• 제목/요약/키워드: SDS micelle

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Micelles in Physical Chemistry Laboratory. Surfactant Catalyzed Oxidation of Glycine by Acidic Permanganate

  • Pare, Brijesh;Kaur, Parwinder;Bhagwat, V.W.;Fogliani, Charles
    • 대한화학회지
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    • 제48권2호
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    • pp.195-202
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    • 2004
  • 미셀 촉매 작용은 이론과 실험 화학 교과내용에서 중요한 부분이다. 산성 용액에서 도데실황산 나트륨(SDS)을 촉매로 한 글리신과 과망가니즈산 칼륨의 반응은 미셀 촉매 작용을 보여주는 반응속도론적 실험으로 적합하며, 고등학교와 대학 학부과정의 물리화학실험에서 사용할 수 있다. 본 연구에서는 이 반응이 계면활성제 존재하에서 반응속도가 빨라지는 것을 관찰하기 위하여 SDS를 넣지 않은 경우와 넣은 경우 모두 실험을 진행하였고, 얻어진 k를 [SDS]에 대하여 도시하였다. SDS의 임계 미셀 농도 이하에서부터 계면활성제에 의한 촉매 효과가 관찰되었는데, 이 선-미셀 촉매 효과는 양의 협동효과에 의한 것임을 알 수 있다. 얻어진 양의 협동지수(n)는 2.37이다. 또한 기질과 산화제의 농도에 따른 반응속도 변화도 논의하였다. 반응은 유사 일차 반응으로 진행되었으며, 글리신과 과망가니즈산 이온의 농도에 각각 일차 반응으로 나타나 전체 반응 차수는 이차 반응이었다. 반응 시간은 3~4시간으로 한 실험 시간에 몇 개의 실험 데이터를 얻을 수 있다. 용액 제조와 실험 과정에 대해서 자세히 기술하였으며, 또한 계면활성제에 의한 촉매 작용의 이론도 논의하였다.

Characterization of CNT-ink and fabrication of a cold cathode using jet-printing technique.

  • Lee, Dae-Sik;Lim, Seong-Chu;Lee, Young-Hee
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2008년도 International Meeting on Information Display
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    • pp.1532-1534
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    • 2008
  • Aquesous carbon nanotubes (CNTs) solutions were prepared using SDS (sodium dodecyl sulfonate) and NADDBS (sodium dodecylbenzene sulfonate). Our inks are found to have the viscosity of 1-2 cps. In addition, the surface tension of inks inversely decreased with increasing surfactant concentration and then saturated at critical micelle concentration (CMC). The low surface tension at CMC gave rise to lower contact angles on Indium layers, resulting in larger printable feature sizes. In the fabrication of cold cathode, jet-printing is feasible to modify and scale up the cathode structures. These feasibilities could contribute jet-printing method to be more adaptable for making large-area cold cathodes.

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Sophorolipid Production by Candida bombicola ATCC 22214 from a Corn-Oil Processing Byproduct

  • KIM , HYUN-SOO;KIM, YOUNG-BUM;LEE, BAEK-SEOK;KIM, EUN-KI
    • Journal of Microbiology and Biotechnology
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    • 제15권1호
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    • pp.55-58
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    • 2005
  • Sophorolipid was produced by Candida bombicola ATCC 22214 from soybean dark oil, a byproduct of soybean oil processing. With a fed-batch culture of C. bombicola for 7 days, 90 g/l of sophorolipid was obtained. The CMC (critical micelle concentration) and minimum surface tension of the sophorolipid in aqueous solution were found to be 150 mg/l and 48 mN/m, respectively. The dispersion capability of sophorolipid was higher than that of the chemical surfactants such as SDS and Brij30. The molar solubility ratio (MSR) of 4-methylnaphthalene was 0.2. Linoleic and oleic acids were the main constituents of the fatty acid composition of the sophorolipid. The sophorolipid showed antimicrobial activity against Propionibacterium acne and Bacillus subtilis.

Separation of Lactoferrin from Model Whey Protein Mixture by Reverse Micelles Formed by Cationic Surfactant

  • Noh, Kyung-Hyun;Rhee, Min-Suk;Imm, Jee-Young
    • Food Science and Biotechnology
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    • 제14권1호
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    • pp.131-136
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    • 2005
  • The selective extraction behavior of lactoferrin (Lf) from whey protein mixture was examined using reverse micelles formed by the cationic surfactant, cetyldimethylammonium bromide (CDAB). The major whey proteins, including ${\beta}$-lactoglobulin, ${\alpha}$-lactalbumin and bovine serum albumin, were solubilized from aqueous phase to organic phase while Lf was recovered in the aqueous phase. The solubilization behaviors of the proteins were manipulated by the process parameters such as the pH and salt concentration of the aqueous phase and the surfactant concentration in the organic phase. Efficient forward extraction was achieved with sodium borate buffer (50 mM, pH 9) containing 50 mM KCl and organic phase containing 100 mM CDAB. Based on SDS-PAGE and densitometry, about 96% of the initial Lf remained in the aqueous phase after forward extraction. The dialyzed Lf fully maintained its bacteriostatic activity against E. coli O157:H7.

