Multi-Stimuli Sensitive Amphiphilic Block Copolymer Assemblies
Open accessAbstract
Stimuli-responsive polymers are arguably the most widely considered systems for a variety of applications in biomedical arena. We report here a novel triple stimuli sensitive block copolymer assembly that responds to changes in temperature, pH and redox potential. Our block copolymer design constitutes an acid-sensitive THP-protected HEMA as the hydrophobic part and a temperature-sensitive PNIPAM as the hydrophilic part with an intervening disulfide bond. The micellar properties and the release kinetics of the encapsulated guest molecule in response to one stimulus as well as combinations of stimuli have been evaluated. Responsiveness to combination of stimuli not only allows for fine-tuning the guest molecule release kinetics, but also provides the possibility of achieving location-specific delivery.
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
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The temperature-sensitive hydrophilic part of nanomicelles is turned to hydrophobic above the low critical solution temperature that transfers the polymer to insoluble in water state which, in turn, leads to the assembly.
“the temperature-sensitive hydrophilic part of nanomicelles is turned to hydrophobic above the low critical solution temperature that transfers the polymer to insoluble in water state which, in turn, leads to the assembly.”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [217]
The Summary says that above the LCST, the hydrophilic block becomes hydrophobic and the polymer becomes insoluble in water, but this results in “no assembly,” not assembly. The Results and Discussion section on thermosensitive behavior likewise reports precipitation on heating. (LLM, conf=0.95)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredThe design of multi stimuli-responsive nanomicelles sensitive to redox potential, pH, and temperature was reported recently.
“For example, the design of multi stimuli-responsive nanomicelles sensitive to redox potential, pH, and temperature was reported recently [217].”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [217]
The hydrophobic part of the structure tetrahydropyran-protected 2-hydroxyethyl methacrylate aimed to respond acidity change, while the hydrophilic part provided by pNIPAM is temperature sensitive and with redox-potential sensitive disulfide bond between them.
“The hydrophobic part of the structure tetrahydropyran-protected 2-hydroxyethyl methacrylate aimed to respond acidity change, while the hydrophilic part provided by pNIPAM is temperature sensitive and with redox-potential sensitive disulfide bond between them.”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [217]
The pH decrease converts acid-sensitive hydrophobic part to hydrophilic and thereby inhibits the assembly.
“The pH decrease, on the other hand, converts acid-sensitive hydrophobic part to hydrophilic and thereby inhibits the assembly.”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [217]
Reducing disulfide bonds in such an environment results in the decomposition of nanomicelles.
“Finally, reducing disulfide bonds in such an environment results in the decomposition of nanomicelles [217].”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [217]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Protective Groups in Organic Synthesis
Greene, T. W., & Wuts, P. G. M. (1999) · Wiley eBooks · doi:10.1002/0471220574 · Cited by 5,677 · see citing works
