2021
DOI: 10.1016/j.ijpharm.2021.120420
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Co-delivery of ciprofloxacin and colistin using microcontainers for bacterial biofilm treatment

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Cited by 5 publications
(6 citation statements)
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“…Each substrate chip, holding 100 microcontainers, was loaded with 1.0 ± 0.2 mg furosemide, corresponding to ≈10 µg per microcontainer. This was a substantially larger loading capacity than previously reported for similarly sized microdevices, which was 1.5 [ 4 ] and 3–5 µg per microdevice, [ 41 ] respectively. This higher loading capacity can be achieved since the structural sidewalls of the microdevices are thinner when fabricated by the custom‐built 3D printer.…”
Section: Resultsmentioning
confidence: 60%
“…Each substrate chip, holding 100 microcontainers, was loaded with 1.0 ± 0.2 mg furosemide, corresponding to ≈10 µg per microcontainer. This was a substantially larger loading capacity than previously reported for similarly sized microdevices, which was 1.5 [ 4 ] and 3–5 µg per microdevice, [ 41 ] respectively. This higher loading capacity can be achieved since the structural sidewalls of the microdevices are thinner when fabricated by the custom‐built 3D printer.…”
Section: Resultsmentioning
confidence: 60%
“…The in vivo pharmacokinetic study presented trends towards delayed and sustained absorption of paracetamol from PCL microcontainers compared to powder in a gelatin capsule as control, with a time until maximum plasma concentration (Tmax) of 59 ± 31 min and 38 ± 26 min, respectively (11). Microcontainers have also been applied to confine amorphous indomethacin to lower the extent of crystallization, and they have shown promising preliminary results for oral delivery of cubosomes in relation to oral vaccine delivery and for eradication of bacterial biofilms (8,(15)(16)(17). Thus, many different applications for microcontainers in oral drug delivery are continuously explored.…”
Section: Introductionmentioning
confidence: 99%
“…[18,[23][24][25][26][27] In a few cases, reservoir-based microdevices have been prepared for oral delivery of multiple drugs, however, without achieving sequential release, but merely simultaneous release of pharmaceutical compounds for therapeutical applications such as drug-resistant infections, diabetes, and cancer. [28][29][30] In one case, the sequential release was obtained from a flat microdevice with separate reservoirs of 5 𝜇m depth in an in vitro cell model, by loading different model drugs in hydrogel matrices using photolithography. However, the developed multi-reservoir microdevice was not evaluated in vivo.…”
Section: Introductionmentioning
confidence: 99%