Amphiphilic block copolymers for drug delivery

Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review

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Long-Circulating and Target-Specific Nanoparticles: Theory to Practice

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Vascular permeability in a human tumor xenograft: molecular size dependence and cutoff size.

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Protein—surface interactions in the presence of polyethylene oxide

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Pluronic® block copolymers as novel polymer therapeutics for drug and gene delivery

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Polymeric micelles—A new generation of colloidal drug carriers

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Advanced drug delivery devices via self-assembly of amphiphilic block copolymers

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Multidrug resistance (MDR) in cancer

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Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS

Maeda, H., Sawa, T., & Konno, T. (2001) · Journal of Controlled Release · doi:10.1016/s0168-3659(01)00309-1 · Cited by 926

Synthesis of Novel Linear PEO‐b‐PS‐b‐PCL Triblock Copolymers by the Combination of ATRP, ROP, and a Click Reaction

He, X., Liang, L., Xie, M., Zhang, Y., Lin, S., & Yan, D. (2007) · Macromolecular Chemistry and Physics · doi:10.1002/macp.200700153 · Cited by 53

Poly(ethylene oxide) (PEO)-based ABC triblock terpolymers – synthetic complexity vs. application benefits

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Micro/nanomachines: what is needed for them to become a real force in cancer therapy?

Reinišová, L., Hermanová, S., & Pumera, M. (2019) · Nanoscale · doi:10.1039/c8nr08022d · Cited by 53

Charge‐Conversion Strategies for Nucleic Acid Delivery

Dutta, K., Das, R., Medeiros, J., Kanjilal, P., & Thayumanavan, S. (2021) · Advanced Functional Materials · doi:10.1002/adfm.202011103 · Cited by 52

Folic acid-decorated PEGylated magnetite nanoparticles as efficient drug carriers to tumor cells overexpressing folic acid receptor

Movileanu, C., Anghelache, M., Turtoi, M., Voicu, G., Neacșu, I. A., Ficai, D., Trusca, R. D., Oprea, O., Ficai, A., Andronescu, E., et al. (2022) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2022.122064 · Cited by 52

Structure, Merits, Gel Formation, Gel Preparation and Functions of Konjac Glucomannan and Its Application in Aquatic Food Preservation

Sun, Y., Xu, X., Wu, Z., Zhou, H., Xie, X., Zhang, Q., Liu, R., & Pang, J. (2023) · Foods · doi:10.3390/foods12061215 · Cited by 51

Micelle-Encapsulated Thiostrepton as an Effective Nanomedicine for Inhibiting Tumor Growth and for Suppressing FOXM1 in Human Xenografts

Wang, M., & Gartel, A. L. (2011) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-11-0536 · Cited by 52

A hyperbranched amphiphilic acetal polymer for pH-sensitive drug delivery

Cao, H., Chen, C., Xie, D., Chen, X., Wang, P., Wang, Y., Song, H., & Wang, W. (2018) · Polymer Chemistry · doi:10.1039/c7py01739a · Cited by 50

Graphene/tri-block copolymer composites prepared via RAFT polymerizations for dual controlled drug delivery via pH stimulation and biodegradation

Song, Z., Xu, Y., Yang, W. R., Cui, L., Zhang, J., & Liu, J. (2015) · European Polymer Journal · doi:10.1016/j.eurpolymj.2015.02.014 · Cited by 50

Polymeric micelle nanoparticles for photodynamic treatment of head and neck cancer cells

Cohen, E. M., Ding, H., Kessinger, C. W., Khemtong, C., Gao, J., & Sumer, B. D. (2010) · Otolaryngology · doi:10.1016/j.otohns.2010.03.032 · Cited by 50

Growth, Shrinking, and Breaking of Pluronic Micelles in the Presence of Drugs and/or β-Cyclodextrin, a Study by Small-Angle Neutron Scattering and Fluorescence Spectroscopy

