journal article·2015-07-01

Rationally Separating the Corona and Membrane Functions of Polymer Vesicles for Enhanced T2 MRI and Drug Delivery

Jingya Qin, Qiuming Liu, Junxue Zhang, Jing Chen, Shuai Chen, Yao Zhao, Jianzhong Du

Publisher page

Abstract

It is an important challenge to in situ grow ultrafine super-paramagnetic iron oxide nanoparticles (SPIONs) in drug carriers such as polymer vesicles (also called polymersomes) while keeping their biodegradability for enhanced T2-weighted magnetic resonance imaging (MRI) and drug delivery. Herein, we present a new strategy by rationally separating the corona and membrane functions of polymer vesicles to solve the above problem. We designed a poly(ethylene oxide)-block-poly(ε-caprolactone)-block-poly(acrylic acid) (PEO43-b-PCL98-b-PAA25) triblock copolymer and self-assembled it into polymer vesicle. The PAA chains in the vesicle coronas are responsible for the in situ nanoprecipitation of ultrafine SPIONs, while the vesicle membrane composed of PCL is biodegradable. The SPIONs-decorated vesicle is water-dispersible, biocompatible, and slightly cytotoxic to normal human cells. Dynamic light scattering, transmission electron microscopy, energy disperse spectroscopy, and vibrating sample magnetometer revealed the formation of ultrafine super-paramagnetic Fe3O4 nanoparticles (1.9 ± 0.3 nm) in the coronas of polymer vesicles. Furthermore, the CCK-8 assay revealed low cytotoxicity of vesicles against normal L02 liver cells without and with Fe3O4 nanoparticles. The in vitro and in vivo MRI experiments confirmed the enhanced T2-weighted MRI sensitivity and excellent metastasis in mice. The loading and release experiments of an anticancer drug, doxorubicin hydrochloride (DOX·HCl), indicated that the Fe3O4-decorated magnetic vesicles have potential applications as a nanocarrier for anticancer drug delivery. Moreover, the polymer vesicle is degradable in the presence of enzyme such as Pseudomonas lipases, and the ultrafine Fe3O4 nanoparticles in the vesicle coronas are confirmed to be degradable under weakly acidic conditions. Overall, this decoration-in-vesicle-coronas strategy provides us with a new insight for preparing water-dispersible ultrafine super-paramagnetic Fe3O4 nanoparticles with promising theranostic applications in biomedicine.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoparticle-Based Drug Delivery · Lanthanide and Transition Metal Complexes · Dendrimers and Hyperbranched Polymers

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science and Engineering, Tongji University, 4800 Caoan Road, Shanghai 201804, China

Beijing National Laboratory for Molecular Sciences; CAS Key Laboratory of Analytical Chemistry for Living Biosystems; Beijing Center for Mass Spectrometry; Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

Shanghai Tenth People’s Hospital, Tongji University School of Medicine, 301 Middle Yanchang Road, Shanghai 200072, China

Funding

Shanghai Municipal Education Commission · Beijing National Laboratory for Molecular Sciences · Shanghai Municipal Government · National Natural Science Foundation of China

References (53)

