• Title/Summary/Keyword: 소염제

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신기능 소염 단백질 분해효소 개발에 관한 연구

  • 노현모
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1993.04a
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    • pp.57-57
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    • 1993
  • 단백질 분해효소는 염증주변에 축적된 파괴조직이나 변성단백질등을 분해하여 염증, 특히 만성염증의 순환을 정상화함으로써 소염제로서 사용되어 왔으며 현재, Chymotrypsin, Trypsin, Promelain, Papain, Serrathiopeptidase, Pronase 등이 소염효소제로써 사용되고 있다. 이들은 주로 미생물 배양액에서 통상적인 방법으로 정제하여 사용하며, 유전자 재조합기술을 사용하여 재조합 균주에서 생산할 경우 그 생산성을 증대시킬수 있을 것이라 기대된다.

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Ignition and Extinction Characteristics of a Low Thrust Combustion Chamber using Green Propellant according to Sequence of the Combustion Test (친환경 추진제를 사용하는 저추력 액체로켓엔진의 연소시험 시퀀스에 따른 점화 및 소염 특성)

  • Kim, Young-Mun;Jeon, Jun-Su;Choi, Yu-Ri;Ko, Young-Sung;Kim, Yoo;Kim, Sun-Jin
    • Proceedings of the Korean Society of Propulsion Engineers Conference
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    • 2009.11a
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    • pp.130-133
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    • 2009
  • The sequence of the propellant supply is very important for the reliable and safe operation of a LRE combustion test. So combustion performance tests were performed to find an optimum test sequence by changing supply time of propellants and purge gas in the moment of ignition and extinction. The liquid rocket engine consisted of a catalytic ignitor and six swirl-coaxial injectors which used hydrogen peroxide and kerosene. Conclusively, an optimum sequence was found for stable combustion in the moment of ignition and extinction.

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압력이 상승하는 고체 추진제 비정상 연소에서 복사열 해석

  • 정호걸;이창진
    • Proceedings of the Korean Society of Propulsion Engineers Conference
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    • 2000.11a
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    • pp.22-22
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    • 2000
  • 고체 추진제에서 연소실 압력이 급격히 변하는 비정상 상태에서의 연소 특성은 정상 상태와 다른 경향을 보인다. 고체 추진 시스템에서 안정적이고 필요한 성능을 얻기 위해서는 이러한 비정상 상태에서 일어나는 현상에 대한 예측이 필요하다. 고체 추진제에서 비정상 연소는 크게 두 가지 경우에 나타나게 된다. 그 중 하나는 소염을 위하여 연소실내 압력강하가 일어나는 경우이며, 다른 하나는 점화 후 압력이 상승하는 경우이다. 급격한 압력 강하로 인한 고체 추진제의 소염에 대하여 그 동안 많은 연구들이 진행되었다.(중략)

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Synthesis and Anti-inflammatory Activity of [2-(Benzothiazol-2-ylimino)-4-oxo-3-phenylthiazolidin-5-yl]-acetic Acid Derivatives

  • Sushilkumar S. Bahekar;Devanand B. Shinde
    • Journal of the Korean Chemical Society
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    • v.47 no.3
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    • pp.237-240
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    • 2003
  • A synthetic method for the title compounds (2a-o) was carried out. The title compounds (2a-o)were prepared by the condensation of various thioureas and maleic anhydride. Anti-inflammatory activities in vivo were evaluated and compared with standard drug diclofenac sodium. Some compounds showed moderate activity. The structures of all the new compounds were established on the basis of $^1H$ NMR and IR spectral data.

Studies on Concurrent Administrations of Herb Preparations (수종의 한방제와 양방 소염제 및 항균제의 병용투여에 관한 연구)

  • Lim, Jong-Pil
    • Journal of Pharmaceutical Investigation
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    • v.17 no.1
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    • pp.31-37
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    • 1987
  • The studies on concurrent administrations of herb preparations(Daesiho-tang, Daehwangmogdanpi-tang, Dohaegseunggi-tang, Baenongsangeub-tang and Jeoryeong-tang) with indomethacin and tetracycline were carried out to investigate the antiinflammatory, antimicrobial, liver-protective and antiulcer activities. The results showed that the concurrent administrations of herb preparations with indomethacin and tetracycline increased significantly the antiinflammatory activities and antimicrobial activities respectively, and also improved the liver-protective activities and antiulcer activities against indomethacin or tetracycline-induced liver defect and Shay ulcers in rats, respectively.

