Llabot Juan Manuel, Manzo Ruben Hilario, Allemandi Daniel Alberto
Departamento de Farmacia, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Cordoba, Argentina.
AAPS PharmSciTech. 2002;3(3):E22. doi: 10.1208/pt030322.
The objective of this work was to design a mucoadhesive tablet with a potential use in the treatment of oral candidosis. A 2-layered tablet containing nystatin was formulated. Lactose CD (direct compression), carbomer (CB), and hydroxypropylmethylcellulose (HPMC) were used as excipients. Tablets were obtained through direct compression. Properties such as in vitro mucoadhesion, water uptake, front movements, and drug release were evaluated. The immediate release layer was made of lactose CD (100 mg) and nystatin (30 mg). The CB:HPMC 9:1 mixture showed the best mucoadhesion properties and was selected as excipient for the mucoadhesive polymeric layer (200 mg). The incorporation of nystatin (33.3 mg) in this layer affected the water uptake, which, in turn, modified the erosion front behavior. Nystatin showed a first-order release. The polymeric layer presented an anomalous kinetic (n = 0.82) when this layer was individually evaluated. The mucoadhesive tablet formulated in this work releases nystatin quickly from the lactose layer and then in a sustained way, during approximately 6 hours, from the polymeric layer. The mixture CB:HPMC 9:1 showed good in vitro mucoadhesion. A swelling-diffusion process modulates the release of nystatin from this layer. A non-Fickian (anomalous) kinetic was observed.
这项工作的目的是设计一种可用于治疗口腔念珠菌病的粘膜粘附片。制备了一种含制霉菌素的双层片。乳糖环糊精(直接压片用)、卡波姆(CB)和羟丙基甲基纤维素(HPMC)用作辅料。通过直接压片获得片剂。对体外粘膜粘附性、吸水性、前沿移动和药物释放等性质进行了评估。速释层由乳糖环糊精(100mg)和制霉菌素(30mg)制成。CB:HPMC 9:1混合物表现出最佳的粘膜粘附性能,被选为粘膜粘附聚合物层(200mg)的辅料。该层中加入制霉菌素(33.3mg)影响了吸水性,进而改变了侵蚀前沿行为。制霉菌素呈一级释放。单独评估该聚合物层时,其呈现出非牛顿动力学(n = 0.82)。本研究中制备的粘膜粘附片制霉菌素从乳糖层快速释放,然后在大约6小时内从聚合物层持续释放。CB:HPMC 9:1混合物表现出良好的体外粘膜粘附性。溶胀-扩散过程调节制霉菌素从该层的释放。观察到非菲克(非牛顿)动力学。