• 한국균학회지
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• 제4권1호
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• pp.53-58
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• 1976

This study was undertaken to investigate the direct effect of three different kinds of steroid to Trichophyton(T.) mentagrophytes growth in vitro. A loopful of T. mentagrophytes was inoculated into Sabouraud's media and Sabouraud's media containing various concentrations of dexamethasone (0.04%-0.00004%) prednisolone (0.25%-0.00025%), triamcinolone acetonide (0.2%-0.0002%), Sabouraud's media containing imidazole nitrate (econasole nitrate) 10 micro gm. per cc. of media, and Sabouraud's media containing econazole nitrate $10{\mu}g$ per cc. of media of various dexamethasone concentrations (0.04%-0.00004%). After inoculation they were left for two weeks at room temparature and the colony diameter were compared between Sabouraud's media and Sabouraud's media containing various concentrations, of three different steroids, Sabouraud's media containing econazole nitrate and Sabouraud's media containing econazole nitrate of various dexamethasone concentrations. For complementary study, hanging slide culture were done between Sabouraud's media and Sabouraud's media containing various dexamethasone concentrations to compare the degree of branching of hyphae and sporulation serially. The study results were as follows: 1. There is no significant difference in growth rate of T. mentcgrophytes between Sabouraud's media and Sabouraud's media containing various concentrations of three different steroids. 2. There is no significant difference in growth rate of T. metagrophytes between Sabouraud's media containing econazole nitrate 10 micro gm per cc. of media and Sabouraud's media containing econazole nitrate 10 micro gm per cc. of media of various dexamethasone concentrations. 3. In hanging slide culture, there is no significant difference in branching of hyphae and sporulation between Sabouraud's media and Sabouraud's media containing various dexamethasone concentrations.

• 한국균학회지
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• 제8권1호
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• pp.1-5
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• 1980

마디풀 전초(全草)의 건조물인 편축의 열수전탕(熱水煎湯)의 여과액으로 증발 농축시킨 추출액을 만들어 대조인 Sabouraud's dextrose arar 배지에 매지 10ml當 편축 추출액 0.5,1,2 및 3ml를 각각 혼합한 배지로서 T. rubrum, T. mentagrophytes, E. floccccosum 및 M. canis 등 4균종을 각각 3종씩 배양하여 그 발육상태를 관찰하므로서 진균발육억제작용의 유무를 검색하여 다음과 같은 성적을 얻었다. 1. E. floccosum은 편축추출물 3ml 혼합의 평판배지 사면배지 및 현적배양에서 거의 완전히 현지한 균발육억제작용을 인정할 수 있었다. 2. T. menagrophytes, T. rubum 및 M. cains에 대해서는 부분적으로 현저한 억제자용과 발육균태(菌苔)의 크기로 보아 반이불(半以不)의 크기로 발육이 억제되는 증정도의 억제효과를 인정하였다.

• 혜화의학회지
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• 제20권2호
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• pp.67-78
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• 2012

Volatile odor substance originating from drying and making dry peel of tangerine from the fruit skin were collected through modern equipment. The anti-microbial activity of the substance against various skin-residing bacteria including acne, dandruff, athelete's foot, and gingivitis inducing microorganisms were tested. Anti-microbial activity was observed in purified oil, where 87 to 92% was D-limonene. Against P. acnes, 103$cfu/m{\ell}$ of P. acnes were suppressed at 0.1% Unshiu oil, and the MIC was measured to be 0.3%. Against P. ovale, a dandruff inducing bacteria, 104$cfu/m{\ell}$were suppressed at 0.1% Unshiu oil, and the MIC was measured to be 0.1%. Against T. rubrum and T. Mentagrophytes, both of which are athelete's foot inducing microorganisms, 83% of T. Mentagrophytes and 99.9% of T. rubrum were suppressed at 0.1% Unshiu oil, and the MIC were 0.3% and 0.05% respectively. Against S. aureus, a skin infection inducing bacteria, 103$cfu/m{\ell}$ of the bacteria were suppressed at 0.1% Unshiu Oil. Against B. subtilis, a non-pathogenic sporulating bacteria, 104$cfu/m{\ell}$ of the bacteria were suppressed at 0.1% Unshiu Oil. Against C. albicans, found in mucous membranes, 104$cfu/m{\ell}$ of the bacteria were suppressed at 0.1% Unshiu Oil. Against Aspergillus niger, an otomycosis inducing microorganism, 99.9% were suppressed at 0.1% Unshiu Oil. The results above indicate that low concentration of purified oil extracted from tangerine had strong antimicrobial activities against bacteria and fungi residing on the skin, and that it may be developed into skin disorder treating products in the future.

