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Method Article

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

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DOI:

10.3791/54422

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October 10th, 2016

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In This Article

Summary

The key steps of living anionic polymerization of phenyl glycidyl ether (PheGE) on methoxy-polyethylene glycol (mPEG-b-PPheGE) are described. The resulting block copolymer micelles (BCMs) were loaded with doxorubicin 14% (wt%) and sustained release of drug over 4 days under physiologically relevant conditions was obtained.

Abstract

In this study, an amphiphilic copolymer that includes a core-forming block with phenyl groups was synthesized by living anionic polymerization of phenyl glycidyl ether (PheGE) on methoxy-polyethylene glycol (mPEG-b-PPheGE). Characterization of the copolymer revealed a narrow molecular distribution (PDI < 1.03) and confirmed the degree of polymerization of mPEG122-b-(PheGE)15. The critical micelle concentration of the copolymer was evaluated using an established fluorescence method with the aggregation behavior evaluated by dynamic light scattering and transmission electronic microscopy. The potential of the copolymer for use in drug delivery applications was evaluated in a preliminary manner including in vitro biocompatibility, loading and release of the hydrophobic anti-cancer drug doxorubicin (DOX). A stable micelle formulation of DOX was prepared with drug loading levels up to 14% (wt%), drug loading efficiencies > 60% (w/w) and sustained release of drug over 4 days under physiologically relevant conditions (acidic and neutral pH, presence of albumin). The high drug loading level and sustained release is attributed to stabilizing π-π interactions between DOX and the core-forming block of the micelles.

Introduction

In aqueous media, amphiphilic block copolymers assemble to form nano-sized block copolymer micelles (BCMs) that consist of a hydrophobic core surrounded by a hydrophilic shell or corona. The micelle core can serve as a reservoir for the incorporation of hydrophobic drugs; while, the hydrophilic corona provides an interface between the core and the external medium. Poly(ethylene glycol) (PEG) and its derivatives are one of the most important classes of polymers and one of the most widely used in drug formulation.1-3 BCMs have proven to be a worthy drug delivery platform with several formulations relying on this technology now in late stage clinical developme....

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Protocol

Anionic polymerization process diagram, showing reagent addition, polymerization, and purification steps.
Figure 1. Schematic showing the nine key steps in the preparation of the mPEG-b-PPheGE copolymer. Please click here to view a larger version of this figure.

1. Preparation of the Reagents under Dry Conditions

  1. Preparation of the reagents.

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Results

Micelle formation via π-π stacking; chemical synthesis, diagram, micelles at 25 nm, DLS graph.
Figure 3. Illustration of the anionic polymerization of phenyl glycidyl ether on mPEG macroinitiator to produce mPEG-b-(PheGE)15 for preparation of block copolymer micelles for loading of doxorubicin.

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Discussion

Due to the good control that anionic polymerization provides over molecular weight it is one of the most applied processes in the industry for the preparation of polymers based on oxirane monomers (PEG and PPG). Optimal and stringent conditions must be used for successful polymerization to be achieved. Rigorous purification of all reagents and appropriate apparatus are essential for the living character of the synthesis. Limitations of the current setup are mostly associated with the transfer technique that relies on can.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

CA acknowledges a Discovery grant from the Natural Sciences and Engineering Research Council of Canada. CA acknowledges a Chair in Pharmaceutics and Drug Delivery from GSK. The authors declare no competing financial interest.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
DMEM/HAMF12Gibco, Life Technologies12500Supplemented with 10% FBS. Warm in 37 °C water bath.
Trypsin-EDTA (0.25%)Sigma-AldrichT4049Warm in 37 °C water bath
Fetal bovine serum (FBS)Sigma-AldrichF1051Canada origin
MDA-MB-468 cell lineATCCHTB-132
MTS tetrazolium reagentPROMEGAG111B
Phenazine ethosulfate (PES)Sigma-AldrichP4544>95%
mPEG5K (Mn 5,400 g/mol)Sigma-Aldrich81323PDI=1.02
Dimethylsolfoxide (DMSO)Sigma-AldrichD4540>99.5%
NaphthaleneSigma-Aldrich147141>99%
Phenyl glycidyl etherSigma-AldrichA32608>85%
BenzophenoneSigma-Aldrich427551>99%
PotassiumSigma-Aldrich451096>98%
TetrahydrofuranCaledon Laboratory Chemicals8900 1ACS
HexaneCaledon Laboratory Chemicals5500 1ACS
Calcium hydride (CaH2)ACPC-0460>99.5%
Diethyl EtherCaledon Laboratory Chemicals1/10/4800ACS
Microplate readerBioTek Instruments
Differential scanning calorimetry (DSC)TA Instruments IncDSC Q100
Gel permeation chromatography (GPC)Waters2695 separation moldule / 2414 detector 2 Columns: Agilent Plgel 5 µm Mixed-D
NMR spectroscopyVarian Mercury 400MHz
Chloroform-dSigma-Aldrich15185899.96%
DMSO-dSigma-Aldrich15691499.96%
Vaccum pumpGardner Denver Welch Vacuum Tech, Inc.Ultimate pressure 1x10-4 torr
Drierit with indicator, 8 meshSigma-Aldrich238988Regenerated at 230 °C for 2 hr

References

  1. Dickerson, T. J., Reed, N. N., Janda, K. D. Soluble Polymers as Scaffolds for Recoverable Catalysts and Reagents. Chemical Reviews. 102, 3325-3344 (2002).
  2. van Heerbeek, R., Kamer, P. C. J., van Leeuwen, P. W. N. M., Reek, J. N. H. Dendrimers as Support for Recoverable Catalysts an....

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