• 멤브레인
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• 제16권1호
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• pp.68-76
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• 2006

본 연구는 투과증발법을 이용하여 수용액 중 미량의 감귤 향 성분을 농축하는 방법으로, 4종류의 실록산계 고분자 복합막을 이용하여 막 종류와 구조에 따른 투과 특성을 살펴보았다. 또한 최적의 막을 선정하여 공급액의 온도와 농도, 순환 유속에 따른 투과 특성을 살펴보고, 이를 resistance-in series model을 이용하여 해석하였다. 4종류의 실록산계 고분자 복합막을 통한 감귤 essence aroma 모델액의 투과 실험에서 지지층이 polyvinylidene fluoride (PVDF)이고 활성층이 polyoctylmethyl siloxane (POMS)인 막이 가장 높은 향 성분 플럭스와 농축계수 값을 나타내었으며, 공급액의 온도와 농도, 순환유속을 변화시키며 투과 실험을 하였다. 그 결과 공급액의 온도와 농도가 증가됨에 따라 향성분의 플럭스는 증가하고 농축계수 값은 감소하였으며 순환유속이 증가됨에 따라 향성분의 플럭스와 농축계수 값 모두 증가하였다.

• 멤브레인
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• 제4권4호
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• pp.197-204
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• 1994

본 연구에서는 hollow fiber 막모듈을 통한 순수 $CH_4,\;CO_2$기체와 $CH_4/CO_2$ 혼합기체의 투과 특성을 살펴 보고, 이를 모사값과 비교하여 보았다. 순수 기체의 투고율은 온도에 따라 Arrhenius type으로 증가하였으며, 활성화에너지는 $CO_2$는 6.61kJ/mol, $CH_4$는 25.26kJ/mol로 나타났다. 혼합기체의 투과에 있어서 투과부의 유량과 $CO_2$ 조성, 그리고 배제부의 $CH_4$조성은 cut의 증가에 따라 증가하였다. 분리인자는 5~20atm의 압력과 cut이 20으로 고정된 상태에서 20~40의 범위에 있었으며, 압력이 증가하고 온도가 감소할수록 증가하는 경향을 나타내었다. 실험결과와 모사결과는 투과부 유량과 $CO_2$조성의 경우 8% 이내에서, 배제부의 $CH_4$조성의 경우 15% 이내에서 일치하였다.

• Korean Membrane Journal
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• 제3권1호
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• pp.69-74
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• 2001

Films of TiO$_2$/SiO$_2$ were deposited on the inner surface of the porous glass support tubes by decomposition of tetraisopropyl titanate (TIPT) and tetraethyl orthosilicate (TEOS) at atmospheric pressure. Dense and hydrogen -permselective membranes were formed at 400-600$\^{C}$. The permeation rates of H$_2$ through the membrane at 600$\^{C}$ were 0.2-0.4 ㎤(STP)/min-㎠ atm and H$_2$:N$_2$permeation ratios were above 1000. The permeation properties of the membranes were investigated at various deposition temperatures and TIPT/TEOS concentrations. Decomposition of TIPT alone at temperatures above 400$\^{C}$ produced porous crystalline TiO$_2$ films and they were not H7-selective. Decomposition of TEOS produced H$_2$-permeable SiO$_2$ films at 400-600$\^{C}$ but film deposition rate was very low. Addition of TIFT to the TEOS stream significantly accelerated the deposition rate and produced highly H$_2$-selective films. Increasing the TIPT/TEOS concentration ratio increased the deposition rate. The TiO$_2$/SiO$_2$ membranes formed at 600 $\^{C}$ have the permeation properties comparable to those of SiO$_2$ membranes produced from TEOS.

• 한국산업융합학회 논문집
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• 제2권1호
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• pp.105-112
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• 1999

Model predicting the respiration rate of pear under modified LDPE film pouch has been developed. The assumptions of the model have three bases; 1) respiration rate is depending on $CO_2$ and $O_2$ concentration in the package, 2) the oxidation of glucose in pear generates carbon dioxides, and 3) gases permeation through the package film bases on the Langmuir adsorption theory and Fick's law. The simulated results agreed fairly well with the experimental data so as this model to be useful in designing the modified atmospheric packaging system.

