• 약학회지
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• 제42권3호
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• pp.290-295
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• 1998

To optimize the formulation of acetaminophen liquid suppository, the effect of additives on the physicochemical properties of liquid suppository base was investigated. The physi cochemical properties of P 407/P 188 (15/15%) (abbreviated in 15/15) and P 407/P l88 (15/20%) (abbreviated in 15/20) were measured after the addition of following additives; 2.5% acetaminophen as an active ingredient, vehicle components (5% ethanol, 5% propylene glycol, 5% glycerin), preservatives (0.1% sodium benzoate, 0,1% methylparahydroxybenzoate, 0.1% propylparahydroxybenzoate) and 1% of sodium chloride as an ionic strength controlling agent. Poloxamer gel was prepared with three different buffer solutions (pH 1.2, 4.0 and 6.8) and the physicochemical properties, gelation temperature, gel strength and bioadhesive force, were determined. In the results, the effect of additives on the physicochemical properties was dependent on their bonding capacities including hydrogen bonding and cross-linking bonding. Because the hydrogen-bonding capacities of acetaminophen, ethanol and propylene glycol were smaller than that of poloxamer, the binding force of poloxamer gel became weak by their putting in between poloxamer gel. Therefore, the gelation temperature (15/15, $35.7^{\circ}C$ vs 37.0, 39.4 $38.2^{\circ}C$; 15/20, $29.2^{\circ}C$ vs 31.2, 32.0, $30.3^{\circ}C$) increased, and gel strength (15/15, 4.03 see vs 2.72, 2.08, 3.12sec; 15/20, 300g vs 50, 50, 200g) and bioadhesive force (15/15, $6.8{\times}10^2\;dyne/cm^2$ vs 3.2, 6.0, $6.0{\times}10^2\;dyne/cm^2$; 15/20, $97.3{\times}10^2\;dyne/cm^2$ vs 11.1, 89.5, $92.0{\times}10^2\;dyne/cm^2$) decreased. Furthermore, the binding force of poloxamer gel became strong due to the hydrogen-bonding capacities of glycerin and the cross-liking bonding of sodium salt. Then, the gelation temperature (15/15, 35.0, $32.1^{\circ}C$; 15/20, 26.0, $21.0^{\circ}C$) decreased, and gel strength (15/15, 6.51 see, 300g; 15/20, 500, 650g) and bioadhesive force (15/15, 7.2, $81.6{\times}10^2\;dyne/cm^2$; 15/20, 112.3, $309.2{\times}10^2\;dyne/cm^2$) increased. The effect of pH on the physicochemical properties of poloxamer gel was dependent on the ingredients with which the buffer solutions were prepared. Poloxamer gels prepared with pH 1.2 and 4.0 buffer solutions had the increasing gelation temperature (15/15, 37.5, $38.1^{\circ}C$; 15/20, 33.1, $34.0^{\circ}C$) and the decreasing gel strength (15/15, 2.98, 3.81sec; 15/20, 200, 200g) and bioadhesive force (15/15, $7.0{\times}10^2dyne/cm^2$; 15/20, $74.0{\sim}88.1{\times}10^2dyne/cm^2$) owing to HCl. Poloxamer gel prepared with pH 6.8 buffer solutions had the decreasing gelation temperature (15/15, $27.2^{\circ}C$; 15/20, $22.3^{\circ}C$) and the increasing gel strength (15/15, 400g; 15/20, 550g) and bioadhesive force (15/15, $207.0{\times}10^2dyne/cm^2$; 15/20, $215.0{\times}10^2dyne/cm^2$) due to the cross-linking bonding of $NaH_2PO_4\;and\;K_2HPO_4$.

