Self-immolative micellar drug delivery: The linker matters
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Redox-responsive polymer-drug conjugate micelles are excellent nanoscale vehicles for self-immolative intracellular drug delivery. To covalently connect the polymer and drug, disulfide-bearing linkers, such as 3,3’-dithiodipropionic acid (DDPA) and 4,4’-dithiodibutyric acid (DDBA), are used. In this paper, we report the influence of linker length on the therapeutic outcome of redox-sensitive conjugate micelles. Curcumin was selected as the model drug and it was conjugated to a multivalent methoxy poly(ethylene glycol)-polylysine copolymer with DDPA or DDBA as the linker. The obtained two polymer-curcumin conjugates were amphiphilic and could self-assemble into micelles that have a hydrodynamic diameter less than 100 nm. The loading of curcumin in both micelles was above 20% (w/w). Irrespective of the linker type, micelle disassembly was observed due to the collapse of the disulfide bond in a reducing environment. However, the rate of curcumin release was much faster with the DDBA linker than with the DDPA linker as the side product was a 5-membered ring with a low ring strain. The linker length-induced variation of curcumin release kinetics caused a significant difference in the intracellular drug concentration and a higher cytotoxicity was witnessed in three model cell lines (HeLa, PC3, and 4T1) for the micelles with a DDBA linker compared to those containing a DDPA linker. As expected, this phenomenon was also observed in HeLa tumor-bearing nude mice in vivo. The current work highlights the significance of linker length in engineering redox-responsive on-demand delivery systems.
Keywordsdrug delivery micelles redox-responsive curcumin polymer-drug conjugate
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- Yu, Q. S.; Wei, Z. K.; Shi, J. Y.; Guan, S. L.; Du, N.; Shen, T.; Tang, H.; Jia, B.; Wang, F.; Gan, Z. H. Polymerdoxorubicin conjugate micelles based on poly(ethylene glycol) and poly(N-(2-hydroxypropyl) methacrylamide): Effect of negative charge and molecular weight on biodistribution and blood clearance. Biomacromolecules 2015, 16, 2645–2655.CrossRefGoogle Scholar
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