• Archives of Pharmacal Research
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• 제26권2호
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• pp.120-123
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• 2003

A method for the determination of terbutaline enantiomers in human urine by capillary elctrophoresis has been developed. Optimum resolution was achieved using 50 mM phosphate buffer, pH 2.5, containing 15 mM of hydroxypropyl-$\beta$-cyclodextrin as a chiral selector. Urine samples were prepared by solid-phase extraction with Sep-pak silica, followed by CE. The assay was linear between 2-250 ng/mL (R = 0.9998 for (S)-(+)-terbutaline and R = 0.9999 for (R)-(-)-terbutaline) and detection limit was 0.8 ng/mL. The intra-day variation ranged between 6.3 and 14.5% in relation to the measured concentration and the inter-day variation was 8.2-20.1%. It has been applied to the determination of (S)-(+)-terbutaline and (R)-(-)-terbutaline in urine from healthy volunteer dosed with racemic terbutaline sulfate.

• Journal of Electrochemical Science and Technology
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• 제8권1호
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• pp.25-34
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• 2017

Concurrent electrocatalysis and sensing of hydrazine, sulfite ions, and nitrite ions in a mixture were studied using electrodes modified by electrodeposited Au nanostructures (NSs). The ${\beta}$-cyclodextrin-mixed silicate sol-gel composite was drop-casted on the electrode surface and nucleation guided by ${\beta}$-cyclodextrin occurred, followed by the electrodeposition of Au NSs. The additive, ${\beta}$-cyclodextrin, played an evident role as a structure-directing agent; thus, small raspberry-like Au NSs were obtained. The modified electrodes were characterized by surface characterization techniques and electrochemical methods. The Au NSs-modified electrodes effciently electrocatalyzed the oxidation of toxic molecules such as hydrazine and sulfite and nitrite ions even in the absence of any other electron transfer mediator or enzyme immobilization. Well-resolved oxidation peaks along with decreased overpotentials were noticed during the electrooxidation process. The fabricated Au nanostructured electrode clearly distinguished the electrooxidation peaks of each of the three analytes from their mixture.

• Journal of Dairy Science and Biotechnology
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• 제25권1호
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• pp.9-13
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• 2007

The present study was carried out to examine the effect of crosslinked ${\beta}$-cyclodextrin(${\beta}$-CD) made by adipic acid on cholesterol removal rate and find the structural change after recycling on SEM observation. The size reduction and morphological changes were found during the recycling process and the profound changes were observed at 8th time reuse. After cholesterol removal in milk, the used crosslinked ${\beta}$-CD was washed for cholesterol dissociation and reused. In recycling study, the cholesterol removal rate at first trial was 92.5% in milk, which was mostly same as that using new crosslinked ${\beta}$-CD(92.4%). With repeated 10th reuse of crosslinked ${\beta}$-CD resulted in 81.4% of cholesterol removal in milk. Similar trend was found in cream and cholesterol removal was 91.5% at 1st trial and 83.4% at 10th trial. In both milk and cream samples, the removal rate at 1st reuse was not significantly different from that at 6th reuse(p>0.05). The present study indicated that crosslinked ${\beta}$-CD made by adipic acid resulted in the effective recycling efficiency, especially up to 6th reuse and morphological modifications were not distinguishable up to 8th reuse.

• Journal of Pharmaceutical Investigation
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• 제20권1호
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• pp.13-18
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• 1990

Hydrocortisone (HC) sustained-release suppositories were prepared by using a solid matrix of methacrylic acid-methacrylic acid methyl ester copolymer $(Eudragit\;L_{100}^{R}:\;EL)$ as a poorly water soluble carrier and polyethylene glycole 1540 (PEG) as an water soluble carrier. HC release rate was controlled by complexation with ${\beta}-cyclodextrin$ $({\beta}-CyD)$ which was confirmed by X-ray diffractometry, IR-spectroscopy and differential scanning calorimetry. Release rate of HC from the EL-PEG matrix suppositories decreased with increase of EL contents. The release rale from $HC-{\beta}-CyD$ complex decreased in the following order: $HC-{\beta}-CyD/PEG$ > HC/PEG > $HC-{\beta}-CyD/EL_{10%}-PEG$ > $HC/EL_{10%}-PEG$ > $HC-{\beta}-CyD/EL_{15%}-PEG$ > $HC/EL_{15%}-PEG$ > $HC-{\beta}-CyD/EL_{20%}-PEG$ > $HC/EL_{20%}-PEG$. The crystallinity of HC in polymer matrix was identified using X-ray diffractometer and the surface of matrix suppositories after release test was examined by scanning electron microscopy. The sustained release of HC from these matrix suppositories was attributed to the network structure of EL.