• 한국임상수의학회지
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• 제8권2호
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• pp.147-152
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• 1991

습도가 높고 환기가 불량하며 비위생적인 우리에서 같이 사육한 두 마리의 어린 염소에서 발생한 진균성피부염의 일차원인이 Trichophyton mentagrophytes이었음을 보고하였다. 두 환축의 진단은 피부소파 시료에 KOH를 사용하여 균요소를 검출하고 3$0^{\circ}C$의 진균배지에서 순수배양하여 균을 분리하여 확인하였다. 한 마리는 안면에서 나머지 한 마리는 목과 귀에서 병변이 발견되었다. 같은 우리에서 사육 중이던 두 마리의 성축에서는 병변이 발견되지 않았다. 더욱이 염소의 주인과 주인가족들에서도 병변이 발견되지 않았다. 두 분리균주를 개량된 sunflower seed medium을 이용하여 유전적 교배실험을 한 결과 둘 다(-) mating type에 속했다. Hair performance test결과 두 균주는 모두 각질용해작용을 나타내었다. 공중위생학적인 중요성과 화학요법에 대해서도 고찰하였다. 감염경로에 대해서는 명확히 밝힐 수 없었다.

• 생명과학회지
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• 제19권1호
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• pp.94-100
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• 2009

GSE와 PSS를 이용한 피부 외용제를 개발하기 위해, 평판 배지확산법 및 액체배지감수성실험을 이용하여 GSE와 PSS의 비듬균(Malassezia furjur, M. restricta), 여드름균(Propionibacterium acnes) 및 무좀균(Trichophyton mentagrophytes, T. rubrum)에 대한 항균 활성을 측정하였다. 평판 배지확산법의 경우 GSE가 $10{\mu}l/disk$일 때 M. furfur, M. restricta. P. acnes, T. mentagrophytes 및 T. rubrum은 각각 1.0, 1.0, 12.0, 15.0, 15.0 mm 였으며, PSS가 $10{\mu}l/disk$일 때에는 각각 7.3, 5.7, 2.0, 0 mm 이었다. 또한 액체배지감수성실험에서 GSE에 대한 MIC 값은 각각 3.91, 3.91, 0.004, 0.024, $0.012{\mu}l/ml$ 이었으며 PSS에 대한 MIC 값은 각각 0.03, 0.03, 0.156, 0.003, $0.012{\mu}l/ml$이었다. 또한 GSE 와 PSS가 함유된 에멀전 시제품을 제조하여 농도별 평판배지확산법을 수행한 결과 그 결과 값은 0.5% 농도에서 각각 5.2, 4.3, 8.0, 9.5, 12.8 mm의 값을 나타내었다. GSE 와 PSS가 실험 대상 균주에 대하여 모두 항균력을 가지고 있었으며 비듬균인 M. furfur와 M. restricta는 GSE 보다는 PSS에서 더 강한 항균력을 보였으며 여드름균인 P. acnes와 무좀균인 T. mentagrophytese 및 T. rubrum은 PSS 보다는 GSE에서 더 강한 항균 활성을 보였다. 그러므로 GSE와 PSS의 각각에 효과적인 균주별 피부질환 외용제 뿐만 아니라 GSE와 PSS를 함께 적용한 광범위한 피부질환 외용제의 응용개발이 가능하리라 사료된다. 또한 에멀전 로션 시제품의 물리화학적 특성을 분석한 결과 pH, 점도, 굴절 및 색도 변화에 있어서 모두 안정성을 보였고 이상의 연구결과를 바탕으로 기능성 화장품과 같은 피부 외용제 제품의 개발 가능성을 확인하였다.

