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Spectral ami ht

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The Spectral AMI HT is a high-throughput hyperspectral imaging system designed for advanced material analysis. It captures detailed spectral data across a wide range of wavelengths, enabling comprehensive characterization of various materials and samples.

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3 protocols using spectral ami ht

1

Photoluminescence Imaging of TiO2 and PA2200

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Samples of PA2200, anatase, and rutile titanium dioxide (Sigma Aldrich, St. Louis, MO, USA), and Nylon-12 (Sigma Aldrich) were charged for 10 s with ambient white light and placed in the light tight chamber of a Spectral advanced molecular imaging high throughput system (Spectral AMI HT, Spectral Instruments Imaging, Tucson, AZ, USA). Then, PL images were acquired with the following parameters: 30 s exposure time, 250 mm field of view, fstop of 1.2, focal-plane of 0 mm, open emission, and 4 × 4 binning. Then, the anatase titanium dioxide and the PA2200 were imaged under similar parameters with the exception of varied emission filters (530, 570, 610, 630, 670, 710, 750, 810, 850, and 870 nm) to create an emission spectrum. All data were plotted on GraphPad Prism version 7 (GraphPad Software, La Jolla, CA, USA).
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2

Myeloperoxidase Activity in Oral Infections

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BALB/c mice (8 to 10 weeks old; 8 mice per group) were injected subcutaneously in the thigh with either 1.5 × 109S. gordonii cells (Sg-only group) or 1.5 × 109S. gordonii cells and 1.5 × 109P. gingivalis cells (Pg+Sg group) in a total volume of 100 μL. After 4 h, each mouse was injected intraperitoneally with 150 μL (40 mg/mL) of IVISbrite MPO 425 chemiluminescent probe in RediJect solution (PerkinElmer). After 10 min of incubation and 300 s of exposure, in vivo imaging was performed using a Spectral Ami HT (Spectral Instruments Imaging). Image validation, acquisition, and data analysis were performed with Aura imaging software.
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3

In Vivo Drug Release Visualization Protocol

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To visualize the drug release mechanics in vivo, we used a fluorescent imaging system (Spectral AMI HT, Spectral Instruments Imaging, LLC., Tucson, AZ, USA). We fabricated three devices with 20 μL of indocyanine green dye (ICG, Fisher Scientific, Waltham, MA, USA). To aid in the quantification of released drug amount, we created a standard curve using the ICG dye with concentrations ranging from 2 μg/mL to 25 μg/mL (SI Fig. 2). We subcutaneously implanted each device into 3 male C57BL/6 mice obtained from an in-house colony. Each animal was anesthetized with an initial injection of Buprenorphine (0.05–0.1 mg/kg) and with 1–3% Isoflurane in 1 L/min O2 during the implantation, device activation, and imaging. For implantation, a 1-mm incision was made in the left dorsum and the skin was separated from underlying connective tissue to create a subcutaneous pocket. The device was then inserted into the pocket and the incision sutured closed. After the implantation, mice were imaged every 10 min for 40 min prior to the activation of the implanted device to quantify any drug leakage. We then activated each device for 60 s using our bespoke magnetic field generator, and each animal was imaged for an additional 30 min post-activation. All procedure were performed with approval from the Purdue Animal Care and Use Committee.
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