• 한국식품영양과학회지
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• 제24권5호
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• pp.811-815
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• 1995

BSA, egg albumin (EA), 그리고 분리대두단백질(SPI)의 Neutrase에 의한 탈아미드화가 용해도에 미치는 영향을 조사하여 보았다. BSA는 탈아미드화로 pH 4~8 사이의 물에 대한 용해도가 천연 BSA에 비하여 98~83%로 감소하였으며, pH 6 부근에서 가장 낮은 용해도를 보았다. 천연 BSA와 탈아미드화된 BSA 모두 0.2M NaCl 용액에서는 100%의 용해도를 보였으나, 산성 1.0M NaCl용액에서는 용해도가 모두 크게 떨어졌다. EA의 용해도는 탈아미드화로 pH3 이하와 6 이상의 수용액에서는 증가하였으나, 산성 NaCl용액에서는 크게 감소하였다. SPI는 탈아미드화로 수용액에서의 용해도가 모든 pH 범위에서 크게 증가하였으나, NaCl용액에 대한 용해도는 pH 6 이상에서는 증가하였고, pH 5 이하에서는 변화가 없었다.

• 한국식품과학회지
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• 제22권3호
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• pp.343-349
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• 1990

pH를 달리한 수용액 및 농도를 달리한 염류수용액에서 들깨종실의 단백질과 phytate의 용해도를 측정하여 단백질로부터 phytate를 제거할 수 있는 조건을 검토하였다. 들깨종실단백질의 용해도는 pH4.0에서 가장 낮은 9.5%로 등전점을 보였고, 그보다 산성 또는 알칼리성쪽으로 갈수록 증가되었다. 반면에 phytate의 용해도는 pH5.0에서 가장 높았으며 그보다 산성 또는 알칼리성쪽으로 갈수록 감소되었다. NaCl 수용액을 처리하였을 때 단백질의 용해도는 pH $3.0{\sim}4.0$ 범위에서 가장 낮았고 pH 6.0 이상에서는 현저히 증가되었다. Phytate의 용해도는 pH$2.0{\sim}5.0$ 범위에서는 약 90%내외로 높았으나 pH6.0 이상에서는 급격히 감소되었다. $Na_2SO_3$ 수용액처리에서는 단백질 용해도가 $pH2.0{\sim}3.0$ 범위에서 가장 낮았고 phytate의 용해도는 $pH5.0{\sim}6.0$에서 최대치를 보였고, 3%의 경우는 전 pH 구간에 걸쳐서 낮았으나 5%와 7%에서는 전 구간에서 높았다. $CaCl_2$ 수용액처리에서는 단백질 용해도가 3% 수용액에서는 전 pH 구간에서 낮았으나 5%와 7%에서는 $pH5.0{\sim}10.0$에서 높은 값을 보였으며 phytate의 용해도는 $pH2.0{\sim}3.0$ 사이에서 최대값을 나타내고 pH4.0이상에서는 급격히 감소하였다. 이상의 결과에서 3% NaCl 용액을 사용하여 pH9.0에서 단백질을 추출하고 pH4.0에서 침전시켰을 때 단백질 수율이 좋고 phytate 잔존량이 가장 적어, 저(低)phytate 분리단백질을 만드는 가장 좋은 조건이었다..

• Asian-Australasian Journal of Animal Sciences
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• 제29권11호
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• pp.1608-1615
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• 2016

This study was conducted to determine the solubility of copper (Cu) in two sources of copper(II) sulfate ($CuSO_4$) including monohydrate and pentahydrate and three sources of dicopper chloride trihydroxide (dCCTH) including ${\alpha}$-form (dCCTH-${\alpha}$), ${\beta}$-form (dCCTH-${\beta}$), and a mixture of ${\alpha}$- and ${\beta}$-form (dCCTH-${\alpha}{\beta}$) at different pH and a 3-step in vitro digestion assay for pigs. In Exp. 1, Cu sources were incubated in water-based buffers at pH 2.0, 3.0, 4.8, and 6.8 for 4 h using a shaking incubator at $39^{\circ}C$. The $CuSO_4$ sources were completely dissolved within 15 min except at pH 6.8. The solubility of Cu in dCCTH-${\alpha}$ was greater (p<0.05) than dCCTH-${\beta}$ but was not different from dCCTH-${\alpha}{\beta}$ during 3-h incubation at pH 2.0 and during 2-h incubation at pH 3.0. At pH 4.8, there were no significant differences in solubility of Cu in dCCTH sources. Copper in dCCTH sources were non-soluble at pH 6.8. In Exp. 2, the solubility of Cu was determined during the 3-step in vitro digestion assay for pigs. All sources of Cu were completely dissolved in step 1 which simulated digestion in the stomach. In Exp. 3, the solubility of Cu in experimental diets including a control diet and diets containing 250 mg/kg of additional Cu from five Cu sources was determined during the in vitro digestion assay. The solubility of Cu in diets containing additional Cu sources were greater (p<0.05) than the control diet in step 1. In conclusion, the solubility of Cu was influenced by pH of digesta but was not different among sources based on the in vitro digestion assay.

