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. Author manuscript; available in PMC: 2010 Dec 1.
Published in final edited form as: Biomaterials. 2009 Sep 17;30(35):6748–6756. doi: 10.1016/j.biomaterials.2009.08.042

Table 2.

Effect of Pluronic and Tetronic coatings on MNP characteristics in vitro

Co-polymer % Co-polymer bound to MNPs* Protein binding Macrophage uptake (µg Fe/µg cell protein)** Diameter of MNPs (nm) and (Polydispersity Index)
Kb n Water Mannitol citrate buffer PBS BSA after 4 h***
Feridex IV 0.111 1.58 0.051 143 (0.29) 126 (0.28) 113 (0.29)
Pluronic F68 6.0 0.046 1.39 0.477 216 (0.12) 255 (0.08) 340 (0.14) 224 (0.08)
Pluronic F108 8.6 0.090 1.55 0.168 206 (0.09) 248 (0.11) 277 (0.17) 223 (0.08)
Pluronic F127 14.5 0.094 1.15 0.222 194 (0.10) 238 (0.08) 257 (0.15) 228 (0.15)
Pluronic L64 4.9 0.082 1.38 0.202 186 (0.10) 243 (0.13) 539 (0.46) 220 (0.12)
Tetronic 904 8.5 0.075 1.48 0.198 196 (0.15) 215 (0.12) 321 (0.21) 202 (0.15)
Tetronic 908 7.5 0.036 1.72 0.190 228 (0.11) 253 (0.11) 257 (0.13) 236 (0.06)
*

Co-polymer bound to MNPs was determined by thermogravimetric analysis.

**

0.1 mg /ml particles incubated with the mouse leukemic monocyte macrophage cell line RAW 264.7.

***

Particle size measured following 4 h incubation in the presence of 100 µg/ml BSA in water. Particle size represents hydrodynamic diameter. Core diameter (measured using transmission electron microscopy) was 10–15 nm. MNPs have negative zeta potentials, typically ranging from −20 to −30 mV.

MNPs, magnetic nanoparticles, PBS, phosphate-buffered saline; BSA, bovine serum albumin.