• Journal of Pharmaceutical Investigation
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• 제34권3호
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• pp.177-183
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• 2004

Recently, studies on intranasal mucosa delivery of influenza vaccine have been actively developed because of lack of pain and ease of administration. We studied on preparation of nanoparticle delivery system using biodegradable polymer as a poly(DL-lactide-co-glycolide) (PLGA) and their binding characteristics with vaccine. Three kinds of PLGA nanoparticles were prepared by spontaneous emulsification solvent diffusion (SESD) method using sodium dodecyl sulfate and sodium laurate as an anionic surfactant and Lutrol F68 (polyethylene glycol-block-polypropylene glycol copolymer) as a nonionic surfactant. The 5-aminofluorescein labeled vaccine was coated on the surface of nanoparticles by ionic complex. The complexes between vaccine and nanoparticles were confirmed by change of the size. After vaccine coating on the surface of anionic nanoparticles, particle size was increased from 174 to 1,040 nm. However the size of nonionic nanoparticles was not more increased than size of anionic nanoparticles. The amount of coated vaccine on the surface of PLGA nanoparticles was $14.32\;{\mu}g/mg$ with sodium dodecyl sulfate, $12.41\;{\mu}g/mg$ with sodium laurate, and $9.47{\mu}g/mg$ with Lutrol F68, respectively. In conclusion, prepared nanoparticles in this study is possible to use as a virus-like nanoparticles and it could be accept in the field of influenza vaccine delivery system.

• Journal of Pharmaceutical Investigation
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• 제37권6호
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• pp.339-347
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• 2007

SMEDDS is mixture of oils, surfactants, and cosurfactants, which are emulsified in aqueous media under conditions of gentle agitation and digestive motility that would be encountered in the gastro-intestinal(GI) tract. The main purpose of this work is to prepare self-microemulsifying drug delivery system(SMEDDS) for oral bioavailability enhancement of a poorly water soluble drug, atorvastatin calcium. Solubility of atorvastatin calcium was determined in various vehicles. Pseudo-ternary phase diagrams were constructed to identity the efficient self-emulsification region and particle size distributions of the resultant micro emulsions were determined using a laser diffraction sizer. Optimized formulations for in vitro dissolution and bioavailability assessment were $Capryol^{(R)}$ 90(50%), Tetraglycol(16%), and $Cremophor^{(R)}$ EL(32%). The release rate of atorvastatin from SMEDDS was significantly higher than the conventional tablet ($Lipitor^{(R)}$), 2-fold. Our studies illustrated the potential use of SMEDDS for the delivery of hydrophobic compounds, such as atorvastatin calcium by the oral route.

• 공업화학
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• 제7권2호
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• pp.379-386
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• 1996

광 이량화 특성을 나타내는 1-methyl-4-[2-(4-diethylacetylphenyl)ethenyl] pridinium methosulfate(SbQ-A염)를 dimethyl sulfate, terephthalaldehyde mono-(diethyl acetal) 및 4-picoline을 이용하여 합성하였다. 합성된 SbQ-A염을 PVA와 반응시켜 동일(MW=77,000-79,000g/mol) 분자량을 가진 PVA내 SbQ의 함량이 다른 PVA-SbQ-H 시료 및 SbQ의 함량은 약 1.3mol%로 같으나 PVA의 분자량이 다른 PVA-SbQ-L들을 합성하였다. Gray scale(GS)법을 이용하여 측정된 PVA-SbQ 수용성 감광성 고분자의 상대감도는 PVA내 SbQ의 함량이 증가함에 따라 증가하였으며, PVA의 분자량이 낮아질수록 감소하였다. PVA-SbQ-H의 경우 SbQ 함량이 2.63mol%인 시료는 PVA에 ammonium dichromate가 혼합된 기존시료보다 90배 증가된 감도를 나타내었다. PVA-SbQ를 사용하여 형광체 슬러리를 제조하고 사진식각공정을 거쳐 형광체의 미세패턴을 형성하였다. 형광체 슬러리 제조시 양이온 계면활성제인 cetyltrimethyl ammonium chloride를 첨가제로 사용하면 형광면의 해상도가 증가됨을 알았다.

