21 research outputs found

    Time-domain monitoring of em exposure during medical device testing

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    This work presents various probes for measuring radio frequency (RF) electric and magnetic fields for real time measurements of the time-varying RF fields used in MRI. A small single loop (2 cm) and short dipole antenna (2 cm) were developed to monitor the near field magnetic and electric exposure during the medical. Theoretical analysis for each designed probes was performed to convert the real time receive signals to the exposed electric and magnetic field. Probes in this study was tuned and matched at center frequency of 127.6 MHz for 3T MRI scanners to improve the accuracy and sensitivity. Probes were fabricated on a single sided PCB, FR4 of thickness 1.57mm and a copper thickness of 35um

    Small footprint high gain and low noise figure preamplifier for 7T MRI scanner

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    This work presents the design and construction of a low input impedance preamplifier with a gain of more than 30 dB and a noise figure of less than 1 dB. It has a low input impedance, around 1Ω. A λ/4 transmission line is used to transform the low input impedance of the preamplifier to a high impedance at the coil to reduce the cross-coupling between coils. In order to test the preamplifier, a single-transmit, single-receive coil was developed at 297.2 MHz. The designed preamplifier can have a footprint as small as 27 mm × 13 mm. Small footprint preamplifiers are crucial where space is at a premium in multichannel coil arrays

    Reliable RF B/E-Field Probes for Time-Domain Monitoring of em Exposure during Medical Device Testing

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    This paper presents electric and magnetic probes to measure radio frequency (RF) electric and magnetic fields for measuring the time-varying RF fields used in magnetic resonance imaging (MRI). A small single loop (2 cm) and short dipole antenna (2 cm) were developed to monitor the near field magnetic and electric exposure during the medical device testing. Theoretical analysis for each designed probe was performed to convert the real time receive signals to the exposed electric and magnetic field. Probes in this paper were tuned and matched at center frequency of 127.6 MHz for 3T MRI scanners to improve the accuracy and sensitivity. Different cables were designed to reduce the E-field pick up and achieving the most accurate measurement setup. Probes were fabricated on a single sided printed circuit board, FR4 of thickness 1.57 mm and a copper thickness of 35μm. The measured S-parameters of the magnetic and electric field probes show less than-44 and-45 dB return loss at 127.6-MHz center frequency of the RF Birdcage

    Collaborative Enhancement of Endothelial Targeting of Nanocarriers by Modulating Platelet-Endothelial Cell Adhesion Molecule-1/CD31 Epitope Engagement

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    Nanocarriers (NCs) coated with antibodies (Abs) to extracellular epitopes of the transmembrane glycoprotein PECAM (platelet endothelial cell adhesion molecule-1/CD31) enable targeted drug delivery to vascular endothelial cells. Recent studies revealed that paired Abs directed to adjacent, yet distinct epitopes of PECAM stimulate each other’s binding to endothelial cells <i>in vitro</i> and <i>in vivo</i> (“collaborative enhancement”). This phenomenon improves targeting of therapeutic fusion proteins, yet its potential role in targeting multivalent NCs has not been addressed. Herein, we studied the effects of Ab-mediated collaborative enhancement on multivalent NC spheres coated with PECAM Abs (Ab/NC, ∼180 nm diameter). We found that PECAM Abs do mutually enhance endothelial cell binding of Ab/NC coated by paired, but not “self” Ab. <i>In vitro</i>, collaborative enhancement of endothelial binding of Ab/NC by paired Abs is modulated by Ab/NC avidity, epitope selection, and flow. Cell fixation, but not blocking of endocytosis, obliterated collaborative enhancement of Ab/NC binding, indicating that the effect is mediated by molecular reorganization of PECAM molecules in the endothelial plasmalemma. The collaborative enhancement of Ab/NC binding was affirmed <i>in vivo</i>. Intravascular injection of paired Abs enhanced targeting of Ab/NC to pulmonary vasculature in mice by an order of magnitude. This stimulatory effect greatly exceeded enhancement of Ab targeting by paired Abs, indicating that ‘“collaborative enhancement”’ effect is even more pronounced for relatively large multivalent carriers <i>versus</i> free Abs, likely due to more profound consequences of positive alteration of epitope accessibility. This phenomenon provides a potential paradigm for optimizing the endothelial-targeted nanocarrier delivery of therapeutic agents
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