• 대한기계학회논문집
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• 제10권1호
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• pp.102-109
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• 1986

본 연구에서는 앞의 여러 연구자들이 시도한 3차원 연쇄기구의 운동해석법을 비교 검토하고, 이중 기호방정식을 이용하여 3차원 연쇄기구의 운동해석을 일반화 하고져 한다. 또 품질향상, 대량생산(mass production) 및 생산가 절하를 위해 만족시키기 위해, 기본해석모델인2차원 연쇄기구에서 3차원연쇄기구로 정밀화 하면서, 가능한 모든 3차원 연쇄기구의 복잡화 되고 있는 현대 기계의 운동요구를 만족시키기 위해, 기본해석모델인 2차원 연쇄기구에서 3차원연쇄기구로 정밀화 하면서, 가능한 모든 3차원 연쇄기구의 운동을 해석 하기 위한 일반해석법을 개발하므로써 해석을 일반화 시키고, 그것을 컴퓨터로 시뮬레이션하여 운동해석을 신빙성있고 신속하게 수행토록 하며, 컴퓨터 결과를 실제모형 즉 구면 4-R 연쇄기구, R-S-S-R 기구 및 3C-R 기구등을 제작하여,실제결과와 비교 검토하므로써 개발된 일반운동해석법의 타당성을 실험적으로 입증 비교 검토하므로써 일반운동해석법의 타당성을 실험적으로 입증하려 한다.

• Smart Structures and Systems
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• 제25권5호
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• pp.605-617
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• 2020

The existence of damages in structures causes changes in the physical properties by reducing the modal parameters. In this paper, we develop a two-stages approach based on normalized Modal Strain Energy Damage Indicator (nMSEDI) for quick applications to predict the location of damage. A two-dimensional IsoGeometric Analysis (2D-IGA), Machine Learning Algorithm (MLA) and optimization techniques are combined to create a new tool. In the first stage, we introduce a modified damage identification technique based on frequencies using nMSEDI to locate the potential of damaged elements. In the second stage, after eliminating the healthy elements, the damage index values from nMSEDI are considered as input in the damage quantification algorithm. The hybrid of Teaching-Learning-Based Optimization (TLBO) with Artificial Neural Network (ANN) and Particle Swarm Optimization (PSO) are used along with nMSEDI. The objective of TLBO is to estimate the parameters of PSO-ANN to find a good training based on actual damage and estimated damage. The IGA model is updated using experimental results based on stiffness and mass matrix using the difference between calculated and measured frequencies as objective function. The feasibility and efficiency of nMSEDI-PSO-ANN after finding the best parameters by TLBO are demonstrated through the comparison with nMSEDI-IGA for different scenarios. The result of the analyses indicates that the proposed approach can be used to determine correctly the severity of damage in beam structures.

• Asian Pacific Journal of Cancer Prevention
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• 제13권12호
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• pp.6435-6439
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• 2012

Chemoresistance to cancer therapy is a major obstacle to the effective treatment of human cancers with cisplatin (DDP), but the mechanisms of cisplatin-resistance are not clear. In this study, we established a cisplatin-resistant human ovarian cancer cell line (COC1/DDP) and identified differentially expressed proteins related to cisplatin resistance. The proteomic expression profiles in COC1 before and after DDP treatment were examined using 2-dimensional electrophoresis technology. Differentially expressed proteins were identified using matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and high performance liquid chromatography-electrospray tandem MS (NanoUPLC-ESI-MS/MS). 5 protein spots, for cytokeratin 9, keratin 1, deoxyuridine triphosphatase (dUTPase), aarF domain containing kinase 4 (ADCK 4) and cofilin1, were identified to be significantly changed in COC1/DDP compared with its parental cells. The expression of these five proteins was further validated by quantitative PCR and Western blotting, confirming the results of proteomic analysis. Further research on these proteins may help to identify novel resistant biomarkers or reveal the mechanism of cisplatin-resistance in human ovarian cancers.

