BNF-Partikel

Bionisierte NanoFerrit-Partikel (BNF-Partikel)

  • werden mittels Core-Shell-Verfahren hergestellt und besitzen einen Kern aus 75-80% (w/w) Magnetit und eine Hülle aus Dextran oder Hydroxyethyl-Stärke,
  • sind mit Durchmessern von 80 nm und 100 nm erhältlich,
  • sind thermisch geblockt bei Raumtemperatur und zeigen spezifische Wechselwirkungen mit magnetischen Wechselfeldern (Dennis et al. 2008 und 2009; Krycka et al., 2011; Bordelon et al., 2011),
  • 100 nm – BNF-Partikel können mit konventionellen Permanentmagneten separiert werden,
  • 80 nm – BNF-Partikel müssen im Hochgradientenmagnetfeld separiert werden oder für mehrere Stunden an einem starken Permanentmagneten,
  • werden mit den Oberflächenfunktionalitäten OH (plain), NH2, PEG-NH2, COOH und PEG-COOH für die kovalente Bindung von Proteinen, Antikörpern oder anderen Molekülen angeboten,
  • sind erhältlich mit kovalent gebundenen Proteinen (Streptavidin, Protein A),
  • können auf Anfrage mit speziellen Antikörpern konjugiert werden,
  • können einfach durch 0,22 µm-Filter filtriert werden.

 

Alle 28 Ergebnisse werden angezeigt

Referenzen
  • C.-T. Yang, P. Korangath, J. Stewart, C. Hu, W. Fu, C. Grüttner, S. E. Beck, F.-H. Lin and R. Ivkov, Systemically delivered antibody-labeled magnetic iron oxide nanoparticles are less toxic than plain nanoparticles when activated by alternating magnetic fields, International Journal of Hyperthermia, 2020, 37(3), 59–75;
  • F. Ahrentorp, A. Astalan, J. Blomgren, C. Jonasson, E. Wetterskog, P. Svedlindh, A. Lak, F. Ludwig, L. J. van IJzendoorn and F. Westphal, Effective particle magnetic moment of multi-core particles, Journal of Magnetism and Magnetic Materials, 2015, 380(221–226;
  • A. Al Faraj, A. Shaik, A. Shaik and B. Al Sayed, Enhanced magnetic delivery of superparamagnetic iron oxide nanoparticles to the lung monitored using noninvasive MR, Journal of Nanoparticle Research, 2014, 16(10), 1–11;
  • A. Attaluri, S. K. Kandala, M. Wabler, H. Zhou, C. Cornejo, M. Armour, M. Hedayati, Y. Zhang, T. L. DeWeese, C. Herman and R. Ivkov, Magnetic nanoparticle hyperthermia enhances radiation therapy: A study in mouse models of human prostate cancer, International Journal of Hyperthermia, 2015, 31(4), 359–374;
  • A. Attaluri, M. Seshadri, S. Mirpour, M. Wabler, T. Marinho, M. Furqan, H. Zhou, S. De Paoli, C. Grüttner, W. Gilson, T. DeWeese, M. Garcia, R. Ivkov and E. Liapi, Image-guided thermal therapy with a dual-contrast magnetic nanoparticle formulation: A feasibility study, International Journal of Hyperthermia, 2016, 1–15;
  • D. E. Bordelon, C. Cornejo, C. Grüttner, F. Westphal, T. L. DeWeese and R. Ivkov, Magnetic nanoparticle heating efficiency reveals magneto-structural differences when characterized with wide ranging and high amplitude alternating magnetic fields, Journal of Applied Physics, 2011, 109(12), 124904;
  • L. Branquinho, C., M. Carrião, S., A. Costa, S. , N. Zufelato, M. Sousa, H. , R. Miotto, R. Ivkov and A. Bakuzis, F. , Effect of magnetic dipolar interactions on nanoparticle heating efficiency: Implications for cancer hyperthermia, Scientific Reports, 2013, 3(2887;
  • L. Cuny, M. P. Herrling, G. Guthausen, H. Horn and M. Delay, Magnetic resonance imaging reveals detailed spatial and temporal distribution of iron-based nanoparticles transported through water-saturated porous media, Journal of contaminant hydrology, 2015, 182(51–62;