• 대한환경공학회지
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• 제22권7호
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• pp.1273-1284
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• 2000

본 연구에서는 한외여과막을 이용하여 수중에 함유되어 있는 부식산의 제거실험을 수행하였다. 한외여과성능에 미치는 공정변수들의 영향이 비선형적으로 서로 얽혀 있기 때문에, 응답표면분석법(RSM)을 이용하여 분리막 공정의 최적화와 각 변수간의 상호관계 및 투과성능에 영향을 미치는 공정변수(압력, 농도, 유량 등)들이 분리성능에 미치는 영향을 분석하였다. 부식산용액의 공정변수에 대한 투과량의 변화는 유입용액의 부식산의 농도가 10ppm, 40ppm 70ppm으로 증가함에 따라 2.56, 2.27, $2.10({\times}10^{-2}cc/cm^2{\cdot}min)$으로 감소하였다. 즉, 순수한 물의 투과량에 비해 각각 17.7%, 26.7%, 32.2%만큼 감소하였으며, 투과부에서의 부식산농도는 0.5, 1.2ppm, 2.1ppm으로 증가하였다. 막내에서의 압력차를 1atm, 2atm, 3atm으로 변화하였을 때, 1atm에서의 투과량보다 각각 66%, 152%로 증가하였으며, 투과부에서의 부식산의 농도도 각각 0.5ppm, 1.5ppm, 3.5ppm으로 증가하였다. 응답표면분석(RSM)에 의하면 공정변수의 최적운전조건은 유입부식산농도 38.8~40ppm, 유입유량 30~30.7cc/min, 압력차는 2atm이었다.

• Journal of Pharmaceutical Investigation
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• 제25권3호spc1호
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• pp.43-51
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• 1995

The in vitro skin permeability of 16 drugs with a wide span of lipophilicity (log P ranging from -0,95 to 4.40) was evaluated with an ethanol/panasate 800 (tricaprylin, P-800) (40/60) lipophilic binary vehicle and an ethanol/water (60/40) hydrophilic binary vehicle with lauric acid, The skin permeability of the drugs was enhanced by the use of the ethanol/P-800 (40/60) binary vehicle or the ethanol/water (60/40) binary vehicle with lauric acid; permeation rate was increased and lag time' was decreased. The relationship between lipophilicity and skin permeation rate of the drugs showed parabolic shapes with their peaks at much greater hydrophilic range compared with other past references. In the in vivo skin absorption of theophylline using abdominal rat skin, the ethanol/P-800 (40/60)-7% (w/w) ethycellulose gel produced a good feature as a sustained-release preparation, and the ethanol/water (60/40)-3 % (w/w) HPMC gel with lauric acid showed the highest BA value. The results suggest that the lipophilicity of a drug is a main factor for prediction of the skin permeability of the drug and that the ethanol/P-800 (40/60) binary vehicle and ethanol/water (60/40) binary vehicle with lauric acid would be good candidates for clinical transdermal application of hydrophilic drugs.

• Journal of Pharmaceutical Investigation
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• 제29권4호
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• pp.343-348
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• 1999

The purpose of this study is to prepare the controlled release adhesive patch containing naproxen. Pressuresensitive adhesive (PSA)-type patch was fabricated by casting of polyisobutylene (PIE.) and mineral oil in toluene. Membrane-controlled release (MCR)-type patch was prepared by the attachment of the controlled release membrane on the PSAtype patch. The membrane was mainly composed of Eudragit, polyethylene glycol(PEG) and glycerin. The drug release profile and skin permeation test with various patches were evaluated in vitro. The release of naproxen from PIE-based PSAtype patch with various loading doses fitted Higuchi's diffusion equation. However, the permeation of naproxen through hairless mouse skin from PSA-type patch followed zero-order kinetics. In MCR-type patch, thickness of controlled release membrane affected on the drug release rate highly. In the composition of membrane, the release rate was decreased as the ratio of Eudragit increased. The drug release from the MCR-type patch followed zero order kinetics. The permeation of naproxen through hairless mouse skin from MCR-type patch showed lag time for the intial release period and didn't fit the zero-order kinetics

• 멤브레인
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• 제5권4호
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• pp.137-144
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• 1995

Hydranautic사의 셀룰로오즈 아세테이트 재질로 된 RO S/W 4040을 이용하여 2성분계의 붕산수용액 및 붕산수에 함유된 실리카의 3성분계 수용액에 대하여 조업온도, 운전압력 및 공급유량 변화가 투과량, 붕산회수율, 실리카 배제율에 미치는 영향에 대한 실험을 수행하였다. 붕산수용액의 경우 35$^{\circ}$C, 20atm 및 원액의 유속이 2.82l/min에서 붕산회수율 및 투과도는 각각 58.7% 및 2.82l/min, 35$^{\circ}$C, 10atm에서는 68.1% 및 1.56l/min이었다. 또한 실리카 및 붕산이 함께 함유된 용액의 경우 35$^{\circ}$C, 3.2atm에서 붕산회수율 69.7%, 실리카 배제율 97.5% 및 투과도 0.47l/min의 결과를 보여주었으며, 35$^{\circ}$C, 20atm에서 원액의 유속이 2.92l/min의 경우 붕산회수율 56.4%, 실리카 배제율 96.1% 및 투과도 2.72l/min의 결과를 보여 주었다.

