Abstract
Interstitial penetration is critical for drug delivery in tumor tissues. To experimentally determine the penetration depth of macromolecules at the steady state, rat fibrosarcoma tissues were sectioned into 600μm slices and incubated in solutions of dextrans with molecular weights of 10 kDa, 70 kDa, and 2000 kDa, respectively. After incubation, 10 μm cross-sections were taken and imaged to determine normalized steady-state concentration profiles as a function of molecular size. 10 kDa dextran had a relatively uniform concentration distribution. However, the concentration profile was nonuniform for 70 kDa dextran and the least uniform for 2000 kDa dextran. Stretching or incubation of tissues in 1 M mannitol solution improved the penetration of macromolecules in tissues. These results indicate that creating more interstitial space by either stretching or reducing cell size improves macromolecule distribution in tissues.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 516-517 |
| Number of pages | 2 |
| Journal | Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings |
| Volume | 1 |
| State | Published - Dec 1 2002 |
| Event | Proceedings of the 2002 IEEE Engineering in Medicine and Biology 24th Annual Conference and the 2002 Fall Meeting of the Biomedical Engineering Society (BMES / EMBS) - Houston, TX, United States Duration: Oct 23 2002 → Oct 26 2002 |
Keywords
- Drug delivery
- Interstitial penetration
ASJC Scopus subject areas
- Signal Processing
- Biomedical Engineering
- Computer Vision and Pattern Recognition
- Health Informatics