  • C. Dennis, A. Jackson, J. Borchers, P. Hoopes, R. Strawbridge, A. Foreman, J. Van Lierop, C. Grüttner and R. Ivkov, Nearly complete regression of tumors via collective behavior of magnetic nanoparticles in hyperthermia, Nanotechnology, 2009, 20(39), 395103;
  • C. Dennis, A. Jackson, J. Borchers, R. Ivkov, A. Foreman, P. Hoopes, R. Strawbridge, Z. Pierce, E. Goerntiz and J. Lau, The influence of magnetic and physiological behaviour on the effectiveness of iron oxide nanoparticles for hyperthermia, Journal of Physics D: Applied Physics, 2008, 41(13), 134020;
  • C. Dennis, A. Jackson, J. Borchers, R. Ivkov, A. Foreman, J. Lau, E. Görnitz and C. Grüttner, The influence of collective behavior on the magnetic and heating properties of iron oxide nanoparticles, Journal of Applied Physics, 2008, 103(7), 07A319;
  • C. L. Dennis, K. L. Krycka, J. A. Borchers, R. D. Desautels, J. van Lierop, N. F. Huls, A. J. Jackson, C. Grüttner and R. Ivkov, Internal magnetic structure of nanoparticles dominates time‐dependent relaxation processes in a magnetic field, Advanced Functional Materials, 2015, 25(27), 4300–4311;
  • J. Fock, C. Jonasson, C. Johansson and M. F. Hansen, Characterization of fine particles using optomagnetic measurements, Physical Chemistry Chemical Physics, 2017, 19(13), 8802–8814;
  • A. Giustini, R. Ivkov and P. Hoopes, Magnetic nanoparticle biodistribution following intratumoral administration, Nanotechnology, 2011, 22(34), 345101;
  • A. J. Giustini, I. Perreard, A. M. Rauwerdink, P. J. Hoopes and J. B. Weaver, Noninvasive assessment of magnetic nanoparticle–cancer cell interactions, Integrative Biology, 2012, 4(10), 1283–1288;
  • A. J. Giustini, A. A. Petryk and P. J. Hoopes, Ionization radiation increases systemic nanoparticle tumor accumulation, Nanomedicine, 2012, 8(6), 818–821;
  • C. Grüttner, K. Müller, J. Teller and F. Westphal, Synthesis and functionalisation of magnetic nanoparticles for hyperthermia applications, International Journal of Hyperthermia, 2013, 29(8), 777–789;
  • L. Gutierrez, R. Costo, C. Grüttner, F. Westphal, N. Gehrke, D. Heinke, A. Fornara, Q. A. Pankhurst, C. Johansson and S. Veintemillas-Verdaguer, Synthesis methods to prepare single-and multi-core iron oxide nanoparticles for biomedical applications, Dalton Transactions, 2015, 44(2943–2952;
  • S. Hapuarachchige, Y. Kato, E. J. Ngen, B. Smith, M. Delannoy and D. Artemov, Non-Temperature Induced Effects of Magnetized Iron Oxide Nanoparticles in Alternating Magnetic Field in Cancer Cells, PLoS ONE, 2016, 11(5), e0156294;
  • M. Hedayati, B. Abubaker-Sharif, M. Khattab, A. Razavi, I. Mohammed, A. Nejad, M. Wabler, H. Zhou, J. Mihalic, C. Grüttner, T. DeWeese and R. Ivkov, An optimised spectrophotometric assay for convenient and accurate quantitation of intracellular iron from iron oxide nanoparticles, International Journal of Hyperthermia, 2017, 1–9;
  • M. Hedayati, O. Thomas, B. Abubaker-Sharif, H. Zhou, C. Cornejo, Y. Zhang, M. Wabler, J. Mihalic, C. Grüttner, F. Westphal, A. Geyt, T. L. DeWeese and R. Ivkov, The effect of cell-cluster size on intracellular nanoparticle-mediated hyperthermia: is it possible to treat microscopic tumors, Nanomedicine, 2012, 8(1), 29–41;
  • A. Jaufenthaler, T. Kornack, V. Lebedev, M. E. Limes, R. Körber, M. Liebl and D. Baumgarten, Pulsed Optically Pumped Magnetometers: Addressing Dead Time and Bandwidth for the Unshielded Magnetorelaxometry of Magnetic Nanoparticles, Sensors, 2021, 21(4), 1212;
