• 대한화장품학회지
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• 제45권3호
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• pp.237-254
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• 2019

본 연구는 친수성 겔화제인 sodium stearate가 수분이 다량 함유된 수중유형의 고형화 자외선 차단제의 경도에 미치는 영향에 관한 연구이다. O/W (oil in water) type의 자외선 차단제는 안정성 및 사용감이 우수하며, W/O (water in oil) type의 자외선 차단제보다 상대적으로 안정화가 용이하다. 고형화 자외선 차단제를 위해 유화제 종류, 전해질과 왁스나 오일 등을 이용하여 안정도를 높이는 방법 등이 연구된 바가 있다. 본 연구에서의 고형화 자외선 차단제 개발은 수분이 40% 이상 함유된 수중유형으로 sodium stearate를 활용하여 경도를 향상시켜 안정화시키고자 하였다. 자외선차단 화장료 경도에 영향을 주는 요인을 분석하기 위하여 반응표면분석법(response surface methodology, RSM)을 사용하였으며, sodium stearate, 폴리올 및 오일을 각 요인으로 하였다. 반응값인 경도는 경도계를 이용하여 측정하였다. 결과적으로 경도에 영향을 주는 3가지 요인 중 특히 sodium stearate가 유의미한 값(p < 0.05)을 보였다. 또한 sodium stearate 함유로 고형화 자외선 차단제의 사용성과 안정성이 증가하는 효과를 보였다.

• 공업화학
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• 제10권8호
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• pp.1216-1220
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• 1999

괴상 중합과 현탁 중합 및 수산화나트륨을 이용한 중화를 통하여 제조된 poly(styrene-co-sodium methacrylate) 이오노머의 가소제로 스테아린산 아연을 첨가하여 열적 성질과 유변학적 성질에 미치는 영향을 조사하였다. 이오노머 중 스테아린산 아연은 이온기 함량에 따라 부분적으로 결정화가 억제됨이 관찰되었다. 이오노머 중 이온기들은 스테아린산 아연을 용해시키고 결정화를 억제하는 것으로 판단되었으며, 이온기 1몰이 0.4~0.6몰의 스테아린산 아연을 용해시키는 것으로 추정할 수 있었다. 용해된 형태의 스테아린산 아연만을 포함한 이오노머는 Cox-Merz 플롯에서 전형적인 균일계의 유변학적 거동을 보였다. 그러나 용해된 스테아린산 아연뿐 아니라 결정성 스테아린산 아연을 포함한 이오노머들은 Cox-Merz 플롯에서 불균일계의유변학적 거동을 보였다.

• Journal of Pharmaceutical Investigation
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• 제38권5호
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• pp.303-311
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• 2008

Highly hydrophobic lubricants including magnesium stearate may hinder water penetration into the tablet core resulting in delayed disintegration of fast disintegrating tablets. Alternative lubricants with equivalent lubricating properties may need to be incorporated into the tablet formulations. Sodium stearyl fumarate, glyceryl behenate and polyethylene glycol were evaluated regarding the tablet ejection energy, mechanical strength and disintegration time using Texture analyzer (TA). Resulting tablets were also compared with different particle sizes of granules and various compression forces. Among the tested lubricants, sodium stearyl fumarate was less sensitive to mixing time and also showed better or competitive tablet properties. During the experiments, TA was found to be very useful tool to investigate the tablet properties.

• 대한화학회지
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• 제55권2호
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• pp.163-168
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• 2011

다양한 농도의 N-methyl acetamide 수용액에서 계면 활성제의 농도에 따른 계면활성제들 (sodium caprylate, sodium laurate, sodium palmitate, sodium stearate, sodium oleate, sodium dodecyl sulphate, lithium dodecyl sulphate)의 몰 전도도 변화를 $30{\pm}0.2^{\circ}C$의 일정온도에서 연구하였다. 각각의 계면활성제에 대한 임계 미셀 농도 (CMC)를 측정하였다. 수용액에 N-methyl acetamide이 공존할 때에는 여러 계면 활성제의 CMC 값이 수용액에서의 CMC 값보다 더 낮고, 미셀 형성에 대한 추진력은 소용매성과 관련되었다. N-methyl acetamide 수용액에서 양쪽성 자기-조직화를 추진하는 계면활성제-용매의 상호작용에 대해 논의하였다. 이 결과들을 설명하기 위하여 미셀 시스템에 대한 열역학적 매개변수들을 추정하였다.

