• Journal of Periodontal and Implant Science
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• 제29권3호
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• pp.483-509
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• 1999

Biodegradable barrier membrane has been demonstrated to have guided bone regeneration capacity on the animal study. The purpose of this study is to evaluate the effects of cultured calvarial cell inoculated on the biodegradable barrier membrane for the regeneration of the artificial bone defect. In this experiment 35 Sprague-Dawley male rats(mean BW 150gm) were used. 30 rats were divided into 3 groups. In group I, defects were covered periosteum without membrane. In group II, defects were repaired using biodegradable barrier membrane. In group III, the defects were repaired using biodegradable barrier membrane seeded with cultured calvarial cell. Every surgical procedure were performed under the general anesthesia by using with intravenous injection of Pentobarbital sodium(30mg/Kg). After anesthesia, 5 rats were sacrificed by decapitation to obtain the calvaria for bone cell culture. Calvarial cells were cultured with Dulbecco's Modified Essential Medium contained with 10% Fetal Bovine Serum under the conventional conditions. The number of cell inoculated on the membrane were $1{\times}10^6$ Cells/ml. The membrane were inserted on the artificial bone defect after 3 days of culture. A single 3-mm diameter full-thickness artificial calvarial defect was made in each animal by using with bone trephine drill. After the every surgical intervention of animal, all of the animals were sacrificed at 1, 2, 3 weeks after surgery by using of perfusion technique. For obtaining histological section, tissues were fixed in 2.5% Glutaraldehyde (0.1M cacodylate buffer, pH 7.2) and Karnovsky's fixative solution, and decalcified with 0.1M disodium ethylene diaminetetraacetate for 3 weeks. Tissue embeding was performed in paraffin and cut parallel to the surface of calvaria. Section in 7${\mu}m$ thickness of tissue was done and stained with Hematoxylin-Eosin. All the specimens were observed under the light microscopy. The following results were obtained. 1 . During the whole period of experiment, fibrous connective tissue was revealed at 1week after surgery which meant rapid soft tissue recovery. The healing rate of defected area into new bone formation of the test group was observed more rapid tendency than other two groups. 2 . The sequence of healing rate of bone defected area was as follows ； test group, positive control, negative control group. 3 . During the experiment, an osteoclastic cell around preexisted bone was not found. New bone formation was originated from the periphery of the remaing bone wall, and gradually extended into central portion of the bone defect. 4 . The biodegradable barrier membrane was observed favorable biocompatibility during this experimental period without any other noticeable foreign body reaction. And mineralization in the newly formed osteoid tissue revealed relatively more rapid than other group since early stage of the healing process. Conclusively, the cultured bone cell inoculated onto the biodegradable barrier membrane may have an important role of regeneration of artificial bone defects of alveolar bone. This study thus demonstrates a tissue-engineering the approach to the repair of bone defects, which may have clinical applications in clinical fields of the dentistry including periodontics.

• 대한약리학회지
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• 제16권2호
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• pp.45-53
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• 1980

