BCD를 섭취한 돼지의 부위별 콜레스테롤 함량

강환구,박병성,Kang, Hwan-Ku,Park, Byung-Sung 한국식품영양과학회 2007 한국식품영양과학회지 Vol.36 No.2

본 연구는 비육말기 돼지에서 베타사이클로덱스트린$\beta$-cyclodextrin의 급여가 돈육의 콜레스테롤 수준을 낮춘다는 것을 나타내고 있다. 120마리의 돼지에게 0, 5, 7, 10%의 $\beta$-cyclodextrin를 함유하는 사료를 35일 간 급여하였다. 혈액 총지질, 중성지방 및 총 콜레스테롤 함량은 $\beta$-cyclodextrin첨가구가 대조구에 비해서 낮게 나타났으며 처리구간 통계적인 유의차가 나타났다(p<0.05). 혈액 100 mL 당 지질은 대조구와 비교할 때 $\beta$-cyclodextrin 5.0%, $\beta$-cyclodextrin 7.0% 및 $\beta$-cyclodextrin 10.0% 첨가구에서 각각 63.22 mg, 73.98 mg, 82.12 mg의 유의적인 감소를 나타냈으며, 중성지방 56.24 mg, 55.48 mg, 60.02 mg, 총콜레스테롤 25.05 mg, 27.17 mg, 30.19 mg의 유의성 있는 감소경향을 보였다(p<0.05). 총스테로이드의 배설은 $\beta$-cyclodextrin 첨가수준이 증가할수록 대조구에 비해서 유의적으로 높게 나타났다(p<0.05). 돼지고기의 부위별, 등지방, 삼겹살, 등심 및 햄의 콜레스테롤 함량은 대조구에 비해서 $\beta$-cyclodextrin 첨가수준이 높아질수록 유의적인 감소경향을 나타냈다(p<0.05). 돼지고기의 콜레스테롤 함량 감소율은 $\beta$-cyclodextrin 첨가구가 대조구와 비교할 때 15.31% 이상의 높은 감소율을 나타냈다(p<0.05). 본 연구 결과는 비육말기 돼지사료 내 $\beta$-cyclodextrin를 혼합 급여하여서 콜레스테롤 함량이 낮아진 새로운 기능성 돈육을 생산할 수 있음을 시사해준다. This study demonstrates that pork cholesterol levels are reduced in fattening stage swine fed $\beta-cyclodextrin({\beta}-cyclodextrin)$. The study subjects were 120 swine fed their respective chow diets containing 0, 5, 7, or 10% $\beta$-cyclodextrin for 35 consecutive days. Plasma total lipids, triglyceride and total cholesterol of the $\beta$-cyclodextrin treated group were significantly lower than those of the control group (p<0.05). The levels of plasma lipid were significantly decreased by 63.22 mg, 73.98 mg, and 82.12 mg in the fattening swine group fed $\beta$-cyclodextrin at 5%, 7%, and 10%, respectively, compared to those in the control group (p<0.05). When 5, 7, and 10% $\beta$-cyclodextrin was administered to fattening swine, the triacylglyceride levels were decreased by 56.24 mg, 55.48 mg, and 60.02 mg, and total cholesterol concentration was reduced by 25.05 mg, 27.17 mg, and 30.19 mg, respectively, compared to those in the control group (p<0.05). Excretion of total steroid significantly (p<0.05) increased with the increasing amount of $\beta$-cyclodextrin supplementation. The cholesterol levels of swine back fat, belly, loin, and ham were significantly decreased with increasing $\beta$-cyclodextrin supplementation (p<0.05). The pork cholesterol was significantly (p<0.05) reduced by 15.31% in the $\beta$-cyclodextrin treated group, compared to that of the control group. These results suggest that feeding $\beta$-cyclodextrin to fattening swine may produce novel functional pork with low cholesterol levels.

