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Fluorescence Characterization of Gold Modified Liposomes with Antisense N-myc DNA Bound to the Magnetisable Particles with Encapsulated Anticancer Drugs (Doxorubicin, Ellipticine and Etoposide)
S. Skalickova, L. Nejdl, J. Kudr, B. Ruttkay-Nedecky, AM. Jimenez, P. Kopel, M. Kremplova, M. Masarik, M. Stiborova, T. Eckschlager, V. Adam, R. Kizek,
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2001
PubMed Central
od 2003
Europe PubMed Central
od 2003
ProQuest Central
od 2001-01-01
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2003-01-01
Health & Medicine (ProQuest)
od 2001-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
26927112
DOI
10.3390/s16030290
Knihovny.cz E-zdroje
- MeSH
- antisense DNA chemie terapeutické užití MeSH
- doxorubicin chemie terapeutické užití MeSH
- elipticiny chemie terapeutické užití MeSH
- etoposid chemie terapeutické užití MeSH
- fluorescence MeSH
- lékové transportní systémy * MeSH
- lidé MeSH
- liposomy chemie terapeutické užití MeSH
- magnetické nanočástice chemie terapeutické užití MeSH
- nádory farmakoterapie MeSH
- protoonkogen n-myc antagonisté a inhibitory genetika MeSH
- zlato chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Liposome-based drug delivery systems hold great potential for cancer therapy. The aim of this study was to design a nanodevice for targeted anchoring of liposomes (with and without cholesterol) with encapsulated anticancer drugs and antisense N-myc gene oligonucleotide attached to its surface. To meet this main aim, liposomes with encapsulated doxorubicin, ellipticine and etoposide were prepared. They were further characterized by measuring their fluorescence intensity, whereas the encapsulation efficiency was estimated to be 16%. The hybridization process of individual oligonucleotides forming the nanoconstruct was investigated spectrophotometrically and electrochemically. The concentrations of ellipticine, doxorubicin and etoposide attached to the nanoconstruct in gold nanoparticle-modified liposomes were found to be 14, 5 and 2 µg·mL(-1), respectively. The study succeeded in demonstrating that liposomes are suitable for the transport of anticancer drugs and the antisense oligonucleotide, which can block the expression of the N-myc gene.
Citace poskytuje Crossref.org
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- $a Skalickova, Sylvie $u Department of Chemistry and Biochemistry, Faculty of Agronomy, Mendel University in Brno, Zemedelska 1, CZ-613 00 Brno, Czech Republic. sylvie.skalickova@gmail.com. Central European Institute of Technology, Brno University of Technology, Technicka 3058/10, CZ-616 00 Brno, Czech Republic. sylvie.skalickova@gmail.com.
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- $a Liposome-based drug delivery systems hold great potential for cancer therapy. The aim of this study was to design a nanodevice for targeted anchoring of liposomes (with and without cholesterol) with encapsulated anticancer drugs and antisense N-myc gene oligonucleotide attached to its surface. To meet this main aim, liposomes with encapsulated doxorubicin, ellipticine and etoposide were prepared. They were further characterized by measuring their fluorescence intensity, whereas the encapsulation efficiency was estimated to be 16%. The hybridization process of individual oligonucleotides forming the nanoconstruct was investigated spectrophotometrically and electrochemically. The concentrations of ellipticine, doxorubicin and etoposide attached to the nanoconstruct in gold nanoparticle-modified liposomes were found to be 14, 5 and 2 µg·mL(-1), respectively. The study succeeded in demonstrating that liposomes are suitable for the transport of anticancer drugs and the antisense oligonucleotide, which can block the expression of the N-myc gene.
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