• 정보처리학회논문지D
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• 제13D권3호
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• pp.383-390
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• 2006

현대의 소프트웨어공학 관련 연구 중에서, 산업계가 궁극적으로 추구하는 수준의 생산성을 제공할 수 있는 기술은 아마도 프로덕트라인 공학이 될 것이다. 지금까지의 소프트웨어공학 기술로는 소프트웨어 개발 분야에 프로덕트라인 기법을 실질적이고 실용적으로 적용하기에는 아직 충분히 성숙하지 못한 것이 사실이다. 본 논문에서는 저자가 산업체에서 접한 과거 3년 동안의 PDA 스마트폰 개발 경험을 바탕으로 실용적 수준의 프로덕트라인 기법을 Model-Driven Architecture(MDA) 접근 방법을 통해 제안한다. 이동 단말 시스템의 경우 단말기 제조사, 목적 사용자 층, 이동 단말 사업자 등에 따라 다양한 형태의 소프트웨어가 존재한다. 특히, 최근에는 단말기 사용자가 직접 느낄 수 있는 지원 기능 구성 및 인터페이스 형식은 매우 다양한 형태가 존재하며, 같은 제조사에 시리즈 제품으로 개발하더라도 이 부분에 대한 변이성이 매우 큰 특징이 있다. 하지만, 전형적인 폰 관련 기능 모듈 즉, 음성호 및 화상전화 기능, 메시지, 주소록, 데이터통신, 카메라 및 멀티미디어 기능, 웹 브라우징 과 같은 큰 기능 묶음에 대한 피처(Feature)들은 자체의 다양한 기능적 요구사항과 함께 피처 간 상호 연관성을 크고 다양한 형태로 구성될 수 있는 특성이 있다. 본 논문에서는 이동 단말기에서 구현해야 하는 다양한 형태의 사용자 소프트웨어의 요구사항에 대해 사용 시나리오 상에서 구분 가능하고 의미 있는 장면의 연속 관계로 정의하여 추후 설계, 구현, 시험 단계에서도 소프트웨어 아키텍쳐 역할을 할 수 있는 개발 기법을 제안한다. 따라서, 요구분석 단계에서도 사용자 인터페이스 관점에서 전반적인 소프트웨어 아키텍쳐에 대해 검증할 수 있게 될 뿐만 아니라 소프트웨어 개발 주기 전 과정에서 그 구조를 사용자 인터페이스 관점에서 유지, 관리 할 수 있는 핵심적인 방법을 제공한다.

• 센서학회지
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• 제24권6호
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• pp.404-411
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• 2015

A stoichiometric mixture of evaporating materials for $BaAl_2Se_4$ single crystal thin films was prepared from horizontal electric furnace. To obtain the single crystal thin films, $BaAl_2Se_4$ mixed crystal was deposited on thoroughly etched semi-insulating GaAs(100) substrate by the Hot Wall Epitaxy (HWE) system. The source and substrate temperatures were $610^{\circ}C$ and $410^{\circ}C$, respectively. The crystalline structure of the single crystal thin films was investigated by the photoluminescence and double crystal X-ray diffraction (DCXD). The carrier density and mobility of $BaAl_2Se_4$ single crystal thin films measured from Hall effect by van der Pauw method are $8.29{\times}10^{-16}cm^{-3}$ and $278cm^2/vs$ at 293 K, respectively. The temperature dependence of the energy band gap of the $BaAl_2Se_4$ obtained from the absorption spectra was well described by the Varshni's relation, $E_g(T)=3.4205eV-(4.3112{\times}10^{-4}eV/K)T^2/(T+232 K)$. The crystal field and the spin-orbit splitting energies for the valence band of the $BaAl_2Se_4$ have been estimated to be 249.4 meV and 263.4 meV, respectively, by means of the photocurrent spectra and the Hopfield quasicubic model. These results indicate that the splitting of the ${\Delta}so$ definitely exists in the ${\Gamma}_5$ states of the valence band of the $BaAl_2Se_4/GaAs$ epilayer. The three photocurrent peaks observed at 10 K are ascribed to the $A_1$-, $B_1$-exciton for n =1 and $C_{31}$-exciton peaks for n=31.