Lipid peroxidation in vitro has been identified as a basic deteriorative reaction in cellular mechanism of aging processes, such as air pollution oxidant damage to cell and to the lung, chlorinated hydrocarbon hepatotoxicity. Many experimental evidences were reported by several investigators that lipid peroxidation could be one of the principle causes for the hepatotoxicity produced by $CCl_4$. It is now reasonably established that $CCl_4$ is activated to a free radical in vivo, that lipid peroxidation occurs very quickly in microsomes prepared from damaged livers, that the peroxidation is associated with loss of enzyme activity of microsomes, and that various antioxidants can protect animals against the hepatotoxic effect of $CCl_4$. Recent studies have drawn attention to some other feature of microsomal lipid peroxidation. Incubation of liver microsomes in the presence of NADPH has led to a loss of cytochrome $P_{450}$. However, the presence of an antioxidant prevented lipid peroxidation and preserved cytochrome $P_{450}$. Decrease of cytochrome $P_{450}$ in microsomes under in vitro incubation can be enhanced by $CCl_4 and these changes were parallel to a loss of microsomal polyunsaturated fatty acid and formation of malonaldehyde. The primary purpose of this experiment was to study the effect of riboflavin tetrabutylate on lipid peroxidation, specially, the relationship between lipid peroxidation and drug metabolizing enzyme system which is located in smooth endoplasmic recticulum as well as the effect of ritoflavin tetrabutylate on drug metabolizing enzyme system of animal treated with $CCl_4$. Albino rats were used for experimental animal. In order to induce drug metabolizing enzyme system, phenobarbital was injected intraperitoneally. $CCl_$ and riboflavin tetrabutylate were given intraperitoneally as solution in olive oil. Microsomal fraction was isolated from liver of animals and TBA value as well as the activity of drug metabolizing enzyme were measured in the microsomal fractions. The results are summerized as following. 1) The secobarbital induced sleeping time of $CCl_4$ treated rat was about 2 times longer than that of the control group. However, the pretreatment with riboflavin tetrabutylate inhibited completely the lengthened sleeping time due to $CCl_4$ treatment. Furthermore TBA value was significantly increased in $CCl_4$ treated rat in comparison to control group tut the increase of TBA value was prevented by the pretreatment with riboflavin tetrabutylate. On the other hand, the activity of hepatic drug metabolizing enzyme was decreased in $CCl_4$ group, however, the pretreatment with riboflavin tetrabutylate also prevented the decrease of the enzyme activity caused by $CCl_4$. 2) The effect of riboflavin tetrabutylate on TBA value and the activity of drug metabolizing enzyme in vitro was similar to in vivo results. Incubation of liver microsome from rat in the presence of $CCl_4$, $Fe^{++}$, or ascorbic acid has led to the marked increase of TBA value, however, the addition of riboflavin tetrabutylate in incubation mixture prevented significantly the increase of TBA value, suggesting the inhibition of lipid peroxidation. In accordance with TBA value, the activity of drug metabolizing enzyme was inhibited in the presence of $CCl_4$, $Fe^{++}$, ascorbic acid but the addition of riboflavin tetrabutylate protected the loss of the enzyme activity in microsome under in vitro incubation.

• 대한핵의학회지
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• 제34권1호
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• pp.82-93
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• 2000

목적: 이 논문에서는 본 연구진이 개발한 소형 감마카메라 시스템에서 사용한 NaI(Tl)섬광결정-위치민감형 광전자증배관 검출기와 각 전자회로에서의 입 출력 신호특성을 조사하고, 시스템 개발을 위해 각 전자회로에서 결정한 변수들에 대하여 고찰하고자 한다. 대상 및 방법: 크기가 $60{\times}60{\times}6mm^3$인 NaI(Tl) 섬광결정을 위치민감형 광전자증배관에 접합하고, 저항 회로와 전치증폭기, 여러 가지 전자회로, 아날로그-디지털 변환기 그리고 개인용 컴퓨터를 이용하여 소형 감마카메라 시스템을 개발하였다. 섬광결정에서 검출된 신호들을 위치민감형 광전자증배관을 통하여 증폭한 후, 전하분할방법으로 34개의 교차된 양극채널 신호를 4개($X^+,\;X^-,\;Y^+,\;Y^-$) 위치신호로 출력시켰다. 출력된 신호를 전치증폭기와 층폭기를 사용하여 증폭 정형하였으며, 핵기기 모듈(nuclear instrument modules, NIMs)을 이용하여 위치신호와 트리거 신호를 처리하였고, 각 단계에서 신호특성을 분석 고찰하였다. 이 신호들을 아날로그-디지털 변환기와 앵거로직을 사용하여 처리한 후, 일반 개인용 컴퓨터에서 그래픽 프로그램을 이용하여 감마카메라 영상을 구현하였다. 결과: 연구에서 분석 고찰한 신호특성을 그림을 통하여 나타내었으며, 이러한 신호처리를 이용하여 개발한 감마카메라는 약 $8{\times}10^3$ counts/sec/${\mu}Ci$의 계수율을 보였다. 140 keV에 대하여 18% FWHM의 에너지 분해능과 X, Y 방향으로 각각 2.2, 2.3 mm FWHM의 내인성 위치 분해능을 나타내었다. 또한 평행구멍형 조준기를 장착한 상태에서 유방모형에 위치한 $2{\sim}7mm$ 직경의 방사능 분포를 정확하게 영상화할 수 있었다. 결론: 이 연구에서 개발한 소형 감마카메라 시스템을 구성하고 있는 각 전자회로에서 결정한 매개변수와 신호특성 고찰결과를 나타내었다. 이 신호처리 시스템 분석을 통하여 감마선 검출을 이용한 영상표현 기술을 확보할 수 있었으며, 소형 감마카메라 개발을 위한 간단한 신호처리 방법을 고안하여 제시하였다.

