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Poly (2-oxazoline) s as polymer therapeutics
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Poly(2‐oxazoline)s (POx) are currently discussed as an upcoming polymer platform for biomaterials design and especially for polymer therapeutics. POx meet specific requirements needed for the development of next‐generation polymer therapeutics such as biocompatibility, high modulation of solubility, variation of size, architecture as well as chemical functionality. Although in the early 1990s first and promising POx‐based systems were presented, the field lay dormant for almost two decades. Only very recently, POx‐based polymer therapeutics came back into the focus of very intensive research. In this review, we give an overview on the chemistry and physicochemical properties of POx and summarize the research of POx–protein conjugates, POx–drug conjugates, POx‐based polyplexes and POx micelles for drug delivery.
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“Poly(2-oxazoline) (POx)-based block copolymers recently gained a lot of interest as novel biomaterials due to their biocompatibility and chemical versatility [44, 45].”
From Polymeric micelles for the delivery of poorly soluble drugs: From nanoformulation to clinical approval. (2020) · cites this paper as [44]
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“One novel drug carrier system that stands apart from the others in that regard is polymeric micelles [11], based on amphiphilic block copolymers of poly(2-alkyl-2-oxazoline)s and specifically the poly[(2-methyl-2-oxazoline)-b-(2-butyl-2-oxazoline)-b-(2-methyl-2-oxazoline)] (P(MeOx-BuOx-MeOx) triblock copolymer [12].”
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Cites
Encyclopedia of polymer science and engineering
Mark, H., & Kroschwitz, J. I. (1985) · Wiley eBooks · Cited by 5,877
Poly(ethylene glycol) in Drug Delivery: Pros and Cons as Well as Potential Alternatives
Knop, K., Hoogenboom, R., Fischer, D., & Schubert, U. S. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200902672 · Cited by 3,533
Block copolymer micelles for drug delivery: design, characterization and biological significance
Kataoka, K., Harada, A., & Nagasaki, Y. (2001) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(00)00124-1 · Cited by 3,506
The dawning era of polymer therapeutics
Duncan, R. (2003) · Nature Reviews Drug Discovery · doi:10.1038/nrd1088 · Cited by 3,312
Designing dendrimers for biological applications
Lee, C., MacKay, J. A., Fréchet, J. M. J., & Szoka, F. C. (2005) · Nature Biotechnology · doi:10.1038/nbt1171 · Cited by 2,046
Structure and design of polymeric surfactant-based drug delivery systems
Torchilin, V. P. (2001) · Journal of Controlled Release · doi:10.1016/s0168-3659(01)00299-1 · Cited by 1,844
Poly(2‐oxazoline)s: A Polymer Class with Numerous Potential Applications
Hoogenboom, R. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200901607 · Cited by 892
Kim, T.-Y., Kim, D.-W., Chung, J.-Y., Shin, S. G., Kim, S.-C., Heo, D. S., Kim, N. K., & Bang, Y.-J. (2004) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-03-0655 · Cited by 821
Kumar, M., Grzelakowski, M., Zilles, J. L., Clark, M. M., & Meier, W. P. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708762104 · Cited by 717
Pluronic® block copolymers for overcoming drug resistance in cancer
Kabanov, A. V., Batrakova, E. V., & Alakhov, V. Y. (2002) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(02)00047-9 · Cited by 637
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1 of the 194 references couldn’t be matched to a known paper.
Research works printed but not linked: 10
- Schwekendiek K., 2006, Synthesis, 18, 2996
- Luxenhofer R., 2006, PMSE Prepr., 95, 283
- Kowalczuk A., 2011, Polym. Int.
- Weber C., 2011, Prog. Polym. Sci.
- Luxenhofer R., 2007, Thesis TU München, Garching
- Harris J. M., 2010, 8th International Symposium on Polymer Therapeutics: From Laboratory to Clinical Practice, 19
- Hruby M., 2010, Macromol. Biosci.