  • S. K. Kandala, E. Liapi, L. L. Whitcomb, A. Attaluri and R. Ivkov, Temperature-controlled power modulation compensates for heterogeneous nanoparticle distributions: a computational optimization analysis for magnetic hyperthermia, International Journal of Hyperthermia, 2018, 1–15;
  • A. Kasten, C. Grüttner, J.-P. Kühn, R. Bader, J. Pasold and B. Frerich, Comparative In Vitro Study on Magnetic Iron Oxide Nanoparticles for MRI Tracking of Adipose Tissue-Derived Progenitor Cells, PloS one, 2014, 9(9), e108055;
  • A. Kasten, B. J. Siegmund, C. Grüttner, J.-P. Kühn and B. Frerich, Tracking of adipose tissue-derived progenitor cells using two magnetic nanoparticle types, Journal of Magnetism and Magnetic Materials, 2015, 380(34–38;
  • K. Kekalo, I. Baker, R. Meyers and J. Shyong, Magnetic Nanoparticles with High Specific Absorption Rate at Low Alternating Magnetic Field, Nano LIFE, 2015, 5(2), 1550002;
  • K. Krycka, A. Jackson, J. Borchers, J. Shih, R. Briber, R. Ivkov, C. Grüttner and C. Dennis, Internal magnetic structure of dextran coated magnetite nanoparticles in solution using small angle neutron scattering with polarization analysis, Journal of Applied Physics, 2011, 109(7), 07B513;
  • D. A. Kuckla, J.-S. Brand, B. Czech, A. Asharion, J. V. Jüttner, I. P. Novoselova, A. Neusch, P. Hagemann, M. Getzlaff and C. Monzel, An efficient magnetothermal actuation setup for fast heating/cooling cycles or long-term induction heating of different magnetic nanoparticle classes, Journal of Physics D: Applied Physics, 2023, 56(50), 505002;
  • T.-A. Le, M. P. Bui and J. J. I. j. o. m. s. Yoon, Theoretical Analysis for Wireless Magnetothermal Deep Brain Stimulation Using Commercial Nanoparticles, 2019, 20(12), 2873;
  • F. Ludwig, O. Kazakova, L. F. Barquin, A. Fornara, L. Trahms, U. Steinhoff, P. Svedlindh, E. Wetterskog, Q. A. Pankhurst and P. Southern, Magnetic, Structural, and Particle Size Analysis of Single-and Multi-Core Magnetic Nanoparticles, Magnetics, IEEE Transactions on, 2014, 50(11), 1–4;
  • B. Mues, B. Bauer, J. Ortega, E. M. Buhl, H. Teller, T. Gries, T. Schmitz-Rode and I. Slabu, Assessing hyperthermia performance of hybrid textile filaments: The impact of different heating agents, Journal of Magnetism and Magnetic Materials, 2021, 519(167486;
  • A. Mukherjee, M. Castanares, M. Hedayati, M. Wabler, B. Trock, P. Kulkarni, R. Rodriguez, R. H. Getzenberg, T. L. DeWeese and R. Ivkov, Monitoring nanoparticle-mediated cellular hyperthermia with a high-sensitivity biosensor, Nanomedicine, 2014, 9(18), 2729–2743;
  • L. Ocker, A. Adamus, L. Hempfling, B. Wagner, R. Vahdad, F. A. Verburg, M. Luster, T. Schurrat, D. Bier, M. J. P. Frank and p. therapy, Hypericin and its radio iodinated derivatives–A novel combined approach for the treatment of pediatric alveolar rhabdomyosarcoma cells in vitro, 2020, 29(101588;
  • A. L. Oei, P. Korangath, K. Mulka, M. Helenius, J. B. Coulter, J. Stewart, E. Velarde, J. Crezee, B. Simons and L. J. Stalpers, Enhancing the abscopal effect of radiation and immune checkpoint inhibitor therapies with magnetic nanoparticle hyperthermia in a model of metastatic breast cancer, International Journal of Hyperthermia, 2019, 36(sup1), 47–63;
  • F. W. Østerberg, G. Rizzi, A. D. Henriksen and M. F. Hansen, Planar Hall effect bridge geometries optimized for magnetic bead detection, Journal of Applied Physics, 2014, 115(18), 184505;
