Nonviral vectors for gene delivery
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTNonviral Vectors for Gene DeliveryMeredith A. Mintzer and Eric E. Simanek*View Author Information Department of Chemistry, Texas A&M University, College Station, Texas 77843* To whom correspondence should be addressed. Tel.: (979) 845-4242. Fax: (979) 845-9452. E-mail: [email protected]Cite this: Chem. Rev. 2009, 109, 2, 259–302Publication Date (Web):December 3, 2008Publication History Received10 June 2008Published online3 December 2008Published inissue 11 February 2009https://pubs.acs.org/doi/10.1021/cr800409ehttps://doi.org/10.1021/cr800409ereview-articleACS PublicationsCopyright © 2008 American Chemical SocietyRequest reuse permissionsArticle Views25002Altmetric-Citations2038LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Chemical structure,Gene delivery,Genetics,Polyethylenimine,Toxicity Get e-Alerts
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Relatively low gene delivery efficiency and transgene expression have been the major barriers in non-viral vectors-based gene therapy.
“So far, relatively low gene delivery efficiency and transgene expression have been the major barriers in non-viral vectors-based gene therapy [76, 77].”
From Non-viral delivery systems for CRISPR/Cas9-based genome editing: challenges and opportunities (2018) · cites this paper as [76]
Non-viral vectors face two main limitations in systemic delivery in vivo: serum stability of polyplexes after systemic administration and relatively low transfection efficiency in targeted tissues after administration.
“There are two main limitations of non-viral vectors-mediated CRISPR/Cas9 delivery in vivo. The first one is the serum stability of polyplexes after systemic administration [73]. The second one is the relatively low transfection efficiency in the targeted tissues after administration in vivo [76, 77].”
From Non-viral delivery systems for CRISPR/Cas9-based genome editing: challenges and opportunities (2018) · cites this paper as [76]
Viruses such as herpes simplex virus and some serotypes of adenovirus could travel through cytoplasm via microtubule-mediated transport.
“Virus such as herpes simplex virus and some serotypes of adenovirus could travel through the cytoplasm via microtubule-mediated transport [76, 193, 194].”
From Non-viral delivery systems for CRISPR/Cas9-based genome editing: challenges and opportunities (2018) · cites this paper as [76]
Cationic polyplexes could move along microtubules by non-specifically interacting with anionic microtubules or motor proteins.
“Cationic polyplexes could move along microtubules by non-specifically interacting with anionic microtubules or motor proteins [76].”
From Non-viral delivery systems for CRISPR/Cas9-based genome editing: challenges and opportunities (2018) · cites this paper as [76]
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- Authors
- Mintzer, M. A., & Simanek, E. E.
- Affiliations
- Texas A&M University (US)
- Corresponding author
- Simanek, Eric E.
- ORCID
- Simanek, Eric E.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2008-12-03
- Volume
- 109
- Issue
- 2
- Pages
- 259-302
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W1998697301
- Cited by
- 2,366
- References
- 553
- Citations by year
- 2026: 32 · 2025: 58 · 2024: 68 · 2023: 66 · 2022: 96 · 2021: 112 · 2020: 105 · 2019: 123 · 2018: 133 · 2017: 170 · 2016: 179 · 2015: 198 · 2014: 217 · 2013: 202 · 2012: 200
- FWCI
- 10.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Chemical Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R01 GM 64560, R01GM064560)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Keywords
- non-viral gene delivery, gene delivery vectors, polyethyleneimine, gene therapy, vector toxicity
- MeSH terms
- Genetic Vectors, Liposomes, Peptides, Polymers, Genetic Therapy, Gene Transfer Techniques, Dendrimers, Nanoparticles
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