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Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
Published on: August 28, 2015
Polymyxin B self-associated with phospholipid nanomicelles
Kenneth S Brandenburg1, Israel Rubinstein, Ruxana T Sadikot
1Department of Bioengineering, University of Illinois at Chicago, IL, USA.
Pharmaceutical Development and Technology
|April 14, 2011
Summary
Polymyxin B (PXB) antibiotic activity decreased when self-associated with PEGylated nanomicelles (SSM). This nanomedicine formation reduced PXB
Area of Science:
- Nanomedicine
- Pharmacology
- Microbiology
Background:
- Polymyxin B (PXB) is a crucial antibiotic for Gram-negative infections.
- Clinical use of PXB is limited by toxicity and protein binding.
- Nanocarrier delivery may overcome PXB limitations.
Purpose of the Study:
- To investigate PXB self-association with PEGylated phospholipid nanomicelles (SSM).
- To evaluate the in vitro bioactivity of PXB-loaded SSM.
Main Methods:
- PXB and SSM (15 nm) were prepared.
- Interactions were analyzed using dynamic light scattering and fluorescence spectroscopy.
- In vitro anti-infective effects were tested against Pseudomonas aeruginosa.
Main Results:
- Approximately four PXB molecules associated with each SSM.
- PXB-SSM showed significantly reduced killing of P. aeruginosa compared to PXB alone.
- Empty SSM did not affect bacterial growth.
Conclusions:
- PXB self-association with SSM mitigated in vitro antibacterial activity.
- PEGylation may hinder PXB's electrostatic interactions with bacterial cell walls.
- Further in vivo studies are needed to assess nanomedicine efficacy.
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