The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Structure−Activity Relationships of Water-Soluble Cationic Methacrylate/Methacrylamide Polymers for Nonviral Gene Delivery
Abstract
A number of water-soluble cationic carriers was evaluated as transfectant. Almost all studied cationic methacrylate/methacrylamide polymers were able to condense the structure of plasmid DNA, yielding polymer/plasmid complexes (polyplexes) with a size of 0.1-0.3 micron and a slightly positive zeta-potential, which can be taken up by cells, e.g., via endocytosis. However, the transfection efficiency and the cytotoxicity of the polymers differed widely: the highest transfection efficiency and cytotoxicity were observed for poly[2-(dimethylamino)ethyl methacrylate], p(DMAEMA). Assuming that polyplexes enter cells via endocytosis, p(DMAEMA) apparently has advantageous properties to escape the endosome. A possible explanation is that, due to its average pK(a) value of 7.5, p(DMAEMA) is partially protonated at physiological pH and might behave as a proton sponge. This might cause a disruption of the endosome, which results in the release of both the polyplexes and cytotoxic endosomal/lysosomal enzymes into the cytosol. On the other hand, the analogues of p(DMAEMA) studied here have a higher average pKa value and have, consequently, a higher degree of protonation and a lower buffering capacity. This might be associated with a lower tendency to destabilize the endosome, resulting in both a lower transfection efficiency and a lower cytotoxicity. Furthermore, molecular modeling showed that, of all studied polymers, p(DMAEMA) has the lowest number of interactions with DNA. We therefore hypothesized that the superior transfection efficiency of p(DMAEMA) containing polyplexes can be ascribed to an intrinsic property of p(DMAEMA) to destabilize endosomes combined with an easy dissociation of the polyplex once present in the cytosol and/or the nucleus.
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Cites
In vitro cytotoxicity of macromolecules in different cell culture systems
Choksakulnimitr, S., Masuda, S., Tokuda, H., Takakura, Y., & Hashida, M. (1995) · Journal of Controlled Release · doi:10.1016/0168-3659(95)00007-u · Cited by 347
2-(dimethylamino)ethyl methacrylate based (co)polymers as gene transfer agents
van de Wetering, P., Cherng, J.-Y., Talsma, H., Crommelin, D. J. A., & Hennink, W. E. (1998) · Journal of Controlled Release · doi:10.1016/s0168-3659(97)00248-4 · Cited by 326
Self-citationvan de Wetering, P., Cherng, J.-Y., Talsma, H., & Hennink, W. E. (1997) · Journal of Controlled Release · doi:10.1016/s0168-3659(97)00059-x · Cited by 268
Self-citationRedundant control of adenovirus late gene expression by early region 4
Bridge, E., & Ketner, G. (1989) · Journal of Virology · doi:10.1128/jvi.63.2.631-638.1989 · Cited by 259
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Peptide-Mediated Gene Delivery: Influence of Peptide Structure on Gene Expression
Wadhwa, M. S., Collard, W. T., Adami, R. C., McKenzie, D. L., & Rice, K. G. (1997) · Bioconjugate Chemistry · doi:10.1021/bc960079q · Cited by 219
Binding of Cationic α-Helical Peptides to Plasmid DNA and Their Gene Transfer Abilities into Cells
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Cited by
Nonviral vectors for gene delivery
Mintzer, M. A., & Simanek, E. E. (2009) · Chemical Reviews · doi:10.1021/cr800409e · Cited by 2,366
Synthetic DNA delivery systems
Luo, D., & Saltzman, W. M. (2000) · Nature Biotechnology · doi:10.1038/71889 · Cited by 1,626
Degradable poly (β-amino esters): synthesis, characterization, and self-assembly with plasmid DNA
Lynn, D. M., & Langer, R. (2000) · Journal of the American Chemical Society · doi:10.1021/ja0015388 · Cited by 924
The great escape: how cationic polyplexes overcome the endosomal barrier
Bus, T., Traeger, A., & Schubert, U. S. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb00967h · Cited by 409
Feng, S.-S., & Huang, G. (2001) · Journal of Controlled Release · doi:10.1016/s0168-3659(00)00364-3 · Cited by 398
Metadata
- Authors
- van de Wetering, P., Moret, E. E., Schuurmans-Nieuwenbroek, N. M. E., van Steenbergen, M. J., & Hennink, W. E.
- Venue
- Bioconjugate Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 1999-06-04
- Volume
- 10
- Issue
- 4
- Pages
- 589-597
- ISSN
- 1043-1802 (ISSN-L)
- 1520-4812
- OpenAlex
- W2070836823
- Cited by
- 428
- References
- 9
- FWCI
- 2.61
- Type
- journal article
- Language
- en
- Open access
- closed
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