• 한국재료학회지
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• 제9권6호
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• pp.583-588
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• 1999

The characteristics of copper thin films and pattern filling capability were investigated by ECD. Prior to deposition of copper film, seed-Cu/Ta(TaN)/$SIO_2$(BPSG)/Si structure was manufactured. Copper deposition was performed with various current waveforms(DC/PC, 1~10,000Hz) and current densities(10~60 mA/$\textrm{cm}^2$) after pretreatment (Oxident removal, wetting) of seed-layer. Conformal pattern filling was performed using PC method with fast deposition rate of 6,000~8,000$\AA$/min. Heat-treated($450^{\circ}C$, 30min) copper films showed good resistivities of 1.8~2.1$\mu$$\Omega$.cm. According to the XRD analysis, (111)-preferred orientation of copper film was found in ECD-Cu/seed-Cu/Ta/$Sio_2$/Si structure. Also, we have successfully achieved to fill via holes with 0.35$\mu\textrm{m}$ width and 4:1 aspect ratio.

• 대한기관식도과학회지
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• 제4권1호
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• pp.64-72
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• 1998

This study aimed at observing the effect of diazepam on the contractility of trachealis muscle isolated from canine trachea, possible involvement of central or peripheral type benzodiazepine receptor, and the calcium related mechanism of action of diazepam. Trachealis muscle strips of 15 mm long were suspended in an isolated organ bath containing 1 ml of physiologic salt solution maintained at $37^{\circ}C$, and aerated with 95% $O_2$ /5% $CO_2$. Isometric myography was performed. Diazepam reduced the basal tone concentration dependently, and this inhibitory action was not affected by neither flumazenil, a central benzodiazepine receptor antagonist, nor PK11195, a peripheral benzodiazepine receptor antagonist. Pretreatment with diazepam showed the inhibitory effect on the concentration-response curves to agonists such as bethanechol, 5-hydroxytryptamine and histamine. Diazepam also caused concentration-related inhibition of contraction with potassium chloride 30 mM. The effect of diazepam on the basal tone and potassium chloride-induced contraction with calcium channel blockers were compared. Similar results were obtained in canine trachealis with verapamil, nifedipine and diltiazem. These results suggest that diazepam relax an airway muscle not via specific receptors but by a similar action as calcium channel blockers in canine trachealis muscle.

• 한국자원식물학회지
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• 제10권1호
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• pp.86-93
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• 1997

본 실험(實驗)은 칼란코에 (Kalanchoe daigremontiana Hamet et Perr.)의 줄기 절편(切片)과 약(葯)을 배양(培養)하여 체세포배(體細胞胚)를 양도(諒導)함에 있어서 여러 식물생장조절물질(植物生長調節物質) 특히. 2,4-D의 효과(效果)를 비교(比較)하고자 실시하였던 바, 두 종류의 절편체에 실시하였던 바, 두 종류의 절편체에 있어서 캘리스 및 체세포배의 유도에 있어 2.4-D는 효과가 없었다. 줄기 절편(切片)으로부터 캘러스의 유도(誘導)는 2,4-D에 비해 IAA와 NAA 첨가(添加)의 경과(境過)에 양호하였으며, 체세포배(體細胞胚)의 유도(誘導)는 배발생(胚發生) 캘러스를 0.1mg/L 1AA와 1.0mg/L BAP 처리구(處理區)인 저농도(低濃度)의 auxin 처리구(處理區)와 식물생장조절물질(植物生長調節物質)이 첨가(添加)되지 않은 배지에 이식(移植)하여 배양(培養)과 경과(境過)에 양호(良好)하였으나. 2,4-D의 처리구(處理區) (0.2-1.0mg/L)에 이식(利殖)하여 배양한 경우에는 일어나지 않았다. 또한, 약(葯)으로부터 캘러스의 유도(誘導)는, 발달단계별(發達段階別)로는 초기 1핵기에서 그리고, 저온(低溫) 처리는 $4^{\circ}C$에서 3일간 전처리(前處理)한 경우(境遇)에 양호(良好)하였고, 2.4-D에 비해 NAA 처리시(處理時)에 양호(良好)하였으며, 그리고 charcoal 처리시(處理時)엔 전혀 일어나지 않았다. 한편 체세포배(體細胞胚)의 유도(誘導)는 줄기절편에서와 같이 2,4-D처리시에는 일어나지 않았으나, 줄기절편의 경우와는 달리 1.0mg/L NAA와 1.0mg/L BAP 처리구와 2.0mg/L NAA와 0.2mg/L BAP 처리구(處理區)인 고농도(高濃度)의 auxin 처리구(處理區)에서 양호(良好)하여, 줄기 절편과 약에 있어서 생장조절물질(生長調節物質)에 대한 반응에 차이(差異)가 다소 있음을 알 수 있었다. 약유래 식물체의 염색체(染色體)조사결과 대부분이 2n=34이었으며, 소수(小數) (5.4%)가 4배체이었다.

