• 제목/요약/키워드: gastric and small intestinal condition

검색결과 4건 처리시간 0.019초

Survival of Double-Microencapsulated Bifidobacterium breve in Milk in Simulated Gastric and Small Intestinal Conditions

  • Jung, Ji-Kang;Kil, Jeung-Ha;Kim, Sang-Kyo;Jeon, Jung-Tae;Park, Kun-Young
    • Preventive Nutrition and Food Science
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    • 제12권1호
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    • pp.58-63
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    • 2007
  • Bifidobacteria are probiotic organisms that provide both flavor and health benefits when incorporated as live cultures into commercial dairy products. Because bifidobacteria are very sensitive to environmental conditions (acids, temperature, oxygen, bile salts, the presence of other cultures, etc.), their viability in human gastrointestinal tract is limited. The microencapsulation of bifidobacteria is a process to protect them against harsh environmental conditions, thereby increasing their viability while passing through human gastrointestinal tract. To confirm the survival rate of microencapsulated Bifidobacterium breve CBG-C2 in milk, their survival rate was compared with several kinds of free bifidobacteria and lactic acid bacteria in commercial yogurt products under simulated gastric and small intestinal conditions. Double-microencapsulation of the bacteria was employed to increase the survival rate during digestion. The outer layer was covered with starch and gelatin to endure gastric conditions, and the inner layer was composed of a hard oil for the upper small intestinal regions. Almost all microencapsulted bifidobacteria in the milk survived longer than the free bifidobacteria and lactic acid bacteria in the commericial yogurt products under the simulated gastric conditions. Numbers of surviving free bifidobacteria and lactic acid bacteria in the commercial products were significantly reduced, however, the viability of the microencapsulated bificobacteria in the milk remained quite stable under gastric and small intestine conditions over 3$\sim$6 hrs. Thus double-microencapsualtion of bifidobacteria in milk is a promising method for improving the survival of bifidobacteria during the digestive process.

웅황과 자황의 소화 반응과 인체내 존재형태에 대한 예측 모델링 (Gastric juice and Realgar and Orpiment Mineral Medicine Reaction; Reaction Path and Speciation Modeling in Human Body)

  • 김선옥;박맹언;신순식;김경철
    • 동의생리병리학회지
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    • 제16권2호
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    • pp.365-372
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    • 2002
  • The mineral medicines mean a sort of mineral or rock for medical treatment and natural material using their chemical components and physical properties. In this study, it was apprehended the mineralogical characteristics of As-bearing group mineral medicines. The extraction test is an vitro test system for predicting the bioavailability of the major and minor elements from mineral medicines and incorporates gastrointestinal tract parameters representative of a human(including stomach and small intestinal pH, stomach mixing time and velocity). The results of the extraction test are used for reaction path modeling in human body. Reaction path modeling in human body can predict digestion with gastric juice as well as bioavailability, speciation. Also, it can predict accumulation of arsenic as pH condition. As the results of the extraction test for digestion, the amounts of Fe extraction was the highest, followed by As, Ca, Ni. In addition, as the results of the reaction path modeling between arsenic compounds and gastric juice using thermodynamic data, when absorbed, major species are followed by H₃As₃S/sub 6/(aq), As₃S/sub 6/ (aq), AsO/sup +/, H₂As₃S/sup 6-/, H₂AsO/sup 3-/, HAs₃S6/sup 2-/, HAsO/sub 3//sup 2-/ and AsO/sub 3//sup 3-/. Specifically the concentration of H₃As₃S/sub 6/(aq) is the highest. As pH increases, the concentration of H₂AsO/sup 3-/, HAsO/sub 3//sup 2-/, HAsO/sub 3//sup 3-/, HAs₃S/sub 6//sup 2-/, H₂As₃S/sup 6-/, and H₃As₃S/sub 6/ increases, whereas the concentration of H₃As₃S/sub 6/ and AsO/sup +/ decreases. On the results of this study, it is able to find out effective and toxic components of poisonous arsenic group of mineral medicines and expected to be widely used for the development of new medicines.

