• 대한수의학회지
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• 제30권1호
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• pp.41-49
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• 1990

These experiments were carried out to develop a novel, simple, and rapid method to determine urinary sulfonamides using fluorescamine by spectrofluorometry. To get optimal conditions for the sulfonamide-fluorescamine reaction, sulfonamides such as sulfamethazine, sulfamerazine, sulfadimethoxine and sulfamonomethoxine, dissolved in buffers with various pH ranges were reacted with various concentrations of fluorescamine. and then, the fluorescence intensity and stability of the fluorophore were measured. To eliminate the interfering substances in urine, the fluorophore in buffers and urine with a definite pH range was extracted with some organic solvents. After then the fluorescence intensity was measured in organic and aquous phases. The results obtained were summarized as follows: 1. The maximal fluorescence of sulfonamides was presented in acidic state, pH 4.5~5.0, at 30 minutes after reaction. 2. The optimal concentration ratio of sulfamethazine and ffuorescamine was more than 1 : 40 in mole. 3. In pH 4.0, the intensity was maximal but was time-dependent, whereas in pH 8.0, the intensity was time-independent. 4. Sulfamethazine-fluorescamine conjugate could be dissolved in some of organic solvents in acidic state such as chloroform, n-butanol, and ethylacetate. 5. Sulfamethazine-flnorescamine conjugate in swine urine coule be extracted with ethylacetate in acidic state, pH 4.0~5.0.

• 지질공학
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• 제3권2호
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• pp.191-201
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• 1993

환원은 심층 지하처분되는 Cr(VI)의 양을 줄이는데 중요한 수단의 하나이다. 이 반응은 pH와 온도에 따라 민감하게 작용하며, 지하심층 처분장의 낮은 pH와 높은 온도는 토양 유기질, 높은 염소이온 농도와 더불어 Cr(VI)의 환원에 좋은 환경을 제공한다. 본 연구에서는 다양한 환경 조건에 따른 토양 유기질과 염소이온에 의한 Cr(VI)의 환원이 조사 되었다. aquifer와 aquitard 샘플은 각각 미국 루이지애나주 세인트 촬스군의 심층 처분장에서 채취되었다. 본 연구에서는 심층처분장을 대표하는 pH(-0.81~2.0), 온도($50^{\circ}C와{\;}70^{\circ}C$), 염소이온 농도(0, 0.26, 0.52 몰)를 이용하였다.

• 약학회지
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• 제34권5호
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• pp.302-310
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• 1990

A study has been made of the Korean bentonite aqueous suspension contrast with American bentonite by means of XRD IR swelling, gel formation and rheogram at various conditions such as concentration, temperature and pH. The Korean bentonite was identified as montmorillonite clay containig a small proprotion of crystoballite and mordenite, and its swelling power were acceptable for requirements of Korean pharmacopeia regulations though its values were not satisfied. Korean bentonite swelled to 10 times and American one did to 15 times compared to its bulkiness of powder. The rheogram of Korean bentonite suspension reveals bulged pseudoplatic flow with yield value at higher concentration and pseudoplastic flow without yield value at lower concentration. The higher the concentration, the greater were the apparent viscosity and hysteresis loop. Korean bentonite suspension showed insignificant temperature dependence on both apparent viscosity and hysteresis loop and it was more temperature dependent on viscosity but less on hysteresis loop than those of American sample. The pH dependence was so high on viscosity that apparent minimum value was near pH 7 and maximum value at pH 3 or 7. The hysteresis loop appeared minimum over the pH range 5-7 and maximum near pH 3 or 11. The Korean bentonite was inferior to the American bentonite in swelling volume, gel formation, thioxotropy, however, it would be possible to improve the quality of Korean bentonite by developing the method of purification for bentonite clay.