Show source-provided references
1. Qiao R. R. · J. Mater. Chem. · 2009 · 19 · 627410.1039/b902394a ↗
2. Jolesz F. A. · Annu. Rev. Med. · 2009 · 60 · 41710.1146/annurev.med.60.041707.170303 ↗
3. Na H. B. · Adv. Mater. · 2009 · 21 · 213310.1002/adma.200802366 ↗
4. Bridot J.-L. · J. Am. Chem. Soc. · 2007 · 129 · 507610.1021/ja068356j ↗
5. Carr D. H. · Lancet · 1984 · 323 · 48410.1016/S0140-6736(84)92852-6 ↗
6. Laurent S. · Chem. Rev. · 2008 · 108 · 206410.1021/cr068445e ↗
7. Szpak A. · J. Nanopart. Res. · 2014 · 16 · 110.1007/s11051-014-2678-6 ↗
8. Do M. A. · Colloids Surf., B · 2014 · 122 · 75210.1016/j.colsurfb.2014.08.015 ↗
9. Lu Z.-R. · Bioconjugate Chem. · 2003 · 14 · 71510.1021/bc0340464 ↗
10. Janib S. M. · Adv. Drug Delivery Rev. · 2010 · 62 · 105210.1016/j.addr.2010.08.004 ↗
11. Bianchi A. · Coordin. Chem. Rev. · 2000 · 204 · 30910.1016/S0010-8545(99)00237-4 ↗
12. Bernstein E. J. · Best Pract. Res., Clin. Rheumatol. · 2012 · 26 · 48910.1016/j.berh.2012.07.008 ↗
13. Sun C. · Adv. Drug Delivery Rev. · 2008 · 60 · 125210.1016/j.addr.2008.03.018 ↗
14. Lu A. H. · Angew. Chem., Int. Ed. · 2007 · 46 · 122210.1002/anie.200602866 ↗
15. Neuberger T. · J. Magn. Magn. Mater. · 2005 · 293 · 48310.1016/j.jmmm.2005.01.064 ↗
16. Liu Q. M. · Macromolecules · 2015 · 48 · 73910.1021/ma502255s ↗
17. Jain T. K. · Biomaterials · 2008 · 29 · 401210.1016/j.biomaterials.2008.07.004 ↗
18. Chandra V. · ACS Nano · 2010 · 4 · 397910.1021/nn1008897 ↗
19. Li D. · Chem. Commun. · 2015 · 51 · 190810.1039/C4CC07985J ↗
20. Sanson C. · ACS Nano · 2011 · 5 · 112210.1021/nn102762f ↗
21. Brigger I. · Adv. Drug Delivery Rev. · 2002 · 54 · 63110.1016/S0169-409X(02)00044-3 ↗
22. Maeda H. · J. Controlled Release · 2000 · 65 · 27110.1016/S0168-3659(99)00248-5 ↗
23. Du J. Z. · Chem. Soc. Rev. · 2011 · 40 · 240210.1039/c0cs00216j ↗
24. Du J. Z. · Soft Matter · 2009 · 5 · 354410.1039/b905635a ↗
25. Gao Z. · Ultrasonics · 2008 · 48 · 26010.1016/j.ultras.2007.11.002 ↗
26. Chi X. D. · J. Am. Chem. Soc. · 2015 · 137 · 144010.1021/ja512978n ↗
27. Huang P. · J. Am. Chem. Soc. · 2014 · 136 · 1174810.1021/ja505212y ↗
28. Hu X. L. · J. Am. Chem. Soc. · 2014 · 137 · 362
29. Zhou C. C. · ACS Macro Lett. · 2013 · 2 · 102110.1021/mz400480z ↗
30. Jones C. H. · Mol. Pharmaceutics · 2013 · 10 · 113810.1021/mp300666s ↗
31. Ye F. · Biomaterials · 2014 · 35 · 388510.1016/j.biomaterials.2014.01.041 ↗
32. Wang H. · Int. J. Pharm. · 2012 · 430 · 34210.1016/j.ijpharm.2012.04.009 ↗
33. Oh J. K. · Prog. Polym. Sci. · 2011 · 36 · 16810.1016/j.progpolymsci.2010.08.005 ↗
34. Hong R. Y. · Biochem. Eng. J. · 2008 · 42 · 29010.1016/j.bej.2008.07.009 ↗
35. Rijcken C. J. F. · J. Controlled Release · 2007 · 120 · 13110.1016/j.jconrel.2007.03.023 ↗
36. Ren T. B. · J. Mater. Chem. · 2012 · 22 · 1232910.1039/c2jm31891a ↗
37. Sanson C. · ACS Nano · 2011 · 5 · 112210.1021/nn102762f ↗
38. Hickey R. J. · ACS Nano · 2013 · 8 · 49510.1021/nn405012h ↗
39. Liu Q. M. · Biomacromolecules · 2014 · 15 · 307210.1021/bm500676e ↗
40. Yang X. Q. · Biomaterials · 2010 · 31 · 906510.1016/j.biomaterials.2010.08.039 ↗
41. Huang J. S. · J. Mater. Chem. · 2006 · 16 · 453510.1039/b609088e ↗
42. Zhang M. · Ion Exch. Adsorpt. · 1995 · 11 · 302
43. Gupta A. K. · Biomaterials · 2005 · 26 · 399510.1016/j.biomaterials.2004.10.012 ↗
44. Schutt W. · Hybridoma · 1997 · 16 · 10910.1089/hyb.1997.16.109 ↗
45. Mahmoudi M. · J. Phys. Chem. B · 2008 · 112 · 1447010.1021/jp803016n ↗
46. Yang X. Y. · J. Mater. Chem. · 2009 · 19 · 271010.1039/b821416f ↗
47. Yang X. Q. · ACS Nano · 2010 · 4 · 680510.1021/nn101670k ↗
48. Lattuada M. · J. Am. Chem. Soc. · 2007 · 129 · 1287810.1021/ja0740521 ↗
49. Berret J. F. · J. Am. Chem. Soc. · 2006 · 128 · 175510.1021/ja0562999 ↗
50. Rohrer M. · Invest. Radiol. · 2005 · 40 · 71510.1097/01.rli.0000184756.66360.d3 ↗
51. Du J. Z. · J. Am. Chem. Soc. · 2005 · 127 · 1798210.1021/ja056514l ↗
52. Żenkiewicz M. · Polym. Test. · 2013 · 32 · 20910.1016/j.polymertesting.2012.10.011 ↗
53. Zou K. D. · Polym. Chem. · 2014 · 5 · 40510.1039/C3PY00966A ↗