• 한국염색가공학회지
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• 제14권1호
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• pp.1-10
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• 2002

The aim of study was to elucidate dyeability and antimicrobial and antifungal activity of silk fabrics dyed with Sophora Radix extracts according to different mordants. Dyes were extracted from Sophora Radix using ethanol. Then, silk fabrics were dyed with extracts two times by post-mordanting method in which the extract was 60%(owf), the mordant was 3%(owf), L.R was 1:20, the temperature was $60~60^\circ{C}$, the time of dyeing was 60min., and the time of mordanting was 60min. The dyeability was evaluated by surface color, K/S values and durability of dye. The skin microorganisms used in this study was S. sureus, B. subtilis, S. epidermidis, P. acnes, P. aeruginosa, E coli, A. niger, C. albicans and T. mentatrophytes. The results are as follows; 1. When mordants were added, K/S value of silk dyed was not improved much and surface color was 2.2Y to 8.8Y in H(hue) value which indicated greenish yellow to raddish yellow 2. The color fastness tests to light, perspiration, dry-cleaning, rubbing, and stain fabric washing show 4~5th degree which were valuated excellent. The color fastness to fade washing was improved to 3~4th degree by addition of $K_2CrO_7$ mordants. 3. Antibacterial activity of silk dyed using no-mordant as well as mordants was excellent on S. aureus, B. subtilis, S.epidermidis and P.acnes, but showed poor antibacterial activities on P.aeruginosa and E.coli such as gram negative baterials 4. Antifungal activity of silk dyed with ethanol extracts was good on A.niger, C.candida and T.mentagrophytes. Especially, on T. mentagrophytes there was no growth of fungus during 72 gous in silk dyed mordanting with $SnCl_2\cdot{2H}_2O$.

• KSBB Journal
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• 제25권2호
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• pp.123-129
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• 2010

An endospore-forming, rod-shaped bacterium was isolated from forest soil samples collected at the Taebaek mountain of Gangwon province, Korea, and taxonomically characterized by physiological, biochemical and phylogenetic methods. Its 16S rRNA sequences showed the maximum similarity of 97% with B. amyloliquefaciens. In addition, the isolate BCNU 2002 was determined to have the ability to produce enzymes such as amylase, protease, gelatinase and catalase. The in vitro antifungal activity of Bacillus sp. BCNU 2002 was also examined against human pathogenic fungi such as Aspergillus niger, Candida albicans, Epidermophyton floccosum, Saccharomyces cerevisiae, Trichophyton mentagrophytes and Trichophyton rubrum. A maximum production level of antifungal substances of Bacillus sp. BCNU 2002 was achieved under aerobic incubation at $28^{\circ}C$ for 7 days in LB broth. BCNU 2002 showed strong antifungal activities against T. mentagrophytes and T. rubrum with the range of percentage inhibition from 56.25 to 63.23%. It was also confirmed that ethylacetate extract of cultured broth showed a strong antifungal activity against A. niger, C. albicans, S. cerevisiae and T. rubrum by agar diffusion method. The peptide fraction also exhibited broad antifungal spectrum against various pathogenic fungi. The minimum inhibitory concentration values for active extracts ranged between 125 ${\mu}g$/mL and 1000 ${\mu}g$/mL.

• 대한수의학회지
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• 제42권3호
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• pp.363-370
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• 2002

