Studying the fragmentation and refinement of diamond powder as well as the diversification in the intergranular stress is crucial to produce a high-quality polycrystalline diamond. In this paper, using different micron-size diamond powders as the initial materials, the samples were compressed under different pressures at ambient temperature. The fragmentation behavior of the diamond powder was investigated by scanning electron microscopy and with a laser particle size analyzer. The results show that the fragmentation of diamond comprises three stages with increasing pressure: (i) fracturing of edges and corners, (ii) cracking of the crystal plane, and (iii) refinement of particle disorder; the particle deformation tends to become relatively stable after a certain pressure. In situ high-pressure synchrotron X-ray diffraction was used to study the intergranular stress distribution under non-hydrostatic compression to 35.1 GPa. A heterogeneous stress distribution was found in compressed diamond bulk, in which under the highest load, the maximum stress reached 69.5 GPa, whereas the minimum stress was only 18.8 GPa.

The potential of using endothelial progenitor cells (EPCs) in novel anticancer therapy and the repair of vascular injury has been increasingly recognized. In the present study, EPCs were labeled with N-alkyl-polyethylenimine 2 kDa (PEI2k)-stabilized superparamagnetic iron oxide (SPIO) to facilitate magnetic resonance imaging (MRI) of EPCs in a mouse lung carcinoma xenograft model. EPCs derived from human peripheral blood were labeled with alkyl-PEI2k/SPIO. The viability and activity of labeled cells were evaluated using proliferation, migration, and tubulogenesis assays. Alkyl-PEI2k/SPIO-labeled EPCs were injected intravenously (group 1) or mixed and injected together with A549 cells subcutaneously (group 2) into groups of six mice with severe combined immunodeficiency. The labeling efficiency with alkyl-PEI2k/SPIO at 7 μg Fe/mL concentration was approximately 100%. Quantitative analysis of cellular iron was 6.062 ± 0.050 pg/cell. No significant effects on EPC proliferation, migration, or tubulogenesis were seen after labeling. Seven-tesla micro-MRI showed the presence of schistic or linear hypointense regions at the tumor margins starting from days 7 to 8 after EPC administration. This gradually extended into the inner tumor layers in group 1. In group 2, tumor growth was accompanied by dispersion of low-signal intensity regions inside the tumor. Iron-positive cells identified by Prussian blue dye were seen at the sites identified using MRI. Human CD31-positive cells and mouse CD31-positive cells were present in both groups. Labeling EPCs with alkyl-PEI2k/SPIO allows noninvasive magnetic resonance investigation of EPC involvement in tumor neovasculature and is associated with excellent biocompatibility and MRI sensitivity.

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