난황의 콜레스테롤 제거에 사용한 $\beta$-Cyclodextrin의 재활용

유익종,최성유,박우문,전기홍 한국축산식품학회 2000 한국축산식품학회지 Vol.20 No.1

The method used to remove cholesterol from egg by using $beta$-cyclodextrin was relatively stable and efficient. The aim of this study was to cost down by recycling $\beta$-cyclodextrin used to remove cholesterol from egg yolk because $\beta$-cyclodextrin was expensive. The solvents used to separate $\beta$-cyclodextrin from $\beta$-cyclodextrin complex containing egg yolk cholesterol were butanol, chloroform, ether, hexane, methanol, 2-propanol and their mixture. The ratio of solvent and complex varied from 2 : 1 to 10 : 1. The condition of mixing time and temperature varied from 30 to 60$^{\circ}C$ and from 10 minutes to 3 hours to remove cholesterol from $\beta$-cyclodextrin complex. When the ratio of choloroform and methanol was 1 : 1, the removal efficiency of cholesterol was 98.8%. The efficiency of cholesterol removal was improved when the ratio of solvent : complex increased to 4 : 1. When mixing time and temperature was up to for 1hr, at 50$^{\circ}C$ respectively, the efficiency of cholesterol removal improved to 99%. It concluded that the efficiency of cholesterol removal of 50% renewed one contained $\beta$-cyclodextrin were 81.1% while the cholesterol removal efficiency of 100% renewed $\beta$-cyclodextrin was 24% if cholesterol removal efficiency of new $\beta$-cyclodextrin were 100%.

Inhibitory Effects of β-Cyclodextrin-Helenalin Complexes on H-TERT Gene Expression in the T47D Breast Cancer Cell Line - Results of Real Time Quantitative PCR

Ghasemali, Samaneh,Nejati-Koshki, Kazem,Akbarzadeh, Abolfazl,Tafsiri, Elham,Zarghami, Nosratollah,Rahmati-Yamchi, Mohamad,Alizadeh, Effat,Barkhordari, Amin,Tozihi, Majid,Kordi, Shirafkan Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.11

Background: Nowadays, the encapsulation of cytotoxic chemotherapeutic agents is attracting interest as a method for drug delivery. We hypothesized that the efficiency of helenalin might be maximized by encapsulation in ${\beta}$-cyclodextrin nanoparticles. Helenalin, with a hydrophobic structure obtained from flowers of Arnica chamissonis and Arnica Montana, has anti-cancer and anti-inflammatory activity but low water solubility and bioavailability. ${\beta}$-Cyclodextrin (${\beta}$-CD) is a cyclic oligosaccharide comprising seven D-glucopyranoside units, linked through 1,4-glycosidic bonds. Materials and Methods: To test our hypothesis, we prepared ${\beta}$-cyclodextrin-helenalin complexes to determine their inhibitory effects on telomerase gene expression by real-time polymerase chain reaction (q-PCR) and cytotoxic effects by colorimetric cell viability (MTT) assay. Results: MTT assay showed that not only ${\beta}$-cyclodextrin has no cytotoxic effect on its own but also it demonstrated that ${\beta}$-cyclodextrin-helenalin complexes inhibited the growth of the T47D breast cancer cell line in a time and dose-dependent manner. Our q-PCR results showed that the expression of telomerase gene was effectively reduced as the concentration of ${\beta}$-cyclodextrin-helenalin complexes increased. Conclusions: ${\beta}$-Cyclodextrin-helenalin complexes exerted cytotoxic effects on T47D cells through down-regulation of telomerase expression and by enhancing Helenalin uptake by cells. Therefore, ${\beta}$-cyclodextrin could be superior carrier for this kind of hydrophobic agent.

Cyanuric Chloride 잔기를 갖는 ${\beta}-Cyclodextrin$ 유도체의 합성과 섬유 방향가공에의 응용

고재훈,박윤철,김진우,김영호,Ko, Jae-Hoon,Park, Yoon-Cheol,Kim, Jin-Woo,Kim, Young-Ho 한국섬유공학회 2007 한국섬유공학회지 Vol.44 No.4

[ ${\beta}$ ]-Cyclodextrin derivative containing cyanuric chloride moiety (${\beta}CD-CC$) was synthesized by a reaction of ${\beta}-cyclodextrin\;({\beta}CD-CC)$ with cyanuric chloride in alkaline condition. FT-IR and UV spectra along with the results of elemental analysis indicated that cyanuric chloride was bound to ${\beta}CD$. Remaining monochlorotriazine group in ${\beta}CD-CC$ was expected to be used as a reactive site for cellulosic fibers. The ${\beta}CD-CC$ could be used as a host material for inclusion complex of various guest molecules. As an example, vanillin, a flavoring agent in foods and others, was included in the ${\beta}CD-CC$ to make a perfume inclusion complex. UV analysis showed that the vanillin-included complex of ${\beta}CD-CC$ released vanillin more slowly than vanillin itself, which reveals that it can be used as a feasible fragrant finishing agent for textiles.