Poly(N-isopropylacrylamide): experiment, theory and application
Schild, H. G. (1992) · Progress in Polymer Science · doi:10.1016/0079-6700(92)90023-r · Cited by 5,162 · see citing works
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 · see citing works
Brunsveld, L., Folmer, B. J. B., Meijer, E. W., & Sijbesma, R. P. (2001) · Chemical Reviews · doi:10.1021/cr990125q · Cited by 3,015 · see citing works
Discher, D., & Eisenberg, A. (2002) · Science · doi:10.1126/science.1074972 · Cited by 2,251 · see citing works
A review of stimuli-responsive nanocarriers for drug and gene delivery
Ganta, S., Devalapally, H., Shahiwala, A., & Amiji, M. M. (2008) · Journal of Controlled Release · doi:10.1016/j.jconrel.2007.12.017 · Cited by 2,157 · see citing works
Water Gelation by Small Organic Molecules
Estroff, L. A., & Hamilton, A. D. (2004) · Chemical Reviews · doi:10.1021/cr0302049 · Cited by 2,038 · see citing works
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 1,824 · see citing works
Stimuli responsive polymers for biomedical applications
Alarcón, C. D. L. H., Pennadam, S. S., & Alexander, C. (2005) · Chemical Society Reviews · doi:10.1039/b406727d · Cited by 1,692 · see citing works
Vriezema, D. M., Comellas-Aragonès, M., Elemans, J. A. A. W., Cornelissen, J. J. L. M., Rowan, A. E., & Nolte, R. J. M. (2005) · Chemical Reviews · doi:10.1021/cr0300688 · Cited by 1,462 · see citing works
Bae, Y., Fukushima, S., Harada, A., & Kataoka, K. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200250653 · Cited by 1,329 · see citing works
Zhang, L., & Eisenberg, A. (1996) · Journal of the American Chemical Society · doi:10.1021/ja953709s · Cited by 1,262 · see citing works
Polymeric micelles—A new generation of colloidal drug carriers
Jones, M.-C., & Leroux, J.-C. (1999) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/s0939-6411(99)00039-9 · Cited by 1,256 · see citing works
Amphiphilic block copolymers for drug delivery
Adams, M. L., Lavasanifar, A., & Kwon, G. S. (2003) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.10397 · Cited by 1,078 · see citing works
Dendritic Catalysts and Dendrimers in Catalysis
Astruc, D., & Chardac, F. (2001) · Chemical Reviews · doi:10.1021/cr010323t · Cited by 1,062 · see citing works
Physical stimuli-responsive polymeric micelles for anti-cancer drug delivery
Rapoport, N. (2007) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2007.05.009 · Cited by 1,002 · see citing works
The role of glutathione in cancer
Balendiran, G. K., Dabur, R., & Fraser, D. A. (2004) · Cell Biochemistry and Function · doi:10.1002/cbf.1149 · Cited by 929 · see citing works
Ion-Induced Morphological Changes in “Crew-Cut” Aggregates of Amphiphilic Block Copolymers
Zhang, L., Yu, K., & Eisenberg, A. (1996) · Science · doi:10.1126/science.272.5269.1777 · Cited by 914 · see citing works
Oxidation-responsive polymeric vesicles
Napoli, A., Valentini, M., Tirelli, N., et al. (2004) · Nature Materials · doi:10.1038/nmat1081 · Cited by 889 · see citing works
Supramolecular Structures from Rod−Coil Block Copolymers
Lee, M., Cho, B., & Zin, W. (2001) · Chemical Reviews · doi:10.1021/cr0001131 · Cited by 759 · see citing works
Applications of thermally reversible polymers and hydrogels in therapeutics and diagnostics
Hoffman, A. S. (1987) · Journal of Controlled Release · doi:10.1016/0168-3659(87)90083-6 · Cited by 747 · see citing works
Smart polymers: Physical forms and bioengineering applications
Kumar, A., Srivastava, A., Galaev, I. Y., et al. (2007) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2007.05.003 · Cited by 743 · see citing works
