Biodegradable microcontainers - towards real life applications of microfabricated systems for oral drug delivery

被引:28
作者
Abid, Zarmeena [1 ,2 ,3 ]
Strindberg, Sophie [1 ,2 ,6 ]
Javed, Madeeha M. [1 ,2 ,3 ]
Mazzoni, Chiara [1 ,2 ,4 ]
Vaut, Lukas [1 ,2 ,4 ]
Nielsen, Line Hagner [1 ,2 ,4 ]
Gundlach, Carsten [5 ]
Petersen, Ritika Singh [1 ,2 ,3 ]
Mullertz, Anette [1 ,2 ,5 ]
Boisen, Anja [1 ,2 ,4 ]
Keller, Stephan S. [1 ,2 ,3 ]
机构
[1] Danish Natl Res Fdn, Copenhagen, Denmark
[2] Villum Fdn, Ctr Intelligent Drug Delivery & Sensing Using Mic, Soborg, Denmark
[3] Tech Univ Denmark, DTU Nanolab, Natl Ctr Nano Fabricat & Characterizat, DK-2800 Lyngby, Denmark
[4] Tech Univ Denmark, Dept Hlth Technol, DTU Hlth Tech, DK-2800 Lyngby, Denmark
[5] Tech Univ Denmark, DTU Phys, Dept Phys, DK-2800 Lyngby, Denmark
[6] Univ Copenhagen, Fac Hlth & Med Sci, Dept Pharm, DK-2100 Copenhagen, Denmark
关键词
POLYMERIC MICROCONTAINERS; BIOADHESIVE MICRODEVICES; BIOAVAILABILITY; MICROSTRUCTURES; FABRICATION; PARTICLES; PLATFORM; RELEASE; DEVICES;
D O I
10.1039/c9lc00527g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microfabrication techniques have been applied to develop micron-scale devices for oral drug delivery with a high degree of control over size, shape and material composition. Recently, microcontainers have been introduced as a novel approach to obtain unidirectional release to avoid luminal drug loss, enhance drug permeation, protect drug payload from the harsh environment of the stomach, and explore the ability for targeted drug delivery. However, in order to eventually pave the way for real life applications of these microfabricated drug delivery systems, it is necessary to fabricate them in biodegradable materials approved for similar applications and with strategies that potentially allow for large scale production. In this study, we for the first time evaluate biodegradable microcontainers for oral drug delivery. Asymmetric poly-epsilon-caprolactone (PCL) microcontainers with a diameter of 300 mu m and a volume of 2.7 nL are fabricated with a novel single-step fabrication process. The microcontainers are loaded with the model drug paracetamol and coated with an enteric pH-sensitive Eudragit (R) S100 coating to protect the drug until it reaches the desired location in the small intestine. In vitro dissolution studies are performed to assess the drug load and release profile of the PCL microcontainers. Finally, in vivo studies in rats showed a higher bioavailability compared to conventional dosage forms and confirm the potential of biodegradable microcontainers for oral drug delivery.
引用
收藏
页码:2905 / 2914
页数:10
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