药品
药物输送
纳米技术
药理学
吸收(声学)
体内
控制释放
生物利用度
生物医学工程
材料科学
医学
生物
生物技术
复合材料
作者
Juliane Fjelrad Christfort,Carmen Milián‐Guimerá,Khorshid Kamguyan,Morten B. Hansen,Line Hagner Nielsen,Lasse Højlund Eklund Thamdrup,Kinga Zór,Anja Boisen
标识
DOI:10.1002/adtp.202200106
摘要
Abstract Combination drug therapy is commonly used to treat cancer, diabetes, cardiovascular conditions, and infections. However, these therapies face challenges associated with patient compliance and toxicology. Over the past decades, microdevices have emerged as a promising candidate for oral delivery allowing for targeted drug delivery with a tunable drug release. In the present work, engineered and monodisperse dual‐compartment microdevices are developed to achieve a physical separation of two drugs followed by a sequential release in the gastrointestinal tract. As proof‐of‐concept, the compartments are sealed with two pH‐sensitive polymers of different thicknesses to control the sequential release of propranolol and furosemide. In vitro release studies and in vivo absorption studies in rats confirm a sequential drug release from the two compartments. Unlike other proposed approaches, it is highly advantageous that the drugs can be loaded directly as powders, and that their release can be tuned via optimized coatings to achieve the desired release and absorption profiles. Conclusively, this study lays a strong foundation for the future use of microdevices to enable co‐delivery of drugs followed by a sequential release in close proximity in the gastrointestinal tract.
科研通智能强力驱动
Strongly Powered by AbleSci AI