• 환경영향평가
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• 제8권1호
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• pp.107-120
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• 1999

This study was performed to survey the general feature of reservoir sediment in Daecheong, Sapkyo and Kumkang reservoir. For investigations, sediments were sampled at four sites in Dae-Cheong and two sites in SapKyo and Kumkang in June and October. The items for investigation are as follows; water content, loss on ignition(IG), porosity of sediment, contents of element such as hydrogen, nitrogen, carbon, phosphorus contents and nutrient release rates. Loss on ignition was measured to determine the contents of organic substance. And its ranges were determined 2.4~16.2% in Daecheong reservoir, 5.6~27.9% in Sapkyo and 4.8~18.7% in Kumkang reservoir. And, total phosphorus contents in sediments were measured $677{\sim}5,238{\mu}g/g$ in Daecheong, $780{\sim}1,417{\mu}g/g$ in Sapkyo and $604{\sim}1,452{\mu}g/g$ in Kumkang reservoir. And release rates of nutrients were calculated $0.05{\sim}8.63mgP/m^2day$ and $4.99{\sim}36.56mgN/m^2day$ in Daecheong, $1.83{\times}10^{-3}{\sim}3.23{\times}10^{-2}mgP/m^2day$ and $1.97{\sim}.22mgN/m^2day$ in Sapkyo, $8.31{\times}10^{-3}{\sim}6.51{\times}10^{-2}mgP/m^2day$ and $0.89{\sim}4.42mgN/m^2day$ in Kumkang reservoir, respectively. And this study attempted to determine the humus level of sediments. As a result of elemental analysis, C/N ratio was determined 3.0~13.1 in Daecheong reservoir, 6.5~13.0 in Sapkyo and 3.6~12.6 in Kumkang reservoir, respectively. From the elemental analysis, humus levels of reservoirs were changed from mesohumic to oligohumic state in all reservoirs.

• 한국수소및신에너지학회논문집
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• 제26권6호
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• pp.659-665
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• 2015

In this study, an experimental investigation is performed for evaluation of a liquid pool spreading model with continuous release. The model considered in this study was developed based on a concept which means that the liquid pool spreading is governed by a balance between an inertia force from gravity and a frictional force from friction with the ground under the whole base of the liquid pool. For evaluation of the model, experimental study is performed. Experimental apparatus is setup for measuring release rate, spreading velocity, and evaporation rate from a liquid pool. The experimental results are compared with results from the model. By applying release and evaporation rates obtained from experiments to solving the model, liquid pool radius variation according to time can be obtained. For evaluation of an effect of friction force in the spreading model, results obtained from the models with and without the friction force are compared with those obtained from the experiments. As a result, it is shown that there exists a large deviation between the results obtained from the model without the friction force and the experimental results. On the other hand, the tendency of liquid pool radius variation according to time is similar between the results obtained from the model without the friction force and the experimental results.

• 해양환경안전학회지
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• 제16권4호
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• pp.361-367
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• 2010

해양구조물 수중부의 해양생물 부착을 방지하는 효과적인 방법으로 방오도료를 사용하고 있다. 트리부틸틴(Tributyltin, TBT) 화합물은 우수한 방오성능을 가져 지금까지 광범위하게 사용해 되어 왔으나, 유해물질 사용금지에 따라 새로운 기술을 적용한 방오도료 개발이 진행되고 있다. 신규 방오도료는 낮은 독성을 가지면서도 우수한 방오성능을 가져야 한다. 본 논문에서는 상용 TBT-free 방오도료 3종(아산화동 함유 자기마모형 도료(Cu SPC AF), 아산화동을 함유하지 않는 자기마모형 도료(Cu-Free SPC AF), Foul-release 실리콘 도료(Foul release AF)의 용출수가 가지는 환경영향성을 조피볼락과 알테미아를 사용하여 평가하였다. 용출수에 대한 급성독성을 조사한 결과 방오도료 용출수의 농도와 생물종의 생존율은 반비례하는 경향을 나타내었으며, 자가마모형 도료가 Foul-release 실리콘 도료보다 상대적으로 높은 급성독성을 가지는 것을 확인할 수 있었다.

• Journal of Pharmaceutical Investigation
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• 제23권2호
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• pp.103-110
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• 1993

Microcapsules(Mc) of cephalexin (CEPH), using Eudragit RS, RL, L, S and polyethylene glycol 1540, were evaluated biopharmaceutically. The area under the curve of CEPH-Eudragit RS/RL Mc administered orally once was larger than that of cephalexin powder twice every 6 hrs. Controlledrelease effectiveness and the absorption rate effectiveness, two important parameters of Vallner's method, of CEPH-Eudragit RS/RL Mc indicate that these Mc can be good sustained-release preparations. And a simple pharmacokinetic model is introduced which allows the gastric emptying and intestinal-transit rates of a drug itself and a solid-state drug contained in Mc. Decreasing $K_r$, without change in $K_a$, showed that the rate-limiting step of absorption moved from absorption step to releasestep.

