Inclusion-Interaction Assembly Strategy for Constructing pH/Redox Responsive Micelles for Controlled Release of 6-Mercaptopurine

Abstract

An inclusion-interaction assembly strategy was used to construct novel pH/redox responsive core-shell micelles with hydrophobic drug as the core and hydrophilic polymer as the shell. At first, a dimer of hydrophobic drug 6-mercaptopurine and a hydrophilic β-CD grafted carboxymethyl chitosan were synthesized. Then, a novel amphiphilic inclusion complex was prepared with the dimer being partially embedded into the cavity of β-CD moiety. It self-assembled into pH/redox responsive core-shell micelles in distilled water. TEM confirmed that the micelles possessed a spherical core-shell configuration with a mean size of about 160 nm. DLS showed that the micelles were stable in aqueous solution. Their particle diameters altered with pH values as well as glutathione (GSH) concentrations and respectively attained a maximum value at pH 6.0 and 20 mM GSH. Release profiles of 6-mercaptopurine showed a low release rate (about 27 wt% after 48 h) in pH 7.4 medium with 10 μM GSH, and a marked increase (over 88 wt% after 48 h) in pH 5.0 medium with 20 mM GSH. In vitro cytotoxicity test showed that the micelles had a dose-dependent toxicity for HeLa cells, indicating a great potential for controlled release of 6-mercaptopurine in tumor cells.

Share and Cite:

