본 연구에서는 가교제인 붕산과 아크릴 수지 바인더에 삼인산(3 인산), 피트산(6 인산) 또는 폴 리인산암모늄(10 인산)을 혼합하여 인계 난연 코팅액을 제조하였다. 제조된 인계 난연 코팅액을 부직포에 각각 코팅하여 높은 난연 효과를 얻었다. 이렇게 제조된 난연성 부직포를 연기밀도기준시험(ASTM E662), 산소한계지수기준시험(ISO E622), 수직연소기준시험(UL 94)을 이용하여 평가하였다. 그들의 난연 효과는 phosphate 그룹의 수에 의해 영향을 받았으며, 천연 또는 합성 바인더 수지에 관계없이 그 효과는 ammonium polyphosphate > phytic acid > triphosphate의 순서로 나타났다. 천연 탄화수소 화합물도 바인더 수지의 난연성을 결정하기 위해 조사되었다. 그 결과 천연 탄화수소 바인 더 수지가 난연성 부직포 제조에 사용될 수 있음을 보여주었다.

본 연구에서는 싸이크론 헥산에서 PVC와 트리에틸디아민 (TEDA), 1,4-디메틸피페라진 (DMP) 및 1,4-비스(이미다졸-1-일메틸)벤젠을 각각 치환반응시켜서3가지 형태의 PVC 멤브레인, AEM-1, AEM-2, and AEM-3를 제조하였다. AEM-1, AEM-2, and AEM-3멤브레인의 성공적인 제조 여부를 이온전도도(S/cm), 물함수율 (%), 접촉각, 이온교환능력 (meq/g), 열분석, SEM 및 XPS 분석 통하여 확인하였다. 또한, 제조된 가교 음이온 PVC멤브레인을 사용하여 유기전해질에서 전기화학 캐퍼 시터 실험을 수행한 결과, 제조된 AEM-1, AEM-2 AEM-3 멤브레인의 경우 유기전해질에서 충/방전 실험결과 매우 안정적임을 확인 할 수 있었다. 이러한 결과로 치환반응 후에 용매 캐시팅법으로 제조 된 PVC기반 멤브레인 (AEM-1, AEM-2, 및 AEM-3)의 경우 유기전기화학캐퍼시터 (슈퍼캐퍼시터)용 분리막으로 사용될 수 있다.

본 논문에서는 다기능성 마스크 팩의 제조 및 이를 이용한 마스크 팩 제조 및 평가에 대한 것이다. 여기서 다 기능성이란 폴리인산에 의한 원적외선 효과, 포접화합물에 의한 기미치료 효과 및 필링효과, 라벤다 추출물에 의한 피부진정 효과를 의미한다. 제조한 다기능성 마스크 팩의 용제에 대한 유해물질의 측정결과 0.001mg/Kg 이하로 검출되었으며, 점도는 280 cP, pH=6.92 이었다. 마스크 시트에 다기능성 용제를 침지시켜 제조한 다기능성 마스크 팩의 원적외선 방사율은 0.882 μm이고 원적외선 방사에너지는 3.40x102 W/mᆞ, 37℃이었다. 다기능성 마스크 팩의 착용 후, 5일간 사용 후의 보습율은 사용전보다 14.5% ~ 35.5% 우수하였으며, 피부 온도는 24 ~ 26℃ 나타내었으며, 30명의 볼란티어 피부접촉 자극성 평가에서도 매우 안정적이었다.

We fabricated glucose oxidase (GOx)-modified biosensor for detection of glucose by physical immobilization of GOx after electrochemical polymerization of the conductive mixture monomers of the 3-thiophenecarboxylic acid (TCA) and thiophene (Th) onto ITO electrode in this study. We confirmed the successfully fabrication of GOx-modified biosensor via FT-IR spectroscopy, SEM, contact angle, and cyclic voltammetry. The fabricated biosensor has the detection limit of 0.1 μM, the linearity of 0.001-27 mM, and sensitivity of 38.75 mAM-1cm-2, respectively. The fabricated biosensor exhibits high interference effects to dopamine, ascorbic acid, and L-cysteine, respectively. From these results, the fabricated GOx-modified biosensor with long linearity and high sensitivity could be used as glucose sensor in human blood sample.

In order to get stabilized pure retinol in skin care cosmetics, developing the three layered matrix bead capsules were studied. This study relates to make a cosmetic composition using the three layered matrix capsule that could increase the stability of the active ingredient. A primary encapsulation, vitamin A (pure retinol) of active ingredient was perfectly capsulated into water-in-oil (Water-in-Oil: W/O) emulsion vesicle using PEG-10 dimethicone copolyol emulsifier. A secondary encapsulation of multiple emulsion of the water-in-oil-in-water (W/O/W) emulsion blending W/O emulsion using sucrose distearate of surfactant was developed using homogenizing emulsifying system. Pure retinol of active ingredient was stably capsulized to inside the W/O/W-multiple emulsion in order to load the triple matrix capsulation. By coating it with a polymer matrix base, encapsulated in the triple layered type, which were developed bead encapsulation of 2~10mm uniformly size. To show beautifully appearance capsulated bead type, these finish particles in this triple matrix layer were developed as a gold, green, dark brown, silver and blue color were encapsulated in the bead types. Structural particle certification of triple matrix layer was observed through SEM analysis. Stability of pure retinol was remained stable more than 99.7% for 30 days at 42°C incubating conditions compared with non-capsule. This technology was applied in different formulations such as various sizes and colors that by applying the skin care cosmetics. In the future, this technology to encapsulate an unstable active ingredient, we expect to be expanded this application in the food and drug as a time delivery system.

