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Ashkin, A., Dziedzic, J. M., Bjorkholm, J. E., and Chu, S., Observation of a single-beam gradient force optical trap for dielectric particles. Opt. Lett., 11:5 (1986), 288–90.CrossRefGoogle ScholarPubMed
[2]
Neuman, K. C. and Nagy, A., Single-molecule force spectroscopy: Optical tweezers, magnetic tweezers and atomic force microscopy. Nat. Methods, 5:6 (2008), 491–505.CrossRefGoogle ScholarPubMed
[3]
Neuman, K. C., Chadd, E. H., Liou, G. F., Bergman, K., and Block, S. M., Characterization of photodamage to Escherichia coli in optical traps. Biophys. J., 77:5(1999), 2856–63.CrossRefGoogle ScholarPubMed
[4]
Sacconi, L., Tolic-Norrelykke, I. M., Stringari, C., Antolini, R., and Pavone, F. S., Optical micromanipulations inside yeast cells. Appl. Opt., 44:11 (2005), 2001–7.CrossRefGoogle ScholarPubMed
[5]
Cherney, D. P., Bridges, T. E., and Harris, J. M., Optical trapping of unilamellar phospholipid vesicles: Investigation of the effect of optical forces on the lipid membrane shape by confocal-raman microscopy. Anal. Chem., 76:17 (2004), 4920–28.CrossRefGoogle ScholarPubMed
[6]
Pauzauskie, P. J., Radenovic, A., Trepagnier, E., Shroff, H., Yang, P. D., and Liphardt, J., Optical trapping and integration of semiconductor nanowire assemblies in water. Nat. Mater., 5:2 (2006), 97–101.CrossRefGoogle ScholarPubMed
[7]
Agarwal, R., Ladavac, K., Roichman, Y., Yu, G. H., Lieber, C. M., and Grier, D. G., Manipulation and assembly of nanowires with holographic optical traps. Opt. Express, 13:22 (2005), 8906–12.CrossRefGoogle ScholarPubMed
[8]
La Porta, A. and Wang, M. D., Optical torque wrench: Angular trapping, rotation, and torque detection of quartz microparticles. Phys. Rev. Lett., 92:19 (2004), 190801.CrossRefGoogle ScholarPubMed
[9]
Block, S. M., Goldstein, L. S. B., and Schnapp, B. J., Bead movement by single kinesin molecules studied with optical tweezers. Nature, 348:6299 (1990), 348–52.CrossRefGoogle ScholarPubMed
[10]
Svoboda, K. and Block, S. M., Force and velocity measured for single kinesin molecules. Cell, 77:5 (1994), 773–84.CrossRefGoogle ScholarPubMed
[11]
Mammen, M., Helmerson, K., Kishore, R., Choi, S. K., Phillips, W. D., and Whitesides, G. M., Optically controlled collisions of biological objects to evaluate potent polyvalent inhibitors of virus-cell adhesion. Chem. Biol., 3:9 (1996), 757–63.CrossRefGoogle ScholarPubMed
[12]
Litvinov, R. I., Shuman, H., Bennett, J. S., and Weisel, J. W., Binding strength and activation state of single fibrinogen-integrin pairs on living cells. Proc. Natl. Acad. Sci. USA, 99:11 (2002), 7426–31.CrossRefGoogle ScholarPubMed
[13]
Wang, M. D., Schnitzer, M. J., Yin, H., Landick, R., Gelles, J., and Block, S. M., Force and velocity measured for single molecules of RNA polymerase. Science, 282:5390 (1998), 902–7.CrossRefGoogle ScholarPubMed
[14]
Neuman, K. C., Abbondanzieri, E. A., Landick, R., Gelles, J., and Block, S. M., Ubiquitous transcriptional pausing is independent of RNA polymerase backtracking. Cell, 115:4 (2003), 437–47.CrossRefGoogle ScholarPubMed
[15]
Shaevitz, J. W., Abbondanzieri, E. A., Landick, R., and Block, S. M., Backtracking by single RNA polymerase molecules observed at near-base-pair resolution. Nature, 426:6967 (2003), 684–7.CrossRefGoogle ScholarPubMed
[16]
Abbondanzieri, E. A., Greenleaf, W. J., Shaevitz, J. W., Landick, R., and Block, S. M., Direct observation of base-pair stepping by RNA polymerase. Nature, 438:7067 (2005), 460–5.CrossRefGoogle ScholarPubMed
[17]
Moffitt, J. R., Chemla, Y. R., Smith, S. B., and Bustamante, C., Recent advances in optical tweezers. Annu. Rev. Biochem., 77 (2008), 205–28.CrossRefGoogle ScholarPubMed
[18]
Hawes, C., Osterrieder, A., Sparkes, I. A., and Ketelaar, T., Optical tweezers for the micromanipulation of plant cytoplasm and organelles. Curr. Opin. Plant Biol., 13:6 (2010), 731–5.CrossRefGoogle ScholarPubMed
[19]
Muller, D. J., Helenius, J., Alsteens, D., and Dufrene, Y. F., Force probing surfaces of living cells to molecular resolution. Nat. Chem. Biol., 5:6 (2009), 383–90.CrossRefGoogle ScholarPubMed
[20]
Zhang, H. and Liu, K. K., Optical tweezers for single cells. J. R. Soc. Interface, 5:24 (2008), 671–90.CrossRefGoogle ScholarPubMed
[21]
Andersson, M., Axner, O., Almqvist, F., Uhlin, B. E., and Fallman, E., Physical properties of biopolymers assessed by optical tweezers: Analysis of folding and refolding of bacterial pili. ChemPhysChem, 9:2 (2008), 221–35.Google ScholarPubMed
[22]
Deniz, A. A., Mukhopadhyay, S., and Lemke, E. A., Single-molecule biophysics: At the interface of biology, physics and chemistry. J. R. Soc. Interface, 5:18 (2008), 15–45.CrossRefGoogle ScholarPubMed
[23]
Herbert, K. M., Greenleaf, W. J., and Block, S. M., Single-molecule studies of RNA polymerase: Motoring along. Annu. Rev. Biochem., 77 (2008), 149–76.CrossRefGoogle ScholarPubMed
[24]
De Vlaminck, I. and Dekker, C., Recent advances in magnetic tweezers. Annu. Rev. Biophys., 41 (2012), 453–72.CrossRefGoogle ScholarPubMed
[25]
Tokarev, A., Aprelev, A., Zakharov, M. N., Korneva, G., Gogotsi, Y., and Kornev, K. G., Multifunctional magnetic rotator for micro and nanorheological studies. Rev. Sci. Instrum., 83:6 (2012), 065110.CrossRefGoogle ScholarPubMed
[26]
Chen, M., Sun, L., Bonevich, J. E., Reich, D. H., Chien, C. L., and Searson, P. C., Tuning the response of magnetic suspensions. Appl. Phys. Lett., 82:19 (2003), 3310–2.CrossRefGoogle Scholar
[27]
Chien, C. L., Sun, L., Tanase, M., et al., Electrodeposited magnetic nanowires: Arrays, field-induced assembly, and surface functionalization. J. Magn. Magn. Mater., 249:1–2 (2002), 146–55.CrossRefGoogle Scholar
[28]
Barbic, M., Magnetic wires in MEMS and bio-medical applications. J. Magn. Magn. Mater., 249:1–2 (2002), 357–67.CrossRefGoogle Scholar
[29]
Hultgren, A., Tanase, M., Chen, C. S., Meyer, G. J., and Reich, D. H., Cell manipulation using magnetic nanowires. J. Appl. Phys., 93:10 (2003), 7554–6.CrossRefGoogle Scholar
[30]
Bentley, A. K., Trethewey, J. S., Ellis, A. B., and Crone, W. C., Magnetic manipulation of copper-tin nanowires capped with nickel ends. Nano. Lett., 4:3 (2004), 487–90.CrossRefGoogle Scholar
[31]
Shevkoplyas, S. S., Siegel, A. C., Westervelt, R. M., Prentiss, M. G., and Whitesides, G. M., The force acting on a superparamagnetic bead due to an applied magnetic field. Lab Chip, 7:10 (2007), 1294–302.CrossRefGoogle Scholar
[32]
Neuman, K. C., Lionnet, T., and Allemand, J. F., Single-molecule micromanipulation techniques. Annu. Rev. Mater. Res., 37 (2007), 33–67.CrossRefGoogle Scholar
[33]
Gosse, C. and Croquette, V., Magnetic tweezers: Micromanipulation and force measurement at the molecular level. Biophys. J., 82:6 (2002), 3314–29.CrossRefGoogle ScholarPubMed
[34]
Charvin, G., Strick, T. R., Bensimon, D., and Croquette, V., Tracking topoisomerase activity at the single-molecule level. Annu. Rev. Biophys. Biomol. Struct., 34 (2005), 201–19.CrossRefGoogle ScholarPubMed
[35]
Strick, T. R., Croquette, V., and Bensimon, D., Single-molecule analysis of DNA uncoiling by a type II topoisomerase. Nature, 404:6780(2000), 901–4.CrossRefGoogle ScholarPubMed
[36]
Celedon, A., I. M. Nodelman, B. Wildt et al., Magnetic tweezers measurement of single molecule torque. Nano. Lett., 9:4 (2009), 1720–5.CrossRefGoogle ScholarPubMed
[37]
Koster, D. A., Croquette, V., Dekker, C., Shuman, S., and Dekker, N. H., Friction and torque govern the relaxation of DNA supercoils by eukaryotic topoisomerase IB. Nature, 434:7033 (2005), 671–4.CrossRefGoogle ScholarPubMed
[38]
Koster, D. A., Palle, K., Bot, E. S. M., Bjornsti, M. A., and Dekker, N. H., Antitumour drugs impede DNA uncoiling by topoisomerase I. Nature, 448:7150 (2007), 213–7.CrossRefGoogle ScholarPubMed