돼지고기의 콜레스테롤 함량 감소에 관한 β-Cyclodextrin의 급여효과

박병성,Park, Byung-Sung 한국식품영양과학회 2006 한국식품영양과학회지 Vol.35 No.3

The main objective of the present study was to determine the effect of dietary ${\beta}-cyclodextrin\;({\beta}CD)$ on reducing the cholesterol content of pork. Twelve swine of 50 kg body weight were randomly distributed into four groups of three heads each and fed experimental diets for 9 weeks until they reached a market weight of 110 kg. They were assigned to the four experimental diets containing 0% (control), 1.5%, 3.0% or 5.0% pure ${\beta}CD$. Daily feed intake, body weight gain and feed efficiency were not significantly different between any of the four group. The plasma total lipid, triacylglycerol and total cholesterol content of the swine in the three ${\beta}CD$-fed groups were significantly (p<0.05) decreased when compared to those in the control group, and were significantly (p<0.05) reduced by 21.80%,55.58% and 27.69%, respectively, in the swine fed on 5% ${\beta}CD$. The cholesterol content of pork belly (mg/100g) was significantly (p<0.05) decreased by 5.33 mg, 12.70 mg and 15.23 mg in the swine maintained on 1.5%, 3.0% and 5.0% ${\beta}CD$, respectively. The cholesterol content of pork belly, when expressed as the rate of reduced cholesterol, was significantly (p<0.05) decreased by 6.44%, 15.36% and 18.42% in groups of 1.5%, 3.0% and 5.0% ${\beta}CD$, respectively, when compared to that of the control group. These results suggest that dietary ${\beta}CD$ may be classified as dietary fiber which can modulate cholesterol metabolism in swine. 본 연구의 주목적은 돼지고기의 콜레스테롤 함량 감소에 관한 사료 내 ${\beta}CD$의 급여 효과를 조사하는 것이었다. 생체중 50 kg의 3원교잡종 거세 수퇘지 12마리를 이용하여서 4처리구 3반복으로 완전임의배치한 후, 시판체중인 110 kg 도달시까지 약 9주 동안 실험사료를 급여하였다. 일일 사료섭취량, 일일 증체량 및 사료효율은 ${\beta}CD$를 첨가하지 않은 대조구와 비교할 때, ${\beta}CD$ 1.5%, 3.0% 및 5.0% 첨가구의 각 처리구간 통계적인 유의차가 나타나지 않았다. 혈액 총지질, 중성지방 및 총콜레스테롤 함량은 대조구와 비교할 때 ${\beta}CD$ 첨가구가 유의적으로 낮아졌으며, 특히 ${\beta}CD$ 5.0% 첨가구에서 각각의 감소율은 21.80%, 55.58% 및 27.69%로서 가장 높게 나타났다(p<0.05). 돼지고기 삼겹살의 콜레스테롤 함량은 대조구와 비교할 때 ${\beta}CD$ 1.5%, 3.0% 및 5.0% 첨가구에서 각각 5.33mg, 12.70mg및 15.23 mg의 유의적인 감소를 나타났으며, 특히 이 값을 콜레스테롤의 감소율로서 나타냈을 때 각각 6.44%, 15.36%, 18.42%로서 유의적인 차이를 나타냈다(p<0.05). 이 결과는 돼지에서 ${\beta}CD$첨가급여가 콜레스테롤 대사를 조절할 수 있는 식이섬유로서 사용될 수 있음을 시사해준다.