• 한국영양학회:학술대회논문집
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• 한국영양학회 1995년도 추계학술대회 초록
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• pp.11-34
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• 1995

Growth hormone (GH) plays a key role in regulating postnatal growth and can stimulate growth of animals by acting directly on specific receptors on the plasma membrane of tissues or indirectly through stimulating insulin-like growth factor (IGF)-I synthesis and secretion by the liver and other tissues. IGF-I and IGF-Ⅱ are polypeptides with structural similarity with proinsulin that stimulate cell proliferation by endocrine, paracrine and autocrine mechanisms. The initial event in the metabolic action of IGFs on target cells appears to be their binding to specific receptors on the plasma membrane. Current evidence indicates that the mitogenic actions of both IGFs are mediated primarily by binding to the type I IGF receptors, and that IGF action is also mediated by interactions with IGF-binding proteins (IGFBPs). Six distinct IGFBPs have been identified that are characterized by cell-specific interaction, transcriptional and post-translational regulation by many different effectors, and the ability to either potentiate or inhibit IGF actions. Nutritional deficiencies can have their devastating consequence during growth. Although IGF-I is the major mediator of GH's action on somatic growth, nutritional status of an organism is a critical regulator of IGF-I and IGFBPs. Various nutrient deficiencies result in decreased serum IGF-I levels and altered IGFBP levels, but the blood levels of GH are generally unchanged or elevated in malnutrition. Effects of protein, energy, vitamin C and D, and zinc on serum IGF and IGFBP levels and tissue mRNA levels were reviewed in the text. Multiple factors are involved in the regulation of intestinal epithelial cell growth and differentiation. Among these factors the nutritional status of individuals is the most important. The intestinal epithelium is an important site for mitogenic action of the IGFs in vivo, with exogenous IGF-I stimulating mucosal hyperplasia. Therefore, the IGF system appears to provide and important mechanism linking nutrition and the proliferation of intestinal epithelial cells. In order to study the detailed mechanisms by which intestinal mucosa is regulated, we have utilized IEC-6 cells, an intestinal epithelial cell line and Caco-2 cells, a human colon adenocarcinoma cell line. Like intestinal crypt cells analyzed in vivo or freshly isolated intestinal epithelial cells, IEC-6 cells and Caco-2 cells possess abundant quatities of both type Ⅰ and type Ⅱ IGF receptors. Exogenous IGFs stimulate, whereas addition of IGFBP-2 inhibits IEC-6 cell proliferation. To investigate whether endogenously secreted IGFBP-2 inhibit proliferation, IEC-6 cells were transfected with a full-length rat IGFBP-2 cDNA anti-sense expression construct. IEC-6 cells transfected with anti-sense IGFBP-2 protein in medium. These cells grew at a rate faster than the control cells indicating that endogenous IGFBP-2 inhibits proliferation of IEC-6 cells, probably by sequestering IGFs. IEC-6 cells express many characteristics of enterocyte, but do not undergo differentiation. On the other hand, Caco-2 cells undergo a spontaneous enterocyte differentiation. On the other hand, Caco-2 cells undergo a spontaneous enterocyte differentiation after reaching confluency. We have demonstrated that Caco-2 cells produce IGF-Ⅱ, IGFBP-2, IGFBP-3, and an as yet unidentified 31,000 Mr IGFBP, and that both mRNA and peptide secretion of IGFBP-2 and IGFBP-3 increased, but IGFBP-4 mRNA and protein secretion decreased after the cells reached confluency. These changes occurred in parallel to and were coincident with differentiation of the cells, as measured by expression of sucrase-isomaltase. In addition, Caco-2 cell clones forced to overexpress IGFBP-4 by transfection with a rat IGFBP-4 cDNA construct exhibited a significantly slower growth rate under serum-free conditions and had increased expression of sucrase-isomaltase compared with vector control cells. These results indicate that IGFBP-4 inhibits proliferation and stimulates differentiation of Caco-2 cells, probably by inhibiting the mitogenic actions of IGFs.