[39]
Zhang, L., T. Petit, Y. Lu et al., Controlled propulsion and cargo transport of rotating nickel nanowires near a patterned solid surface. ACS Nano, 4:10(2010), 6228–34.CrossRefGoogle Scholar
[40]
Tierno, P., Golestanian, R., Pagonabarraga, I., and Sagues, F., Controlled swimming in confined fluids of magnetically actuated colloidal rotors. Phys. Rev. Lett., 101:21 (2008), 218304.CrossRefGoogle ScholarPubMed
[41]
Gao, W., Sattayasamitsathit, S., Manesh, K. M., Weihs, D., and Wang, J., Magnetically powered flexible metal nanowire motors. J. Am. Chem. Soc., 132:41 (2010), 14403–5.CrossRefGoogle ScholarPubMed
[42]
Fan, D. L., Cammarata, R. C., and Chien, C. L., Precision transport and assembling of nanowires in suspension by electric fields. Appl. Phys. Lett., 92:9 (2008), 093115.CrossRefGoogle Scholar
[43]
Fan, D. L., Zhu, F. Q., Cammarata, R. C., and Chien, C. L., Electric tweezers. Nano Today, 6:4 (2011), 339–54.CrossRefGoogle Scholar
[44]
Jones, T. B., Electromechanics of Particles, 1st edn (Cambridge: Cambridge University Press, 1995).CrossRefGoogle Scholar
[45]
Smith, P. A., C. D. Nordquist, T. N. Jackson et al., Electric-field assisted assembly and alignment of metallic nanowires. Appl. Phys. Lett., 77:9 (2000), 1399–401.CrossRefGoogle Scholar
[46]
Krupke, R., Hennrich, F., von Lohneysen, H., and Kappes, M. M., Separation of metallic from semiconducting single-walled carbon nanotubes. Science, 301:5631 (2003), 344–7.CrossRefGoogle ScholarPubMed
[47]
Fan, D. L., Zhu, F. Q., Cammarata, R. C., and Chien, C. L., Controllable high-speed rotation of nanowires. Phys. Rev. Lett., 94:24 (2005), 247208.CrossRefGoogle Scholar
[48]
Fan, D. L., Z. Yin, R. Cheong et al., Subcellular-resolution delivery of a cytokine through precisely manipulated nanowires. Nat. Nanotech., 5:7 (2010), 545–51.CrossRefGoogle ScholarPubMed
[49]
Fan, D. L., Zhu, F. Q., Xu, X. B., Cammarata, R. C., and Chien, C. L., Electronic properties of nanoentities revealed by electrically driven rotation. Proc. Natl. Acad. Sci. USA., 109:24 (2012), 9309–13.CrossRefGoogle ScholarPubMed
[50]
Xu, X. B., Kim, K., Li, H. F., and Fan, D. L., Ordered arrays of raman nanosensors for ultrasensitive and location predictable biochemical detection. Adv. Mater., 24:40 (2012), 5457–63.Google ScholarPubMed
[51]
Edwards, B., Engheta, N., and Evoy, S., Electric tweezers: Experimental study of positive dielectrophoresis-based positioning and orientation of a nanorod. J. Appl. Phys., 102:2 (2007), 024913.CrossRefGoogle Scholar
[52]
Edwards, B., Engheta, N., and Evoy, S., Theory of simultaneous control of orientation and translational motion of nanorods using positive dielectrophoretic forces. J. Appl. Phys., 98:12 (2005), 124314.CrossRefGoogle Scholar
[53]
Fan, D. L., Zhu, F. Q., Cammarata, R. C., and Chien, C. L., Manipulation of nanowires in suspension by ac electric fields. Appl. Phys. Lett., 85:18 (2004), 4175–7.CrossRefGoogle Scholar
[54]
Edwards, B., Mayer, T. S., and Bhiladvala, R. B., Synchronous electrorotation of nanowires in fluid. Nano. Lett., 6:4 (2006), 626–32.CrossRefGoogle Scholar
[55]
Chiou, P. Y., Ohta, A. T., and Wu, M. C., Massively parallel manipulation of single cells and microparticles using optical images. Nature, 436:7049 (2005), 370–2.CrossRefGoogle ScholarPubMed
[56]
Jamshidi, A., P. J. Pauzauskie, P. J. Schuck et al., Dynamic manipulation and separation of individual semiconducting and metallic nanowires. Nat. Photon., 2:2 (2008), 86–9.CrossRefGoogle ScholarPubMed
[57]
Paxton, W. F., Sen, A., and Mallouk, T. E., Motility of catalytic nanoparticles through self-generated forces. Chem. Eur. J., 11:22 (2005), 6462–70.CrossRefGoogle ScholarPubMed
[58]
Paxton, W. F., K. C. Kistler, C. C. Olmeda et al., Catalytic nanomotors: Autonomous movement of striped nanorods. J. Am. Chem. Soc., 126:41 (2004), 13424–31.CrossRefGoogle ScholarPubMed
[59]
Sundararajan, S., Lammert, P. E., Zudans, A. W., Crespi, V. H., and Sen, A., Catalytic motors for transport of colloidal cargo. Nano. Lett., 8:5 (2008), 1271–6.CrossRefGoogle ScholarPubMed
[60]
Laocharoensuk, R., Burdick, J., and Wang, J., Carbon-nanotube-induced acceleration of catalytic nanomotors. ACS Nano, 2:5 (2008), 1069–75.CrossRefGoogle ScholarPubMed
[61]
Demirok, U. K., Laocharoensuk, R., Manesh, K. M., and Wang, J., Ultrafast catalytic alloy nanomotors. Angew. Chem. Int., 47:48 (2008), 9349–51.CrossRefGoogle ScholarPubMed
[62]
Kagan, D., P. Calvo-Marzal, S. Balasubramanian et al., Chemical sensing based on catalytic nanomotors: Motion-based detection of trace silver. J. Am. Chem. Soc., 131:34 (2009), 12082–3.CrossRefGoogle ScholarPubMed
[63]
Kagan, D., R. Laocharoensuk, M. Zimmerman et al., Rapid delivery of drug carriers propelled and navigated by catalytic nanoshuttles. Small, 6:23 (2010), 2741–7.CrossRefGoogle ScholarPubMed
[64]
Valadares, L. F., Y.-G. Tao, N. S. Zacharia et al., Catalytic nanomotors: Self-propelled sphere dimers. Small, 6:4 (2010), 565–72.CrossRefGoogle ScholarPubMed
[65]
Baraban, L., D. Makarov, R. Streubel et al., Catalytic janus motors on microfluidic chip: Deterministic motion for targeted cargo delivery. ACS Nano, 6:4 (2012), 3383–9.CrossRefGoogle ScholarPubMed
[66]
Fournier-Bidoz, S., Arsenault, A. C., Manners, I., and Ozin, G. A., Synthetic self-propelled nanorotors. Chem. Commun., 4 (2005), 441–3.Google Scholar
[67]
Gibbs, J. G. and Zhao, Y. P., Design and characterization of rotational multicomponent catalytic nanomotors. Small, 5:20 (2009), 2304–8.CrossRefGoogle ScholarPubMed
[68]
Kline, T. R., Paxton, W. F., Mallouk, T. E., and Sen, A., Catalytic nanomotors: Remote-controlled autonomous movement of striped metallic nanorods. Angew. Chem. Int., 44:5 (2005), 744–6.CrossRefGoogle ScholarPubMed
[69]
Burdick, J., Laocharoensuk, R., Wheat, P. M., Posner, J. D., and Wang, J., Synthetic nanomotors in microchannel networks: Directional microchip motion and controlled manipulation of cargo. J. Am. Chem. Soc., 130:26 (2008), 8164–5.CrossRefGoogle ScholarPubMed
[70]
Sundararajan, S., Sengupta, S., Ibele, M. E., and Sen, A., Drop-off of colloidal cargo transported by catalytic Pt-Au nanomotors via photochemical stimuli. Small, 6:14 (2010), 1479–82.CrossRefGoogle ScholarPubMed
[71]
Catchmark, J. M., Subramanian, S., and Sen, A., Directed rotational motion of microscale objects using interfacial tension gradients continually generated via catalytic reactions. Small, 1:2 (2005), 202–6.CrossRefGoogle ScholarPubMed
[72]
Wu, J., Balasubramanian, S., Kagan, D., Manesh, K. M., Campuzano, S., and Wang, J., Motion-based DNA detection using catalytic nanomotors. Nature Communications, 1 (2010), 36.CrossRefGoogle ScholarPubMed
[73]
Ding, X. Y., S.-C. Lin, B. Kiraly et al., On-chip manipulation of single microparticles, cells, and organisms using surface acoustic waves. Proc. Natl. Acad. Sci. USA., 109:28 (2012), 11105–9.CrossRefGoogle ScholarPubMed
[74]
Franke, T., Braunmuller, S., Schmid, L., Wixforth, A., and Weitz, D. A., Surface acoustic wave actuated cell sorting (SAWACS). Lab Chip, 10:6 (2010), 789–94.CrossRefGoogle Scholar
[75]
Rezk, A. R., Qi, A., Friend, J. R., Li, W. H., and Yeo, L. Y., Uniform mixing in paper-based microfluidic systems using surface acoustic waves. Lab Chip, 12:4 (2012), 773–9.CrossRefGoogle ScholarPubMed
[76]
Shi, J. J., Mao, X. L., Ahmed, D., Colletti, A., and Huang, T. J., Focusing microparticles in a microfluidic channel with standing surface acoustic waves (SSAW). Lab Chip, 8:2 (2008), 221–3.CrossRefGoogle Scholar
[77]
Juan, M. L., Righini, M., and Quidant, R., Plasmon nano-optical tweezers. Nat. Photon., 5:6 (2011), 349–56.CrossRefGoogle Scholar
[78]
