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008181129s2018 ||| | | | eng d
020 ▼a 9780438151697
035 ▼a (MiAaPQ)AAI10746412
035 ▼a (MiAaPQ)uiowa:15480
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0491 ▼f DP
0820 ▼a 615
1001 ▼a Allen, Rondine Joni-Ann.
24510 ▼a Development of PEG-peptide Scavenger Receptor Inhibitors for Non-viral Gene Delivery: An In-depth Analysis into the Properties which Influence Liver Uptake.
260 ▼a [S.l.] : ▼b The University of Iowa., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 190 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Adviser: Kevin Rice.
5021 ▼a Thesis (Ph.D.)--The University of Iowa, 2018.
520 ▼a Gene therapy can potentially treat a wide range of diseases ranging from inherited diseases to cancer. The successful use of nucleic acids to treat genetic diseases is limited by rapid capture and degradation of the nanoparticle by Kupffer cells
520 ▼a PEG-peptides were found to inhibit scavenger receptors on the surface of Kupffer cells by forming albumin nanoparticles when intravenously dosed. This work explores the development of potent, low-molecular weight PEG-peptide inhibitors. In order
520 ▼a Other properties including spatial distribution of leucine, hydrophobicity and peptide length were also explored to determine their effect on liver uptake. Hydrophobic peptides resulted in the formation of micelles which were inactive as scaveng
590 ▼a School code: 0096.
650 4 ▼a Pharmaceutical sciences.
650 4 ▼a Pharmacology.
690 ▼a 0572
690 ▼a 0419
71020 ▼a The University of Iowa. ▼b Pharmacy.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0096
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14996891 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자 ▼b 관리자