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Polymeric Micelles for Delivery of Poorly Water-Soluble Compounds
Abstract
Amphiphilic polymers assemble into nanoscopic supramolecular core-shell structures, termed polymeric micelles, which are under extensive study for drug delivery. There are several reasons for this growing interest. Polymeric micelles maybe safe for parenteral administration relative to existing solubilizing agents (for instance, Cremophor EL), permitting an increase in the dose of potent yet toxic and poorly water soluble compounds. Polymeric micelles solubilize important poorly water-soluble compounds, such as amphotericin B (AmB), propofol, paclitaxel, and photosensitizers. A major factor in drug solubilization is the compatibility of a drug and a core of a polymeric micelle. In this context, we may consider Pluronics, poly(ethylene glycol) (PEG)-phospholipid conjugates, PEG-b-poly(ester)s, and PEG-b-poly(L-amino acid)s for drug delivery. Polymeric micelles may circulate for prolonged periods in blood, evade host defenses, and gradually release drug. Thus, they may show a preferential accumulation at sites of disease such as solid tumors. Polymeric micelles inhibit p-glycoprotein at drug-resistant tumors, gastrointestinal tract, and blood/brain barrier, perhaps providing a way to overcome drug resistance in cancer and increase drug absorption from the gut and drug absorption into the brain. Lastly, polymeric micelles may reduce the self-aggregation of polyene antibiotics, key membrane-acting drugs used to combat life-threatening systemic fungal diseases. In this way, they may reduce its dose-limiting toxicity without a loss of antifungal activity.
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“The major benefit of polyester over other polymers is that a wide range of polyesters was approved for biomedical usage, such as poly(lactic acid) (PLA), poly(ε-caprolactone) (PCL), poly(propylene oxide) (PPO), poly(trimethylene carbonate) (PTMC), and poly(lactic-co-glycolic acid) (PLGA) [69].”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [69]
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Items 201–300 of 502
Organometallic polymeric carriers for redox triggered release of molecular payloads
Jańczewski, D., Song, J. C., Csányi, E., Kiss, L., Blazsó, P., Katona, R. L., Deli, M. A., Gros, G., Xu, J., & Vancso, G. J. (2012) · Journal of Materials Chemistry · doi:10.1039/c2jm15755a · Cited by 41
Preparation of Propolis Nanofood and Application to Human Cancer
Kim, D.-M., Lee, G., Aum, S.-H., & Kim, H. (2008) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.31.1704 · Cited by 41
RetractedPillai, 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
Nanoparticles Based on Modified Polysaccharides
Namazi, H., Fathi, F., & Heydari, A. (2012) · InTech eBooks · doi:10.5772/34795 · Cited by 42
“Starch, chitosan, dextran, cyclodextrin, cellulose and pullulan are polysaccharides that have been modified with various reactants and after the modification step the nanoparticles based on modified polysaccharides were prepared with using various methods (Onyuksel et al., 2003; Aumelas et al., 2007; Ragauskas et al.,…”
MethodZhang, Y., Wang, X., Wang, J., Zhang, X., & Zhang, Q. (2011) · Pharmaceutical Research · doi:10.1007/s11095-011-0381-1 · Cited by 40
“Micelles are widely used as nanocarriers because of their efficacy in encapsulating a large amount of hydrophobic drugs within the inner core, their stability in the blood circulation and their ability to gradually release the loaded drugs (8).”
