Increasing the density of nanomedicines improves their ultrasound-mediated delivery to tumours
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F15%3A00444229" target="_blank" >RIV/61389013:_____/15:00444229 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.jconrel.2015.05.265" target="_blank" >http://dx.doi.org/10.1016/j.jconrel.2015.05.265</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jconrel.2015.05.265" target="_blank" >10.1016/j.jconrel.2015.05.265</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Increasing the density of nanomedicines improves their ultrasound-mediated delivery to tumours
Popis výsledku v původním jazyce
Nanomedicines have provided fresh impetus in the fight against cancer due to their selectivity and power. However, these agents are limited when delivered intravenously due to their rapid clearance from the bloodstream and poor passage from the bloodstream into target tumours. Here we describe a novel stealthing strategy which addresses both these limitations and thereby demonstrate that both the passive and mechanically-mediated tumour accumulation of the model nanomedicine adenovirus (Ad) can be substantially enhanced. In our strategy gold nanoparticles were thoroughly modified with 2 kDa polyethyleneglycol (PEG) and then linked to Ad via a single reduction-cleavable 5 kDa PEG. The resulting Ad?gold?PEG construct was compared to non-modified Ad or conventionally stealthed Ad?poly[N-(2-hydroxypropyl)methacrylamide] (Ad?PHPMA). Notably, although Ad?gold?PEG was of similar size and surface charge to Ad?PHPMA the increase in density, resulting from the inclusion of the gold nanoparticles
Název v anglickém jazyce
Increasing the density of nanomedicines improves their ultrasound-mediated delivery to tumours
Popis výsledku anglicky
Nanomedicines have provided fresh impetus in the fight against cancer due to their selectivity and power. However, these agents are limited when delivered intravenously due to their rapid clearance from the bloodstream and poor passage from the bloodstream into target tumours. Here we describe a novel stealthing strategy which addresses both these limitations and thereby demonstrate that both the passive and mechanically-mediated tumour accumulation of the model nanomedicine adenovirus (Ad) can be substantially enhanced. In our strategy gold nanoparticles were thoroughly modified with 2 kDa polyethyleneglycol (PEG) and then linked to Ad via a single reduction-cleavable 5 kDa PEG. The resulting Ad?gold?PEG construct was compared to non-modified Ad or conventionally stealthed Ad?poly[N-(2-hydroxypropyl)methacrylamide] (Ad?PHPMA). Notably, although Ad?gold?PEG was of similar size and surface charge to Ad?PHPMA the increase in density, resulting from the inclusion of the gold nanoparticles
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CE - Biochemie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/EE2.3.30.0029" target="_blank" >EE2.3.30.0029: BIOPOL: BIOpolymerní POstdoktorandská Laboratoř a vzdělávácí centrum</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Controlled Release
ISSN
0168-3659
e-ISSN
—
Svazek periodika
210
Číslo periodika v rámci svazku
28 July
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
9
Strana od-do
10-18
Kód UT WoS článku
000356238700002
EID výsledku v databázi Scopus
2-s2.0-84929611293