• 약학회지
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• 제57권6호
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• pp.442-447
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• 2013

The aim of the present study was to improve commercial twice-a-day Acebrophylline formulation to once-a-day new formulation to improve patient compliances. To develop the double-layered tablet, the sustained release layer was prepared using Eudragit$^{(R)}$ L100-55 and Carnauba wax. The sustained release layer has shown delayed release rates in pH 1.2 which comparable to that of performed in pH 6.8 buffer. In the comparative pharmacokinetic study with commercialized Surfolase$^{(R)}$, the present double-layered Acebrophylline tablet has shown similar pharmacokinetic parameters of AUC, $C_{max}$ and $T_{max}$ values.

• Asian-Australasian Journal of Animal Sciences
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• 제25권6호
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• pp.852-860
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• 2012

An Antarctic bacterial isolate displaying extracellular ${\alpha}$-galactosidic activity was named Paenibacillus sp. LX-20 based on 16S rRNA gene sequence analysis. Optimal activity for the LX-20 ${\alpha}$-galactosidase occurred at pH 6.0-6.5 and $45^{\circ}C$. The enzyme immobilized on the smart polymer Eudragit L-100 retained 70% of its original activity after incubation for 30 min at $50^{\circ}C$, while the free enzyme retained 58% of activity. The enzyme had relatively high specificity for ${\alpha}$-D-galactosides such as p-nitrophenyl-${\alpha}$-galactopyranoside, melibiose, raffinose and stachyose, and was resistant to some proteases such as trypsin, pancreatin and pronase. Enzyme activity was almost completely inhibited by $Ag^+$, $Hg^{2+}$, $Cu^{2+}$, and sodium dodecyl sulfate, but activity was not affected by ${\beta}$-mercaptoethanol or EDTA. LX-20 ${\alpha}$-galactosidase may be potentially useful as an additive for soybean processing in the feed industry.

• Bulletin of the Korean Chemical Society
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• 제32권4호
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• pp.1298-1302
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• 2011

This study describes the development of an electrochemical array immunochip for the detection of IgG. Interdigitated immunochip platforms were fabricated by sputtering gold on a glass wafer by using MEMS process and then were coated with Eudragit S100, an enteric polymer, forming an insulating layer over the working area of immunochips. The breakdown of the polymer layer was exemplified by the catalytic action of urease which, in the presence of urea, caused an alkaline pH change. This subsequently caused an increase of the double layer capacitance of the underlying electrode. Used in conjunction with a competitive immunoassay format, this allowed the ratio of initial to final electrode capacitance to be directly linked with the concentration of analyte, i.e. IgG. Responses to IgG could be detected at IgG concentration as low as $250\;ngmL^{-1}$ and showed good linearity up to IgG concentration as high as $20\;{\mu}gmL^{-1}$.

• 한국식품과학회지
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• 제34권5호
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• pp.856-861
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• 2002

유산균의 활용성을 증진시키기 위한 방안으로서 건식 Hybridization system을 이용하여 장용성 피복재로 유산균분말의 표면처리를 실시하였다. 전자현미경 관찰 결과 표면처리는 유산균의 표면을 매끄러운 구형의 모양으로 변화시켰으며 표면처리를 통한 분체복합화 과정에서 유산균의 활력은 유의적인 변화없이 유지되었다. 또한 유산균의 내염성은 처리여부에 따른 유의적 변화를 보이지 않음으로써 표면처리 과정 중 유산균 세포막의 물리적 손상은 일어나지 않은 것으로 판단된다. 표면처리된 유산균의 내산성은 처리전후에 차이를 나타내지 않았으나 이는 균주 자체의 높은 내산성에 기인한 것으로 판단된다. 표면처리 후의 유산균은 유의적으로 높은 열저항성을 보여 표면처리가 유산균의 내열성 향상을 위하여 활용될 수 있는 가능성을 나타냈다. 조사된 장용성 피복재 중 Sureteric은 다른 피복재에 비하여 우수한 표면 처리 효과를 보였으며 유산균분말의 표면처리를 위한 적합한 처리조건은 유산균의 초기입도가 $100{\sim}200\;{\mu}m$, 유산균:피복재의 혼합비율(w/w)은 9 : 1, 처리속도는 15,000 rpm, 3분이었다.