Thermodynamic and Kinetic Stability of DSPE-PEG(2000) Micelles in the Presence of Bovine Serum Albumin
Authors:
- 9 September 2010
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 114 (39) , 12632-12640
Abstract
This work investigated the stability of DSPE-PEG(2000) micelles in the presence of bovine serum albumin (BSA). DSPE-PEG(2000) was found to exist in equilibrium among monomeric, micellar, and BSA-bound states, and this equilibrium shifted toward the BSA-bound state when the temperature increased from 20 to 37 °C. The micellar state is thermodynamically unstable at both temperatures when the concentration of BSA approaches that of DSPE-PEG(2000), and micelle breakup occurs with a first-order time constant of 130 ± 9 min at 20 °C and 7.8 ± 1.6 min at 37 °C. Thus, previous targeting experiments that demonstrate synergistic effects in multiply functionalized DSPE-PEG(2000) micelles are likely due to targeting that occurs on a timescale faster than that of micelle breakup. Micelle breakup was limited by diffusion at 20 °C whereas at 37 °C monomer desorption from the micelle was the rate-limiting step. These findings give clear guidance concerning the lifetimes of micelles that may be used as diagnostic and therapeutic nanoparticles.Keywords
This publication has 24 references indexed in Scilit:
- Targeting atherosclerosis by using modular, multifunctional micellesProceedings of the National Academy of Sciences, 2009
- Targeting of albumin-embedded paclitaxel nanoparticles to tumorsNanomedicine: Nanotechnology, Biology and Medicine, 2009
- Stable and Potent Polyvalent Anthrax Toxin Inhibitors: Raft-Inspired Domain Formation in Liposomes that Contain PEGylated LipidsChemistry – A European Journal, 2008
- Structural Study of BSA/Poly(ethylene glycol) Lipid Conjugate ComplexesThe Journal of Physical Chemistry B, 2007
- Complex Formation of Bovine Serum Albumin with a Poly(ethylene glycol) Lipid ConjugateBiomacromolecules, 2007
- Raftlike Polyvalent Inhibitors of the Anthrax Toxin: Modulating Inhibitory Potency by Formation of Lipid MicrodomainsAngewandte Chemie International Edition, 2007
- Statistical pattern matching facilitates the design of polyvalent inhibitors of anthrax and cholera toxinsNature Biotechnology, 2006
- Detailed Structure of Hairy Mixed Micelles Formed by Phosphatidylcholine and PEGylated Phospholipids in Aqueous MediaLangmuir, 2005
- Crystal structures of human serum albumin complexed with monounsaturated and polyunsaturated fatty acidsJournal of Molecular Biology, 2001
- Crystallographic analysis reveals common modes of binding of medium and long-chain fatty acids to human serum albumin 1 1Edited by R. HuberJournal of Molecular Biology, 2000