001     9565
005     20240619091746.0
024 7 _ |2 pmid
|a pmid:20567774
024 7 _ |2 DOI
|a 10.1039/b923147a
024 7 _ |2 WOS
|a WOS:000277315800015
024 7 _ |2 MLZ
|a AccardoMMMPTRAAAM2010
037 _ _ |a PreJuSER-9565
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Biochemistry & Molecular Biology
100 1 _ |0 P:(DE-HGF)0
|a Accardo, A.
|b 0
245 _ _ |a Peptide modified nanocarriers for selective targeting of bombesin receptors
260 _ _ |a Cambridge
|b Royal Society of Chemistry
|c 2010
300 _ _ |a 878 - 887
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |0 20661
|a Molecular BioSystems
|v 6
|x 1742-206X
|y 5
500 _ _ |a We thank Prof. Helmut Maecke, University Hospital Basel, Switzerland for the helpful discussions and suggestions. We are indebted to EMIL, European Molecular Imaging Laboratories, for financial support. Some of us (LP, GM, AR) wish to thank the Forschungszentrum Julich for provision of beam time.
520 _ _ |a The present work describes new supramolecular aggregates obtained by co-assembling two different amphiphilic molecules, one containing the bioactive bombesin peptide (BN), or a scramble sequence, and the other, the DOTA chelating agent, (C18)(2)DOTA, capable of forming stable complexes with the radioactive (111)In(III) isotope. The peptide in the amphiphilic monomer is spaced by the lipophilic moiety through ethoxylic spacers of different length: a shorter spacer with five units of dioxoethylene moieties in (C18)(2)L5-peptide, or a longer spacer consisting of a Peg3000 residue in (C18)(2)Peg3000-peptide. Structural characterization by SANS and DLS techniques indicates that, independently from the presence of the peptide containing monomer in the final composition, the predominant aggregates are liposomes of similar shape and size with a hydrodynamic radius R(h) around 200 nm and bilayer thickness, d, of 4 nm. In vitro data show specific binding of the (111)In-(C18)(2)DOTA/(C18)(2)L5-[7-14]BN 90:10 liposomes in receptor expressing cells. However, the presence of the Peg3000 unit on the external liposomal surface, could hide the peptide and prevent the receptor binding. In vivo experiments using (111)In-(C18)(2)DOTA/(C18)(2)L5-[7-14]BN show the expected biological behavior of aggregates of such size and molecular composition, moreover there is an increase in concentration of the GRPR targeting aggregate in the tumors compared to control at the 48 h time point evaluated (2.4% ID/g versus 1.6% ID/g).
536 _ _ |0 G:(DE-Juel1)FUEK505
|2 G:(DE-HGF)
|a BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
|c P45
|x 0
536 _ _ |0 G:(DE-Juel1)FUEK415
|a Großgeräte für die Forschung mit Photonen, Neutronen und Ionen (PNI)
|c P55
|x 1
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Cell Line, Tumor
650 _ 2 |2 MeSH
|a Chelating Agents: chemistry
650 _ 2 |2 MeSH
|a Heterocyclic Compounds, 1-Ring: chemistry
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Liposomes: chemistry
650 _ 2 |2 MeSH
|a Models, Theoretical
650 _ 2 |2 MeSH
|a Molecular Structure
650 _ 2 |2 MeSH
|a Peptides: chemistry
650 _ 2 |2 MeSH
|a Peptides: metabolism
650 _ 2 |2 MeSH
|a Receptors, Bombesin: metabolism
650 _ 7 |0 0
|2 NLM Chemicals
|a Chelating Agents
650 _ 7 |0 0
|2 NLM Chemicals
|a Heterocyclic Compounds, 1-Ring
650 _ 7 |0 0
|2 NLM Chemicals
|a Liposomes
650 _ 7 |0 0
|2 NLM Chemicals
|a Peptides
650 _ 7 |0 0
|2 NLM Chemicals
|a Receptors, Bombesin
650 _ 7 |0 60239-18-1
|2 NLM Chemicals
|a 1,4,7,10-tetraazacyclododecane- 1,4,7,10-tetraacetic acid
650 _ 7 |2 WoSType
|a J
693 _ _ |0 EXP:(DE-MLZ)KWS2-20140101
|1 EXP:(DE-MLZ)FRMII-20140101
|5 EXP:(DE-MLZ)KWS2-20140101
|6 EXP:(DE-MLZ)NL3ao-20140101
|a Forschungs-Neutronenquelle Heinz Maier-Leibnitz
|e KWS-2: Small angle scattering diffractometer
|f NL3ao
|x 0
700 1 _ |0 P:(DE-HGF)0
|a Mansi, R.
