Skeletal muscle satellite cell migration to injured tissue measured with 111In-oxine and high-resolution SPECT imaging.

The delivery of adult skeletal muscle stem cells, called satellite cells, to several injured muscles via the circulation would be useful, however, an improved understanding of cell fate and biodistribution following their delivery is important for this goal to be achieved. The objective of this study was to evaluate the ability of systemically delivered satellite cells to home to injured skeletal muscle using single-photon emission computed tomography (SPECT) imaging of (111)In-labeled satellite cells. Satellite cells labeled with (111)In-oxine and green fluorescent protein (GFP) were injected intravenously after bupivicaine-induced injury to the tibialis anterior muscle. Animals were imaged with a high-resolution SPECT system called FastSPECT II for up to 7 days after transplantation. In vivo FastSPECT II imaging demonstrated a three to five-fold greater number of transplanted satellite cells in bupivicaine-injured muscle as compared to un-injured muscle after transplantation; a finding that was verified through autoradiograph analysis and quantification of GFP expression. Satellite cells also accumulated in other organs including the lung, liver, and spleen, as determined by biodistribution measurements. These data support the ability of satellite cells to home to injured muscle and support the use of SPECT and autoradiograph imaging techniques to track systemically transplanted (111)In labeled satellite cells in vivo, and suggest their homing may be improved by reducing their entrapment in filter organs.

Kinetic behavior of polymer-coated long-period-grating fiber-optic sensors.

A new method of analysis employing the time-dependent response of long-period-grating (LPG) fiber-optic sensors is introduced. The current kinetic approach allows analysis of the time-dependent wavelength shift of the sensor, in contrast to previous studies, in which the LPG sensing element has been operated in an equilibrium mode and modeled with Langmuir adsorption behavior. A detailed kinetic model presented is based on diffusion of the analyte through the outer protective membrane coating into the affinity coating, which is bound to the fiber cladding. A simpler phenomenological approach presented is based on measurement of the slope of the time-dependent response of the LPG sensor. We demonstrate the principles of the kinetic methods by employing a commercial Cu+2 sensor with a carboxymethylcellulose sensing element. The detailed mathematical model fits the time-dependent behavior well and provides a means of calibrating the concentration-dependent time response. In the current approach, copper concentrations below parts per 10(6) are reliably analyzed. The kinetic model allows early-time measurement for low concentrations of the analyte, where equilibration times are long. This kinetic model should be generally applicable to other affinity-coated LPG fiber-optic sensors.