TY - JOUR
T1 - From concept to in vivo testing
T2 - Microcontainers for oral drug delivery
AU - Mazzoni, Chiara
AU - Tentor, Fabio
AU - Strindberg, Sophie Andersen
AU - Nielsen, Line Hagner
AU - Keller, Stephan Sylvest
AU - Alstrøm, Tommy Sonne
AU - Gundlach, Carsten
AU - Müllertz, Anette
AU - Marizza, Paolo
AU - Boisen, Anja
PY - 2017/12/28
Y1 - 2017/12/28
N2 - This work explores the potential of polymeric micrometer sized devices (microcontainers) as oral drug delivery systems (DDS). Arrays of detachable microcontainers (D-MCs) were fabricated on a sacrificial layer to improve the handling and facilitate the collection of individual D-MCs. A model drug, ketoprofen, was loaded into the microcontainers using supercritical CO2 impregnation, followed by deposition of an enteric coating to protect the drug from the harsh gastric environment and to provide a fast release in the intestine. In vitro, in vivo and ex vivo studies were performed to assess the viability of the D-MCs as oral DDS. D-MCs improved the relative oral bioavailability by 180% within 4 h, and increased the absorption rate by 2.4 times compared to the control. This work represents a significant step forward in the translation of these devices from laboratory to clinic.
AB - This work explores the potential of polymeric micrometer sized devices (microcontainers) as oral drug delivery systems (DDS). Arrays of detachable microcontainers (D-MCs) were fabricated on a sacrificial layer to improve the handling and facilitate the collection of individual D-MCs. A model drug, ketoprofen, was loaded into the microcontainers using supercritical CO2 impregnation, followed by deposition of an enteric coating to protect the drug from the harsh gastric environment and to provide a fast release in the intestine. In vitro, in vivo and ex vivo studies were performed to assess the viability of the D-MCs as oral DDS. D-MCs improved the relative oral bioavailability by 180% within 4 h, and increased the absorption rate by 2.4 times compared to the control. This work represents a significant step forward in the translation of these devices from laboratory to clinic.
KW - Enteric coating
KW - Microtechnology
KW - Oral drug delivery
KW - Supercritical impregnation
U2 - 10.1016/j.jconrel.2017.10.013
DO - 10.1016/j.jconrel.2017.10.013
M3 - Journal article
C2 - 29054373
AN - SCOPUS:85032678984
VL - 268
SP - 343
EP - 351
JO - Journal of Controlled Release
JF - Journal of Controlled Release
SN - 0168-3659
ER -