Quidant, R., Plasmonic tweezers: The strength of surface plasmons. MRS Bull., 37:8 (2012), 739–44.CrossRefGoogle Scholar
[79]
Righini, M., Zelenina, A. S., Girard, C., and Quidant, R., Parallel and selective trapping in a patterned plasmonic landscape. Nat. Phys., 3:7 (2007), 477–80.CrossRefGoogle Scholar
[80]
Zhang, W. H., Huang, L. N., Santschi, C., and Martin, O. J. F., Trapping and sensing 10 nm metal nanoparticles using plasmonic dipole antennas. Nano. Lett., 10:3 (2010), 1006–11.CrossRefGoogle ScholarPubMed
[81]
Pang, Y. J. and Gordon, R., Optical trapping of a single protein. Nano. Lett., 12:1 (2012), 402–6.CrossRefGoogle ScholarPubMed
[82]
Torchilin, V. P., Passive and active drug targeting: Drug delivery to tumors as an example. Handb. Exp. Pharmacol., 197 (2010), 3–53.CrossRefGoogle Scholar
[83]
Yasukawa, T., H. Kimura, Y. Tabata et al., Active drug targeting with immunoconjugates to choroidal neovascularization. Curr. Eye. Res., 21:6 (2000), 952–61.CrossRefGoogle ScholarPubMed
[84]
Andrä, W., Häfeli, U. O., Hergt, R., and Misri, R., Application of magnetic particles in medicine and biology. In Kronmüller, H. and Parkin, S., eds., The Handbook of Magnetism and Advanced Magnetic Materials– Novel Materials (Chichester: John Wiley & Sons Ltd., 2007), pp. 2536–68.Google Scholar
[85]
Häfeli, U. O., Magnetic nano- and microparticles for targeted drug delivery. In Arshady, R. and Kono, K., eds., Smart Nanoparticles in Nanomedicine – The MML Series (London: Kentus Books, 2006), pp. 77–126.Google Scholar
[86]
Lu, A. H., Salabas, E. L., and Schuth, F., Magnetic nanoparticles: Synthesis, protection, functionalization, and application. Angew. Chem. Int. Ed. Engl., 46:8 (2007), 1222–44.CrossRefGoogle ScholarPubMed
[87]
Wang, X., Zhuang, J., Peng, Q., and Li, Y., A general strategy for nanocrystal synthesis, Nature, 437 (2005), 121–4.CrossRefGoogle ScholarPubMed
[88]
Redl, F. X., C. T. Black, G. C. Papaefthymiou et al., Magnetic, electronic, and structural characterization of nonstoichiometric iron oxides at the nanoscale. J. Am. Chem. Soc., 126:44 (2004), 14583–99.CrossRefGoogle ScholarPubMed
[89]
Sun, S., H. Zeng, D. B. Robinson et al., Monodisperse MFe2O4 (M = Fe, Co, Mn) nanoparticles.J. Am. Chem. Soc., 126:1 (2004), 273–9.CrossRefGoogle ScholarPubMed
[90]
Butter, K., Philipse, A. P., and Vroege, G. J., Synthesis and properties of iron ferrofluids.J. Magn. Magn. Mater., 252 (2002), 1–3.CrossRefGoogle Scholar
[91]
Jana, N. R., Chen, Y., and Peng, X., Size- and shape-controlled magnetic (Cr, Mn, Fe, Co, Ni) oxide nanocrystals via a simple and general approach.Chem. Mater., 16:20 (2004), 3931–5.CrossRefGoogle Scholar
Ge, S., X-Y. Shi, K. Sun et al., A facile hydrothermal synthesis of iron oxide nanoparticles with tunable magnetic properties. J. Phys. Chem. C Nanomater. Interfaces, 113:31 (2009), 13593–9.CrossRefGoogle ScholarPubMed
[94]
Martínez, G., Malumbres, A., Mallada, R.et al., Use of a polyol liquid collection medium to obtain ultrasmall magnetic nanoparticles by laser pyrolysis.Nanotechnology, 23:42 (2012), 425605.CrossRefGoogle ScholarPubMed
[95]
Schneider, T., Zhao, H., Jackson, J. K., Chapman, G. H., Dykes, J., and Häfeli, U. O., Use of hydrodynamic flow focusing for the generation of biodegradable camptothecin-loaded polymer microspheres. J. Pharm. Sci., 97:11 (2008), 4943–54.CrossRefGoogle ScholarPubMed
[96]
Sandhu, A., Handa, H., and Abe, M., Synthesis and applications of magnetic nanoparticles for biorecognition and point of care medical diagnostics. Nanotechnology, 21:44 (2010), 442001.CrossRefGoogle ScholarPubMed
[97]
Weissleder, R., D. D. Stark, B. L. Engelstad et al., Superparamagnetic iron oxide: Pharmacokinetics and toxicity. AJR Am. J. Roentgenol., 152:1 (1989), 167–73.CrossRefGoogle ScholarPubMed
[98]
Häfeli, U. O., Aue, J., and Damani, J., The biocompatibility and toxicity of magnetic particles. In Zborowski, M. and Chalmers, J. J., eds., Magnetic Cell Separation (Amsterdam: Elsevier, 2007), pp. 163–224.CrossRefGoogle Scholar
[99]
Reddy, L. H., Arias, J. L., Nicolas, J., and Couvreur, P., Magnetic nanoparticles: Design and characterization, toxicity and biocompatibility, pharmaceutical and biomedical applications. Chem. Rev., 112:11 (2012), 5818–78.CrossRefGoogle ScholarPubMed
[100]
Lopez, A., Gutierrez, L., and Lazaro, F. J., The role of dipolar interaction in the quantitative determination of particulate magnetic carriers in biological tissues. Phys. Med. Biol., 52:16 (2007), 5043–56.CrossRefGoogle ScholarPubMed
[100]
Lopez, A., Gutierrez, L., and Lazaro, F. J., The role of dipolar interaction in the quantitative determination of particulate magnetic carriers in biological tissues. Phys. Med. Biol., 52:16 (2007), 5043–56.CrossRefGoogle ScholarPubMed
[101]
Misri, R., Saatchi, K., Ng, S. S., Kumar, U., and Hafeli, U. O., Evaluation of (111)In labeled antibodies for SPECT imaging of mesothelin expressing tumors. Nucl. Med. Biol., 38:6 (2011), 885–96.CrossRefGoogle ScholarPubMed
[102]
Misri, R., Meier, D., Yung, A. C., Kozlowski, P., and Hafeli, U. O., Development and evaluation of a dual-modality (MRI/SPECT) molecular imaging bioprobe. Nanomedicine, 8:6 (2012), 1007–16.Google ScholarPubMed
[103]
Sakulkhu, U., Preparation of coated nanoparticles and investigation of their behavior in biological environment. Unpublished Ph.D. thesis, École Polytechnique Fédérale deLausanne (2013).
[104]
Zborowski, M., Magnetic cell separation (Laboratory Techniques in Biochemistry and Molecular Biology), (Amsterdam: Elsevier, 2007).Google Scholar
[105]
Zborowski, M. and Chalmers, J. J., Rarecell separation and analysis by magnetic sorting. Anal. Chem., 83:21 (2011), 8050–6.CrossRefGoogle Scholar
[106]
Kim, E., Lee, K., Huh, Y-M., and Haam, S., Magnetic nanocomplexes and the physiological challenges associated with their use for cancer imaging and therapy.J. Mater. Chem. B, 1 (2013), 729–39.CrossRefGoogle Scholar
[107]
Yang, J., C-H. Lee, J. Park et al., Antibody conjugated magnetic PLGA nanoparticles for diagnosis and treatment of breast cancer.J. Mater. Chem., 17 (2007), 2695–9.CrossRefGoogle Scholar
[108]
Kaittanis, C., Santra, S., and Perez, J. M., Role of nanoparticle valency in the nondestructive magnetic-relaxation-mediated detection and magnetic isolation of cells in complex media. J. Am. Chem. Soc., 131:35 (2009), 12780–91.CrossRefGoogle ScholarPubMed
[109]
Gaster, R. S., D. A. Hall, C. H. Nielsen et al., Matrix-insensitive protein assays push the limits of biosensors in medicine. Nat. Med., 15:11 (2009), 1327–32.CrossRefGoogle Scholar
[110]
Puertas, S., Moros, M., Fernández-Pacheco, R., Ibarra, M. R., Grazú, V., and Fuente, J. M. d. l., Designing novel nano-immunoassays: Antibody orientation versus sensitivity.J. Phys. D: Appl. Phys., 43:47 (2010), 474012.CrossRefGoogle Scholar
[111]
Puertas, S., P. Batalla, M. Moros et al., Taking advantage of unspecific interactions to produce highly active magnetic nanoparticle-antibody conjugates. ACS Nano, 5:6 (2011), 4521–8.CrossRefGoogle ScholarPubMed
[112]
Misri, R., Saatchi, K., and Hafeli, U. O., Nanoprobes for hybrid SPECT/MR molecular imaging. Nanomedicine (Lond.), 7:5 (2012), 719–33.CrossRefGoogle ScholarPubMed
[113]
Vazquez, M., Luna, C., Morales, M. P., Sanz, R., Serna, C. J., and Mijangos, C., Magnetic nanoparticles: Synthesis, ordering and properties. Physica B, 354 (2004), 71–9.CrossRefGoogle Scholar
[114]
Gold, L., Brown, D., He, Y., Shtatland, T., Singer, B. S., and Wu, Y., From oligonucleotide shapes to genomic SELEX: Novel biological regulatory loops. Proc. Natl. Acad. Sci. USA., 94:1 (1997), 59–64.CrossRefGoogle ScholarPubMed
[115]
Gold, L. and Ringquist, S., Systematic evolution of ligands by exponential enrichment: Solution SELEX, USA Patent 5567588 (1995).
