4.6 Article

Delaying Anticancer Drug Delivery by Self-Assembly and Branching Effects of Minimalist Dendron-Drug Conjugates

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 25, Issue 41, Pages 9586-9591

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201801092

Keywords

anticancer agents; dendrimers; drug delivery; nanomedicine; paclitaxel

Funding

  1. French National Research Agency [ANR Lasernanobio 10Blan91902]
  2. DGOS (SIRIC label) [INCa-DGOS-Inserm 6038]
  3. A*MIDEX [ANR-11-IDEX-0001-02]
  4. LASERNANOCANCER project of the ITMO Plan Cancer 2014-2019 INSERM program [PC201420]
  5. GRAVITY project of the ITMO Plan Cancer 2014-2019 INSERM program [PC201613]

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Self-assembly of a covalently-bound lipophilic drug to a dendronic scaffold for making organic nanoparticles is reported as a proof of concept in nanovectorization. A minimalist structural approach with a small PEG-dendron conjugated to paclitaxel (PTX), incorporating safe succinic and gallic acids, is efficient to provide the expected anticancer bioactivity, but also significantly retards and targets intracellular delivery of PTX in 2D and 3D lung cancer cell cultures. A branching effect of dendrons is crucial, when compared to linear PTX conjugates. Transmission electron microscopy (TEM) and dynamic light-scattering (DLS) studies indicate the formation of stable, low-disperse nanoparticles at 10(-5)m in H(2)0, which could also be responsible for the biological effects. An ultrasensitive LC-MS/MS method was used for the determination of intracellular PTX concentration over time, along with the survival rates of cancer cells. Similarly, cell survival assays were successfully correlated to a 3D cell culture with spheroids for mimicking tumors, when treated with PTX conjugates. Our work opens the way to a full evaluation program required for new chemical entities.

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