- Schulz A., 2012, Polym. Prepr., 53, 354
- Schulz A., 2012, Polym. Prepr., 53, 305
- Bender J. C. M. E., 2011, PCT Int. Appl. WO 2011/002285
Cited by
Sorted by citations
Items 301–400 of 470
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Alkattan, N., Alasmael, N., Ladelta, V., Khashab, N. M., & Hadjichristidis, N. (2023) · Nanoscale Advances · doi:10.1039/d3na00116d · Cited by 13
Kampmann, A., Luksin, M., Pretzer, I., & Weberskirch, R. (2016) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201600108 · Cited by 12
Wang, Y., Shen, H., Zhou, L., Hu, F., Xie, S., & Jiang, L. (2016) · Catalysis Science & Technology · doi:10.1039/c6cy00448b · Cited by 12
Poly(L-glutamic acid)-co-poly(ethylene glycol) block copolymers for protein conjugation
Maso, K., Grigoletto, A., Raccagni, L., Bellini, M., Marigo, I., Ingangi, V., Suzuki, A., Hirai, M., Kamiya, M., Yoshioka, H., et al. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.05.015 · Cited by 12
Jung, N., Diehl, F., & Jonas, U. (2020) · Polymers · doi:10.3390/polym12081767 · Cited by 12
Kirila, T. Y., Smirnova, A. V., Aseyev, V. O., Теньковцев, А. В., Tenhu, H. J., & Филиппов, А. П. (2021) · Polymers · doi:10.3390/polym13091429 · Cited by 12
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Hu, F., Du, G., Ye, L., Zhu, Y., Wang, Y., & Jiang, L. (2016) · Polymer · doi:10.1016/j.polymer.2016.08.089 · Cited by 11
Fer, G. L., Cœur, C. L., Guigner, J., Amiel, C., & Volet, G. (2017) · Langmuir · doi:10.1021/acs.langmuir.7b00471 · Cited by 11
Baheti, P., Rheinberger, T., Gimello, O., Bouilhac, C., Wurm, F. R., Lacroix‐Desmazes, P., & Howdle, S. M. (2020) · Green Chemistry · doi:10.1039/d0gc00819b · Cited by 12
Drews, M., Trötschler, T. M., Bauer, M., Guntupalli, A., Beichel, W., Gentischer, H., Mülhaupt, R., Kerscher, B., & Bíro, D. (2021) · ACS Applied Polymer Materials · doi:10.1021/acsapm.1c01171 · Cited by 11
Warne, N. M., Elbourne, A. J., Tran, M., Finnegan, J. R., Feeney, O. M., & Kempe, K. (2023) · Polymer Chemistry · doi:10.1039/d3py00399j · Cited by 11
Li, A., Zhang, J., Xu, Y., Liu, J., & Feng, S. (2014) · Chemistry - A European Journal · doi:10.1002/chem.201402836 · Cited by 11
Zhang, G., Ohta, Y., & Yokozawa, T. (2017) · Macromolecular Rapid Communications · doi:10.1002/marc.201700586 · Cited by 11
Mahmoud, A., Rajakanthan, A., & Kempe, K. (2017) · Polymer Chemistry · doi:10.1039/c7py01912b · Cited by 11
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Özköse, U. U., Yılmaz, Ö., & Alptürk, O. (2019) · Polymer Bulletin · doi:10.1007/s00289-019-03038-w · Cited by 11
Complex Temperature and Concentration Dependent Self-Assembly of Poly(2-oxazoline) Block Copolymers
Trinh, L. T. T., Hiorth, M., Hoogenboom, R., & Kjøniksen, A. (2020) · Polymers · doi:10.3390/polym12071495 · Cited by 11
Schoolaert, E., Merckx, R., Becelaere, J., Everaerts, M., Guyse, J. F. R. V., Sedláček, O., Geest, B. G. D., den Mooter, G. V., D’hooge, D., Clerck, K. D., et al. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c00970 · Cited by 11
Subasic, C. N., Ardana, A., Chan, L. J., Huang, F., Scoble, J. A., Butcher, N. J., Meagher, L., Chiefari, J., Kaminskas, L. M., & Williams, C. C. (2021) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2021.121075 · Cited by 11
Sano, K., Bao, L., Suzuno, N., Kannaka, K., Yamasaki, T., Munekane, M., & Mukai, T. (2019) · ACS Applied Polymer Materials · doi:10.1021/acsapm.8b00238 · Cited by 11
Morgese, G., Verbraeken, B., Ramakrishna, S. N., Gombert, Y., Cavalli, E., Rosenboom, J., Zenobi‐Wong, M., Spencer, N. D., Hoogenboom, R., & Benetti, E. M. (2018) · Angewandte Chemie · doi:10.1002/ange.201805620 · Cited by 13
Beudert, M., Hahn, L., Horn, A. H. C., Hauptstein, N., Sticht, H., Meinel, L., Luxenhofer, R., Gutmann, M., & Lühmann, T. C. (2022) · Journal of Controlled Release · doi:10.1016/j.jconrel.2022.04.028 · Cited by 10