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Simultaneous Analysis of Several Non-Steroidal Anti-Inflammatory Drugs in Urine by Gas Chromatograph/Negative Chemical Ionization-Mass Spectrometry (기체 크로마토그래프-질량분석법을 이용한 뇨중 비스테로이드성 소염진통제 (NSAIDs)의 동시 분석법)

  • Myung, Seung-Woon;Park, Joon-Ho;Kim, Myung-Soo;Cho, Hyun-Woo
    • Analytical Science and Technology
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    • v.12 no.6
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    • pp.571-576
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    • 1999
  • Screening method for NSAIDs (Hon-Steroidal Anti-Inflammatory Drugs) in urine was developed using GC/NCI-MS. Derivatized six fenamates with pentafluoropropionic anhydride showed high sensitivity in NCI-MS. The conditions of the derivatization reaction and chromatographic conditions were established for screening with a trace analysis. Limit of detection was in the range of 4-25 pg/mL. This method may be used to the equine doping analysis for NSAIDs and forensic analysis.

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Current Guidelines for Non-Steroidal Anti-Inflammatory Drugs (비스테로이드 소염제의 최신 사용 지침)

  • Park, Min-Gyue;Yoo, Jae-Doo;Lee, Kyu-Ho
    • Journal of the Korean Orthopaedic Association
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    • v.55 no.1
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    • pp.9-28
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    • 2020
  • Non-steroidal anti-inflammatory drugs (NSAIDs) are the most commonly used drugs worldwide for chronic pain, such as arthritis, and there are many different types depending on their composition and mechanism. After long-term use, various side effects can occur, such as gastrointestinal and cardiovascular complications. With a similar analgesic effect to that of traditional non-selective NSAIDs, cyclooxygenase-2-selective NSAIDs have been highly anticipated, because they could complement gastrointestinal tolerance. On the other hand, because of concerns about cardiovascular safety in 2004 and 2005, and the license withdrawals of rofecoxib and valdecoxib, the interest in the side effects of NSAIDs is increasing. Therefore, it is important to use the necessary drugs at a minimum, considering the side effects and interactions of each drug. This study examined the side effects and characteristics of each NSAID that may occur and reviewed the recent research and guidelines related to the use of non-selective NSAIDs and cyclooxygenase-2-selective NSAIDs.

Studies on the Production of Serratiopeptidase from Serratia Culture (세라티아 배양에 의한 세라티오펩티다아제의 생산에 관한 연구)

  • 노현수;박호진;이병룡
    • Microbiology and Biotechnology Letters
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    • v.20 no.2
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    • pp.207-212
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    • 1992
  • An anti-inflammatory agent, serratiopeptidase, was produced from the culture of the Serratia marcescens. The effects of carbon sources, nitrogen sources and inducers on the production were investigated. Citrate was found to be inhibitory in the production of serratiopeptidase. The enzyme was synthesized in the synthetic medium without inducers, albeit low level of synthesis. But the synthesis was increased by the addition of proteinaceous substrate and leucine. Induction of extracellular proteinase by its end-product was discovered, which is not common in the proteinase synthesis in the bacteria. By the glucose fed-batch culture, we found the possible catabolite repression on the production of serratiopeptidase.

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A Case of Eosinophilic Pneumonia with Ibuprofen as the Suspected Etiology (Ibuprofen이 원인으로 추정되는 호산구성 폐렴 1예)

  • Cho, Sung Yeon;Lee, Yang Deok;Cho, Yongseon;Kim, Jeong Nyum;Han, Minsoo
    • Tuberculosis and Respiratory Diseases
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    • v.55 no.2
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    • pp.206-210
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    • 2003
  • Eosinophilic lung diseases are heterogenous disorder which are characterized by the presence of pulmonary symptoms or an abnormal chest radiograph accompanied by inflammatory cellular infiltrates in the airways and lung parenchyma which contain large numbers of eosinophils. The incidence of drug-induced pulmonary disorder is increasing, with at least 40 drug entities having been reported to cause this pulmonary disease. However, nonsteroidal anti-inflammatory drugs (NSAIDs) are rarely mentioned in the lists of drugs in published articles describing drug induced eosinophilic pneumonia. The following is a case of eosinophilic pneumonia that we believe was related to ibuprofen therapy.