• 공업화학
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• 제10권7호
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• pp.974-978
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• 1999

면섬유에 대한 정련제로서 NP-7(polyoxyethylene(7) nonylphenyl ether) 및 TDA-7((polyoxyethylene(7) tridecyl ether)을 인산에스테르화 반응시켜 PAPE(sodium polyoxyethylene alkyl phosphoric ester)형 음이온 계면활성제인 sodium polyoxyethylene(7) nonylphenyl phosphoric ester(CPB-1)와 sodium polyoxyethylene(7) tridecyl phosphoric ester(CPB-2)를 각각 합성하였다. 합성한 CPB-1과 CPB-2를 기존의 상용제품인 Ultravon GP(GP)와 각 기능별로 성능을 비교하였다. 그 결과 상온 및 $100^{\circ}C$에서의 억포 및 파포력이 CPB-2>CPB-1>GP의 순으로 CPB-2의 기포가 가장 적었고, 또한 가장 빨리 파포되어졌다. 증류수에서의 침윤효과는 CPB-1>GP>CPB-2의 순으로 나타났으나, 실제 일반 정련에서 많이 사용하는 1.2 wt % NaOH 수용액에서의 침윤효과는 전반적으로 CPB-2가 가장 우수한 것으로 나타났다. 섬유가공시의 정련조건인 알카리 상태에서의 안정성은 $CPB-2{\geq}CPB-1$>GP의 순으로 나타났으며, 재흡수력 실험결과 CPB-2>CPB-1>GP의 순으로 CPB-2의 정련력이 가장 우수한 것으로 나타났다.

• Asian Pacific Journal of Cancer Prevention
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• 제13권5호
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• pp.2379-2383
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• 2012

Objective: To investigate possible signal pathway involvement in multi-drug resistant P-glycoprotein (P-gp) expression induced by cyclooxygenase-2 (COX-2) in a human gastric adenocarcinoma cell line stimulated with pacliaxel (TAX). Methods: The effects of TAX on SGC7901 cell growth with different doses was assessed by MTT assay, along with the effects of the COX-2 selective inhibitor NS-398 and the nuclear factor-KB (NF-KB) pathway inhibitor pyrrolidine dithiocarbamate (PDTC). Influence on COX-2, NF-KB p65 and P-gp expression was determined by Western blotting. Results: TAX, NS-398 and PDTC all reduced SGC7901 growth, with dosedependence. With increasing dose of TAX, the expression of COX-2, p65 and P-gp showed rising trends, this being reversed by NS-398. PDTC also caused decrease in expression of p65 and P-gp over time. Conclusion: COX-2 may induce the expression of P-gp in SGC7901 cell line via the NF-kappa B pathway with pacliaxel stimulation.

• 통합자연과학논문집
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• 제5권1호
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• pp.18-21
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• 2012

The resistance of tumour cells against cytotoxic drug is significant limitation in successful chemotherapeutic treatment of cancer. To date, no crystal structure is available for human P-gp. We developed homology model for human P-gp NBD2 by using coordinates of transporter associated protein (TAP1). Docking study was performed for 8-geranyl-chrysin (Flavonoids) inhibitor in the NBD2 model. Ligand-protein interactions were determined which indicates that the 8-geranyl chrysin shares two overlapping sites in the cytosolic domains of P-gp, the ATP site and a hydrophobic steroid-binding site.

• Biomolecules & Therapeutics
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• 제24권2호
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• pp.199-205
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• 2016

This study aimed to investigate the in vivo relevance of P-glycoprotein (P-gp) in the pharmacokinetics and adverse effect of phenformin. To investigate the involvement of P-gp in the transport of phenformin, a bi-directional transport of phenformin was carried out in LLC-PK1 cells overexpressing P-gp, LLC-PK1-Pgp. Basal to apical transport of phenformin was 3.9-fold greater than apical to basal transport and became saturated with increasing phenformin concentration ($2-75{\mu}M$) in LLC-PK1-Pgp, suggesting the involvement of P-gp in phenformin transport. Intrinsic clearance mediated by P-gp was $1.9{\mu}L/min$ while passive diffusion clearance was $0.31{\mu}L/min$. Thus, P-gp contributed more to phenformin transport than passive diffusion. To investigate the contribution of P-gp on the pharmacokinetics and adverse effect of phenformin, the effects of verapamil, a P-gp inhibitor, on the pharmacokinetics of phenformin were also examined in rats. The plasma concentrations of phenformin were increased following oral administration of phenformin and intravenous verapamil infusion compared with those administerd phenformin alone. Pharmacokinetic parameters such as $C_{max}$ and AUC of phenformin increased and CL/F and Vss/F decreased as a consequence of verapamil treatment. These results suggested that P-gp blockade by verapamil may decrease the phenformin disposition and increase plasma phenformin concentrations. P-gp inhibition by verapamil treatment also increased plasma lactate concentration, which is a crucial adverse event of phenformin. In conclusion, P-gp may play an important role in phenformin transport process and, therefore, contribute to the modulation of pharmacokinetics of phenformin and onset of plasma lactate level.