[116]
Farokhzad, O. C., Karp, J. M., and Langer, R., Nanoparticle-aptamer bioconjugates for cancer targeting. Expert. Opin. Drug Del., 3:3 (2006), 311–24.CrossRefGoogle ScholarPubMed
[117]
Gu, F., L-F. Zhang, B. A. Teply et al., Precise engineering of targeted nanoparticles by using self-assembled biointegrated block copolymers. Proc. Natl. Acad. Sci. USA., 105:7 (2008), 2586–91.CrossRefGoogle ScholarPubMed
[118]
Wang, A. Z.et al., Superparamagnetic iron oxide nanoparticle-aptamer bioconjugates for combined prostate cancer imaging and therapy. ChemMedChem, 3:9 (2008), 1311–5.CrossRefGoogle ScholarPubMed
[119]
Chen, H. W., C. D. Medley, K. Sefah et al., Molecular recognition of small-cell lung cancer cells using aptamers. ChemMedChem, 3:6 (2008), 991–1001.CrossRefGoogle ScholarPubMed
[120]
Bamrungsap, S., Shukoor, M. I., Chen, T., Sefah, K., and Tan, W., Detection of lysozyme magnetic relaxation switches based on aptamer-functionalized superparamagnetic nanoparticles. Anal. Chem., 83:20 (2011), 7795–9.CrossRefGoogle ScholarPubMed
[121]
Bamrungsap, S., T. Chen, M. I. Shukoor et al., Pattern recognition of cancer cells using aptamer-conjugated magnetic nanoparticles. ACS Nano, 6:5 (2012), 3974–81.CrossRefGoogle ScholarPubMed
[122]
Lim, E. K., B. Kim, Y. Choi et al., Aptamer-conjugated magnetic nanoparticles enable efficient targeted detection of integrin αvβ3 via magnetic resonance imaging. J. Biomed. Mater. Res. A, 102:1(2014), 49–59.CrossRefGoogle ScholarPubMed
[123]
Lopez-Colon, D., Jimenez, E., You, M., Gulbakan, B., and Tan, W., Aptamers: Turning the spotlight on cells. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol., 3:3 (2011), 328–40.CrossRefGoogle ScholarPubMed
[124]
Mann, S., Hannington, J. P., and Williams, R. J. P., Phospholipid vesicles as a model system for biomineralization.Nature, 324 (1986), 565–7.CrossRefGoogle ScholarPubMed
[125]
Meldrum, F. C., Heywood, B. R., and Mann, S., Magnetoferritin: In vitro synthesis of a novel magnetic protein. Science, 257:5069 (1992), 522–3.CrossRefGoogle ScholarPubMed
[126]
Tresilwised, N., P. Pithayanukul, O. Mykhaylyk et al., Boosting oncolytic adenovirus potency with magnetic nanoparticles and magnetic force. Mol. Pharm., 7:4 (2010), 1069–89.CrossRefGoogle ScholarPubMed
[127]
Huh, Y-M., E-S. Lee, J-H. Lee et al., Hybrid nanoparticles for magnetic resonance imaging of target-specific viral gene delivery.Adv. Mater., 19:20 (2007), 3109–12.Google Scholar
[128]
Nishimura, K., Hasegawa, M., Ogura, Y., Nishi, T., Kataoka, K., and Handa, H., 4°C preparation of ferrite nanoparticles having protein molecules immobilized on their surfaces.J. Appl. Phys., 91:10 (2002), 8555–6.CrossRefGoogle Scholar
[129]
Nishio, K., N. Gokon, M. Hasegawa et al., Identification of a chemical substructure that is immobilized to ferrite nanoparticles (FP).Colloids Surf. B, 54:2 (2007), 249–53.CrossRefGoogle ScholarPubMed
[130]
Hatanaka, S., Matsushita, N., Abe, M., Nishimura, K., Hasegawa, M., and Handa, H., Direct immobilization of fluorescent dyes onto ferrite nanoparticles during their synthesis from aqueous solution.J. Appl. Phys., 93:10 (2003), 7569–70.CrossRefGoogle Scholar
[131]
Vanderhoff, J. W., Micale, F. J., and Krumrine, P. H., Continuous flow electrophoresis. In Righetti, P. G., Oss, C. J. Van, and Vanderhoff, J. W., eds., Electrokinetic Separation Methods (Amsterdam: Elsevier/North-Holland Biomedical Press, 1979), pp. 121–41.Google Scholar
[132]
Zborowski, M., Magnetophoresis. In Zborowski, M. and Chalmers, J. J., eds., Magnetic Cell Separation (Amsterdam: Elsevier, 2007), pp. 105–18.Google Scholar
[133]
Iacob, G., Rotariu, O., Strachan, N. J. C., and Häfeli, U. O., Magnetizable needles and wires – modeling an efficient way to target magnetic microspheres in vivo.Biorheology, 41:5 (2004), 599–612.Google ScholarPubMed
[134]
Rotariu, O., Iacob, G., Strachan, N. J. C., and Chiriac, H., Simulating the embolization of blood vessels using magnetic microparticles and acupuncture needle in a magnetic field.Biotechnol. Progr., 20 (2004), 299–305.CrossRefGoogle Scholar
[135]
Chen, H., Ebner, A. D., Rosengart, A. J., Kaminski, M. D., and Ritter, J. A., Analysis of magnetic drug carrier particle capture by a magnetizable intravascular stent: 1. Parametric study with single wire correlation.J. Magn. Magn. Mater., 284 (2004), 181–94.CrossRefGoogle Scholar
[136]
Forbes, Z. G., Yellen, B. B., Halverson, D. S., Fridman, G., Barbee, K. A., and Friedman, G., Validation of high gradient magnetic field based drug delivery to magnetizable implants under flow.IEEE Trans. Biomed. Eng., 55:2 (2008), 643–9.CrossRefGoogle ScholarPubMed
[137]
Furlani, E. P. and Ng, K. C., Analytical model of magnetic nanoparticle transport and capture in the microvasculature. Phys. Rev. E, 73:6 (2006) 061919.CrossRefGoogle ScholarPubMed
[138]
Gerber, R., Takayasu, M., and Friedlaender, F. J., Generalization of HGMS theory: The capture of ultra-fine particles.IEEE Trans. Magn., 19 (1983), 2115–7.CrossRefGoogle Scholar
[139]
Takayasu, M., Gerber, R., and Friedlaender, F. J., Magnetic separation of submicron particles.IEEE Trans. Magn., 19:5 (1983), 2112–4.CrossRefGoogle Scholar
[140]
Goll, D. and Kronmüller, H., High-performance permanent magnets.Naturwissenschaften, 87 (2000), 423–38.CrossRefGoogle ScholarPubMed
[141]
Avilés, M. O., Chen, H., Ebner, A. D., Rosengart, A. J., Kaminski, M. D., and Ritter, J. A., In vitro study of ferromagnetic stents for implant assisted magnetic drug targeting.J. Magn. Magn. Mater., 311:1 (2007), 306–311.CrossRefGoogle Scholar
[142]
Polyak, B., I. Fishbein, M. Chorny et al., High field gradient targeting of magnetic nanoparticle-loaded endothelial cells to the surfaces of steel stents. Proc. Natl. Acad. Sci. USA., 105:2 (2008), 698–703.CrossRefGoogle ScholarPubMed
[143]
Hournkumnuard, K. and Natenapit, M., Magnetic drug targeting by ferromagnetic microwires implanted within blood vessels.Med. Phys., 40:6 (2013), 062302.CrossRefGoogle ScholarPubMed
[144]
McCloskey, K. E., Chalmers, J. J., and Zborowski, M., Magnetophoretic mobilities correlate to antibody binding capacities.Cytometry, 40:4 (2000), 307–15.3.0.CO;2-H>CrossRefGoogle ScholarPubMed
[145]
Moore, L. R., M. Zborowski, M. Nakamura et al., The use of magnetite-doped polymeric microspheres in calibrating cell tracking velocimetry.J. Biochem. Bioph. Meth., 44:1–2 (2000), 115–30.CrossRefGoogle ScholarPubMed
[146]
Nakamura, M., Zborowski, M., Lasky, L. C., Margel, S., and Chalmers, J. J., Theoretical and experimental analysis of the accuracy and reproducibility of cell tracking velocimetry.Exp. Fluids, 30 (2001), 371–80.CrossRefGoogle Scholar
[147]
Schneider, T., L. R. Moore, Y. Jing et al., Continuous flow magnetic cell fractionation based on antigen expression level.J. Biochem. Bioph. Meth., 68:1 (2006), 1–21.CrossRefGoogle ScholarPubMed
[148]
Schneider, T., Karl, S., Moore, L. R., Chalmers, J. J., Williams, P. S., and Zborowski, M., Sequential CD34 cell fractionation by dipole magnetophoresis.Analyst, 135:1 (2010), 62–70.CrossRefGoogle ScholarPubMed
[149]
Robinson, A. L., New magnets enhance synchrotron radiation. Science, 219:4590 (1983), 1309–11.CrossRefGoogle ScholarPubMed
[150]