For the development of diagnostic polymerase chain reaction (PCR) to fungal infection by dermatophytes Trichophyton and Microsporum, detection of the fungal DNA by PCR and analysis of the DNA pattern were undertaken in the present study. A total of 15 strains were tested and those consisted of 3 reference strains and 12 isolates such as: reference strains of T mentagrophytes (downy type, ATCC 9533), T rubrum (IFO 6204) and M gypseum (ATCC 9083), and each isolate of T mentogrophytes (powdery type), T mentagrophytes (granular type), T mentogrophytes (purple-red type), T rubrum, T raubitschekii, T tonsurans, T equinum, T ajelloi, T verrucosum, M cookei, M nanum and M gypseum. The DNA were purely isolated from all strains of Trichophyton spp. and Microsporum spp. by a simple method partly consisted of disruption of fungal cells by lyophilization and grinding and extraction of fungal DNA without phenol treatment which is a routine procedure in DNA isolation. For the detection of fungal DNAs, optimal condition of PCR was determined as preheating once at $94^{\circ}C$ for 5 min, 35 cycles of denaturation at $94^{\circ}C$ for 1 min, annealing at $38^{\circ}C$ for 1 min and polymerization at $72^{\circ}C$ for 2 min, and 1 cycle of final extension at $72^{\circ}C$ for 5 min. In PCR using arbitrary primers AP-1 (5' ACCCGACCTG3') and AP-2 (5' ACGGGCCAGT3'), DNAs in various numbers and sizes were detected from different species of Trichophyton and Microsporum, while DNAs in similar size were also detected in all strains of Trichophyton spp. and Microsporum spp. There were unique DNAs observed from certain dermatophytes by AP-1 such as 1,900 bases in T rubrum, 950 and 1,100 bases in T raubitscheldi, 2,100 bases in T equinum, 400 bases in T verrucosum and 1,150 bases in M gypseum. The unique DNAs were also observed by AP-2 such as 1,200 bases in T ajelloi, 250 bases in T verrucosum, 1,150 bases in M cookei and 2,000 bases in M nanum. The results indicated that PCR can detect a specific DNA from certain Trychophyton and Microsporum spp, which can be the information for further development of diagoomc PCR to dennatophytes.

• Journal of the Korean Wood Science and Technology
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• 제34권3호
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• pp.46-55
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• 2006

본 연구는 피부사상균에 항진균 활성을 보이는 편백정유에 대하여 이를 구성하고 있는 mono- 및 sesquiterpene 성분들 중 어떠한 성분들에 의해 항진균 활성이 나타나는지 탐색하고 성분들 간의 synergy 효과가 존재하는지 알아보고자 피부사상균인 Trichophyton mentagrophytes (KCTC6077), Microsporum canis (KCTC6591), Microsporum gypseum에 대하여 디스크확산법, 한천희석법을 이용하여 항진균 활성을 평가, 비교하였다. Column chromatography를 이용하여 편백정유를 7개(A, B, C, D, E, F, G)로 분획하고, 각각의 분획들에 대하여 한천희석법을 이용하여 T. mentagrophytes에 대한 항진균 활성을 실험한 결과, 분획 D, E, F, G의 항진균 활성이 높았다. GC/MS 분석을 실시하여 높은 항진균 활성을 나타내는 분획의 주성분을 확인하고 그 중 monoterpene인 borneol, linalool, ${\alpha}$-terpineol과, sesquiterpene인 ${\alpha}$-cedrol, nerolidol, ${\beta}$-eudesmol을 선택하였다. 단일 terpene의 항진균 활성 비교 시 monoterpene보다 sesquiterpene이 더 높은 활성을 보였다. 높은 활성을 보이는 sesquiterpene의 단일 및 혼합 성분들과 편백정유의 분획 중 항진균 활성이 높고 sesquiterpene의 함유량이 높은 분획 F의 비교 시, sesquiterpene의 조합 성분들이 높은 항진균 활성을 나타냈다. 이는 sesquiterpene 성분들의 혼합에 의하여 항진균 활성의 synergy 효과가 발현됨을 의미하였다.

• 약학회지
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• 제35권4호
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• pp.308-313
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• 1991

The synthesis of 1-[(2-phenyl-1, 3-benzodioxol-2-yl)methyl]-1H-imidazole derivatives is described starting with 2-bromoacetophenones and catechols. 1-[(2-Phenyl-1, 3-benzodioxol-2-yl)methyl]-1H-imidazole (9-$_{12}$) showed potent broad-spectrum activity, not only against Candida species but also Cr. neofortnans, S. cerevisiae and T. mentagrophytes.