BackgroundLiu, G., Li, M., Zhu, C., Jin, Q., Zhang, Z., & Ji, J. (2014) · Macromolecular Bioscience · doi:10.1002/mabi.201400162 · Cited by 41
Cao, Y., Liu, M., Zhang, K., Zu, G., Kuang, Y., Tong, X., Xiong, D., & Pei, R. (2016) · Biomacromolecules · doi:10.1021/acs.biomac.6b01437 · Cited by 39
Mahdaviani, P., Bahadorikhalili, S., Nigjeh, M. N., et al. (2017) · Materials Science and Engineering C · doi:10.1016/j.msec.2017.05.126 · Cited by 39
Bobde, Y., Biswas, S., & Ghosh, B. (2020) · Reactive and Functional Polymers · doi:10.1016/j.reactfunctpolym.2020.104561 · Cited by 40
Richter, A., Olbrich, C., Krause, M., & Kissel, T. (2010) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2010.01.032 · Cited by 38
Kaneo, Y., Taguchi, K., Tanaka, T., et al. (2014) · Journal of Drug Delivery Science and Technology · doi:10.1016/s1773-2247(14)50072-x · Cited by 38
Nanoassembled Capsules as Delivery Vehicles for Large Payloads of High Relaxivity Gd3+ Agents
Plush, S. E., Woods, M., Zhou, Y.-F., Kadali, S. B., Wong, M. S., & Sherry, A. D. (2009) · Journal of the American Chemical Society · doi:10.1021/ja906981w · Cited by 39
ten Cate, M. G. J., & Börner, H. G. (2007) · Macromolecular Chemistry and Physics · doi:10.1002/macp.200600666 · Cited by 40
Bioconjugates to specifically render inhibitorswater-soluble
Hirsch, A. K. H., Diederich, F., Antonietti, M., & Börner, H. G. (2009) · Soft Matter · doi:10.1039/b915928b · Cited by 38
Li, Y., Zhang, X., Zhu, J., Cheng, H. L., Cheng, S., & Zhuo, R. ‐. (2007) · Nanotechnology · doi:10.1088/0957-4484/18/21/215605 · Cited by 38
Kardys, A. Y., Bharali, D. J., & Mousa, S. A. (2013) · Journal of Nanotechnology · doi:10.1155/2013/768724 · Cited by 38
Barros, S. D. M., Whitaker, S. K., Sukthankar, P., Avila, L. A., Gudlur, S., Warner, M., Beltrão, E. I. C., & Tomich, J. M. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2016.02.027 · Cited by 41
“In most micellar assemblies, the molecular weight of PEG tends to exceed that of the hydrophobic coreforming block [73].”
He, Q., Gao, Y., Zhang, L., et al. (2011) · Journal of Materials Chemistry · doi:10.1039/c1jm13598h · Cited by 37
Tao, L., Chan, J. W., & Uhrich, K. E. (2015) · Journal of Bioactive and Compatible Polymers · doi:10.1177/0883911515609814 · Cited by 40
Lamch, Ł., Kulbacka, J., Dubińska–Magiera, M., Saczko, J., & Wilk, K. A. (2019) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2019.02.014 · Cited by 37
Kim, S. C., Yoon, H. J., Lee, J. W., Yu, J.-W., Park, E., & Chi, S. (2005) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2005.01.011 · Cited by 37
PLGA-PEG-RA-based polymeric micelles for tumor targeted delivery of irinotecan
Emami, J., Maghzi, P., Hasanzadeh, F., Sadeghi, H., Mirian, M., & Rostami, M. (2018) · Pharmaceutical Development and Technology · doi:10.1080/10837450.2017.1340950 · Cited by 36
Tang, L., Jin, J., Zhang, S., Mao, Y., Sun, J. Z., Yuan, W. Z., Zhao, H., Xu, H., Qin, A., & Tang, B. Z. (2009) · Science China Chemistry · doi:10.1007/s11426-009-0119-7 · Cited by 36
Enhanced in vivo antitumor efficacy of fenretinide encapsulated in polymeric micelles
Okuda, T., Kawakami, S., Higuchi, Y., Satoh, T., Oka, Y., Yokoyama, M., Yamashita, F., & Hashida, M. (2009) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2009.01.019 · Cited by 36
Sharma, R., Yadav, V. R., Jha, S., Dighe, S., & Jain, S. (2024) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2024.122196 · Cited by 37
Self‐Assembled Micelles Based on PEG‐Polypeptide Hybrid Copolymers for Drug Delivery
Hua, S., Li, Y., Liu, Y., Xiao, W., Li, C., Huang, F., Zhang, X., & Zhuo, R. (2009) · Macromolecular Rapid Communications · doi:10.1002/marc.200900473 · Cited by 36
Richter, A., Olbrich, C., Krause, M., Hoffmann, J., & Kissel, T. (2010) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2010.02.010 · Cited by 35
Podduturi, V. P., Magaña, I. B., O’Neal, D. P., et al. (2013) · Computer Methods and Programs in Biomedicine · doi:10.1016/j.cmpb.2013.06.011 · Cited by 35
“lthough particle size is a factor in delivery and aggregation ill lead to much larger particles, NP aggregates formed within he body are quickly removed from the blood circulation by the iver and spleen [45,46].”