• Journal of Pharmaceutical Investigation
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• 제29권3호
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• pp.227-234
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• 1999

Solid dispersions were prepared to increase the dissolution rate of biphenyl dimethyl dicarboxylate (DDB) using water-soluble carriers such as povidone, copolyvidone, $2-hydroxypropyl-{\beta}-cyclodextrin (HPCD)$, sodium salicylate or sodium benzoate by solvent evaporation method. Solid dispersions were characterized by infrared spectrometry, differential scanning calorimetry (DSC) and powder X-ray diffractometry, dissolution and permeation studies. DDB tablets (7.5 mg) were prepared by compressing the powder mixtures composed of solid dispersions, lactose, com starch, crospovidone and magnesium stearate using a single-punch press. DDB capsules (7.5 mg) were also prepared by filling the mixtures in empty hard gelatin capsules (size No.1). From the DSC and powder x-ray diffractometric studies, it was found that DDB was amorphous in the HPCD or copolyvidone solid dispersions. Dissolution rates after 10 min of DDB alone and solid dispersions (1 : 10) in sodium benzoate, sodium salicylate and copolyvidone were 11.8, 23.5, 22.8 and 82.5%, respectively. Dissolution rates of DDB after 30 min from 1 : 10 and 1 : 20 copolyvidone solid dispersions were 80.5 and 95.0%, respectively. For the DDB tablets prepared using solid dispersions (1 : 20), the initial dissolution rate was dependent on carrier material, and was ranked in order, $Kollidon\;30\;{\ll}$ copolyvidone < HPCD. For the HPCD solid dispersion tablets, dissolution rate reached 97.4% after 15 min, but thereafter slowly decreased to 80.7% after 2 hr due to the precipitation of DDB. However, in the case of copolyvidone solid dispersion tablets, dissolution increased linearly and reached 93.4% after 2 hr. Reducing the volume of test medium from 900 to 300 ml markedly decreased the dissolution rate of the tablets containing 1 : 20 HPCD solid dispersions and 1 : 10 copolyvidone solid dispersion. For 1 : 20 copolyvidone solid dispersion tablets, there was no significant change in dissolution rate up to 1 hr with different volumes of test medium. Preparation of the copolyvidone solid dispersion (1 : 20) in capsules markedly delayed the dissolution (31.2 % after 2hr) due to the limited diffusion within capsules. The permeation rate $(13.4\;g/cm^2\;after\;8\;hr)$ of DDB through rabbit duodenal mucosa from copolyvidone solid dispersion (1 : 10) was markedly enhanced, when compared with drug alone or physical mixtures. From overall findings, DDB formulations containing copolyvidone solid dispersions (1 : 20) could be used to remarkably improve the dissolution rate in dosage form of powders and tablets.

• Journal of Pharmaceutical Investigation
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• 제20권4호
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• pp.223-228
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• 1990

The contribution of endogenous transport systems to the blood-brain barrier (BBB) transport of basic and acidic drugs was studied by using a carotid injection technique in rats and an isolated bovine cerebrovascular disease state were compared between the normotensive rats (WKY) and stroke-prone spontaneously hypertensive rats (SHRSP) which have been well established as an animal model with pathogenic similarities to humans. Basic drugs such as eperisone, thiamine and scopolamine inhibited, in a concentration dependent manner the in vivo uptake of $[{^3}H]choline$ through BBB, whereas amino acids and acidic drugs such as salicylic acid and valproic acid did not inhibit the uptake. The uptake of $[^3H]choline$ by B-CAP increased with time and showed a remarkable temperature dependency. The uptake of $[^3H]choline$ by B-CAP showed the very similar inhibitory effects as observed in the in vivo brain uptake, and was competitively inhibited by a basic drug, eperisone. The in vivo BBB uptakes of $[^3H]acetic$ acid and $[^{14}C]salicylic$ acid were dependent on pH of the injectate and the concentration of drugs. Several acidic drugs such such as salicylic acid, benzoic acid and valproic acid inhibited the in vivo uptake of $[^3H]acetic$ acid, whereas amino acid, choline and a basic drug such as eperisone did not inhibit the uptake. The uptake of acetic acid by B-CAP was competitively inhibited by salicylic acid. The permeability surface area product (PS) through BBB for $[^3H]choline$ in SHRSP was significantly lower than that in WKY. The concentration of choline in the brain dialysate in SHRSP was about half of that in WKY, while no significant difference was observed in the plasma concentration of choline between SHRSP and WKY. No significant difference was observed in the transport of monocarboxylic acids, glucose and neutral amino acid through BBB between SHRSP and WKY. From these results, it was concluded that BBB transport system of choline contributes to the transport of basic drugs through BBB, that acidic drugs can be transported via a moncarboxylic acid BBB transport system and that the specific dysfuntion of the BBB choline transport in SHRSP was ascribed to the reduction of the maximum velocity of choline concentration in the brain interstitial fluids.

