Literature DB >> 23486314

Evaluation of polymeric gene delivery nanoparticles by nanoparticle tracking analysis and high-throughput flow cytometry.

Ron B Shmueli1, Nupura S Bhise, Jordan J Green.   

Abstract

Non-viral gene delivery using polymeric nanoparticles has emerged as an attractive approach for gene therapy to treat genetic diseases(1) and as a technology for regenerative medicine(2). Unlike viruses, which have significant safety issues, polymeric nanoparticles can be designed to be non-toxic, non-immunogenic, non-mutagenic, easier to synthesize, chemically versatile, capable of carrying larger nucleic acid cargo and biodegradable and/or environmentally responsive. Cationic polymers self-assemble with negatively charged DNA via electrostatic interaction to form complexes on the order of 100 nm that are commonly termed polymeric nanoparticles. Examples of biomaterials used to form nanoscale polycationic gene delivery nanoparticles include polylysine, polyphosphoesters, poly(amidoamines)s and polyethylenimine (PEI), which is a non-degradable off-the-shelf cationic polymer commonly used for nucleic acid delivery(1,3) . Poly(beta-amino ester)s (PBAEs) are a newer class of cationic polymers(4) that are hydrolytically degradable(5,6) and have been shown to be effective at gene delivery to hard-to-transfect cell types such as human retinal endothelial cells (HRECs)(7), mouse mammary epithelial cells(8), human brain cancer cells(9) and macrovascular (human umbilical vein, HUVECs) endothelial cells(10). A new protocol to characterize polymeric nanoparticles utilizing nanoparticle tracking analysis (NTA) is described. In this approach, both the particle size distribution and the distribution of the number of plasmids per particle are obtained(11). In addition, a high-throughput 96-well plate transfection assay for rapid screening of the transfection efficacy of polymeric nanoparticles is presented. In this protocol, poly(beta-amino ester)s (PBAEs) are used as model polymers and human retinal endothelial cells (HRECs) are used as model human cells. This protocol can be easily adapted to evaluate any polymeric nanoparticle and any cell type of interest in a multi-well plate format.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23486314      PMCID: PMC3622088          DOI: 10.3791/50176

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  16 in total

1.  Imaging in solution of (Lys)(16)-containing bifunctional synthetic peptide/DNA nanoparticles for gene delivery.

Authors:  Louise Collins; Michael Kaszuba; John W Fabre
Journal:  Biochim Biophys Acta       Date:  2004-04-07

2.  Evaluating the intracellular stability and unpacking of DNA nanocomplexes by quantum dots-FRET.

Authors:  Yi-Ping Ho; Hunter H Chen; Kam W Leong; Tza-Huei Wang
Journal:  J Control Release       Date:  2006-09-22       Impact factor: 9.776

3.  Virus-sized self-assembling lamellar complexes between plasmid DNA and cationic micelles promote gene transfer.

Authors:  B Pitard; O Aguerre; M Airiau; A M Lachagès; T Boukhnikachvili; G Byk; C Dubertret; C Herviou; D Scherman; J F Mayaux; J Crouzet
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

4.  The relationship between terminal functionalization and molecular weight of a gene delivery polymer and transfection efficacy in mammary epithelial 2-D cultures and 3-D organotypic cultures.

Authors:  Nupura S Bhise; Ryan S Gray; Joel C Sunshine; Soe Htet; Andrew J Ewald; Jordan J Green
Journal:  Biomaterials       Date:  2010-07-31       Impact factor: 12.479

Review 5.  Polymers for gene delivery across length scales.

Authors:  David Putnam
Journal:  Nat Mater       Date:  2006-06       Impact factor: 43.841

6.  Biodegradable polymeric vectors for gene delivery to human endothelial cells.

Authors:  Jordan J Green; Julie Shi; Eugene Chiu; Elizaveta S Leshchiner; Robert Langer; Daniel G Anderson
Journal:  Bioconjug Chem       Date:  2006 Sep-Oct       Impact factor: 4.774

7.  2011 Rita Schaffer lecture: nanoparticles for intracellular nucleic acid delivery.

Authors:  Jordan J Green
Journal:  Ann Biomed Eng       Date:  2012-03-27       Impact factor: 3.934

8.  Non-viral gene delivery nanoparticles based on poly(β-amino esters) for treatment of glioblastoma.

Authors:  Stephany Y Tzeng; Hugo Guerrero-Cázares; Elliott E Martinez; Joel C Sunshine; Alfredo Quiñones-Hinojosa; Jordan J Green
Journal:  Biomaterials       Date:  2011-05-04       Impact factor: 12.479

9.  Plasmid DNA size does not affect the physicochemical properties of lipoplexes but modulates gene transfer efficiency.

Authors:  P Kreiss; B Cameron; R Rangara; P Mailhe; O Aguerre-Charriol; M Airiau; D Scherman; J Crouzet; B Pitard
Journal:  Nucleic Acids Res       Date:  1999-10-01       Impact factor: 16.971

10.  Small-Molecule End-Groups of Linear Polymer Determine Cell-type Gene-Delivery Efficacy.

Authors:  Joel Sunshine; Jordan J Green; Kerry P Mahon; Fan Yang; Ahmed A Eltoukhy; David N Nguyen; Robert Langer; Daniel G Anderson
Journal:  Adv Mater       Date:  2009-08-15       Impact factor: 30.849

View more
  1 in total

1.  Differential polymer structure tunes mechanism of cellular uptake and transfection routes of poly(β-amino ester) polyplexes in human breast cancer cells.

Authors:  Jayoung Kim; Joel C Sunshine; Jordan J Green
Journal:  Bioconjug Chem       Date:  2013-12-20       Impact factor: 4.774

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.