• The Korean Journal of Physiology
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• 제3권2호
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• pp.9-16
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• 1969

It is well known that a number of -SH and -SS containing substances afford a certain measure of protection against radiation effects in many biological systems, and it is conceivable that inherent -SH levels in Ehrlich ascites tumour (ELD)cells may be of decisive improtance with respect to the development of cellular radiation injury. So far, little effort has been directed to elucidate the changes in levels of different -SH and -SS groups in ELD cells when the tumour-bearing whole animal was subjected to the sublethal dose of X-irradiation. The present study was designed to bring some lights in the possible changes of and relationship between various sulfhydryl levels, such as P-SH, NP-SH and NP-SS, as well as the content of protein and cell volume of ELD cells, after subjecting the ELD mice to 1,200 r of X-irradiation. The animals used in this experiment were all mixed bred mice of $20{\sim}25\;gm$ in body weight (approximately 2 months old) irrespective of sex. 12 mice in one experiment were inoculated intraperitoneally with 0.2 ml of ascites tumour cells $(2{\times}10^6\;cells)$, and on the 7th day of the tumour growth, they were X-irradiated with 1,200 r, using the conventional X-ray machine under the following conditions: 200 Kv at 15 mA, 0.5 mm Cu filter, target-skin distance: 50 cm. Radiation dose was measured with the the Philip integrating dosimeter. At 24, 36, 48 and 60 hours after the X-irradiation, the mice were killed by cervical dislocation, and the tumours were taken out. Freshly withdrawn ascites tumours were placed in ice, and immediately the cell concentration was measured with the Coulter Cell Counter (Model B), and the hematocrit of the tumour cells were also determined. Cell volume was thus calculated by the cell concentration and hematocrit value. P-SH content of ELD cells was measured potentiometrically according to the method of Calcutt & Doxey, and NP-SH and NP-SS contents were measured spectrophotometrically by the method described by Ellman. Protein content of ELD cells was determined with the Folin phenol reagent by Lowry et al. Altogether, 48 experimental mice were used, and 12 mice with the only exception of X-irradiation were used as the control. Results obtained indicate that the contents of all the cellular sulfhydryl groups as well as cell volume and protein content of the ELD cells increase significantly as time progresses after the sub-lethal X-ray dose of 1,200 r was given and that all the increase is in a lineal fashion. The regression lines of the relative values, (i. e., taking each control value as 1) of all the values obtained, and the regression lines of cell volume, protein and NP-SH are identical, whereas those of NP-SS and P-SH appear to be widely seperated. However, the difference of those two lines (NP-SS & P-SH) were found to be not significant statistically (p>0.05). Therefore, it can be concluded from the above results that all the values examined increase in a lineal fashion with no statistically significant difference among them. Also, with the radiation dose of 1,200 r, the ELD cell becomes enlarged and swollen progressively up to 60 hours post-irradiation and it becomes more than two times of the original normal size at 60 hours after the irradiation, and up to this stage, it seems apparent that the cell division has been slow due to the X-irradiation applied in this experiment. It is well understandable that the contents of NP-SH, NP-SS, P-SH and protein of the ELD cells increase in parallel with the increase of the cell volume by the X-ray does used, but it also seems interesting to note that all the cellular substances tested show no appreciable difference in the pattern of increase.

