• 한국추진공학회지
• /
• 제15권4호
• /
• pp.85-93
• /
• 2011

아크 채널 모델을 이용하여 플라즈마 온도를 매개로 플라즈마 입력전력과 전류 조건에 따른 간극 반지름(R) 및 간극팩 묶음 길이(L) 변수 계산이 가능한 해석해를 유도하고 이를 이용하여 300 A 전류조건에서 0.4 MW 급 분절형 아크 플라즈마 토치에 대한 해석적 설계 변수 해석을 수행하였다. 해석 결과, R��${\leq}$ 7.5 mm, L ${\leq}$ 1.25 m 인 범위에 대해, L이 길어지거나 R이 작아질 때, 플라즈마 온도는 비례하여 증가하는 경향을 가지고 있음을 알 수 있었으며, 그 이상의 범위에서는 증가하다 감소하는 비선형 현상이 존재하여 주어진 전류 및 전력조건에서 아크 플라즈마의 형성이 불가능하거나 불안정할 것으로 예측되었다. 이와 같은 결과를 바탕으로 입력전류가 300 A 일 때, 아크 플라즈마 온도를 안정적으로 구현할 수 있을 것이라 여겨지는 0.4 MW 급 분절형 아크 플라즈마 토치의 간극 반지름 R 및 간극팩 묶음 길이 L의 설계범위를 각각 5.5 mm ${\leq}$ R ${\leq}$ 7.5 mm, 0.25 m ${\leq}$ L ${\leq}$ 0.5 m 범위로 제안하였다.

• The Korean Journal of Pain
• /
• 제21권1호
• /
• pp.44-50
• /
• 2008

Background: The use of regional local anesthetics or opioids during laparoscopic cholecystectomy (LC), in combination with general anesthesia, has been investigated in several interventional studies. Methods: We studied a total of 240 (n = 60, each) patients who were undergoing LC, and they received local infiltration and intraperitoneal instillation with normal saline or 0.25% levobupivacaine 60 ml. Group R (S) received infiltration of normal saline 20 ml before incision and at the end of surgery and then 40 ml intraperitoneal instillation after removal of the gall bladder under remifentanil-based anesthesia. Group R (L) received 0.25% levobupivacaine instead of normal saline in the same method like group R (S). Group S (S) received the same method as group R (S) under sevoflurane based anesthesia in place of remifentanil. Group S (L) received 0.25% levobupivacaine instead of normal saline with the same method as group S (S). Pain was assessed on a visual analog scale at 1, 6, 12 and 24 hours after operation. Results: The pain intensity of Group R (L) was significantly lower than that of group R (S), and the the incisional pain of group S (L) was significantly lower than that of group S (S) in the first six hours. The time delay to first operative analgesics in group R (S) and group S (S) was significantly shorter than that of group R (L) and group S (L). Conclusions: Infiltration and instillation of levobupivacaine reduced the postoperative pain and remifentanil did not increase the pain severity and opioid requirement when performing the LC.

• 한국응용과학기술학회지
• /
• 제32권4호
• /
• pp.781-788
• /
• 2015

본 연구에서는 건조된 까마중(Solanum nigrum L.) 전초의 50% 에탄올 추출물, 에틸아세테이트 분획, 아글리콘 분획을 이용하여 항산화 실험을 진행하였다. 1,1-diphenyl-2-picrylhydrazyl(DPPH)을 이용한 자유라디칼 소거 활성($FSC_{50}$)은 50% 에탄올 추출물, 에틸아세테이트 분획, 아글리콘 분획에서 각각 $215.46{\mu}g/mL$, $42.43{\mu}g/mL$, $52.28{\mu}g/mL$이였다. Luminol-의존성 화학발광법을 이용한 $Fe^{3+}-EDTA/H_2O_2$ 계에서의 총항산화능($OSC_{50}$) 평가에서, 까마중 50% 에탄올 추출물은 $25.25{\mu}g/mL$, 에틸아세테이트 분획은 $7.05{\mu}g/mL$, 아글리콘 분획은 $6.25{\mu}g/mL$를 나타냈다. $^1O_2$로 유도된 적혈구 세포손상에 대한 보호효과 측정에서는 까마중 50% 에탄올 추출물 및 아글리콘 분획은 $5{\sim}25{\mu}g/mL$ 농도에서는 세포보호효과를 나타냈으나 높은 농도에서는 세포보호 활성을 나타내지 않았다. 이러한 결과를 통해 까마중 추출물 및 분획물들은 항산화 활성을 가지고 있지만, 세포 수준에서는 비교적 높은 농도에서 활성산소로 유도된 세포 손상을 촉진할 수도 있음을 시사한다. 따라서 화장품 등에 까마중 추출물을 응용할 때는 사용상 주의가 필요한 것으로 판단된다.