  • J. Pearce, A. Giustini, R. Stigliano and P. Jack Hoopes, Magnetic Heating of Nanoparticles: The Importance of Particle Clustering to Achieve Therapeutic Temperatures, Journal of Nanotechnology in Engineering and Medicine, 2013, 4(1), 0110071–01100714;
  • I. Perreard, D. Reeves, X. Zhang, E. Kuehlert, E. Forauer and J. Weaver, Temperature of the magnetic nanoparticle microenvironment: estimation from relaxation times, Physics in medicine and biology, 2014, 59(5), 1109;
  • A. A. Petryk, A. J. Giustini, R. E. Gottesman, P. A. Kaufman and P. J. Hoopes, Magnetic nanoparticle hyperthermia enhancement of cisplatin chemotherapy cancer treatment, International Journal of Hyperthermia, 2013, 29(8), 845–851;
  • A. A. Petryk, A. J. Giustini, R. E. Gottesman, B. S. Trembly and P. J. Hoopes, Comparison of magnetic nanoparticle and microwave hyperthermia cancer treatment methodology and treatment effect in a rodent breast cancer model, International Journal of Hyperthermia, 2013, 29(8), 819–827;
  • F. Ranzinger, M. P. Herrling, S. Lackner, V. W. Grande, A. Baniodeh, A. K. Powell, H. Horn and G. Guthausen, Direct surface visualization of biofilms with high spin coordination clusters using Magnetic Resonance Imaging, Acta biomaterialia, 2016, 31(167–177;
  • D. B. Reeves and J. B. Weaver, Magnetic nanoparticle sensing: decoupling the magnetization from the excitation field, Journal of physics D: Applied physics, 2014, 47(4), 045002;
  • S. Sepehri, J. Andersson, V. Schaller, C. Grüttner, M. Stading and C. Johansson, Remote Sensing of the Nano-Rheological Properties of Soft Materials Using Magnetic Nanoparticles and Magnetic AC Susceptometry, Nanomaterials, 2022, 13(1), 67;
  • A. Sharma, E. Cressman, A. Attaluri, D. Kraitchman and R. Ivkov, Current Challenges in Image-Guided Magnetic Hyperthermia Therapy for Liver Cancer, Nanomaterials, 2022, 12(2768;
  • B. J. Siegmund, A. Kasten, J.-P. Kühn, K. Winter, C. Grüttner and B. Frerich, MRI-tracking of transplanted human ASC in a SCID mouse model, Journal of Magnetism and Magnetic Materials, 2017, 427(151–155;
  • F. Soetaert, S. K. Kandala, A. Bakuzis and R. Ivkov, Experimental estimation and analysis of variance of the measured loss power of magnetic nanoparticles, Scientific Reports, 2017, 7(1), 6661;
  • T. Sriviriyakul, S. Bogren, V. Schaller, C. Jonasson, J. Blomgren, F. Ahrentorp, P. Lopez-Sanchez, M. Berta, C. Grüttner and L. Zeng, Nanorheological studies of xanthan/water solutions using magnetic nanoparticles, Journal of Magnetism and Magnetic Materials, 2019, 473(268–271;
  • R. V. Stigliano, F. Shubitidze, K. Kekalo, I. Baker, A. J. Giustini and P. J. Hoopes, Understanding mNP Hyperthermia for cancer treatment at the cellular scale, Proceedings - Society of Photo-Optical Instrumentation Engineers, 2013, 8584(85840E;
  • M. Wabler, W. Zhu, M. Hedayati, A. Attaluri, H. Zhou, J. Mihalic, A. Geyh, T. L. DeWeese, R. Ivkov and D. Artemov, Magnetic resonance imaging contrast of iron oxide nanoparticles developed for hyperthermia is dominated by iron content, International Journal of Hyperthermia, 2014, 30(3), 192–200;
  • J. B. Weaver and E. Kuehlert, Measurement of magnetic nanoparticle relaxation time, Med. Phys., 2012, 39(5), 2765–2770;