• KSBB Journal
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• 제15권5호
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• pp.444-451
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• 2000

Nonliving methanotrophic biomass was used as biosorbent to remove lead which is one of representative pollutants in metal-bearing wastewater. Solution pH, maximum uptake, biosorbent dose and ionic strength were considered as major factors for adsorption experiments. The optimum pH range for lead removal was increased 3.8∼11.0 for methanotrophic biomass compared to biosorbent-free control, pH of 8.4∼11.2. Removal efficiency of lead by methanotrophic biomass was pH dependent, but less sensitive than that of control. In isotherm experiments with 0.2g biosorbent/L at initial solution pH 5.0, methanotrophic biomass took up lead from aqueous solutions to the extent of 1085 mg/g biomass. Removal amount of lead increased with an increase of biomass dose. According to biomass dose for initial 1000 mg Pb/L at initial pH 5.0, the optimum amount of biomass for maximum lead removal per unit methanotrophic biomass was 0.2 g biomass/L. As a result of scanning electron microscope (SEM) micrographs equipped with energy dispersive spectroscopy (EDS), lead removal by methanotrophic biomass seemed to be through adsorptions on the surface of methanotrophic biomass and exopolymers around the biomass. EDS spectra confirmed that lead adsorption appeared on the biomass and exopolymers that may be effective to lead removal comparing before and after contact with lead. Removal efficiency of lead was slightly affected by ionic strength up to 2.0 M of NaCl and NaNO$_3$respectively.

• Journal of Pharmaceutical Investigation
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• 제17권3호
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• pp.127-133
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• 1987

Dissolution characteristics and urinary excreted amount of commercially available three brands of sulfisoxazole tablets were investigated in order to elucidate the in vitro-in vivo correlations and relative bioavailability in humans. All the tablets tested met the K.P. IV and the USP XXI specifications for tablet weight variation, content uniformity, disintegration and dissolution. The disintegration and dissolution rate constants of sulfisoxazole tablets in pH 2.0 HCl-KCl buffer were reduced more significantly (p<0.05) than those in diluted HCl $(1{\rightarrow}12.5)$ and pH 6.5 phosphate buffer. It seemed to be attributed to the pH dependent solubility of sulfisoxazole. We could see that the relative bioavailability of brand B to sulfisoxazole powder was about 90% and that its value was higher than those of other two brands from the urinary excretion data obtained from eight healthy male volunteers by means of Latin square cross over design. No useful correlation was observed between the in vitro and in vivo studies in this experiment.

• 한국생명과학회:학술대회논문집
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• 한국생명과학회 2003년도 제39회 학술심포지움
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• pp.129-129
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• 2003

• Bulletin of the Korean Chemical Society
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• 제30권6호
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• pp.1401-1404
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• 2009

• 약학회지
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• 제46권3호
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• pp.168-173
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• 2002

The physicochemical properties of aloesin, which has been recently found to reduce renal toxicity induced by cis-platin, were studied including solubility, partition coefficient ( $P_{c}$ ), osmolality, and stability. The solubility of aloesin was about 500 mg/mι, and the $P_{c}$ value for n-octanol/water was 1.01 $\pm$ 0.03. The degradation of aloesin followed the pseudo-first-order kinetics and was dependent on temperature, pH and ionic strength. From the pH-rate profile, the optimal pH was found to be 2.0~3.0. Some metal ions increased the degradation rate in the rank order of M $n^{2+}$ ＞ F $e^{3+}$ ＞ C $u^{2+}$ ＞ F $e^{2+}$. On the other hand, other metal ions such as B $i^{3+}$, $Ba^{2+}$, Z $n^{2+}$, N $i^{2+}$, $Co^{2+}$ and $Mg^{2+}$ did not show the unfavorable effects. After autoclaving, aloesin contents remaining were 81.8~98.8% of initial concentrations depending on pH. The most stable pH was 3.98 in the autoclaving. Osmolality increased linearly as concentration increased.sed.creased.sed.

• Fibers and Polymers
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• 제4권2호
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• pp.66-70
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• 2003

Temporarily solubilized azo disperse dyes based on 1,2-substituted indoles were synthesized and characterized. Dispersant-free dyeing of polyester by using the synthesized dyes has been investigated. The colour yields of the dyes on the polyester fabric were found to be highly dependent on the dyeing pH, optimum results being obtained at pH 5. The dyes exhibited good to excellent fastness properties on polyester while lightfastness was moderate.

• 한국인쇄학회지
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• 제20권1호
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• pp.45-53
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• 2002

The removal of chelated copper from anthraquinone dyes by cementation on powdered iron was studied. The removal of chelated copper was found to be a function of solution pH, amount of NTA and iron, and reaction temperature. In the presence of NTA, reaction rate of cementation was found to be strongly dependent on reaction temperature, solution pH, amount of NTA and amount of iron powder. These experimental results can be explained successfully by the distribution of complexed copper iron in solutions.