Stimuli‐Responsive Polymeric Systems for Biomedical Applications
Mano, J. F. (2008) · Advanced Engineering Materials · doi:10.1002/adem.200700355 · Cited by 667 · see citing works
Thermally on-off switching polymers for drug permeation and release
Okano, T., Bae, Y. H., Jacobs, H. A., & Kim, S. W. (1990) · Journal of Controlled Release · doi:10.1016/0168-3659(90)90138-j · Cited by 616 · see citing works
Fuhrhop, J., & Wang, T. (2004) · Chemical Reviews · doi:10.1021/cr030602b · Cited by 605 · see citing works
pH-Sensitive Vesicles Based on a Biocompatible Zwitterionic Diblock Copolymer
Du, J., Tang, Y., Lewis, A. L., & Armes, S. P. (2005) · Journal of the American Chemical Society · doi:10.1021/ja056514l · Cited by 603 · see citing works
pH-Responsive Copolymer Assemblies for Controlled Release of Doxorubicin
Gillies, E. R., & Fréchet, J. M. J. (2005) · Bioconjugate Chemistry · doi:10.1021/bc049851c · Cited by 551 · see citing works
Stimuli-Responsive Supramolecular Assemblies of Linear-Dendritic Copolymers
Gillies, E. R., Jonsson, T. B., & Fréchet, J. M. J. (2004) · Journal of the American Chemical Society · doi:10.1021/ja0463738 · Cited by 549 · see citing works
Functional copolymers of N-isopropylacrylamide for bioengineering applications
Rzaev, Z. M. O., Dinçer, S., & Pişkın, E. (2007) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2007.01.006 · Cited by 528 · see citing works
Xia, Y., Yin, X., Burke, N. A. D., & Stöver, H. D. H. (2005) · Macromolecules · doi:10.1021/ma050261z · Cited by 503 · see citing works
A New Design for Light-Breakable Polymer Micelles
Jiang, J., Tong, X., & Zhao, Y. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0521019 · Cited by 460 · see citing works
PEG-SS-PPS: Reduction-Sensitive Disulfide Block Copolymer Vesicles for Intracellular Drug Delivery
Cerritelli, S., Velluto, D., & Hubbell, J. A. (2007) · Biomacromolecules · doi:10.1021/bm070085x · Cited by 444 · see citing works
Yin, X., Hoffman, A. S., & Stayton, P. S. (2006) · Biomacromolecules · doi:10.1021/bm0507812 · Cited by 417 · see citing works
Takae, S., Miyata, K., Oba, M., Ishii, T., Nishiyama, N., Itaka, K., Yamasaki, Y., Koyama, H., & Kataoka, K. (2008) · Journal of the American Chemical Society · doi:10.1021/ja800336v · Cited by 400 · see citing works
Synthetic Micelle Sensitive to IR Light via a Two-Photon Process
Goodwin, A. P., Mynar, J. L., Ma, Y., Fleming, G. R., & Fréchet, J. M. J. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0523035 · Cited by 352 · see citing works
An, Z., Shi, Q., Tang, W., et al. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0756974 · Cited by 341 · see citing works
Light-induced gene transfer from packaged DNA enveloped in a dendrimeric photosensitizer
Nishiyama, N., Iriyama, A., Jang, W., Miyata, K., Itaka, K., Inoue, Y., Takahashi, H., Yanagi, Y., Tamaki, Y., Koyama, H., et al. (2005) · Nature Materials · doi:10.1038/nmat1524 · Cited by 340 · see citing works
Monitoring disulfide bond formation in the eukaryotic cytosol
Østergaard, H., Tachibana, C., & Winther, J. R. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200402120 · Cited by 333 · see citing works
Ahmed, F., Pakunlu, R. I., Srinivas, G., Brannan, A. K., Bates, F. S., Klein, M. L., Minko, T., & Discher, D. E. (2006) · Molecular Pharmaceutics · doi:10.1021/mp050103u · Cited by 330 · see citing works
pH-Responsive Vesicles Based on a Hydrolytically Self-Cross-Linkable Copolymer