  • J. B. Weaver, X. Zhang, E. Kuehlert, S. Toraya-Brown, D. B. Reeves, I. M. Perreard and S. N. Fiering, Magnetic Nanoparticle Quantitation with Low Frequency Magnetic Fields: Compensating for Relaxation Effects, Nanotechnology, 2013, 24(32), 325502–325502;
  • K. Witte, K. Müller, C. Grüttner, F. Westphal and C. Johansson, Particle size-and concentration-dependent separation of magnetic nanoparticles, Journal of Magnetism and Magnetic Materials, 2017, 427(320–324;
  • P. L. Zadnik, C. A. Molina, R. Sarabia-Estrada, M. L. Groves, M. Wabler, J. Mihalic, E. F. McCarthy, Z. L. Gokaslan, R. Ivkov and D. Sciubba, Characterization of intratumor magnetic nanoparticle distribution and heating in a rat model of metastatic spine disease: Laboratory investigation, Journal of Neurosurgery: Spine, 2014, 20(6), 740–750;
  • D. C. Baiu, N. S. Artz, M. R. McElreath, B. D. Menapace, D. Hernando, S. B. Reeder, C. Grüttner and M. Otto, High specificity targeting and detection of human neuroblastoma using multifunctional anti-GD2 iron-oxide nanoparticles, Nanomedicine, 2015, 10(19), 2973–2988;
  • B. Behnam Azad, S. R. Banerjee, M. Pullambhatla, S. Lacerda, C. A. Foss, Y. Wang, R. Ivkov and M. G. Pomper, Evaluation of a PSMA-targeted BNF nanoparticle construct, Nanoscale, 2015, 7(10), 4432–4442;
  • Z. Boekelheide, J. T. Miller, C. Grüttner and C. L. Dennis, The effects of intraparticle structure and interparticle interactions on the magnetic hysteresis loop of magnetic nanoparticles, Journal of Applied Physics, 2019, 126(4), 043903;
  • F. Gaffron, A. Tilch, C. Grüttner, A. Kowalski, M. Kramer and U. Teichgräber, Challenges in Tracking of Fluorochrome-Labelled Nanoparticles in Mice via Whole Body NIRF Imaging, Nanomaterials, 2020, 10(3), 596;
  • C. Grüttner, K. Müller and J. Teller, Comparison of Strain-Promoted Alkyne-Azide Cycloaddition with Established Methods for Conjugation of Biomolecules to Magnetic Nanoparticles, Magnetics, IEEE Transactions on, 2013, 49(1), 172–176;
  • P. Korangath, J. D. Barnett, A. Sharma, E. T. Henderson, J. Stewart, S.-H. Yu, S. K. Kandala, C.-T. Yang, J. S. Caserto and M. Hedayati, Nanoparticle interactions with immune cells dominate tumor retention and induce T cell–mediated tumor suppression in models of breast cancer, Science Advances, 2020, 6(13), eaay1601;
  • C. Ndong, S. Toraya-Brown, K. Kekalo, I. Baker, T. U. Gerngross, S. N. Fiering and K. E. Griswold, Antibody-mediated targeting of iron oxide nanoparticles to the folate receptor alpha increases tumor cell association in vitro and in vivo, International Journal of Nanomedicine, 2015, 10(2595;
  • E. J. Ngen, B. Behnam Azad, S. Boinapally, A. Lisok, M. Brummet, D. Jacob, M. G. Pomper and S. R. Banerjee, MRI Assessment of Prostate-Specific Membrane Antigen (PSMA) Targeting by a PSMA-Targeted Magnetic Nanoparticle: Potential for Image-Guided Therapy, Molecular pharmaceutics, 2019, 16(5), 2060–2068;
  • F. W. Østerberg, G. Rizzi, T. Zardán Gómez de la Torre, M. Strömberg, M. Strømme, P. Svedlindh and M. Hansen, Measurements of Brownian relaxation of magnetic nanobeads using planar Hall effect bridge sensors, Biosensors and Bioelectronics, 2013, 40(1), 147–152;
  • S. Schrittwieser, B. Pelaz, W. J. Parak, S. Lentijo-Mozo, K. Soulantica, J. Dieckhoff, F. Ludwig, A. Guenther, A. Tschöpe and J. Schotter, Homogeneous biosensing based on magnetic particle labels, Sensors, 2016, 16(6), 828;
