• 제목/요약/키워드: sonication

검색결과 382건 처리시간 0.022초

Effects of Heat Processing Time on Total Phenolic Content and Antioxidant Capacity of Ginseng Jung Kwa

  • Oh, Chang-Ho;Kim, Gyo-Nam;Lee, Sang-Hyun;Lee, Jung-Sook;Jang, Hae-Dong
    • Journal of Ginseng Research
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    • 제34권3호
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    • pp.198-204
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    • 2010
  • Korean ginseng (Panax ginseng C.A. Meyer) preserved in syrup, known as ginseng Jung Kwa (GJK), is a popular traditional snack in Korea. We investigated the effects of heat processing time on total phenolic content and antioxidant capacity of GJK. Water extract was prepared from GJK with different heat processing times, 3 hours (GJK-3), 6 hours (GJK-6), or 12 hours (GJK-12), with sonication for 2 hours. The GJK extract contained total phenolic content in the following order: GJK-12 (2.28%)>GJK-6 (1.57%)>GJK-3 (1.29%). Both the peroxy and hydroxyl radical-scavenging activity and cellular antioxidant capacity of GJK extract was significantly enhanced with increasing heat processing time. The hydroxyl radical-scavenging activity of GJK-12 extract was greater than that of the GJK-3 and GJK-6 extracts, consistent with metal chelating capacity and reducing capacity. In a cellular model, the GJK extract effectively reduced 2,2'-azobis(2-amidinopropane) dihydrochloride, $Cu^{2+}$-, and $H_2O_2$-induced oxidative stress, with GJK-12 and GJK-6 extracts demonstrating greater cellular antioxidant capacity than the GJK-3 extract. These results suggest that heat processing time can contribute to the antioxidant capacity of GJK and that GJK extract may have the potential to be used as an effective dietary antioxidant to prevent oxidative stress-related diseases.

개발 과수용 농약방제복의 반복세탁에 따른 부위별 농약 방호성능의 변화 (Change of the Protection Efficiency in Each Part of Developed Pesticide-Proof Clothes by Repeated Washings)

  • 신정화;황경숙;이효현
    • 한국지역사회생활과학회지
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    • 제22권4호
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    • pp.615-621
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    • 2011
  • This study was conducted to evaluate of the protection efficiency in each part of developed pesticide-proof clothes by repeated washings. We investigated the effect of repeated laundering on mechanical properties of pesticide-proof clothes (not washed vs 5 times washed). We also examined pesticide infiltration rate into the pesticide-proof clothes by repeated laundering. The patches(TCL paper, surface area 50cm2)were attached to the inside of pesticide-proof clothes(head, chest, right upper-arm, right forearm, left thigh, left calf, back) which subjects had dressed in during pesticide spraying. The patches were detached from working clothes after work. For the extraction of pesticide in pesticide-proof clothes, sonication was applied for 30 min with methanol. The gas chromatography/mass spectrometry (GC/MS) was applied to identify the pesticide component. The results of this study are as follows: The force strength, water-vapour resistance and surface wetting resistance of pesticide-proof clothes decreased 5 times more in washed clothes. The concentration of pesticide was the highest in the head area of pesticide-proof clothes. In seven parts of TLC paper attached to the pesticide proof clothes, the concentration of pesticide was higher in the left thigh. The penetration part and concentration of pesticide increased as washing was repeated. Therefore the conclusion which can be drawn from this study is this: protection efficiency of pesticide-proof clothes decrease by repeated washings.

The effects of proteins released from silk mat layers on macrophages

  • Kim, Ju-Won;Jo, You-Young;Kweon, Hae Yong;Kim, Dae-Won;Kim, Seong-Gon
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제40권
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    • pp.10.1-10.6
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    • 2018
  • Background: The objective of this study was to evaluate the changes in gene expression after incubation of cells with proteins released from different silk mat layers. Methods: A silk cocoon from Bombyx mori was separated into four layers of equal thickness. The layers were numbered from 1 to 4 (from the inner to the outer layer). The proteins were released by sonication of a silk mat layer in normal saline. The concentration of proteins was determined by spectrophotometry. They were incubated with RAW264.7 cells, and changes in the expression of genes were evaluated by cDNA microarray analysis and quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR). Results: Layer 1 and 4 groups had higher protein concentrations compared to those in layer 2 and 3 groups. The genes associated with inflammation and angiogenesis showed significantly higher expression in layer 1 and 4 groups. The results of qRT-PCR were in agreement with those of the cDNA microarray analysis. Conclusions: The silk mat from the middle portion of the silkworm cocoon yielded a lower protein release and caused an insignificant change in the expression of genes that are associated with inflammation and angiogenesis.

