• The Journal of Advanced Prosthodontics
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• 제7권6호
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• pp.454-459
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• 2015

PURPOSE. To determine whether the fracture strengths and failure types differed between metal and zirconia frameworks veneered with pressable or layering ceramics. MATERIALS AND METHODS. A phantom molar tooth was prepared and duplicated in 40 cobalt-chromium abutments. Twenty metal (IPS d.SIGN 15, Ivoclar, Vivadent, Schaan, Liechtenstein) and 20 zirconia (IPS e.max ZirCAD, Ivoclar) frameworks were fabricated on the abutments. Each framework group was randomly divided into 2 subgroups according to the veneering material: pressable and layering ceramics (n=10). Forty molar crowns were fabricated, cemented onto the corresponding abutments and then thermocycled ($5-55^{\circ}C$, 10,000 cycles). A load was applied in a universal testing machine until a fracture occurred on the crowns. In addition, failure types were examined using a stereomicroscope. Fracture load data were analyzed using one-way ANOVA and Tukey HSD post-hoc tests at a significance level of 0.05. RESULTS. The highest strength value was seen in metal-pressable (MP) group, whereas zirconia-pressable (ZP) group exhibited the lowest one. Moreover, group MP showed significantly higher fracture loads than group ZP (P=.015) and zirconia-layering (ZL) (P=.038) group. No significant difference in fracture strength was detected between groups MP and ML, and groups ZP and ZL (P>.05). Predominant fracture types were cohesive for metal groups and adhesive for zirconia groups. CONCLUSION. Fracture strength of a restoration with a metal or a zirconia framework was independent of the veneering techniques. However, the pressing technique over metal frameworks resisted significantly higher fracture loads than zirconia frameworks.

• 한국식품저장유통학회지
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• 제21권3호
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• pp.427-433
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• 2014

생강나무 줄기와 초피 과피의 60% ethanol과 열수 추출물의 식중독 균에 대한 항균 활성과 추출물의 열안정성에 대하여 알아보았다. 100 mg/mL의 농도에서 생강나무 줄기의 60% ethanol 추출물은 MRSA에 대하여 31.50 mm, 열수추출물은 S. aureus에 대해 25.5 mm의 생육 저해환을 보이며 가장 높은 항균활성을 보였으며, B. cereus에 대해서는 가장 낮은 항균활성을 보였다. 같은 농도에서 초피 과피의 60% ethanol 추출물의 항균효과는 S. aurues와 B. cereus에 대해 25 mm의 생육 저해환을 나타냈으며, 열수추출물은 S. aurues 에 대해 22 mm의 생육저해환을 나타내 항균 효과가 가장 크게 나타났으며, E. coli 에 대해서는 낮은 항균활성을 나타내었다. 생강나무 줄기와 초피 과피의 60% ethanol, 열수 추출물 모두 농도가 낮아짐에 따라 생육 저해환의 크기가 작아지는 현상을 보였으며, ethanol추출물이 열수 추출물에 비해 다소 높은 항균력을 나타냈다. 또 추출물의 열안정성 실험에서 열처리군과 비열처리군(대조구)을 비교했을 때 항균 효과가 감소하지 않는 것으로 보아 생강나무 줄기와 초피 과피 추출물은 열에 안정하다고 판단된다. 본 연구 결과 생강나무 줄기와 초피 과피 추출물에 미생물 부패 방지에 효과적인 항균 물질이 함유되어 있으며 비교적 열에 안정하므로 천연보존료로서 산업적 응용이 가능할 것이라 사료된다.

• 한국농공학회지
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• 제20권1호
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• pp.4592-4598
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• 1978