• Journal of Pharmaceutical Investigation
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• 제38권2호
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• pp.111-117
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• 2008

To overcome the solubility of poorly water-soluble drug, the formation of solid dispersion using a spray-dryer with polymeric material, that can potentially enhance the dissolution rate extend of drug absorption was considered in this study. $Eudragit^{(R)}$ E100 as carrier for solid dispersion is acrylate copolymer that soluble in acidic buffer solutions (below pH 5.0). It was used to increase dissolution of atorvastatin calcium as a water-insoluble drug in acidic environments. In this study, a spray-dryer was used to prepare solid dispersion of atorvastatin calcium and $Eudragit^{(R)}$ E100 for purpose of improving the solubility of drug. Atorvastatin calcium and $Eudragit^{(R)}$ E100 were dissolved in ethanol and spray-dryed. DSC and XRD were used to analyze the crystallinity of the sample. It was found that atorvastatin calcium is amorphous in the $Eudragit^{(R)}$ E100 solid dispersion. FT-IR was used to analyze the salt formation by interaction between atorvastatin calcium and $Eudragit^{(R)}$ E100. Comparative dissolution study exhibited better dissolution characteristics than the commercial drug ($Lipitor^{(R)}$) as control. The dissolution rate of atorvastatin calcium was markedly increased in solid dispersion system in simulated gastric juice (pH 1.2). This study proposed that this solid dispersion system improved the bioavailability of poorly water-soluble atorvastatin calcium.

• 센서학회지
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• 제7권4호
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• pp.254-262
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• 1998

수정진동자(QCM)위에 네 종류의 프탈로시아닌($MPc(OEH)_8$, M ${\equiv}$ Cu, Co, Sn, $H_2$) LB박막을 여러 층 적층시킨 후 순수한 질소 분위기 하에서 $NO_2$에 노출시켜 그 농도를 정량화 하였다. 사용한 네 종류의 프탈로시아닌 중에서 중심위치에 금속 이온이 자리하지 않은 $H_2Pc(OEH)_8$ 감응막이 $NO_2$에 대하여 가장 민감한 것으로 나타났다. 그러나 이 박막은 $NO_2$에 노출된 후 질소로 퍼지해도 처음의 주파수를 회복하지 못하는 비가역적인 흡착 양상을 보였다. NMR과 FTIR 스펙트럼 조사 결과 비가역적인 흡착은 빙고링과 프탈로시아닌 곁가지의 결합부위인 ether 그룹에서 일어나는 것으로 판명되었다. 따라서 비가역적으로 흡착이 일어나는 부분을 미리 고농도에서 포화시키는 방법으로 박막을 전처리 한 후 반복실험에 사용하였다. $CuPc(OEH)_8$박막 사용 시 수십 ppm 수준부터 4 ppm의 $NO_2$ 농도까지 정량화가 가능하였고 $H_2Pc(OEH)_8$ 박막의 경우에는 수 ppm부터 35 ppb까지의 낮은 농도까지 정량화가 가능하였다. 또한, 실제 대기 조건을 모사하기 위하여 운반기체를 순수한 질소 대신 공기로 교체하여 $H_2Pc(OEH)_8$ 감응막의 성능을 실험한 결과 산소의 영향으로 센싱 가능 한계가 수백 ppb 수준으로 증가하였다. 습기가 운반기체에 포함된 경우 감지 성능에 매우 큰 영향을 미쳤다.

• 센서학회지
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• 제2권1호
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• pp.3-10
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• 1993

Chemical bath deposition 방법으로 다결정 CdS 박막을 세라믹 기판 위에 성장시킨 다음 온도를 변화시켜 열처리하고 X-선 회절무늬를 측정하여 결정구조를 밝혔다. $550^{\circ}C$로 열처리한 시료의 경우 X-선 회절무늬로부터 외삽법에 의해 $a_{o}$와 $c_{o}$는 각각 $4.1364{\AA}$과 $6.7129{\AA}$인 육방정계임을 알았다. 이 때 낱알크기는 약 $0.35{\mu}m$이었다. Van der Pauw 방법으로 Hall 효과를 측정하여 운반자 농도와 이동도의 온도의존성을 연구하였다. 이동도는 33 K에서 150 K까지는 압전산란에 의하여, 150 K에서 293 K 까지는 곽성광학산란에 의하여 감소하는 경향을 나타냈다. 광전도 셀의 특성으로 스펙트럼 응답, 감도(${\gamma}$), 최대허용소비전력 및 응답 시간을 측정하였다.

