College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA.
AAPS PharmSciTech. 2013 Jun;14(2):475-84. doi: 10.1208/s12249-012-9891-3. Epub 2013 Mar 2.
The aim of this work was to investigate the influence of particles on the properties of polymethacrylate films intended for buccal delivery. A solvent casting method was used with Eudragit RS and RL (ERS and ERL, respectively) as film-forming rate-controlling polymers, with caffeine as a water-soluble model drug. The physicochemical properties of the model films for a series of formulations with increasing concentrations of caffeine were determined in terms of morphology, mechanical and mucoadhesive properties, drug content uniformity, and drug release and associated kinetics. Typically regarded as non-mucoadhesive polymers, ERS and mainly ERL, were found to be good mucoadhesives, with ERL01 exhibiting a work of mucoadhesion (WoA) of 118.9 μJ, which was about five to six times higher than that observed for commonly used mucoadhesives such as Carbopol(®) 974P (C974P, 23.9 μJ) and polycarbophil (PCP, 17.4 μJ). The mucoadhesive force for ERL01 was found to be significantly lower yet comparable to C974P and PCP films (211.1 vs. 329.7 and 301.1 mN, respectively). Inspection of cross-sections of the films indicated that increasing the concentration of caffeine was correlated with the appearance of recrystallized agglomerates. In conclusion, caffeine agglomerates had detrimental effects in terms of mucoadhesion, mechanical properties, uniformity, and drug release at large particle sizes. ERL series of films exhibited very rapid release of caffeine while ERS series showed controlled release. Analysis of release profiles revealed that kinetics changed from a diffusion controlled to a first-order release mechanism.
本工作旨在研究粒子对颊用聚甲基丙烯酸酯膜性能的影响。采用溶剂浇铸法,以 Eudragit RS 和 RL(分别为 ERS 和 ERL)为成膜控速聚合物,以咖啡因作为水溶性模型药物。通过考察一系列含有不同咖啡因浓度的模型膜的形态、力学和粘膜黏附性能、药物含量均匀性以及药物释放和相关动力学,确定了模型膜的物理化学性质。ERS 和 ERL 通常被认为是非粘膜黏附性聚合物,但被发现是良好的粘膜黏附剂,其中 ERL01 的粘膜黏附功(WoA)为 118.9 μJ,约为常用粘膜黏附剂 Carbopol(®) 974P(C974P,23.9 μJ)和聚卡波非(PCP,17.4 μJ)的五到六倍。研究发现,ERL01 的粘膜黏附力虽然较低,但与 C974P 和 PCP 膜相当(分别为 211.1、329.7 和 301.1 mN)。对膜的横截面进行检查表明,咖啡因浓度的增加与结晶团聚体的出现有关。总之,大粒径的咖啡因团聚体对粘膜黏附性、力学性能、均匀性和药物释放有不利影响。ERL 系列薄膜表现出非常快速的咖啡因释放,而 ERS 系列则表现出控制释放。对释放曲线的分析表明,释放动力学从扩散控制转变为一级释放机制。