• Bulletin of the Korean Chemical Society
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• 제35권8호
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• pp.2487-2493
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• 2014

Dimeric ${\beta}$-cyclodextrin linked by a thioether bridge was synthesized from a reaction of mono-6-iodo-6-deoxy-${\beta}$-cyclodextrin with sodium sulfide, and the structure was analyzed using nuclear magnetic resonance spectroscopy and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. The effects of thioether-bridged dimeric ${\beta}$-CD on the aqueous solubility of flavonols (myricetin, quercetin, and kaempferol) were investigated by ultraviolet-visible spectroscopy. The aqueous solubility of myricetin, quercetin, and kaempferol were enhanced 33.6-, 12.4-, and 10.5-fold following the addition of 9 mM of thioether-bridged dimeric ${\beta}$-CD. In comparison, the aqueous solubility of myricetin, quercetin, and kaempferol were enhanced 5.4-, 3.3-, and 2.7-fold using the same concentration of monomeric ${\beta}$-cyclodextrin. Furthermore, the formation of flavonol/thioether-bridged dimeric ${\beta}$-CD inclusion complexes was confirmed with nuclear magnetic resonance, Fourier-transform infrared spectroscopy, differential scanning calorimetry, and scanning electron microscopy. The results showed that the nature of the complexes significantly differed from that of free flavonols. Herein, we suggest that the thioether-bridged dimeric ${\beta}$-CD can act as an effective complexing agent for flavonols.

• 한국전산구조공학회논문집
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• 제17권3호
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• pp.279-293
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• 2004

등방성 혹은 비등방성 적층복합판 및 쉘의 선형 정적 문제와 자유진동 해석이 새로운 변형률 변위 관계가 도입된 개선된 9절점 쉘 요소에 의하여 수행되었다. 그 관계에서 새롭게 추가된 휨 변형률과 변위사이의 관계 항들에 의한 효과는 비틀어진 보 문제에서 검토되었다. 정식화의 전 과정을 통해, 식들의 모든 항들은 자연 좌표계에 기초하고 있다. 가정 자연 변형률 방법이 막 잠김과 전단 잠김 거동을 제거하기 위하여 사용하였다. 적층 복합판 및 쉘의 고유치의 계산을 위해 Lanczos방법을 사용하였고 질량행렬을 구성하기 위하여 Gauss적분법을 사용하였다. 정식화의 유효성을 평가하기 위해 수치 예제를 해석적 해와 비교하였으며, 제시된 결과는 자유진동 조건하에서 적층체의 거동을 이해하는데 유용할 것이다.

• 지질공학
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• 제26권3호
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• pp.325-330
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• 2016

현재 경주 중저준위방사성폐기물 처분장(이하 '경주방폐장')에서는 2단계 표층처분시설이 계획중에 있으며, 포화대에 위치한 1단계 처분시설과는 달리 불포화대 상부에 위치하게 된다. 단열을 포함하는 불포화대의 특성상 지하수 및 용질의 대부분이 단열을 통해 이동할 것으로 예상된다. 따라서 불포화 암반 매질에 대한 정밀한 해석을 위하여 단열망 연속체와 암반 매질 연속체를 구분하여 해석하는 TOUGH2 전산코드의 meshmaker 모듈의 MINC 기법을 활용하였다. TOUGH2 MINC 기법의 기존 국내 연구 사례가 미미하여 본 연구에서는 MINC를 이용한 mesh 구성 방법에 대한 절차를 개발하였으며, 단열 연속체와 암반매질 연속체의 k-field를 생성하였다. 이와 같이 생성된 도메인은 향후 이중 연속체를 기반으로 경주방폐장의 지하수 유동 및 오염물질 이동 등에 활용될 뿐만 아니라 단열이 발달한 암반에서 단열-암반매질 연결성을 고려한 단열망 유동 특성을 분석하는데 참고가 될 것으로 기대한다.

• KSBB Journal
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• 제11권1호
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• pp.30-36
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• 1996

Cyclosporin A 고정화배양과 현탁배양의 결과를 바탕으로 각각의 배양의 경우에 따른 비성장속도의 포도당에 대한 Monod 속도식을 제안하고 그에 필요 한 매개변수들을 구하였다. 고정화 배양이 현탁배양 에 비해 높은 ${\mu}m$와 낮은 Km 값을 갖는 것으로 나 타났는데 이는 고정화 균체의 우수한 활성과 기질에 대한 높은 친화도에 기 인한 것으로 보인다. 고정상 발효의 경우, 구한 매개변수들을 담체내에서의 물질 전달 및 반응속도의 정도를 나타내는 효율인자 값을 계산하는데 이용하였다. 중요한 고정화 공정변수인 담체크기, 균체부하의 정도가 기질의 확산저항에 미 치는 영향을 고려하여 효율인자값을 계산한 결과, 적절한 담체의 크기는 반경 $100 ~ 500{\mu}m$로 나타났 다. 고정화세포배양시 담체내의 균체의 균일한 분포 및 활성도의 유지를 위해서, 적정한 담체입자크기를 결정한 후 균체부하량을 조절하여 고정화 공정을 운 영하는 것이 중요한 것요로 판명되었다.