• 항공우주정책ㆍ법학회지
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• 제28권1호
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• pp.3-54
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• 2013

현재 주요 항공기술 선진국들은 군용기에서 거둔 무인항공기의 성공을 그 성장성과 효용성에 주목하고 민간 부문으로 확대하려는 노력을 경주하고 있으며 그 결과 민간 무인항공기 시장은 2020년 경에는 그 시장규모를 약 88억불에 달할 것으로 보면서 앞으로 가장 유망한 시장의 하나가 될 것으로 예상하고 있다. 그 용도도 원격탐사, 통신중계, 환경감시, 기상관측, 국경감시, 산불감시, 위험지역 정찰, 치안, 교통, 재난구호 지원활동 등 다양한 분야에 걸쳐 있다. 그러나 현재의 항공교통체계는 유인항공기 위주로 운용되고 있는 실정이어서 조종사가가 탑승하지 않는 무인항공기의 등장으로 무인항공기 운용을 고려한 조정이 필요하게 되었으며 그 조정에 필수적으로 수반하는 것이 법제화 작업이다. 현재 무인항공기 운용에 관한 법제화 작업은 전 세계적으로 ICAO가 중심이 되어 표준화 작업을 진행 중에 있으며 미국, 영국, 호주 등 국가는 개별적으로 법 규정을 마련하여 운용 중에 있다. 본 논문에서는 ICAO산하의 무인항공기시스템연구그룹(UASSG)의 활동과 무인항공기 법제화에 앞서가고 있는 미국, 영국, 호주의 법제화를 소개 하였다. 이중 미국의 경우는 2012년 2월14일에 오바마 대통령이 미국의 국가공역에서의 무인항공기를 운용하도록 하는 제반 법령 및 규정을 2015년 9월30일 시한으로 제정하도록 하는 법안에 서명함으로서 가장 적극적이다. 우리나라의 경우는 현재 국내 항공법상의 정의 규정과 비행허가에 관한 일부 사항을 제외하고는 운용에 관한 규정은 거의 전무한 상태라고 할 수 있다. 그러나 현실에 있어서는 군사용 및 민간 무인항공기가 실제 개발 운용되고 있는 실정이며 국토교통부에서는 상업용 민간무인항공기 개발을 우리나라의 항공기 제작 및 수출부문에 있어 가장 국제경쟁력 있는 분야로 보아 적극적으로 추진할 계획이어서 국내적으로도 무인항공기 운용을 위한 제반 사항에 대한 법제화가 필요하게 되었다. 무인항공기 운용을 위한 법제화 작업 중 가장 중요하다고 생각되는 부분은 (1)공역사용, (2)항공종사자 자격인증, (3)무인항공기 감항인증 및 기술기준인증 등 이지만 이외에도 (4)무인항공기 등 관련 사항에 대한 정의 규정, (5)무인항공기의 분류체계, (6)탑재장비 및 탑재서류, (7)통신, (8)비행규칙, (9)무인항공기 항공종사자 교육훈련, (10)보안, (11)보험, (12)기타 법제화가 필요한 사항으로 나누어 법제화 작업이 이루어져야 한다고 본다. 이와 함께 우리나라도 2012년 12월에 UASSG에 참가하였으므로 국제기준의 수립에 능동적이고도 주도적으로 참여하여 국제 사회에 기여함은 물론 무인항공기와 관련된 국제 관련 법령의 동향과 선진국의 사례를 파악하여 무인항공기 운용을 위한 국내 관련 법령을 선진형으로 제정 정비하는 법제화 작업을 병행하여야 할 것으로 본다.