  • T. Zardan Gomez de la Torre, M. Strömberg, C. Russell, J. Göransson, M. Nilsson, P. Svedlindh and M. Stromme, Investigation of immobilization of functionalized magnetic nanobeads in rolling circle amplified DNA coils, J. Phys. Chem. B, 2010, 114(3707–3713;
  • Y. Zhu, K. Kekalo, C. NDong, Y. Y. Huang, F. Shubitidze, K. E. Griswold, I. Baker and J. X. Zhang, Magnetic‐Nanoparticle‐Based Immunoassays‐on‐Chip: Materials Synthesis, Surface Functionalization, and Cancer Cell Screening, Advanced Functional Materials, 2016, 26(3953–3972;
  • J. Fock, M. Parmvi, M. Strömberg, P. Svedlindh, M. Donolato and M. F. Hansen, Comparison of optomagnetic and AC susceptibility readouts in a magnetic nanoparticle agglutination assay for detection of C-reactive protein, Biosensors and Bioelectronics, 2016, 88(94–100;
  • E. J. Ngen, L. Wang, Y. Kato, B. Krishnamachary, W. Zhu, N. Gandhi, B. Smith, M. Armour, J. Wong and K. Gabrielson, Imaging transplanted stem cells in real time using an MRI dual-contrast method, Scientific reports, 2015, 5(13628;
  • A. Al Faraj, A. Shaik, S. Afzal, S. Al-Muhsen and R. Halwani, Specific targeting and noninvasive magnetic resonance imaging of an asthma biomarker in the lung using polyethylene glycol functionalized magnetic nanocarriers, Contrast media & molecular imaging, 2015, 11(3), 172–183;
  • C. Grüttner, K. Müller, J. Teller, F. Westphal, A. R. Foreman and R. Ivkov, Synthesis and antibody conjugation of magnetic nanoparticles with improved specific power absorption rates for alternating magnetic field cancer therapy, J. Magn. Magn. Mat., 2007, 311(1), 181–186;
  • A. Natarajan, C. Grüttner, R. Ivkov, G. DeNardo, G. Mirick, A. Yuan, A. Foreman and S. DeNardo, NanoFerrite particle based radioimmunonanoparticles: binding affinity and in vivo pharmacokinetics, Bioconjugate chemistry, 2008, 19(6), 1211–1218;
  • J. Zhang, A. H. Dewilde, P. Chinn, A. R. Foreman, S. Barry, D. Kanne and S. J. Braunhut, Herceptin-directed nanoparticles activated by an alternating magnetic field selectively kill HER-2 positive human breast cancer cells in vitro via hyperthermia, Int. J. Hyperthermia, 2011, 27(7), 682–697;
  • R. S. Bejhed, T. Z. G. de la Torre, M. Donolato, M. F. Hansen, P. Svedlindh, M. Strömberg, R. S. Bejhed, T. Z. G. de la Torre, M. Donolato, M. F. Hansen, P. Svedlindh and M. Strömberg, Turn-on optomagnetic bacterial DNA sequence detection using volume-amplified magnetic nanobeads, Biosensors and Bioelectronics, 2015, 66(405–411;
  • R. S. Bejhed, M. Strømme, P. Svedlindh, A. Ahlford and M. Strömberg, Magnetic nanobeads present during enzymatic amplification and labeling for a simplified DNA detection protocol based on AC susceptometry, AIP Advances, 2015, 5(12), 127139;
  • J. Blomgren, F. Ahrentorp, D. Ilver, C. Jonasson, S. Sepehri, A. Kalaboukhov, D. Winkler, T. Zardán Gómez de la Torre, M. Strømme and C. Johansson, Development of a Sensitive Induction-Based Magnetic Nanoparticle Biodetection Method, Nanomaterials, 2018, 8(11), 887;
  • P. H. D. da Fonseca, W. D. T. Antunes and S. I. P. C. de Freitas, Characterisation of bacterial-nanoparticle interactions via STORM and SEM: Optimising magnetic labelling strategies for biosensor integration, Sensors and Actuators Reports, 2025, 100430;
  • M. Donolato, P. Antunes, R. S. Bejhed, T. Zardán Gómez de la Torre, F. W. Østerberg, M. Strömberg, M. Nilsson, M. Strømme, P. Svedlindh and M. F. Hansen, Novel readout method for molecular diagnostic assays based on optical measurements of magnetic nanobead dynamics, Analytical chemistry, 2015, 87(3), 1622–1629;