• 폴리머
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• 제36권4호
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• pp.486-493
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• 2012

칼콘기를 포함하는 광가교성 sulfonated polyimide(SPI) 전해질 고분자를 칼콘기를 가지는 실란 커플링제가 처리된 알루미나 전극에 도포하여 습도센서를 제조하였다. SPI 필름 중 bis(tetramethyl)ammonium 2,2'-benzidinedisulfonate($Me_4N$-BDS)/4,4'-diaminochalcone(DAC)/pyromellitic dianhydride(PA)= 90/10/100 이루어진 습도센서는 20과 95 %RH 영역에서 4.48부터 $2.1k{\Omega}$까지 변화하며 좋은 직선성(Y = -0.04528X+7.69446, $R^2=0.99675$)을 보여주었다. 33 %RH와 94 %RH 사이에서 흡습과 제습과정의 응답속도는 약 79초이며, 가교화된 SPI 필름은 습도를 빠르게 검지할 수 있는 매우 효율적인 감습재료이다. 온도 의존성 계수는 $-0.49%RH/^{\circ}C$이며 습도센서로서 응용시 온도 보상이 필요하다. 또한 센서의 기재를 칼콘을 포함하는 실란 커플링제로 처리한 센서는 가교와 동시에 기재에 접합되어 480시간 이상 내수성, 고온과 고습 안정성 및 장기 안정성이 뛰어남을 알 수 있었다. 이렇게 가교화된 SPI는 상용화된 센서보다 우수한 특성을 보이는 재료로서 응용 가능성을 보여주었다.

• The Korean Journal of Physiology
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• 제24권1호
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• pp.67-76
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• 1990

The contractile mechanisms of serotonin were investigated in the renal artery of a rabbit. The helical strips of isolated renal artery were immersed in the normal or $Ca^{2+}$-free tris-buffered Tyrode's solution, which was equilibrated with 100% $O_{2}$ at $35^{\circ}C$. The contraction by serotonin or norepinephrine (NE) began at $1{\times}10^{-7}\;M$ and reached the maximal contraction at $1{\times}10^{-5}\;M$. The maximal contraction by serotonin corresponded to $58.1{\pm}4.2%$ of maximal contraction by NE. Cyproheptadine, a serotonin receptor blocker, shifted the concentration-response curve to the right without any reduction in the maximum response but shifted that of NE to the right with reduction in maximum response. And phentolamine, an ${\alpha}-receptor$ blocker, shifted the concentration-response curve of serotonin or NE without any reduction in maximum responses. The $pA_{2}$ values for cyproheptadine against serotonin and NE were $10.35{\pm}0.04$ and $8.45{\pm}0.13$, respectively. The $pA_{2}$ values for phentolamine against serotonin and NE were $6.87{\pm}0.04$ and $8.14{\pm}0.08$, respectively. after the pretreatment with 6-hydroxydopamine, the contraction induced by 100 mM $K^{+}$, tyramine and serotonin reduced to $83.0{\pm}2.0$, $26.8{\pm}6.2$ and $82.0{\pm}3.5%$ of control, respectively. The contraction by serotonin in the $Ca^{2+}$-free Tyrode's solution was increased and sustained with the addition of $Ca^{2+}$ extracellulary. The serotonin-sensitive intracellular $Ca^{2+}$ pool was depleted completely by the pretreatment with NE, but the NE-sensitive intracellular $Ca^{2+}$ pool was depleted partially by the pretreatment with serotonin. From the above results, it is suggested that the contraction induced by serotonin in the renal artery of a rabbit may be due to mechanisms in which serotonin acts directly on specific serotonin receptors and also acts indirectly on ${\alpha}-adrenoceptors$ by displacing NE from neuronal stores.

