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Issue 20, 2013
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Hyaluronan degrading silica nanoparticles for skin cancer therapy

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Abstract

We report the first nanoformulation of Hyaluronidase (Hyal) and its enhanced adjuvant effect over the free enzyme. Hyaluronic acid (HA) degrading enzyme Hyal was immobilized on 250 nm silica nanoparticles (SiNP) maintaining specific activity of the enzyme via the layer-by-layer self-assembly technique. This process was characterized by dynamic light scattering (DLS), zeta potential, infrared and UV-Vis spectroscopy, transmission electron microscopy (TEM) and enzymatic activity measurements. The nanoparticles were tested in vivo as adjuvants of carboplatin (CP), peritumorally injected in A375 human melanoma bearing mice and compared with the non-immobilized enzyme, on the basis of equal enzymatic activity. Alcian Blue staining of A375 tumors indicated large overexpression of hyaluronan. At the end of the experiment, tumor volume reduction with SiNP-immobilized Hyal was significantly enhanced compared to non-immobilized Hyal. Field emission scanning electron microscopy (FE-SEM) images together with energy dispersive X-ray spectroscopy (EDS) spectra confirmed the presence of SiNP on the tumor. We mean a proof of concept: this extracellular matrix (ECM) degrading enzyme, immobilized on SiNP, is a more effective local adjuvant of cancer drugs than the non-immobilized enzyme. This could prove useful in future therapies using other or a combination of ECM degrading enzymes.

Graphical abstract: Hyaluronan degrading silica nanoparticles for skin cancer therapy

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Publication details

The article was received on 29 May 2013, accepted on 30 Jul 2013 and first published on 01 Aug 2013


Article type: Paper
DOI: 10.1039/C3NR02787B
Citation: Nanoscale, 2013,5, 9690-9698
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    Hyaluronan degrading silica nanoparticles for skin cancer therapy

    P. Scodeller, P. N. Catalano, N. Salguero, H. Duran, A. Wolosiuk and G. J. A. A. Soler-Illia, Nanoscale, 2013, 5, 9690
    DOI: 10.1039/C3NR02787B

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