Du, J., & Armes, S. P. (2005) · Journal of the American Chemical Society · doi:10.1021/ja054755n · Cited by 315 · see citing works
Bulmuş, V. (2003) · Journal of Controlled Release · doi:10.1016/j.jconrel.2003.06.001 · Cited by 290 · see citing works
Synthesis of Reversible Shell Cross-Linked Micelles for Controlled Release of Bioactive Agents
Li, Y., Lokitz, B. S., Armes, S. P., & McCormick, C. L. (2006) · Macromolecules · doi:10.1021/ma0604035 · Cited by 277 · see citing works
A new approach towards acid sensitive copolymer micelles for drug delivery
Gillies, E. R., & Fréchet, J. M. J. (2003) · Chemical Communications · doi:10.1039/b304251k · Cited by 252 · see citing works
Glucose-oxidase Based Self-Destructing Polymeric Vesicles
Napoli, A., Boerakker, M. J., Tirelli, N., Nolte, R. J. M., Sommerdijk, N. A. J. M., & Hubbell, J. A. (2004) · Langmuir · doi:10.1021/la0357054 · Cited by 241 · see citing works
A New Class of Biochemically Degradable, Stimulus‐Responsive Triblock Copolymer Gelators
Li, C., Madsen, J., Armes, S. P., & Lewis, A. L. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200600324 · Cited by 236 · see citing works
Oupický, D., Parker, A. L., & Seymour, L. W. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016440n · Cited by 232 · see citing works
Crystal Design of Barium Sulfate using Double-Hydrophilic Block Copolymers
Qi, L., Cölfen, H., & Antonietti, M. (2000) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(20000204)39:3 · Cited by 226 · see citing works
Henry, S. M., ElSayed, M. E. H., Pirie, C. M., et al. (2006) · Biomacromolecules · doi:10.1021/bm060143z · Cited by 216 · see citing works
Temperature-Sensitive Dendritic Micelles
Aathimanikandan, S. V., Savariar, E. N., & Thayumanavan, S. (2005) · Journal of the American Chemical Society · doi:10.1021/ja054542y · Cited by 215 · see citing works
Self-citationJONES, R. A., Cheung, C., Black, F. E., Zia, J. K., Stayton, P. S., Hoffman, A. S., & Wilson, M. R. (2003) · Biochemical Journal · doi:10.1042/bj20021945 · Cited by 212 · see citing works
Jiang, X., Lavender, C. A., Woodcock, J. W., & Zhao, B. (2008) · Macromolecules · doi:10.1021/ma7028105 · Cited by 208 · see citing works
Tong, Z., Zeng, F., Xu, Z. G., et al. (1999) · Macromolecules · doi:10.1021/ma990062d · Cited by 205 · see citing works
Aoshima, S., & Kanaoka, S. (2007) · Advances in polymer science · doi:10.1007/12_2007_120 · Cited by 205 · see citing works
Chiu, H., Lin, Y., Huang, Y., et al. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200704078 · Cited by 202 · see citing works
Zhou, Z., Li, Z., Ren, Y. J., Hillmyer, M. A., & Lodge, T. P. (2003) · Journal of the American Chemical Society · doi:10.1021/ja036551h · Cited by 176 · see citing works
Sundararaman, A., Stephan, T., & Grubbs, R. B. (2008) · Journal of the American Chemical Society · doi:10.1021/ja8052688 · Cited by 172 · see citing works
Sweet Talking Double Hydrophilic Block Copolymer Vesicles
Pasparakis, G., & Alexander, C. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200801098 · Cited by 161 · see citing works
Seleno Compounds and Glutathione Peroxidase Catalyzed Decomposition ofS-Nitrosothiols
Hou, Y., Guo, Z., Li, J., & Wang, P. G. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.1620 · Cited by 153 · see citing works
Arimori, S., Davidson, M. G., Fyles, T. M., et al. (2004) · Chemical Communications · doi:10.1039/b404937c · Cited by 145 · see citing works
Hydrogels for site-specific oral drug delivery: synthesis and characterization
BRØNDSTED, H. V., & Kopec̆ek, J. (1991) · Biomaterials · doi:10.1016/0142-9612(91)90056-g · Cited by 141 · see citing works
