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Tumour homing peptide-functionalized porous silicon nanovectors for cancer therapy
Tekijät: Kinnari PJ, Hyvonen MLK, Makila EM, Kaasalainen MH, Rivinoja A, Salonen JJ, Hirvonen JT, Laakkonen PM, Santos HA
Kustantaja: ELSEVIER SCI LTD
Julkaisuvuosi: 2013
Journal: Biomaterials
Tietokannassa oleva lehden nimi: BIOMATERIALS
Lehden akronyymi: BIOMATERIALS
Numero sarjassa: 36
Vuosikerta: 34
Numero: 36
Aloitussivu: 9134
Lopetussivu: 9141
Sivujen määrä: 8
ISSN: 0142-9612
DOI: https://doi.org/10.1016/j.biomaterials.2013.08.034
Verkko-osoite: http://www.scopus.com/inward/record.url?eid=2-s2.0-84883806964∂nerID=40&md5=aa6ff9084a390044ea44d6f9e1b3c9c3
Tiivistelmä
Tumour targeting nanoparticles (NPs) have demonstrated great potential for enhancing anticancer drug delivery to tumour sites and for reducing the side effects of chemotherapy. However, many nano-particulate delivery systems still lack efficient tumour accumulation. In this work, we present a porous silicon (PSi) nanovector functionalized with a tumour-homing peptide, which targets the mammary-derived growth inhibitor (MDGI) expressing cancer cells both in vitro and in vivo, thereby enhancing the accumulation of the NPs in the tumours. We demonstrated that the tumour homing peptide (herein designated as CooP) functionalized thermally hydrocarbonized PSi (THCPSi) NPs homed specifically to the subcutaneous MDGI-expressing xenograft tumours. The THCPSi-CooP NPs were stable in human plasma and their uptake by MDGI-expressing cancer cells measured by confocal microscopy and flow cytometry was significantly increased compared to the non-functionalized THCPSi NPs. After intravenous injections into nude mice bearing MDGI-expressing tumours, effective targeting was detected and THCPSi-CooP NPs showed similar to 9-fold higher accumulation in the tumour site compared to the control THCPSi NPs. Accumulation of both NPs in the vital organs was negligible. (C) 2013 Elsevier Ltd. All rights reserved.
Tumour targeting nanoparticles (NPs) have demonstrated great potential for enhancing anticancer drug delivery to tumour sites and for reducing the side effects of chemotherapy. However, many nano-particulate delivery systems still lack efficient tumour accumulation. In this work, we present a porous silicon (PSi) nanovector functionalized with a tumour-homing peptide, which targets the mammary-derived growth inhibitor (MDGI) expressing cancer cells both in vitro and in vivo, thereby enhancing the accumulation of the NPs in the tumours. We demonstrated that the tumour homing peptide (herein designated as CooP) functionalized thermally hydrocarbonized PSi (THCPSi) NPs homed specifically to the subcutaneous MDGI-expressing xenograft tumours. The THCPSi-CooP NPs were stable in human plasma and their uptake by MDGI-expressing cancer cells measured by confocal microscopy and flow cytometry was significantly increased compared to the non-functionalized THCPSi NPs. After intravenous injections into nude mice bearing MDGI-expressing tumours, effective targeting was detected and THCPSi-CooP NPs showed similar to 9-fold higher accumulation in the tumour site compared to the control THCPSi NPs. Accumulation of both NPs in the vital organs was negligible. (C) 2013 Elsevier Ltd. All rights reserved.
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