• Journal of Pharmaceutical Investigation
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• 제37권3호
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• pp.131-135
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• 2007

A previous report recently demonstrated that ultrasound-induced hyperthermia (USHT:0.4 watts (W)/$cm^2$ at $41^{\circ}C$) could increase cellular uptake of P-glycoprotein (P-gp) substrates in P-gp expressing cancer cell lines. Since P-gp plays a major role in limiting drug permeability in the multi-drug resistant (MDR) cells, studies were conducted to elucidate the mechanism of USHT on cellular accumulation of P-gp and non-P-gp substrate in MDR cells. To accomplish this aim, we studied the effects of USHT on the accumulation of P-gp substrate, R123 and non-P-gp substrate, antipyrine in MDR cells. We demonstrated that USHT increased permeability of hydrophobic molecules (R123 and $[^{14}C]$-antipyrine). The enhanced permeability is reversible and size-dependent as USHT produces a much larger effect on cellular accumulation of $[^{14}C]$-antipyrine (MW 188) than that of R123 (MW 380.8). These results suggest that USHT could affect MDR cells more sensitive than BBMECs. Also, the present results point to the potential use of USHT to increase cellular uptake of P-gp recognized substrates, mainly anti-cancer agents into cancer cells.

• 한국환경생태학회지
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• 제12권3호
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• pp.259-270
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• 1998

본 연구는 산지의 수자원보전량 평가용 수문유출모형의 개발을 위한 중요한 기초연구로서 우리나라 주요 수종인 소나무와 상수리나무에 대한 수간류 및 수관통과우의 물수지식과 수문학적 특성을 밝히고자 수행하였다. 영남대학교 자연자원대학 부속 용성연습림과 영남대학교 교내 야산에 각각 수관통과우 및 수간류 관측용 야외 실험지를 설치하고, 1995년 9월에서 1998년 6월까지 약 2년 10개월 사이에 이 지역에 내린 다수의 단위강우에 대한 두 수종의 임내우 수량배분을 조사하였다. 그 결과 임외의 단위강우에 응답하는 두 수종의 수문학적 특성과 임내우 물수지식을 요약하면 다음과 같다. 1. 소나무에 있어서 수관통과우와 수간류의 총량은 각각 임외우의 73.8%와 0.8%이였으며 상수리나무는 각각 임외우의 76.9%와 3.8%로 관측되었다. 2. 소나무에 있어서 임외우(Gp)에 대한 수간류(S$_{f}$)와 수관통과우(T$_{f}$)의 회귀식은 각각 S$_{f}$ = 0.01GP -2.05 ($r^2$=0.54) T$_{f}$ = 0.79Gp - 26.04 ($r^2$=0.92)로, 임내우(N$_{r}$)와는 N$_{r}$ = 0.81Gp - 28.09 (r2=0.92)로 추정하였다. 이와 같이 소나무에 있어서 수간류와 수관통과우는 임외우의 양에 정비례하여 증가하였다. 3. 상수리나무에 있어서 임외우(Gp)에 대한 수간류(S$_{f}$)와 수관통과우(T$_{f}$)의 회귀식은 각각 S$_{f}$ = 0.03Gp + 12.25 ($r^2$=0.74) T$_{f}$ = 0.78Gp + 19.75 ($r^2$=0.96)로, 임내우(N$_{r}$)와는 N$_{r}$ = 0.81Gp + 31.99 ($r^2$=0.96)로 구해졌는데 소나무보다 상수리나무에 있어서 수간류와 수관통과우의 증가폭이 더 큰 것으로 나타났다. 4. 수간류 및 수관통과우와 그 영향인자로 평가된 수관투영면적(CA). 흉고직경(DBH), 임외우량(Gp)과의 내부상관분석을 한 결과, 소나무 수간류에는 임외우＞수관투영면적＞흉고직경의 순으로, 상수리나무 수간류에는 임외우＞흉고직경＞수관투영면적의 순으로 상관계수 값이 높았다. 그리고 소나무와 상수리나무의 수관통과우는 임외우＞수관투영면적＞흉고직경의 순으로 상관계수 값이 높았다.상관계수 값이 높았다.

