Abstract
Oridonin (ORI)-loaded Nanostructured lipid carriers (NLC) were prepared by emulsionevaporation and low temperaturesolidification technique, and evaluated for morphological observation, particle size, zeta potential and in vitro drug release. Next, the characteristics of biodistribution and pharmacokinetics in vivo were examined. The average particle size of resultant NLC was 245.2nm and the zeta potential was found to be -38.77 mV. The in vivo characteristics of ORI-loaded NLC were studied after intravenous administration using Kunming strain mice as experimental animals. An ORI control solution was studied parallelly. In tested organs, the distribution of ORI-loaded NLC to liver was higher than that of free drug. ORI-loaded NLC showed higher AUC (area under tissue concentrationtime curve) values and circulated in the blood stream for a longer time compared with ORI solution. These results support the potential applications of NLC for the delivery of ORI. © 2012 Informa Healthcare USA, Inc.
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Zheng, D., Dai, W., Zhang, D., Duan, C., Jia, L., Liu, Y., & Zhang, Q. (2012). In vivo studies on the oridonin-loaded nanostructured lipid carriers. Drug Delivery, 19(6), 286–291. https://doi.org/10.3109/10717544.2012.704096
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