|
|
|
|
LEADER |
01000naa a22002652 4500 |
001 |
NLM210533544 |
003 |
DE-627 |
005 |
20231224011831.0 |
007 |
cr uuu---uuuuu |
008 |
231224s2011 xx |||||o 00| ||eng c |
024 |
7 |
|
|a 10.1021/la201160y
|2 doi
|
028 |
5 |
2 |
|a pubmed24n0702.xml
|
035 |
|
|
|a (DE-627)NLM210533544
|
035 |
|
|
|a (NLM)21819046
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a Goldenbogen, Björn
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a Reduction-sensitive liposomes from a multifunctional lipid conjugate and natural phospholipids
|b reduction and release kinetics and cellular uptake
|
264 |
|
1 |
|c 2011
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
500 |
|
|
|a Date Completed 29.12.2011
|
500 |
|
|
|a Date Revised 21.11.2013
|
500 |
|
|
|a published: Print-Electronic
|
500 |
|
|
|a Citation Status MEDLINE
|
520 |
|
|
|a © 2011 American Chemical Society
|
520 |
|
|
|a The development of targeted and triggerable delivery systems is of high relevance for anticancer therapies. We report here on reduction-sensitive liposomes composed of a novel multifunctional lipidlike conjugate, containing a disulfide bond and a biotin moiety, and natural phospholipids. The incorporation of the disulfide conjugate into vesicles and the kinetics of their reduction were studied using dansyl-labeled conjugate 1 in using the dansyl fluorescence environmental sensitivity and the Förster resonance energy transfer from dansyl to rhodamine-labeled phospholipids. Cleavage of the disulfide bridge (e.g., by tris(2-carboxyethyl)phosphine (TCEP), dithiothreitol (DTT), l-cysteine, or glutathione (GSH)) removed the hydrophilic headgroup of the conjugate and thus changed the membrane organization leading to the release of entrapped molecules. Upon nonspecific uptake of vesicles by macrophages, calcein release from reduction-sensitive liposomes consisting of the disulfide conjugate and phospholipids was more efficient than from reduction-insensitive liposomes composed only of phospholipids. The binding of streptavidin to the conjugates did not interfere with either the subsequent reduction of the disulfide bond of the conjugate or the release of entrapped molecules. Breast cancer cell line BT-474, overexpressing the HER2 receptor, showed a high uptake of the reduction-sensitive doxorubicin-loaded liposomes functionalized with the biotin-tagged anti-HER2 antibody. The release of the entrapped cargo inside the cells was observed, implying the potential of using our system for active targeting and delivery
|
650 |
|
4 |
|a Journal Article
|
650 |
|
4 |
|a Research Support, Non-U.S. Gov't
|
650 |
|
7 |
|a Disulfides
|2 NLM
|
650 |
|
7 |
|a Fluoresceins
|2 NLM
|
650 |
|
7 |
|a Lipids
|2 NLM
|
650 |
|
7 |
|a Liposomes
|2 NLM
|
650 |
|
7 |
|a Biotin
|2 NLM
|
650 |
|
7 |
|a 6SO6U10H04
|2 NLM
|
650 |
|
7 |
|a Doxorubicin
|2 NLM
|
650 |
|
7 |
|a 80168379AG
|2 NLM
|
650 |
|
7 |
|a fluorexon
|2 NLM
|
650 |
|
7 |
|a V0YM2B16TS
|2 NLM
|
700 |
1 |
|
|a Brodersen, Nicolai
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Gramatica, Andrea
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Loew, Martin
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Liebscher, Jürgen
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Herrmann, Andreas
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Egger, Holger
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Budde, Bastian
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Arbuzova, Anna
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 27(2011), 17 vom: 06. Sept., Seite 10820-9
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
|
773 |
1 |
8 |
|g volume:27
|g year:2011
|g number:17
|g day:06
|g month:09
|g pages:10820-9
|
856 |
4 |
0 |
|u http://dx.doi.org/10.1021/la201160y
|3 Volltext
|
912 |
|
|
|a GBV_USEFLAG_A
|
912 |
|
|
|a SYSFLAG_A
|
912 |
|
|
|a GBV_NLM
|
912 |
|
|
|a GBV_ILN_22
|
912 |
|
|
|a GBV_ILN_350
|
912 |
|
|
|a GBV_ILN_721
|
951 |
|
|
|a AR
|
952 |
|
|
|d 27
|j 2011
|e 17
|b 06
|c 09
|h 10820-9
|