• Journal of Pharmaceutical Investigation
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• 제36권5호
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• pp.315-320
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• 2006

Silymarin showed P-glycoprptein(P-gp) inhibitory activity as much as verapamil, a well-known P-gp inhibitor, by decreasing $IC_{50}$ value of daunomycin(DNM)($16.0{\pm}0.7{\mu}M$), increasing the DNM accumulation($224.9{\pm}3.2%$), and decreasing DNM efflux($58.5{\pm}6.7%$), concurrently. In this study, we clarified the mechanism of action of silymarin for P-gp inhibitory function. First, silymarin may bind to the ATP-binding site and thus, prevent ATP hydrolysis. Second, the P-gp inhibitory activity of silymarin is not related to changing the cellular P-gp level. Third, the cytotoxicity of silymarin was increased in the presence of verapamil, reflecting that silymarin is a competent P-gp substrate against verapamil in the P-gp-overexpressed adriamycin-resistant MCF-7 breast cancer(MCF-7/ADR) cells. Conclusively, silymarin had the P-gp inhibitory activity through the action of competent binding to the P-gp substrate-binding site. Therefore, silymarin can be a good candidate for safe and effective MDR reversing agent in clinical chemotherapy by administering concomitantly with anticancer drugs.

• Advances in environmental research
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• 제4권2호
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• pp.83-104
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• 2015

Air Quality Index (AQI) is a pointer to broadcast short term air quality. This paper presents one day ahead AQI forecasting on seasonal basis for three major cities in Maharashtra State, India by using Artificial Neural Networks (ANN) and Genetic Programming (GP). The meteorological observations & previous AQI from 2005-2008 are used to predict next day's AQI. It was observed that GP captures the phenomenon better than ANN and could also follow the peak values better than ANN. The overall performance of GP seems better as compared to ANN. Stochastic nature of the input parameters and the possibility of auto-correlation might have introduced time lag and subsequent errors in predictions. Spectral Analysis (SA) was used for characterization of the error introduced. Correlational dependency (serial dependency) was calculated for all 24 models prepared on seasonal basis. Particular lags (k) in all the models were removed by differencing the series, that is converting each i'th element of the series into its difference from the (i-k)"th element. New time series is generated for all seasonal models in synchronization with the original time line & evaluated using ANN and GP. The statistical analysis and comparison of GP and ANN models has been done. We have proposed a promising approach of use of GP coupled with SA for real time prediction of seasonal multicity AQI.

• Journal of Pharmaceutical Investigation
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• 제14권2호
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• pp.86-91
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• 1984

A ginseng preparation (GP) consisting of ginseng ex., lycium fructus ex., four kinds of vitamines and caffein was evaluated for acute toxicity and general pharmacology. Average lethal doses $(LD_{50})$ of GP in male mice were 2,988mg/kg (i.p.) and more than 3g/kg (p.o.). In dosage of 300 and 900mg/kg (p.o.) showed no analgesic activity in both tests of the writhing method induced by acetic acid and of tail pressure method and no effect on the pentetrazole-induced convulsion. However, it appeared to have a hypothermic action only in dose of 900mg/kg. The duration of hypnosis induced by hexobarbital sodium in mice was shortened by GP, being probably due to caffein. GP Produced no marked contraction of isolated ileum and uterus in high concentrations of up to $1{\pm}10^{-3}g/ml$. These results suggested that GP did not show any considerable central nervous depressant activity and exhibited very weak actue toxicity in mice.

• International Journal of Advanced Culture Technology
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• 제4권4호
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• pp.57-63
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• 2016

In this paper, we propose the optimized binarization in the GP-GPU. Because the binarinztion is esily paralledlized, we propose two ways of binary operations that utilize GP-GPU. The first method was to divide data load, subtraction and conversion, data store. The second method was processed collectibely. The second method was 2.52 times faster than the first method. After synthesizing the GP-GPU to the FPGA, the GP-GPU on the binarization were compared with the binarization on the ODROID XU. The binarization on the GP-GPU was 1.89 times faster than the binarization on the ODROID XU.