Combined Delivery of Temozolomide and Anti-miR221 PNA Using Mesoporous Silica Nanoparticles Induces Apoptosis in Resistant Glioma Cells

被引:112
作者
Bertucci, Alessandro [1 ,2 ,3 ,4 ]
Prasetyanto, Eko Adi [1 ,2 ,3 ]
Septiadi, Dedy [1 ,2 ,3 ]
Manicardi, Alex [4 ]
Brognara, Eleonora [5 ]
Gambari, Roberto [5 ]
Corradini, Roberto [4 ]
De Cola, Luisa [1 ,2 ,3 ]
机构
[1] Univ Strasbourg, Inst Sci & Ingn Supramol, F-67000 Strasbourg, France
[2] Univ Strasbourg, IcFRC, F-67000 Strasbourg, France
[3] CNRS, F-67000 Strasbourg, France
[4] Univ Parma, Dipartimento Chim, I-43124 Parma, Italy
[5] Univ Ferrara, Dipartimento Sci Vita & Biotecnol, I-44121 Ferrara, Italy
基金
欧洲研究理事会;
关键词
PEPTIDE-NUCLEIC-ACIDS; DRUG-DELIVERY; CO-DELIVERY; BREAST-CANCER; IN-VIVO; BIOLOGICAL-ACTIVITY; SIRNA; THERAPY; GLIOBLASTOMA; NANOCARRIERS;
D O I
10.1002/smll.201500540
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mesoporous silica nanoparticles (MSNPs), 100 nm in size, incorporating a Cy5 fluorophore within the silica framework, are synthesized and loaded with the anti-cancer drug temozolomide (TMZ), used in the treatment of gliomas. The surface of the particles is then decorated, using electrostatic interactions, with a polyarginine-peptide nucleic acid (R8-PNA) conjugate targeting the miR221 microRNA. The multi-functional nanosystem thus obtained is rapidly internalized into glioma C6 or T98G cells. The anti-miR activity of the PNA is retained, as confirmed by reverse transcription polymerase chain reaction (RT-PCR) measurements and induction of apoptosis is observed in temozolomide-resistant cell lines. The TMZ-loaded MSNPs show an enhanced pro-apoptotic effect, and the combined effect of TMZ and R8-PNA in the MSNPs shows the most effective induction of apoptosis (70.9% of apoptotic cells) thus far achieved in the temozolomide-resistant T98G cell line.
引用
收藏
页码:5687 / 5695
页数:9
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