Valero, M., & Dreiss, C. A. (2010) · Langmuir · doi:10.1021/la100596q · Cited by 50

A novel diblock copolymer of (monomethoxy poly [ethylene glycol]-oleate) with a small hydrophobic fraction to make stable micelles/polymersomes for curcumin delivery to cancer cells

Moghadam, V. E., Nomani, A., Zamani, M., Yazdani, Y., Najafi, F., & Sadeghizadeh, M. (2014) · International Journal of Nanomedicine · doi:10.2147/ijn.s63762 · Cited by 51

Preparation, characterization, and evaluation of amphotericin B-loaded MPEG-PCL-g-PEI micelles for local treatment of oral Candida albicans

Zhou, L., Zhang, P., Chen, Z., Cai, S., Jing, T., Fan, H., Mo, F., Zhang, J., & Lin, R. (2017) · International Journal of Nanomedicine · doi:10.2147/ijn.s124264 · Cited by 50

Polymeric Nanomaterials

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Amphiphilic Poly( l -lactide)-b-dendritic Poly( l -lysine)s Synthesized with A Metal-Free Catalyst and New Dendron Initiators: Chemical Preparation and Characterization

Yang, L., Li, Q., Li, F., Zhang, H., Jia, L., Yu, J., Fang, Q., & 曹阿民 (2005) · Biomacromolecules · doi:10.1021/bm050602g · Cited by 52

Synthesis, reactivity, and pH-responsive assembly of new double hydrophilic block copolymers of carboxymethyldextran and poly(ethylene glycol)

Hernandez, O. S., Soliman, G. M., & Winnik, F. M. (2006) · Polymer · doi:10.1016/j.polymer.2006.12.036 · Cited by 50

Clinical Applications of Targeted Nanomaterials

Kumar, A., Shahvej, S., Yadav, P. K., Modi, U., Yadav, A. K., Solanki, R., & Bhatia, D. D. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17030379 · Cited by 53

Anionic poly (lactic acid)-polyurethane micelles as potential biodegradable drug delivery carriers

Zhang, J., Wu, M., Yang, J., Wu, Q., & Jin, Z. (2008) · Colloids and Surfaces A Physicochemical and Engineering Aspects · doi:10.1016/j.colsurfa.2008.12.025 · Cited by 49

Current taxane formulations and emerging cabazitaxel delivery systems

Sun, B., Straubinger, R. M., & Lovell, J. F. (2018) · Nano Research · doi:10.1007/s12274-018-2171-0 · Cited by 50

Mitochondria-targeting self-assembled nanoparticles derived from triphenylphosphonium-conjugated cyanostilbene enable site-specific imaging and anticancer drug delivery

Kim, K. Y., Jin, H., Park, J. H., Jung, S. H., Lee, J. H., Park, H., Kim, S. K., Bae, J., & Jung, J. H. (2017) · Nano Research · doi:10.1007/s12274-017-1728-7 · Cited by 49

KE108-conjugated unimolecular micelles loaded with a novel HDAC inhibitor thailandepsin-A for targeted neuroendocrine cancer therapy

Chen, G., Jaskula‐Sztul, R., Harrison, A. D., Dammalapati, A., Xu, W., Cheng, Y., Chen, H., & Gong, S. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.04.029 · Cited by 48

Poly(methyl methacrylate)−Poly(caprolactone) AB and ABA Block Copolymers by Combined Ring-Opening Polymerization and Atom Transfer Radical Polymerization

Schappacher, M., Fur, N. L., & Guillaume, S. M. (2007) · Macromolecules · doi:10.1021/ma070417q · Cited by 47

Physical Confinement Impacts Cellular Phenotypes within Living Materials

Priks, H., Butelmann, T., Illarionov, A., Johnston, T. G., Fellin, C. R., Tamm, T., Nelson, A., Kumar, R., & Lahtvee, P. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c00335 · Cited by 47

EGFP-EGF1 protein-conjugated PEG–PLA nanoparticles for tissue factor targeted drug delivery

