INTENDED USE Diagnostic Kit for Cardiac Troponin I(fluorescence immunochromatographic assay) is a fluorescence immunochromatographic assay for the quantitative detection of Cardiac Troponin I (cTnI) in human serum or plasma, it is used for auxiliary diagnosis of AMI(Acute Myocardial Infarction). All positive sample must be confirmed by other methodologies. This test is intended for healthcare professional use only.

SUMMARY cTnI levels increased several hours after Myocardial infarction occurred, peaked at 12-16 hours, and remained elevated 4-9 days after Myocardial infarction occurred. The global definition of the third myocardial infarction in 2012:The preferred biomarker-cTn(I or T),has high myocardial tissue specificity and high clinical sensitivity. Changes in the concentration of cTn are essential to the diagnosis of AMI

PRINCIPLE OF THE PROCEDURE The membrane of the test device is coated with anti cTnI antibody on the test region and goat anti rabbit IgG antibody on the control region. Lable pad are coated by fluorescence labeled anti cTnI antibody and rabbit IgG in advance. When testing positive sample, the cTnI antigen in sample combine with fluorescence labeled anti cTnI antibody, and form immune mixture. Under the action of the immunochromatography, the complex flow in the direction of absorbent paper, when complex passed the test region, it combined with anti cTnI coating antibody, forms new complex.cTnI level is positively correlated with fluorescence signal, and the concentration of cTnI in sample can be detected by fluorescence immunoassay assay.

REAGENTS AND MATERIALS SUPPLIED

MATERIALS REQUIRED BUT NOT PROVIDED Sample collection container,timer

SAMPLE COLLECTION AND STORAGE 1.The samples tested can be serum, heparin anticoagulant plasma or EDTA anticoagulant plasma. 2.According to standard techniques collect sample. Serum or plasma sample can be kept refrigerated at 2-8℃ for 7days and cryopreservation below -15°C for 6 months. 3.All sample avoid freeze-thaw cycles.

ASSAY PROCEDURE Please read the instrument operation manual and package insert before testing. 1.Lay aside all reagents and samples to room temperature. 2.Open the Portable Immune Analyzer(WIZ-A101), enter the account password login according to the operation method of the instrument, and enter the detection interface. 3.Scan the dentification code to confirm the test item. 4.Take out the test card from the foil bag. 5.Insert the test card into the card slot, scan the QR code, and determine the test item. 6.Add 40μL serum or plasma sample to sample diluent, and mix well.. 7.Add 80μL sample solution to sample well of the card. 8.Click the "standard test" button, after 15 minutes, the instrument will automatically detect the test card, it can read the results from the display screen of the instrument, and record/print the test results. 9.Refer to the instruction of Portable Immune Analyzer(WIZ-A101).

EXPECTED VALUES cTnI <0.3ng/mL It is recommended that each laboratory establish its own normal range representing its patient population.

TEST RESULTS AND INTERPRETATION .The above data is the result of cTnI reagent test, and it is suggested that each laboratory should establish a range of cTnI detection values suitable for the population in this region. The above results are for reference only. .The results of this method are only applicable to the reference ranges established in this method, and there is no direct comparability with other methods. .Other factors can also cause errors in detection results, including technical reasons, operational errors and other sample factors.

STORAGE AND STABILITY 1.The kit is 18 months shelf-life from the date of manufacture. Store the unused kits at 2-30°C. DO NOT FREEZE. Do not use beyond the expiration date. 2.Do not open the sealed pouch until you are ready to perform a test, and the single-use test is suggested to be used under the required environment (temperature 2-35℃, humidity 40-90%) within 60 mins as quickly as possible. 3.Sample diluent is used immediately after being opened.

WARNINGS AND PRECAUTIONS .The kit should be sealed and protected against moisture. .All positive specimens shall be validated by other methodologies. .All specimens shall be treated as potential pollutant. .DO NOT use expired reagent. .DO NOT interchange reagents among kits with different lot No.. .DO NOT reuse test cards and any disposable accessories. .Misoperation, excessive or little sample can lead to result deviations.

LIMITATION .As with any assay employing mouse antibodies, the possibility exists for interference by human anti-mouse antibodies (HAMA) in the specimen. Specimens from patients who have received preparations of monoclonal antibodies for diagnosis or therapy may contain HAMA. Such specimens may cause false positive or false negative results. .This test result is only for clinical reference, should not serve as the only basis for clinical diagnosis and treatment, the patients clinical management should be comprehensive consideration combined with its symptoms, medical history, other laboratory examination, treatment response, epidemiology and other information. .This reagent is only used for serum and plasma tests. It may not obtain accurate result when used for other samples such as saliva and urine and etc.

PERFORMANCE CHARACTERISTICS

REFERENCES

Key to symbols used:

	In Vitro Diagnostic Medical Device
	Manufacturer
	Store at 2-30℃
	Expiration Date
	Do Not Reuse
	CAUTION
	Consult Instructions For Use