• 한국지능시스템학회:학술대회논문집
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• 한국퍼지및지능시스템학회 1993년도 Fifth International Fuzzy Systems Association World Congress 93
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• pp.975-976
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• 1993

This talk presents the overview of the author's research and development activities on fuzzy inference hardware. We involved it with two distinct approaches. The first approach is to use application specific integrated circuits (ASIC) technology. The fuzzy inference method is directly implemented in silicon. The second approach, which is in its preliminary stage, is to use more conventional microprocessor architecture. Here, we use a quantitative technique used by designer of reduced instruction set computer (RISC) to modify an architecture of a microprocessor. In the ASIC approach, we implemented the most widely used fuzzy inference mechanism directly on silicon. The mechanism is beaded on a max-min compositional rule of inference, and Mandami's method of fuzzy implication. The two VLSI fuzzy inference chips are designed, fabricated, and fully tested. Both used a full-custom CMOS technology. The second and more claborate chip was designed at the University of North Carolina(U C) in cooperation with MCNC. Both VLSI chips had muliple datapaths for rule digital fuzzy inference chips had multiple datapaths for rule evaluation, and they executed multiple fuzzy if-then rules in parallel. The AT & T chip is the first digital fuzzy inference chip in the world. It ran with a 20 MHz clock cycle and achieved an approximately 80.000 Fuzzy Logical inferences Per Second (FLIPS). It stored and executed 16 fuzzy if-then rules. Since it was designed as a proof of concept prototype chip, it had minimal amount of peripheral logic for system integration. UNC/MCNC chip consists of 688,131 transistors of which 476,160 are used for RAM memory. It ran with a 10 MHz clock cycle. The chip has a 3-staged pipeline and initiates a computation of new inference every 64 cycle. This chip achieved an approximately 160,000 FLIPS. The new architecture have the following important improvements from the AT & T chip: Programmable rule set memory (RAM). On-chip fuzzification operation by a table lookup method. On-chip defuzzification operation by a centroid method. Reconfigurable architecture for processing two rule formats. RAM/datapath redundancy for higher yield It can store and execute 51 if-then rule of the following format: IF A and B and C and D Then Do E, and Then Do F. With this format, the chip takes four inputs and produces two outputs. By software reconfiguration, it can store and execute 102 if-then rules of the following simpler format using the same datapath: IF A and B Then Do E. With this format the chip takes two inputs and produces one outputs. We have built two VME-bus board systems based on this chip for Oak Ridge National Laboratory (ORNL). The board is now installed in a robot at ORNL. Researchers uses this board for experiment in autonomous robot navigation. The Fuzzy Logic system board places the Fuzzy chip into a VMEbus environment. High level C language functions hide the operational details of the board from the applications programme . The programmer treats rule memories and fuzzification function memories as local structures passed as parameters to the C functions. ASIC fuzzy inference hardware is extremely fast, but they are limited in generality. Many aspects of the design are limited or fixed. We have proposed to designing a are limited or fixed. We have proposed to designing a fuzzy information processor as an application specific processor using a quantitative approach. The quantitative approach was developed by RISC designers. In effect, we are interested in evaluating the effectiveness of a specialized RISC processor for fuzzy information processing. As the first step, we measured the possible speed-up of a fuzzy inference program based on if-then rules by an introduction of specialized instructions, i.e., min and max instructions. The minimum and maximum operations are heavily used in fuzzy logic applications as fuzzy intersection and union. We performed measurements using a MIPS R3000 as a base micropro essor. The initial result is encouraging. We can achieve as high as a 2.5 increase in inference speed if the R3000 had min and max instructions. Also, they are useful for speeding up other fuzzy operations such as bounded product and bounded sum. The embedded processor's main task is to control some device or process. It usually runs a single or a embedded processer to create an embedded processor for fuzzy control is very effective. Table I shows the measured speed of the inference by a MIPS R3000 microprocessor, a fictitious MIPS R3000 microprocessor with min and max instructions, and a UNC/MCNC ASIC fuzzy inference chip. The software that used on microprocessors is a simulator of the ASIC chip. The first row is the computation time in seconds of 6000 inferences using 51 rules where each fuzzy set is represented by an array of 64 elements. The second row is the time required to perform a single inference. The last row is the fuzzy logical inferences per second (FLIPS) measured for ach device. There is a large gap in run time between the ASIC and software approaches even if we resort to a specialized fuzzy microprocessor. As for design time and cost, these two approaches represent two extremes. An ASIC approach is extremely expensive. It is, therefore, an important research topic to design a specialized computing architecture for fuzzy applications that falls between these two extremes both in run time and design time/cost. TABLEI INFERENCE TIME BY 51 RULES {{{{Time }}{{MIPS R3000 }}{{ASIC }}{{Regular }}{{With min/mix }}{{6000 inference 1 inference FLIPS }}{{125s 20.8ms 48 }}{{49s 8.2ms 122 }}{{0.0038s 6.4㎲ 156,250 }} }}