  • M. Donolato, P. Antunes, T. Z. G. de la Torre, E.-T. Hwu, C.-H. Chen, R. Burger, G. Rizzi, F. G. Bosco, M. Strømme and A. Boisen, Quantification of rolling circle amplified DNA using magnetic nanobeads and a Blu-ray optical pick-up unit, Biosensors and Bioelectronics, 2015, 67(649–655;
  • A. Engström, T. Z. G. de la Torre, M. Strømme, M. Nilsson and D. Herthnek, Detection of rifampicin resistance in Mycobacterium tuberculosis by padlock probes and magnetic nanobead-based readout, PloS one, 2013, 8(4), e62015;
  • S. W. Gordon-Wylie, C. Grüttner, H. Teller and J. B. Weaver, Using magnetic nanoparticles and protein/protein interactions to measure pH at the nanoscale, IEEE Sensors Letters, 2020, 1–1;
  • H. Khurshid, Y. Shi, B. L. Berwin and J. B. Weaver, Evaluating blood clot progression using magnetic particle spectroscopy, Medical physics, 2018, 45(7), 3258–3263;
  • G. A. S. Minero, J. Fock, J. S. McCaskill and M. F. Hansen, Optomagnetic detection of DNA triplex nanoswitches, Analyst, 2017, 142(4), 582–585;
  • G. A. S. Minero, C. Nogueira, G. Rizzi, B. Tian, J. Fock, M. Donolato, M. Strömberg and M. F. Hansen, Sequence-specific validation of LAMP amplicons in real-time optomagnetic detection of Dengue serotype 2 synthetic DNA, Analyst, 2017, 142(18), 3441–3450;
  • F. W. Østerberg, G. Rizzi, M. Donolato, R. S. Bejhed, A. Mezger, M. Strömberg, M. Nilsson, M. Strømme, P. Svedlindh and M. F. Hansen, On-Chip Detection of Rolling Circle Amplified DNA Molecules from Bacillus Globigii Spores and Vibrio Cholerae, Small, 2014, 10(14), 2877–2882;
  • M. Strömberg, T. Zardán Gómez de la Torre, M. Nilsson, P. Svedlindh and M. Strømme, A magnetic nanobead-based bioassay provides sensitive detection of single- and biplex bacterial DNA using a portable AC susceptometer, Biotechnology Journal, 2014, 9(1), 137–145;
  • B. Tian, R. S. Bejhed, P. Svedlindh and M. Strömberg, Blu-ray optomagnetic measurement based competitive immunoassay for Salmonella detection, Biosensors and Bioelectronics, 2016, 77(32–39;
  • B. Tian, Y. Han, E. Wetterskog, M. Donolato, M. F. Hansen, P. Svedlindh and M. Strömberg, MicroRNA Detection through DNAzyme-Mediated Disintegration of Magnetic Nanoparticle Assemblies, J ACS sensors, 2018, 3(9), 1884–1891;
  • B. Tian, X. Liao, P. Svedlindh, M. Strömberg and E. Wetterskog, Ferromagnetic Resonance Biosensor for Homogeneous and Volumetric Detection of DNA, ACS sensors, 2018, 3(6), 1093–1101;
  • B. Tian, J. Ma, T. Zardán Gómez de la Torre, A. d. m. Bálint, M. Donolato, M. F. Hansen, P. Svedlindh and M. Strömberg, Rapid Newcastle Disease Virus Detection Based on Loop-Mediated Isothermal Amplification and Optomagnetic Readout, Acs Sensors, 2016, 1(10), 1228–1234;
  • B. Tian, Z. Qiu, J. Ma, T. Z. G. de la Torre, C. Johansson, P. Svedlindh and M. Strömberg, Attomolar Zika virus oligonucleotide detection based on loop-mediated isothermal amplification and AC susceptometry, Biosensors and Bioelectronics, 2016, 86(420–425;
  • R. Uddin, R. Burger, M. Donolato, J. Fock, M. Creagh, M. F. Hansen and A. Boisen, Lab-on-a-disc agglutination assay for protein detection by optomagnetic readout and optical imaging using nano-and micro-sized magnetic beads, Biosensors and Bioelectronics, 2016, 85(351–357;
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