• Restorative Dentistry and Endodontics
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• 제15권1호
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• pp.88-96
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• 1990

The purpose of this study was to investigate the fluoride release and solubility of glass ionomer cement associated with three pH media. For this study, GC Fuji II discs (20.0mm in diameter ${\times}$ 1.5mm thick) were immersed in pH 4.0 lactic acid, pH 7.0 distilled water and pH 10.0 KOH solutions for 1, 7, 14 and 28 days. The amount of fluoride release from the cement into three pH media were measured by fluoride specific ion electrode and the solubility was measured by weight loss of discs. The results were as follows: 1. The lower was the pH of media, the more was the amount of release of fluoride. 2. The amount of fluoride release was increased with time lapse. 3. After I day, the solubility was the highest, and after 7 days that was the least. 4. The lower was the pH of media, the more was the solubility, but there was no statistical difference in solubility according to the pH change.

• Applied Biological Chemistry
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• 제29권2호
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• pp.212-218
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• 1986

pH를 달리한 수용액 및 농도를 달리한 염류수용액에서 평지 종실의 단백질과 phytate의 용해도를 측정하여 단백질로부터 phytate를 제거할 수 있는 조건을 검토하였다. 1. 평지종실의 단백질과 phytate의 용해도에 미치는 pH의 영향을 측정한 결과 단백질의 용해도는 pH 5.0에저 가장 은 20.9%로 등전점을 보였고, 그 보다 산성 또는 알칼리 쪽으로 갈수록 그 용해도가 증가되어 pH 11.5에서 94.%로 가장 높았다. Phytate의 용해도는 pH 6.0에서 가장 높았으며 (61.0%) 알칼리 쪽에서 더 급격히 감소되어 pH 11.5에서는 그 용해도가 1.3%였다. 2. 단백질과 phytate의 용해도에 미치는 염류의 영향을 보면 NaCl 수용액을 처리하였을 때 단백질의 용해도는 $pH\;6.0{\sim}8.0$ 이상에서 높은 값을 보였고, 염의 농도별 차이는 크지 않았다. Phytate의 용해도는 pH 6.0이하에서는 높았으나 그 이상의 pH에서는 급격히 감소되어 pH 8.0 이상에서 6.0% 이하로 떨어졌다. $CaCl_2$ 수용액 처리에서는 단백질 용해도가 $pH\;6.0{\sim}8.0$ 부근에서 최대치를 보이나 전 pH구간에서 큰 변화를 보이지 않았다. Phytate의 용해도는 $pH\;3.0{\sim}4.0$ 부근에서 최대치를 보이고 그 이상의 pH에서는 급격히 감소되어 $pH\;5.0{\sim}6.0$에서 7% 이하로 떨어졌다. 그리고 염의 농도가 높을수록 더 낮은 pH에서부터 감소를 보였다. $Na_2SO_3$ 처리에서 단백질의 용해도는 pH가 높아짐에 따라 계속 증가되어 pH 11.5에서 84% 이상이었고 phytate의 용해도는 $pH\;5.0{\sim}8.0$의 부근에서 최대치를 보이며 농도가 높을수록 더 높은 pH에서 최대치가 나타났다. 염의 농도에 따라 알칼리 쪽에서의 감소 양상이 달라졌다. 3. 저(低) $Ca^{2+}$이온 처리에서 phytate의 용해도는 pH 7.0 이상에서 $Ca^{2+}$이온의 농도별로 별차이 없이 낮았고 농도가 증가됨에 따라서 더 낮은 pH에서 최대치를 보였다. 단백질의 용해도는 pH 11.5에서 보면 $1mM\;Ca^{2+}$이온 농도에서 가장 높게 나타났다. 이상의 결과에서 증류수 또는 $1mM\;Ca^{2+}$수용액을 용매로 하여 pH 11.5에서 단백질을 추출하고 pH 5.0에서 침전시킬 때 평지종실단백질로부터 Phytate를 제거하는 효과가 가장 좋다는 것을 알 수 있다.