$\beta$-시클로덱스트린($\beta$-Cyclodextrin)의 결합 특성과 벤젠의 생물학적 분해에의 적용에 대한 연구

최종규,손현석,조경덕 한국환경보건학회 2002 한국환경보건학회지 Vol.28 No.5

Recently, surfactants were frequently used in order to desorb the hydrophobic organic compounds (HOCs) from soil and to enhance the bioavailability. Among them, -cyclodextrin ($\beta$-CD) is one of those. This study was performed to investigate the binding characteristics between benzene and $\beta$-CD and to examine the bioavailability of benzene. First, we investigated binding characteristics between benzene and $\beta$-CD in water and water/soil system. Then, we examined the effect of $\beta$-CD on the biodegradation of benzene in water and water/soil system. Experimental results on the binding characteristics showed that $\beta$-CD resulted in an efficient complex formation with benzene. As -CD concentration increased, the benzene concentration complexed with $\beta$-CD rapidly increased to 30-40% initial benzene added, and reached the equilibrium. We also investigated the effect of $\beta$-CD on the desorption of benzene from soil in the water/soil system. As $\beta$-CD concentration increased, benzene concentration desorbed into water increased up to 90%. How-ever, in its application to biodegradation of benzene in water and water/soil system, the biodegradation rate of benzene did not improved in the presence of $\beta$-CD compared with in the absense of $\beta$-CD. This result indicated that $\beta$-CD was more preferentially used as a carbon source than benzene. Therefore, for remediation of benzene contaminated soils, $\beta$-CD can be used as a surfactant to desert benzene from soil, and then ex-situ chemical treatment can be applied for the remediation.

${\beta}$-cyclodextrin 및 가교제 처리에 의한 면직물의 방향가공

허종태,이경주,박병기,정용식,Huh, Jong-Tea,Lee, Kyung-Ju,Pak, Pyong-Ki,Chung, Yong-Sik 한국섬유공학회 2007 한국섬유공학회지 Vol.44 No.2

[ ${\beta}$ ]-cyclodextrin having an inclusion property was applied to perfumed finishing of textile goods. ${\beta}$-cyclodextrin was treated on the cotton fabric with polycarboxylic acid such as citric acid and butanetetracarboxylic acid. The fact that ${\beta}$-cyclodextrin is covalently bound to cotton fabric with butanetetracarboxylic acid was confirmed by IR spectrum, TGA thermogram, and dyeing with basic dye. In case of citric acid, the result was not satisfactory, which was supported by laundering durability experiment. When cotton fabric treated with crosslinking agent and ${\beta}$-cyclodextrin was compared with cotton fabric treated with only crosslinking agent, they gave similar values in dry wrinkle recovery angle. Perfumed finishing with ${\beta}$-cyclodextrin including perfume was possible.

Comparison of Inhibitory Effects of 17-AAG Nanoparticles and Free 17-AAG on HSP90 Gene Expression in Breast Cancer

Ghalhar, Masoud Gandomkar,Akbarzadeh, Abolfazl,Rahmati, Mohammad,Mellatyar, Hassan,Dariushnejad, Hassan,Zarghami, Nosratallah,Barkhordari, Amin Asian Pacific Journal of Cancer Prevention 2014 Asian Pacific journal of cancer prevention Vol.15 No.17

Background: HSP90 may be overexpressed in cancer cells which are greatly dependent on Hsp90 function. Geldanamycin derivative 17 allylamino-17-demethoxygeldanamycin (17-AAG) inhibits the function and expression of HSP90. 17-AAG has poor water-solubility which is a potential problem for clinical practice. In this study for improving the stability and solubility of molecules in drug delivery systems we used a ${\beta}$-cyclodextrin-17AAG complex. Materials and Methods: To assess cytotoxic effects of ${\beta}$-cyclodextrin-17AAG complexes and free 17AAG, colorimetric cell viability (MTT) assays were performed. Cells were treated with equal concentrations of ${\beta}$-cyclodextrin- 17AAG complex and free 17AAG and Hsp90 gene expression levels in the two groups was compared by real-time PCR. Results: MTT assay confirmed that ${\beta}$-cyclodextrin- 17AAG complex enhanced 17AAG cytotoxicity and drug delivery in T47D breast cancer cells. The level of Hsp90 gene expression in cells treated with ${\beta}$-cyclodextrin- 17AAG complex was lower than that of cells treated with free 17AAG (P=0.001). Conclusions: The results demonstrated that ${\beta}$-cyclodextrin- 17AAG complexes are more effective than free 17AAG in down-regulating HSP90 expression due to enhanced ${\beta}$-cyclodextrin-17AAG uptake by cells. Therefore, ${\beta}$-cyclodextrin could be superior carrier for this kind of hydrophobic agent.

