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AAPS Pharmscitech|September 3, 2011
Radiation and ethylene oxide terminal sterilization experiences with drug eluting stent productsByron J Lambert, Todd A Mendelson, Michael D CravenAAPS Pharmscitech|October 5, 2011
De-risking pharmaceutical tablet manufacture through process understanding, latent variable modeling, and optimization technologiesKoji Muteki, Vidya Swaminathan, Sonja S Sekulic, et al.AAPS Pharmscitech|October 29, 2011
Preparation, statistical optimization, and in vitro characterization of insulin nanoparticles composed of quaternized aromatic derivatives of chitosanReza Mahjub, Farid Abedin Dorkoosh, Mohsen Amini, et al.AAPS Pharmscitech|July 13, 2011
The application of the Accelerated Stability Assessment Program (ASAP) to quality by design (QbD) for drug product stabilityKenneth Craig WatermanAAPS Pharmscitech|November 1, 2011
Investigation of PLLA/PCL blends and paclitaxel release profilesErde Can, Gokce Udenir, Ayse Irem Kanneci, et al.AAPS Pharmscitech|August 4, 2011
Preparation, characterization, pharmacokinetics and tissue distribution of solid lipid nanoparticles loaded with tetrandrineSu Li, Zhaoshuai Ji, Meijuan Zou, et al.AAPS Pharmscitech|August 24, 2011
Quality-by-design case study: investigation of the role of poloxamer in immediate-release tablets by experimental design and multivariate data analysisGoldi Kaul, Jun Huang, Ramarao Chatlapalli, et al.AAPS Pharmscitech|September 1, 2011
In vitro and in vivo investigation of drug-eluting implants for the treatment of periodontal diseaseFu-Ying Lee, Dave W Chen, Chih-Chien Hu, et al.AAPS Pharmscitech|September 1, 2011
Formulation and evaluation of in situ gelling systems for intranasal administration of gastrodinZheng Cai, Xiangrong Song, Feng Sun, et al.AAPS Pharmscitech|October 19, 2011
The effect of the chopper on granules from wet high-shear granulation using a PMA-1 granulatorLauren Briens, Ryan LoganPageof 486