• 대한화장품학회지
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• 제36권2호
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• pp.93-97
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• 2010

본 연구에서는 샴푸에 널리 사용되는 양이온성 폴리머 중, 양이온성 구아 폴리머를 선택적으로 사용하여, 다양한 성능평가를 통해 0.7 % 질소함량 이상의 치환도와 190~200 cps사이의 점도를 가지는 새로운 양이온성 구아 폴리머를 개발하였다. 성능평가로는 헹굼 시 모발 부드러움(Wet combing ability), 폴리머의 잔존정도와 실리콘의 흡착정도를 측정하였으며 최종적으로 관능평가를 실시하였다. 본 연구에서 개발된 양이온성 구아 폴리머를 배합하면 샴푸 사용감을 최적화할 수 있을 것이다.

• 멤브레인
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• 제16권4호
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• pp.294-302
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• 2006

은 고분자 전해질은 올레핀/파리핀 혼합물 분리에 매우 효과적인 분리막 재료이다. 이는 고분자 매질속에 녹아 있는 은이온이 올레핀과 선택적, 가역적 반응을 통해 올레핀만을 분리막속으로 통과시키기 때문이다. 그러나 이러한 은 고분자 전해질 분리막은 실제 공정에 응용되기에는 다소 약한 장시간 운전 성능 안정성을 보인다. 즉 분리 성능이 시간이 지남에 따라 점차 감소되는데 이는 은이온이 은 나노입자로 환원되기 때문이다. 따라서 본 연구에서는 poly(vinyl pyrrolidone) (PVP)와 $AgBF_4$로 이루어진 고분자 전해질막의 안정성을 향상시키고자 비이온 계면활성제인 $C_{18}H_{35}(OCH_2CH_2)_{20}OH$ (Brij98)를 첨가제로 사용하였다. 분리막속에서 은이온의 은 나노입자로의 환원현상을 원자전자 현미경과 자외선 분광학을 이용하여 분석하였다. 그 결과 Brij98이 첨가된 분리막의 경우 은 나노입자의 성장이 늦춰졌으며, 프로판/프로핀렌 선택도가 장시간 유지됨을 알 수 있었다.

• Journal of Pharmaceutical Investigation
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• 제36권4호
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• pp.271-276
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• 2006

Felodipine, a calcium-antagonist of dihydropyridine type, is a poorly water soluble drug and has very low bioavailability. As preceding studies, use of solid dispersion systems and surfactants(solubilizers) has been suggested to increase dissolution and to improve bioavailability of felodipine. But in case of solid dispersion systems, large amount of toxic organic solvents should be used and manufacturing process time become longer than conventional process. In case of using surfactants, as time elapsed, decreasing of dissolution rate of felodipine due to crystallization has been reported. In this study, Copovidon as a hydrophilic polymer and $Transcutol^{\circledR}$ as a surfactant were combined to formulations if order to increase dissolution of felodipine and conventional wet granulation process were applied to manufacturing of formulations. The effect of Copovidon and $Transcutol^{\circledR}$ on the dissolution oi felodipine was investigated in-vitro. When Copovidon and $Transcutol^{\circledR}$ used simultaneously, the dissolution rate of felodipine was prominently increased compared with when used separately and the maximum increase in the dissolution of felodipine was 5.8 fold compared to control. This is most probably due to synergy effect by combination of Copovidon and $Transcutol^{\circledR}$. Felodipine sustained release tablets were successfully formulated using several grades of HPMC as a release retarding agent. The stability of felodipine sustained release tablet was evaluated after storage at accelerated condition($40^{\circ}C/75%\;RH$) for 6months in HDPE(High density polyethylene) bottle. Neither significant degradation nor change of dissolution rate for felodipine was observed after 6months. In conclusion, felodipine sustained release tablet was successfully formulated and dissolution of felodipine, poorly water soluble drug, was prominently increased and also stability was guaranteed by using combination system of hydrophilic polymer and surfactant.

