The largest database of trusted experimental protocols

Noa 280i

Manufactured by GE Healthcare

The NOA 280i is a nitric oxide analyzer designed for the measurement of nitric oxide (NO) concentrations in various applications. It utilizes a chemiluminescence detection method to provide accurate and reliable measurements of NO levels.

Automatically generated - may contain errors

5 protocols using noa 280i

1

Nitric Oxide Release Study from Gauze

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 1

The materials and methods employed in these experiments are now described.

A NORS solution was prepared at a nitrite strength of 0.3% w/v and pH 3.7. Once ready, a 3×3 in gauze was dipped into the solution, lightly squeezed to discard excess liquid and placed in a “Hath Bath” device (FIG. 1). At different time points, the NO that was being released was measured with a chemiluminescence analyzer (NOA 280i, General Electric, CO).

The results of the experiments are now described.

FIG. 2 shows the amount of NO detected at 3, 8, 15 min as well as 3, 4 (2A) and 24 (2B) hours. The X scale is TIME (minutes) from start on measuring point (showing pre-measuring amount as 0-0.1 ppm) and Y scale showing amount of NO (measured in ppb).

The Chemiluminescent analyzer has a sample draws rate of 200 cc per min and thus, there is an initial peak and reduction in NO concentration following that. The “Hathback” may not be completely sealed and thus some NO may “escape”. However, release of NO was still detected 24 hours after gauze was saturated with the NORS solution.

+ Open protocol
+ Expand
2

Nitric Oxide Measurement in Endothelial Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemiluminescence measurement of nitrite ion accumulation in cell culture supernatant, which is directly proportional to nitric oxide production, was conducted with a Sievers® NOA 280i high-performance liquid chromatography with fluorescence detection (General Electric, Boulder, CO) as previously described.11 (link) HLMVEC monolayers were treated with TNFα (20 ng/ml) in the absence or presence of different concentrations of ropivacaine (1 nM, 1 μM, or 100 μM). For some experiments, the cells were pretreated with the NOS inhibitor N5-(1-iminoethyl)-l-ornithine dihydrochloride (l-NIO; Cayman Chemical, Ann Arbor, MI) for 1 h before the application of TNFα.
+ Open protocol
+ Expand
3

Photolytic NO Release from PetACrONO

Check if the same lab product or an alternative is used in the 5 most similar protocols
Photolysis
of PetACrONO was
carried out in isobutyronitrile solution. The NO release was determined
by entraining the photolysis solution contained in a “Y”
cell with medical-grade air, which then flowed to a Sievers Nitric
Oxide Analyzer (NOA, GE model NOA-280i), where it was detected and
quantified via a calibrated chemiluminescence technique (SI Figure S1). (In each case, the entraining gas
was purged through a solvent bubbler prior to entering the photolysis
cell to reduce evaporative losses.) The photoexcitation source was
either the 365 nm emission from a 200 W high-pressure mercury lamp
isolated with an interference filter or the 451 nm light from a Luxeon
blue light-emitting diode (LED) (SI Figure S2). Excitation intensities at 365 nm were determined by ferrioxalate
actinometry,47 (link) while those at 451 nm were
determined with a power meter (Newport model 8442 PE). Excitation
intervals were controlled using a Uniblitz shutter, and quantum yields
of NO release (ΦNO) were determined by evaluating
the NO released and recorded using the NOA software (“Liquid”)
for varied excitation intervals. The slope of a plot of NO released
vs total light absorbed by the solution gives ΦNO (SI Figure S3).
+ Open protocol
+ Expand
4

Nitrite and Nitrate Quantification in Biological Fluids

Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemiluminescence analysis has been widely recognized as a reliable method for nitrite and nitrate quantification in biological fluids [[40] (link), [41] (link), [42] (link)]. Based on the highly sensitive ozone-chemiluminescence method, its sensitivity reaches 1 pmol (1 nM for a 1 mL injection) for liquid samples. A Nitric Oxide Analyzer 280i (NOA 280i, GE) was applied to measure the levels of nitrite and nitrate in this study. Reducing reagents employed were the triiodide ion for nitrite detection, and vanadium trichloride (VCl3) solution containing 1 M HCl for nitrate quantification. Duplicate injections of standard solutions into the NOA purge vessel were performed. The NOA instrument passed daily calibration when calibration curves were obtained with R2 > 0.999.
Comparison among the three pretreatment methods was performed via injection of each sample six times in order to evaluate the recovery ratio and RSD. Detection of each serum sample was immediately carried out after pretreatment, while samples stayed on ice during measurement. Assays for every group sample were repeated in triplicate.
+ Open protocol
+ Expand
5

Nitric Oxide and Nitrous Oxide Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Nitric oxide and nitrous oxide (NO and N2O) were analyzed on an Agilent series 6890 gas chromatograph (Agilent, USA) equipped with a Porapak Q and a Molecular sieve column, coupled to a thermal conductivity detector and a mass spectrometer (MS; Agilent 5975 Cinert MSD; Agilent, USA) as described before (Ettwig et al., 2008 (link)). For all gas analyses, 100 μl gas samples were injected into the gas chromatograph. Furthermore, nitric oxide production was monitored directly from the gas outlet of the reactors using a nitric oxide analyzer (NOA 280i, GE) with a suction rate of 11.6 ml.min−1.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!