Self-citationPoly(2-oxazoline)-Based Thermoresponsive Stomatocytes
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Multi-responsive hollow nanospheres self-assembly by amphiphilic random copolymer and azobenzene
Wang, Y., Hu, L., Yin, Q., Du, K., Zhang, T., & Yin, Q. (2019) · Polymer · doi:10.1016/j.polymer.2019.04.071 · Cited by 10
An ε-caprolactone-derived 2-oxazoline inimer for the synthesis of graft copolymers
Kim, J., Waldron, C., Cattoz, B., & Becer, C. R. (2020) · Polymer Chemistry · doi:10.1039/d0py01092h · Cited by 10
Abbrent, S., Mahun, A., Dušková‐Smrc̆ková, M., Kobera, L., Konefał, R., Černoch, P., Dušek, K., & Brus, J. (2021) · RSC Advances · doi:10.1039/d1ra01509e · Cited by 10
Schoolaert, E., Merckx, R., Becelaere, J., Rijssegem, S., Hoogenboom, R., & Clerck, K. D. (2021) · Advanced Functional Materials · doi:10.1002/adfm.202106859 · Cited by 10
A Facile Synthesis of 2-Oxazolines via Dehydrative Cyclization Promoted by Triflic Acid
Yang, T., Huang, C., Jia, J., Wu, F., & Ni, F. (2022) · Molecules · doi:10.3390/molecules27249042 · Cited by 10
Morrow, J. P., Mazrad, Z. A. I., Warne, N. M., Ayton, S., Bush, A. I., & Kempe, K. (2024) · Biomacromolecules · doi:10.1021/acs.biomac.3c01106 · Cited by 10
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Chroni, A., Mavromoustakos, T., & Pispas, S. (2021) · Macromol—A Journal of Macromolecular Research · doi:10.3390/macromol1030014 · Cited by 11
Bardoula, V., Leclercq, L., Hoogenboom, R., & Nardello‐Rataj, V. (2022) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2022.11.018 · Cited by 10
Frateur, O., Becelaere, J., Merckx, R., Guyse, J. F. R. V., Purino, M. A., Hoogenboom, R., & Clerck, K. D. (2024) · European Polymer Journal · doi:10.1016/j.eurpolymj.2024.113076 · Cited by 9
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Summers, G. J., Maseko, R. B., & Summers, C. A. (2014) · Polymer International · doi:10.1002/pi.4776 · Cited by 9
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Engel, N., Dirauf, M., Czaplewska, J. A., Nischang, I., Gottschaldt, M., & Schubert, U. S. (2024) · Royal Society Open Science · doi:10.1098/rsos.231008 · Cited by 8
Cvek, M., Ilčíková, M., Mrlík, M., Skopalová, K., Vesel, A., Masař, M., & Humpolíček, P. (2024) · Applied Surface Science · doi:10.1016/j.apsusc.2024.161548 · Cited by 8
Hahn, D., Sonntag, J. M., Lück, S., Maitz, M. F., Freudenberg, U., Jordan, R., & Werner, C. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202101327 · Cited by 8
Self-citationGhoderao, P. N. P., Lee, C., & Byun, H. (2023) · Chemical Engineering Science · doi:10.1016/j.ces.2023.118566 · Cited by 8
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Milborne, B., Arafat, A., Layfield, R., Thompson, A., & Ahmed, I. (2020) · Recent Progress in Materials · doi:10.21926/rpm.2002012 · Cited by 8
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Kalinova, R. G., Yordanov, Y., Tzankov, B., Tzankova, V., Yoncheva, K., & Dimitrov, I. V. (2020) · Reactive and Functional Polymers · doi:10.1016/j.reactfunctpolym.2020.104763 · Cited by 8
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Zahoranová, A., & Kronek, J. (2015) · doi:10.1002/9781119041559.ch10 · Cited by 8
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Bansal, K. K., Sasso, L., Makwana, H., Awwad, S., Brocchini, S., & Alexander, C. (2016) · Wiley eBooks · doi:10.1002/9783527800681.ch10 · Cited by 8
Pyzhov, V. S., Бахрушина, Е. О., Gegechkori, V., Smirnov, V. V., Evzikov, G. Y., Kartashova, A. K., Zubareva, I. M., Krasnyuk, I. I., & Краснюк, И. И. (2026) · Polymers · doi:10.3390/polym18060681 · Cited by 7
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Keckeis, P., Zeller, E., Jung, C., Besirske, P., Kirner, F., Ruiz‐Agudo, C., Schlaad, H., & Cölfen, H. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202101327 · Cited by 7
