Nimodipine-loaded mixed micelles: formulation, compatibility, pharmacokinetics, and vascular irritability study.

Abstract

BACKGROUND:

The clinical application of nimodipine (NIM) is limited by several unfavorable properties, which are induced by its low aqueous solubility. In the present study, nimodipine-loaded egg phosphatidylcholine-sodium glycocholate mixed micelles (NIM-EPC-SGC-MMs) were prepared to improve the water solubility of NIM, thus allowing it to be more applicable for clinical use.

METHODS:

NIM-EPC-SGC-MMs were prepared using the coprecipitation method and the factors influencing formulation quality were optimized. After formulation, water solubility, solubilizing efficiency, drug loading, particle size, physical compatibility, pharmacokinetics, and vascular irritability were determined.

RESULTS:

The mean size of the NIM-EPC-SGC-MMs was 6.099 ± 0.048 nm under optimized conditions. The water solubility of NIM in EPC-SGC-MMs was enhanced 250-fold compared with free NIM. The physical compatibility, pharmacokinetic, and vascular irritability studies showed that, in comparison to the commercially available NIM injections, NIM-EPC-SGC-MMs presented better physical compatibility, the same pharmacokinetic profile, and less risk of local vascular irritation and phlebitis.

CONCLUSION:

EPC-SGC-MMs represent a promising new formulation suitable for the intravenous delivery of NIM.

• Authors: Xu Song, Yu Jiang, Chunjuan Ren, Xun Sun, Qiang Zhang, Tao Gong, Zhirong Zhang
• Journal: International journal of nanomedicine (Int J Nanomedicine) Vol. 7 Pg. 3689-99 ( 2012) ISSN: 1178-2013 [Electronic] New Zealand
• PMID: 22888228 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Micelles
• Phosphatidylcholines
• Nimodipine
• Glycocholic Acid

Topics

• Animals
• Drug Stability
• Ear (blood supply)
• Edema (chemically induced)
• Glycocholic Acid (chemistry, pharmacokinetics, toxicity)
• Hydrogen-Ion Concentration
• Male
• Micelles
• Nimodipine (chemistry, pharmacokinetics, toxicity)
• Particle Size
• Phlebitis (chemically induced)
• Phosphatidylcholines (chemistry, pharmacokinetics, toxicity)
• Rabbits
• Rats
• Rats, Wistar
• Solubility
• Veins (drug effects)