Mei, H., Shi, W., Pang, Z., Wang, H., Lu, W., Jiang, X., Deng, J., Guo, T., & Hu, Y. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.03.055 · Cited by 46

Soybean β-Conglycinin Nanoparticles for delivery of hydrophobic nutraceuticals

Levinson, Y., Israeli-Lev, G., & Livney, Y. D. (2014) · Food Biophysics · doi:10.1007/s11483-014-9341-8 · Cited by 47

Smart triblock dendritic unimolecular micelles as pioneering nanomaterials: Advancement pertaining to architecture and biomedical applications

Tambe, P., Kumar, P., Paknikar, K. M., & Gajbhiye, V. (2019) · Journal of Controlled Release · doi:10.1016/j.jconrel.2019.02.026 · Cited by 46

Self-Assembly of Soluplus in Aqueous Solutions: Characterization and Prospectives on Perfume Encapsulation

Sofroniou, C., Baglioni, M., Mamusa, M., Resta, C., Doutch, J., Smets, J., & Baglioni, P. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c01087 · Cited by 46

Current development of cabazitaxel drug delivery systems

Sun, B., Lovell, J. F., & Zhang, Y. (2022) · Wiley Interdisciplinary Reviews Nanomedicine and Nanobiotechnology · doi:10.1002/wnan.1854 · Cited by 45

Polymer Micelle Formulations of Proteasome Inhibitor Carfilzomib for Improved Metabolic Stability and Anticancer Efficacy in Human Multiple Myeloma and Lung Cancer Cell Lines

Ao, L., Reichel, D., Hu, D., Jeong, H., Kim, K. B., Bae, Y., & Lee, W. (2015) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.115.226993 · Cited by 46

Dual Stimuli-Responsive Polymer Prodrugs Quantitatively Loaded by Nanoparticles for Enhanced Cellular Internalization and Triggered Drug Release

Huang, M., Zhao, K., Wang, L., Lin, S., Li, J., Chen, J., Zhao, C., & Ge, Z. (2016) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5b12227 · Cited by 45

Inducing angiogenesis with the controlled release of nitric oxide from biodegradable and biocompatible copolymeric nanoparticles

Yang, C., Hwang, H. H., Jeong, S., Seo, D., Jeong, Y., Lee, D. Y., & Lee, K. (2018) · International Journal of Nanomedicine · doi:10.2147/ijn.s174989 · Cited by 45

Nano drug delivery systems in upper gastrointestinal cancer therapy

Salapa, J., Bushman, A., Lowe, K., & Irudayaraj, J. (2020) · Nano Convergence · doi:10.1186/s40580-020-00247-2 · Cited by 45

Thermoreversible Micelle Formation Using a Three-Armed Star Elastin-like Polypeptide

Ghoorchian, A., Cole, J. T., & Holland, N. B. (2010) · Macromolecules · doi:10.1021/ma100285v · Cited by 44

Biodegradable Micelles Capable of Mannose‐Mediated Targeted Drug Delivery to Cancer Cells

Yin, L., Chen, Y., Zhang, Z., Yin, Q., Zheng, N., & Cheng, J. (2015) · Macromolecular Rapid Communications · doi:10.1002/marc.201400650 · Cited by 44

Self-assembled mPEG–PCL-g–PEI micelles for simultaneous codelivery of chemotherapeutic drugs and DNA: synthesis and characterization in vitro

Qian, Z. (2012) · International Journal of Nanomedicine · doi:10.2147/ijn.s28932 · Cited by 44

Polymers and hydrogels for local nucleic acid delivery

Fliervoet, L. A. L., Engbersen, J. F. J., Schiffelers, R. M., Hennink, W. E., & Vermonden, T. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb01795f · Cited by 44

Structural and therapeutic properties of Pluronic® P123/F127 micellar systems and their modulation by salt and essential oil