Structure of CT16 in the C-terminal of Amyloid Precursor Protein Studied by NMR Spectroscopy

  • Lee, Kyoung-Ik;Baek, Dong-Ha;Shin, Song-Yub;Kim, Yang-Mee
    • 한국자기공명학회논문지
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    • 제8권1호
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    • pp.19-27
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    • 2004
  • C-terminal fragments of APP (APP-CTs), that contain complete Abeta sequence, are found in neuritic plaques, neurofibrillary tangles and the cytosol of lymphoblastoid cells obtained from AD patients. CT16, Lys649-Asp664 (KKQYTSIHHGVVEVD) has been known as the most toxic part in the C-terminal fragment of amyloid precursor protein (APP). The solution structure of CT16 was investigated using NMR spectroscopy in various membrane-mimicking environments. According to Circular Dichroim (CD) spectra, CT16 has a random structure in aqueous solution, while conformational change was induced by addition of TFE and SDS micelle. Tertiary structure as determined by NMR spectroscopy shows that CT16 has a ${\beta}$-turn conformation in trifluoroethanol-containing aqueous solution.

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Catalytic Properties of Phospholipase D using Phosphatidic Acid as an Activator

  • Eun-hie Koh;Myung-Un Chol;Kwanyoung Jung
    • Bulletin of the Korean Chemical Society
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    • 제10권6호
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    • pp.595-599
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    • 1989
  • The effects of phosphatidic acid(PA) on the activity of phospholipase D were examined in detail. The enzyme activity was examined in the liposome system containing phosphatidylcholine and PA, which was suspended in a desired buffer solution by ultrasonication. The substrate of large unilamella vesicle (LUV) state by ultrasonication was more effective on the enzyme activity than that of multilamella vesicle(MLV) by water-bath type sonication. The most effective molar ratio of PC-PA liposome for enzyme activity was found to be 1:0.7. The other optimum conditions were found 5 mM $Ca^{2+}$ ion, pH 6.6, and incubation temperature of $27^{\circ}C. K_m \;and \;V_{max}$ values were estimated to be 1.43 mM and 0.8 $nmole/min/{\mu}g$ protein respectively. These properties in a PC-PA liposome system were compared with those in a PC-SDS mixed micelle system. The effects of other phospholipids and organic phosphates on the enzyme activity were also examined.

Benoxaprofen-photosensitization Decomposition of Tryptophan Peptides in Aqueous Micellar Systems

  • Yoon, Min-Joong;Lee, Ki-Hwan
    • Bulletin of the Korean Chemical Society
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    • 제8권4호
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    • pp.261-264
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    • 1987
  • Benoxaprofen (2-(4-chlorophenyl)-${\alpha}$ -methyl-5-benzoxazole acetic acid) is a nonsteroidal anti-inflammatory drug that causes acute cutaneous phototoxicity. The ability of benoxaprofen (BXP) and its photoproduct, decarboxybenoxaprofen (DBXP) to photosensitize the decomposition of tryptophan was evaluated in various media such as water, ethanol and aqueous micellar dispersions of surfactants. The weak photosensitization of BXP in water was found to be enhanced in cationic CTAB micelle system, but yielded little difference in anionic SDS micelles. In ethanol solution, BXP was determined to photosensitize the decomposition of tryptophan, but no photosensitization was observed with DBXP. All of these results implicate that the anion radical of BXP may play a major role in the photosensitization in hydrophobic micellar phase, forming superoxide through interaction with oxygen as demonstrated by observation that the photosensitization was inhibited by superoxide dismutase.

담즙산염과의 고체분산체로부터 로바스타틴의 용출 및 십이지장 점막 투과 특성 (Dissolution and Duodenal Permeation Characteristics of Lovastatin from Bile Salt Solid Dispersions)