• 한국응용과학기술학회지
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• 제41권2호
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• pp.318-328
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• 2024

본 연구에서는 수크로스 스테아레이트(SS)의 유화력과 가용화력을 좀 더 향상시키기 위해, sodium deoxycholate (SDOC)와 PEG-40 hydrogenated castor oil (HCO)와의 혼합 조성물을 구성하였다. 혼합물의 최적 조성을 구하기 위해 혼합물 실험 계획법을 도입하여 실험을 진행하고, 실험에서 얻은 데이터를 회귀 분석하여 혼합물 조성의 변화가 혼합물의 특성에 미치는 영향을 살펴보았다. SS에 SDOC만을 첨가했을 때 코코넛 오일에 대한 유화력이 가장 향상되고, HCO만을 첨가했을 때는 가용화력이 가장 향상된 반면, 에스테르 오일인 cetyl ethylhexanoate (CEH)에 대한 유화력은 SDOC와 HCO를 함께 첨가했을 때 가장 크게 향상됨을 알 수 있었다. 코코넛 오일 및 CEH 각각에 대한 유화력과 가용화력, 3개의 특성치에 대한 동시 최적화를 실시한 결과, 최적의 계면활성제 혼합 조성은 SS 0.7939, SDOC 0.0586, HCO 0.1475로 구해졌다.

• Journal of Pharmaceutical Investigation
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• 제32권2호
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• pp.95-101
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• 2002

Matrix tablets of nifedipine (NP) were prepared with Eudragit, diluent (lactose or Ca. phosphate) and Mg. stearate employing two different preparation methods (wet granulation and direct compression) to develop its sustained-release dosage forms. The effects of various formulation factors on the dissolution rate of the drug were investigated. Dissolution test was studied in pH 6.8 phosphate buffer containing 1% sodium lauryl sulfate using the paddle method. Formulation factors were the type and content of Eudragit, the type of diluent and the tablet preparation method. The optimum formula of NP matrix tablet, which resulted in a similar dissolution profile to that from Adalat Oros used as a reference, was 30 mg NP, 10% Eudragit RS, 2% Mg. stearate and an adequate quantity of lactose to yield 500 mg weight using the wet granulation method.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1997년도 춘계학술대회
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• pp.118-118
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• 1997

Solid dispersions were used to increase the dissolution rate of biphenyl dimethyl dicarboxylate (DDB) in water, with the ultimate goal of optimizing its bioavailability when incoporated into pharmaceuticals. Carriers used were Kollidon 30, Kollidon VA 64, 2-hydroxypropyl-${\beta}$-cyclodextrin (HPCD), sodium salicylate or sodium benzoate. DDB solid dispersions were prepared at drug to carrier proportions ranging from 1 : 5 to 1 : 20 (w/w) by solvent evaporation method. DDB tablets (7.5 mg) were prepared by compressing the powder mixture composed of solid dispersions, lactose, corn starch, crospovidone and magnesium stearate using a single-punch press. DDB capsules (7.5 mg) were prepared by filing the mixture into empty hard gelatin capsules (size #1). Dissolution studies of DDB from powdered solid dispersions, tablets and capsules were performed in 900 $m\ell$ of water at 100 rpm and 37$^{\circ}C$ by the paddle method. The dissolved amount was assayed by HPLC and expressed as the mean(%)of three determinations.