• 센서학회지
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• 제2권1호
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• pp.81-86
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• 1993

Chemical bath deposition 방법으로 다결정 CdSe 박막을 세라믹 기판 위에 성장시킨 다음 온도를 변화시켜 열처리하고 X-선 회절무늬를 측정하여 결정구조를 밝혔다. $450^{\circ}C$로 열처리한 시료가 X-선 회절무늬로 부터 외삽법에 의해 $a_{o}$와 $c_{o}$는 각각 $4.302{\AA}$과 $7.014{\AA}$인 육방정계임을 알았다. 이 때 낱알크기는 약 $0.3{\mu}m$이었다. Van der Pauw 방법으로 Hall 효과를 측정하여 운반자 농도와 이동도의 온도의존성을 연구하였다. 이동도는 33 K에서 200 K까지는 압전산란에 의하여, 200K에서 293 K까지는 극성광학산란에 의하여 감소하는 경향을 나타냈다. 광전도 셀의 특성으로 스텍트럼 응답, 감도(${\gamma}$), 최대허용소비전력 및 응답 시간을 측정하였다.

• 센서학회지
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• 제2권1호
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• pp.109-115
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• 1993

승화방법으로 광전도체의 CdS 단결정을 성장하였고 외삽법으로 구한 $a_{o}$와 $c_{o}$의 격자상수 값은 각각 $4.131{\underline{8}}{\AA}$과 $6.712{\underline{2}}{\AA}$임을 알았다. Hall 측정값으로 부터 상온에서의 CdS 단결정의 운반자 농도와 이동도는 각각${\sim}10^{23}m^{-3}$ 과 $2.93{\times}10^{-2}m^{2}$/V sec이였으며 온도에 따른 이동도 변화는 33 K에서 150 K까지는 $T^{1/2}$에 따라 증가하는 경향이 있고 180 K에서 상온까지는 $T^{-2}$에 따라 감소한 경향이 나타났다. 광전류 측정으로부터 나타난 단파장대의 봉우리는 진성전이에 기인하는 봉우리였으며 이 봉우리의 에너지 값은 CdS 광전도체에 에너지 밴드 갭과 동일한 값을 나타냄을 알았다.

• 한국수정란이식학회지
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• 제14권3호
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• pp.203-210
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• 1999

In this stuyd, the effect of the dominant follicle aspiration for the superovulatory response in HanWoo was investigated. The criterion for the presence or absence of a dominant follicle based on their morphological examination. The dominant follicle was aspirated 48hr before the onset of superovulation treatment by 6.5MHz convex probe connected with a carrier and superovulation induced by FSH (Super-Ov Tyrer, Texas, U.S.A) adminstered twic a day s.c. over 4 day in a decreasing regimen. From 13 HanWoo scanned daily to determine the presence and growth of the dominant follicle, its an average diameter of 15.4mm was measured and an average diameter of corpora lutea was 18.7mm on day of follicular aspiration. In the experiment, a follicular remove by ultrasound-guided aspiration, the ovarian response was significantly enhanced when animals were superovulated in the aspiation of a dominant follicle compare with animals superovulated non-aspiration of a dominat follicle. In the aspiration of a dominant follicle donors yieleded more corpora lutea(14.4$\pm$4.7 vs 8.6$\pm$3.4) and transferable embryos(8.9$\pm$4.2 vs 5.4$\pm$2.7) than control. In cows in which the dominant follicle had been aspirated under sonographical control 2 days before superovuation, the number of corpus lutea and transferable embryos were significantly enhanced compared with animals superovulated in the presence of a dominant follicle (14.4$\pm$4.7 vs 6.9$\pm$2.7, ; 8.9$\pm$4.2 vs 3.3$\pm$1.6). After 7 days of artificial insemination, the embryos at 7 days were cllected by uterine flushing after dominant follicle insemination, the embryos at 7 days were collected by uterine flushing after dominant follicle aspiration and superovulation treatment, and evaluated their quality by morphological criteria. Sixteen embryos with excellent and good grade were transferred into 8 recipient cows. Six pregnancies were identified at 60 and 120 days of gestation by rectal palpations. In conclusion, the present study showed that 1) the presence or absence of a dominant follicle signficicnatly affects superovulatory responses, and 2) ultrasound-guided follicular aspiration of the dominant follicle and superovuation treatment provides an accurate and procedure to increase ovarian responses in HanWoo.