  • 전인구
    • Journal of Pharmaceutical Investigation
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    • 제39권2호
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    • pp.97-106
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    • 2009
  • Although lovastatin (LS) is widely used in the treatment of hypercholesterolemia, its bioavailability is known to be around 5%. This study was aimed to increase the solubility and dissolution-permeation rates of LS using solid dispersions (SDs) with bile salts. The solubilities of LS in water, aqueous bile salt solutions and non-aqueous vehicles were determined, and effects of bile salts on the cellulose or duodenal permeation of LS from SDs were evaluated using a horizontal permeation system. SDs were prepared at various ratios of LS to carriers, such as sodium deoxycholate (SDC), sodium glycocholate (SGC) and/or 2-hydroxypropyl-$\beta$-cyclodextrin (HPCD). The addition of bile salts (25 mM) in water increased markedly the solubility of LS by the micellar solubilization. Some non-aqueous vehicles were effective in solubilizing LS. From differential scanning calorimetric studies, it was found that the crystallinity of LS in SDs disappeared, indicating a formation of amorphous state. The SDs showed markedly enhanced dissolution compared with those of their physical mixtures (PMs) and drug alone. In the dissolution-permeation studies using a cellulose membrane, the donor and receptor solutions were maintained as a sink condition using pH 7.0 phosphate buffer containing 0.05% sodium lauryl sulfate (SLS). The flux of LS alone was nearly same as that of LS-SDC-HPCD (1:3:6) PM. However, the flux of LS-SDC-HPCD (1:3:6) SD slightly increased compared with drug alone and PM, suggesting that entrapment of LS in micelles does not significantly hinder the permeation across cellulose membrane. In the dissolution-duodenal permeation studies using a LS-HPCD-SDC (1:3:6) SD, the addition of various bile salts in donor solutions (25 mM) enhanced the permeation of LS markedly, and the fluxes were found to be $0.69{\pm}0.41$, $0.87{\pm}0.51$, $0.84{\pm}0.46$, $0.47{\pm}0.17$ and $0.68{\pm}0.32{\mu}g/cm^2/hr$ for sodium cholate (SC), SDC, SGC, sodium taurodeoxycholate (STDC) and sodium taurocholate (STC), respectively. The stepwise increase of donor SGC concentration increased the flux dose-dependently. From the relationship of donor SGC concentration and flux, the concentration of SGC initiating the permeation across the duodenal mucosa was calculated to be 11.1 mM, which is nearly same as the critical micelle concentration (CMC, 11.6 mM) of SGC. However, with no addition of bile salts and below CMC, the permeation was very limited and irratic, indicating that LS itself is very poor permeable. Higher protions of bile salt in SD such as LS-SDC or LS-SGC (1 : 49 and 1 : 69) showed highly promoted fluxes. In conclusion, SD systems with bile salts, which may form their micelles in intestinal fluids, might be a promising means for providing enhanced dissolution and intestinal permeation of practically insoluble and non-absorbable LS.

계면촬성제 첨가에 따른 지하수 폭기법의 폭기효율 변화 연구 (Surfactant Aided Air-sparging for Groundwater Remediation)

  • 소효은;최경민;이승재;김헌기
    • 자원환경지질
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    • 제35권5호
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    • pp.421-428
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    • 2002
  • 계면활성제를 사용하여 지하수의 표면장력을 인위적으로 감소하였을 때, 감소된 표면장력이 지하수 폭기시의 폭기 영향권 및 VOC 제거 효율에 미치는 영향을 실험실 규모의 실험을 통하여 규명하였다. 내경 9.5 cm, 길이 100 cm의 유리 컬럼에 계면활성제(sodium dodecyl sulfate, SDS) 및 toluene 100 ppm 포함하는 물로 채운 후 일정한 속도로 공기를 주입하였을 때의 toluene의 제거 속도를 측정하였다. 또한 같은 컬럼에 토양(모래)이 채워진 상태에서 동일한 실험을 반복하였다. 토양이 존재하지 않는 상태에서의 stripping에 의한 toluene의 제거 속도는 표면장력의 감소(계면 활성제 농도의 증가)에 따라 증가하는 것으로 나타났으며, 토양이 존재하는 경우에도 비슷한 결과를 나타내었다. 2차원 유리 상자에 모래와 SBS를 포함하는 물을 채운 후 일정한 공기 유속을 유지하였을 때, 폭기의 영향권(공기의 침투영역)은 물의 표면장력 감소에 따라 현저히 증가하는 것으로 나타났다. 특히 SDS의 critical micelle concentration(CMC)보다 훨씬 낮은 농도에서 폭기 영향권이 최대화하는 것으로 밝혀졌다. 본 연구결과는 폭기에 의한 지하수 오염물질 중, 특히 휘발성 유기오염물질의 제거 공정의 효율을 증대하는데 기여할 것으로 생각된다.

Rana box를 포함한 Brevinin-1 및 Thanatin의 구조-상생활성 상관관계 (Structure-antibiotic Acitivity Relationships of Brevinin-1 and Thanatin Containing Rana Box)

  • 신송엽;강주현;이동건;장소윤;서무열;함경수
    • 한국미생물·생명공학회지
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    • 제27권6호
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    • pp.440-445
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    • 1999
  • In order to investigate structure-antibiotic activity relationships of brevinin-1 and thanatin containing Rana box composed of basic loop formed by disulfide bridge in their arboxy terminus, thanatin, brevinin 1 and their analogues (T-B1, T-B2 and B-T) in which their Rana box sequence exchanged was designed and synthesized by the solid phase method using Fmoc-chemistry. The basic sequence of Rana box of thanatin had more significant effect on both antibacterial and antifungal activity than that of brevinin 1. The tail sequence (QRM) of thanatin was found to be important in its antibacterial and antifungal activity. Rana box sequence of brevinin-1 did not have a significant effect on its antitumor and phospholipid vesicle-aggregating activities. Brevinin-1 showed stronger $\alpha$-helical structure in the membrane-mimicking environment such as SDS micelle than thanatin. A remarkable increase in a-helicity of bervinin-1 plays more important role in antibiotic activity than that of thanatin. Furthermore, antibacterial activity of thanatin against E. coli resulted from the disruptive effect against the outer cell membrane of E. coli.

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