• Advances in Computational Design
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• 제2권3호
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• pp.123-141
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• 2017

Solving a system of linear or non-linear equations is required to analyze any kind of structures. There are many ways to solve a system of equations, and they can be classified as implicit and explicit techniques. The explicit methods eliminate round-off errors and use less memory. The dynamic relaxation method (DR) is one of the powerful and simple explicit processes. The important point is that the DR does not require to store the global stiffness matrix, for which it just uses the residual loads vector. In this paper, a new approach to the DR method is expressed. In this approach, the damping, mass and time steps are similar to those of the traditional method of dynamic relaxation. The difference of this proposed method is focused on the method of calculating the damping. The proposed method is expressed such that the time step is constant, damping is equal to zero except in steps with maximum energy and the concentrated damping can be applied to minimize the energy of system in this step. In this condition, the calculation of damping in all steps is not required. Then the volume of computation is reduced. The DR method for form-finding of membrane structures is employed in this paper. The form-finding of the three plans related to the membrane structures with different loading is considered to investigate the efficiency of the proposed method. The numerical results show that the convergence rate based on the proposed method increases in all cases than other methods.

• Asian Pacific Journal of Cancer Prevention
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• 제16권14호
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• pp.5779-5785
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• 2015

The present study was designed to investigate cholangiocarcinoma (CCA) antibodies in hamster serum. Hamster CCA cell lines were processed using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. A candidate biomarker was confirmed by immunoprecipitation and western blot, and was further analyzed using ELISA and sera from normal control hamsters, hamsters with opisthorchiasis and hamsters with various stages of CCA, as well as from CCA patients and healthy individuals. One candidate marker was identified as $HSP90{\alpha}$, as indicated by a high level of anti-$HSP90{\alpha}$ in hamster CCA sera. It was found that the levels of anti-$HSP90{\alpha}$ were specifically elevated in the sera of hamsters with CCA compared with other groups and progressively increased with the clinical stage. At the cut-off point of 0.4850 on the receiver operating characteristic curve, anti-$HSP90{\alpha}$ could discriminate CCA from healthy control groups with a sensitivity of 76.2%, specificity of 71.4% and total accuracy 75.5%. In the present study, we have shown that anti-$HSP90{\alpha}$ may be a potential useful serum biomarker to discriminate CCA cases from healthy persons.

• Asian Pacific Journal of Cancer Prevention
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• 제14권10호
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• pp.5789-5795
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• 2013

Background: The high mobility group box 1 (HMGB1) protein is a widespread nuclear protein present in most cell types. It typically locates in the nucleus and functions as a nuclear cofactor in transcription regulation. However, HMGB1 can also localize in the cytoplasm and be released into extracellular matrix, where it plays critical roles in carcinogenesis and inflammation. However, it remains elusive whether HMGB1 is relocated to cytoplasm in clear cell renal cell carcinoma (ccRCC). Methods: Nuclear and cytoplasmic proteins were extracted by different protocols from 20 ccRCC samples and corresponding adjacent renal tissues. Western blotting and immunohistochemistry were used to identify the expression of HMGB1 in ccRCC. To elucidate the potential mechanism of HMGB1 cytoplasmic translocation, HMGB1 proteins were enriched by immunoprecipitation and analyzed by mass spectrometry (MS). Results: The HMGB1 protein was overexpressed and partially localized in cytoplasm in ccRCC samples (12/20, 60%, p<0.05). Immunohistochemistry results indicated that ccRCC of high nuclear grade possess more HMGB1 relocation than those with low grade (p<0.05). Methylation of HMGB1 at lysine 112 in ccRCC was detected by MS. Bioinformatics analysis showed that post-translational modification might affect the binding ability to DNA and mediate its translocation. Conclusion: Relocation of HMGB1 to cytoplasm was confirmed in ccRCC. Methylation of HMGB1 at lysine 112 might the redistribution of this cofactor protein.