BackgroundIn vivo evaluation of novel chitosan graft polymeric micelles for delivery of paclitaxel
Liu, J., Li, H., Chen, D., Jin, X., Zhao, X., Zhang, C., & Ping, Q. N. (2010) · Drug Delivery · doi:10.3109/10717544.2010.520355 · Cited by 34
“In our research, a considerable amount of PTX in micelle accumulated in kidney, which was a nonRES organ, suggesting that it may be the increased kidney elimination of micelle.”
BackgroundInfluentialTănase, M. A., Soare, A. C., Diţu, L.-M., et al. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14102137 · Cited by 33
“Pluronics® micelles have been extensively studied as carriers for many antitumoral drugs [13] as well as for antimicrobial substances [14].”
BackgroundCai, L., Qiu, N., Li, X., Luo, K., Chen, X., Yang, L., He, G., Wei, Y., & Chen, L. (2011) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2011.01.042 · Cited by 33
Bawazir, W. A., Al-Mahmood, M. A., Almalki, R. S., et al. (2023) · Arabian Journal of Chemistry · doi:10.1016/j.arabjc.2023.105436 · Cited by 32
Lila, A. S. A., Kiwada, H., & Ishida, T. (2014) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b13-00540 · Cited by 34
Lamch, Ł., Tylus, W., Jewgiński, M., Latajka, R., & Wilk, K. A. (2016) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.6b10267 · Cited by 32
Dimchevska, S., Geškovski, N., Koliqi, R., Matevska-Geshkovska, N., Gómez‐Vallejo, V., Szczupak, B., Sebastian, E. S., Llop, J., Hristov, D. R., Monopoli, M. P., et al. (2017) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2017.05.054 · Cited by 32
Polymeric Micelles as Drug Delivery System: Recent Advances, Approaches, Applications and Patents
Jain, A., Bhardwaj, K., & Bansal, M. (2023) · Current Drug Safety · doi:10.2174/1574886318666230605120433 · Cited by 36
Nastruzzi, C., Capretto, Mazzitelli, Brognara, Lampronti, Carugo, Hill, M., Zhang, X., & Gambari, R. (2012) · International Journal of Nanomedicine · doi:10.2147/ijn.s25657 · Cited by 31
Polymeric Micelles for the Delivery of Poorly Soluble Drugs
Biswas, S., Vaze, O. S., Movassaghian, S., & Torchilin, V. P. (2013) · Wiley eBooks · doi:10.1002/9781118444726.ch14 · Cited by 37
“As the concentration of the surfactant drops below the CMC, micelles dissociate into unimers to re-establish the unimer-micelle thermodynamic equilibrium [113].”
BackgroundInfluentialEffects of pluronic F68 micellization on the viability of neuronal cells in culture
Samith, V. D., Miño, G., Ramos‐Moore, E., & Arancibia‐Miranda, N. (2013) · Journal of Applied Polymer Science · doi:10.1002/app.39426 · Cited by 30
Biamphiphilic triblock copolymer micelles as a multifunctional platform for anticancer drug delivery
Zhu, W. J., Li, Y., Liu, L., Zhang, W., Chen, Y., & Xi, F. (2010) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.32985 · Cited by 30
Akiba, I., Takechi, A., Sakou, M., Handa, M., Shinohara, Y., Amemiya, Y., Yagi, N., & Sakurai, K. (2012) · Macromolecules · doi:10.1021/ma300461d · Cited by 30
Bony, B. A., Miller, H. A., Tarudji, A. W., Gee, C. C., Sarella, A., Nichols, M. G., & Kievit, F. M. (2020) · ACS Omega · doi:10.1021/acsomega.0c01890 · Cited by 32
Fahmy, S. A., Issa, M. Y., Saleh, B. M., Meselhy, M. R., & Azzazy, H. M. E.-S. (2021) · ACS Omega · doi:10.1021/acsomega.1c00455 · Cited by 31
Brief overview of nanoparticulate therapy in cancer
Wakaskar, R. R. (2017) · Journal of drug targeting · doi:10.1080/1061186x.2017.1347175 · Cited by 29
“of various drugs while located on the cell membrane [3,4].”