• 한국음향학회지
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• 제36권6호
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• pp.387-393
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• 2017

베타 사이클로덱스트린(${\beta}$-Cyclodextrin, ${\beta}$-CD)(호스트)과 벤조산 유도체(게스트)의 수용액에 대하여 $25^{\circ}C$, 광대역 주파수영역(0.2 MHz ~ 50 MHz)에서 초음파 흡수계수를 측정하여 호스트와 게스트의 복합체 형성반응의 속도론적 연구를 행하였다. 특히 본 연구에서는 1 MHz이하의 초음파 흡수측정이 중요하다. ${\beta}$-CD와 벤조산 유도체의 상호작용에 의한 초음파 완화는 수 MHz영역에서 단일 완화현상의 전형적인 스펙트럼을 보였다. 단일완화현상의 원인은 ${\beta}$-CD와 벤조산 유도체의 복합체 형성반응에 의한 화학평행의 혼란상태에 의한것으로 해석하였다. 게스트 농도에 따른 완화주파수의 의존성으로부터 붕괴 속도상수($k_b=7.48{\times}10^6M^{-1}s^{-1}$), 평형상수($K=68.6M^{-1}$)를 결정하였다. 그리고 파장당 최대흡수치의 의존성으로부터 반응에 의한 표준체적변화(${\Delta}V=10.6{\times}10^{-6}m^3mol^{-1}$)를 구하였다. 또한 게스트 분자의 소수성 그룹이 복합체의 안정성에 중요한 역할을 하는 것을 알았다.

• Journal of Pharmaceutical Investigation
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• 제25권3호
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• pp.227-237
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• 1995

Omeprazole(OMP) complexes such as inclusion complexes of OMP with $hydroxypropyl-{\beta}-cyclodextrin$(HPCD) and ${\beta}-cyclodextrin({\beta}-CD)$, OMP-cholestyramine(CHL) and OMP-ethylenediamine(OMP-ED) were prepared, respectively. The partition coefficients in Witepsol H-15 /pH 7.4 phosphate buffer solution of OMP complexes$(OMP-HPCD;\;3.69{\pm}0.26,\;OMP-{\beta}-CD;\;4.08{\pm}0.21,\;OMP-CHL;\;4.36{\pm}0.25\;and\;omeprazole\;sodium(OMP-Na);\;3.64{\pm}0.37)$ were higher than that of OMP $(2.66{\pm}0.47)$. OMP was not completely dissolved until even 3 hrs, but all the OMP complexes studied were released about 100% in 20 min. The rectal suppositories containing OMP or each above OMP complex were prepared using Witepsol H-15 base, and their dissolution and stability were examined, and pharmacokinetic study were investigated after their rectal administrations to the rabbits. While the suppository containing OMP was released only less than 60% in 150 min, $OMP-{\beta}-CD$, OMP-CHL, OMP-Na and OMP-ED suppositories were all released about 65% in 20 min. Especially, OMP-HPCD suppository released OMP about 70% in 10 min. All the additives such as sodium laurylsulfate, eglumine, arginine and PVP increased drug release from OMP-HPCD suppository to some extent. The decomposition rate constants of OMP in the suppositories were $9.117{\times}10^{-3}\;day^{-l}$ for OMP suppository, $2.121{\times}10^{-2}$ for OMP-HPCD, $1.607{\times}10^{-2}$ for $OMP-{\beta}-CD$, $9.26{\times}10^{-3}$ for OMP-Na, $6.769{\times}10^{-3}$ for OMP-CHL and $5.58{\times}10^{-3}\;day^{-l}$ for OMP-ED suppository, respectively. Additives such as arginine, eglumine and ED had some stabilizing effect for OMP-HPCD, OMP-CHL and OMP-Na suppositories, respectively. After 6 month-storage at $30^{\circ}C$, 75% RH, OMP-CHL suppository was most stable. The values of Tmax for OMP-HPCD and OMP-Na suppositories were $11.7{\pm}2.36\;and\;11.4{\pm}2.56\;min$, respectively. The values of Cmax for OMP-HPCD and OMP-CHL suppository were $2.31\;{\mu}g/ml\;(p<0.01)\;and\;1.89\;{\mu}g/ml\;p<0.01)$, respectively. The values of AUC for OMP and $OMP-{\beta}-CD$ suppository were $61.9{\pm}25.79\;and\;68.6{\pm}29.48\;{\mu}g\;{\cdot}\;min/ml$, and the corresponding values for OMP-HPCD and OMP-CHL were $106.1{\pm}43.16\;(p<0.05)\;and\;127.3{\pm}42.52\;{\mu}g\;{\cdot}\;min/ml(p<0.01)$, respectively. The above results indicate the OMP-HPCD and OMP-CHL suppositories have the excellent bioavailabilties in vivo study.