Ganguly, R., Kumar, S., Tripathi, A., Basu, M., Verma, G., Sarma, H. D., Chaudhari, D., Aswal, V. K., & Melo, J. S. (2020) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2020.113231 · Cited by 47

Photocontrollable release and enhancement of photodynamic therapy based on host–guest supramolecular amphiphiles

Xu, L., Zhang, W., Cai, H., Liu, F., Wang, Y., Gao, Y., & Zhang, W. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb01363a · Cited by 43

Radiolabeling polymeric micelles for in vivo evaluation: a novel, fast, and facile method

Laan, A. C., Santini, C., Jennings, L., de Jong, M., Bernsen, M. R., & Denkova, A. G. (2016) · EJNMMI Research · doi:10.1186/s13550-016-0167-x · Cited by 44

Types of Nanomaterials and Corresponding Methods of Synthesis

Aguilar, Z. P. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-385089-8.00002-9 · Cited by 47

Synthesis and characterization of polyion complex micelles between poly(ethylene glycol)-grafted poly(aspartic acid) and cetyltrimethyl ammonium bromide

Chen, W., Chen, H., Hu, J., Yang, W., & Wang, C. (2006) · Colloids and Surfaces A Physicochemical and Engineering Aspects · doi:10.1016/j.colsurfa.2005.11.084 · Cited by 43

Activatable Cell Penetrating Peptide-Conjugated Nanoparticles with Enhanced Permeability for Site-Specific Targeting Delivery of Anticancer Drug

Xia, H., Gu, G., Hu, Q., Liu, Z., Jiang, M., Kang, T., Miao, D., Song, Q., Yao, L., Tu, Y., et al. (2013) · Bioconjugate Chemistry · doi:10.1021/bc300520t · Cited by 43

Acetals moiety contained pH-sensitive amphiphilic copolymer self-assembly used for drug carrier

Lu, J., Li, N., Xu, Q., Ge, J., Lu, J., & Xia, X. (2010) · Polymer · doi:10.1016/j.polymer.2009.12.034 · Cited by 42

Montmorillonite-PLGA nanocomposites as an oral extended drug delivery vehicle for venlafaxine hydrochloride

Jain, S., & Datta, M. (2014) · Applied Clay Science · doi:10.1016/j.clay.2014.06.006 · Cited by 42

Structural changes in block copolymer micelles induced by cosolvent mixtures

Kelley, E. G., Smart, T. P., Jackson, A., Sullivan, M. O., & Epps, T. H. I. (2011) · Soft Matter · doi:10.1039/c1sm05506b · Cited by 44

Characterization and application of mixed micellar assemblies of PEO-PPO star block copolymers for solubilization of hydrophobic anticancer drug and in vitro release

Pillai, S. A., Sharma, A. K., Desai, S. M., Sheth, U. V., Bahadur, A., Ray, D., Aswal, V. K., & Kumar, S. (2020) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2020.113543 · Cited by 41

Polymer-based nanocarriers to transport therapeutic biomacromolecules across the blood-brain barrier

Romero‐Ben, E., Goswami, U., Soto-Cruz, J., Mansoori-Kermani, A., Mishra, D., Martín‐Saldaña, S., Ugartemendia, J. M., Sosnik, A., Calderón, M., Beloqui, A., et al. (2025) · Acta Biomaterialia · doi:10.1016/j.actbio.2025.02.065 · Cited by 48

A coarse-grained model for polyethylene glycol polymer

Wang, Q., Keffer, D. J., & Nicholson, D. M. (2011) · The Journal of Chemical Physics · doi:10.1063/1.3664623 · Cited by 40

Combination antitumor effects of micelle-loaded anticancer drugs in a CT-26 murine colorectal carcinoma model

Na, H. S., Lim, Y. K., Jeong, Y., Lee, H. S., Lim, Y. J., Kang, M., Cho, C., & Lee, H. C. (2009) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2009.08.041 · Cited by 41

pH-Responsive Aggregates from Double Hydrophilic Block Copolymers Carrying Zwitterionic Groups. Encapsulation of Antiparasitic Compounds for the Treatment of Leishmaniasis