BackgroundDrozdek, S., Szeremeta, J., Lamch, Ł., et al. (2016) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.6b04301 · Cited by 29
Cheng, C., Wei, H., Zhang, X., Cheng, S., & Zhuo, R. (2008) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31770 · Cited by 29
Polymeric Nanomedicines in Diabetic Wound Healing: Applications and Future Perspectives
Chen, Z., Chan, K., Li, X., Li, G., Ma, Y., Huang, C.-W., Lu, Y., Wang, L., & Piao, C. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s514000 · Cited by 32
“61 For instance, dual temperature/pH-sensitive nanogels have been developed using temperature-responsive poly(N-isopropylacrylamide) P(NIPAAm) and N, N-dimethylaminoethyl methacrylate (DMAEMA), which contains amino groups that exhibit pH-responsive behavior to facilitate the release of anticancer…”
Sedush, N. G., Kadina, Y. A., Razuvaeva, E. V., Puchkov, A. A., Shirokova, E. M., Gomzyak, V. I., Kalinin, K. T., Kulebyakina, A. I., & Чвалун, С. Н. (2021) · Nanobiotechnology Reports · doi:10.1134/s2635167621040121 · Cited by 28
Novel methods of targeted drug delivery: the potential of multifunctional nanoparticles
Akbulut, M. E. S., D’Addio, S. M., Gindy, M. E., & Prud’homme, R. K. (2009) · Expert Review of Clinical Pharmacology · doi:10.1586/ecp.09.4 · Cited by 28
Synthesis and characterization of modified starch hydrogels for photodynamic treatment of cancer
Saboktakin, M. R., Tabatabaie, R. M., Ostovarazar, P., Maharramov, A. M., & Рамазанов, М. А. (2012) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2012.06.024 · Cited by 28
Jin, W., Xu, P., Zhan, Y., Shen, Y., Kirk, E. A. V., Alexander, B. M., Murdoch, W. J., Liu, L., & Isaak, D. D. (2007) · Drug Delivery · doi:10.1080/10717540601036856 · Cited by 28
“…drug conjugates of water-soluble polymers (Senter and Kopecek 2004; Vicent and Duncan 2006) and dendrimers (Gillies and Frechet 2005), liposomes (Torchilin 2005), and micelles (Gaucher et al. 2005; Kwon 2003) via the enhanced permeation and retention effect (EPR) of tumors (Maeda et al. 2003).”