• 대한수의학회지
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• 제44권1호
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• pp.15-21
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• 2004

This paper describes the development of $^{99m}Tc$ tricarbonyl cysteine as potential renal function diagnostic radiopharmaceutical and evaluation of its biological characteristics using experimental animals. l-Cysteine was labeled efficiently with $^{99m}Tc$ tricarbonyl precursor $([^{99m}Tc(CO)_3(H_2O)_3)]^{+})$ under 30 min heating at ${75^{\circ}C}$. Labeling yield and stability were analyzed by high performance liquid chromatography (HPLC). The biodistribution property of $^{99m}Tc$ tricarbonyl cysteine in mice and its dynamic imaging profiles in rabbits were carried out. To investigate the excretion mechanism of $^{99m}Tc$ tricarbonyl cysteine, tubular transport inhibition test with probenecid was adopted. $^{99m}Tc$ tricarbonyl cysteine was obtained with a high labeling yield under the moderate condition. The results of biodistribution experiments of $^{99m}Tc$ tricarbonyl cysteine in ICR mice at 3 and 90 min provided that $^{99m}Tc$ tricarbonyl cysteine was very highly accumulated in the kidney and bladder, thereby almost 99% of $^{99m}Tc$ tricarbonyl cysteine was excreted within 90 min post injection. The same results were confirmed by the whole body dynamic images for 30 minutes and static images in rabbits at given time intervals after injection. Renogram of $^{99m}Tc$ tricarbonyl cysteine in rabbits showed that its $T_{max}$ and $T_{1/2}$ of $^{99m}Tc$ tricarbonyl cysteine were $2.33{\pm}0.56$ and $4.30{\pm}0.79$ min, respectively. The $T_{max}$ of $^{99m}Tc$ tricarbonyl cysteine with probenecid pretreatment was $2.30{\pm}0.17$ min, whereas $T_{1/2}$ of that with probenecid pretreatment was $17.0{\pm}32.47$ min. $T_{1/2}$ of $^{99m}Tc$ tricarbonyl cysteine with probenecid pretreatment was significantly different, as compared to the result without probenecid (p<0.0001). The results showed that the excretion of $^{99m}Tc$ tricarbonyl cysteine was extremely affected by probenecid. Therefore, $^{99m}Tc$ tricarbonyl cysteine was rapidly excreted from the kidney principally by the tubular secretion.

• 생명과학회지
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• 제19권9호
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• pp.1226-1231
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• 2009

