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Morphology and mean particle diameter were determined using a JEM-2100F microscope (JEOL, Freising, Germany).
BET surface area and average pore diameter were determined using a Micrometrics Tristar II surface area and porosity analyzer.
Surface morphology and MWCNT diameter were determined using high-resolution transmission electron microscopy (HR TEM, JEOL Jem-2100).
A thickness of 3,530 nm and pore sizes ranging from 25 to 45 nm in diameter were determined using scanning electron microscopy (data not shown).
Cell concentration, viability and average cell diameter were determined using the Vi-CELL™ XR device (Beckman Coulter).
Particle size distribution and mean diameter were determined using an N5 Submicron Particle Size Analyzer (Beckman, USA) [ 18].
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Particle diameter was determined using a Nicomp 380ZLS particle sizing system.
Maximal aneurysm diameter was determined using two independent methods: (1) measured manually, from cross-sectional computed tomography (XSCT) angiograms and (2) calculated from quantitative three-dimensional computed tomography (3DCT) data as orthonormal diameter.
The average cell diameter was determined using an automated cell counter (Invitrogen, Darmstadt, Germany) in a separate experiment.
The growth cone diameter was determined using ImageJ by measuring from the lateral edges of lamellipodia at the widest point of the growth cone, excluding filopodia.
Longitudinal electrocardiograph-gated end-diastolic images were acquired and the arterial diameter was determined using automatic edge-detection software (Vascular Tools, Coralville, IA).
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