• Bulletin of the Korean Chemical Society
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• 제10권2호
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• pp.172-177
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• 1989

Stereoselective solvolyses of optically active activated esters in the aggregate system of optically active polymeric surfactants containing imidazole and benzene moieties were performed. The catalyst polymers employed were copolymers of N-methacryloyl-L-histidine methyl ester (MHis) with N,N-dimethyl-N-hexadecyl-N-[10-(p-methacryloylo xyphenoxycarbonyl)-decyl]ammonium bromide(DEMAB). In the solvolyses of N-carbobenzoxy-D- and L-phenylalanine p-nitrophenyl esters (D-NBP and L-NBP) by polymeric catalysts, copoly(MHis-DEMAB) exhibited not only increased catalytic activity but also enhanced enantioselectivity as the mole ${\%}$ of surfactant monomers in the copolymers increased. The polymeric catalysts showed noticeable enantioselective solvolyses toward D- and L-NBP of the substrates employed. As the reaction temperature was lowered for the solvolyses of D- and L-NBP with the catalyst polymer containing 3.5 mole ${\%}$ of MHis, the increased reaction rate and enhanced enantioselectivity were observed. The coaggregative systems of the polymer and monomeric surfactants were also investigated. In the case of coaggregate system consisted of 70 mole ${\%}$ of cetyldimethylethylammonium bromide with polymeric catalyst showed maximum enantioselective catalysis, viz., $k_{cat}(L)/k_{cat}(D)$ = 2.85. The catalyst polymers in the sonicated solvolytic solutions were confirmed to form large aggregate structure by electron microscopic observation.

• 설비공학논문집
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• 제12권3호
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• pp.251-257
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• 2000

District heating and cooling systems offer highly efficient energy utilization and maintenance by centralizing heat management. More pumping power, however, is required because the water has to travel long distance from heat source to the users. In the present study, a trace of drag reduction additives is added to the District Cooling system to achieve a significant drag reduction and save pumping power. Water-soluble polymers, surfactants, and environment-friendly degradable polymers are used as effective drag reducing additives. Time dependent percent drag reductions are compared for various additive solutions at 100 wppm concentration for different water velocity. Without as an anionic surfactant, copolymer was most effective in percent drag reduction. It is found that there exists an optimal condition when copolymer is mixed with SDS. An environment-friendly degradable polymer, xanthan gum, is found to be a significant drag reduction additive. Ice slurry systems, can give less pressure drops compared with chilled water system for certain condtions. Drag reduction additives were also effective for the ice slurry system.

• 대한화장품학회지
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• 제33권2호
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• pp.93-97
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• 2007

일반적으로 음이온 계면활성제는 효소의 disulfide bond를 분해시켜 효소의 활성이 없어진다. 따라서 특정한 캡슐에 효소를 포집하여 안정도를 증대시킨다. 본 연구에서는 polyethylene glycol (PEG), polypropylene glycol (PPG), 그리고 PEG-PPG-PEG block copolymer 등의 폴리올을 이용하여 papain 효소의 안정도를 증대시켰다. Energy dispersive spectroscopy (EDS)와 confocal laser scanning microscope (CLSM) 분석을 통하여 폴리올은 고분자층과 효소의 중간에 위치하며, 이들은 완충액으로 작용하여 효소의 안정도를 증대시키는 것으로 확인하였다. 또한, 이온 복합체를 이용하여 다층 캡슐을 제조하여 wash-off 형태의 세정제에 응용하였다. 세정제 내에서 계면활성제와 물은 효소캡슐의 표면에 분산되었으며, 캡슐의 중앙부분으로 서서히 침투되었다. 반면에 본 연구에서 사용된 sodium lauroyl sarcosinate와 polyguaternium-6는 물이 효소부분으로 침투하지 않는 것을 in vivo 시험을 통하여 확인하였다.

• Korean Chemical Engineering Research
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• 제61권4호
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• pp.570-575
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• 2023

Targeted anticancer drug delivery systems are needed to enhance therapeutic efficacy by selectively delivering drugs to tumor cells while minimizing off-target effects, improving treatment outcomes and reducing toxicity. In this study, a silica-based nanocarrier capable of targeting drug delivery to cancer cells was developed. First, silica nanoparticles were synthesized by the Stöber method using the surfactant cetyltrimethylammonium bromide (CTAB). Increasing the ratio of EtOH in the solvent produced uniformly spherical silica nanoparticles. Washing the nanoparticles removed unreacted residues, resulting in a non-toxic carrier for drug delivery in cells. Upon surface modification, the pH-responsive polymer, polyethyleneimine (PEI) exhibited slow doxorubicin release at pH 7.4 and accelerated release at pH 5.5. By exploiting this feature, we developed a system capable of targeted drug release in the acidic tumor microenvironment.