• Journal of Pharmaceutical Investigation
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• 제25권1호
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• pp.37-46
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• 1995

The experiment was designed to investigate the sustained release dosage form of silymarin (SL) from chitosan (CS) carrier. Solid dispersed system was prepared by mixing the drug with chitosan. This solid dispersed system was cross-linked by glutaraldehyde, formaldehyde, acetaldehyde and butylaldehyde, respectively. The dissolution rates of these preparations were compared with each other in vitro. The silymarin was mired with anionic alginate gel and bead was prepared by dropping this mixture to cationic chitosan solution including calcium chloride. Chitosan encapsulated alginate bead after drying in the oven was investigated for the dissolution rate. The dissolution rate of SL-CS mixture was delayed with increase in the amounts of CS and the concentration of aldehyde. The effect on the delay of dissolution rate was in the increasing order of formaldehyde, glutaraldehyde, acetaldehyde, butylaldehyde. The dissolution rate of chitosan encapsulated alginate bead was parallel with the concentration of chitosan in diluted hydrochloric acid solution and delayed with increase in the concentration of chitosan in phosphate buffer solution.

• 약학회지
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• 제40권6호
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• pp.679-683
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• 1996

The current study evaluates the capacity of eugenol to regulate immediate allergic reaction by control of histamine release. Administrations of eugenol (1M/kg, i.p.) at 60 min b efore and 5, 10 min after the compound 48/80 treatment (8mg/kg, i.p.) were shown the mortality rates as 0, 44.4, and 77.8%, respectively. A 60 min before administered group revealed a significant inhibition of serum histamine release compared with those of 5 and 10 min after the compound 48/80 injection. Eugenol (6-48mM) was also showed a dose-dependent activity on the compound 48/80-induced histamine release from the highly purified population of Alcian Blue-positive peritonea] mast cells. These results indicate that in vitro treatment with exogenous eugenol inhibited the active response of mast cell populations and modulated its characteristics.

• 한국정밀공학회지
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• 제27권10호
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• pp.69-76
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• 2010

This study examined how the fracture toughness is affected according to the variation of the initial crack length and the fiber arranged angle using FEA method and experimental method. Therefore, the energy release rates were calculated and compared by J-integral method and VCCT(Virtual Crack Closure Technique). The results of fracture toughness test verified these results. At this time, the locus method was used in order to determine the energy release rate. When the results of FEA were compared with those of experiment, all of those decreased with the increase of angle between load and the fiber arranged direction. The decrease was due to reducing maximum load and stiffness, and the reason of reduction has been judged that the inplane shear stress.

• Journal of Pharmaceutical Investigation
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• 제28권4호
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• pp.249-255
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• 1998

Solid Lipid Nanoparticle(SLN), one of the colloidal carrier systems, has many advantages such as good biocompatibility, low toxicity and stability. In this paper, the effects of drug lipophilicity and surfactant on the drug loading capacity, particle size and drug release profile were examined. SLNs were prepared by homogenization of melted lipid dispersed in an aqueous surfactant solution. Ketoprofen, ibuprofen and pranoprofen were used as model drugs and tweens and poloxamers were tested for the effect of surfactant. Mean particle size of prepared SLNs was ranged from 100 to 150nm. The drug loading capacity was improved with the most lipophilic drug and low concentration of surfactant. Particle size and polydispersity of SLNs were changed according to the used lipid and surfactant. The rates of drug release were controlled by the loading drug and surfactant concentration. SLN system with effective drug loading efficiency and proper particle size for the intravenous or oral formulation can be prepared by selecting optimum drug and surfactant.

• 한국운동역학회지
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• 제23권1호
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• pp.1-9
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• 2013

The purpose of this study was to provide information on athletes' characteristics and advantages and disadvantages by analyzing the kinematic factors having a decisive influence on competitive abilities such as release conditions in the delivery phase on major Korean javelin athletes. Two supported javelin throwers of the Korean national team participated in this study. The total average time required of the delivery phase was 0.31(${\pm}0.016$). The athletes' release angle was 33.2 to 41.7 degrees. The attack angle varied widely from -3.5 to 5.9 degrees. The Javelin heights of Subject A and B were 95.9 and 89.2%Ht. The average stride length were 180.6 and 176.7cm. The center of mass velocity of LFD and REL was relatively low in all the subjects. The average deceleration rates of center of mass velocity of Subject A and B were 57.2 and 48.9%lose. The left knee angles of Subject A and B were 160.1 and 155.5 degrees in LFD, 153.0 and 164.0 degrees in REL. The joint velocity of upper limb segments was relatively low in all the subjects. The maximum average wrist velocity of Subject A and B was 18.2 and 16.3 m/s in REL.

• 한국임상약학회지
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• 제8권2호
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• pp.143-146
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• 1998

Acetaminophen (APAP) suppositories with active ingredients, i.e., polyethylene glycol (PEG), Witepsol H-15 (WH), were prepared for hospital use and investigated on their drug release characteristics and pharmacokinetics. WH was employed as oil-soluble base with an aim of reducing fragility and mucosa irritancy that are common drawbacks found in PEG suppositories. Also hollow type suppository was tried as compared with conventional type suppository. Drug release tests revealed that in most formulations, more than $80\%$ of loaded APAP were released within 20 minutes, except for APAP-WH hollow type suppositories. Significant differences in the plasma concentration profile were observed among four type suppositories. $T_{max}$ of APAP-PEG and APAP-WH suppositories were 90 and 60 minutes, respectively, in hollow types. APAP-WH hollow type suppositories demonstrated fast absorption rates of APAP as compared with those of APAP-PEG suppositories. No burst effect was observed from APAP-WH suppository in contrast to APAP conventional type suppository, whereas AUCs of all the suppositories were similar. APAP-WH hollow type suppository may be an useful dosage form for hospital use.