• 대한화장품학회지
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• 제30권1호
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• pp.129-133
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• 2004

In vitro method는 in vivo results를 예측하기 위해 사용되어지는 것이 가장 큰 목적이므로 지급까지 in vitro SPF test는 여러 formulations를 screen 하거나 self-tanners의 activity에 미치는 cosmetic ingredients의 영향을 연구하는 데에 이용되어져 왔다. In vitro SPF test는 신속하고 객관적이며 적은 비용으로 사람에게 in vivo test를 하기에 앞서 protective formulas를 pre-screen 하며, 따라서 in vitro test가 유용하게 원하는 역할을 하기 위해서는 in vitro SPF 평가법의 정확성이 무엇보다 중요하다. 본 연구에서는 건조시간을 15분으로 고정하면서 기존에 사용해온 substrate인 Transpore$^{(R)}$ tape을 이용, 도포 방법을 개선하기 위한 시도를 하였다. 우선 기존 시험법의 분석을 통한 현 수준을 파악하고, 사용되고 있는 Transpore$^{(R)}$ tape의 외측으로부터 일정 부위만 사용하도록 개선하였다. 또한 다양한 시도를 통해 광원의 scan 부위에만 국소적으로 도포하는 방법이 도포시 발생하는 오차를 줄일 수 있음을 확인하였으며, 개선된 시험법을 이용하여 반복성과 선형성이 뛰어난 시험 결과를 얻어낼 수 있었다. 통계 패키지 분석을 통한 시험법의 신뢰성 검토에서도 우수한 결과를 보여 이와 같은 시험법을 통해 in vivo와 in vitro SPF의 보다 정확한 예측 시스템 관계를 구축할 수 있을 것으로 기대한다.

• 대한수의학회지
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• 제32권2호
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• pp.181-194
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• 1992

Two hundred and eighty nine strains of Yersinia enterocolitica isolated from healthy pigs were tested for the presence of 40~50 Megadalton virulence-associated plasmids and plasmidmediated in vitro virulence-associated properties, i.e., congo red uptake, calcium dependency, autoagglutination, CRMOX reaction, crystal violet binding and pyrazinamidase reaction. The correlationships between in vitro virulence-associated properties and the presence of 220 Kdalton outer membrane protein(OMP) were examined in strains with or without virulence-associated plasmids. The correlationships between the presence of plasmids on the production of the OMP and the expression of in vitro virulence-associated properties were studied with $CRMOX^+$ strains and acridine orangecured $CRMOX^-$ mutants. The results were as follows : 1. Of the in vitro virulence-associated tests with 289 strains of Y enterocolitica, 275 strains (95.2%) were positive for pyrazinamidase test, and followed by in order of crystal violet binding test, 226 (79.2% ) ; CRMOX test, 190 (65.7%) ; autoagglutination test, 1.85(64.0%) : calcium dependency test, 86 (29.8%) and congo red uptake test, 47(16.3%). 2. The correlationship between autoagglutination and CRMOX test(r=0.90) was highly significant (p<0.01). 3. In 190 strains(65.7%) bearing the virulence-associated plasmids(MW 40~50 Mdalton), the correlation between the presence of plasmids and their in vitro virulence-associated properties were highest with CRMOX test(r=0.93) and followed by in orders of AAG test(0.81), CV test(0.46), PYZ test(0.37) and CD test(0.18), but no correlationship between the presence of plasmids and CR test(-0.11). 4. The $CRMOX^+$ strains produced the 220 Kdalton OMP when they were cultured at $37^{\circ}C$, but not at $26^{\circ}C$. The presence of 220 Kdalton OMP was correlated significantly with in vitro virulence properties and the presence of virulence-associated plasmid, respectively. 5. In the isogenic $CRMOX^-$ mutant strains, of which plasmid were cured by treatment with acridine orange not only in vitro virulence-associated properties(CR 100%, CD 100%, AAG 82.6%, CV 58.3%) disappeared but also 220 Kdalton OMP(100%) was not produced. These results indicate that the positive CRMOX reaction is plasmid-mediated and the CRMOX test is potential as an in vitro virulence tests with Y enterocolitica.

• 대한수의학회지
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• 제38권3호
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• pp.589-594
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• 1998

The in vitro screening tests against the in vitro cultivated $L_3$ of Ascaris suum (in vitro $L_3$), which were cultivated from the embryonated egg to third-stage larva on 7 days in culture(DIC) and the in vivo rat's lung-derived $L_3$ of Ascaris suum (in vivo $L_3$), which were recovered from the lungs of rat on 7 days after infection, carried out in order to compare the anthelmintic efficacy of in vitro $L_3$ and that of in vivo $L_3$ in RPMI medium 1640 with 5% bovine calf serum. And also a screening test of efficacy against adult worms of Trichuris suis performed. The efficacies of screening tests were as follows : 1. The screening efficacies of abamectin and ivermectin against the in vitro $L_3$ were all 100% at the 10ppm concentration in RPMI medium 1640 on 5 DIC. 2. The screening efficacies of abamectin and ivermectin against the in vivo $L_3$ were all 100% at the 20ppm on 5 DIC or at 40ppm on 3 DIC. 3. The screening efficacies of abamectin and ivermectin against the adult worms of Trichuris suis were all 100% at 20ppm on 4 DIC. And therefore, the in vitro cultivated $L_3$ of Ascaris suum were used in the screening test as well as the in vivo rat's lung-derived $L_3$ of Ascaris suum. And also the adult worms such as Trichuris suis and filaroids which is small size and difficult to cultivate to vitro, were used in the screening test in vitro.

