izpis_h1_title_alt

Polymer-mediated delivery of siRNAs to hepatocellular carcinoma : variables affecting specificity and effectiveness
ID Farra, Rossella (Avtor), ID Musiani, Francesco (Avtor), ID Perrone, Francesca (Avtor), ID Čemažar, Maja (Avtor), ID Kamenšek, Urška (Avtor), ID Tonon, Federica (Avtor), ID Abrami, Michela (Avtor), ID Ručigaj, Aleš (Avtor), ID Grassi, Mario (Avtor), ID Pozzato, Gabriele (Avtor), ID Bonazza, Deborah (Avtor), ID Zanconati, Fabrizio (Avtor), ID Forte, Giancarlo (Avtor), ID El Boustani, Maguie (Avtor), ID Scarabel, Lucia (Avtor), ID Garziera, Marica (Avtor), ID Russo Spena, Concetta (Avtor), ID De Stefano, Lucia (Avtor), ID Salis, Barbara (Avtor), ID Toffoli, Giuseppe (Avtor), ID Rizzolio, Flavio (Avtor), ID Grassi, Gabriele (Avtor), ID Dapas, Barbara (Avtor)

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Izvleček
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.

Jezik:Angleški jezik
Ključne besede:optimized drug delivery, anticancer drugs, HCC, siRNA
Vrsta gradiva:Članek v reviji
Tipologija:1.02 - Pregledni znanstveni članek
Organizacija:FKKT - Fakulteta za kemijo in kemijsko tehnologijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2018
Št. strani:24 str.
Številčenje:Vol. 23, iss. 4, art. 777
PID:20.500.12556/RUL-131823 Povezava se odpre v novem oknu
UDK:602.6/.7
ISSN pri članku:1420-3049
DOI:10.3390/molecules23040777 Povezava se odpre v novem oknu
COBISS.SI-ID:2895739 Povezava se odpre v novem oknu
Datum objave v RUL:04.10.2021
Število ogledov:751
Število prenosov:191
Metapodatki:XML RDF-CHPDL DC-XML DC-RDF
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Gradivo je del revije

Naslov:Molecules
Skrajšan naslov:Molecules
Založnik:MDPI
ISSN:1420-3049
COBISS.SI-ID:18462981 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:01.04.2018

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:izboljšana dostava učinkovin, onkološka zdravila, rak jeter, hepatocelularni rak

Projekti

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Beneficentia Stiftung

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Italian Minister of Instruction, University and Research
Številka projekta:20109PLMH2

Financer:Drugi - Drug financer ali več financerjev
Program financ.:MIUR, FFABR

Financer:Drugi - Drug financer ali več financerjev
Program financ.:University of Trieste, FRA

Financer:Drugi - Drug financer ali več financerjev
Program financ.:POR FESR
Akronim:BIOFLUO

Financer:Drugi - Drug financer ali več financerjev
Program financ.:POR FESR
Akronim:ATeNA

Financer:EC - European Commission
Program financ.:European Social Fund

Financer:EC - European Commission
Program financ.:European Regional Development Fund
Številka projekta:CZ.02.1.01/0.0/0.0/15_003/0000492
Akronim:MAGNET

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