항콜린에스테라아제 살충제 음독 후 발생한 창자벽공기낭증과 문맥장간막정맥가스 1례 (Pneumatosis Cystoides Intestinales and Portomesenteric Venous Gas following Anticholinesterase Pesticide Poisoning)

  • 이숙희;이경우;정진희
    • 대한임상독성학회지
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    • 제15권1호
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    • pp.56-59
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    • 2017
  • Pneumatosis cystoides intestinalis and portomesenteric venous gas are uncommon radiological findings, but are found commonly in cases of bowel ischemia, or as a result of various non-ischemic conditions. A 72-year-old man visited an emergency center with altered mental status 2 hours after ingestion of an unknown pesticide. On physical examination, he showed the characteristic hydrocarbon or garlic-like odor, miotic pupils with no response to light, rhinorrhea, shallow respiration, bronchorrhea, and sweating over his face, chest and abdomen. Laboratory results revealed decreased serum cholinesterase, as well as elevated amylase and lipase level. We made the clinical diagnosis of organophosphate poisoning in this patient based on the clinical features, duration of symptoms and signs, and level of serum cholinesterase. Activated charcoal, fluid, and antidotes were administered after gastric lavage. A computerized tomography scan of the abdomen with intravenous contrast showed acute pancreatitis, poor enhancement of the small bowel, pneumatosis cystoides intestinalis, portomesenteric venous gas and ascites. Emergent laparotomy could not be performed because of his poor physical condition and refusal of treatment by his family. The possible mechanisms were believed to be direct intestinal mucosal damage by pancreatic enzymes and secondary mucosal disruption due to bowel ischemia caused by shock and the use of inotropics. Physicians should be warned about the possibility of pneumatosis cystoides intestinalis and portomesenteric venous gas as a complication of pancreatitis following anticholinesterase poisoning.

광물성 약재(광물약)의 표준화에 관한 연구 (Standardization Studies for the Oriental Mineral Medicine)

  • 김선옥;박맹언
    • 자원환경지질
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    • 제48권3호
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    • pp.187-197
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    • 2015
  • 광물성 약재(광물약)는 오랜 기간 동안 주로 중국, 한국 등 동양의 전통의학에서 화학성분이나 물리적인 성질이 질병치료나 건강 증진에 이용되어 왔던 단일 광물, 암석 및 생물화석 등을 의미한다. 광물성 약재는 산지의 지질특성, 기후 및 지표 환경에 의해 광물학적 특성이 달라지며, 광물의 조직, 수반광물, 정제 방법에 따라 약재로서의 효용성이 달라진다. 특히, 광물성 약재에 함유되어 있는 광물조성, 주성분 및 미량성분의 차이는 광물약의 약효와 유해성에 영향을 준다. 그러므로 광물약의 분석방법과 전처리 및 제조과정에 대한 표준화가 매우 중요하다. 광물성 약재에 함유된 유해 금속 원소는 수치(법제)나 탕약 제조 등 약제의 전처리 과정과 위와 장에서의 소화과정에서 성분이 변화되어 용출량이 결정되기 때문에 체내와 대응되는 조건에서의 적절한 시험방법을 정립하여, 그 결과에 의해 위액용출도, 인체흡수도, 안정성과 위해성이 평가되어야 한다. 또한, 광물성 약재의 안정성과 위해성을 평가할 수 있는 연구결과로 유효성분과 독성 물질의 체내 존재량을 예측할 수 있어야 한다. 연구에서 제안된 광물성 약재의 표준화 방법은 광물약의 개발과 활용에 유용한 기초자료로 이용될 뿐만 아니라, 광물성 약재의 품질 표준을 규격화 하는 기준을 제시해줄 것으로 기대된다.