The purpose of this research is to find out mathemetically an economical intake water depth in the design of head works through the derivation of some formulas. For the performance of the purpose the following formulas were found out for the design intake water depth in each flow type of intake sluice, such as overflow type and orifice type. (1) The conditional equations of !he economical intake water depth in .case that weir body is placed on permeable soil layer ; (a) in the overflow type of intake sluice, {{{{ { zp}_{1 } { Lh}_{1 }+ { 1} over {2 } { Cp}_{3 }L(0.67 SQRT { q} -0.61) { ( { d}_{0 }+ { h}_{1 }+ { h}_{0 } )}^{- { 1} over {2 } }- { { { 3Q}_{1 } { p}_{5 } { h}_{1 } }^{- { 5} over {2 } } } over { { 2m}_{1 }(1-s) SQRT { 2gs} }+[ LEFT { b+ { 4C TIMES { 0.61}^{2 } } over {3(r-1) }+z( { d}_{0 }+ { h}_{0 } ) RIGHT } { p}_{1 }L+(1+ SQRT { 1+ { z}^{2 } } ) { p}_{2 }L+ { dcp}_{3 }L+ { nkp}_{5 }+( { 2z}_{0 }+m )(1-s) { L}_{d } { p}_{7 } ] =0}}}} (b) in the orifice type of intake sluice, {{{{ { zp}_{1 } { Lh}_{1 }+ { 1} over {2 } C { p}_{3 }L(0.67 SQRT { q} -0.61)}}}} {{{{ { ({d }_{0 }+ { h}_{1 }+ { h}_{0 } )}^{ - { 1} over {2 } }- { { 3Q}_{1 } { p}_{ 6} { { h}_{1 } }^{- { 5} over {2 } } } over { { 2m}_{ 2}m' SQRT { 2gs} }+[ LEFT { b+ { 4C TIMES { 0.61}^{2 } } over {3(r-1) }+z( { d}_{0 }+ { h}_{0 } ) RIGHT } { p}_{1 }L }}}} {{{{+(1+ SQRT { 1+ { z}^{2 } } ) { p}_{2 } L+dC { p}_{4 }L+(2 { z}_{0 }+m )(1-s) { L}_{d } { p}_{7 }]=0 }}}} where, z=outer slope of weir body (value of cotangent), h1=intake water depth (m), L=total length of weir (m), C=Bligh's creep ratio, q=flood discharge overflowing weir crest per unit length of weir (m3/sec/m), d0=average height to intake sill elevation in weir (m), h0=freeboard of weir (m), Q1=design irrigation requirements (m3/sec), m1=coefficient of head loss (0.9∼0.95) s=(h1-h2)/h1, h2=flow water depth outside intake sluice gate (m), b=width of weir crest (m), r=specific weight of weir materials, d=depth of cutting along seepage length under the weir (m), n=number of side contraction, k=coefficient of side contraction loss (0.02∼0.04), m2=coefficient of discharge (0.7∼0.9) m'=h0/h1, h0=open height of gate (m), p1 and p4=unit price of weir body and of excavation of weir site, respectively (won/㎥), p2 and p3=unit price of construction form and of revetment for protection of downstream riverbed, respectively (won/㎡), p5 and p6=average cost per unit width of intake sluice including cost of intake canal having the same one as width of the sluice in case of overflow type and orifice type respectively (won/m), zo : inner slope of section area in intake canal from its beginning point to its changing point to ordinary flow section, m: coefficient concerning the mean width of intak canal site,a : freeboard of intake canal. (2) The conditional equations of the economical intake water depth in case that weir body is built on the foundation of rock bed ; (a) in the overflow type of intake sluice, {{{{ { zp}_{1 } { Lh}_{1 }- { { { 3Q}_{1 } { p}_{5 } { h}_{1 } }^{- {5 } over {2 } } } over { { 2m}_{1 }(1-s) SQRT { 2gs} }+[ LEFT { b+z( { d}_{0 }+ { h}_{0 } )RIGHT } { p}_{1 }L+(1+ SQRT { 1+ { z}^{2 } } ) { p}_{2 }L+ { nkp}_{5 }}}}} {{{{+( { 2z}_{0 }+m )(1-s) { L}_{d } { p}_{7 } ]=0 }}}} (b) in the orifice type of intake sluice, {{{{ { zp}_{1 } { Lh}_{1 }- { { { 3Q}_{1 } { p}_{6 } { h}_{1 } }^{- {5 } over {2 } } } over { { 2m}_{2 }m' SQRT { 2gs} }+[ LEFT { b+z( { d}_{0 }+ { h}_{0 } )RIGHT } { p}_{1 }L+(1+ SQRT { 1+ { z}^{2 } } ) { p}_{2 }L}}}} {{{{+( { 2z}_{0 }+m )(1-s) { L}_{d } { p}_{7 } ]=0}}}} The construction cost of weir cut-off and revetment on outside slope of leeve, and the damages suffered from inundation in upstream area were not included in the process of deriving the above conditional equations, but it is true that magnitude of intake water depth influences somewhat on the cost and damages. Therefore, in applying the above equations the fact that should not be over looked is that the design value of intake water depth to be adopted should not be more largely determined than the value of h1 satisfying the above formulas.