Karanikolopoulos, N., Pitsikalis, M., Hadjichristidis, N., Georgikopoulou, K., Calogeropoulou, T., & Dunlap, J. R. (2007) · Langmuir · doi:10.1021/la0628827 · Cited by 42

Synthesis and self‐assembling of poly(N‐isopropylacrylamide‐block‐poly( L ‐lactide)‐block‐poly(N‐isopropylacrylamide) triblock copolymers prepared by combination of ring‐opening polymerization and atom transfer radical polymerization

Hu, Y., Darcos, V., Monge, S., & Li, S. (2013) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.26721 · Cited by 41

Etoposide-loaded biodegradable amphiphilic methoxy (poly ethylene glycol) and poly (epsilon caprolactone) copolymeric micelles as drug delivery vehicle for cancer therapy

Mohanty, A. K., Dilnawaz, F., Mohanty, C., & Sahoo, S. K. (2010) · Drug Delivery · doi:10.3109/10717541003720688 · Cited by 41

Size effects of self-assembled block copolymer spherical micelles and vesicles on cellular uptake in human colon carcinoma cells

Chang, T., Lord, M. S., Bergmann, B., Macmillan, A., & Stenzel, M. H. (2014) · Journal of Materials Chemistry B · doi:10.1039/c3tb21751e · Cited by 38

Recombinant Amphiphilic Protein Micelles for Drug Delivery

Kim, W., Xiao, J., & Chaikof, E. L. (2011) · Langmuir · doi:10.1021/la202864x · Cited by 40

Polysorbate 80 and Cremophor EL Micelles Deaggregate and Solubilize Nystatin at the Core–Corona Interface

Croy, S., & Kwon, G. S. (2005) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.20301 · Cited by 40

Functionalization of nanoparticles in specific targeting and mechanism release

Adamo, G., Campora, S., & Ghersi, G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-46142-9.00003-7 · Cited by 43

Development and characterization of morin hydrate-loaded micellar nanocarriers for the effective management of Alzheimer’s disease

Singh, M., Thakur, V. R., Deshmukh, R. R., Sharma, A., Rathore, M. S., Kumar, A., & Mishra, N. (2018) · Journal of Microencapsulation · doi:10.1080/02652048.2018.1441916 · Cited by 40

Amphiphilic PEG/alkyl‐grafted comb polylactides

Jiang, X., Vogel, E. B., Smith, M. R., & Baker, G. L. (2007) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.22268 · Cited by 40

Bioimaging guided pharmaceutical evaluations of nanomedicines for clinical translations

Tuguntaev, R. G., Hussain, A., Fu, C., Chen, H., Tao, Y., Huang, Y. H., Liu, L., Liang, X., & Guo, W. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01451-4 · Cited by 41

A Hybrid Silica Nanoreactor Framework for Encapsulation of Hollow Manganese Oxide Nanoparticles of Superior T1 Magnetic Resonance Relaxivity

Hsu, B. Y. W., Ng, M., Zhang, Y., Wong, S. Y., Bhakoo, K. K., Li, X., & Wang, J. (2015) · Advanced Functional Materials · doi:10.1002/adfm.201501269 · Cited by 39

Effects of amphiphilic PCL–PEG–PCL copolymer addition on 5-fluorouracil release from biodegradable PCL films for stent application

Lu, F., Lei, L., Shen, Y., Hou, J., Chen, W., Li, Y., & Guo, S. (2011) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2011.07.020 · Cited by 39

Polymeric‐Micelle‐Based Nanomedicine for siRNA Delivery

Liu, X., Sun, C., Yang, X., & Wang, J. (2013) · Particle & Particle Systems Characterization · doi:10.1002/ppsc.201200061 · Cited by 39

