Abstract
The aim of the present study was to evaluate the utility of pullulan acetate microparticles (PAMs), chitosan micropaticles (CMs), and dipalmitoylphosphatidyl-serine-liposomes (PS-Lip) as oral carriers for delivery to the intestinal Peyer's patches (PPs). To monitor PP delivery after oral administration, PAMs, CMs, and PS-Lip were radiolabeled with 99mTc. Radiolabeling efficiencies of the particles were 95 ± 2.5% (PAMs), 87 ± 4.3% (CMs), and 77.2 ± 5.8% (PS-Lip). In delivery studies to the PPs, the percentage of PS-Lip taken up to the PPs was 3.8 × 10 -3 ± 0.3% of the administered dose with PS-Lip group showed significantly high uptake compared to the PAM and CM groups. These results suggest that PS-Lip may be used as a potential system for developing an oral delivery carrier.
| Original language | English |
|---|---|
| Pages (from-to) | 884-889 |
| Number of pages | 6 |
| Journal | Drug Development Research |
| Volume | 67 |
| Issue number | 12 |
| DOIs | |
| State | Published - 2006.12 |
Keywords
- Tc
- Liposomes
- Microparticles
- Oral drug delivery systems
- Peyer's patch
Quacquarelli Symonds(QS) Subject Topics
- Pharmacy & Pharmacology
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