BackgroundLactic acid‐ and carbonate‐based crosslinked polymeric micelles for drug delivery
Danquah, M. K., Fujiwara, T., & Mahato, R. I. (2012) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.26392 · Cited by 28
Polymeric Micelles as Carriers for Nerve-Highlighting Fluorescent Probe Delivery
Hackman, K. M., Doddapaneni, B. S., Barth, C. W., Wierzbicki, I. H., Alani, A. W. G., & Gibbs, S. L. (2015) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.5b00582 · Cited by 28
Micellization and sustained drug release behavior of EC-g-PPEGMA amphiphilic copolymers
Tan, J., Li, Y., Liu, R., Kang, H., Wang, D., Ma, L., Liu, W., Wu, M., & Huang, Y. P. (2010) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2010.02.017 · Cited by 27
Self-assembly and characterization of Pluronic P105 micelles for liver-targeted delivery of silybin
Li, X., Huang, Y., Chen, X., Zhou, Y., Zhang, Y. H., Li, P., Liu, Y., Sun, Y., Zhao, J., & Wang, F. (2009) · Journal of drug targeting · doi:10.3109/10611860903062062 · Cited by 27
UV and Near-IR Triggered Release from Polymeric Micelles and Nanoparticles
Alatorre‐Meda, M., Alvarez‐Lorenzo, C., Concheiro, Á., & Taboada, P. (2013) · Royal Society of Chemistry eBooks · doi:10.1039/9781849736800-00304 · Cited by 28
Pluronic Nanotechnology for Overcoming Drug Resistance
Chowdhury, P., Nagesh, P. K. B., Kumar, S., Jaggi, M., Chauhan, S. C., & Yallapu, M. M. (2017) · Nanomedicine and nanotoxicology · doi:10.1007/978-981-10-5864-6_9 · Cited by 30
Nanomedicine advances in cancer therapy
Hinge, N. S., Pandey, M. M., Singhvi, G., Gupta, G., Mehta, M., Satija, S., Gulati, M., Dureja, H., & Dua, K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818471-4.00008-x · Cited by 30
Passive diffusion of polymeric surfactants across lipid bilayers
Mathot, F., Schanck, A. N., Bambeke, F. V., et al. (2007) · Journal of Controlled Release · doi:10.1016/j.jconrel.2007.03.015 · Cited by 26
“Such polymeric micelles have been mainly investigated for parenteral administration of anticancer drugs [1] [2] [3].”
Saboktakin, M. R., Tabatabaie, R. M., Maharramov, A. M., & Рамазанов, М. А. (2011) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2011.08.031 · Cited by 26
Hiller, W., Engelhardt, N., Kampmann, A., Degen, P., & Weberskirch, R. (2015) · Macromolecules · doi:10.1021/acs.macromol.5b00149 · Cited by 25
Chen, X., Zhang, Y., Zhao, P., Chen, Y., Zhou, Y., Wang, S., & Yin, L. (2019) · Drug Development and Industrial Pharmacy · doi:10.1080/03639045.2019.1701002 · Cited by 26
Ahmed, S., Rehman, S. U., & Tabish, M. (2022) · OpenNano · doi:10.1016/j.onano.2022.100051 · Cited by 25
Interfacial micellar phase transfer using amphiphilic invertible polymers
Hevus, I., Kohut, A., & Voronov, A. S. (2011) · Polymer Chemistry · doi:10.1039/c1py00399b · Cited by 25
Richter, A., Wiedekind, A., Krause, M., Kissel, T., Haag, R., & Olbrich, C. (2010) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2010.02.008 · Cited by 25
Ziraksaz, Z., Nomani, A., Soleimani, M., et al. (2013) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2013.03.035 · Cited by 25
“This makes the ction of these dendritic units more versatile, allowing for drugs o be encapsulated or attached to the surface or peripheral groups hat modulate the solubility and toxicity (Liu and Frechet, 1999; venson and Tomalia, 2005).”
BackgroundNanomicelles in Diagnosis and Drug Delivery∗
Trinh, H. M., Joseph, M. A., Cholkar, K., Mitra, R., & Mitra, A. K. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-42978-8.00003-6 · Cited by 33
Rasolonjatovo, B., Gomez, J., Même, W., Gonçalves, C., Huin, C., Bennevault, V., Gall, T. L., Montier, T., Lehn, P., Cheradame, H., et al. (2014) · Biomacromolecules · doi:10.1021/bm5016656 · Cited by 24
Qiao, Y., Zhan, C., Wang, C., Shi, X., Yang, J., He, X., Ji, E., Yu, Z., Yan, C., & Wu, H. (2020) · Journal of Materials Chemistry B · doi:10.1039/d0tb01682a · Cited by 25
Potential Role of Carbon Nanomaterials in the Treatment of Malignant Brain Gliomas
Caffo, M., Curcio, A., Rajiv, K., Caruso, G., Venza, M., & Germanò, A. (2023) · Cancers · doi:10.3390/cancers15092575 · Cited by 24
“Furthermore, the majority of chemotherapeutic agents are poorly soluble and are mixed with toxic solvents [19].”
