Hombach Juliane, Palmberger Thomas F, Bernkop-Schnürch Andreas
Department of Pharmaceutical Technology, Institute of Pharmacy, Leopold-Franzens-University Innsbruck, Innsbruck, Austria.
J Pharm Sci. 2009 Feb;98(2):555-64. doi: 10.1002/jps.21457.
The purpose of the present study was to design and evaluate a novel vaginal delivery system for nystatin based on mucoadhesive polymers. L-Cysteine and cysteamine, respectively, were covalently attached to poly(acrylic acid), and the two different thiolated polymers were evaluated in vitro regarding their swelling behavior, mucoadhesive properties and release behavior. Tablets comprising these thiolated polymers and nystatin demonstrated a high stability in vaginal fluid simulant pH 4.2 and an increase in weight by swelling whereas control tablets comprising unmodified poly(acrylic acid) disintegrated and dissolved. The mucoadhesion time of tablets on freshly excised bovine vaginal mucosa on a rotating cylinder and the total work of adhesion of gels and tablets increased significantly due to the formation of disulfide bonds between the thiolated polymer and cysteine rich subdomaines of the mucus layer. The drug nystatin was released more slowly out of thiomer tablets and gels than out of PAA control tablets and gels. Therefore these thiolated polymers are promising delivery systems for nystatin providing a prolonged residence time and a sustained drug release in vitro under physiological relevant conditions.
本研究的目的是设计并评估一种基于粘膜粘附聚合物的新型制霉菌素阴道给药系统。分别将L-半胱氨酸和半胱胺共价连接到聚丙烯酸上,并对这两种不同的硫醇化聚合物的溶胀行为、粘膜粘附性能和释放行为进行了体外评估。含有这些硫醇化聚合物和制霉菌素的片剂在pH 4.2的阴道液模拟物中表现出高稳定性,且因溶胀而重量增加,而含有未改性聚丙烯酸的对照片剂则崩解并溶解。由于硫醇化聚合物与粘液层富含半胱氨酸的亚结构域之间形成二硫键,片剂在旋转圆筒上新鲜切除的牛阴道粘膜上的粘膜粘附时间以及凝胶和片剂的总粘附功显著增加。与从聚丙烯酸对照片剂和凝胶中释放相比,制霉菌素从硫醇聚合物片剂和凝胶中释放得更慢。因此,这些硫醇化聚合物是有前景的制霉菌素给药系统,在生理相关条件下可提供延长的停留时间和体外持续药物释放。