Gohy, J., Antoun, S., & Jérôme, R. (2001) · Macromolecules · doi:10.1021/ma010535s · Cited by 119 · see citing works
Triggered release of hydrophilic agents from plasmologen liposomes using visible light or acid
Anderson, V. C., & Thompson, D. H. (1992) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(92)90183-m · Cited by 117 · see citing works
pH-Responsive Shell Cross-Linked Nanoparticles with Hydrolytically Labile Cross-Links
Li, Y., Du, W., Sun, G., et al. (2008) · Macromolecules · doi:10.1021/ma801737p · Cited by 106 · see citing works
Triggered release of siRNA from poly(ethylene glycol)-protected, pH-dependent liposomes
Auguste, D. T., Furman, K., WONG, A., Fuller, J. E., Armes, S. P., Deming, T. J., & Langer, R. (2008) · Journal of Controlled Release · doi:10.1016/j.jconrel.2008.06.004 · Cited by 106 · see citing works
You, Y., Zhou, Q.-H., Manickam, D. S., et al. (2007) · Macromolecules · doi:10.1021/ma071176p · Cited by 105 · see citing works
Thermally Responsive Polymer Vesicles
Morishima, Y. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200603405 · Cited by 103 · see citing works
You, Y., & Oupický, D. (2006) · Biomacromolecules · doi:10.1021/bm060635b · Cited by 101 · see citing works
Sun, K. H., Sohn, Y. S., & Jeong, B. (2006) · Biomacromolecules · doi:10.1021/bm060512r · Cited by 100 · see citing works
Persigehl, P., Jordan, R., & Nuyken, O. (2000) · Macromolecules · doi:10.1021/ma0007381 · Cited by 97 · see citing works
pH-Sensitive Polymer Nanospheres for Use as a Potential Drug Delivery Vehicle
Jung, J., Lee, I., Lee, E. H., et al. (2007) · Biomacromolecules · doi:10.1021/bm700517z · Cited by 92 · see citing works
Tunable Disassembly of Micelles Using a Redox Trigger
Ghosh, S., Irvin, K., & Thayumanavan, S. (2007) · Langmuir · doi:10.1021/la700981z · Cited by 88 · see citing works
Self-citationElSayed, M. E. H., Hoffman, A. S., & Stayton, P. S. (2005) · Journal of Controlled Release · doi:10.1016/j.jconrel.2005.01.009 · Cited by 88 · see citing works
Manickam, D. S., & Oupický, D. (2006) · Bioconjugate Chemistry · doi:10.1021/bc060104k · Cited by 88 · see citing works
pH-Sensitivity of the E3/K3 Heterodimeric Coiled Coil
Apostolovic, B., & Klok, H. (2008) · Biomacromolecules · doi:10.1021/bm800746e · Cited by 88 · see citing works
A Facile Method for the Synthesis of Cleavable Block Copolymers from ATRP-Based Homopolymers
Klaikherd, A., Ghosh, S., & Thayumanavan, S. (2007) · Macromolecules · doi:10.1021/ma071852n · Cited by 86 · see citing works
Self-citationYeh, P., Kopečková, P., & Kopeček, J. (1994) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.1994.080320904 · Cited by 79 · see citing works
Delivery of siRNA mediated by histidine-containing reducible polycations
Stevenson, M., Ramos-Perez, V., Singh, S., et al. (2008) · Journal of Controlled Release · doi:10.1016/j.jconrel.2008.05.014 · Cited by 76 · see citing works
Synthesis and Characterization of Cross-Linked Reverse Micelles
Jung, H. M., Price, K. E., & McQuade, D. T. (2003) · Journal of the American Chemical Society · doi:10.1021/ja0271983 · Cited by 75 · see citing works
Neiser, M. W., Muth, S., Kolb, U., Harris, J. R., Okuda, J., & Schmidt, M. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200353259 · Cited by 75 · see citing works
ElSayed, M. E. H., Hoffman, A. S., & Stayton, P. S. (2004) · Journal of Controlled Release · doi:10.1016/j.jconrel.2004.08.032 · Cited by 70 · see citing works
Polymer ligands that can regulate reaction temperature in “smart” catalysts
