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Evolution from Covalent to Self-Assembled PAMAM-Based Dendrimers as Nanovectors for siRNA Delivery in Cancer by Coupled in Silico-Experimental Studies. Part II: Self-Assembled siRNA Nanocarriers

Laurini, Erik
•
Marson, Domenico
•
Aulic, Suzana
altro
Pricl, Sabrina
2019
  • journal article

Periodico
PHARMACEUTICS
Abstract
In part I of this review, the authors showed how poly(amidoamine) (PAMAM)-based dendrimers can be considered as promising delivering platforms for siRNA therapeutics. This is by virtue of their precise and unique multivalent molecular architecture, characterized by uniform branching units and a plethora of surface groups amenable to effective siRNA binding and delivery to e.g., cancer cells. However, the successful clinical translation of dendrimer-based nanovectors requires considerable amounts of good manufacturing practice (GMP) compounds in order to conform to the guidelines recommended by the relevant authorizing agencies. Large-scale GMP-standard high-generation dendrimer production is technically very challenging. Therefore, in this second part of the review, the authors present the development of PAMAM-based amphiphilic dendrons, that are able to auto-organize themselves into nanosized micelles which ultimately outperform their covalent dendrimer counterparts in in vitro and in vivo gene silencing.
DOI
10.3390/pharmaceutics11070324
WOS
WOS:000478995100027
Archivio
http://hdl.handle.net/11368/2947303
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85071377461
https://www.mdpi.com/1999-4923/11/7/324
Diritti
open access
license:creative commons
license:creative commons
license uri:http://creativecommons.org/licenses/by/4.0/
license uri:http://creativecommons.org/licenses/by/4.0/
FVG url
https://arts.units.it/bitstream/11368/2947303/4/pharmaceutics-11-00324_compressed.pdf
Soggetti
  • PAMAM dendrimer

  • RNAi therapeutic

  • amphiphilic dendron

  • gene silencing

  • nanovector

  • self-assembling

  • siRNA delivery

Web of Science© citazioni
9
Data di acquisizione
Mar 26, 2024
Visualizzazioni
9
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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