• 한국가축번식학회지
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• 제16권4호
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• pp.289-299
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• 1993

돼지 난포내의 각 구성분들에 대해 10% SDS-PAGE와 IEF를 이용한 이차원 전기영동을 실시하여 세포 및 난포액 구성분의 구조단백질상을 분석하였다. 난자-난구세포 복합체를 호르몬과 15%의 FCS가 포함된 M16 배양액으로 39$^{\circ}C$, 5% CO2 상태에서 35시간 동안 체외배양하였다. 배양 전후의 난자, 투명대 및 난구세포와 난포 크기별로 회수된 난포액들을 각각 분리 회수하여 구조단백질상을 분석하였으며, Silver 염색과 CBB 염색으로 분석이 가능한 각 구성분의 적정 시료량을 조사하였다. 한편 난포 구성분들에 있어서 난자는 분자량이 25와 114kd, 난구세포는 20, 33, 58, 78 및 112kd, 투명대는 65kd, 그리고 난포액은 18, 76, 92, 152 및 187kd 단백질을 세포특이단백질로 가지고 있음이 확인되었다. 특히 난자의 경우 성숙에 따라 구조단백질상의 변화가 확인된 반면, 난구세포에서는 차이가 없었다. 또한 난포액은 난포의 크기에 따라서는 단백질상의 차이가 없었으나 호르몬 처리 여부에 따라서는 이차원 전기영동상에서 몇가지 단백질에서 차이가 확인되었고, 난포세포들도 폐쇄 여부에 따라 단백질 조성에 차이를 보였다. 따라서 본 실험에서는 전기영동에 필요한 시료의 양과 준비 방법을 확립하여 각 난포 구성분들의 단백질상 분석에 대한 기초자료를 확립하였으며, 이상의 결과는 앞으로 진행될 단백질의 생합성 분석이나 면역화학학적 분석에 유용하게 이용될 수 있을 것이다.

• 대한환경공학회지
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• 제27권12호
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• pp.1327-1331
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• 2005

본 연구에서는 해안연약지반의 현장토(준설점토)를 차수층에 이용하기 위해 첨가되는 고화재에 의한 수화열을 저감하기 위한 방안을 모색하고자 산업부산물로 년간 다량 배출되는 고로슬래그를 이용하였다. 실험결과, 고로슬래그를 첨가한 준설혼합토(준설점토 95% w+시멘트 5% w)의 경우 고화재에 의한 초기수화반응열을 저감하는 것으로 나타났는데 이는 불투수성인 aluminosilicate 피막이 고로슬래그의 표면을 코팅하였기 때문으로 판단된다. 따라서 고화재의 수화반응에 따른 수화열에 의해 발생될 수 있는 매립지 차수층의 미세균열을 산업부산물인 고로슬래그가 저감해 줄 수 있을 것으로 판단된다.

• Clinical and Experimental Reproductive Medicine
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• 제27권4호
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• pp.345-351
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• 2000