Hayden, M. E. and Häfeli, U. O., “Magnetic bandages” for targeted delivery of therapeutic agents.J. Phys. Condens. Mat., 18:38 (2006), S2877–91.CrossRefGoogle Scholar
[151]
Häfeli, U. O., Gilmour, K., Zhou, A., Lee, S., and Hayden, M. E., Modeling of magnetic bandages for drug targeting: Button vs. Halbach arrays.J. Magn. Magn. Mater., 311:1 (2007), 323–9.CrossRefGoogle Scholar
[152]
Hoyos, M., Moore, L., Williams, P. S., and Zborowski, M., The use of a linear Halbach array combined with a step-SPLITT channel for continuous sorting of magnetic species.J. Magn. Magn. Mater., 323:10 (2011), 1384–8.CrossRefGoogle ScholarPubMed
[153]
Ijiri, Y., Poudel, C., Williams, P. S., Moore, L. R., Orita, T., and Zborowski, M., Inverted linear halbach array for separation of magnetic nanoparticles.IEEE Trans. Magn., 49:7 (2013) 3449–52.CrossRefGoogle ScholarPubMed
[154]
Sarwar, A., Nemirovski, A., and Shapiro, B., Optimal Halbach permanent magnet designs for maximally pulling and pushing nanoparticles.J. Magn. Magn. Mater., 324:5 (2012), 742–54.CrossRefGoogle ScholarPubMed
[155]
Krause, K., U. Adamu, M. Weber et al., German stereotaxis-guided percutaneous coronary intervention study group: First multicenter real world experience. Clin. Res. Cardiol., 98:9 (2009), 541–7.CrossRefGoogle Scholar
[156]
Carpi, F., Kastelein, N., Talcott, M., and Pappone, C., Magnetically controllable gastrointestinal steering of video capsules. IEEE Trans. Biomed. Eng., 58:2 (2011), 231–4.CrossRefGoogle ScholarPubMed
[157]
Rinaldi, C., Franklin, T., Zahn, M., and Cader, T., Magnetic nanoparticles in fluid suspension: ferrofluid applications. In Schwarz, J. A., Contescu, C. I., and Putyera, K., eds., Encyclopedia of Nanoscience and Nanotechnology (Oxford: Taylor & Francis Group Ltd., 2004), pp. 1731–48.Google Scholar
[158]
Dutz, S. and Hergt, R., Magnetic nanoparticle heating and heat transfer on a microscale: Basic principles, realities and physical limitations of hyperthermia for tumour therapy. Int. J. Hyperther., 29:8 (2013), 790–800.CrossRefGoogle ScholarPubMed
Jordan, A., R. Scholz, K. Maier-Hauff et al., Presentation of a new magnetic field therapy system for the treatment of human solid tumors with magnetic fluid hyperthermia.J. Magn. Magn. Mater., 225 (2001), 118–26.CrossRefGoogle Scholar
[161]
Johannsen, M., U. Gneveckow, L. Eckelt et al., Clinical hyperthermia of prostate cancer using magnetic nanoparticles: Presentation of a new interstitial technique. Int. J. Hyperther., 21:7 (2005), 637–47.CrossRefGoogle ScholarPubMed
[162]
Johannsen, M., U. Gneveckow, K. Taymoorian et al., Morbidity and quality of life during thermotherapy using magnetic nanoparticles in locally recurrent prostate cancer: Results of a prospective phase I trial. Int. J. Hyperthermia, 23:3 (2007), 315–23.CrossRefGoogle ScholarPubMed
[163]
Johannsen, M., U. Gneveckow, B. Thiesen et al., Thermotherapy of prostate cancer using magnetic nanoparticles: Feasibility, imaging, and three-dimensional temperature distribution. Eur. Urol., 52:6 (2007), 1653–61.CrossRefGoogle ScholarPubMed
[164]
Maier-Hauff, K., R. Rothe, R. Scholz et al., Intracranial thermotherapy using magnetic nanoparticles combined with external beam radiotherapy: Results of a feasibility study on patients with glioblastoma multiforme. J. Neurooncol., 81:1 (2007), 53–60.CrossRefGoogle ScholarPubMed
[165]
Johannsen, M., Thiesen, B., Wust, P., and Jordan, A., Magnetic nanoparticle hyperthermia for prostate cancer. Int. J. Hyperther., 26:8 (2010), 790–5.CrossRefGoogle ScholarPubMed
[166]
van Landeghem, F. K., K. Maier-Hauff, A. Jordan et al., Post-mortem studies in glioblastoma patients treated with thermotherapy using magnetic nanoparticles. Biomaterials, 30:1 (2009), 52–7.CrossRefGoogle ScholarPubMed
[167]
Krishnan, S., Diagaradjane, P., and Cho, S. H., Nanoparticle-mediated thermal therapy: Evolving strategies for prostate cancer therapy. Int. J. Hyperther., 26:8 (2010), 775–89.CrossRefGoogle ScholarPubMed
[168]
Maier-Hauff, K., F. Ulrich, D. Nestler et al., Efficacy and safety of intratumoral thermotherapy using magnetic iron-oxide nanoparticles combined with external beam radiotherapy on patients with recurrent glioblastoma multiforme. J. Neurooncol., 103:2 (2011), 317–24.CrossRefGoogle ScholarPubMed
[169]
Nakamura, T., Konno, K., Moroné, T., Tsuya, N., and Hatano, M., Magneto-medicine: Biological aspects of ferromagnetic fine particles.J. Appl. Phys., 42:4 (1971), 1320–44.CrossRefGoogle Scholar
[170]
Senyei, A. E. and Widder, K. J., Drug targeting: Magnetically responsive albumin microspheres – a review of the system to date. Gynecol. Oncol., 12:1 (1981), 1–13.CrossRefGoogle ScholarPubMed
[171]
Lim, E. K., Huh, Y. M., Yang, J., Lee, K., Suh, J. S., and Haam, S., pH-triggered drug-releasing magnetic nanoparticles for cancer therapy guided by molecular imaging by MRI. Adv. Mater., 23:21 (2011), 2436–42.CrossRefGoogle ScholarPubMed
[172]
Nowicka, A. M., A. Kowalczyk, A. Jarzebinska et al., Progress in targeting tumor cells by using drug-magnetic nanoparticles conjugate. Biomacromolecules, 14:3 (2013), 828–33.CrossRefGoogle ScholarPubMed
[173]
Chorny, M., I. Fishbein, B. B. Yellen et al., Targeting stents with local delivery of paclitaxel-loaded magnetic nanoparticles using uniform fields. Proc. Natl. Acad. Sci. USA., 107:18 (2010), 8346–51.CrossRefGoogle ScholarPubMed
[174]
Li, M., Neoh, K. G., Wang, R., Zong, B. Y., Tan, J. Y., and Kang, E. T., Methotrexate-conjugated and hyperbranched polyglycerol-grafted Fe(3)O(4) magnetic nanoparticles for targeted anticancer effects. Eur. J. Pharm. Sci., 48:1–2 (2013), 111–20.CrossRefGoogle Scholar
[175]
Bleul, R., R. Thiermann, G. U. Marten et al., Continuously manufactured magnetic polymersomes: A versatile tool (not only) for targeted cancer therapy.Nanoscale, 5:23 (2013), 11385–93.CrossRefGoogle ScholarPubMed
[176]
Alexiou, C., R. J. Schmid, R. Jurgons et al., Targeting cancer cells: Magnetic nanoparticles as drug carriers. Eur. Biophys. J., 35:5 (2006), 446–50.CrossRefGoogle ScholarPubMed
[177]
Hsieh, D. S., Langer, R., and Folkman, J., Magnetic modulation of release of macromolecules from polymers. Proc. Natl. Acad. Sci. USA., 78:3 (1981), 1863–7.CrossRefGoogle ScholarPubMed
[178]
Edelman, E. R., Kost, J., Bobeck, H., and Langer, R., Regulation of drug release from polymer matrices by oscillating magnetic fields. J. Biomed. Mater. Res., 19:1 (1985), 67–83.CrossRefGoogle ScholarPubMed
[179]
Edelman, E. R., Fiorino, A., Grodzinsky, A., and Langer, R., Mechanical deformation of polymer matrix controlled release devices modulates drug release. J. Biomed. Mater. Res., 26:12 (1985), 1619–31.Google Scholar
[180]
Pirmoradi, F. N., Jackson, J. K., Burt, H. M., and Chiao, M., A magnetically controlled MEMS device for drug delivery: Design, fabrication, and testing. Lab Chip, 11:18 (2011), 3072–80.CrossRefGoogle Scholar
[181]
Pirmoradi, F. N., Jackson, J. K., Burt, H. M., and Chiao, M., On-demand controlled release of docetaxel from a battery-less MEMS drug delivery device. Lab Chip, 11:16 (2011), 2744–52.CrossRefGoogle ScholarPubMed
[182]
Dengler, M., K. Saatchi, J. P. Dailey et al., Targeted delivery of magnetic cobalt nanoparticles to the eye following systemic administration.AIP Conf. Proc., 1311 (2010), 329–36.CrossRefGoogle Scholar
