Department of Pharmaceutical Sciences
College of Pharmacy
University of Nebraska Medical Center
986025 Nebraska Medical Center
Omaha, NE 68198-6025
- Pharmacy Doctorate Students
- Pharmaceutical Sciences 570: Bioavailability & Bioequivalence, rate processes of drug release, drug absorption, parenterals, biotechnology-derived products, nasal, pulmonary and opthalmic delivery.
- Pharmaceutical Sciences Graduate Students
- Quantitative Pharmaceutical Sciences 845: DNA, RNA and proteins
- Pharm Chem for Drug Delivery 826: Surface modification of micro and nanospheres, synthesis of biodegradable nanogels
- Innovative Drug Delivery Systems 851: Biological barriers to drug delivery
- Physical Pharmacy 885: Mass transfer
Dr. Vetro's research interests are in developing novel synthetic targeted drug and gene delivery nanocarriers for the anti-angiogenesis treatment of cancer, improving development paradigms for targeted bioimaging and drug delivery nanocarriers and developing subunit vaccines based on the novel adjuvant, EP67.
- Ye Z, Abdelmoaty MM, Ambardekar VV, Curran SM, Dyavar SR, Arnold LL, Cohen SM, Kumar D, Alnouti Y, Coulter DW, Singh RK, Vetro JA (2021). Preliminary Preclinical Study of Chol-DsiRNA Polyplexes Formed with PLL-PEG[5K] for the RNAi-Based Therapy of Breast Cancer. Nanomedicine NBM. 33: 102363.
- Alshammari AM, Smith DD; Parriott J; Stewart JP, Curran SM; McCulloh RJ, Barry PA, Iyer SS, Palermo N, Phillips JA, Dong Y, Ronning DR, Vennerstrom JL, Sanderson SD, Vetro JA (2020). Targeted Amino Acid Substitution Overcomes Scale-Up Challenges with the Human C5a-Derived Decapeptide Immunostimulant EP67. ACS Infect Dis. 6: 1169-1181.
- Tallapaka SB, Karuturi BVK, Yeapuri P, Curran SM, Phillips JA, Smith DD, Sanderson SD, Vetro JA (2019). Surface conjugation of EP67 to biodegradable nanoparticles increases the generation of long-lived mucosal and systemic memory T-cells by encapsulated protein vaccine after respiratory immunization and subsequent T-cell-mediated protection against respiratory infection. Int J Pharm. 565: 242-257.
- Ambardekar VV, Wakaskar RR, Ye Z, Curran SM, McGuire TR, Coulter DW, Singh RK, Vetro JA (2018). Complexation of Chol-DsiRNA in place of Chol-siRNA greatly increases the duration of mRNA suppression by polyplexes of PLL(30)-PEG(5K) in primary murine syngeneic breast tumors after i.v. administration. Int J Pharm. 543: 130-138.
- Karuturi VK, Tallapaka SB, Yeapuri P, Curran SM, Sanderson SD, Vetro JA. Encapsulation of an EP67-conjugated CTL peptide vaccine in nanoscale biodegradable particles increases the efficacy of respiratory immunization and affects the magnitude and memory subsets of vaccine-generated mucosal and systemic CD8+ T cells in a diameter-dependent manner (2017). Mol Pharm. DOI: 10.1021/acs.molpharmaceut.6b01088
- Bala Vamsi K. Karuturi, Shailendra B. Tallapaka, Joy A. Phillips, Sam D. Sanderson, Joseph A. Vetro (2015). Preliminary evidence that the novel host-derived immunostimulant EP67 can act as a mucosal adjuvant. Clinical Immunology 161: 251–259.
- Wakaskar RR, Bathena SPR, Tallapaka SB, Ambardekar VV, Gautam N, Thakare R, Simet SM, Curran SM, Dong Y, Vetro JA (2014). “Peripherally cross-linking the shell of core-shell polymer micelles decreases premature release of physically loaded combretastatin A4 in whole blood and increases its mean residence time and subsequent potency against primary murine breast tumors after IV administration.” Pharm Res. DOI: 10.1007/s11095-014-1515-z.
- Ambardekar VV, Wakaskar RR, Sharma B, Bowman J, Vayaboury W, Singh RK and Vetro JA (2013). "The efficacy of nuclease-resistant Chol-siRNA in primary breast tumors following complexation with PLL-PEG(5K)."Biomaterials 34(20): 4839-4848.
- Ambardekar VV, Han HY, Varney ML, Vinogradov SV, Singh RK and Vetro JA (2011). "The modification of siRNA with 3' cholesterol to increase nuclease protection and suppression of native mRNA by select siRNA polyplexes."Biomaterials 32(5): 1404-1411.
- Batrakova EV, Bronich TK, Vetro JA and Kabanov AV (2006). Polymeric micelles as drug carriers. Nanoparticulates as drug carriers. V. P. Torchilin. London, UK, Imperial College Press: 57-93.