BackgroundMassoumi, B., Abdollahi, M., Fathi, M., Entezami, A. A., & Hamidi, S. (2013) · Journal of Polymer Research · doi:10.1007/s10965-012-0047-7 · Cited by 24
Tokarska, K., Lamch, Ł., Piechota, B., Żukowski, K., Chudy, M., Wilk, K. A., & Brzózka, Z. (2020) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2020.111981 · Cited by 24
Pharmaceutical Micelles: Combining Longevity, Stability, and Stimuli Sensitivity
Carstens, M. G., Rijcken, C. J. F., van Nostrum, C. F., & Hennink, W. E. (2008) · Fundamental biomedical technologies · doi:10.1007/978-0-387-76554-9_9 · Cited by 26
“…(Adams et al., 2003; Allen et al., 1999; Gaucher et al., 2005; Jones and Leroux, 1999; Kabanov et al., 1992; Kataoka et al., 2001; Kreuter, 2006; Kwon, 2003; Lavasanifar et al., 2002b; Liu et al., 2007; Moghimi et al., 2001; Nishiyama and Kataoka, 2006; Torchilin, 2001, 2006; Yokoyama et al.,…”
BackgroundAmphiphilic Polymethacrylate‐ and Polystyrene‐Based Chemical Delivery Systems for Damascones
Berthier, D. L., Trachsel, A., Fehr, C., Ouali, L., & Herrmann, A. (2005) · Helvetica Chimica Acta · doi:10.1002/hlca.200590249 · Cited by 24
Nanosized ZSM-5 will improve photodynamic therapy using Methylene blue
Kariminezhad, H., Habibi, M., & Mirzababayi, N. (2015) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2015.03.013 · Cited by 23
Jin, X., Asghar, S., Zhang, M., et al. (2018) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2018.09.025 · Cited by 22
Targeted nano-drug delivery system for glioblastoma therapy: In vitro and in vivo study
Hassanzadeganroudsari, M., Soltani, M., Heydarinasab, A., Apostolopoulos, V., Akbarzadehkhiyavi, A., & Nurgali, K. (2020) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2020.102039 · Cited by 22
Formulation and evaluation of glimepiride solid dispersion tablets
Gill, B., Kaur, T., Kumar, S., & Gupta, G. D. (2010) · Asian Journal of Pharmaceutics · doi:10.4103/0973-8398.72121 · Cited by 29
Jiang, S., Mou, Y., He, H., Yang, D., Qin, L., Zhang, F., & Zhang, P. (2019) · Drug Development and Industrial Pharmacy · doi:10.1080/03639045.2019.1660365 · Cited by 20
“The hydrophobic drugs are trapped in hydrophobic nuclear centers by hydrophobic interactions (such as hydrogen bonds or covalent bonds) and hydrophilic chains extend into water (hydrogen bonds) to form micelles shells of a certain thickness [4,5].”
BackgroundDutra, J. A. P., Luiz, M. T., Tavares, A. G., Filippo, L. D. D., Carvalho, S. G., & Chorilli, M. (2022) · Current Pharmaceutical Design · doi:10.2174/1381612828666220603152918 · Cited by 20
Poša, M. (2018) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2018.02.035 · Cited by 20
KABIR‐UD‐DIN, K., Khan, A. B., & Naqvi, A. Z. (2012) · Journal of Solution Chemistry · doi:10.1007/s10953-012-9884-6 · Cited by 20
“Drug delivery systems which have attracted much attention for their potential to improve the pharmacological properties of drugs include nanocapsules [1], cell ghost [2], liposomes [3] and micelles [4, 5].”
BackgroundEfficient entrapment of poorly water-soluble pharmaceuticals in hybrid nanoparticles
Ishihara, T., Goto, M., Kanazawa, H., Higaki, M., & Mizushima, Y. (2008) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.21605 · Cited by 20
“JOURNAL O most of these agents are never used clinically because of their low bioavailability and unanticipated side effects.(1,2) In order to expand the utility of such compounds for various applications, it is necessary to establish a technique for solubilizing them and controlling their biodistribution.”