Intracellular Guest Exchange between Dynamic Supramolecular Hosts

Swaminathan, S., Fowley, C., McCaughan, B., Cusido, J., Callan, J. F., & Raymo, F. M. (2014) · Journal of the American Chemical Society · doi:10.1021/ja500285p · Cited by 39

An experimental rheological phase diagram of a tri-block co-polymer in water validated against dissipative particle dynamics simulations

Pasquino, R., Droghetti, H., Carbone, P., Mirzaagha, S., Grizzuti, N., & Marchisio, D. L. (2019) · Soft Matter · doi:10.1039/c8sm01959b · Cited by 40

Polymeric micelles based on poly(ethylene oxide) and α-carbon substituted poly(ɛ-caprolactone): An in vitro study on the effect of core forming block on polymeric micellar stability, biocompatibility, and immunogenicity

Garg, S. M., Vakili, M. R., & Lavasanifar, A. (2015) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2015.05.015 · Cited by 38

Characterization of polyoxyalkylene block copolymers by combination of different chromatographic techniques and MALDI-TOF-MS

Malik, M. I., Trathnigg, B., Bartl, K., & Saf, R. (2009) · Analytica Chimica Acta · doi:10.1016/j.aca.2009.11.017 · Cited by 38

Micelles from Amphiphilic Block Copolyphosphates for Drug Delivery

Zhai, X., Huang, W., Liu, J., Pang, Y., Zhu, X., Zhou, Y., & Yan, D. (2011) · Macromolecular Bioscience · doi:10.1002/mabi.201100163 · Cited by 38

Micelles with surface conjugated RGDpeptide and crosslinked polyurea core viaRAFT polymerization

Duong, H. T. T., Nguyen, T., & Stenzel, M. H. (2009) · Polymer Chemistry · doi:10.1039/b9py00210c · Cited by 40

Comparison of surfactants at solubilizing, forming and stabilizing nanoemulsion of hesperidin

Liao, Y., Zhong, L., Liu, L., Xie, L., Tang, H., Zhang, L., & Li, X. (2020) · Journal of Food Engineering · doi:10.1016/j.jfoodeng.2020.110000 · Cited by 38

Novel Pentablock Copolymers as Thermosensitive Self-Assembling Micelles for Ocular Drug Delivery

Alami-Milani, M., Zakeri‐Milani, P., Valizadeh, H., Salehi, R., Salatin, S., Naderinia, A., & Jelvehgari, M. (2017) · Advanced Pharmaceutical Bulletin · doi:10.15171/apb.2017.003 · Cited by 38

Use of Degradable and Nondegradable Nanomaterials for Controlled Release

Khairunizam, W., Yang, L., & Padavan, D. T. (2007) · Nanomedicine · doi:10.2217/17435889.2.4.483 · Cited by 39

Bioinspired core‐crosslinked micelles from thymine‐functionalized amphiphilic block copolymers: Hydrogen bonding and photo‐crosslinking study

Kaur, G., Chang, S. L. Y., Bell, T. D. M., Hearn, M. T. W., & Saito, K. (2011) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.24853 · Cited by 37

Amphiphilic block copolymers featuring a reversible hetero Diels-Alder linkage

Langer, M., Brandt, J., Lederer, A., Goldmann, A. S., Schacher, F. H., & Barner‐Kowollik, C. (2014) · Polymer Chemistry · doi:10.1039/c4py00644e · Cited by 37

Molecular dynamics study on the interaction between doxorubicin and hydrophobically modified chitosan oligosaccharide

Shan, P., Shen, J., Xu, D., Shi, L., Gao, J., Lan, Y.-W., Wang, Q., & Wei, X.-H. (2014) · RSC Advances · doi:10.1039/c4ra01199f · Cited by 37

Dual redox-triggered shell-sheddable micelles self-assembled from mPEGylated starch conjugates for rapid drug release

Chen, M., Gao, C., Lü, S., Chen, Y., & Liu, M. (2016) · RSC Advances · doi:10.1039/c5ra23618e · Cited by 37