Bergbreiter, D. E., Mariagnanam, V. M., & Zhang, L. (1995) · Advanced Materials · doi:10.1002/adma.19950070116 · Cited by 44 · see citing works
Maeda, Y., Taniguchi, N., & Ikeda, I. (2001) · Macromolecular Rapid Communications · doi:10.1002/1521-3927(20011101)22:17 · Cited by 42 · see citing works
Liu, Y., Lü, J., & Shao, Y. (2006) · Macromolecular Bioscience · doi:10.1002/mabi.200600007 · Cited by 35 · see citing works
Thermally-Induced (Re)shaping of Core−Shell Nanocrystalline Particles
Zhang, Q., Clark, C. G., Wang, M., et al. (2002) · Nano Letters · doi:10.1021/nl025653n · Cited by 34 · see citing works
Self-Assembled Micelles of Amphiphilic Polysilane Block Copolymers
Sanji, T., Kitayama, F., & Sakurai, H. (1999) · Macromolecules · doi:10.1021/ma990556a · Cited by 34 · see citing works
Nonionic Surfactant-Mediated Affinity Cloud-Point Extraction of Vancomycin
Lee, C., & Su, W.-D. (1999) · Separation Science and Technology · doi:10.1081/ss-100100835 · Cited by 32 · see citing works
Arvinte, T., Bui, T. T. T., Dahab, A. A., et al. (2004) · Analytical Biochemistry · doi:10.1016/j.ab.2004.05.045 · Cited by 30 · see citing works
Postfabrication encapsulation of model protein drugs in a negatively thermosensitive hydrogel
Zhang, Y., Zhu, W. J., Wang, B., et al. (2005) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.20310 · Cited by 28 · see citing works
Boubakari, Bracht, K., Neumann, C., et al. (2004) · Archiv der Pharmazie · doi:10.1002/ardp.200400620 · Cited by 27 · see citing works
Preconcentration of Phenanthrene from Aqueous Solution by a Slightly Hydrophobic Nonionic Surfactant
Li, J., Bai, R., & Chen, B. (2004) · Langmuir · doi:10.1021/la035975m · Cited by 21 · see citing works
Säily, V. M. J., Ryhänen, S. J., Lankinen, H., et al. (2006) · Langmuir · doi:10.1021/la052398o · Cited by 19 · see citing works
Control of heme peptide activity by using phase transition polymers modified with inhibitors
Komori, K., Matsui, H., & Tatsuma, T. (2004) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2004.09.003 · Cited by 16 · see citing works
ChemInform Abstract: Supramolecular Material with Electroactive Chemical Functions.
Tew, G. N., Pralle, M. U., & Stupp, S. I. (2000) · ChemInform · doi:10.1002/chin.200016026 · Cited by 1 · see citing works
Flagged first, then by citations
Research works printed but not linked: 4
- [3](a) Okano T Bae YH Jacobs H Kim SW J. Controlled Release 1990 11 255 265 (b) Hoffman AS J. Controlled Release 1987 6 297 305 (c) Brønsdsted H Kopecek J Biomaterials 1991 12 584 592 1772957 (d) Yeh P Kopečková P Kopeček J J. Polym. Sci., Polym. Chem 1994 32 1627 1637 (e) Ganta S Devalapally H Shahiwala A Amiji M J. Controlled Release 2008 126 187 204 18261822 (f) Kataoka K Harada A Nagasaki Y Adv. Drug Delivery Rev 2001 47 113 131 11251249 (g) Rapoport N Prog. Polym. Sci 2007 32 962 990
- [11](a) Mariagnanam VM Zhang L Bergbreiter DE Adv. Mater 1995 7 69 71 (b) Komori K Matsui H Tatsuma T Bioelectrochemistry 2005 65 129 134 15713563
- [12](a) Lee C-K Su W-D Sep. Sci. Technol 1999 34 3267 3277 (b) Li J-L Bai R Chen B-H Langmuir 2004 20 6068 6070 16459631
- [21]Ostergaard H Tachibana C Winther JR J. Cell Biol 2004 166 337 345 15277542 PMC2172265
Cited by
Sorted by citations
Redox-responsive polymers for drug delivery: from molecular design to applications
Huo, M., Yuan, J., Tao, L., & Wei, Y. (2014) · Polym. Chem. · doi:10.1039/c3py01192e · Cited by 561 · see citing works
Advances in redox-responsive drug delivery systems of tumor microenvironment
