Abstract:
A method for inactivating biofilm is provided, which inactivates the biofilm in an improved disinfecting power using the supercritical fluid in a short time. A method for inactivating biofilm using the supercritical fluid comprises: a step for positioning an object in which the biofilm is formed in the surface at the high pressure container; and a step for inactivating biofilm by bringing the biofilm into contact with the supercritical fluid. The biofilm using the supercritical fluid is exposed to the supercritical fluid in the state that it is not dipped in the aqueous medium and the moisture is adhered. The supercritical fluid comprises the supercritical carbon dioxide, and the supercritical nitrous oxide or their mixture fluid.
Abstract:
A method for visualizing nucleotide and analyzing polarity thereof is provided to be applied to select a DNA sequence for a PCR primer or a DNA probe, search a restriction site from DNA, differentiate a promoter region from exon and intron from a genomic DNA(gDNA), and search for genetic mutation and be effectively used to decipher a DNA code cipher through an electrostatic structure of the DNA code. A method for visualizing nucleotide and analyzing polarity thereof comprises the steps of: (a) visualizing nucleotide bases of A, G, T or U, and C in a sequence to mark A as an upper empty semicircle, G as an upper full semicircle, T or U as a lower empty semicircle, and C as a lower full semicircle based on the horizon; (b) putting together a continuous arrangement of pyrimidine(s)-purine(s) from an arrangement of a sequence proceeding from 5' end to 3' end of the marked nucleotide and dividing it into a nucleotide segment; and (c) calculating a nucleotide total base pair binding energy(total DHE/DS), a nucleotide segment average base pair binding energy(average DHE/DS), and a nucleotide segment polarity base pair binding energy(polarity DHE/DS) regarding the divided nucleotide segments using a migration pattern of electrons inside of the nucleotide.
Abstract:
A method for drying cefpodoxime proxetil is provided to obtain the cefpodoxime proxetil with almost no remaining solvent with reduced cost and drying time by performing a drying process using a saturated liquid CO2, which is relatively cheap, harmless to human body and non-reactive with a product. A method for drying cefpodoxime proxetil comprises a step of removing at least one remaining organic solvent selected from the group consisting of diisopropylether, ethyl acetate and dichloromethane by circulating saturated liquid carbon dioxide using a reboiler and a condenser without using a power unit such as a pump during a process of preparing the cefpodoxime proxetil.
Abstract:
가압 액체, 초임계유체 및 그들의 혼합물을 사용하여 아크릴산과 수분이 제거된 초 흡수성 중합체의 제조방법이 개시되어 있다. 이를 수행하기 위해서는 중합 반응으로 형성된 초 흡수성 중합체에 가압 액체, 초임계 유체 또는 이들의 혼합물을 제공한다. 이후, 가압 액체, 초임계 유체 또는 이들의 혼합물을 이용한 추출 공정을 수행하여 중합반응으로 형성된 초 흡수 중합체 내에 잔류하는 아크릴산과 수분을 추출한다. 이로 인해, 상기 추출공정으로 형성된 초 흡수성 중합체는 아크릴산 잔류량이 20 내지 500ppm인 초 흡수성 중합체로 형성된다. 초 흡수성 중합체, 잔류 용매, 초임계, 이산화탄소
Abstract:
PURPOSE: A method for sterilizing beverages using nitrous oxide is provided to control the pH change of beverages and to sterilize beverages with sterilizing power in a short time using liquid or supercritical nitrous oxide. CONSTITUTION: A method for sterilizing beverages using nitrous oxide comprises the steps of: positioning liquid beverages inside a high pressure container; sterilizing microbe existing in beverages without the pH change of beverages by contacting with liquid or supercritical nitrous oxide in the pressure of 40 - 500bar; and stirring two phases while contacting with liquid or supercritical nitrous oxide.
Abstract:
Acetaminophen fine particles are provided to control the crystal polymorphism of drug by diversifying parameters in manufacturing the particles and to be usable for an immediate release analgesic composition due to improved elution rate. A method for manufacturing acetaminophen fine particles comprises (a) a step for preparing the solution by dissolving acetaminophen in ethylacetate or tetrahydrofurane; (b) a step for preparing the acetaminophen fine particles by mixing carbon dioxide of 0-45 °C and 35-200 pressure(atm) and the solution obtained from the (a) step in a precipitator; (c) a step for removing an organic solvent remaining in particles by using the supercritical carbon dioxide of 0-45 °C and 35-200 pressure(atm); and (d) a step for collecting the fine particles generated through the pressure reduction of the inside of the precipitator.
Abstract:
A supercritical fluid extraction method is provided to prevent the crushing of rice through maintaining moisture content in brown rice and to selectively extract only a fat ingredient, by adding water as an assistant solvent to a supercritical carbon dioxide used as an extraction solvent in a process of manufacturing functional brown rice removed with a fat ingredient of the surface of brown rice. A supercritical fluid extraction method without the crushing of rice extracts fat ingredient from brown rice by using supercritical carbon dioxide as a main solvent and water as an assistant solvent. The supercritical state of carbon dioxide is characterized in that the temperature is 31-60 deg.C, the pressure is 100-350 bar, the density of supercritical carbon dioxide is 0.6-1.0 g / cm^3, and the weight fraction of carbon dioxide to added water is 0.001 - 0.005.