Dr. Sunny  M. Ogbomo
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Dr. Sunny M. Ogbomo

QA/QC Associate
Premium Waters Inc, USA


Highest Degree
PostDoc Fellow in Materials Science from University of Nebraska-Lincoln, USA

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Area of Interest:

Chemistry
100%
Drug Delivery Systems
62%
Organic Chemistry
90%
Magnetic Material
75%
Polymer Science
55%

Research Publications in Numbers

Books
0
Chapters
0
Articles
0
Abstracts
0

Selected Publications

  1. Shi, W., S.M. Ogbomo, N.K. Wagh, Z. Zhou and Y. Jia et al., 2014. The influence of linker length on the properties of cathepsin S cleavable177 Lu-labeled HPMA copolymers for pancreatic cancer imaging. Biomaterials, 35: 5760-5770.
  2. Zhou, Z., S.K. Brusnahan, Y. Jia, S.M. Ogbomo, W. Shi, N.K. Wagh and J.C. Garrison, 2013. Synthesis and in vitro and in vivo evaluation of hypoxia-enhanced 111 in-bombesin conjugates for prostate cancer imaging. J. Nuclear Med., 54: 1605-1612.
  3. Ogbomo, S.M., W. Shi, N.K. Wagh, Z. Zhou, S.K. Brusnahan and J.C. Garrison, 2013. 177Lu-labeled HPMA copolymers utilizing cathepsin B and S cleavable linkers: Synthesis, characterization and preliminary in vivo investigation in a pancreatic cancer model. Nuclear Med. Biol., 40: 606-617.
  4. Wagh, N.K., Z. Zhou, S.M. Ogbomo, W. Shi, S.K. Brusnahan and J.C. Garrison, 2012. Development of hypoxia enhanced 111in-labeled Bombesin conjugates: Design, synthesis and in vitro evaluation in PC-3 human prostate cancer. Bioconjugate Chem., 23: 527-537.
    CrossRef  |  Direct Link  |  
  5. Ogbomo, S.M., K. Chapman, C. Webber, R. Bledsoe and N.A. D'Souza, 2009. Benefits of low kenaf loading in biobased composites of poly (L‐lactide) and kenaf fiber. J. Applied Polymer Sci., 112: 1294-1301.
    CrossRef  |  Direct Link  |  
  6. Dagnon, K.L., S. Ambadapadi, A. Shaito, S.M. Ogbomo and V. DeLeon et al., 2009. Poly (L‐lactic acid) nanocomposites with layered double hydroxides functionalized with ibuprofen. J. Applied Polymer Sci., 113: 1905-1915.
    CrossRef  |  Direct Link  |  
  7. Ogbomo, S.M. and D.J. Burnell, 2006. cis-3, 5-Cyclohexadiene-1, 2-diol derivatives: Facial selectivity in their Diels-Alder reactions with ethylenic, acetylenic and azo dienophiles. Org. Biomol. Chem., 4: 3838-3848.
    Direct Link  |