Publications (70) View all
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Article: Evaluation of brain tumor vessels specific contrast agents for glioblastoma imaging.
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ABSTRACT: A mouse model of glioblastoma multiforme was used to determine the accumulation of a targeted contrast agent in tumor vessels. The contrast agent, consisting of superparamagnetic iron oxide coated with dextran, was functionalized with an anti-insulin-like-growth-factor binding protein 7 (anti-IGFBP7) single domain antibody. The near infrared marker, Cy5.5, was also attached for an in vivo fluorescence study. A 9.4T magnetic resonance imaging (MRI) system was used for in vivo studies on days 10 and 11 following tumor inoculation. T(2) relaxation time was used to measure the accumulation of the contrast agent in the tumor. Changes in tumor to brain contrast because of active targeting were compared with a nontargeted contrast agent. Effective targeting was confirmed with near infrared measurements and fluorescent microscopic analysis. The results showed that there was a statistically significant (P < .01) difference in normalized T(2) between healthy brain and tumor tissue 10 min, 1 h, and 2 h point postinjection of the anti-IGFBP7 single domain antibody targeted and nontargeted iron oxide nanoparticles. A statistical difference remained in animals treated with targeted nanoparticles 24 h postinjection only. The MRI, near infrared imaging, and fluorescent microscopy studies showed corresponding spatial and temporal changes. We concluded that the developed anti-IGFBP7-iron oxide single domain antibody-targeted MRI contrast agent selectively binds to abnormal vessels within a glioblastoma. T(2)-weighted MRI and near infrared imaging are able to detect the targeting effects in brain tumors.Neuro-Oncology 01/2012; 14(1):53-63. · 5.72 Impact Factor -
Article: Collagen I scaffolds cross-linked with beta-glycerol phosphate induce osteogenic differentiation of embryonic stem cells in vitro and regulate their tumorigenic potential in vivo.
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ABSTRACT: Embryonic stem cells (ESCs) have the potential to differentiate into all tissues of the adult organism. This, along with the ability for unlimited self-renewal, positions these cells for regenerative medicine approaches based on tissue engineering strategies. With the objective of developing a treatment regime for skeletal injuries and diseases, this study presents a novel protocol that effectively induces ESC differentiation into osteogenic and chondrogenic lineages while concurrently eliminating observed tumorigenicity during the period of observation after transplantation in vivo. Exposure to a collagen I matrix polymerized with beta-glycerol phosphate (BGP) induced the osteogenic differentiation of the ESCs with an efficiency of >80% without purification and/or lineage-specific cell selection. Furthermore, when the collagen I matrix was supplemented with chondroitin sulfate, chondrogenesis was promoted instead of osteogenesis. Interestingly, without purification of the differentiated cells from the collagen I matrix, these constructs did not lead to the formation of teratomas or tumors when implanted subcutaneously in a severe combined immunodeficiency (SCID). Furthermore, if undifferentiated ESCs were mixed with collagen I and then injected immediately (i.e., without previous in vitro differentiation), again, no teratomas or tumors were observed, whereas undifferentiated ESCs without collagen scaffolds all produced teratomas in this bioassay system. These results suggest that collagen I scaffolds not only induce osteogenic differentiation of ESCs, but also prevent ESCs from producing unwanted tumors when injected in vivo.Tissue Engineering Part A 12/2011; 18(9-10):1014-24. · 4.64 Impact Factor -
Article: The functional microstructure of tendon collagen revealed by high-field MRI.
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ABSTRACT: T(2) was used in this study to assess tendon microstructure. Two unloaded digital extensor tendons were bent such that their long axes were imaged throughout 180° with respect to B(0) . T(2) -weighted images reveal periodic banding (∼200 μm) when tendons were oriented at ±55° with respect to B(0) . Five pairs of tendons were used to study the influence of load on T2W MRI: one tendon of each pair was loaded with a 7.8-N mass, and both tendons were fixed in formalin then imaged at 55° to B(0) . MRI banding was present in the unloaded, but not loaded, tendons. In unloaded tendons, polarized-light microscopy revealed collagen crimp with a periodicity similar to MRI. In loaded tendons, there was a strain-induced extinction of periodicity on both MRI and polarized-light microscopy. These studies confirm that crimp is detectable by high-field MRI and could serve as an in vivo index of physiological strains in collagenous tissues. Magn Reson Med, 2011. © 2011 Wiley-Liss, Inc.Magnetic Resonance in Medicine 08/2011; 66(2):spcone. · 2.96 Impact Factor -
Article: The functional microstructure of tendon collagen revealed by high-field MRI.
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ABSTRACT: T2 was used in this study to assess tendon microstructure. Two unloaded digital extensor tendons were bent such that their long axes were imaged throughout 180° with respect to B0. T2-weighted images reveal periodic banding (∼200 μm) when tendons were oriented at ±55° with respect to B0. Five pairs of tendons were used to study the influence of load on T2W MRI: one tendon of each pair was loaded with a 7.8-N mass, and both tendons were fixed in formalin then imaged at 55° to B0. MRI banding was present in the unloaded, but not loaded, tendons. In unloaded tendons, polarized-light microscopy revealed collagen crimp with a periodicity similar to MRI. In loaded tendons, there was a strain-induced extinction of periodicity on both MRI and polarized-light microscopy. These studies confirm that crimp is detectable by high-field MRI and could serve as an in vivo index of physiological strains in collagenous tissues.Magnetic Resonance in Medicine 06/2011; 66(2):520-7. · 2.96 Impact Factor -
Article: Response to Letter to the Editor: "Structural and functional changes of the articular surface measured by atomic force microscopy".
Journal of biomechanics 06/2011; 44(9):1825-6. · 2.66 Impact Factor
