Abstract
Lomerizine is a calcium channel blocker that selectively blocks L- and T-type Ca2+ channels, but it is effectively insoluble under physiological conditions. Herein we show that lomerizine can be released from a nanoparticle-based carrier by intracellular protonation in PC12 cells, suppressing Ca2+ influx in these cells in response to glutamate.
| Original language | English |
|---|---|
| Pages (from-to) | 8587-8590 |
| Journal | RSC Advances |
| Volume | 2 |
| Early online date | 25 Jul 2012 |
| DOIs | |
| Publication status | Published - 2012 |