Carboxyl-terminated PAMAM dendrimer interaction with 1-palmitoyl-2-oleoyl phosphocholine bilayers
Polyanionic polymers and liposomes have a great potential use as individual drug delivery systems and greater potential as a combined drug delivery system. Thus, it is important to better understand the interactions of polymers with phospholipid bilayers. A mechanistic study of the interaction betwe...
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Published in: | Biochimica et biophysica acta Vol. 1838; no. 1; pp. 445 - 455 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Netherlands
Elsevier B.V
01-01-2014
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Subjects: | |
Online Access: | Get full text |
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Summary: | Polyanionic polymers and liposomes have a great potential use as individual drug delivery systems and greater potential as a combined drug delivery system. Thus, it is important to better understand the interactions of polymers with phospholipid bilayers. A mechanistic study of the interaction between carboxyl-terminated poly(amidoamine) (PAMAM) dendrimers with 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) bilayer using fluorescence leakage and quartz crystal microbalance with dissipation monitoring (QCMD) was conducted. Fluorescence leakage experiments demonstrated that carboxyl-terminated generation 2 (G2-COOH) dendrimers caused increased liposome leakage with increasing dendrimer concentration over a 0 to 20μM range. Generation 5 (G5-COOH), on the other hand, reduced leakage over the same concentration range, presumably by increasing lipid packing. QCMD and atomic force microscopy (AFM) measurements demonstrated that G2-COOH interacting with supported bilayers resulted in small defects with some mass loss and no adsorption. In contrast, G5-COOH interaction with a bilayer resulted in adsorption and local bilayer swelling.
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•G2 and G5 carboxyl-terminated dendrimers and POPC interactions were evaluated.•G2 created defects that resulted in increased leakage in liposomes.•G5 binding increased lipid packing in liposomes and local swelling in SPB. |
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ISSN: | 0005-2736 0006-3002 1879-2642 |
DOI: | 10.1016/j.bbamem.2013.08.012 |