http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SA-116370790-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-721
filingDate 2016-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_225c46e15e74316178e62e7987b6ba83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b44c512caa36a29b73bd33b26115da88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_623644d95fd7cc8571c2c9c7f284a3d8
publicationDate 2017-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SA-116370790-B1
titleOfInvention A spectroscopic method for measuring hemoglobin impairment due to smoking
abstract The spectrophotometric method for the measurement of smoking-induced impairment of hemoglobin is based on reduced tryptophan concentration and elevated concentrations of the biomolecules nicotinamide adenine dinucleotide (NADH), flavin adenine dinucleotide (FAD), and porphyrin in the present invention for hemoglobin impairment. The method includes the steps of obtaining a blood sample from a smoking patient; separate blood plasma from samples; Obtain synchronous excitation spectra (SXS) of blood plasma with a spectrofluorometer at 70 nm assay and 10 nm; comparison of a patient's synchronous excitation spectra (SXS) with synchronous excitation spectra (SXS) for normal control samples; The diagnosis of hemoglobin impairment is when the maximum excitability of nicotinamide adenine dinucleotide (NADH), flavin adenine dinucleotide (FAD), and porphyrin is between 30% and 70% above the maximum for these metabolites in normal comparison samples, or when the maximum excitability of For tryptophan is 60% of the comparison sample
priorityDate 2015-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 20.