Interactions of Pluronic nanocarriers with 2D and 3D cell cultures: Effects of PEO block length and aggregation state

Arranja, A., Denkova, A. G., Morawska, K., Waton, G., Vlierberghe, S. V., Dubruel, P., Schosseler, F., & Mendes, E. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.01.014 · Cited by 37

Functional nanostructured materials based on self-assembly of block copolymers

Bai, W., & Ross, C. A. (2016) · MRS Bulletin · doi:10.1557/mrs.2016.1 · Cited by 36

Tailoring Polymersome Bilayer Permeability Improves Enhanced Permeability and Retention Effect for Bioimaging

Lai, M.-H., Lee, S., Smith, C. E., Kim, K., & Kong, H. (2014) · ACS Applied Materials & Interfaces · doi:10.1021/am502822n · Cited by 39

Drug loading and release kinetics in polymeric micelles: Comparing dynamic versus unimolecular sugar-based micelles for controlled release

Tao, L., Chan, J. W., & Uhrich, K. E. (2015) · Journal of Bioactive and Compatible Polymers · doi:10.1177/0883911515609814 · Cited by 40

Nanoparticles for cosmetic use and its application

Chiari‐Andréo, B. G., de Almeida-Cincotto, M. G. J., Oshiro, J. A., Taniguchi, C. Y. Y., Chiavacci, L. A., & Isaac, V. L. B. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816504-1.00013-2 · Cited by 38

NIR Light‐Induced ATRP for Synthesis of Block Copolymers Comprising UV‐Absorbing Moieties

Kütahya, C., Meckbach, N., Strehmel, V., Gutmann, J. S., & Strehmel, B. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202001099 · Cited by 37

New poly(lactic-co-glycolic acid) derivatives: Modular polymers with tailored properties

Dailey, L. A., & Kissel, T. (2005) · Drug Discovery Today Technologies · doi:10.1016/j.ddtec.2005.05.017 · Cited by 37

Behavior of a Styrene Oxide−Ethylene Oxide Diblock Copolymer/Surfactant System: A Thermodynamic and Spectroscopy Study

de Castro, E. D. M., Taboada, P., & Mosquera, V. (2005) · The Journal of Physical Chemistry B · doi:10.1021/jp044766n · Cited by 37

Synthesis and Self-Aggregation of Poly(2-ethyl-2-oxazoline)-Based Photocleavable Block Copolymer: Micelle, Compound Micelle, Reverse Micelle, and Dye Encapsulation/Release

Jana, S., Saha, A., Paira, T. K., & Mandal, T. K. (2016) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.5b10019 · Cited by 37

Zwitterionic Polyester-Based Nanoparticles with Tunable Size, Polymer Molecular Weight, and Degradation Time

Palmiero, U. C., Maraldi, M., Manfredini, N., & Moscatelli, D. (2018) · Biomacromolecules · doi:10.1021/acs.biomac.8b00127 · Cited by 36

Photo‐ and pH‐Responsive Polycarbonate Block Copolymer Prodrug Nanomicelles for Controlled Release of Doxorubicin

Kalva, N., Uthaman, S., Augustine, R., Jeon, S. H., Huh, K. M., Park, I., & Kim, I. (2020) · Macromolecular Bioscience · doi:10.1002/mabi.202000118 · Cited by 36

Structure and Interactions in Micellar Solutions: Molecular Simulations of Pluronic L64 Aqueous Solutions

Bedrov, D., Smith, G. D., & Yoon, J. (2007) · Langmuir · doi:10.1021/la700742z · Cited by 36

Micelles based on amphiphilic PCL‐PEO triblock and star‐shaped diblock copolymers: Potential in drug delivery applications

Quaglia, F., Ostacolo, L., Nese, G., Canciello, M., Rosa, G. D., Ungaro, F., Palumbo, R., Rotonda, M. I. L., & Maglio, G. (2008) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31804 · Cited by 36

