Abstract:
The present invention relates to a biomarker composition for diagnosing stomach cancer and a method for diagnosing stomach cancer using the same. According to an embodiment of the present invention, the biomarker composition for diagnosing stomach cancer and the method using the biomarker composition for diagnosing stomach cancer are usefully used for diagnosing a suspected stomach cancer patient.
Abstract:
PURPOSE: A method for simultaneously detecting nucleotides in blood plasma using a capillary electrophoresis-mass spectrometer is provided to effectively separate nine kinds of nucleotides from a blood plasma specimen by securing optimal analyzing conditions of the capillary electrophoresis-mass spectrometer. CONSTITUTION: A method for simultaneously detecting nucleotides in blood plasma includes the following: protein is removed from the blood plasma; the blood plasma without the protein passes through a micelle electrokinetically capillary chromatography column which is adjusted with a surfactant containing developing solvent; and the treated blood plasma is analyzed by a capillary electrophoresis-mass spectrometer. The protein is removed using 50-70% of an ethanol solution containing ethylene diamine tetraacetic acid(EDTA). The concentration of the EDTA is in a range between 1 and 5 mM. The surfactant is a cationic surfactant. The developing solvent is an ammonium acetate buffer solution. The concentration of the ammonium acetate buffer solution is in a range between 10 and 60 nM.
Abstract:
PURPOSE: A method for simultaneously analyzing cholesterol, oxysterol, and bile acid in urine is provided to treat diseases and to prevent side effect. CONSTITUTION: A method for simultaneously detecting cholesterol, oxysterol, and bile acid in urine comprises a step of TMS(trimethylsilylation) derivatization of cholesterol, oxysterol, and bile acid contained in a urine sample. The simultaneous detection comprises: a process of treating enzyme to the urine sample for hydrolyzation; and a process of solvent extraction. The enzyme is beta-glucuronidase or arylsulfatase. They used solvent is a mixture solution of ethyl acetate and n-hexane, ethyl ether, or t-butyl methyl ether.
Abstract:
PURPOSE: Provided is a method for detecting estriol 3-glucuronide and estriol 16-glucuronide, which has no need of pretreating urine samples, ensures high analytical sensitivity even with a small amount of sample and gives excellent operation property. CONSTITUTION: The method for detecting estriol 3-glucuronide and estriol 16-glucuronide in urine by using HPLC comprises the steps of: introducing a urine sample into a concentration column(5) in which proteins and analytically undesirable materials are removed from the sample and the sample is concentrated in the presence of buffered triethylamine solution as an eluting solvent; and terminating the introduction of the buffered triethylamine solution after the completion of the concentration step, introducing acetonitrile as an eluting solvent to elute the concentrated estriol 3-glucuronide and estriol 16-glucuronide out of the concentration column, and then introducing the eluted materials into an analytic column(6) to perform analysis for concentration. In the method, the kind of eluting solvent is determined by a switching valve(3). Additionally, injection of the sample into the concentration column(5) and ejection of the concentrated sample from the concentration column(5) are determined by another switching valve(4).
Abstract:
PURPOSE: Provided is a method of detecting vitamin E in the serum which extracts the vitamin E from the serum, and provides optimum analyzing conditions with selective and excellent sensitivity to the high performance liquid chromatography and ultraviolet ray absorber. CONSTITUTION: A method of detecting the vitamin E in the serum comprises the steps of: treating the serum by a buffer solution containing 0.075-0.2M of salt with pH4.0-5.5; extracting the vitamin E from the treated serum by diethyl ether; and analyzing the concentration of the extracted vitamin E by a high performance liquid chromatography with a ultraviolet ray absorber. The serum is derived from livestock, the buffer solution from phosphoric acid or acetic acid, and the salt from NaCl.
Abstract:
본발명은시토크롬 P450 이소효소에특이적으로반응하는기질을포함하는가스크로마토그래피를이용한시토크롬 P450(Cytochrome P450) 이소효소활성분석용조성물을제공함으로써, 가스크로마토그래피질량분석을통해다양한시토크롬 P450 이소효소들의활성을동시에측정할수 있다. 따라서, 본발명은한약탕재와같은다성분을포함하는복합물에서의약물의상호작용을효율적으로측정할수 있는시스템을제공할수 있다.