• Journal of the Korean Data and Information Science Society
• /
• 제3권1호
• /
• pp.25-31
• /
• 1992

Some results relating to $C_{0}(R)\;and\;L^{1}(R)$ spaces with application to kernel density estimators will be introduced. First, random elements in $C_{0}(R)\;and\;L^{1}(R)$ are discussed. Then, complete convergence limit theorems are given to show that these results can be used in establishing uniformly consistency and $L^{1}$ consistency.

• 대한기계학회:학술대회논문집
• /
• 대한기계학회 2005년도 창립60주년 기념 추계 학술대회
• /
• pp.25.1-25.1
• /
• 2005

• 한국임상약학회지
• /
• 제16권1호
• /
• pp.28-33
• /
• 2006

The stability of cefditoren in three kinds of oral liquid preparations at 4 and $25^{\circ}C$ was studied for 90 days. Two tablets of 100 mg cefditoren pivoxil were mixed with 200 mL of each oral liquid syrup, which is Pebron syrup (oxolamine citrate 10 mg/mL), $Mucopect^{(R)}$ syrup (ambroxol hydrochloride 3 mg/mL) or $Tyrenol^{(R)}$ suspension (acetaminophen encapsulated 32 mg/mL). Three samples of each formulation were refrigerated $(4^{\circ}C)$ and three were stored at room temperature $(25^{\circ}C)$. At predetermined time, samples were assayed by stability-indicating HPLC method. The chromatographic analysis after deliberate degradation showed no evidence of any breakdown product likely to interfere with the chromatographic peak of the parent substance. The relation between cefditoren pivoxil concentration and peak area was linear from 10 to $150{\mu}g/mL\;(r^2=0.9998)$. The analysis method was precise, with coefficients of variation no greater than 3.6%. Cefditoren was stable in $Mucopect^{(R)}$ syrup up to 4 weeks regardless of the temperature; in $Tyrenol^{(R)}$ suspension and Pebron syrup, it was stable for at least 28 and 45 days, and 7 and 45 days at 25 and $4^{\circ}C$, respectively. The percentages of initial cefditoren concentration remaining after 90 days were $51.5{\pm}1.8\;and\;80.9{\pm}5.6%,\;61.7{\pm}7.8\;and\;70.2{\pm}7.3%,\;and\;39.9{\pm}3.2\;and\;81.4{\pm}5.5%$ in $Mucopect^{(R)}$ syrup, $Tyrenol^{(R)}$ suspension and $Pebron^{(R)}$ syrup at 25 and $4^{\circ}C$, respectively. The pH variations of all test solutions were minimal, which was within 0.5. The results indicated that the stability of cefditoren was significantly affected by liquid solutions mixed with cefditoren, and storage tempertature.

• 한국환경보건학회지
• /
• 제10권2호
• /
• pp.89-97
• /
• 1984

The possible effects of garlic (Aliium sativurn L.) extract on growth and aflatoxin production by Aspergillus parasiticus R- 716 were investigated. Various solvent extracts of garlic strongly inhibited growth and sporulation by Aspergillus parasiticus R-716, and effective solvents used for extraction of garlic were chloroform, benzene, and water-chloroform. The growth and aflatoxin production decreased with the increase in extract concentration, and extract equivalent 1.5g of raw garlic weight in 25ml SLS medium completely inhibited, and at a level of 1.25g garlic, total aflatoxin was reduced 64% (472 ${\mu}g$/25ml) of that produced in the control (1, 352 ${\mu}g$/25 ml). During cultivation inhibitory rate of growth was reduced from 89.1% to 40% and aflatoxin $B_2$, $G_1$ production increased with the laps of time. Especially garlic extract appeared to have a stimulatory effect on lipid accumulation on the contrary aflatoxin production.