• 한국정보전자통신기술학회논문지
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• 제11권2호
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• pp.144-149
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• 2018

인공부화기 내에 종란이 입란하여 18일간 발생기를 거쳐 발육기로 이란을 한다. 발생기 동안 계태아 무게 손실은 곧 기실형성과 상관되며 적당한 기실 형성은 곧 건강한 초생추와 입란 대비 부화율과도 연결된다. 그러나 국내 부화장의 부화기에는 현재 무게를 측정하는 장치 없이 부화실장과 관계자의 경험과 발육기로 이란시 표준 무게 측정으로 결과적 측면을 습득하는 것이 현실이다. 그로 인하여 부화 중 조기 폐사, 약추, 병약한 초생추 발생이 빈번한 실정이다. 종란 중량 감소를 모니터링하는 것은 발육장치기 안에서의 무게 변화에 따른 병아리 품질과 부화율 성과를 얻는 데에 절대적으로 중요하다. 종란의 크기와 난각질, 노계 군에 따라 수분 손실은 각기 다르다. 발육기 안에서 무게 변화를 실시간 측정하고 그에 따른 환기 변화를 최적화하여 부화율의 증가를 기대할 수 있으며 부화 시 전체 무게의 10~13% 감소를 컨트롤할 수 있는 실시간 측정 시스템의 개발 필요성이 대두된다. 본 연구를 통한 시스템은 기존의 입란과 이란시 직접적으로 일회성을 체크하는 방식으로 발육 기간 내에는 계태아 수분 증발 측정 제어가 불가능하여 부화율에 영향을 못 미치는 시스템과 달리 아두이노 스케치 보드에 로드셀 4개를 병렬로 연결하고 실시간으로 휴대폰, 컴퓨터를 연결하기 위해 Hyper-terminal 프로그램을 이용하여 AT-command 명령어를 활용하여 정상적으로 연동하였다. 블루투스의 통신속도는 15200으로 설정하여 아두이노와 Hyper-terminal 프로그램의 통신 속도를 맞춰주었다. 실시간 모니터링을 하여 인공부화기 내의 계태아 무게의 변화를 육안으로 확인할 수 있도록 시스템을 설계하였다. 이와 같은 방법으로 종란의 부화율 상승 및 건강상태의 향상을 목표로 하였으며 실시간 모니터링으로 인하여 사용자의 편의성을 확대하고자 하였다.

• Journal of the Korean Wood Science and Technology
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• 제36권3호
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• pp.1-8
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• 2008