Guo, X., Cheng, Y., Zhao, X., Luo, Y., Chen, J., & Yuan, W.-E. (2018) · Journal of Nanobiotechnology · doi:10.1186/s12951-018-0398-2 · Cited by 459 · see citing works
Zhang, Q., Re Ko, N., & Kwon Oh, J. (2012) · Chemical Communications · doi:10.1039/c2cc32408c · Cited by 395 · see citing works
pH-sensitive poly (histidine)-PEG/DSPE-PEG co-polymer micelles for cytosolic drug delivery
Wu, H., Zhu, L., & Torchilin, V. P. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2012.08.072 · Cited by 355 · see citing works
Bacteria‐Responsive Multifunctional Nanogel for Targeted Antibiotic Delivery
Xiong, M., Li, Y., Bao, Y., Yang, X., Hu, B., & Wang, J. (2012) · Advanced Materials · doi:10.1002/adma.201202847 · Cited by 299 · see citing works
Polymeric micelles: authoritative aspects for drug delivery
Kulthe, S. S., Choudhari, Y. M., Inamdar, N. N., & Mourya, V. (2012) · Designed Monomers and Polymers · doi:10.1080/1385772x.2012.688328 · Cited by 235 · see citing works
Enzyme Sensitive Synthetic Polymer Micelles Based on the Azobenzene Motif
Rao, J., & Khan, A. (2013) · Journal of the American Chemical Society · doi:10.1021/ja407514z · Cited by 207 · see citing works
Recent Advances in Nanomicelles Delivery Systems.
Tawfik, S. M., Azizov, S., Elmasry, M. R., Sharipov, M., & Lee, Y.-I. (2020) · Nanomaterials · doi:10.3390/nano11010070 · Cited by 156 · see citing works
“For example, the design of multi stimuli-responsive nanomicelles sensitive to redox potential, pH, and temperature was reported recently [217].”
BackgroundMultiple stimuli-responsive polymeric micelles for controlled release
Dong, J., Wang, Y., Zhang, J., Zhan, X., Zhu, S., Yang, H., & Wang, G. (2013) · Soft Matter · doi:10.1039/c2sm27116h · Cited by 116 · see citing works
Multicompartment Micelle Morphology Evolution in Degradable Miktoarm Star Terpolymers
Saito, N., Liu, C., Lodge, T. P., & Hillmyer, M. A. (2010) · ACS Nano · doi:10.1021/nn9016873 · Cited by 95 · see citing works
- Authors
- Klaikherd, A., Nagamani, C., & Thayumanavan, S.
- Affiliations
- University of Massachusetts Amherst (US)
- Corresponding author
- Thayumanavan, S.
- ORCID
- Thayumanavan, S.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2009-03-16
- Volume
- 131
- Issue
- 13
- Pages
- 4830-4838
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- PMC
- PMC2693022
- OpenAlex
- W1992741184
- Cited by
- 594
- References
- 94
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 15 · 2023: 10 · 2022: 10 · 2021: 26 · 2020: 24 · 2019: 35 · 2018: 32 · 2017: 54 · 2016: 45 · 2015: 51 · 2014: 65 · 2013: 49 · 2012: 57
- FWCI
- 24.80
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of the American Chemical Society (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- ScholarWorks@UMassAmherst (University of Massachusetts Amherst) (submittedVersion)
- Scholarworks (University of Massachusetts Amherst) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM065255)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- stimuli-responsive polymers, amphiphilic block copolymers, thermoresponsive polymers, pH-responsive polymers, redox-responsive polymers, poly(N-isopropylacrylamide), HEMA, disulfide bonds, micelles, controlled release kinetics
- MeSH terms
- Acids, Acrylamides, Acrylic Resins, Drug Carriers, Hydrogen-Ion Concentration, Kinetics, Methacrylates, Micelles, Magnetic Resonance Spectroscopy, Oxazines, Oxidation-Reduction, Polymers, Pyrans, Temperature, Water, Hydrophobic and Hydrophilic Interactions
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