• Journal of Dairy Science and Biotechnology
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• 제23권2호
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• pp.115-123
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• 2005

Microcapsules consisting of natural, biodegradable polymers for controlled and/or sustained core release applications are needed. Physicochemical properties of whey proteins suggest that they may be suitable wall materials in developing such microcapsules. The objectives of the research were to develop water-insoluble, whey protein-based microcapsules containing a model water-soluble drug using a chemical cross-linking agent, glutaraldehyde, and to investigate core release from these capsules at simulated physiological conditions. A model water soluble drug, theophylline, was suspended in whey protein isolate (WPI) solution. The suspension was dispersed in a mixture of dichloromethane and hexane containing 1% biomedical polyurethane. Protein matrices were cross-linked with 7.5-30 ml of glutaraldehyde-saturated toluene (GAST) for 1-3 hr. Microcapsules were harvested, washed, dried and analyzed for core retention, microstructure, and core release in enzyme-free simulated gastric fluid (SGF) and simulated intestinal fluid(SIF) at $37^{\circ}C$. A method consisting of double emulsification and heat gelation was also developed to prepare water-insoluble, whey protein-based microcapsules containing anhydrous milkfat (AMF) as a model apolar core. AMF was emulsified into WPI solution (15${\sim}$30%, pH 4.5-7.2) at a proportion of 25${\sim}$50%(w/w, on dry basis). The oil-in-water emulsion was then added and dispersed into corn oil ($50^{\circ}C$) to form an O/W/O double emulsion and then heated at $85^{\circ}C$ for 20 min for gelation of whey protein wall matrix. Effects of emulsion composition and pH on core retention, microstructure, and water-solubility of microcapsules were determined. Overall results suggest that whey proteins can be used in developing microcapsules for controlled and sustained core release applications.

• 멤브레인
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• 제28권5호
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• pp.326-331
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• 2018

축전식 탈염(capacitive deionization)에 이용할 수 있는 폴리페닐렌 옥사이드(PPO) 음이온 교환막의 가교결합에 대해 조사하였다. 브롬화와 아민화 반응단계를 거쳐 PPO 음이온 교환 고분자를 제조하고 비스페놀 A 디글리시딜에테르(BADGE), m-페닐렌디아민(m-PDA), 헥사메틸렌디아민(HMDA) 등으로 가교하였다. 가교에 따른 겔화되는 시간은 HMDA > m-PDA > BADGE 순으로 짧았으며, 일정한 함량 이상으로 실온에서 가교하면 1-메틸피롤리돈(NMP)과 같은 비양성자성 용매(aprotic solvent)에 녹지 않아 내화학성이 증대되었다. 가교제(BADGE) 함량에 따른 음이온 교환막의 이온 교환 용량과 함수율을 측정하고 비교하였다. HMDA 용액에 침적하여 표면 가교한 PPO 음이온 교환막을 축전식 탈염에 적용한 결과 그 탈염 성능은 가교하지 않은 막과 비교하여 흡착단계의 초기 부분을 제외하고 거의 차이가 없었다.

• Journal of the Korean Wood Science and Technology
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• 제23권3호
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• pp.33-39
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• 1995

To accelerate the cure of phenolic resin adhesives for plywood, the complexation with melamine resin and the addition of cure-accelerating agents were discussed. The hot-pressing temperature and time of phenol resin could be decreased by complexation with melamine resin. but the wet glue-joints strength of phenol melamine resin was lower than that of ordinary phenol resin in case of plywood using spruce veneer at core layer. Among the tested cure-accelerating agents. the sodium carbonate showed the greatest effect on shortening gelation time of phenolic resin. In addition, in the manufacturing scale test, the hot-pressing time of phenol resin with the addition of 5 parts sodium carbonate could be shortened about 20% compared with ordinary phenol resin which had same glue-joints properties.

• 한국세라믹학회지
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• 제31권5호
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• pp.499-504
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• 1994

PbTiO3 thin films were prepared by sol-gel spin coating method using metal alkoxide and diethanolamine (DEA). The precipitation of the PbTiO3 sol occurred at pH 7.3 with HNO3 addition, regardless of the amount of DEA. The gelation time of the PbTiO3 sol was reduced with increasing amount of HNO3 and/or water. When the PbTiO3 films prepared by 0.2 molar coating solution were annealed at $650^{\circ}C$ for 30 min, dense and single phase perovskite films were obtained. Dielectric constant and loss tangent of the film were 239 and 0.01 at 1 kHz, respectively.

