nitrogen adsorption/desorption. Then, we constructed an ion-crosslinked network using CCS and PVA employed with the solution casting method, and sodium tripolyphosphate (TPP) was used as a hydrogen bond crosslinking agent. The formulation was optimized through Box-Behnken design, where the impact of the proportion of the ingredients on the quality of the films was evaluated entirely. Herein, folding endurance, swelling, tensile strength, and adhesion force were selected as response variables. Morphology, mechanical, spectroscopic, thermal, and safety of CCS-PVA-TPP-FSM@HMSNs films were also investigated. The release and permeability behaviors of CCS-PVA-TPP-FSM@HMSNs films were evaluated by in vitro drug release, across isolated porcine buccal and TR146 cell model. The CCS-PVA-TPP-FSM@HMSNs films showed outstanding mechanical properties, suitable bioadhesion, high drug loading, significant sustained-release properties, and improved permeability. In pharmacokinetic study with golden hamster models, the relative bioavailability was increased by 191.54%, and the absolute bioavailability was 82.20%. In summary, this study provides evidence that this innovative CCS-PVA-TPP-FSM@HMSNs films could be a promising and industrialized buccal drug delivery system.
黏膜黏附型颊膜(MBFs)因其具有制备技术简单和患者顺应性较好等优势,成为最有前途的颊黏膜给药系统。MBFs 的机械性能和黏膜黏附性对于其成功应用以及制造和管理至关重要。在本研究中,我们使用羧甲基壳聚糖(CCS)和聚乙烯醇(PVA)制备了负载呋塞米(FSM)的中空介孔硅纳米粒子载药离子交联双层膜(CCS-PVA-TPP-FSM@HMSNs),用于 FSM 的颊黏膜给药。首先通过 SEM、TEM 和氮气吸附/解吸对负载 FSM 的中空介孔硅纳米粒子(FSM@HMSNs)进行了表征。然后,我们通过溶液浇铸法构建了 CCS 和 PVA 的离子交联网络,并使用三聚磷酸钠(TPP)作为氢键交联剂。通过 Box-Behnken 设计对配方进行了优化,其中评估了成分比例对薄膜质量的影响。在此,选择折叠耐力、溶胀度、拉伸强度和粘附力作为响应变量。还研究了 CCS-PVA-TPP-FSM@HMSNs 薄膜的形态、力学、光谱、热学和安全性。通过体外药物释放、在分离的猪颊黏膜和 TR146 细胞模型上评估 CCS-PVA-TPP-FSM@HMSNs 薄膜的释放和渗透性行为。CCS-PVA-TPP-FSM@HMSNs 薄膜表现出优异的力学性能、合适的生物黏附性、高载药量、显著的缓释性能和改善的渗透性。在金黄地鼠模型的药代动力学研究中,相对生物利用度增加了 191.54%,绝对生物利用度为 82.20%。总之,本研究为这种创新的 CCS-PVA-TPP-FSM@HMSNs 薄膜作为一种有前途的工业化颊黏膜给药系统提供了证据。