The present in vitro study was conducted to examine the effect of buffer solubility of eight protein feeds (coconut meal, distillers grain, sesame meal, perilla meal, soy source cake, rape seed meal, soybean meal and lupine) on the fermentation characteristics, degradability of dry matter (DM) and crude protein (CP), and methane (CH4) production by rumen microbes. Buffer extraction increased pH (P<0.05 ~ p<0.001) of the culture solution but tended to lower ammonia- N concentration for all protein feeds. Total volatile fatty acids(VFAs) and each VFAs concentrations in all incubation was decreased by buffer extraction (P<0.01 ~ P<0.001). Also, molar proportion of acetate in 1h (P<0.001), 3h (P<0.01) and 12h (P<0.05) incubations and molar proportion of propionate in 1h (P<0.001), 3h (P<0.01), 6h (P<0.05) and 12h (P<0.05) were decreased by buffer extraction. But molar proportion of butyrate in 1h (P<0.001), 3h (P<0.01) and 6h (P<0.05) were increased by buffer extraction. The in vitro effective degradability of dry matter (P<0.001) and CP (P<0.001) was decreased by buffer extraction. The methane production (P<0.01~P<0.001) in all incubation was decreased by buffer extraction. The results from in the current study might be useful for diet formulation to improve the feed efficiency of the ruminant animals without massive loss of major nutrients.

An enantioselective recognition of D- and L-tryptophan (Trp)-b-cyclodextrin (CD) inclusion complex was performed using electrochemical and FT-Raman spectroscopic analysis. From the electrochemical analysis, the selectivity coefficient (KDL) of b-CD inclusion complexes was found higher than that of the D- and L-Trp in phosphate buffered saline (PBS, pH=7.0) solution. The percentage of enantioselectivity (I%ee) for peak current of D-Trp-b-CD inclusion complexes was observed higher than that of L-Trp-b-CD inclusion complexes in PBS solution. From Raman spectroscopy, chemical shift difference (D, cm-1) for the C=C stretch, ring vibration, and ring breathing of D-Try-b-CD inclusion complex were observed higher than that of L-Trp-b-CD inclusion complex. The electrochemical and Raman spectroscopic analyses were found very useful for chiral detection of racemic amino acid in the presence of b-CD.

이 연구는 경표피흡수를 위하여 큐빅액정의 자기조직체의 형성에 관한 것이다. 복수 수산기 (-OH)를 가지는 친수부에 4개의 메칠 그룹을 가지는 양친매성지질인 diglyceryl phytylacetate (DGPA) 를 합성하여 다양한 성능평가를 수행하였다. DGPA의 유화력은 1%의 적은 농도에서도 고 내상의 물을 함유하는 안정한 W/O water-in-oil)에멀젼이 유지되었다. DGPA, dimethicone (2CS), water의 3성분 계의 특정영역에서, 안정한 큐빅상의 액정이 형성되었다. 3상 구조도 작성을 통하여 큐빅 액정영역, 헥 사고날 영역, 물과 헥사고날이 혼제된 영역, 역미셀 영역을 확인하였고, SAXS (small angled x-ray scattering)분석을 통하여 그 구조를 증명하였다. 화장품의 응용으로, 큐보좀 (cubosome)에 10%의 마그 네슘아스코르빌포스페이트, 5％의 피리독신트리헥사데카노에이트를 봉입하여 캡슐화하였다. 큐보좀의 occlusive 효과는 역미셀(reverse micelle)보다 1.7배 우수한 효과를 가졌다. 큐보좀을 분산제인 poloxamer를 사용하여 W/O 에멀젼을 만든 것으로부터 큐빅구조의 액정상으로 회복되는 것을 새롭게 발견하였다. 따라서, DGPA의 양친매성지질의 특성을 이용하여, 큐빅상의 액정을 형성하는 기재로써 화 장품 산업과 의약품분야에서 경표피흡수제로써 응용이 가능할 것으로 기대된다.

