材料科学
聚乙烯醇
聚乳酸
扫描电子显微镜
溶解试验
生物医学工程
剂型
溶解
生物利用度
盐酸普萘洛尔
控制释放
色谱法
化学工程
纳米技术
复合材料
化学
药理学
聚合物
普萘洛尔
医学
乙基纤维素
内科学
工程类
作者
Abdulsalam A. Alqahtani,Abdul Aleem Mohammed,Farhat Fatima,Mohammed Muqtader Ahmed
出处
期刊:Polymers
[MDPI AG]
日期:2023-08-26
卷期号:15 (17): 3554-3554
被引量:14
标识
DOI:10.3390/polym15173554
摘要
Three-dimensional printing has revolutionized drug manufacturing and has provided a solution to the limitations associated with the conventional manufacturing method by designing complex drug delivery systems with customized drug release profiles for personalized therapies. The present investigation aims to design a gastric floating tablet with prolonged gastric floating time and sustained drug release profile. In the present study, a gastro retentive floating device (GRFD) was designed and fabricated using a fused deposition modelling (FDM)-based 3D printing technique. This device acts as a multifunctional dosage form exhibiting prolonged gastric retention time and sustained drug release profile with improved oral bioavailability in the upper gastrointestinal tract. Commercial polyvinyl alcohol (PVA) and polylactic acid (PLA) filaments were used to design GRFD, which was comprised of dual compartments. The outer sealed compartment acts as an air-filled chamber that imparts buoyancy to the device and the inner compartment is filled with a commercial propranolol hydrochloride immediate-release tablet. The device is designed as a round-shaped shell with a central opening of varying size (1 mm, 2 mm, 3 mm, and 4 mm), which acts as a drug release window. Scanning electron microscope (SEM) images were used to determine morphological characterization. The in vitro buoyancy and drug release were evaluated using the USP type II dissolution apparatus. All the designed GRFDs exhibit good floating ability and sustained drug release profiles. GRFDs fabricated using PLA filament show maximum buoyancy (>24 h) and sustained drug release for up to 10 h. The floating ability and drug release from the developed devices were governed by the drug release window opening size and the filament material affinity towards the gastric fluid. The designed GRFDs show great prospects in modifying the drug release characteristics and could be applied to any conventional immediate-release product.
科研通智能强力驱动
Strongly Powered by AbleSci AI