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AAPS Pharmscitech|May 7, 2008
Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000S Biswal, J Sahoo, P N Murthy, et al.AAPS Pharmscitech|October 16, 2016
Tetramethylpyrazine-Loaded Hydrogels: Preparation, Penetration Through a Subcutaneous-Mucous-Membrane Model, and a Molecular Dynamics SimulationHongmei Xia, Yinxiang Xu, Zhiqing Cheng, et al.AAPS Pharmscitech|October 8, 2016
Acceptability of Mini-Tablets in Young Children: Results from Three Prospective Cross-over StudiesViviane KlingmannAAPS Pharmscitech|October 8, 2016
Assessment Methodology for Process Validation Lifecycle Stage 3ANaheed Sayeed-Desta, Ajay Babu Pazhayattil, Jordan Collins, et al.AAPS Pharmscitech|February 11, 2014
Nanoemulsions in translational research-opportunities and challenges in targeted cancer therapySrinivas Ganta, Meghna Talekar, Amit Singh, et al.AAPS Pharmscitech|May 27, 2008
Formulation of controlled-release baclofen matrix tablets. II. Influence of some hydrophobic excipients on the release rate and in vitro evaluationHamdy Abdelkader, Ossama Youssef Abdalla, Hesham SalemAAPS Pharmscitech|June 5, 2008
The use of beta-cyclodextrin in the manufacturing of disintegrating pellets with improved dissolution performancesLucia Zema, Luca Palugan, Alessandra Maroni, et al.AAPS Pharmscitech|February 12, 2014
Liposomal oxymatrine in hepatic fibrosis treatment: formulation, in vitro and in vivo assessmentShujuan Zhang, Jun Wu, Hua Wang, et al.AAPS Pharmscitech|March 1, 2014
Best practices for the development, scale-up, and post-approval change control of IR and MR dosage forms in the current quality-by-design paradigmGlenn A Van Buskirk, Satish Asotra, Christopher Balducci, et al.AAPS Pharmscitech|February 22, 2014
Considerations for a Pediatric Biopharmaceutics Classification System (BCS): application to five drugsShivani V Gandhi, William Rodriguez, Mansoor Khan, et al.Pageof 486