de Menezes, R. N. L., & Felisberti, M. I. (2021) · Polymer Chemistry · doi:10.1039/d1py00730k · Cited by 7
Kadokawa, J. (2023) · Gels · doi:10.3390/gels9060432 · Cited by 7
Göppert, N. E., Quader, S., Guyse, J. F. R. V., Weber, C., Kataoka, K., & Schubert, U. S. (2023) · Biomacromolecules · doi:10.1021/acs.biomac.3c00934 · Cited by 7
Bardoula, V., Leclercq, L., Hoogenboom, R., & Nardello‐Rataj, V. (2024) · Colloids and Surfaces A Physicochemical and Engineering Aspects · doi:10.1016/j.colsurfa.2024.134634 · Cited by 7
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Çelebi, O., Barnes, S. R., Narang, G. S., Kellogg, D., Mecham, S. J., & Riffle, J. S. (2014) · Polymer · doi:10.1016/j.polymer.2014.11.005 · Cited by 7
Kang, M., Cho, M., Kim, S., & Youk, J. H. (2017) · Fibers and Polymers · doi:10.1007/s12221-017-7309-2 · Cited by 8
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Fam, S. Y., Chee, C. F., Yong, C. Y., Ho, K. L., Mariatulqabtiah, A. R., Lau, H. Y., & Tan, W. S. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194903 · Cited by 7
Özköse, U. U., Gülyüz, S., Khalily, M. P., Özçubukçu, S., Bozkır, A., Taşdelen, M. A., Alptürk, O., & Yılmaz, Ö. (2020) · Journal of Applied Polymer Science · doi:10.1002/app.50286 · Cited by 7
The Chemistry of Poly(2‐oxazoline)s
Verbraeken, B., Monnery, B. D., Lava, K., & Hoogenboom, R. (2018) · Wiley eBooks · doi:10.1002/0471440264.pst626.pub2 · Cited by 11
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Merckx, R., Dhaware, V., Leiske, M. N., Clerck, K. D., & Hoogenboom, R. (2024) · Chemistry of Materials · doi:10.1021/acs.chemmater.4c00277 · Cited by 6
Cho, W. H., Kim, H., Yoo, S., Lee, S. M., Kim, T. J., & Lee, J. (2025) · Journal of Pharmaceutical Investigation · doi:10.1007/s40005-025-00733-x · Cited by 6
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Zabihi, F., Beyranvand, S., Mohammadi, Z., Zeinivand, M., Dezfoulian, O., Farjanikish, G., Achazi, K., Chong, C., Rancan, F., Vogt, A., et al. (2026) · Biomaterials · doi:10.1016/j.biomaterials.2025.123974 · Cited by 6
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Simon, L., Reichel, L. S., Benkhaled, B. T., Devoisselle, J., Catrouillet, S., Eberhardt, J., Hoeppener, S., Schubert, U. S., Brendel, J. C., Morille, M., et al. (2024) · Macromolecular Bioscience · doi:10.1002/mabi.202400148 · Cited by 6
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Kosakowska, K. A., Dimitrov, P., Panambur, G., & Grayson, S. M. (2017) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.28495 · Cited by 6
Zhang, H., Sun, Y., Zhou, T., Yu, Q., Yang, Z., Cai, Z., & Cang, H. (2019) · International Journal of Polymeric Materials · doi:10.1080/00914037.2018.1525550 · Cited by 6
Yadav, R., Kahlon, N. K., Kumar, S., Devunuri, N., & Venkatesu, P. (2021) · Polymer · doi:10.1016/j.polymer.2021.123871 · Cited by 7
Leiske, M. N., Kuenneth, C., Breuck, J. D., Geest, B. G. D., & Hoogenboom, R. (2023) · Macromolecular Chemistry and Physics · doi:10.1002/macp.202300200 · Cited by 6
Hydrolyzed Poly(2‐plenyl‐2‐oxazoline)s in Aqueous Media and Biological Fluids
Vlassi, E., Papagiannopoulos, A., & Pispas, S. (2018) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201800047 · Cited by 7
Crosslinkable/functionalizable poly(2-oxazoline)based micelles
Rossegger, E., Pirolt, F., Hoeppener, S., Schubert, U. S., Glatter, O., & Wiesbrock, F. (2019) · European Polymer Journal · doi:10.1016/j.eurpolymj.2019.109305 · Cited by 6
Broeck, E. V. D., Verbraeken, B., Dedecker, K., Cnudde, P., Vanduyfhuys, L., Verstraelen, T., Hecke, K. V., Jerca, V. V., Çatak, Ş., Hoogenboom, R., et al. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c00865 · Cited by 6
Kazemi, M., Nazarabi, M., Niazi, Z., & Ashjari, M. (2021) · International Journal of Polymeric Materials · doi:10.1080/00914037.2021.1963723 · Cited by 6