Objective: Hatching of the blastocyst from the zona pellucida (ZP) is a key event in mammalian implantation. In vivo, two factors have been identified as possible mediators of hatching: lysis of the ZP by substances elaborated either from the embryo or female reproductive tract and pressure exerted on the zona by expansion of the blastocyst. Two methods of zona manipulation were already in use to enhance the ability of embryos to hatch: mechanical PZD and chemical ZD by acidic Tyrode's solution. But several controversies of each method have been reported. The purpose of this study was to investigate the effect of pronase for mouse embryo hatching. Methods: Mouse embryos were obtained following ovulation induction of $F_1$ animals. Fresh and cryo-thawed morula embryos were exposed to 0.5, 1.0, 2.0, 5.0 ${\mu}g/ml$ pronase in Ham's F10 for 72 hrs. Main outcome measures were the rates of partial hatching and completely hatched blastocysts, and cell number of it. Results: In fresh and cryo-thawed group, the rates of completely hatched blastocyst were significantly higher in 5 ${\mu}g/ml$ pronase treatment group than control group. There was no difference in completely hatched blastocyst total cell number between pronase treatment group and control group. This suggest that pronase treatment did not harmful in mouse embryo development. In pronase treatment group, zona pellucida were thinner than control group. Conclusion: The addition of pronase to culture media may accelerate the hatching of embryo. So, enzymatic treatment of the zona may provide a valuable and effective assisted hatching technique for human in-vitro fertilization-embryo transfer.

• Clinical and Experimental Reproductive Medicine
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• 제28권2호
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• pp.147-153
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• 2001

Objective: The present study was performed to investigate the efficiency of partial laser assisted hatching (p-LAH; lased 1/2 ZP width from ZP edge) on hatching of mouse blastocysts. Methods: We used non-contact $1.48{\mu}m$ diode laser (MTM, Switzland) to create a precise hole on zona pellucida. 2-cell embryos were collected from the mouse (ICR) oviduct at 48 hours after hCG administration. Collected 2-cell embryos were cultured in the P-1 medium supplemented with 0.4% BSA. For experiments, embryos at 8-cell stage were used after $20{\sim}22$ hours in culture. After conventional (c-LAH) or partial laser assisted hatching, the embryos were further cultured in P-1 medium supplemented with 0.4% BSA for 3 days. To compare efficiency of complete and partial laser assisted hatching, hatching rate, hatching time and blastocyst diameter and zona pellucida thickness at hatching time were investigated. Embryos were examined every 12 hours. Blastocyst diameter and zona pellucida thickness at hatching time were measured with an ocular micrometer. Results: Hatching rates of p-LAH group (84.2%) was significantly higher than that of control group (39.3%), but there was no difference between the p-LAH (84.2%) and c-LAH (91.2%). p-LAH group was hatched 12 hours earlier than control group, but hatched 12 hours later than c-LAH group. The diameter of blastocyst at hatching time of p-LAH group ($113.1{\pm}6.4{\mu}m$) was smaller than that of control group ($122.2{\pm}5.0{\mu}m$), but larger than that of c-LAH group ($102.2{\pm}2.7{\mu}m$). Zona pellucida thickness at hatching time of p-LAH group ($6.4{\pm}0.9{\mu}m$) was thicker than that of control group ($4.5{\pm}1.5{\mu}m$), but thinner than that of c-LAH group ($10.0{\pm}0.8{\mu}m$). Conclusion: These results suggest that p-LAH may maintains the cell arrangement of early embryos to ensure successful development and prevent precocious hatching of blastocyst when compare to c-LAH and conventional (acidic tyrode) AH. Thus, p-LAH may provide a valuable and effective AH technique for human ART program.

• 한국식품영양과학회지
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• 제42권5호
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• pp.663-669
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• 2013

인삼과 마찬가지로 많은 사포닌을 함유하고 있는 인삼꽃의 이용 가치를 증진시키기 위한 연구의 일환으로 Bacillus subtilis(BS), Lactobacillus plantarum(LP), Lactobacillus casei(LC), Candida utilis(CU), Saccharomyces cerevisiae strain CHY1011(Y1), Saccharomyces cerevisiae strain ZP 541(Y2), 혼합발효(M) 등의 여러 유용 미생물을 이용하여 인삼꽃을 발효시킨 후 미생물별 인삼꽃 발효물에 대한 항산화 활성 변화를 탐색하였다. 총 페놀함량 측정 결과 무발효 추출물은 인삼꽃 발효물에 비해 유의적(p<0.05)으로 높은 값을 보였으며, 발효 균주 중에서는 BS로 발효한 발효물이 가장 높은 값을 나타내었다. DPPH radical 소거활성 및 ABTS radical 소거활성 측정 결과 BS 발효물이 유의적으로 가장 높은 활성을 나타내었으나, FRAP value(10 mg/mL)는 무발효 추출물의 활성이 가장 높게 나왔으며 BS 발효물과는 유의차를 보이지 않았다. 환원력 측정 결과, 대체적으로 무발효 추출물에 비해 미생물 발효물에서 높은 활성을 나타내었으며 LC 발효물이 높은 활성을 나타내었다. 따라서 여러 유용미생물을 이용한 인삼꽃 발효의 경우 Bacillus subtilis를 이용하여 발효할 경우 다른 균주들을 이용하는 것보다 항산화 활성 증진에 우수한 효과를 나타낼 것으로 사료되며 다른 생리활성 증진 효과에 대한 연구가 좀 더 진행되어져야 할 것이다.