• 한국마이크로전자및패키징학회:학술대회논문집
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• 한국마이크로전자및패키징학회 2002년도 춘계 기술심포지움 논문집
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• pp.152-157
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• 2002

The cure and rheological behavior of Diglycidyl ether of bisphenol F, catalyzed by four kinds of imidazoles and a Nadic methyl anhydride curing agent were studied using a differential scanning calorimeter (DSC) and rheometer. The isothermal traces were employed to analyze cure reaction. The DGEBF/anhydride conversion profiles showed autocatalyzed reaction characterized by maximum conversion rate at 20~40 % of the reaction. The rate constants obtained from isothermal test showed temperature dependance, but reaction order did not. The order of reaction (m+n) was calculated to be close to 3. The measurements of viscosity and relation time in the presence of inorganic fillers were carried out at different isothermal curing temperatures. The viscosity and gelation time increased with filler content at the same isothermal temperature.

• International Journal of Industrial Entomology and Biomaterials
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• 제27권2호
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• pp.312-316
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• 2013

Caffeine is a thermogenic agent that can be used in weight loss products. In order to achieve a sustained release of caffeine, silk fibroin (SF) film was uses as carrier. It has been shown that the loading method of caffeine into SF film affected the uniform distribution of caffeine in the SF film. When caffeine was added directly into SF solution, gelation has been occurred immediately and prevented the uniform distribution of caffeine. On the other hand, caffeine was dissolved in methanol in order to load the caffeine in SF film and crystallize the SF film at the same time. However, due to the fast evaporation of methanol, caffeine was recrystallized on the surface of SF film rather than penetrating into the film. Finally, caffeine was loaded into pre-crystallized SF film and uniform distribution of caffeine could be achieved. There was an initial burst of caffeine during the first 15 min, but after that a sustained release was achieved.

• 공업화학
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• 제17권4호
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• pp.420-425
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• 2006

Propylene oxide (PPO)를 gelation agent로 한 졸-겔법으로 입자가 균일하고 자기적 특성이 우수한 $MO{\cdot}Fe_{12}O_{18}$ (M/Ba and Sr)의 구조식을 가지는 M-type hexagonal ferrite를 제조하였다. 본 방법으로 얻은 졸-겔용액은 매우 안정적인 분산상태를 보이며, $Fe^{3+}$의 겔화가 진행되고, 생성된 $Fe_2O_3$의 표면에서 $Ba^{2+}$ 또는 $Sr^{2+}$의 겔화가 진행되는 것으로 설명될 수 있어서, +3가 이하의 금속이라도 +3가 이상의 금속 존재 하에는 겔화가 가능한 것을 확인하였다. 또한, 기존 방법과 비교하여 값싼 원료를 사용하며, 반응 시간도 1 min 이내로 짧아지는 장점이 있다. 본 제조법으로 얻어진 분말은 기왕에 발표된 문헌 값과 비교하면 $150^{\circ}C$ 이상 낮은 열처리 온도에서 최고의 자기적 특성을 나타냈으며, 향상된 자기적 특성을 보였다. Sr-ferrite의 경우 최대포화자화 값 74.4 emu/g, 보자력 값 6198 Oe을, Ba-ferrite의 경우도 최대포화자화 값 68.1 emu/g, 보자력 값 5155 Oe을 보였다. 이들은 기존에 발표된 문헌 값과 비교하면 각각 10%와 5% 이상 증가된 보자력 값을 나타내어, 고밀도 자기기록재료에 적합함을 확인하였다. 제조된 분말은 1차 건조 분말의 경우 3~5 nm의 입자들이 응집된 50 nm 정도의 구형입자가 생성되고, 열처리 후에는 500 nm 정도의 고른 크기를 가진 육각판상형 입자가 생성된다.