|b 1
700 1 _ |0 P:(DE-HGF)0
|a Mirisco, A.
|b 2
700 1 _ |0 P:(DE-HGF)0
|a Mangiapia, G.
|b 3
700 1 _ |0 P:(DE-HGF)0
|a Paduano, L.
|b 4
700 1 _ |0 P:(DE-HGF)0
|a Tesauro, D.
|b 5
700 1 _ |0 P:(DE-Juel1)VDB4342
|a Radulescu, A.
|b 6
|u FZJ
700 1 _ |0 P:(DE-HGF)0
|a Aurilio, M.
|b 7
700 1 _ |0 P:(DE-HGF)0
|a Aloj, L.
|b 8
700 1 _ |0 P:(DE-HGF)0
|a Arra, C.
|b 9
700 1 _ |0 P:(DE-HGF)0
|a Morelli, G.
|b 10
773 _ _ |0 PERI:(DE-600)2188635-0
|a 10.1039/b923147a
|g Vol. 6, p. 878 - 887
|p 878 - 887
|q 6<878 - 887
|t Molecular BioSystems
|v 6
|x 1742-206X
|y 2010
856 7 _ |u http://dx.doi.org/10.1039/b923147a
909 C O |o oai:juser.fz-juelich.de:9565
|p VDB
913 1 _ |0 G:(DE-Juel1)FUEK505
|b Schlüsseltechnologien
|k P45
|l Biologische Informationsverarbeitung
|v BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
|x 0
913 1 _ |0 G:(DE-Juel1)FUEK415
|b Struktur der Materie
|k P55
|l Großgeräteforschung mit Photonen, Neutronen und Ionen
|v Großgeräte für die Forschung mit Photonen, Neutronen und Ionen (PNI)
|x 1
913 2 _ |0 G:(DE-HGF)POF3-623
|1 G:(DE-HGF)POF3-620
|2 G:(DE-HGF)POF3-600
|a DE-HGF
|b Forschungsbereich Materie
|l In-house research on the structure, dynamics and function of matter
|v Neutrons for Research on Condensed Matter
|x 0
914 1 _ |y 2010
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |0 I:(DE-Juel1)VDB784
|d 31.12.2010
|g IFF
|k IFF-4
|l Streumethoden
|x 0
920 1 _ |0 I:(DE-Juel1)VDB785
|d 31.12.2010
|g IFF
|k IFF-5
|l Neutronenstreuung
|x 1
920 1 _ |0 I:(DE-Juel1)JCNS-20121112
|k Jülich Centre for Neutron Science JCNS (JCNS) ; JCNS
|l JCNS
|x 2
970 _ _ |a VDB:(DE-Juel1)119485
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)PGI-4-20110106
980 _ _ |a I:(DE-Juel1)ICS-1-20110106
980 _ _ |a I:(DE-Juel1)JCNS-1-20110106
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-Juel1)JCNS-2-20110106
980 _ _ |a I:(DE-Juel1)JCNS-SNS-20110128
980 _ _ |a I:(DE-Juel1)JCNS-ILL-20110128
981 _ _ |a I:(DE-Juel1)JCNS-2-20110106
981 _ _ |a I:(DE-Juel1)IBI-8-20200312
981 _ _ |a I:(DE-Juel1)JCNS-1-20110106
981 _ _ |a I:(DE-Juel1)PGI-4-20110106
981 _ _ |a I:(DE-Juel1)ICS-1-20110106
981 _ _ |a I:(DE-Juel1)JCNS-2-20110106
981 _ _ |a I:(DE-Juel1)JCNS-SNS-20110128
981 _ _ |a I:(DE-Juel1)JCNS-ILL-20110128


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21