• Clinical and Experimental Reproductive Medicine
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• 제25권2호
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• pp.123-128
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• 1998

Implantation rates remain low following human in vitro fertilization (IVF). Suboptimal culture conditions may limit the ability of embryos to hatch as blastocysts, and artificial opening of the zona pellucida has been proposed as a means to promote subsequent hatching (assisted hatching). In this study, assisted hatching (AH) by zona drilling using acidic Tyrode's solution was performed in 320 patients, due to their age of more than 38 years (group A), the thick zona pellucida (group Z; $ZP\geq0.18{\mu}m$), and failures in implantation more than 3 times in previous IVF-ET trial (group P). This study was designed firstly, to study the effects of AH on the outcomes of IVF-ET according to the indications and secondly, to verify the appropriate application of AH. The results were as follows; 1. There was no difference in pregnancy rate between AH group (26.6%) and non-AH group (26.5%). 2. Assisted hatching (AH) showed significantly higher pregnancy rate of the patients with thick zona pellucid a than those of the patients with age factor and with the history of repeated implantation failure. But in the patients with age factor only, AH resulted in higher pregnancy rate. 3. Interestingly, the patients with complex factors including zona factor (Z: 33.9%; ZA: 30.4%; ZP: 31.6%; ZAP: 21.4%) showed higher pregnancy rates than other complex factors excluding zona factor (A: 24.4%, P: 0%; AP: 10.8%). From these results, AH is more helpful to the patients with thick zona pellucida rather than patients with older age and/or previous repeated implantation failure.

• Clinical and Experimental Reproductive Medicine
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• 제43권1호
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• pp.9-14
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• 2016

Objective: Autophagy contributes to the clearance and recycling of macromolecules and organelles in response to stress. We previously reported that vitrified mouse oocytes show acute increases in autophagy during warming. Herein, we investigate the potential role of Atg7 in oocyte vitrification by using an oocyte-specific deletion model of the Atg7 gene, a crucial upstream gene in the autophagic pathway. Methods: Oocyte-specific Atg7 deficient mice were generated by crossing Atg7 floxed mice and Zp3-Cre transgenic mice. The oocytes were vitrified-warmed and then subjected to in vitro fertilization and development. The rates of survival, fertilization, and development were assessed in the Atg7 deficient oocytes in comparison with the wildtype oocytes. Light chain 3 (LC3) immunofluorescence staining was performed to determine whether this method effectively evaluates the autophagy status of oocytes. Results: The survival rate of vitrified-warmed $Atg7^{f/f}$;Zp3-Cre ($Atg7^{d/d}$) metaphase II (MII) oocytes was not significantly different from that of the wildtype ($Atg7^{f/f}$) oocytes. Fertilization and development in the $Atg7^{d/d}$ oocytes were significantly lower than the $Atg7^{f/f}$ oocytes, comparable to the $Atg5^{d/d}$ oocytes previously described. Notably, the developmental rate improved slightly in vitrified-warmed $Atg7^{d/d}$ MII oocytes when compared to fresh $Atg7^{d/d}$ oocytes. LC3 immunofluorescence staining showed that this method can be reliably used to assess autophagic activation in oocytes. Conclusion: We confirmed that the LC3-positive signal is nearly absent in $Atg7^{d/d}$ oocytes. While autophagy is induced during the warming process after vitrification of MII oocytes, the Atg7 gene is not essential for survival of vitrified-warmed oocytes. Thus, induction of autophagy during warming of vitrified MII oocytes seems to be a natural response to manage cold or other cellular stresses.