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Model 55 2222

Manufactured by Harvard Apparatus
Sourced in United States

The Model 55-2222 is a laboratory instrument manufactured by Harvard Apparatus. This device is designed for general laboratory use, but its core function is not available in the provided information. A more detailed and unbiased description cannot be provided without additional specifics about the product.

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4 protocols using model 55 2222

1

Coronary Stenosis Induction via Catheter

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Anesthesia was induced with Telazol (4.4 mg/kg), Ketamine (2.2 mg/kg), and Xylazine (2.2 mg/kg), and was maintained with 1.5–2.5% Isoflurane (Highland Medical Equipment, Temecula, CA and Baxter, Deerfield, IL). Sheaths were placed (AVANTI®, Cordis Corporation, Miami Lakes, FL) in both femoral veins for intravenous adenosine and contrast administration. In three of the animals, an extra sheath was placed in the right carotid artery to pass a Judkins Right (JR) catheter (Cordis Corporation, Miami Lakes, FL) into the left coronary ostium. A pressure wire (PrimeWire PRESTIGE® Pressure Guide Wire, Volcano Corp, Rancho Cordova, CA) was then advanced into the distal LAD. A balloon was passed over the wire into the mid LAD and was used to generate several levels of sub-occlusive stenosis with FFR (ComboMap, Volcano Corp., Rancho Cordova, CA) severities of 0.7–0.9 under maximal vasodilation (240 µg adenosine/kg/min, Model 55-2222, Harvard Apparatus, Holliston, MA). Beta blockers were not administered for heart rate control and nitroglycerin was not administered during CTA.
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2

Evaluating Lumen Patency of Catheters

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Flow testing was used to check for lumen patency. A pCLE imaging probe was inserted into the central imaging lumen of each catheter and advanced until the probe exited the distal end of the catheter to ensure that the lumen was un-occluded. The imaging probe was then removed. A 100ml syringe was then placed in a syringe pump (Model# 55-2222, Harvard Apparatus,) and an inline pressure transducer (PRESS-S-000, Pendotech) was attached between the syringe and one of the TLBC fluid lumens. The pressure transducer was connected to a data acquisition system (PC mounted National Instruments NI USB-6211) as well as a 5V DC power source. The syringe pump was set to flow air through the catheter fluid lumen at a rate of 15 ml/min. Pressure readings were sampled at 100 Hz and pressure / time curves generated for each catheter (SignalView2009, National Instruments). Upon completion of the test, the syringe and syringe pump were reset, and the test was repeated for the other lumen of the catheter. 35 catheters in four sample lots were tested.
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3

Dynamic CT Imaging of Myocardial Perfusion

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For each animal, one or two rest acquisitions were performed, followed by one to three stress acquisitions, all with the same CT settings. For each stress acquisition, adenosine was infused intravenously for 3 min prior to and throughout imaging (240 μg adenosine/kg/min, Model 55-2222, Harvard Apparatus, Holliston, MA, USA). For each rest and stress acquisition, 1 mL/kg of contrast material (Isovue 370, Bracco Diagnostics, Princeton, NJ, USA) was injected (5 mL/s, Empower CTA, Acist Medical Systems, Eden Prairie, MN, USA) followed by a saline chaser (0.5 mL/kg) at the same rate. ECG-gated volume scans were acquired dynamically with a 320-slice CT scanner (Aquilion One, Toshiba America Medical Systems, Tustin, CA, USA) over 20–30 s to capture base and peak of the aortic enhancement, as shown in Fig. 1a, b. All volume scans were acquired as full projection data at 100 kVp and 200 mA with a rotation time of 0.35 s, a collimation of 320 × 0.5 mm, and a cranio-caudal coverage of 16 cm. A minimum 10-min delay was employed between consecutive acquisitions to allow for adequate clearance of contrast material and, if used, adenosine. All volume scans were retrospectively reconstructed at 75% of the R-R interval using an adaptive iterative dose reduction three-dimensional reconstruction [24 (link)], an FC03 kernel, and a voxel size of 0.43 × 0.43 × 0.5 mm.
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4

Micro-Free-Flow Electrophoresis Separation

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Separation buffer was pumped into the device using syringe pumps (Model # 55– 2222, Harvard Apparatus, Holliston, MA) at 0.6 mL/min. The sample stream exited the nLC column at 300 nL/min and was introduced directly into the μFFE channel for further separation (See Figure 2A). During μFFE dye separations, the right electrode was grounded and a +60 V separation potential was applied to the left electrode using a power supply (PS310, Stanford Research Systems INC, Sunnyvale, CA). Tefzel® Tubing (1/16” OD × 0.040”, IDEX Health and Science, Oak Harbor, WA) was connected directly to the printed access ports on the ABS μFFE device using modified commercially available fittings (6–32 coned finger tight ferrules, IDEX, Science, Oak Harbor,WA) and o-rings.
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