The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
Novel gene delivery systems
Abstract
Gene therapy is an emerging field in medical and pharmaceutical sciences because of its potential in treating chronic diseases like cancer, viral infections, myocardial infarctions, and genetic disorders. Application of gene therapy is limited because of lack of suitable methods for proper introduction of genes into cells and therefore, this is an area of interest for most of the researchers. To achieve successful gene therapy, development of proper gene delivery systems could be one of the most important factors. Several nonviral and viral gene transfer methods have been developed. Even though the viral agents have a high transferring efficiency, they are difficult to handle due to their toxicity. To overcome the safety problems of the viral counterpart, several nonviral in vitro and in vivo gene delivery systems are developed. Out of these, the most promising and latest systems include polymer-based nonviral gene carriers, dendrimers, and physical means like electroporation, microinjection, etc., Shunning of possible immunogenicity and toxicity, and the feasibility of repeated administration are some of the merits of nonviral gene delivery systems over viral gene delivery. An ideal nonviral gene carrying system should possess all these merits without any compromise to its gene transferring efficiency. The viral gene delivery systems include lytic and nonlytic vectors for drug delivery. Inspite of its toxicity they are still preferred because of their long term expression, stability, and integrity. This review explores the recent developments and relevancy of the novel gene delivery systems in gene therapy.
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“Even though said techniques are widely used in research labs, these shortcomings combined with low efficiency limit their use in human gene therapy [143,144].”
From CRISPR-Cas: Converting A Bacterial Defence Mechanism into A State-of-the-Art Genetic Manipulation Tool (2019) · cites this paper as [143]
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Citations
Cites
Electroporation: theory and methods, perspectives for drug delivery, gene therapy and research
Gehl, J. (2003) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2003.01093.x · Cited by 973
Current status of polymeric gene delivery systems☆
PARK, T., JEONG, J., & KIM, S. (2006) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2006.03.007 · Cited by 944
A Polyamidoamine Dendrimer-Capped Mesoporous Silica Nanosphere-Based Gene Transfection Reagent
Radu, D. R., Lai, C.-Y., Jeftinija, K., Rowe, E. W., Jeftinija, S., & Lin, V. S.-Y. (2004) · Journal of the American Chemical Society · doi:10.1021/ja046275m · Cited by 840
Adenoviral gene delivery can reprogram human fibroblasts to induced pluripotent stem cells
Zhou, W., & Freed, C. R. (2009) · Stem Cells · doi:10.1002/stem.201 · Cited by 538 · cited 1×
“[4] Most of the adenoviral gene delivery is being aimed for cancer chemotherapy.”
Micelles and nanoparticles for ultrasonic drug and gene delivery
Husseini, G. A., & Pitt, W. G. (2008) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2008.03.008 · Cited by 468
Swift, S., Lorens, J., Achacoso, P., & Nolan, G. P. (1999) · Current Protocols in Immunology · doi:10.1002/0471142735.im1017cs31 · Cited by 313
A novel magnetic crystal–lipid nanostructure for magnetically guided in vivo gene delivery
Namiki, Y., Namiki, T., Yoshida, H., Ishii, Y., Tsubota, A., Koido, S., Nariai, K., Mitsunaga, M., Yanagisawa, S., Kashiwagi, H., et al. (2009) · Nature Nanotechnology · doi:10.1038/nnano.2009.202 · Cited by 243
Exosomes as nano-theranostic delivery platforms for gene therapy
Tan, A., Rajadas, J., & Seifalian, A. M. (2013) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2012.06.014 · Cited by 242
Chlorotoxin Labeled Magnetic Nanovectors for Targeted Gene Delivery to Glioma
Kievit, F. M., Omid Veiseh, A., Fang, C., Bhattarai, N., Lee, D., Ellenbogen, R. G., & Zhang, M. (2010) · ACS Nano · doi:10.1021/nn1008512 · Cited by 228
Akhtar, S., & Benter, I. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.03.010 · Cited by 219
Research works printed but not linked: 3
- Peng, 2012, Short noncoding DNA fragment improve efficiencies of in vivo electroporation-mediated gene transfer, J Gene Med, 563
- Cao, 2012, Gene gun bombardment with DNA-coated golden particles enhanced the protective effect of a DNA vaccine based on thioredoxin glutathione reductase of Schistosoma japonicum, J Biomed Biotecnol, 1
- Ginsberg AA, Shen X, Hutnick NA, Weiner DB. Improvement of DNA vaccines by electroporation. Available from: http://www.researchgate.net/publication/225843247_Improvement_of_DNA_Vaccines_by_Electroporation [Last accessed on 2012 Nov 26].
Cited by
Lee, C. S., Bishop, E. S., Zhang, R., Yu, X., Farina, E. M., Yan, S., Zhao, C., Zeng, Z., Shu, Y., Wu, X., et al. (2017) · Genes & Diseases · doi:10.1016/j.gendis.2017.04.001 · Cited by 691
Loureiro, A., & da Silva, G. J. (2019) · Antibiotics · doi:10.3390/antibiotics8010018 · Cited by 129
Metadata
- Authors
- Valsalakumari, J., Baby, J., Bijin, E., Constantine, I., Manjila, S., & Pramod, K.
- Venue
- International Journal of Pharmaceutical Investigation
- Publisher
- Manuscript Technomedia LLP
- Published
- 2013
- Volume
- 3
- Issue
- 1
- Pages
- 1
- ISSN
- 2230-973X
- PMC
- PMC3687232
- Cited by
- 48
- References
- 44
- Language
- en
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- Valsalakumari, J., Baby, J., Bijin, E., Constantine, I., Manjila, S., & Pramod, K. (2013). Novel gene delivery systems. International Journal of Pharmaceutical Investigation. https://doi.org/10.4103/2230-973x.108958
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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