• 대한핵의학회지
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• 제9권1호
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• pp.5-9
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• 1975

• 대한화장품학회지
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• 제19권1호
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• pp.57-76
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• 1993

기기의 광독성 유발 물질 및 자외선 차단제 그리고 수종의 천연물에 대해 in-vitro 와 in-vivo에서 광독성 시험을 하였다. In-vitro시험은 C. albicans와 S. typhymurium TA 98을 이용 광독성 시험을 하였으며, 광조사는 시료, 시료와 미생물 모두 각각의 시료와 미생물 조사하는 방법을 사용하여 비교하여 보았다. 조사 방법에 따른 유의성은 관찰되지 않았는데, 제한된 시료를 사용했다는 것도 여러 원인 중에 하나가 될 수 있다. 한편 사용된 두 균주의 감수성은 C. albicans에 비해 S. typhimurium TA 98을 이용했을 때 높게 나타났고, S. typhimurium TA 98을 이용한 in-vitro method(Method I)와 in-vivo method를 시험 결과 측면에서 볼 때 상관 관계가 높게 나타났다.

• Journal of Pharmaceutical Investigation
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• 제20권3호
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• pp.115-119
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• 1990

The reaction rates, duration times and neutralizing capacities of the antacids which are frequently used in Korean market and three different commercial combination products were evaluated in vitro by Fuchs method and Johnson-duncan method, respectively. In vivo tests of combination products were determined in the fasted state of rat by Aspiration method. Comparing the result of in vitro test with that of in vivo test, the maximal pH was lowered by 2-3 value and the durational time increased by two folds in vivo test. Each antacid composition and combination products from three phamaceutical companies (A, B, and C) were studied, respectively. The duration times measured by Fuchs method were double compared to those by Johnson-Duncan method. A and C preparation maintained the pH range from 3 to 7 for 60 min by Fuchs method. In vovo test, maximum pH of A, B and C preparation was 6.50, 3.65, 2.65 and duration time of those was 200, 500, 0 min, respectively.

• 대한화장품학회:학술대회논문집
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• 대한화장품학회 2003년도 IFSCC Conference Proceeding Book II
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• pp.528-528
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• 2003

The present study was undertaken to develop the in vitro sun protection factor(SPF) test method having good correlation with in vivo method using human. 8% homomentyl salicylate, P3 reference standard and commercially available sunscreen products were measured by the in vitro method using SPF 290S analyzer, and the SPFs were compared with the SPFs measured by in vivo test method. In vitro SPFs of 8% HMS and P3 reference standard were 4.59 $\pm$ 0.12 and 14.94 $\pm$ 0.83. There are good correspondence, correlation coefficients were 0.9506 and 0.9769 respectively, between the in vitro and in vivo SPFs for the sunscreen creams and lotions. Correlation coefficients of makeup base/liquid foundation, lotion labled with "shake before use" and compact powder were 0.8812, 0.8632 and 0.5984 respectively. The optimum mixture ratio of compact powder and cream base represents 1:0.8. These results suggest that the in vitro SPF test method will be able to be used as an alternative method for in vivo SPF in case of lotion and cream.

• Journal of Pharmaceutical Investigation
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• 제30권1호
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• pp.27-32
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• 2000

Various release test methods have been applied for the evaluation of nicotine release in vitro from commercial patches. However, whether and how the release data reflect the permeation of nicotine across the skin, is not fully elucidated. To predict in vivo bioavailability from in vitro release tests, correlation between in vitro release and in vitro skin permeation was assessed in the present study. Release of nicotine from three commercial patches was measured for 24 hours under nine experimental conditions which were classified depending on the apparatus (i.e., paddle over disk, cylinder and reciprocating holder) and dissolution media (i.e., phosphate buffer pH 7.4, water and the 1 % phosphoric acid pH 1.5). In vitro permeation of nicotine from the patches across the human cadaver skin was also measured using a diffusion cell. The release of nicotine was better explained by the Higuchi's equation rather than by the first order rate equation. Correlation between the release rate and the in vitro skin permeation differed among the patches. However, in general, the cylinder method, in which water is used as a dissolution medium, showed the highest correlation among the nine release test conditions.

• 한국식품과학회지
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• 제29권4호
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• pp.804-807
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• 1997

제일제당주식회사에서는 미생물발효법을 이용하여 palatinose를 대량생산하게 되었다. Palatinose 산물의 안전성을 확인하기 위하여 1) Salmonella typhimurium을 이용한 미생물복귀돌연변이시험, 2) Chinese Hamster Lung (CHL) 세포를 이용한 in vitro 염색체이상시험을 실시하였다. Palatinose 및 palatinose syrup은 미생물복귀돌연변이 시험에서 10 mg/plate의 용량까지 복귀돌연변이를 유발하지 않았으며, CHL 세포에서도 5 mg/mL 농도에서 염색체이상을 유발하지 않았다. 이 결과는 palatinose 산물들이 위의 in vitro 변이원성시험계에서 돌연변이원성을 나타내지 않음을 보여준다.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.404.2-404.2
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• 2002

The present study was undertaken to develop the in vitro sun protection factor(SPF) test method having good correlation with in vivo method using human. 8% homomentyl salicylate. P3 reference standard and commercially available sunscreen products were measured by the in vitro method using SPF 290S analyzer. and the SPFs were compared with the SPFs measured by in vivo test method. In vitro SPFs of 8% HMS and P3 reference standard were 4.59$\pm$0.12 and 14.94$\pm$0.83. (omitted)