NMR Spectroscopic Analysis on the Chiral Recognition of Noradrenaline by β-Cyclodextrin ( β-CD) and Carboxymethyl- β-cyclodextrin (CM- β-CD)

Lee, Sang-Hoo,Yi, Dong-Heui,Jung, Seung-Ho Korean Chemical Society 2004 Bulletin of the Korean Chemical Society Vol.25 No.2

${\beta}$-CD and CM- ${\beta}$-CD as chiral NMR shift agents were used to resolve the enantiomers of noradrenaline (NA). The stoichiometry of each complex formed between the CDs and the enantiomers of NA was found to be 1 : 1 through the continuous variation plots. The binding constants (K) of the complexes were determined from $^1H$ NMR titration curves. This result indicated that both ${\beta}$-CD and CM- ${\beta}$-CD formed the complexes with the S(+)-NA more preferentially than its R(-)-enantiomer. The K values for the complexes with ${\beta}$-CD ($K_{S(+)}$ = 537 $M^{-1}$ and $K_{R(-)}$ = 516 $M^{-1}$ was larger than those with CM- ${\beta}$-CD ($K_{S(+)}$ = 435 $M^{-1}$ and $K_{R(-)}$ = 313 $M^{-1}$), however, enantioselectivity (${\alpha}$) of S(+)- and R(-)-NA to CM- ${\beta}$-CD ( ${\alpha}$ = 1.38) was larger than that to ${\beta}$-CD ( ${\alpha}$ = 1.04), indicating that CM- ${\beta}$-CD was the better chiral NMR solvating agents for the recognition of the enantiomers of NA. Two dimensional rotating frame nuclear Overhauser enhancement spectroscopy (ROESY) experiments were also performed to explain the binding properties in terms of spatial fitting of the NA molecule into the macrocyclic cavities.

${\beta}$-시클로덱스트린과의 포접에의한 디플로페낙나트륨의 용해도 및 생체흡수율 증가

이경태,김종환,김주일,김승조,서희경,서성훈,Lee, Kyung-Tae,Kim, Jong-Hwan,Kim, Joo-Il,Kim, Seung-Jo,Seo, Hee-Kyoung,Seo, Seong-Hoon 한국약제학회 1996 Journal of Pharmaceutical Investigation Vol.26 No.3

Inclusion complexes of diclofenac sodium with ${\beta}-cyclodextrin$ were prepared in aqueous solution, alkaline solution and solid phase. The interaction of diclofenac sodium with ${\beta}-cyclodextrin$ in pH 9.0 alkaline solution was evaluated by the solubility method and the instrumental analysis such as thermal analysis, infrared spectroscopy, X-ray diffractometry. The solubility of diclofenac sodium was increased linearly with the increase in the concentration of ${\beta}-cyclodextrin$up to 0.15 mol and showed that the aqueous solubility rate of diclofenac sodium was significantly increased by complex with ${\beta}-cyclodextrin$. The optimum composition of this complex was one molecule of ${\beta}-cyclodextrin$ included 1.59 molecular weight of diclofenac sodium as a guest molecule. The pharmacokinetic parameters of the diclofenac sodium and the complex with ${\beta}-cyclodextrin$ were studied in rats by oral route. $T_{max}$ between drug alone and inclusion complex showed significant difference to be 120 minute and 20 minute respectively. Both of $C_{max}$ and AUC of inclusion complex was about 40% higher than drug alone. It is estimated from the data in this study that complexation of diclofenac sodium with ${\beta}-cyclodextrin$ increased the absorption rate and improved the bioavalability of the diclofenac sodium by the formation of a water-soluble complexes.