$^1H-NMR$을 이용한 한약재의 품질 평가 방법 확립;진피의 Hesperidin 정량분석 (Quantitative Analysis of Quality Control of Natural Medicine by $^1H-NMR$ Spectrometry-Quantitative Analysis of Hesperidin from Citrus unshiu)

  • 안은미;백미영
    • 대한본초학회지
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    • 제23권3호
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    • pp.27-32
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    • 2008
  • Objectives : In this paper, we describe that $^1H-NMR$ spectroscopy may be superior to the conventional HPLC for the quantitative analysis of hesperidin from Citrus unshiu. Methods : $^1H-NMR$ spectra (400 MHz) were recorded in $DMSO-d_6$ using a Varian UNITY Inova AS 400 FT NMR spectrometer. One hundred milligram of powdered Citrus unshiu was weighed out and mixed with 1 ml of $DMSO-d_6$ with sonication for 30 min (room temperature). The extracts were filtrated through a 0.45 ${\mu}m$ PVDF filter and 0.5 ml of filtrated extract used for quantitative $^1H-NMR$ measurement (added 1 mg of dimethyl terephthalate as internal standard). The quantity of hesperidin was calculated by the ratio of the intensity of the compound to the known amount of internal standard. For HPLC analysis, the half gram of plant material was extracted with 60 ml of MeOH for 2 hours. The extracts were made 100 ml volume and analyzed by a Waters HPLC system using a YMC ODS column. The total flow rate was 1.0 ml/min with a sample volume 10 ${\mu}l$ and UV detection at 280nm. Results : The contents of hesperidin in Citrus unshiu was determined $5.33{\pm}0.06$% in the quantitative $^1H-NMR$ method and $5.15{\pm}0.12%$ in HPLC method. Using the quantitative $^1H-NMR$ the contents of hesperidin can be determined in much shorter time than the conventional HPLC measurements. Conclusions : From those results, the advantages of quantitative $^1H-NMR$ analysis are that can be analyzed to identify and quantify, and no reference compounds required for calibration curve. Besides, it allows rapid and simple quantification for hesperidin with an analysis time for only 10 min without any pre-purification steps.

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막유화 다중 에멀젼을 이용한 생분해성 폴리카프로락톤(PCL) 마이크로캡슐의 제조 (Preparation of Biodegradable PCL Microcapsules Using Multiple Emulsions by Membrane Emulsification)

  • 지연주;염경호
    • 멤브레인
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    • 제27권6호
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    • pp.511-518
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    • 2017
  • 막유화(membrane emulsification, ME)는 SPG 막과 같이 균일한 크기의 세공을 갖는 막을 사용하여 좁은 입도분포의 에멀젼을 제조하는 기술이다. 본 연구에서는 막유화법으로 형성시킨 다중 에멀젼을 사용하여 폴리카프로락톤(PCL) 마이크로캡슐의 제조를 연구하였다. 먼저 초음파 유화기로 $W_1/O$ 단일 에멀젼을 제조한 후, premix 막유화를 적용하여 $W_1/O/W_2$ 다중 에멀젼을 형성시킨 후 용매 증발을 통해 모델 약물인 BSA가 담지된 PCL 마이크로캡슐을 제조하였다. 연속상에 대한 분산상의 비율(D/C ratio), PCL 농도, 유화제 농도, 모델 약물의 농도, 막간 압력차 등 막유화 변수가 제조된 마이크로캡슐의 입경과 입도 분포에 미치는 영향을 실험하였다. Premix-ME를 적용하여 평균 입경 $5{\sim}6{\mu}m$의 균일한 크기를 갖는 모델 약물 BSA의 함침량이 약 26%인 다중 코어형 PCL 마이크로캡슐을 제조할 수 있었다.