• 약학회지
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• 제42권1호
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• pp.59-69
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• 1998

To increase the solubility of quercetin, which is a practically insoluble flavonoid of Ginkgo biloba leaf, the effects of nonaqueous vehicles. Their cosolvents, water-sol uble polymers and modified cyclodextrins (CDs) were observed. Polyethylene glycols, diethyleneglycol monoethyl ether, and their cosolvents with water showed a good solvency toward quercetin. Also the aqueous solutions of povidone, copolyvidone and Cremophor RH 40 was effective in solubilizing quercetin. Complex formation of quercetin with ${\beta}$-cyclodextrin (${\beta}$-CD), dimethyl-${\beta}$-cyclodextiin (DMCD), 2-hydroxypropyl-${\beta}$-cyclodextrin (HPCD) and ${\beta}$-cyclodextrin sulfobutyl ether (SBCD) in water was investigated by solubility method at $37^{\circ}C$. The addition of CDs in water markedly increased the solubility of quercetin with increasing the concentration. AL type phase solubility diagrams were obtained with CDs studied. Solubilizaton efficiency by CDs was in the order of SBCD >> DMCD > HPCD > ${\beta}$-CD. The dissolution rates of quercetin from solid dispersions with copolyvidone, povidone and HPCD were much faster than those of drug alone and corresponding physical mixtures, and exceeded the equilibrium solubility (3.03${\pm}1.72{\mu}$g/ml). The permeation of quercetin through duodenal mucosa did not occur even in the presence of enhancers such as bile salts, but the permeation was observed when the mucus layer was scraped off. This was due to the fact that quercetin had a strong binding to mucin ($58.5{\mu}$g/mg mucin). However rutin was permeable to the duodenal mucosa. The addition of enhancer significantly increased the permeation of rutin in the order of sodium glycocholate.

• 분석과학
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• 제11권3호
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• pp.179-188
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• 1998

15여종의 페놀 유도체들의 용량인자는 씨클로덱스트린의 농도, 이동상 중 유기용매의 종류와 농도, 온도 등에 영향을 받았다. 페놀유도체들의 머무름은 ${\alpha}$-, ${\beta}$-씨클로덱스트린과의 내포착물 형성에 기인하며, ${\alpha}$-씨클로덱스트린보다 ${\beta}$-씨클로덱스트린을 첨가하였을 때가 내포착물 형성이 훨씬 효과적이었다. 또한 시료의 머무름에 영향을 주는, MeOH, MeCN, THF 유기용매 중 메탄올 용액에서 내포착물 형성효과가 가장 강하고, 메탄올 용액의 농도가 증가할수록 k'값이 감소하였다. $[CD]_T$에 대한 용량인자를 구하여 내포착물의 해리상수, $K_D$값을 측정하고, $pK_D$를 메탄올농도에 대해 도시한 직선의 절편으로부터 100% 물에서의 $K_D$값을 구하였다. 한편, 분리인자, ${\alpha}$는 씨클로덱스트린의 농도뿐만 아니라 $K_D$값 등에 상당히 영향을 받기 때문에, 씨클로덱스트린을 이동상에 첨가하고, 이동상 중 유기용매의 농도와 컬럼온도를 조절하여 페놀 유도체의 몇 가지 이성질체들을 이상적으로 분리하였다.