[183]
Yanai, A., Häfeli, U. O., Metcalfe, A. L.et al., Focused magnetic stem cell targeting to the retina using superparamagnetic iron oxide nanoparticles. Cell Transplant., 21:6 (2012), 1137–48.CrossRefGoogle ScholarPubMed
[184]
Gregory-Evans, K., Bashar, A. E., and Laver, C., Use of magnetism to enhance cell transplantation success in regenerative medicine. Regen. Med., 8:1 (2013), 1–3.CrossRefGoogle ScholarPubMed
[185]
Bashar, A. E., A. Metcalfe, A. Yanai et al., Influence of iron oxide nanoparticles on innate and genetically modified secretion profiles of mesenchymal stem cells.IEEE Trans. Magn., 49:1 (2013), 389–393.CrossRefGoogle ScholarPubMed
[186]
Plank, C., Anton, M., Rudolph, C., Rosenecker, J., and Krotz, F., Enhancing and targeting nucleic acid delivery by magnetic force. Expert. Opin. Biol. Ther., 3:5 (2003), 745–58.CrossRefGoogle ScholarPubMed
[187]
Mykhaylyk, O., Antequera, Y. S., Vlaskou, D., and Plank, C., Generation of magnetic nonviral gene transfer agents and magnetofection in vitro. Nat. Protoc., 2:10 (2007), 2391–411.CrossRefGoogle ScholarPubMed
[188]
Jenkins, S. I., Pickard, M. R., and Chari, D. M., Magnetic nanoparticle mediated gene delivery in oligodendroglial cells: A comparison of differentiated cells versus precursor forms.Nano Life, 3:2 (2012), 1243001.CrossRefGoogle Scholar
[189]
Vlaskou, D.et al., Magnetic and Acoustically Active Lipospheres for Magnetically Targeted Nucleic Acid Delivery.Adv. Funct. Mater., 20 (2010), 3881–3894.CrossRefGoogle Scholar
[190]
Riegler, J., Wells, J. A., Kyrtatos, P. G., Price, A. N., Pankhurst, Q. A., and Lythgoe, M. F., Targeted magnetic delivery and tracking of cells using a magnetic resonance imaging system. Biomaterials, 31:20 (2010), 5366–71.CrossRefGoogle ScholarPubMed
[191]
Honig, D., DeRouchey, J., Jungmann, R., Koch, C., Plank, C., and Radler, J. O., Biophysical characterization of copolymer-protected gene vectors. Biomacromolecules, 11:7 (2010), 1802–9.CrossRefGoogle ScholarPubMed
[192]
Mayes, E., Douek, M., and Pankhurst, Q. A., Surgical magnetic systems and tracers for cancer staging. In Thanh, N. T. K., ed. Magnetic Nanoparticles – From Fabrication to Clinical Applications (Boca Raton: CRC Press – Taylor & Francis Group, 2012) pp. 541–55.Google Scholar
[193]
Krishnan, K. M., Biomedical nanomagnetics: A spin through possibilities in imaging, diagnostics, and therapy.IEEE Trans. Magn., 46:7 (2010), 2523–58.CrossRefGoogle Scholar
[194]
Duncan, R. and Gaspar, R., Nanomedicine(s) under the microscope. Mol. Pharm., 8:6 (2011), 2101–41.CrossRefGoogle ScholarPubMed
[195]
Svenson, S., Theranostics: Are we there yet?, Mol. Pharmaceutics, 10:3 (2013), 848–56.CrossRefGoogle ScholarPubMed
[196]
Zhou, J., Zhang, J., and Gao, W., Enhanced and selective delivery of enzyme therapy to 9L-glioma tumor via magnetic targeting of PEG-modified, beta-glucosidase-conjugated iron oxide nanoparticles. Int. J. Nanomed., 9 (2014), 2905–17.Google ScholarPubMed
[197]
Arias, J. L., Gallardo, V., Ruiz, M. A., and Delgado, A. V., Magnetite/poly(alkylcyanoacrylate) (core/shell) nanoparticles as 5-fluorouracil delivery systems for active targeting. Eur. J. Pharm. Biopharm., 69:1 (2008), 54–63.CrossRefGoogle ScholarPubMed
[198]
Arias, J. L., Lopez-Viota, M., Delgado, A. V., and Ruiz, M. A., Iron/ethylcellulose (core/shell) nanoplatform loaded with 5-fluorouracil for cancer targeting. Colloids Surf. B, 77:1 (2010), 111–6.CrossRefGoogle ScholarPubMed
[199]
Hua, M. Y., H. L. Liu, H. W. Yang et al., The effectiveness of a magnetic nanoparticle-based delivery system for BCNU in the treatment of gliomas. Biomaterials, 32:2 (2011), 516–27.CrossRefGoogle ScholarPubMed
[200]
Qu, J. B., Shao, H. H., Jing, G. L., and Huang, F., PEG-chitosan-coated iron oxide nanoparticles with high saturated magnetization as carriers of 10-hydroxycamptothecin: Preparation, characterization and cytotoxicity studies. Colloids Surf. B, 102 (2013), 37–44.CrossRefGoogle ScholarPubMed
[201]
Ding, G. B., Wang, Y., Guo, Y., and Xu, L., Integrin alpha(V)beta(3)-targeted magnetic nanohybrids with enhanced antitumor efficacy, cell cycle arrest ability, and encouraging anti-cell-migration activity. ACS Appl. Mater. Interfaces, 6:19 (2014), 16643–52.CrossRefGoogle ScholarPubMed
[202]
Li, F. R., Yan, W. H., Guo, Y. H., Qi, H., and Zhou, H. X., Preparation of carboplatin-Fe@C-loaded chitosan nanoparticles and study on hyperthermia combined with pharmacotherapy for liver cancer. Int. J. Hyperther., 25:5 (2009), 383–91.CrossRefGoogle Scholar
[203]
Saboktakin, M. R., Tabatabaie, R. M., Amini, F. S., Maharramov, A., and Ramazanov, M. A., Synthesis and in-vitro photodynamic studies of the superparamagnetic chitosan hydrogel/chlorin E6 nanocarriers. Med. Chem., 9:1 (2013), 112–7.Google ScholarPubMed
[204]
Gupta, R. and Bajpai, A. K., Magnetically guided release of ciprofloxacin from superparamagnetic polymer nanocomposites. J. Biomater. Sci. Polym. Ed., 22:7 (2011), 893–918.CrossRefGoogle ScholarPubMed
[205]
Unterweger, H., R. Tietze, C. Janko et al., Development and characterization of magnetic iron oxide nanoparticles with a cisplatin-bearing polymer coating for targeted drug delivery. Int. J. Nanomed., 9 (2014), 3659–76.Google ScholarPubMed
[206]
Manju, S. and Sreenivasan, K., Enhanced drug loading on magnetic nanoparticles by layer-by-layer assembly using drug conjugates: Blood compatibility evaluation and targeted drug delivery in cancer cells. Langmuir, 27:23 (2011), 14489–96.CrossRefGoogle ScholarPubMed
[207]
Mikhaylova, M., Stasinopoulos, I., Kato, Y., Artemov, D., and Bhujwalla, Z. M., Imaging of cationic multifunctional liposome-mediated delivery of COX-2 siRNA. Cancer Gene Ther., 16:3 (2009), 217–26.CrossRefGoogle ScholarPubMed
[208]
Du, X., K. Chen, S. Kuriyavar et al., Magnetic targeted delivery of dexamethasone acetate across the round window membrane in guinea pigs. Otol. Neurotol., 34:1 (2013), 41–7.CrossRefGoogle ScholarPubMed
[209]
Ling, Y., Wei, K., Luo, Y., Gao, X., and Zhong, S., Dual docetaxel/superparamagnetic iron oxide loaded nanoparticles for both targeting magnetic resonance imaging and cancer therapy. Biomaterials, 32:29 (2011), 7139–50.CrossRefGoogle ScholarPubMed
[210]
Gao, X., Y. Luo, Y. Wang et al., Prostate stem cell antigen-targeted nanoparticles with dual functional properties: In vivo imaging and cancer chemotherapy. Int. J. Nanomed., 7 (2012), 4037–51.Google ScholarPubMed
[211]
Mi, Y., Liu, X., Zhao, J., Ding, J., and Feng, S. S., Multimodality treatment of cancer with herceptin conjugated, thermomagnetic iron oxides and docetaxel loaded nanoparticles of biodegradable polymers. Biomaterials, 33:30 (2012), 7519–29.CrossRefGoogle ScholarPubMed
[212]
Guo, M., Que, C., Wang, C., Liu, X., Yan, H., and Liu, K., Multifunctional superparamagnetic nanocarriers with folate-mediated and pH-responsive targeting properties for anticancer drug delivery. Biomaterials, 32:1 (2011), 185–94.CrossRefGoogle ScholarPubMed
[213]
Nasongkla, N., E. Bey, J. Ren et al., Multifunctional polymeric micelles as cancer-targeted, MRI-ultrasensitive drug delivery systems. Nano Lett., 6:11 (2006), 2427–30.CrossRefGoogle ScholarPubMed
[214]