페닐케톤뇨증은 상염색체 열성으로 유전되며, phenylalanine-4-hydroxylase (PAH, EC 1.14.16.1)의 돌연변이에 의해 효소 불활성화를 초래하는 질환이다. 최근 유전자 재조합된 phenylalanine ammonia-lyse (PAL)에 의한 효소 대체요법이 보고된 바 있다. 이 효소를 경구용 약제로 개발하기 위하여 효소활성을 나타내기 위한 최적 조건들을 알아야 하며, 위장관내 소화효소에 의해 분해되지 않는 구조적 안정성을 유지하여야 한다. 따라서 본 연구에서는 PAL의 생화학적 특성을 규명하고, 이를 바탕으로 위장관내 소화효소로부터 저항할 수 있는 변이형들을 만들고자 하였으며, 이러한 구조적 변화를 통하여 효소의 특이 활성도가 유지될 수 있는지를 보고자 하였다. PAL의 특이 활성도를 측정하였고, 효소 활성을 나타내기 위한 최적 pH, 온도 변화에 따른 효소 활성도, 단백분해효소에 의한 활성도 변화를 측정하였다. PAL의 Vmax는 페닐알라닌과 티로신에 대하여 각각 1.77, $0.47{\mu}mol$/ mg x protein로 나타났으며, Km은 페닐알라닌에 대하여 $4.77{\times}10^{-4}\;M$,티로신에 대하여 $4.37{\times}10^{-4}\;M$로 나타났다. 또한 pH 8.5에서 가장 높은 활성을 나타내었는데, 이는 소장의 평균 pH와 유사하다. PAL의 효소 활성은 $-80^{\circ}C$에서 5개월 동안 유지되었으며, $4^{\circ}C$에서 1주일 동안 93.4%의 활성을 유지하였다. PAL은 키모트립신에 의해 쉽게 분해되었으며, 이보다 약한 정도로 트립신, elastase, carboxypeptidase A, B에 의해 분해 되었다. 췌장 소화효소에 대한 저항성을 증가시키기 위하여 트립신, 키모트립신 절단부위 아미노산을 변이시켜 유전자 변이형을 만들었고, 효소 활성도를 측정하였다. 6개의 유전자 변이형은 모두 저하된 효소 활성도를 나타내었는데, Y110H는 0.084, Y110A와 Y110L은 0, R123A는 0.11, R123H는 0.074, R123Q는 0.033으로 나타났다. 이러한 결과는 트립신 및 키모트립신 절단부위 아미노산이 PAL의 효소 활성에 필수적인 역할을 하고 있음을 나타낸다. PAL 변이형은 단백분해작용으로부터 보호할 수 있는 전처치 방법이지만, 페닐알라닌을 효과적으로 저하시키기 위해서 효소활성을 유지할 수 있는 다음 단계의 처치가 필요하다.

• Journal of Chest Surgery
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• 제16권2호
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• pp.199-212
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• 1983

The inhibition/influences of adenine compounds on the heart have been described repeatedly by many investigators, since the first report by Druny and Szent-Gyorgyi [1929]. These studies have shown that adenosine and adenine nucleotides have an over-all effect similar to that of acetylcholine [ACh] by slowing and weakening the heartbeat. The basic cellular and membrane events underlying the inhibitory action of adenosine on sinus rate, however, are not well understood. Furthermore, the physiological role of adenosine in regulation of the heartbeat remains still to be elucidated. Therefore, this study was undertaken in order to examine the response of rabbit SA node to adenosine and to compare the response to that of ACh. Isolated SA node preparation, whole atrial pair, or left atrlal strip was used in each experiment. Action potentials of SA node were recorded through the intracellular glass microelectrodes, which were filled with 3M KCI and had resistance of 30-50 M. All experiments were performed in a bicarbonate-buffered Tyrode solution which was aerated with 3% $CO_2-97%$ $O_2$ gas mixture and kept at $35^{\circ}C$. Spontaneous firing rate of SA node at 35C [Mean + SEM, n=16] was 154 + 3.3 beats/min. The parameters of action potentials were: maximum astolic potential [MDP], -731.7mV: overshoot [OS], 9 + 1.4mV; slope of pacemaker potential [SPP], 94 3.0mV/sec.Adenosine suppressed the firing rate of SA node in a dose dependent manner. This inhibitory effect appeared at the concentration of $10^{-6}M$ and was potentiated in parallel with the increase in adenosine concentration. Changes in action potential by adenosine were dose-dependent increase of MDP and decrease of SPP until $10^{-4}$. Above this concentration, however, the amplitude of action potential decreased markedly due to the simultaneous decrease of both MDP and OS. All these effects of adenosine were not affected by pretreatment of atropine [2mg/l] and propranolol [$5{\times}10^{-6}M$]. ACh [$10^{-6}M$] responses on action potential were similar to those of adenosine by increasing MDP and decreasing SPP. These effects of ACh disappeared by pretreatment of atropine [2mg/1]. Inhibition/effects of adenosine and ACh on sinus rate were enhanced synergistically with the simultaneous administration of adenosine and ACh. Marked decrease of overshoot potential was the most prominent feature on action potential. Dipyridamole [DPM], which is known to block the adenosine transport across cell membrane, definitely potentiated the action of adenosine . Adenosine suppressed the sinus rate and atrial contractility in the same dosage range, even in the reserpinized preparation. Above` results suggest that adenosine suppresses pacemaker activity, like ACh, by acting directly on the membrane of SA node, increasing MDP and decreasing SPP.

