Flexible cyclic siloxane core enhances the transfection efficiency of polyethylenimine-based non-viral gene vectors. Issue 42 (25th August 2015)
- Record Type:
- Journal Article
- Title:
- Flexible cyclic siloxane core enhances the transfection efficiency of polyethylenimine-based non-viral gene vectors. Issue 42 (25th August 2015)
- Main Title:
- Flexible cyclic siloxane core enhances the transfection efficiency of polyethylenimine-based non-viral gene vectors
- Authors:
- Uritu, Cristina M.
Calin, Manuela
Maier, Stelian S.
Cojocaru, Corneliu
Nicolescu, Alina
Peptanariu, Dragos
Constantinescu, Cristina Ana
Stan, Daniela
Barboiu, Mihail
Pinteala, Mariana - Abstract:
- Abstract : cD4 H –AGE–PEI conjugates, with a favorable balance between hydrophilic and hydrophobic moieties, are promising carriers for gene delivery. Abstract : Transfection of nucleic acid molecules, large enough to interfere with the genetic mechanisms of active cells, can be performed by means of small carriers, able to collectively collaborate in generating cargocomplexes that could be involved in passive mechanisms of cellular uptake. The present work describes the synthesis, characterization, and evaluation of transfection efficacy of a conjugate molecule, which comprises a cyclic siloxane ring (2, 4, 6, 8-tetramethylcyclotetrasiloxane, cD4 H ) as the core, and, on average, 3.76 molecules of 2 kDa polyethyleneimine (PEI) as cationic branches, with an average molecular mass of 7.3 kDa. As demonstrated by in silico molecular modeling and dynamic simulation, the conjugate molecule (cD4 H –AGE–PEI) tends to adopt an asymmetric structure, specific for amphipathic molecules (confirmed by a log P value of −1.902 ± 0.06), that favors a rapid interaction with nucleic acids. The conjugate and the polyplexes with the pEYFP plasmid were proved to be non-cytotoxic, and capable of ensuring transfection yields better than 30%, on HEK 293T cell culture, superior to the value obtained using the SuperFect® reagent. We presume that the increased transfection efficacy originates in the ability of the conjugate to locally tightly encompass pDNA molecules by electrostatic interactionAbstract : cD4 H –AGE–PEI conjugates, with a favorable balance between hydrophilic and hydrophobic moieties, are promising carriers for gene delivery. Abstract : Transfection of nucleic acid molecules, large enough to interfere with the genetic mechanisms of active cells, can be performed by means of small carriers, able to collectively collaborate in generating cargocomplexes that could be involved in passive mechanisms of cellular uptake. The present work describes the synthesis, characterization, and evaluation of transfection efficacy of a conjugate molecule, which comprises a cyclic siloxane ring (2, 4, 6, 8-tetramethylcyclotetrasiloxane, cD4 H ) as the core, and, on average, 3.76 molecules of 2 kDa polyethyleneimine (PEI) as cationic branches, with an average molecular mass of 7.3 kDa. As demonstrated by in silico molecular modeling and dynamic simulation, the conjugate molecule (cD4 H –AGE–PEI) tends to adopt an asymmetric structure, specific for amphipathic molecules (confirmed by a log P value of −1.902 ± 0.06), that favors a rapid interaction with nucleic acids. The conjugate and the polyplexes with the pEYFP plasmid were proved to be non-cytotoxic, and capable of ensuring transfection yields better than 30%, on HEK 293T cell culture, superior to the value obtained using the SuperFect® reagent. We presume that the increased transfection efficacy originates in the ability of the conjugate to locally tightly encompass pDNA molecules by electrostatic interaction mediated by the short PEI branches, and consequently to expose the siloxane hydrophobic moiety, which decreases the interaction energy with the lipid layers. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 3:Issue 42(2015)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 3:Issue 42(2015)
- Issue Display:
- Volume 3, Issue 42 (2015)
- Year:
- 2015
- Volume:
- 3
- Issue:
- 42
- Issue Sort Value:
- 2015-0003-0042-0000
- Page Start:
- 8250
- Page End:
- 8267
- Publication Date:
- 2015-08-25
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5tb01342a ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1475.xml