Zhang, J. and Misra, R. D., Magnetic drug-targeting carrier encapsulated with thermosensitive smart polymer: Core-shell nanoparticle carrier and drug release response. Acta Biomater., 3:6 (2007), 838–50.CrossRefGoogle ScholarPubMed
[215]
Chen, L. B., Zhang, F., and Wang, C. C., Rational synthesis of magnetic thermosensitive microcontainers as targeting drug carriers. Small, 5:5 (2009), 621–8.CrossRefGoogle ScholarPubMed
[216]
Purushotham, S., P. E. J. Chang, H. Rumpel et al., Thermoresponsive core-shell magnetic nanoparticles for combined modalities of cancer therapy. Nanotechnology, 20:30 (2009), 305101.CrossRefGoogle ScholarPubMed
[217]
Purushotham, S. and Ramanujan, R. V., Thermoresponsive magnetic composite nanomaterials for multimodal cancer therapy. Acta Biomater., 6:2 (2010), 502–10.CrossRefGoogle ScholarPubMed
[218]
Pradhan, P., J. Giri, F. Rieken et al., Targeted temperature sensitive magnetic liposomes for thermo-chemotherapy. J. Control. Release, 142:1 (2010), 108–21.CrossRefGoogle ScholarPubMed
[219]
Rahimi, M., A. Wadajkar, K. Subramanian et al., In vitro evaluation of novel polymer-coated magnetic nanoparticles for controlled drug delivery. Nanomedicine, 6:5 (2010), 672–80.Google ScholarPubMed
[220]
Yallapu, M. M., Foy, S. P., Jain, T. K., and Labhasetwar, V., PEG-functionalized magnetic nanoparticles for drug delivery and magnetic resonance imaging applications. Pharm. Res., 27:11 (2010), 2283–95.CrossRefGoogle ScholarPubMed
[221]
Yang, X., J. J. Grailer, I. J. Rowland et al., Multifunctional SPIO/DOX-loaded wormlike polymer vesicles for cancer therapy and MR imaging. Biomaterials, 31:34 (2010), 9065–73.CrossRefGoogle ScholarPubMed
[222]
Zou, P., Y. Yu, Y. A. Wang et al., Superparamagnetic iron oxide nanotheranostics for targeted cancer cell imaging and pH-dependent intracellular drug release. Mol. Pharm., 7:6 (2010), 1974–84.CrossRefGoogle ScholarPubMed
[223]
Chang, Y., X. Meng, Y. Zhao et al., Novel water-soluble and pH-responsive anticancer drug nanocarriers: Doxorubicin-PAMAM dendrimer conjugates attached to superparamagnetic iron oxide nanoparticles (IONPs). J. Colloid Interface Sci., 363:1 (2011), 403–9.CrossRefGoogle Scholar
[224]
Chao, X., L. Guo, Y. Zhao et al., PEG-modified GoldMag nanoparticles (PGMNs) combined with the magnetic field for local drug delivery. J. Drug Target., 19:3 (2011), 161–70.CrossRefGoogle ScholarPubMed
[225]
Chen, T., M. I. Shukoor, R. Wang et al., Smart multifunctional nanostructure for targeted cancer chemotherapy and magnetic resonance imaging. ACS Nano, 5:10 (2011), 7866–73.CrossRefGoogle ScholarPubMed
[226]
Fan, T., Li, M., Wu, X., and Wu, Y., Preparation of thermoresponsive and pH-sensitivity polymer magnetic hydrogel nanospheres as anticancer drug carriers. Colloids Surf. B, 88:2 (2011), 593–600.CrossRefGoogle ScholarPubMed
[227]
Liao, C., Sun, Q., Liang, B., Shen, J., and Shuai, X., Targeting EGFR-overexpressing tumor cells using Cetuximab-immunomicelles loaded with doxorubicin and superparamagnetic iron oxide. Eur. J. Radiol., 80:3 (2011), 699–705.Google ScholarPubMed
[228]
Yang, X., H. Hong, J. J. Grailer et al., cRGD-functionalized, DOX-conjugated, and 64Cu-labeled superparamagnetic iron oxide nanoparticles for targeted anticancer drug delivery and PET/MR imaging. Biomaterials, 32:17 (2011), 4151–60.CrossRefGoogle Scholar
[229]
Akbarzadeh, A., Mikaeili, H., Zarghami, N., Mohammad, R., Barkhordari, A., and Davaran, S., Preparation and in vitro evaluation of doxorubicin-loaded Fe(3)O(4) magnetic nanoparticles modified with biocompatible copolymers. Int. J. Nanomed., 7 (2012), 511–26.Google ScholarPubMed
[230]
Allard-Vannier, E., S. Cohen-Jonathan, J. Gautier et al., Pegylated magnetic nanocarriers for doxorubicin delivery: A quantitative determination of stealthiness in vitro and in vivo. Eur. J. Pharm. Biopharm., 81:3 (2012), 498–505.CrossRefGoogle ScholarPubMed
[231]
Gautier, J., E. Munnier, A. Paillard et al., A pharmaceutical study of doxorubicin-loaded PEGylated nanoparticles for magnetic drug targeting. Int. J. Pharm., 423:1 (2012), 16–25.CrossRefGoogle ScholarPubMed
[232]
Huang, C., Z. Tang, Y. Zhou et al., Magnetic micelles as a potential platform for dual targeted drug delivery in cancer therapy. Int. J. Pharm., 429:1–2 (2012), 113–22.CrossRefGoogle ScholarPubMed
[233]
Kaaki, K., Hervé-Aubert, K., Chiper, M.et al., Magnetic nanocarriers of doxorubicin coated with poly(ethylene glycol) and folic acid: Relation between coating structure, surface properties, colloidal stability, and cancer cell targeting. Langmuir, 28:2 (2012), 1496–505.CrossRefGoogle ScholarPubMed
[234]
Li, D., Tang, J., Guo, J., Wang, S., Chaudhary, D., and Wang, C., Hollow-core magnetic colloidal nanocrystal clusters with ligand-exchanged surface modification as delivery vehicles for targeted and stimuli-responsive drug release. Chemistry, 18:51 (2012), 16517–24.Google ScholarPubMed
[235]
Wang, H., S. Wang, Z. Liao et al., Folate-targeting magnetic core-shell nanocarriers for selective drug release and imaging. Int. J. Pharm., 430:1–2 (2012), 342–9.CrossRefGoogle Scholar
[236]
Chiang, W. H., W. C. Huang, C. W. Chang et al., Functionalized polymersomes with outlayered polyelectrolyte gels for potential tumor-targeted delivery of multimodal therapies and MR imaging. J. Control. Release, 168:3 (2013), 280–8.CrossRefGoogle ScholarPubMed
[237]
Glover, A. L., J. B. Bennett, J. S. Pritchett et al., Magnetic heating of iron oxide nanoparticles and magnetic micelles for cancer therapy. IEEE Trans. Magn., 49:1 (2013), 231–235.CrossRefGoogle ScholarPubMed
[238]
Pourjavadi, A., Hosseini, S. H., Alizadeh, M., and Bennett, C., Magnetic pH-responsive nanocarrier with long spacer length and high colloidal stability for controlled delivery of doxorubicin. Colloids Surf. B, 116C (2013), 49–54.Google Scholar
[239]
Sahoo, B., Devi, K. S., Banerjee, R., Maiti, T. K., Pramanik, P., and Dhara, D., Thermal and pH responsive polymer-tethered multifunctional magnetic nanoparticles for targeted delivery of anticancer drug. ACS Appl. Mater. Interfaces, 5:9 (2013), 3884–93.CrossRefGoogle ScholarPubMed
[240]
Ao, L., B. Wang, P. Liu et al., A folate-integrated magnetic polymer micelle for MRI and dual targeted drug delivery. Nanoscale, 6:18 (2014), 10710–6.CrossRefGoogle ScholarPubMed
[241]
Davaran, S., S. Alimirzalu, K. Nejati-Koshki et al., Physicochemical characteristics of Fe3O4 magnetic nanocomposites based on Poly(N-isopropylacrylamide) for anti-cancer drug delivery. Asian Pac. J. Cancer Prev., 15:1 (2014), 49–54.CrossRefGoogle ScholarPubMed
[242]
Park, J. H., H. J. Cho, H. Y. Yoon et al., Hyaluronic acid derivative-coated nanohybrid liposomes for cancer imaging and drug delivery. J. Control. Release, 174 (2014), 98–108.CrossRefGoogle ScholarPubMed
[243]
Sadighian, S., Rostamizadeh, K., Hosseini-Monfared, H., and Hamidi, M., Doxorubicin-conjugated core-shell magnetite nanoparticles as dual-targeting carriers for anticancer drug delivery. Colloids Surf. B, 117 (2014), 406–13.CrossRefGoogle ScholarPubMed
[244]
Scialabba, C., Licciardi, M., Mauro, N., Rocco, F., Ceruti, M., and Giammona, G., Inulin-based polymer coated SPIONs as potential drug delivery systems for targeted cancer therapy. Eur. J. Pharm. Biopharm., 88:3 (2014), 695–705.CrossRefGoogle ScholarPubMed