BackgroundHafezi, M., & Sharif, F. (2012) · Langmuir · doi:10.1021/la303686h · Cited by 19
Salvador-Morales, C. (2011) · Frontiers in Bioscience-Elite · doi:10.2741/398 · Cited by 19
“Many potential pharmaceuticals with high biological activity are never used clinically because of their low bioavailability and unanticipated side effects (63, 64).”
BackgroundAl-Abboodi, A. S., AL-QUBAISI, M. S., Abdullah, R., Abdul, A. B., Taufiq‐Yap, Y. H., & Yeap, S. K. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17101653 · Cited by 19
“In addition, absence of selectivity and short blood circulation time of chemotherapy agents, which in turn, will damage not only cancer cells but also normal and healthy tissue [28].”
BackgroundRikiyama, K., Horiuchi, T., Koga, N., et al. (2018) · Polymer · doi:10.1016/j.polymer.2018.09.047 · Cited by 19
Langer, R. (2012) · Frontiers in Bioscience-Elite · doi:10.2741/e398 · Cited by 19
Synthesis of amphiphilic polysiloxanes and their properties for formation of nano-aggregates
Iwakiri, N., Nishikawa, T., Kaneko, Y., et al. (2009) · Colloid & Polymer Science · doi:10.1007/s00396-009-2005-4 · Cited by 19
Nanostructured systems for transbuccal drug delivery
Franz‐Montan, M., de Araújo, D. R., Ribeiro, L. N. D. M., de Melo, N. F. S., & de Paula, E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-47720-8.00005-5 · Cited by 22
Propofol induced micelle formation in aqueous block copolymer solutions
Dwyer, C., Viebke, C., & Meadows, J. (2004) · Colloids and Surfaces A Physicochemical and Engineering Aspects · doi:10.1016/j.colsurfa.2004.11.020 · Cited by 19
Development of nanoparticulate systems with action in breast and ovarian cancer: nanotheragnostics
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Modified chitosan derivative micelle system for natural anti-tumor product gambogic acid delivery
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Zhang, J., Liu, J., Zhao, Y., Wang, G., & Zhou, F. (2014) · Expert Opinion on Drug Delivery · doi:10.1517/17425247.2014.945417 · Cited by 17
“However, overlarge micelles may only have a moderate effect because large size will lead to a poor intratumor penetration [26].”
BackgroundLiveri, M. L. T., Licciardi, M., Sciascia, L., Giammona, G., & Cavallaro, G. (2012) · The Journal of Physical Chemistry B · doi:10.1021/jp211973s · Cited by 17
Polymer Nanomaterials for Drug Delivery Across the Blood Brain Barrier
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“They are of particular interest because of their small particle size, their efficiency in entrapping a satisfactory amount of hydrophobic drug within the inner core, their stability in the circulation and their ability to gradually release the drug ( 14 ).”
Background
Metadata
- Authors
- Kwon, G. S.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- Kwon, Glen S.
- ORCID
- Kwon, Glen S.
- Venue
- Critical Reviews in Therapeutic Drug Carrier Systems
- Publisher
- Begell House
- Published
- 2003
- Volume
- 20
- Issue
- 5
- Pages
- 357-403
- ISSN
- 0743-4863 (ISSN-L)
- OpenAlex
- W2082105104
- Cited by
- 502
- References
- 0
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 12 · 2023: 15 · 2022: 17 · 2021: 13 · 2020: 20 · 2019: 15 · 2018: 26 · 2017: 28 · 2016: 24 · 2015: 20 · 2014: 28 · 2013: 36 · 2012: 35
- FWCI
- 8.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Critical Reviews in Therapeutic Drug Carrier Systems (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (AI-43346-06)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Surfactants and Colloidal Systems
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Drug Solubulity and Delivery Systems
- Keywords
- polymeric micelles, poorly water-soluble drugs, drug solubilization, drug delivery, amphotericin B, propofol, paclitaxel, photosensitizers, poloxamer, tumor targeting, P-glycoprotein inhibition, drug resistance, polyene antibiotics, antifungal agents, parenteral administration
- MeSH terms
- Drug Stability, Pharmaceutical Preparations, Humans, Micelles, Pharmacokinetics, Polyethylene Glycols, Solubility, Surface-Active Agents, Water, Poloxamer
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