• The Plant Pathology Journal
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• 제26권4호
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• pp.353-359
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• 2010

In order to control postharvest spoilage of satsuma mandarin fruits, rhizobacteria were isolated from soil samples. The Pantoea agglomerans strain 59-4 (Pa 59-4) which suppresses the decay of mandarin fruit by green and blue mold, was tested for the control efficacy and its mode of action was investigated. Pa 59-4 inhibited infection by green and blue mold on wounded mandarins, which were artificially inoculated with a spore suspension of Penicillium digitatum and P. italicum with control efficacies of 85-90% and 75-80%, respectively. The biocontrol efficacy was increased by raising the concentration of cells to between $10^8$ and $10^9\;cfu/ml$, and pretreatment with the antagonist prevented subsequent infection by green mold. The population of Pa 59-4 was increased more than 10 fold during the 24 hr incubation at $20^{\circ}C$, indicating that colonization of the wound site might prevent the infection by green mold. Despite poor antifungal activity, the Pa 59-4 isolate completely inhibited the germination and growth of P. digitatum spores at $1{\times}10^8\;cfu/ml$. We argue that the control efficacy was mediated by nutrient competition. Overall, the effective rhizobacterium, Pa 59-4, was shown to be a promising biocontrol agent for the postharvest spoilage of mandarin fruits by green and blue mold.

• 한국자원식물학회지
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• 제21권5호
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• pp.368-373
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• 2008

물레나물 약유래 캘러스로부터 신초 재분화에 미치는 저온 전처리 및 식물생장조절물질의 효과를 조사하기 약배양을 실시하였다. 약유래 캘러스 유도 및 식물체 재분화에 미치는 식물생장조절제의 효과를 조사하기 위해 2,4-D, NAA, BA 및 TDZ를 8종류로 혼합한 1/2 MS 배지에 약배양을 실시한 결과 물레나물은 식물생장소절물질에 의존적인 식물로 배지내 식물생장조절물질이 첨가되지 않으면 캘러스가 형성되지 않았다. 2,4-D가 포함된 배지에서 약유래 캘러스 형성이 양호하였으며 2.0mg/L 9,4-D단용 처리에서 캘러스 형성율이 52.6%로 가장 높았으며 지속적 캘러스의 증식 및 shoot 분화는 0.1mg/L 2,4-D와 1.0mg/L BA 혼용처리가 효과적이었다. 2.0mg/L 2,4-D 단용처리에 의해 형성된 캘러스로부터 부정적 다수의 신초분화에 미치는 TDZ와 BA 효과를 조사한 결과 1.0mg/L TDZ 처리구에서 단 한개의 shoot가 분화된 것을 제외하고는 갤러스가 갈변되어 효과적이지 못하였으나 모든 BA 처리구에서 갤러스는 shoot가 분화되어 TDZ에 비해 효과적이었다. 특히 3.0mg/L BA 처리구에서는 캘러스 모두 shoo4로 분화되어 다수의 multishoot가 형성되어 가장 효과적이었다. 개화 1주일전의 화뢰를 $5^{\circ}C$ 에서 8일간, 15일간 저온 전처리 하여 0.1mg/L 2,4-D와 1.0 mg/L BA 혼용처리된 DIS 배지에 배양한 결과 무처리에 비해 처기구에서 약의 생육기간이 길었으며 특히 $5^{\circ}C$ 15일간 저온처리한 약이 배양기간 동안 지속적으로 캘러스 및 부정 shoot를 형성하여 저온처리 효과가 있었다.