• 한국식품과학회지
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• 제31권6호
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• pp.1477-1483
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• 1999

양파의 향기성분을 보존 또는 제거할 목적으로 양파냄새를 masking하거나 제거하는 물질을 양파즙에 처리하여 관능검사를 실시하였고, pyruvate와 thiosulfinate를 측정하였으며 Solid Phase Micro Extraction(SPME)/GC법을 이용하여 휘발성 향기성분의 변화를 조사하였다. 생양파즙의 주요 향기성분은 dipropyl tetrasulfide, 1-propenyl propyl trisulfide, methyl propyl trisulfide, dipropyl trisulfide 등이었다. 다시마, 미역, 김, 규조토를 첨가한 양파즙의 휘발성 향기성분은 대조군과 비교하였을 때 모든 향기성분이 다소 감소하는 경향이었으나 활성탄과 ${\beta}-cyclodextrin$ 첨가군은 거의 모든 향기성분이 제거되었다. 여러 가지 첨가물의 농도를 달리하여 양파즙에 첨가하여 관능검사를 실시한 결과 양파 냄새는 감소하였으며 p<0.05 수준에서 유의적으로 차이가 나타났다. 해조류를 첨가한 군의 pyruvate와 thiosulfinate 함량은 대조군과 차이가 없었으나 활성탄을 첨가한 양파즙의 경우, 그 함량이 크게 감소하였다. 이상의 결과, 다시마, 미역, 김 등의 해조류 처리군은 양파의 향기성분과 매운맛 성분을 보존하면서 관능적으로 양파냄새를 masking하는 효과를 나타내었고, ${\beta}-cyclodextrin$과 활성탄은 양파에 존재하는 많은 휘발성 향기성분과 복합물을 형성하거나 홉착하여 양파냄새를 제거한 것으로 사료되어 진다.

• Reproductive and Developmental Biology
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• 제35권3호
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• pp.265-271
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• 2011

This study was undertaken to find out the effect of methyl-beta-cyclodextrin (MBCD) on cold shock and membrane cholesterol quantity of sperm during the freezing process in miniature pigs. For this study, semen ejaculated from PWG M-type miniature pig was diluted that freezing solution (with egg yolk group) and m-Modena B (without egg yolk group) treated with 0, 1, 5, 10 and 20 mM MBCD before freezing process. The diluted semen was monitored sperm ability at room temperature, after cooled until $5^{\circ}C$ and after forzen-thawed for cold shock test of spermatozoa. Also, membrane cholesterol of sperm was extracted by folch solution at the same time sperm ability was assessed for viability and acrosomal status. The membrane cholesterol quantity was measured by thin-layer chromatography (TLC) method. The result, viability and acrosome integrity in semen diluted without egg yolk groups were decreased at all temperature range by increasing of MBCD concentration. In particular, sperm of egg yolk group was showed that significantly higher viability and lower acrosome damage when treated with 5 mM MBCD (p<0.05). The results of TLC experiment, cholesterol amounts were increased with MBCD cocentration in egg yolk, and decreased with MBCD concentration in m-Modena B. In cryopreservation efficiency, there was no significant difference at viability, and acrosomal state of sperm in 5 mM MBCD concentration was significantly lower in acrosome damage than other groups (p<0.05). Therefore, the addition MBCD in egg yolk was protected spermatozoa from cold shock injury. This protective effect of MBCD may be due to addition of sperm membrane cholesterol.