2000
DOI: 10.1016/s0165-022x(00)00085-3
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The use of magnetite-doped polymeric microspheres in calibrating cell tracking velocimetry

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Cited by 49 publications
(42 citation statements)
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“…Recipes for the creation of monodisperse polymer latex and microspheres exist; heterocoagulation of nanoparticles (17)(18)(19) or the direct precipitation of magnetic materials (20)(21)(22) onto the surfaces of monosized latex results in magnetic latex, monodisperse in size. Further polymerization of a polymer layer to cap the latex surface creates hydrophobic (18) or hydrophilic (23) magnetic latex.…”
Section: Introductionmentioning
confidence: 99%
“…Recipes for the creation of monodisperse polymer latex and microspheres exist; heterocoagulation of nanoparticles (17)(18)(19) or the direct precipitation of magnetic materials (20)(21)(22) onto the surfaces of monosized latex results in magnetic latex, monodisperse in size. Further polymerization of a polymer layer to cap the latex surface creates hydrophobic (18) or hydrophilic (23) magnetic latex.…”
Section: Introductionmentioning
confidence: 99%
“…We have relied on magnetophoretic mobility as a basis of continuous magnetic cell sorting methods and instrumentation during our past studies [10, 11]. The high sensitivity of the CTV technique to single cell motion allowed us to determine the relationship between surface antigen expression and the immunomagnetic superparamagnetic iron oxide (SPION) label binding [9], and to measure the difference in the MM distributions between RBCs differing in the hemoglobin magnetic moment [5]. The different MM obtained for paramagnetic and non-paramagnetic erythrocytes agreed with values calculated on the basis of bulk hemoglobin content and red blood cell magnetic susceptibility measurements by Gouy’s method [11], superconducting quantum interference device (SQUID) [12] and nuclear magnetic resonance (NMR) methods [13].…”
Section: Methodsmentioning
confidence: 99%
“…The magnetophoretic mobility of the spores was measured using our in house instrument, Cell Tracking Velocimetry, CTV (Chalmers et al, 1999;Moore et al, 2000;Zhang et al, 2005). Figure 1A presents an overview of the CTV system, while Figure 1B presents an enlarged view of the analysis region where the value of B ranges from 1.5 to 1.875 T, and the gradient, dB/dy, decreases correspondingly to the increase in B such that the product, dB 2 /dy, varies from 0.36 to 0.37 and back down to 0.36 T 2 /mm (between y ¼ À7 and À9 mm, Fig.…”
Section: Methodsmentioning
confidence: 99%