Controlling Membrane Phase Separation of Polymersomes for Programmed Drug Release

Shuai Chen; Erik Jan Cornel; Jian-Zhong Du

doi:10.1007/s10118-022-2683-7

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Controlling Membrane Phase Separation of Polymersomes for Programmed Drug Release

RESEARCH ARTICLE | Updated：2022-08-19

- Controlling Membrane Phase Separation of Polymersomes for Programmed Drug Release
- Controlling Membrane Phase Separation of Polymersomes for Programmed Drug Release
- 高分子科学（英文版） 2022年40卷第9期页码：1006-1015
- Affiliations：
  
  a.Department of Orthopedics, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai 200072, China
  b.Department of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai 201804, China
- Author bio：
  
  jzdu@tongji.edu.cn
- Funds：
  
  J. D. is financially supported by the National Natural Science Fund for Distinguished Young Scholars (No. 21925505) and Shanghai International Scientific Collaboration Fund (No. 21520710100). E. J. C. is supported by the National Natural Science Foundation of China (No. 22101207), the China Postdoctoral Science Foundation (No. 2020M671197) and International Postdoctoral Exchange Fellowship Program.
- DOI：10.1007/s10118-022-2683-7
  中图分类号：
- 收稿：2021-10-21，
  
  修回：2021-12-10，
  
  录用：2021-12-14，
  
  网络首发：2022-02-23，
  
  纸质出版：2022-09-01
- Accepted：
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Chen, S.; Cornel, E. J.; Du, J. Z. Controlling membrane phase separation of polymersomes for programmed drug release. Chinese J. Polym. Sci. 2022, 40, 1006–1015

Shuai Chen, Erik Jan Cornel, Jian-Zhong Du. Controlling Membrane Phase Separation of Polymersomes for Programmed Drug Release[J]. Chinese Journal of Polymer Science, 2022, 40(9): 1006-1015.
Chen, S.; Cornel, E. J.; Du, J. Z. Controlling membrane phase separation of polymersomes for programmed drug release. Chinese J. Polym. Sci. 2022, 40, 1006–1015 DOI： 10.1007/s10118-022-2683-7.

Shuai Chen, Erik Jan Cornel, Jian-Zhong Du. Controlling Membrane Phase Separation of Polymersomes for Programmed Drug Release[J]. Chinese Journal of Polymer Science, 2022, 40(9): 1006-1015. DOI： 10.1007/s10118-022-2683-7.

摘要

We proposed a new strategy to control the drug release rate of polymersomes by controlling membrane phase separation. This was achieved by employing membrane-forming blocks with different molecular architectures and cross-linking degrees. This work shed light on the design of programmed drug release vehicles.

Abstract

Programmed release of small molecular drugs from polymersomes is of great importance in drug delivery. A significant challenge is to adjust the membrane permeability in a well-controlled manner. Herein

we propose a strategy for controlling membrane phase separation by photo-cross-linking of the membrane-forming blocks with different molecular architectures. We synthesized three amphiphilic block copolymers with different membrane-forming blocks

which are poly(ethylene oxide)

-poly((

-caprolactone)

stat

-((

-(cinnamoyloxymethyl)-1

3-triazol)caprolactone)

) (PEO

-P(CL

stat

-CTCL

))

PEO

-P(CL

108

stat

-CTCL

)

and PEO

-PCTCL

-PCL

. These polymers were self-assembled into polymersomes using either a solvent-switch or powder rehydration method

and the obtained polymersomes were characterized by dynamic light scattering and transmission electron microscopy. Then the phase separation patterns within the polymersome membranes were investigated by mesoscopic dynamics (MesoDyn) simulations. To further confirm the change of the membrane permeability that resulted from the phase separation within the membrane

doxorubicin

as a small molecular drug

was loaded and released from the polymersomes. Due to the incompatibility between membrane-forming moieties (PCTCL and PCL)

phase separation occurs and the release rate can be tuned by controlling the membrane phase pattern or by photo-cross-linking. Moreover

besides the compacting effect by formation of chemical bonds in the membrane

the cross-linking process can act as a driving force to facilitate the rearrangement and re-orientation of the phase pattern

which also influences the drug release behavior by modulating the cross-membrane distribution of the amorphous PCTCL moieties. In this way

the strategy of focusing on the membrane phase separation for the preparation of the polymersomes with finely tunable drug release rate can be envisioned and designed accordingly

which is of great significance in the field of delivery vehicles for programmed drug release.

关键词

Keywords

references

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