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Polymer-mediated delivery of siRNAs to hepatocellular carcinoma : variables affecting specificity and effectiveness
ID
Farra, Rossella
(
Author
),
ID
Musiani, Francesco
(
Author
),
ID
Perrone, Francesca
(
Author
),
ID
Čemažar, Maja
(
Author
),
ID
Kamenšek, Urška
(
Author
),
ID
Tonon, Federica
(
Author
),
ID
Abrami, Michela
(
Author
),
ID
Ručigaj, Aleš
(
Author
),
ID
Grassi, Mario
(
Author
),
ID
Pozzato, Gabriele
(
Author
),
ID
Bonazza, Deborah
(
Author
),
ID
Zanconati, Fabrizio
(
Author
),
ID
Forte, Giancarlo
(
Author
),
ID
El Boustani, Maguie
(
Author
),
ID
Scarabel, Lucia
(
Author
),
ID
Garziera, Marica
(
Author
),
ID
Russo Spena, Concetta
(
Author
),
ID
De Stefano, Lucia
(
Author
),
ID
Salis, Barbara
(
Author
),
ID
Toffoli, Giuseppe
(
Author
),
ID
Rizzolio, Flavio
(
Author
),
ID
Grassi, Gabriele
(
Author
),
ID
Dapas, Barbara
(
Author
)
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MD5: 042DABD70206C24FE6A10208C6FFD946
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http://www.mdpi.com/1420-3049/23/4/777
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Abstract
Despite the advances in anticancer therapies, their effectiveness for many human tumors is still far from being optimal. Significant improvements in treatment efficacy can come from the enhancement of drug specificity. This goal may be achieved by combining the use of therapeutic molecules with tumor specific effects and delivery carriers with tumor targeting ability. In this regard, nucleic acid-based drug (NABD) and particularly small interfering RNAs (siRNAs), are attractive molecules due to the possibility to be engineered to target specific tumor genes. On the other hand, polymeric-based delivery systems are emerging as versatile carriers to generate tumor-targeted delivery systems. Here we will focus on the most recent findings in the selection of siRNA/polymeric targeted delivery systems for hepatocellular carcinoma (HCC), a human tumor for which currently available therapeutic approaches are poorly effective. In addition, we will discuss the most attracting and, in our opinion, promising siRNA-polymer combinations for HCC in relation to the biological features of HCC tissue. Attention will be also put on the mathematical description of the mechanisms ruling siRNA-carrier delivery, this being an important aspect to improve effectiveness reducing the experimental work.
Language:
English
Keywords:
optimized drug delivery
,
anticancer drugs
,
HCC
,
siRNA
Work type:
Article
Typology:
1.02 - Review Article
Organization:
FKKT - Faculty of Chemistry and Chemical Technology
Publication status:
Published
Publication version:
Version of Record
Year:
2018
Number of pages:
24 str.
Numbering:
Vol. 23, iss. 4, art. 777
PID:
20.500.12556/RUL-131823
UDC:
602.6/.7
ISSN on article:
1420-3049
DOI:
10.3390/molecules23040777
COBISS.SI-ID:
2895739
Publication date in RUL:
04.10.2021
Views:
948
Downloads:
229
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Record is a part of a journal
Title:
Molecules
Shortened title:
Molecules
Publisher:
MDPI
ISSN:
1420-3049
COBISS.SI-ID:
18462981
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
01.04.2018
Secondary language
Language:
Slovenian
Keywords:
izboljšana dostava učinkovin
,
onkološka zdravila
,
rak jeter
,
hepatocelularni rak
Projects
Funder:
Other - Other funder or multiple funders
Funding programme:
Beneficentia Stiftung
Funder:
Other - Other funder or multiple funders
Funding programme:
Italian Minister of Instruction, University and Research
Project number:
20109PLMH2
Funder:
Other - Other funder or multiple funders
Funding programme:
MIUR, FFABR
Funder:
Other - Other funder or multiple funders
Funding programme:
University of Trieste, FRA
Funder:
Other - Other funder or multiple funders
Funding programme:
POR FESR
Acronym:
BIOFLUO
Funder:
Other - Other funder or multiple funders
Funding programme:
POR FESR
Acronym:
ATeNA
Funder:
EC - European Commission
Funding programme:
European Social Fund
Funder:
EC - European Commission
Funding programme:
European Regional Development Fund
Project number:
CZ.02.1.01/0.0/0.0/15_003/0000492
Acronym:
MAGNET
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