볼트 간격에 따른 국내산 낙엽송 집성재 이중 볼트접합부의 내력성능을 검토하기 위하여 휨 type 전단강도실험을 실시하였다. 전단시편은 강판삽입형 볼트접합부 시편으로서 볼트구멍은 볼트직경(12 mm, 16 mm), 볼트 개수(단일 볼트 : Control, 이중 볼트), 볼트 열 방향(섬유평행 : Type-A, 섬유직교 : Type-B) 그리고 볼트 간격(Type-A : 4 d, 7 d, Type-B : 3 d, 5 d)을 달리하여 제작하였다. 조건에 따른 볼트접합부의 강도성능과 파괴형상을 비교, 검토하였다. 설계표준(KBCS, 2000)시 볼트간격이 감소된 기준허용전단내력에 대한 저감계수를 산출하였다. 본 연구의 결과는 다음과 같다. 1) 단일 볼트접합부와 Type-A의 이중 볼트접합부의 볼트 한 개당 지압응력은 볼트의 직경, 볼트 간격과 비례 관계를 보여주었다. Type-B의 지압응력은 볼트의 직경이 증가할 때 감소하였고, 볼트 간격이 증가할 때 2~10% 정도 감소하였다. 2) 단일 볼트접합부와 Type-A의 이중 볼트접합부의 파괴형상은 연단거리 방향으로 할렬파단이 일어났다. Type-B의 경우 볼트간격이 3 d일 때 인장부위 볼트가 압축부위 볼트보다 더 굴곡되었고 인장부위볼트에서 할렬파단이 시작되었다. 5 d 시편의 경우 인장부위와 압축부위 볼트의 굴곡은 비슷하게 나타났으며, 압축부위볼트에서 할렬파단이 시작되었다. 3) 설계표준시 기준볼트 간격(Type A : 7 d, Type B : 5 d)에 따른 항복하중을 무차원화시켜 저감계수를 산출하였다. 12 mm 볼트접합부의 경우 Type-A인 볼트 간격 4d와 단일 볼트접합부의 저감계수는 각각 0.87, 0.55였고 Type-B인 볼트 간격 3 d와 단일 볼트접합부의 저감계수는 0.91, 0.55였다. 16 mm 볼트접합부의 경우 Type-A인 볼트 간격 4 d와 단일 볼트접합부의 저감계수는 0.96, 0.76이었고 Type-B인 볼트 간격 3 d, 단일 볼트접합부의 저감계수는 0.91, 0.77이었다.

• 한국엔터테인먼트산업학회논문지
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• 제15권7호
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• pp.225-233
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• 2021

본 연구는 정상인을 대상으로 건강을 위한 유산소 능력과 관계가 깊은 하지에 혈류제한 유산소 훈련을 시행함으로써 하지 근활성도와 운동신경원을 정량적으로 비교·분석하여 효과적인 혈류제한 운동프로그램의 효용성을 제시하는 기초자료를 제공하고자 한다. 압력 정도가 140 mmHg으로 혈류제한하여 트레드밀 위에서 유산소 운동을 적용한 집단 10명을 실험군I, 트레드밀 위에서 유산소 운동만 적용한 집단을 11명을 대조군으로 각각 무작위 배치한 후, 트레드밀에서 4주간, 주 3회, 1일 1회, 1회 30분간 중재 프로그램을 시행하였다. 중재 전 표면근전도를 활용하여 근활성도와 운동신경원을 측정하여 분석하였다. 연구 결과는 실험군I의 집단 내 전후 비교에서 넙다리곧은근, 넙다리두갈래근, 앞정강근 및 장딴지근의 근활성도가 유의하게 증가하였다(p<.001). 대조군의 집단 내 전후 비교에서는 넙다리곧은근, 넙다리두갈래근, 앞정강근 및 장딴지근의 근활성도가 유의하게 증가하였다(p<.001). 집단 간 변화 비교에서는 넙다리곧은근의 활성도가 유의한 차이가 있었다(p<.05). 하지 혈류제한과 병행하여 유산소운동을 접목하는 것은 엘리트선수 육성과 관절이 약한 노인 등 재활 트레이닝에 기능적인 활동을 회복시킬 수 있는 부상방지 운동프로그램 등으로 발전시킬 수 있을 것이며, 향후 연구에서 이러한 결과를 바탕으로 하여 정상인이 아닌 대상의 영역을 확대하고, 압력강도에 따른 다각적인 연구들이 필요할 것으로 사료된다.