• Korean Chemical Engineering Research
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• 제59권2호
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• pp.219-224
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• 2021

Ion flotation is an efficient method to remove metal ions from aqueous solution. In this work, ion flotation was applied to calcium removal from aqueous solution. The parameters used included sodium stearate (SS) and sodium dodecyl sulfate (SDS) as collectors, 1-butanol and 1-propanol as frothers, pH, and air-flow rate. An L16 orthogonal array was chosen according to the mentioned factors and levels, and experimental tests were conducted according to the Taguchi orthogonal array. The results showed that all of the factors except one had significant effect on the flotation performance. The percentage contribution of parameters showed that type of frother and type of collector made the greatest (43.14%) and the lowest (9.86%) contribution, respectively. In optimal conditions, the recovery of Ca (II) ion was 45.67%. Also, the results illustrated that the Taguchi method could predict calcium removal from aqueous solution by ion flotation with 2.63%. This study showed that the use of ion flotation was an effective method for Ca (II) ion removal from aqueous solution.

• 열처리공학회지
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• 제37권1호
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• pp.16-22
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• 2024

The conventional degreasing process involves removing oil and contaminants at temperatures above 80℃, resulting in excessive energy consumption, increased process costs, and environmental issues. In this study, we aimed to find the optimal degreasing conditions for the pre-treatment process of electro-galvanizing cold-rolled steel sheets, conducted efficiently at room temperature without the need for a separate heating device. To achieve this, we developed a room temperature degreasing solution and a brush-type degreasing tool, aiming to reduce energy consumption and normalize the decrease in degreasing efficiency caused by temperature reduction. Alkaline degreasing solution were prepared using KOH, SiO₂, NaOH, Na₂CO₃, and Sodium Lauryl Sulfate, with KOH and NaOH as the main components. To enhance the degreasing performance at room temperature, we manufactured additives including sodium oleate, sodium stearate, sodium palmitate, sodium lauryl sulfate, ammonium lauryl sulfate, silicone emulsion, and EDTA-Na. Room temperature additives were added to the alkaline degreasing solution in quantities ranging from 0.1 to 20 wt.%, and the uniformity of degreasing and the adhesion of the galvanized layer were evaluated through Dyne Test, T-bending Test, OM, SEM, and EDS analyses. The results indicated that the optimal degreasing solution composition consisted of NaOH (30 g/L), Na₂CO₃ (30 g/L), SLS (6 g/L), and room temperature additives (≤1 wt%).

• Journal of Pharmaceutical Investigation
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• 제41권4호
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• pp.217-225
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• 2011

The aim of this work was to prepare porous osmotic pump tablets for controlled delivery of Aceclofenac. Aceclofenac solid dispersion was prepared to improve the solubility by using the drug - carrier (Mannitol) ratio of 1:1. The osmotic pump tablets were prepared using the solid dispersed product of Aceclofenac. The formulation contains potassium chloride as osmotic agent, cellulose acetate as semipermeable membrane, poly ethylene glycol (PEG 4000) as pore former and sodium lauryl sulphate (SLS) as solubility enhancer. The formulations were designed by the general factors such as osmotic agent and pore former. All formulations were evaluated for various physical parameters and, the in vitro release studies were conducted as per USP. The drug release kinetic studies such as zero order, first order, and Higuchi and Korsmeyer peppas were determined and compared. All the formulations gave more controlled release compared to the marketed tablet studied. Numerical optimization techniques were applied to found out the best formulation by considering the parameter of in vitro drug release kinetics and dissolution profile standards. It was concluded that the porous osmotic pump tablets (F7) composed of Aceclofenac solid dispersion/Potassium chloride/Lactose/Sodium lauryl sulphate/Magnesium Stearate (400/40/95/10/5, mg/tab) and coating composition with Cellulose acetate/ PEG 4000 (60/40 %w/w) is the most satisfactory formulation. The porous osmotic pump tablets provide prolonged, controlled, and gastrointestinal environment-independent drug release.