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Liu, K., Ye, L., Wang, Y., Du, G., & Jiang, L. (2018) · Polymers · doi:10.3390/polym10091004 · Cited by 6
Guan, X., Jana, S., Tomita, T., Ogoshi, T., Woisel, P., & Hoogenboom, R. (2025) · Macromolecules · doi:10.1021/acs.macromol.4c02456 · Cited by 5
Biodegradable and water-soluble polymers in block copolymer architectures
Azhdari, S., Gröschel, A. H., & Wurm, F. R. (2025) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2025.111749 · Cited by 5
Morrow, J. P., Pizzi, D., Mazrad, Z. A. I., Bush, A. I., & Kempe, K. (2023) · Biomaterials Science · doi:10.1039/d2bm02087d · Cited by 5
Amgoth, C., Patra, S., Wasnik, K., Maity, P., & Paik, P. (2023) · Journal of Applied Polymer Science · doi:10.1002/app.53854 · Cited by 5
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Mees, M. A., McAllister, T. D., Curia, S., Howdle, S. M., & Hoogenboom, R. (2023) · Macromolecules · doi:10.1021/acs.macromol.2c02443 · Cited by 5
Synthesis and evaluation of pseudopeptide chiral stationary phases for enantioselective resolution
Shen, H., Du, G., Liu, K., Ye, L., Xie, S., & Jiang, L. (2017) · Journal of Chromatography A · doi:10.1016/j.chroma.2017.08.082 · Cited by 5
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Venturini, P., Fleutot, S., Cleymand, F., Hauet, T., Dupin, J., Ghanbaja, J., Martinez, H., Robin, J., & Lapinte, V. (2018) · ChemistrySelect · doi:10.1002/slct.201802234 · Cited by 5
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Arsenie, L. V., Bangoura, M. A., Ramonda, M., Merindol, R., Hespel, L., Blanquer, S., Azemar, F., & Lapinte, V. (2025) · Progress in Organic Coatings · doi:10.1016/j.porgcoat.2025.109096 · Cited by 4
Atılkan, N., Schlaad, H., Nur, Y., & Hacaloğlu, J. (2013) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201300524 · Cited by 4
Amphiphilic Heterograft Copolymers Bearing Biocompatible/Biodegradable Grafts
Glaive, A.-S., Cœur, C. L., Guigner, J., Amiel, C., & Volet, G. (2024) · Langmuir · doi:10.1021/acs.langmuir.3c02772 · Cited by 4
Liu, Y., Xue, Y., Tang, J., Zhang, P., Liu, C., Wu, D., & Liu, J. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c17267 · Cited by 4
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Metadata
- Authors
- Luxenhofer, R., Han, Y., Schulz, A., Tong, J., He, Z., Kabanov, A. V., & Jordan, R.
- Affiliations
- Technische Universität Dresden (DE)
- Wuhan University of Technology (CN)
- University of Nebraska Medical Center (US)
- Center for Regenerative Therapies Dresden (DE)
- Corresponding author
- Luxenhofer, Robert
- Jordan, Rainer
- Venue
- Macromolecular Rapid Communications
- Publisher
- Wiley
- Published
- 2012-08-03
- Volume
- 33
- Issue
- 19
- Pages
- 1613-1631
- ISSN
- 1022-1336 (ISSN-L)
- 1521-3927
- PMC
- PMC3608391
- OpenAlex
- W2065735911
- Cited by
- 470
- References
- 194
- Citations by year
- 2026: 22 · 2025: 21 · 2024: 28 · 2023: 23 · 2022: 28 · 2021: 42 · 2020: 43 · 2019: 43 · 2018: 47 · 2017: 39 · 2016: 42 · 2015: 37 · 2014: 28 · 2013: 23 · 2012: 3
- FWCI
- 1.39
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Macromolecular Rapid Communications (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- China Scholarship Council
- Zentrum für Regenerative Therapien Dresden
- National Cancer Institute (U01 CA116591, U01CA151806, R01CA116591)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Keywords
- poly(2-oxazoline), polymer therapeutics, biocompatibility, protein-polymer conjugates, polymer-drug conjugates, polyplexes, micelles, drug delivery, biomaterials
- MeSH terms
- Biocompatible Materials, Drug Carriers, Pharmaceutical Preparations, Micelles, Oxazoles, Polymers, Proteins, Nanomedicine, Nanoparticles
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