Stoddart Mechanostereochemistry Group

 

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Stoddart Mechanostereochemistry Group
 

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Haiyan Li

haiyanli@northwestern.edu

Postdoctoral Fellow

Hometown: NeiMongol, China

Joined group: 2016


Education:

Ph.D., Pharmaceutics (2009) Shenyang Pharmaceutical University
B.Sc., Pharmaceutics (2005) Shenyang Pharmaceutical University

Publications:

1. Chi L, Wu D, Li Z, Zhang M, Liu H, Wang C, Gui S, Geng M*, Li H*, Zhang J*. Modified Release and Improved Stability of Unstable BCS II Drug by Using Cyclodextrin Complex as Carrier To Remotely Load Drug into Niosomes. Mol Pharm. 2016, 13(1):113-24.
2. Chi L, Liu R, Guo T, Wang M, Liao Z, Wu L, Li H*, Wu D*, Zhang J*. Dramatic improvement of the solubility of pseudolaric acid B by cyclodextrin complexation: Preparation, characterization and validation. Int J Pharm. 2015, 479(2):349-356.
3. Zhang J, Li H, Sun L, Wang C. Determination of the kinetic rate constant of cyclodextrin supramolecular systems by high performance affinity chromatography. A chapter in: Senta Reichelt (ed.), Affinity Chromatography in Methods in Molecular Biology. Springer, 2015, 1286:309-19.
4. Wang C, Ge J, Zhang J, Guo T, Chi L, He Z, Xu X, York P*, Sun L*, Li H*. Multianalyte determination of the kinetic rate constants of drug-cyclodextrin supermolecules by high performance affinity chromatography. J Chromatogr A. 2014, 1359:287-95.
5. Li X, Li H, Xiao Q, Wang L, Wang M, Lu X, York P, Shi S, Zhang J. Two-way effects of surfactants on Pickering emulsions stabilized by the self-assembled microcrystals of -cyclodextrin and oil. Phys Chem Chem Phys. 2014, 16(27):14059-69.
6. Li H, Ge J, Guo T, Yang S, He Z, York P, Sun L, Xu X, Zhang J. Determination of the kinetic rate constant of cyclodextrin supramolecular systems by high performance affinity chromatography. J Chromatogr A. 2013, 1305:139-48.
7. Li H, Yin X, Ji J, Sun L, Shao Q, York P, Xiao T, He Y, Zhang J. Microstructural investigation to the controlled release kinetics of monolith osmotic pump tablets via synchrotron radiation X-ray microtomography. Int J Pharm. 2012, 427(2):270-5.
8. Li H, Chen Z, Xu X, Sui X, Guo T, Liu W, Zhang J. Predicting human plasma protein binding of drugs using plasma protein interaction QSAR analysis (PPI-QSAR). Biopharm Drug Dispos. 2011, 32(6):333-42.
9. Li H, Sun J, Wang Y, Sui X, Sun L, Zhang J, He Z. Structure-based in silico model profiles the binding constant of poorly soluble drugs with -cyclodextrin. Eur J Pharm Sci. 2011, 42(1-2):55-64.

 

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