Tan, M. , Zheng, H. , Zhang, X. , Yu, Z. , Ye, Z. , Shi, L. and Ding, K. (2015) Inclusion-Interaction Assembly Strategy for Constructing pH/Redox Responsive Micelles for Controlled Release of 6-Mercaptopurine. Materials Sciences and Applications, 6, 605-616. doi: 10.4236/msa.2015.67063.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] Zhang, J., et al. (2005) Temperature Sensitive Poly[N-isopropylacrylamide-co-(acryloylβ-cyclodextrin)] for Improved Drug Release. Macromolecular Bioscience, 5, 192-196.
http://dx.doi.org/10.1002/mabi.200400167
[2] Thorsteinn, L. and Dominique, D. (2007) Cyclodextrin and Their Pharmaceutical Applications. International Journal of Pharmaceutics, 329, 1-11.
http://dx.doi.org/10.1016/j.ijpharm.2006.10.044
[3] He, H., Chen, S., Zhou, J., Dou, Y., Song, L., Che, L., Zhou, X., Chen, X., Jia, Y., Zhang, J., Li, S. and Li, X. (2013) Cyclodextrin-Derived pH-Responsive Nanoparticles for Delivery of Paclitaxel. Biomaterials, 34, 5344-5358.
http://dx.doi.org/10.1016/j.biomaterials.2013.03.068
[4] Yuan, Z., Ye, Y., Gao, F., Yuan, H., Lan, M., Lou, K. and Wang, W. (2013) Chitosan-Graft-β-Cyclodextrin Nanoparticles as a Carrier for Controlled Drug Release. International Journal of Pharmaceutics, 446, 191-198.
http://dx.doi.org/10.1016/j.ijpharm.2013.02.024
[5] Zhang, J. and Ma, P. (2013) Cyclodextrin-Based Supramolecular Systems for Drug Delivery: Recent Progress and Future Perspective. Advanced Drug Delivery Reviews, 65, 1215-1233.
http://dx.doi.org/10.1016/j.addr.2013.05.001
[6] Wang, J. and Jiang, M. (2006) Polymeric Self-Assembly into Micelles and Hollow Spheres with Multiscale Cavities Driven by Inclusion Complexation. Journal of American Chemical Society, 128, 3703-3708.
http://dx.doi.org/10.1021/ja056775v
[7] Zheng, H., Rao, Y., Yin, Y., Xiong, X., Xu, P. and Lu, B. (2011) Preparation, Characterization, and in Vitro Drug Release Behavior of 6-Mercaptopurine-carboxymethyl Chitosan. Carbohydrate Polymer, 83, 1952-1958.
http://dx.doi.org/10.1016/j.carbpol.2010.10.069
[8] Gong, X., Yin, Y., Huang, Z., Lu, B., Xu, P., Zheng, H., Xiong, F., Xu, H., Xiong, X. and Gu, X. (2012) Preparation, Characterization and in Vitro Release Study of a Glutathione-Dependent Polymeric Prodrug Cis-3-(9H-purin-6-ylthio)- acrylic acid-graft-carboxymethyl chitosan. International Journal of Pharmaceutics, 436, 240-247.
http://dx.doi.org/10.1016/j.ijpharm.2012.06.043
[9] Chang, D., Lei, J., Cui, H., Lu, N., Sun, Y., Zhang, X., Gao, C., Zheng, H. and Yin, Y. (2012) Disulfide Cross-Linked Nanospheres from Sodium Alginate Derivative for Inflammatory Bowel Disease: Preparation, Characterization, and in Vitro Drug Release Behavior. Carbohydrate Polymer, 88, 663-669.
http://dx.doi.org/10.1016/j.carbpol.2012.01.020
[10] Gao, C., Liu, T., Dang, Y., Yu, Z., Wang, W., Guo, J., Zhang, X., He, G., Zheng, H., Yin, Y. and Kong, X. (2014) pH/Redox Responsive Core Cross-Linked Nanoparticles from Thiolated Carboxymethyl Chitosan for in Vitro Release Study of Methotrexate. Carbohydrate Polymer, 111, 964-970.
http://dx.doi.org/10.1016/j.carbpol.2014.05.012
[11] Wang, W., Yang, H., Kong, X., Ye, Z., Yin, Y., Zhang, X., He, G., Xu, P. and Zheng, H. (2014) Hydrogen-Bonding Strategy for Constructing pH-Sensitive Core-Shell Micelles with Hydrophilic Polymer as the Shell and Hydrophobic Drug as the Core. RSC Advances, 4, 28499-28503.
http://dx.doi.org/10.1039/c4ra03716b
[12] Schafer, F.Q. and Buettner, G.R. (2001) Redox Environment of the Cell as Viewed through the Redox State of the Glutathione Disulfide/Glutathione Couple. Free Radical Biology Medicine, 30, 1191-1212.
http://dx.doi.org/10.1039/c4ra03716b
[13] Zacchigna, M., Cateni, F., Di-Luca, G. and Drioli, S. (2007) A Simple Method for the Preparation of PEG-6-mercap- topurine for Oral Administration. Bioorganic & Medicinal Chemistry, 17, 6607-6609.
http://dx.doi.org/10.1016/j.bmcl.2007.09.064
[14] Chen, Y., Peng, C. and Lu, Y. (2015) Responsiveness and Release Characteristic of Semi-IPN Hydrogels Consisting of Nano-Sized Clay Crosslinked Poly(Dimethylaminoethyl Methacrylate) and Linear Carboxymethyl Chitosan. Journal of Nanoscience and Nanotechnology, 15, 164-171.
http://dx.doi.org/10.1166/jnn.2015.8768
[15] Gerweck, L.E. and Seetharaman, K. (1996) Cellular pH Gradient in Tumor versus Normal Tissue: Potential Exploitation for Treatment of Cancer. Cancer Research, 56, 1194-1198.
[16] Doerr, I.L., Wempen, I., Clarke, D.A. and Fox, J.J. (1961) Thiation of Nucleosides. III. Oxidation of 6-Mercaptopu- rines. Journal of Organic Chemistry, 26, 3401-3409.
http://dx.doi.org/10.1021/jo01067a093
[17] Rajendiran, N., Mohandoss, T. and Sankaranarayanan, R.K. (2014) Nanostructure Formed by Cyclodextrin Covered Procainamide through Supramolecular Self-Assembly—Spectral and Molecular Modeling Study. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 136, 875-883.
http://dx.doi.org/10.1016/j.saa.2014.09.108
[18] Arti, M., Manisha, S. and Deepak, S. (2011) Investigation of the Binding of Roxatidine Acetate Hydrochloride with Cyclomaltoheptaose (β-Cyclodextrin) Using IR and NMR Spectroscopy. Carbohydrate Research, 346, 1809-1813.
http://dx.doi.org/10.1016/j.carres.2011.07.003
[19] Warayuth, S., Onanong, N., Pattarapond, G., Somsak, S., Issara, S., Apinan, S., Satit, P. and Uracha, R. (2012) Water-Soluble β-Cyclodextrin Grafted with Chitosan and Its Inclusion Complex as a Mucoadhesive Eugenol Carrier. Carbohydrate Polymer, 89, 623-631.
http://dx.doi.org/10.1016/j.carbpol.2012.03.060
[20] Yuan, P., Chengde, L., Zhongxing, Z., Kerh, L., Jianhai, C. and Jun, L. (2011) Chitosan-Graft-(PEI-β-Cyclodextrin) Copolymers and Their Supramolecular PEGylation for DNA and siRNA Delivery. Biomaterials, 32, 8328-8341.
http://dx.doi.org/10.1016/j.biomaterials.2011.07.038

Copyright © 2023 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.