Risk based in vitro performance assessment of extended release abuse deterrent formulations基于风险的缓释滥用威慑制剂的体外性能评估INTERNATIONAL JOURNAL OF PHARMACEUTICSIF5.22016-03-0132OAAI
United States Food and Drug Administration and Department of Defense Shelf-Life Extension Program of Pharmaceutical Products: Progress and PromiseJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82014-05-0125PREAI
Analytical Methods for the Evaluation of Melamine ContaminationJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82014-02-014PREAI
Challenges of pediatric formulations: A FDA science perspectiveINTERNATIONAL JOURNAL OF PHARMACEUTICSIF5.22013-11-0115PREAI
Development and Validation of a HPLC Method for Dissolution and Stability Assay of Liquid-Filled Cyclosporine Capsule Drug ProductsAAPS PHARMSCITECHIF42013-06-1314OAAI
Process analytical technology to understand the disintegration behavior of alendronate sodium tabletsJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82013-05-018OAAI
FDA: Contribution to developing pediatric formulations and transatlantic collaborationINTERNATIONAL JOURNAL OF PHARMACEUTICSIF5.22012-10-011PREAI
Influence of Formulation and Processing Factors on Stability of Levothyroxine Sodium PentahydrateAAPS PHARMSCITECHIF42010-05-0857OAAI
Comparative stability of repackaged metoprolol tartrate tabletsINTERNATIONAL JOURNAL OF PHARMACEUTICSIF5.22010-01-0112PREAI
Difference in the Lubrication Efficiency of Bovine and Vegetable-Derived Magnesium Stearate During TablettingAAPS PHARMSCITECHIF42009-04-2410OAAI
Disintegration of Highly Soluble Immediate Release Tablets: A Surrogate for DissolutionAAPS PHARMSCITECHIF42009-04-2340OAAI
Real-time on-line blend uniformity monitoring using near-infrared reflectance spectrometry: A noninvasive off-line calibration approachJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSISIF3.12009-01-0174PREAI
Functionality of Magnesium Stearate Derived from Bovine and Vegetable Sources: Dry Granulated TabletsJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82008-12-0114PREAI
Comparison of the stability of split and intact gabapentin tabletsINTERNATIONAL JOURNAL OF PHARMACEUTICSIF5.22008-02-0115PREAI
Development and application of a validated HPLC method for the analysis of dissolution samples of gabapentin drug productsJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSISIF3.12008-01-0140PREAI
Development and application of a validated HPLC method for the determination of gabapentin and its major degradation impurity in drug productsJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSISIF3.12007-04-0150PREAI
Effect of the variation in the ambient moisture on the compaction behavior of powder undergoing roller-compaction and on the characteristics of tablets produced from the post-milled granulesJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82005-10-0128PREAI
Influence of ambient moisture on the compaction behavior of microcrystalline cellulose powder undergoing uni-axial compression and roller-compaction: A comparative study using near-infrared spectroscopyJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82005-10-0174PREAI
Real-time near-infrared monitoring of content uniformity, moisture content, compact density, tensile strength, and Young's modulus of roller compacted powder blends实时近红外监测碾压粉末混合物的含量均匀性，水分含量，压实密度，拉伸强度和杨氏模量JOURNAL OF PHARMACEUTICAL SCIENCESIF3.82005-07-01107PREAI
Nondestructive measurements of the compact strength and the particle-size distribution after milling of roller compacted powders by near-infrared spectroscopyJOURNAL OF PHARMACEUTICAL SCIENCESIF3.82004-04-0178PREAI
个人简介
教育背景
工作经历
荣誉奖项
未登录.png){kind=icon}
未登录个人简介教育背景工作经历荣誉奖项
研究方向