[245]
Tian, Y., Jiang, X., Chen, X., Shao, Z., and Yang, W., Doxorubicin-loaded magnetic silk fibroin nanoparticles for targeted therapy of multidrug-resistant cancer. Adv. Mater., 26:43 (2014), 7393–8.CrossRefGoogle ScholarPubMed
[246]
Unsoy, G., Khodadust, R., Yalcin, S., Mutlu, P., and Gunduz, U., Synthesis of Doxorubicin loaded magnetic chitosan nanoparticles for pH responsive targeted drug delivery. Eur. J. Pharm. Sci., 62 (2014), 243–50.CrossRefGoogle ScholarPubMed
[247]
Shen, J. M., F. Y. Gao, T. Yin et al., cRGD-functionalized polymeric magnetic nanoparticles as a dual-drug delivery system for safe targeted cancer therapy. Pharmacol. Res., 70:1 (2013), 102–15.CrossRefGoogle ScholarPubMed
[248]
Wadajkar, A. S.et al., Multifunctional particles for melanoma-targeted drug delivery. Acta. Biomater., 8:8 (2012), 2996–3004.CrossRefGoogle ScholarPubMed
[249]
Shevtsov, M. A., B. P. Nikolaev, L. Y. Yakovleva et al., Superparamagnetic iron oxide nanoparticles conjugated with epidermal growth factor (SPION-EGF) for targeting brain tumors. Int. J. Nanomed., 9 (2014), 273–87.Google ScholarPubMed
[250]
Su, W.et al., PEG/RGD-modified magnetic polymeric liposomes for controlled drug release and tumor cell targeting. Int. J. Pharm., 426:1–2 (2012), 170–81.CrossRefGoogle ScholarPubMed
[251]
Yuk, S. H.et al., Glycol chitosan/heparin immobilized iron oxide nanoparticles with a tumor-targeting characteristic for magnetic resonance imaging. Biomacromolecules, 12:6 (2011), 2335–43.CrossRefGoogle ScholarPubMed
[252]
Zhang, J., Shin, M. C., and Yang, V. C., Magnetic targeting of novel heparinized iron oxide nanoparticles evaluated in a 9L-glioma mouse model. Pharm. Res., 31:3 (2014), 579–92.CrossRefGoogle Scholar
[253]
Cinteza, L. O., Ohulchanskyy, T. Y., Sahoo, Y., Bergey, E. J., Pandey, R. K., and Prasad, P. N., Diacyllipid micelle-based nanocarrier for magnetically guided delivery of drugs in photodynamic therapy. Mol. Pharm., 3:4 (2006), 415–23.CrossRefGoogle ScholarPubMed
[254]
Shen, J. M., L. Xu, Y. Lu et al., Chitosan-based luminescent/magnetic hybrid nanogels for insulin delivery, cell imaging, and antidiabetic research of dietary supplements. Int. J. Pharm., 427:2 (2012), 400–9.CrossRefGoogle ScholarPubMed
[255]
Chen, S., Y. Li, C. Guo et al., Temperature-responsive magnetite/PEO-PPO-PEO block copolymer nanoparticles for controlled drug targeting delivery. Langmuir, 23:25 (2007), 12669–76.CrossRefGoogle ScholarPubMed
[256]
Cheong, S-J., C-M. Lee, S-L. Kim et al., Superparamagnetic iron oxide nanoparticles-loaded chitosan-linoleic acid nanoparticles as an effective hepatocyte-targeted gene delivery system. Int. J. Pharm., 372:1–2 (2009), 169–76.CrossRefGoogle ScholarPubMed
[257]
Ragheb, R. R., D. Kim, A. Bandyopadhyay et al., Induced clustered nanoconfinement of superparamagnetic iron oxide in biodegradable nanoparticles enhances transverse relaxivity for targeted theranostics. Magn. Reson. Med., 70:6 (2013), 1748–60.CrossRefGoogle ScholarPubMed
[258]
Krukemeyer, M. G., Krenn, V., Jakobs, M., and Wagner, W., Magnetic drug targeting in a rhabdomyosarcoma rat model using magnetite-dextran composite nanoparticle-bound mitoxantrone and 0.6 tesla extracorporeal magnets – sarcoma treatment in progress. J. Drug Target., 20:2 (2012), 185–93.CrossRefGoogle Scholar
[259]
Majd, M. Heidariet al., Specific targeting of cancer cells by multifunctional mitoxantrone-conjugated magnetic nanoparticles. J. Drug Target., 21:4 (2013), 328–40.Google Scholar
[260]
Ciofani, G., Genchi, G. G., Guardia, P., Mazzolai, B., Mattoli, V., and Bandiera, A., Recombinant human elastin-like magnetic microparticles for drug delivery and targeting. Macromol. Biosci., 14:5 (2014), 632–42.CrossRefGoogle ScholarPubMed
[261]
Jiang, X., X. Sha, H. Xin et al., Self-aggregated pegylated poly (trimethylene carbonate) nanoparticles decorated with c(RGDyK) peptide for targeted paclitaxel delivery to integrin-rich tumors. Biomaterials, 32:35 (2011), 9457–69.CrossRefGoogle Scholar
[262]
Luo, B., S. Xu, A. Luo et al., Mesoporous biocompatible and acid-degradable magnetic colloidal nanocrystal clusters with sustainable stability and high hydrophobic drug loading capacity. ACS Nano, 5:2 (2011), 1428–35.CrossRefGoogle ScholarPubMed
[263]
Chen, Y. C., Lee, W. F., Tsai, H. H., and Hsieh, W. Y., Paclitaxel and iron oxide loaded multifunctional nanoparticles for chemotherapy, fluorescence properties, and magnetic resonance imaging. J. Biomed. Mater. Res. A, 100:5 (2012), 1279–92.Google ScholarPubMed
[264]
Filippousi, M., S. A. Papadimitriou, D. N. Bikiaris et al., Novel core-shell magnetic nanoparticles for Taxol encapsulation in biodegradable and biocompatible block copolymers: Preparation, characterization and release properties. Int. J. Pharm., 448:1 (2013), 221–30.CrossRefGoogle ScholarPubMed
[265]
Shen, J. M., Yin, T., Tian, X. Z., Gao, F. Y., and Xu, S., Surface charge-switchable polymeric magnetic nanoparticles for the controlled release of anticancer drug. ACS Appl. Mater. Interfaces, 5:15 (2013), 7014–24.CrossRefGoogle ScholarPubMed
[266]
Jiao, Y., Sun, Y., Tang, X., Ren, Q., and Yang, W., Tumor- targeting multifunctional rattle-type theranostic nanoparticles for MRI/NIRF bimodal imaging and delivery of hydrophobic drugs. Small, 11:16 (2015). 1962–74CrossRefGoogle ScholarPubMed
[267]
Singh, A., Dilnawaz, F., Mewar, S., Sharma, U., Jagannathan, N. R., and Sahoo, S. K., Composite polymeric magnetic nanoparticles for co-delivery of hydrophobic and hydrophilic anticancer drugs and MRI imaging for cancer therapy. ACS Appl. Mater. Interfaces, 3:3 (2011), 842–56.CrossRefGoogle ScholarPubMed
[268]
Oliveira, R. R., Ferreira, F. S., Cintra, E. R., Branquinho, L. C., Bakuzis, A. F., and Lima, E. M., Magnetic nanoparticles and rapamycin encapsulated into polymeric nanocarriers. J. Biomed. Nanotechnol., 8:2 (2012), 193–201.CrossRefGoogle ScholarPubMed
[269]
Kirthivasan, B., Singh, D., Bommana, M. M., Raut, S. L., Squillante, E., and Sadoqi, M., Active brain targeting of a fluorescent P-gp substrate using polymeric magnetic nanocarrier system. Nanotechnology, 23:25 (2012), 255102.CrossRefGoogle ScholarPubMed
[270]
Namiki, Y., T. Namiki, H. Yoshida et al., A novel magnetic crystal-lipid nanostructure for magnetically guided in vivo gene delivery. Nat. Nanotechnol., 4:9 (2009), 598–606.CrossRefGoogle ScholarPubMed
[271]
Kumar, S., Jana, A. K., Dhamija, I., and Maiti, M., Chitosan-assisted immobilization of serratiopeptidase on magnetic nanoparticles, characterization and its target delivery. J. Drug Target., 22:2 (2014), 123–37.CrossRefGoogle ScholarPubMed
[272]
Chen, Y., W. Wang, G. Lian et al., Development of an MRI-visible nonviral vector for siRNA delivery targeting gastric cancer. Int. J. Nanomed., 7 (2012), 359–68.Google ScholarPubMed
[273]
Majd, M. Heidari, D. Asgari, J. Barar et al., Tamoxifen loaded folic acid armed PEGylated magnetic nanoparticles for targeted imaging and therapy of cancer. Colloids Surf. B, 106 (2013), 117–25.Google Scholar
[274]
Kempe, M., H. Kempe, I. Snowball et al., The use of magnetite nanoparticles for implant-assisted magnetic drug targeting in thrombolytic therapy. Biomaterials, 31:36 (2010), 9499–510.CrossRefGoogle ScholarPubMed