• 한국식품조리과학회지
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• 제9권4호
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• pp.278-283
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• 1993

This study was attempted to investigate the effects of enzymatic modification of milk protein with protease on functional properties. The selected functional properties were solubility, emulsifying activity (EA), emulsion stability(ES), foam expansion(FE), and foam stability(FS). These properties were measu-red from pH 3.0 to pH 8.0. The proteases used in this study were iaolated from Meju(fermemted soybean) and had specific activity of 250 units/㎎ protein at pH 7.0, 1600 units of pretense was used for 1gr. of skim milk protein. Skim milk showed 30.5％ degree of hydrolysis for 1 hr. and 36.4% degree of hydrolysis for 3.5 hrs. of protease treatment at pH 7.0. Solubility of native skim milk, control, 1 hr. and 3.5 hrs. groups were 3.37, 3.64, 10.21, 14.34％o at pH 4.0 respcetively. The emulsifying activity of native skim milk, control, 1 hr. and 3.5 hrs. groups were 38.8,42.0,43.0,46.7ft at pH 4.0, respectively. Enzymatic modification resulted in the increase of solubility and emulsifying activity at pH 4.0. However at pH 5.0 emulsifying activity of 1 hr. and 3.5 hr. group were lower than native skim milk and control groups. 1 hr. protease treatment was found to be most effective way of increasing foam expansion at pH 4.0 to 6.0. It was supported that, protease treated skim milk can be used to improve solubility, emulsifying activity, foam expansion at acid pH. meju protease. skim milk, solubility, emulsion, foam.

• 한국식품조리과학회지
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• 제6권3호통권12호
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• pp.9-15
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• 1990

Peanut prptein isolate was tested for the purpose of finding out the effect of pH, Sodium Chloride concentration and heat treatment on the solubility, surface hydrophobicity, foam expansion and foam stability. The solubility of peanut protein isolate was affected by pH and showed the lowest value at pH 4.5. When the peanut protein isolate was heated, the solubility decreased at pH 3 and pH 7 but at pH 9 solubility increased. At all pH range, solubility decreased as NaCl was added. The surface hydrophobicity of peanut protein isolate showed the highest value at pH 1.5. Generally, at acidic pH range the surface hydrophobicity was high, but at alkaline region, the surface hydrophobicity increased as the temperature increased. And when NaCl was added, the surface hydrophobicity was also increased. Foam expansion of peanut protein isolate was no significant difference among the values about pH. When the peanut protein was heated and NaCl was added, foam expansion was increased at pH 7. Foam stability was significantly low at pH 4.5 and foam stability was increased at acidic pH region below pH 4.5. At pH 7 and pH 9, heat treatment above $60^{\circ}C$ increased foam stability. When NaCl was added, foam stability was significantly increased at pH 3 and pH 7.

• 한국식품조리과학회지
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• 제9권1호
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• pp.43-51
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• 1993