An in vitro study was conducted to determine the effects of defaunation (removal of protozoa) and forage sources (rice straw, ryegrass and tall fescue) on ruminal fermentation characteristics, methane (CH4) production and degradation by rumen microbes. Sodium lauryl sulfate, as a defaunation reagent, was added into the mixed culture solution to remove ruminal protozoa at a concentration of 0.375 mg/ml. Pure cellulose (0.64 g, Sigma, C8002) and three forage sources were incubated in the bottle of culture solution of mixed rumen microbes (faunation) or defaunation for up to 24 h. The concentration of ammonia-N was high under condition of defaunation compared to that from faunation in all incubations (p<0.001). Total VFA concentration was increased at 3, 6 and 12 h (p<0.05~p<0.01) but was decreased at 24 h incubation (p<0.001) under condition of defaunation. Defaunation decreased acetate (p<0.001) and butyrate (p<0.001) proportions at 6, 12 and 24 h incubation times, but increased propionate (p<0.001) proportion at all incubation times for forages. Effective degradability of dry matter was decreased by defaunation (p<0.001). Defaunation not only decreased total gas (p<0.001) and CO2 (p<0.01~0.001) production at 12 and 24 h incubations, but reduced CH4 production (p<0.001) at all incubation times for all forages. The CH4 production, regardless of defaunation, in order of forage sources were rice straw > tall fescue > ryegrass > cellulose (p<0.001) up to 24 h incubation.

Two-types of ionically modified multi-walled carbon nanotube (MWNTs) based sensors were developed by radiationinduced graft polymerization using vinyl monomers such as 3-(butyl imidazol)-2-(hydroxyl)propyl methyl methacrylate and 1-[(4-ethenylphenyl)methyl]-3-buthyl-imidazolium chloride with ionic properties, in aqueous solution at room temperature. Subsequently, the tyrosinase-immobilized biosensor was fabricated by a hand-casting of the ionic property-modified MWNTs, tyrosinase, and chitosan solution as a binder onto ITO glass surface. The sensing ranges of the tyrosinase-biosensor for phenol in phosphate buffer solution was in the range of 0.005~0.2 mM. The total phenolic compounds mainly such as caffeine of the tyrosinase-immobilized biosensor for commercial coffee were also determined.

Gingival overgrowth can cause dental occlusion and seriously interfere with mastication, speech, and dental hygiene. It is observed in 25 to 81% of renal transplant patients treated with cyclosporine A (CsA). CsA-induced gingival overgrowth (CIGO) is caused by quantitative alteration of the extracellular matrix components, particularly collagen. However, the molecular mechanisms involved in the pathogenesis of CIGO remain poorly understood, despite intense clinical and laboratory investigations. The aim of the present work is to identify differentially expressed genes closely associated with CIGO. Human gingival fibroblasts were isolated by primary explant culture of gingival tissues from five healthy subjects (HGFs) and two patients with the CIGO (CIGO-HGFs). The proliferative activity of CsA-treated HGFs and CIGO-HGFs was examined using the MTT assay. The identification of differentially expressed genes in CsA-treated CIGO-HGF was performed by differential display reverse transcriptase-polymerase chain reaction (RT-PCR) followed by DNA sequencing. CsA significantly increased the proliferation of two HGFs and two CIGO-HGFs, whereas three HGFs were not affected. Seven genes, including the beta subunit of prolyl 4-hydroxylase (P4HB) and testican 1, were upregulated by CsA in a highly proliferative CIGO-HGF. The increased P4HB and testican-1 mRNA levels were confirmed in CsA-treated CIGO-HGFs by semiquantitative RT-PCR. Furthermore, CsA increased type I collagen mRNA levels and suppressed MMP-2 mRNA levels, which are regulated by P4HB and testican-1, respectively. These results suggest that CsA may induce gingival overgrowth through the upregulation of P4HB and testican-1, resulting in the accumulation of extracellular matrix components.

참깨줄기의 반쪽부분(部分)만이 특징적으로 변색(變色)되며 결국은 식물체전체(植物體全體)가 고사(枯死)되는 병미(病微)이 장려품종(奬勵品種)인 광산(廣産)깨와 풍년(豊年)깨가 심겨진 포장(圃場)에서 관찰(觀察)되었다. 병미(病微)은 처음에 줄기의 한쪽 부분(部分)만이 수침상(水浸狀)의 줄무늬(條斑)형태(形態)로 변색(變色)되며, 병징후기(病徵後期)에는 변색부위상(變色部位上)에 황백색(黃白色)선홍색(鮮紅色)의 Fusarium 포자퇴(胞子堆)들이 많이 형성(形成)된다. Fusarium oxysporum에 감염(感染)된 참깨 유묘(幼苗)에서는 주로 시들음 증상(症狀)이 나타나지만, 성묘(成苗)에서는 토양접종(土壞接種)이나 상처접종(傷處接種)에 의해 줄기반쪽썩음증상(症狀)을 재현(再現)시킬 수 있었다. 본(本) 병해(病害)는 주로 생육후기(生育後期)인 7월하순(月下旬) 경에 많이 발생(發生)된다. 참깨줄기반쪽썩음증상(症狀)에서 분리(分離)한 Fusarium oxysporum의 균학적(菌學的) 특성(特性)을 이미 참께시들음병(病)에서 보고(報告)되어 있는 Fusarium 균(菌)들과 비교(比較)한 결과(結果) 본(本) 균(菌)은 F. oxysporum f. sp. sesame로 생각된다.