Area of Interest:

Pharmacology and Toxicology

100%

Pharmaceutical Sciences

62%

Pharmacokinetics

90%

Biopharmacy

75%

Metabolism

55%

Research Publications in Numbers

Books
0

Chapters
0

Articles
0

Abstracts
0

Selected Publications

Wu, Z., S. Wang, X. Peng, C. Lu, X. Ye and B. Wu, 2016. Altered cisatracurium pharmacokinetics and pharmacodynamics in patients with congenital heart defects. Drug Metab. Dispos., 44: 75-82.
CrossRef | Direct Link |
Dong, D., H. Sun, Z. Wu, B. Wu, Y. Xue and Z. Li, 2016. A validated ultra-performance liquid chromatography-tandem mass spectrometry method to identify the pharmacokinetics of SR8278 in normal and streptozotocin-induced diabetic rats. J. Chromatogr., 1020: 142-147.
CrossRef | Direct Link |
Wu, Z., X. Zhang, Z. Ma and B. Wu, 2015. Establishment of pharmacophore and VolSurf models to predict the substrates of UDP-glucuronosyltransferase1A3. Xenobiotica, 45: 653-662.
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Wu, Z., H. Liu and B. Wu, 2015. Regioselective glucuronidation of gingerols by human liver microsomes and expressed UDP-glucuronosyltransferase enzymes: Reaction kinetics and activity correlation analyses for UGT1A9 and UGT2B7. J. Pharm. Pharmacol., 67: 583-596.
CrossRef | Direct Link |
Sun, H., T. Zhang, Z. Wu and B. Wu, 2015. Warfarin is an Effective Modifier of Multiple UDP-glucuronosyltransferase (UGT) Enzymes: Evaluation of its Potential to Alter the Pharmacokinetics of Zidovudine. J. Pharm. Sci., 104: 244-256.
CrossRef | Direct Link |
Liu, H.M., Z.F. Wu, Z.G. Ma and B.J. Wu, 2014. Glucuronidation of macelignan by human liver microsomes and expressed UGT enzymes: Identification of UGT1A1 and 2B7 as the main contributing enzymes. Biopharmaceut. Drug Dispos., 35: 513-524.
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