• 환경생물
• /
• 제37권3호
• /
• pp.372-379
• /
• 2019

해산규조류(Skeletonema cosatatum)의 개체군성장률(r)을 사용하여 연안 유기오염물질인 phenanthrene (PHE)과 zinc undecylenate (ZU)의 독성평가를 실시하였다. S. costatum을 PHE(0, 25, 50, 100, 200, 300 mg L^-1)와 ZU(0, 5, 10, 15, 20, 25 mg L^-1)에 각각 96시간 노출한 이후에 r을 산출하였고, 대조구의 r은 0.04보다 높아 시험기준에 적합하였다. S. costatum의 r은 PHE 50, ZU 10mg L^-1 이상의 농도에서 대조구 대비 유의하게 감소하기 시작해 PHE와 ZU의 농도가 증가할수록 감소되는 농도의존성을 나타냈으며, 최고농도인 300과 25mg L^-1 농도에서는 r이 나타나지 않았다. PHE와 ZU에 노출된 S. costatum r의 반수영향농도(EC₅₀)은 136.13, 16.95 mg L^-1, 무영향농도(NOEC)는 25, 5 mg L^-1, 최소영향농도(LOEC)는 50, 10 mg L^-1로 나타났다. 본 연구결과, 해양생태계 내에서 S. costatum의 r은 PHE 50 mg ^-1, ZU 10 mg L^-1 이상의 농도에서 독성영향으로 감소할 것으로 판단되며, PHE와 ZU의 기준농도 설정을 위한 기초자료로 유용하게 사용될 것이다.

• 한국임상약학회지
• /
• 제22권2호
• /
• pp.176-180
• /
• 2012

The stability of triamcinolone in three kinds of oral liquid syrups at 4 and $25^{\circ}C$ was studied for 21 days. Twenty tablets of 4 mg triamcinolone were mixed with 100 mL of each oral liquid syrup, which is Levotuss$^{(R)}$Syrup (levodropropizine 6 mg/mL), Ucerax$^{(R)}$Syrup (hydroxyzine 2 mg/mL), and Xyzal$^{(R)}$Liquid (levocetirizine 0.5 mg/mL). The chromatographic analysis after deliberate degradation showed no evidence of any breakdown product likely to interfere with the chromatographic peak of the parent substance. The relationship between triamcinolone concentrations and peak areas was linear from 50 to 1000 ${\mu}g/mL$ ($r^2$ = 0.9998). The analysis method was precise, with coefficients of variation no greater than 5.4%. Triamcinolone was stable for up to 14 and 21 days in Levotuss$^{(R)}$Syrup at 25 and $4^{\circ}C$, respectively; in Ucerax$^{(R)}$Syrup and Xyzal$^{(R)}$Syrup, it was stable for at least 21 days at both temperatures. The percentages of initial triamcinolone concentration remaining after 21 days were $72.3{\pm}3.2$ and $94.9{\pm}6.0%$ and $93.2{\pm}4.9$ and $92.4{\pm}5.7%$, and $92.6{\pm}1.2$ and $92.7{\pm}2.2%$ in Levotuss$^{(R)}$Syrup, Ucerax$^{(R)}$Syrup, and Xyzal$^{(R)}$Syrup at 25 and $4^{\circ}C$, respectively. The pH variations of all test solutions were within 0.8. Based on the results, it was concluded that triamcinolone in three oral liquid syrups which are Levotuss$^{(R)}$syrup, Ucerax$^{(R)}$syrup and Xyzal$^{(R)}$syrup was chemically and physically stable in both states of refrigeration and room temperature for at least 14 days.

• 약학회지
• /
• 제49권6호
• /
• pp.443-448
• /
• 2005

Diosgenin (25 (R) - spirost-5-en-3$\beta$ -ol) was oxidized with 2,3-dichloro -5,6-dicyano-1,4-benzoquinone to form 25(R)-1,4,6-spirostatrien-3-one (1) as rigid cyclic $\alpha$,$\beta$-unsaturated carbonyl compound. This compound was reacted with $H_{2}O_{2}$, m-chloroperoxybenzoic acid (mCPBA), NaOCl in the presence with (R,R)- or (S,S)-Jacobsen catalyst, tert-butyl-hydroperoxide (TBHP) in Mo$(CO)_{6}$, and in VO $(acac)_{2}$ catalyst, respectively, 25(R) -1,4,6-spirostatrien -3-one (1) was reduced with $NaBH_{4}$ L-Selectride, $LiAIH_{4}$,$BH_{3}$ $\cdot$$(CH_{3})_{2}S$, Superhydride, Red-Al, and lithium tri-tert-butoxyaluminium hydride. And 25(R)-4,6-spirostadien-3$\beta$-ol (4) was treated with $H_{2}O_{2}$, mCPBA, TBHP in D - (-) - and L-(+)-diisopropyltar-trate and $Ti(OiPr)_{4}$ condition (Sharpless asymmetric epoxidation), TBHP in $Mo(CO)_{6}$, and in $VO(acac)_{2}$ catalyst, respectively.