Tailored biopolymer capsules for colon-specific drug delivery: A 3D printing perspective
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
40348186
DOI
10.1016/j.xphs.2025.103815
PII: S0022-3549(25)00268-0
Knihovny.cz E-zdroje
- Klíčová slova
- 3D printed capsules, Colitis, Colonic drug delivery system, Microbiota-triggered release mechanism, Pectin, Personalized medicine,
- MeSH
- 3D tisk * MeSH
- algináty chemie MeSH
- aplikace orální MeSH
- biopolymery chemie MeSH
- chitosan chemie MeSH
- deriváty hypromelózy chemie MeSH
- kofein aplikace a dávkování chemie farmakokinetika MeSH
- kolon * metabolismus účinky léků MeSH
- lékové transportní systémy * metody MeSH
- lidé MeSH
- pektiny chemie MeSH
- prasata MeSH
- příprava léků metody MeSH
- rozpustnost MeSH
- tobolky chemie MeSH
- uvolňování léčiv MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- algináty MeSH
- biopolymery MeSH
- chitosan MeSH
- deriváty hypromelózy MeSH
- kofein MeSH
- pektiny MeSH
- tobolky MeSH
The present study aims to develop capsules employing hot melt extrusion (HME) and fused deposition modeling (FDM) three-dimensional (3D) printing approach. The primary objective was to establish a colon drug delivery system (CDDS) based on multiple release mechanisms. In the study, 3D printed hydroxypropylmethylcellulose (HPMC) based capsules containing polysaccharides (alginate, chitosan pectin from citrus and pectin from apple) were used to provide a time-triggered and microbiota-triggered release mechanism. Thirteen capsule compositions were tested, and physico-chemical properties, disintegration time, dissolution characteristic (lag time) and 50 days accelerated stability were assessed. In addition, an enteric coating by Eudragit S was tested to enhance protection against the gastric environment. Disintegration time of the capsule under in vivo conditions was verified in healthy volunteers by oral administration of the caffeine-loaded capsule and determination of the first-appearance time of caffeine in the saliva. Furthermore, in vivo monitoring of the transition time in piglets was performed by X-ray examination after oral administration of BaSO4-loaded capsules. Optimal capsule composition was identified as HPMC and pectin from citrus in 80:20 wt% ratio. Printed capsules showed suitable physico-chemical properties, lag time and stability. Minimal drug release in the upper gastrointestinal tract (∼5 %) for the first 8-10 h was ensured by both coated and uncoated capsules. In addition, as demonstrated by the in vivo transition time monitoring assay, with accelerated passage of the capsule through the gastrointestinal tract, degradation is significantly accelerated (∼4 h) by a microbiota-triggered mechanism, effectively targeting the colon. Using 3D printing, a colonic-specific drug delivery system was prepared that could potentially be suitable for treating patients with various intestinal physiological conditions.
Citace poskytuje Crossref.org