Journal
CHEMISTRY OF MATERIALS
Volume 24, Issue 16, Pages 3197-3211Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cm301556b
Keywords
platinum drugs; polymeric micelles; cross-linked micelles; acid degradable nanoparticles; cellular uptake
Funding
- ARC (Australian Research Council) [FT0991273, DP1092694]
- Australian government
- Centre for Advanced Macromolecular Design (CAMD)
- UNSW Analytical Centre
- Australian Research Council [FT0991273, DP1092694] Funding Source: Australian Research Council
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Well-defined and nontoxic cross-linked polymeric micelles, containing either permanent or acid degradable cross-linkers, Were employed for efficient intracellular delivery of cisplatin. The self-assembled structures were generated from triblock copolymers of poly(oligo(ethylene glycol) methylether methacrylate)-block-poly(N-hydroxysuccinic methacrylate)-block-poly(1,1-di-tert-butyl 3-(2-(methacryloyloxy)ethyl) butane-1,1,3-tricarboxylate) (POEGMEMA-b-PNHSMA-b-PMAETC) loaded with cisplatinum. The polymeric micelles were subsequently cross-linked via a reaction between pendant activated esters at the nexus core of the triblock copolymer using acid degrdabale ketal diamino cross-linkers. An in vitro study confirmed that both uncross-linked and cross-linked micelles prior to the loading of the platinum drug were nontoxic against OVCAR-3 cells even at high polymer concentration (around 300 mu g mL(-1)). The drug loaded cross-linked platinum polymeric micelles were superior to the uncross-linked platinum polymeric micelles in terms of cytotoxicity against OVCAR-3, due to a higher cellular uptake. Although there was no significant difference in cytotoxicity of cross-linked platinum polymeric micelles using different cross-linkers (permanent and acid cleavable) after 72 h of exposure, the difference was noticeable after 24 h of incubation, highlighting a much higher activity for acid degradable crosslinked micelles with conjugated platinum drugs. Moreover, the clonogenic assay suggested that cross-linked, micelle loaded platinum drugs, in contrast to uncross-linked micelles, can effectively inhibit the OVCAR-3 cell regrowth for an extended period of time (10 days), even at very low micellar concentrations. In summary, acid degradable. linkers ensure high cellular uptake compared to uncross-linked micelles but also lead to a faster drug action in comparison to a permanently cross-linked micelle.
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