Larry L. Augsburger
Affiliations: | University of Maryland School of Medicine, Baltimore, MD, United States |
Area:
Pharmaceutical ChemistryWebsite:
http://www.pharmtech.com/larry-l-augsburger-phd-0Google:
"Larry Louis Augsburger"Bio:
https://www.researchgate.net/profile/Larry_Augsburger
https://doi.org/10.1002/jps.2600570417
Mean distance: (not calculated yet)
Parents
Sign in to add mentorRalph Frederick Shangraw | grad student | 1967 | University of Maryland | |
(Aerosolfoams : the relationship of bubble size to foam rheology and a preliminary study of the rheology of pressurized emulsions.) |
Children
Sign in to add traineeSusan H. Kopelman | grad student | 2001 | University of Maryland Medical School |
Huijeong A. Hahm | grad student | 2002 | University of Maryland Medical School |
Xiaohong Pan | grad student | 2002 | University of Maryland Medical School |
Wendy I. Wilson | grad student | 2004 | University of Maryland Medical School |
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Publications
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Moolchandani V, Augsburger LL, Gupta A, et al. (2016) To investigate the influence of machine operating variables on formulations derived from lactose types in capsule filling: part 2. Drug Development and Industrial Pharmacy. 42: 624-35 |
Moolchandani V, Augsburger LL, Gupta A, et al. (2015) Characterization and selection of suitable grades of lactose as functional fillers for capsule filling: part 1. Drug Development and Industrial Pharmacy. 41: 1452-63 |
Jung HA, Augsburger LL. (2012) Application of a novel automatic disintegration apparatus for the development and evaluation of a direct compression rapidly disintegrating tablet. Drug Development and Industrial Pharmacy. 38: 825-36 |
Cantor SL, Hoag SW, Augsburger LL. (2009) Formulation and characterization of a compacted multiparticulate system for modified release of water-soluble drugs--Part II theophylline and cimetidine. Drug Development and Industrial Pharmacy. 35: 568-82 |
Cantor SL, Hoag SW, Augsburger LL. (2009) Formulation and characterization of a compacted multiparticulate system for modified release of water-soluble drugs--part 1--acetaminophen. Drug Development and Industrial Pharmacy. 35: 337-51 |
Jin P, Madieh S, Augsburger LL. (2008) Selected physical and chemical properties of Feverfew (Tanacetum parthenium) extracts important for formulated product quality and performance. Aaps Pharmscitech. 9: 22-30 |
Pan X, Julian T, Augsburger L. (2008) Increasing the dissolution rate of a low-solubility drug through a crystalline-amorphous transition: a case study with indomethacin [correction of indomethicin]. Drug Development and Industrial Pharmacy. 34: 221-31 |
Xie L, Wu H, Shen M, et al. (2008) Quality-by-design (QbD): effects of testing parameters and formulation variables on the segregation tendency of pharmaceutical powder measured by the ASTM D 6940-04 segregation tester. Journal of Pharmaceutical Sciences. 97: 4485-97 |
Jin P, Madieh S, Augsburger LL. (2007) The solution and solid state stability and excipient compatibility of parthenolide in feverfew. Aaps Pharmscitech. 8: E105 |
Madieh S, Simone M, Wilson W, et al. (2007) Investigation of drug-porous adsorbent interactions in drug mixtures with selected porous adsorbents. Journal of Pharmaceutical Sciences. 96: 851-63 |