6/2008-present Associate professor, College of Life Science and Technology, HUST
5/1987-5/2008 Medicine teaching and drug discovery in Hubei University of Chinese Medicine and Wuhan Institute of Technology.
 Chengwen Mao, Jiangling Wan, Huabing Chen, Huibi Xu, Xiangliang Yang. The composition of oil phase modulates venous irritation of lipid emulsion-loaded diallyl trisulfide. Drug development and Industrial Pharmacy, 2010, 36 (6): 698-704.
 Chengwen Mao, Jiangling Wan, Huabing Chen, Huibi Xu, Xiangliang Yang. Emulsifiers' composition modulates venous irritation of the nanoemulsions as a lipophilic and venous irritant drug delivery system. AAPS Pharmscitech, 2009, 10 (3): 1058-1064.
 Xiaozhi Zhao, Dongsheng Mou, Jiangling Wan, Huibi Xu, Xiangliang Yang. A novel method for the separation and determination of non-encapsulated pyrene in plasma and its application in pharmacokinetic studies of pyrene-loaded MPEG-PLA based nanoparticles . Nanotechnology, 2009, 20(12): 125701.
 Wei Wang, Wei Xiong, Jiangling Wan, Xiaohui Sun, Huibi Xu, Xiangliang Yang. The decrease of PAMAM dendrimer-induced cytotoxicity by PEGylation via attenuation of oxidative stress. Nanotechnology, 2009, 20(10): 105103.
 Xiaozhi Zhao, Jiangling Wan, Huibi Xu, Xiangliang Yang. An improved HPLC method with fluorescence detection for the determination of pyrene in rat plasma and its pharmacokinetics. Journal of Pharmaceutical and Biomedical Analysis, 2008, 48(4): 1237-1242.
 Huabing Chen, Jiangling Wan（共同第一作者）, Yirui Wang, Dongsheng Mou, Huibi Xu, Xiangliang Yang. A facile nanoaggregation strategy for oral delivery of hydrophobic drugs by utilizing acid-base neutralization reactions. Nanotechnology, 2008, 19(37): 375104.
 Tao Yi, Jiangling Wan, Huibi Xu, Xiangliang Yang. A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs. European Journal of Pharmaceutics and Biopharmaceutics, 2008, 70(2): 439-444.
 Tao Yi, Jiangling Wan, Huibi Xu, Xiangliang Yang. Controlled poorly soluble drug release from solid self-microemulsifying formulations with high viscosity hydroxypropylmethylcellulose. European Journal of Pharmaceutical Sciences. 2008, 34(4-5): 274-280.