• 보존과학회지
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• 제37권6호
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• pp.801-806
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• 2021

전통 접착 소재인 아교의 사용성과 해초 추출물 카라기난의 겔화 현상을 개선하기 위해 두 재료를 혼합하여 목재 보존용 액상형 접착제를 제조하였으며, 9종의 천연 및 합성 접착제와의 물성 비교를 통해 적용 가능성을 확인하였다. 제조한 목재 접착제는 15 wt% 아교 수용액과 λ-carrageenan, 항균제, 소포제 등을 혼합하였으며, 1.80 Mpa의 최대 접착 강도를 확인하였다. 비교 결과 5종의 전통 천연 접착 성분(수용액)과 Polyvinyl acetate 기반 접착제 1종보다 우수한 접착 강도가 나타났으며, 총호기성생성균수와 유해성(TVOC, HCHO, 중금속) 시험 결과 불검출로 항균성과 안정성을 확인하였다.

• 한국산림과학회지
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• 제77권3호
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• pp.294-302
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• 1988

본(本) 실험(實驗)은 낙엽송(落葉松)(Larix leptolepsis) 수피(樹皮)로부터 추출(抽出)한 수피추출물(樹皮抽出物)의 특성(特性)을 조사(調査)하고 그들 추출물(抽出物)의 접착제화(接着劑化)의 가능성(可能性)을 평가(評價)하기 위해 실행되었다. 수율(收率)과 반응도(反應度)의 측정(測定)을 통해 온도(溫度) 및 시간(時間)의 영향(影響)과 탄산화(炭酸化) 및 설폰화(化)의 효과(效果)를 조사하였다. 목재접착제(木材接着劑)로의 적용(適用) 가능성(可能性)을 구명하기 위해서는 33% 농도(濃度)에서 점도(粘度)와 겔화시간(化時間)을 측정(測定)하였다. 그 결과(結果)는 다음과 같다. 1. 수율(收率)과 반응도(反應度)가 모두 높은 $80^{\circ}C$에서 120분(分)의 추출(抽出)이 적정온도(適正溫度) 및 시간(時問)이었다. 2. 탄산화(炭酸化)는 1% $Na_2CO_3$에서 설폰화(化)는 1% $Na_2SO_3$ : $NaHSO_3$와 0.25% $Na_2SO_3$에서 가장 큰 효과(效果)를 얻었으며 이들중 0.25% $Na_2SO_3$에 의한 설폰화(化)가 수율(收率)과 반응도(反應度)를 가장 크게 증가시켰다. 3. 온수추출액(溫水抽出液)의 수율(收率)은 17.2%이며 1% NaOH와 5% NaOH 추출액(抽出液)의 수율(收率)은 각각(各各) 38.6%와 44.6%이었다. 4. 온수추출액(溫水抽出液)의 반응도(反應度)는 68.8%로 가장 높았으며 1% NaOH와 5% NaOH 추출액(抽出液)의반응도(反應度)는 각각(各各) 49.3%와 25.8%이었다. 5. 각(各) 추출액(抽出液)은 33% 농도(濃度)에서 점도변화(粘度變化)가 매우 심했다. 특히 1% NaOH 추출액(抽出液)은 점도(粘度)가 매우 높았으며 5% NaOH 추출액(抽出液)은 오히려 점도(粘度)가 낮았다. 6. 추출액(抽出液)의 겔화시간(化時間)은 pH 7-10에서 가장 낮은 값을 나타냈으며 pH 4에서 가장 높은 값을 나타냈다. 파라포름알데히드의 이용(利用)은 37% 포름알데히드보다 겔화시간(化時間)을 더 연장시켜 주었다. 7. 온수추출(溫水抽出)의 설폰화(化)와 1% NaOH 추출(抽出)의 설폰화(化)를 제외(除外)한 다른 추출방법(抽出方法)은 높은 점도(粘度)(1% NaOH 추출(抽出))와 비경화성(比硬化性)(5% NaOH 추출(抽出), 5% NaOH 추출(抽出)의 설폰화(化)) 때문에 부적합한 것으로 밝혀졌다. 8. 접착제로(接着劑)로의 이용(利用)이 적합한 것으로 나타난 추출액(抽出液) 중 온수추출(溫水抽出)과 온수추출(溫水抽出)의 설폰화(化)는 반응도(反應度)가 뛰어난 반면 1% NaOH 추출(抽出)의 설폰화(化)는 비율면(比率面)에서 유리(有利)한 것으로 나타났다.