The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Tuning the Hemolytic and Antibacterial Activities of Amphiphilic Polynorbornene Derivatives
Open accessAbstract
Amphiphilic cationic polynorbornene derivatives, soluble in water, were prepared from modular norbornene monomers, with a wide range of molecular weights (M(n) = 1600-137 500 g/mol) and narrow polydispersities (PDI = 1.1-1.3). The antibacterial activity determined by growth inhibition assays and the hemolytic activity against human red blood cells were measured and compared to determine the selectivity of the polymers for bacterial over mammalian cells. The effects of monomer repeat unit hydrophobicity and polymer molecular weight on antibacterial and hemolytic activities were determined. The hydrophobicity of the repeat unit was observed to have dramatic effects on antibacterial and hemolytic activities. Lipid membrane disruption activities of the polymers was confirmed by measuring polymer-induced dye leakage from large unilamellar vesicles. By tuning the overall hydrophobicity of the polymer through random copolymerizations of modular norbornene derivatives, highly selective, nonhemolytic antibacterial activities were obtained. For appropriate monomer composition, selectivity against bacteria versus human red blood cells was determined to be over 100.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Antimicrobial peptides of multicellular organisms
Zasloff, M. (2002) · Nature · doi:10.1038/415389a · Cited by 8,457
The Development of L2X2RuCHR Olefin Metathesis Catalysts: An Organometallic Success Story
Trnka, T. M., & Grubbs, R. H. (2001) · Accounts of Chemical Research · doi:10.1021/ar000114f · Cited by 3,561
Handbook of Metathesis: Catalyst Development
(2003) · Wiley eBooks · doi:10.1002/9783527619481 · Cited by 1,671
Antibacterial agents based on the cyclic d,l-α-peptide architecture
Fernandez-Lopez, S., Kim, H.-S., Choi, E. C., Delgado, M., Granja, J. R., Khasanov, A., Kraehenbuehl, K., Long, G., Weinberger, D. A., Wilcoxen, K. M., et al. (2001) · Nature · doi:10.1038/35086601 · Cited by 938
Mode of action of linear amphipathic α-helical antimicrobial peptides
Oren, Z., & Shai, Y. (1998) · Biopolymers · doi:10.1002/(sici)1097-0282(1998)47:6<451::aid-bip4>3.0.co;2-f · Cited by 848
Buchmeiser, M. R. (2000) · Chemical Reviews · doi:10.1021/cr990248a · Cited by 796
Stiriba, S.-E., Frey, H., & Haag, R. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020415)41:8<1329::aid-anie1329>3.0.co;2-p · Cited by 672
Non-haemolytic β-amino-acid oligomers
Porter, E. A., Wang, X., Lee, H.-S., Weisblum, B., & Gellman, S. H. (2000) · Nature · doi:10.1038/35007145 · Cited by 671
Oren, Z., & Shai, Y. (1997) · Biochemistry · doi:10.1021/bi962507l · Cited by 416
Dathe, M., Schümann, M., Wieprecht, T., Winkler, A., Beyermann, M., Krause, E., Matsuzaki, K., Murase, O., & Bienert, M. (1996) · Biochemistry · doi:10.1021/bi960835f · Cited by 409
Cited by
Polymeric materials with antimicrobial activity
Muñoz-Bonilla, A., & Fernández-García, M. (2012) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2011.08.005 · Cited by 1,221
Silver bromide nanoparticle/polymer composites: dual action tunable antimicrobial materials
Sambhy, V., MacBride, M. M., Peterson, B. R., & Sen, A. (2006) · Journal of the American Chemical Society · doi:10.1021/ja061442z · Cited by 748
Antimicrobial polymers: mechanism of action, factors of activity, and applications
Timofeeva, L., & Kleshcheva, N. (2011) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2920-9 · Cited by 579
Cationic Antimicrobial Polymers and Their Assemblies
Carmona-Ribeiro, A., & De Melo Carrasco, L. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14059906 · Cited by 532
Baruah, B., Gabriel, G. J., Akbashev, M. J., & Booher, M. E. (2013) · Langmuir · doi:10.1021/la305068p · Cited by 391
Kuroda, K., Caputo, G. A., & DeGrado, W. F. (2009) · Chemistry – A European Journal · doi:10.1002/chem.200801523 · Cited by 346
Chin, W., Zhong, G., Pu, Q., Yang, C., Lou, W., De Sessions, P. F., Periaswamy, B., Lee, A., Liang, Z. C., Ding, X., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03325-6 · Cited by 331
Biomimetic antimicrobial polymers: recent advances in molecular design
Ergene, C., Yasuhara, K., & Palermo, E. F. (2018) · Polymer Chemistry · doi:10.1039/c8py00012c · Cited by 312
Antimicrobial hydrogels: A new weapon in the arsenal against multidrug-resistant infections
Ng, V. W. L., Chan, J. M. W., Sardon, H., Ono, R. J., García, J. M., Yang, Y. Y., & Hedrick, J. L. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.10.028 · Cited by 279
Hemocompatibility of hydrophilic antimicrobial copolymers of alkylated 4-vinylpyridine
Allison, B. C., Applegate, B. M., & Youngblood, J. P. (2007) · Biomacromolecules · doi:10.1021/bm7004627 · Cited by 129
Cationic polymers and their self-assembly for antibacterial applications
Deka, S., Sharma, A., & Kumar, P. (2015) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026615666150330110602 · Cited by 82
King, A., Chakrabarty, S., Zhang, W., Zeng, X., Ohman, D. E., Wood, L. F., Abraham, S., Rao, R., & Wynne, K. J. (2014) · Biomacromolecules · doi:10.1021/bm401794p · Cited by 72
Chakrabarty, S., King, A., Kurt, P., Zhang, W., Ohman, D. E., Wood, L. F., Lovelace, C., Rao, R., & Wynne, K. J. (2011) · Biomacromolecules · doi:10.1021/bm101381y · Cited by 37
Metadata
- Authors
- Ilker, M. F., Nüsslein, K., Tew, G. N., & Coughlin, E. B.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2004-11-13
- Volume
- 126
- Issue
- 48
- Pages
- 15870-15875
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W1986286007
- Cited by
- 502
- References
- 23
- FWCI
- 6.14
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.