Buckwheat protein isolate was tested for the effects of pH, addition of sodium chloride and heat treatment on solubility, emulsion capacities, emulsion stability, surface hydrophobicity, foam capacities and foam stability. The solubility of buckwheat protein isolate was affected by pH and showed the lowest value at pH 4.5, the isoelectric point of buckwheat protein isolate. The solubility significantly as the pH value reached closer to either ends of the pH, i.e., pH 1.0 and 11.0. The effects of NaCl concentration on solubility were as follows; at pH 2.0, the solubility significantly decreased when NaCl was added; at pH 4.5, it increased above 0.6 M; at pH 7.0 it increased; and at pH 9.0 it decreased. The solubility increased above $80^{\circ}C$, at all pH ranges. The emulsion capacity was the lowest at pH 4.5. It significantly increased as the pH approached higher acidic or alkalic regions. At pH 2.0, when NaCl was added, the emulsion capacity decreased, but it increased at pH 4.5 and showed the maximum value at pH 7.0 and 9.0 with 0.6 M and 0.8 M NaCl concentrations. Upon heating, the emulsion capacity decreased at acidic pH's but was maximised at pH 7.0 and 9.0 on $60^{\circ}C$ heat treatment. The emulsion stability was the lowest at pH 4.5 but increased with heat treatment. At acidic pH, the emulsion stability increased with the increase in NaCl concentration but decreased at pH 7.0 and 9.0. Generally, at other pH ranges, the emulsion stability was decreased with increased heating temperature. The surface hydrophobicity showed the highest value at pH 2.0 and the lowest value at pH 11.0. As NaCl concentrationed, the surface hydrophobicity decreased at acidic pH. The NaCl concentration had no significant effects on surface hydrophobicity at pH 7.0, 9.0 except for the highest value observed at 0.8 M and 0.4 M. At all pH ranges, the surface hydrophobicity was increased, when the temperature increased. The foam capacity decreased, with increased in pH value. At acidic pH, the foam capacity was decreased with the increased in NaCl concentration. The highest value was observed upon adding 0.2 M or 0.4 M NaCl at pH 7.0 and 9.0. Heat treatments of $60^{\circ}C$ and $40^{\circ}C$ showed the highest foam capacity values at pH 2.0 and 4.5, respectively. At pH 7.0 and 9.0, the foam capacity decreased with the increased in temperature. The foam stability was not significantly related to different pH values. The addition of 0.4 M NaCl at pH 2.0, 7.0 and 9.0 showed the highest stability and the addition of 1.0 M at pH 4.5 showed the lowest. The higher the heating temperature, the lower the foam stability at pH 2.0 and 9.0. However, the foam stability increased at pH 4.5 and 7.0 before reaching $80^{\circ}C$.

• Journal of Pharmaceutical Investigation
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• 제30권1호
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• pp.33-37
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• 2000

One of the methods to increase the solubility of a drug is to use complexation with a cyclodextrin. Due to the hydrophobic nature of the interior cavity of the cyclodextrin, it has been known that undissociated lipophilic drugs can be included within the cyclodextrin by hydrophobic interaction. Recently, inclusion of hydrophilic or dissociated form of a drug has been investigated. In this study, the synergism of pH and complexation with $hydroxypropy-{\beta}-cyclodextrin\;(HP\;{\beta}\;CD)$ to increase the solubility of two oxicam derivatives was investigated. In addition, the effect of partition coefficient of dissociated and undissociated form of the drug on the extent of complexation with HP ${\beta}$ CD was studied. The solubility was measured by equilibrium solubility method. The solubility of tenoxicam and piroxicam increased exponentially with an increase in solution pH above the pKa of the drug in the presence and absence of HP ${\beta}$ CD. The solubility of the drugs increased linearly as a function of HP ${\beta}CD$ concentration at fixed pH. Although the stability constant of ionized species is less than that of the unionized species, the concentration of the ionized drug complex is greater than that of the unionized drug complex due to higher concentration of ionized species at pH 7.3.

• Applied Biological Chemistry
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• 제32권4호
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• pp.321-326
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• 1989

탈지들깨종자박의 질소용해도는 $pH\;4.0{\sim}5.0$에서 최저수준을 보였으며, pH11.0에서는 92.3%로 최고용해도를 나타내었다. Phytate의 용해도는 pH 4.8에서 최고수준을 나타내었으며 $pH\;8.0{\sim}11.0$에서는 $9.4{\sim}8.3%$로 낮은 값을 나타내었다. 원심력이 추출액 중의 질소량의 변화에 미치는 영향는 미미하였으나 phytate의 양과 혼탁도는 원심력의 증가에 따라 감소하다가 8,000 rpm 이상에서 거의 일정수준을 유지하였다. 추출온도의 상승$(5{\sim}60^{\circ}C)$에 따라 종자박의 졸소 및 phytate의 용해도는 증가하였으나 증가폭은 미미하였다. pH 0.5에서 $CaCl_2$의 첨가는 phytate의 용해도를 크게 감소시켰는데 $50mM\;CaCl_2$ 용액에서는 거의 0%에 가까운 용해도를 나타내었다. 들깨종자 분리단백질의 질소 및 phytate의 용해도는 pH의 상승에 따라 모두 증가하는 경향을 보였다. 그러나 pH 11.1에서 10mM $CaCl_2$ 첨가는 phytate의 용해도를 80.5%에서 약 10%로 감소시켰다. 탈지들깨종자박의 조단백질과 phytate 함량은 각각 60.1%와 5.0%였으며, 분리단백질은 각각 89.6%와 1.1%였다.