이중 유제 방법으로 제조된 PLGA 미립자들과 반구체:특성과 라니티딘(ranitidine)의 방출 양상 (PLGA particles and half-shells prepared by double emulsion method: characterization and release profiles of ranitidine )

  • 남대식;김성철;강수용;오돈치멕문크자갈;심영기;이우경
    • Journal of Pharmaceutical Investigation
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    • 제38권2호
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    • pp.99-104
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    • 2008
  • PLGA micro/nano particles encapsulating ranitidine as a hydrophilic model drug were prepared by the double-emulsion solvent evaporation method. Surface morphology investigation by scanning electron microscope (SEM) showed that the emulsification by sonication could produce nanoparticles, whereas microparticles were prepared using high speed homogenizer. Moreover, while nanohalf-shell structure instead of spherical nanoparticle could be produced by adding poloxamer into oil phase (MC) with PLGA 504H, the addition of poloxamer didn't change particle shape in case of PLGA 502H. On the other hand, microparticle with poloxamer had more surface pores than those without poloxamer. The size and polydispersity (PDI) of particles were determined by particle size analyzer. Effective diameters of particles were in the range of $400{\sim}800\;nm$ and $1200{\sim}3300\;nm$ in case of nanoparticles and microparticles, respectively. Encapsulation efficiencies were in the range of $1.2{\sim}2.9%$. The addition of poloxamer produced the particles with higher encapsulation efficiency. In vitro release study in phosphate buffer (pH 7.4) at $37^{\circ}C$ showed common large initial burst release. However, the relative slower release profile could be observed in case of microparticles. Poloxamer addition increased the release rate, which was thought to be related to the increased surface area of particles.

연쇄구균의 세포벽 단백질이 L929 세포의 미세구조 변화에 미치는 영향에 관한 연구 (THE EFFECT OF CELL WALL PROTEINS OF STREPTOCOCCUS SPECIES ON MICROSTRUCTURAL CHANGES OF L929 CELLS)

  • 오세홍;임미경
    • Restorative Dentistry and Endodontics
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    • 제20권2호
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    • pp.549-576
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    • 1995
  • Bacteria are one of the most important causative agents of the pulpal and periapical diseases. Streptococci are one of the most frequently isolated facultative anarerobic bacteria in the infected root canals. Bacterial cell wall components have a direct effect in the pathogenesis of the pulpal and periapical infections. Hyaluronidase produced by bacteria has been implicated in dissemination of the diseases. The purpose of this study was to evaluate the effect of cell wall extract of streptococci on the L929 cells using inverted microscope and the transmission electron microscopy (TEM). Hyaluronidase production of streptococcal strains were investigated to determine the correlation between the severity of cell damage and the activity of enzymes. Bacterial cell wall extracts of S. sanguis, S. mitis and S. uberis isolated from infected root canals and ATCC type strains of S. mutans (ATCC 10449) and E. faecalis (ATCC 19433) were prepared by sonication and confirmed with SDS-PAGE. Silver stain of SDS-PAGE of sonic extract was efficient at $100{\mu}g$/ml concentration of cell wall protein, while Coomasie blue stain was efficient at $100{\mu}g$/ml concentration. Inverted microscope showed that sonic extract-treated L929 cells were round and detached from the substratum while others lost their fibroblastic shapes. Transmission electron microscopic examination revealed that streptococcal extracts induced death of L929 cells. Sonic extracts of streptococci had variable effect on microstructure of L929 cells. significant chromatin condensation was observed in the nucleus of the cells. Disappearance of cell surface microvilli and nuclear fragments with dense chromatin were observed. The cell nucleus had an irregular shape and numerous large vacuoles were seen in the cytoplasm and some breaks of the cell membrane could be seen. Cell organelles were in various stages of destruction and cristae of mitochondria were disoriented or disappeared. Eighteen strains of streptococci did not produce hyaluronidase.