Characterization of self-assembling copolymers in aqueous solutions using Electron Paramagnetic Resonance and Fluorescence spectroscopy

Beghein, N., Rouxhet, L., Dinguizli, M., Brewster, M. E., Ariën, A., Véronique Préat, A., Habib, J.-L., & Gallez, B. (2006) · Journal of Controlled Release · doi:10.1016/j.jconrel.2006.10.028 · Cited by 36

Spontaneous Self‐Assembly and Micellization of Random Copolymers in Organic Solvents

Sadeghi, I., & Asatekin, A. (2017) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201700226 · Cited by 36

Bioderived Lipoic Acid-Based Dynamic Covalent Nanonetworks of Poly(disulfide)s: Enhanced Encapsulation Stability and Cancer Cell-Selective Delivery of Drugs

Mondal, A. K., Das, S., Ali, S. M., Kolay, S., Sengupta, A., & Molla, M. R. (2023) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.2c00493 · Cited by 35

Molecular Insights on Morphology, Composition, and Stability of Mixed Micelles Formed by Ionic Surfactant and Nonionic Block Copolymer in Water Using Coarse-Grained Molecular Dynamics Simulations

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Cellulose ether derivatives: a new platform for prodrug formation of fluoroquinolone antibiotics

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PLMA‐b‐POEGMA amphiphilic block copolymers: Synthesis and self‐assembly in aqueous media

Skandalis, A., & Pispas, S. (2016) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.28379 · Cited by 35

In-vitro cytotoxic activities of poly(2-ethyl-2-oxazoline)-based amphiphilic block copolymers prepared by CuAAC click chemistry

Gülyüz, S., Özköse, U. U., Koçak, P., Telci, D., Yılmaz, Ö., & Taşdelen, M. A. (2017) · eXPRESS Polymer Letters · doi:10.3144/expresspolymlett.2018.13 · Cited by 35

Thymol polymeric nanoparticle synthesis and its effects on the toxicity of high glucose on OEC cells: involvement of growth factors and integrin-linked kinase

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DNA-functionalised blend micelles: mix and fix polymeric hybrid nanostructures

Kwak, M., Musser, A. J., Lee, J., & Herrmann, A. P. (2010) · Chemical Communications · doi:10.1039/c0cc00855a · Cited by 35

Thermo- and pH-Responsive Copolymers Bearing Cholic Acid and Oligo(ethylene glycol) Pendants: Self-Assembly and pH-Controlled Release

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Tunable thermo-responsive P(NIPAAm-co-DMAAm)-b-PLLA-b-P(NIPAAm-co-DMAAm) triblock copolymer micelles as drug carriers

Hu, Y., Darcos, V., Monge, S., Li, S., Zhou, Y., & Su, F. (2014) · Journal of Materials Chemistry B · doi:10.1039/c3tb21793k · Cited by 34

Self-assemblies of the six-armed star triblock ABC copolymer: pH-tunable morphologies and drug release

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Significance of Amphiphilic Block Copolymer Micelles and its Characteristics

Joshi, T. (2017) · International Journal of Trend in Scientific Research and Development · doi:10.31142/ijtsrd2316 · Cited by 2

Amphiphilic block copolymer micelles for nanoscale drug delivery

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Amphiphilic Block Copolymer Based Nanocarriers for Drug and Gene Delivery

Xiong, X.-B., & Lavasanifar, A. (2011) · Fundamental biomedical technologies · doi:10.1007/978-94-007-1248-5_10 · Cited by 5

Engineering of amphiphilic block copolymers for polymeric micellar drug and gene delivery

Xiong, X.-B., Falamarzian, A., Garg, S. M., & Lavasanifar, A. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.04.028 · Cited by 271

ABC Micelles for Drug Delivery — Nanoscopic Vehicles for Potent Yet Toxic and Poorly Water-Soluble Compounds

Kwon, G. S. (2006) · International Conference on MEMS, NANO, and Smart Systems · doi:10.1109/icmens.2004.1508913