• Journal of Pharmaceutical Investigation
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• 제29권3호
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• pp.227-234
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• 1999

Solid dispersions were prepared to increase the dissolution rate of biphenyl dimethyl dicarboxylate (DDB) using water-soluble carriers such as povidone, copolyvidone, $2-hydroxypropyl-{\beta}-cyclodextrin (HPCD)$, sodium salicylate or sodium benzoate by solvent evaporation method. Solid dispersions were characterized by infrared spectrometry, differential scanning calorimetry (DSC) and powder X-ray diffractometry, dissolution and permeation studies. DDB tablets (7.5 mg) were prepared by compressing the powder mixtures composed of solid dispersions, lactose, com starch, crospovidone and magnesium stearate using a single-punch press. DDB capsules (7.5 mg) were also prepared by filling the mixtures in empty hard gelatin capsules (size No.1). From the DSC and powder x-ray diffractometric studies, it was found that DDB was amorphous in the HPCD or copolyvidone solid dispersions. Dissolution rates after 10 min of DDB alone and solid dispersions (1 : 10) in sodium benzoate, sodium salicylate and copolyvidone were 11.8, 23.5, 22.8 and 82.5%, respectively. Dissolution rates of DDB after 30 min from 1 : 10 and 1 : 20 copolyvidone solid dispersions were 80.5 and 95.0%, respectively. For the DDB tablets prepared using solid dispersions (1 : 20), the initial dissolution rate was dependent on carrier material, and was ranked in order, $Kollidon\;30\;{\ll}$ copolyvidone < HPCD. For the HPCD solid dispersion tablets, dissolution rate reached 97.4% after 15 min, but thereafter slowly decreased to 80.7% after 2 hr due to the precipitation of DDB. However, in the case of copolyvidone solid dispersion tablets, dissolution increased linearly and reached 93.4% after 2 hr. Reducing the volume of test medium from 900 to 300 ml markedly decreased the dissolution rate of the tablets containing 1 : 20 HPCD solid dispersions and 1 : 10 copolyvidone solid dispersion. For 1 : 20 copolyvidone solid dispersion tablets, there was no significant change in dissolution rate up to 1 hr with different volumes of test medium. Preparation of the copolyvidone solid dispersion (1 : 20) in capsules markedly delayed the dissolution (31.2 % after 2hr) due to the limited diffusion within capsules. The permeation rate $(13.4\;g/cm^2\;after\;8\;hr)$ of DDB through rabbit duodenal mucosa from copolyvidone solid dispersion (1 : 10) was markedly enhanced, when compared with drug alone or physical mixtures. From overall findings, DDB formulations containing copolyvidone solid dispersions (1 : 20) could be used to remarkably improve the dissolution rate in dosage form of powders and tablets.

• Journal of Pharmaceutical Investigation
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• 제36권5호
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• pp.299-304
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• 2006

The aim of this study was to investigate the effect of deformable liposomes with sodium cholate on the skin permeation and skin deposition of arbutin, a hydrophilic skin-whitening agent. Various compositions of liposomes were prepared by the extrusion method. Particle size distribution and entrapment efficiency were determined by the laser light scattering and the gel permeation chromatography, respectively. The in vitro rat skin permeation and deposition of arbutin in various skin layers were investigated using the Keshary-Chien diffusion cells at $37^{\circ}C$. The average particle size of the deformable liposomes ranged from 217.4 to 117.4 nm, depending on the composition. The entrapment efficiency was dependent on surfactant concentration and loading dose of arbutin. The permeation rate of 5% arbutin in deformable liposomes was $8.91({\pm}1.33){\mu}g/cm^2/h$, and was not significantly different from 5% arbutin aqueous solution $[9.82({\m}0.86){\mu}g/cm^2/h]$. The deposition of arbutin was $43.34({\pm}12.13)$ and $16.99({\pm}7.83){\mu}g/cm^2$ in stratum corneum layer and epidermis/dermis layer, respectively, after 12 h of permeation study. These results are consistent with several earlier studies for the localization effect of liposomal formulations in stratum corneum, and demonstrated the feasibility of the deformable liposomes as a promising carrier for the skin deposition of hydrophilic skin-whitening compounds.