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초음파가 조사되는 용융 혼합에 의한 폴리카보네이트/스티렌-아크릴로니트릴 혼합물의 상용화 (Compatibilization of PC/SAN Blends via Ultrasound-irradiated Melt Mixing)

  • 김형수
    • 폴리머
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    • 제28권3호
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    • pp.225-231
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    • 2004
  • 폴리 카보네이트와 스티렌-아크릴로니트릴 공중합체, 그리고 이들의 혼합물이 혼합기에서 용융 가공되는 동안 고강도 초음파를 조사하였다. 순수한 고분자의 경우에 용융상태에서 가해진 초음파 에너지에 의하여 용융점도가 감소되었으며, 혼합물에서는 분산상의 크기가 감소하는 것으로 확인되었다. 초음파 조사에 따른 성분 고분자의 용융점도 저하는 가공 중에 거대 라디칼이 생성된 것과 관련이 있으며, 이들의 상호 결합으로 말미암아 폴리 카보네이트/스티렌-아크릴로니트릴 혼합물의 상용화가 진행됨을 알 수 있었다. 전체적인 상용화의 효과는 혼합물의 형태학과 기계적 성질을 측정함으로 평가하였다. 총 조사 시간 5분 중에서 약 3분을 전후하여 분산상의 크기가 현저하게 감소하였고 혼합이 끝난 시료를 20$0^{\circ}C$에서 약 10분간 방치한 후의 형태학은 초음파로 처리된 경우에 매우 안정한 상 구조를 유지하였다. 아울러 파단 신율과 인장강도와 같은 기계적 성질이 현저하게 향상되는 결과를 바탕으로, 고강도 초음파를 이용한 용융 혼합은 별도의 상용화제의 투입 없이 비상용계 고분자 혼합물을 상용화할 수 있는 효과적인 방법으로 판단되었다.

초음파 표면개질에 의한 CDI 전극용 술폰화 염화비닐(PVC) 멤브레인의 제조 및 특성 (Preparation and Properties of Sulfonated Polyvinylchloride (PVC) Membrane for Capacitive Deionization Electrode by Ultra Sonication Modification)

  • 황치원;오창민;황택성
    • 접착 및 계면
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    • 제15권1호
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    • pp.1-8
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    • 2014
  • 이온 교환막은 전기투석, 확산투석, Redox flow 전지, 연료전지 등 다양하고 넓은 분야에서 사용되고 있다. 초음파를 이용하여 만들어진 PVC 양이온 교환막을 시간을 변화시켜 가면서 술폰화 반응에 의해 제조하였다. 술폰화제로 황산을 사용하였으며, 술폰화 PVC 양이온 교환막의 기본구조와 특성을 FT-IR, EDX, Water uptake, 이온교환용량(IEC), 전기저항(ER), 전도도, 이온수송수 및 표면 morphology를 SEM 분석하였다. FT-IR 스펙트럼 분석결과 술폰화 PVC 양이온 교환막에 술폰산기가 도입되었음을 확인하였으며 멤브레인의 Water uptake, IEC, 전기 저항 및 ion transport number의 최대값은 각각 40.2%, 0.87 meq/g, $35.2{\Omega}{\cdot}cm^2$ 및 0.88이었다.

비집속 회분저주파를 이용한 Dunaliella salina 세포 파쇄 (Cell Disruption of Dunaliella salina using Batch Low Frequency Non-Focused Ultrasound)

  • 최준혁;김광호;박종락;정상화
    • 한국기계가공학회지
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    • 제20권10호
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    • pp.63-71
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    • 2021
  • Using fossil fuels in existing industrial systems causes a variety of social problems. Recently, many studies have been conducted on bio-refineries, which aim to actively utilize biomass to reduce the use of fossil fuels and solve various social problems. Among them, research using microalgae as a third-generation biomass has attracted considerable attention. Microalgae use inorganic matter to produce organic matter, and cell destruction is necessary to extract useful organic materials from microalgae. The extracted organic materials are currently used in various industrial fields. Numerous cell-destruction methods exist. We have investigated cell disruption by sonication, especially its efficiency. Ultrasound is a sound wave with frequencies above 20 kHz, and destroys cells by sending high energy through a cavitation that occurs, according to the characteristics of the sound wave. The Dunaliella salina microalgae used in this study was cultured in a flat-type photobioreactor. Experiments were performed using a batch low-frequency processing device. Logistic model was applied to analyze the results of cell-destruction experiments using ultrasound. The proper conditions for the most efficient cell destruction were OD 1.4(microalgae concentration)), 54watt(output power) and 200mL(microalgae capacity).