• 한국임상수의학회지
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• 제27권5호
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• pp.565-568
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• 2010

설파퀴녹살린과 트리메토프림 합제는 닭콕시듐병의 예방과 치료목적으로 널리 사용하고 있으나, 닭에서의 잔류에 관한 연구보고는 미흡하다. 본 연구에서는 음수첨가용 액제로 신규 개발된 설파퀴녹살린 및 트리메토프림 합제 (설파퀴녹살린, 100 g/L; 트리메토프림, 33.4 g/L)를 육계에 음수 리터당 본제 0.75 mL 및 1.5 mL를 3일간 투여한 후 살처분하여 가식부위내 잔류농도를 액체크로마토그래프/질량분석기를 이용하여 측정하였다. 그 결과 약물 투여 후 7일째에는 모든 가식부위내에서 설파퀴녹살린 및 트리메토프림은 검출되지 않았다. 따라서 신규 음수첨가용 액제인 설파퀴녹살린 및 트리메토프림 합제의 휴약기간은 최소 5일 이상으로 설정되어야 할 것이다.

• Journal of Pharmaceutical Investigation
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• 제22권2호
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• pp.105-113
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• 1992

To improve the solubility and dissolution rate of trimethoprim (TMP), which is slightly soluble drug, its inclusion complexes were prepared and studied in this experiment. Inclusion complexes of TMP with ${\beta}-cyclodextrin$ and ${\beta}-cyclodextrin$ polymer (CDPS) were prepared according to Fenyvesi method. These were compared with TMP and its physical mixture with CDPS. Water, diluted hydrochloric acid and phosphate buffer solution were used as dissolution media. And accelerated stability test was studied at $50,\;70\;and \;80^{\circ}C$. It was found that solubility and dissolution rate of inclusion complexes were increased in water. Especially, the solubility and dissolution rate of TMP was found to be markedly increased by inclusion complexation with CDPS. In stability test, ${\beta}-cyclodextrin$ inclusion complexes were more or less stable than TMP alone. This tendency was not led in CDPS. Consequently, CDPS was useful in increasing dissolution rate and stability of TMP.

• Journal of Pharmaceutical Investigation
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• 제17권3호
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• pp.135-139
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• 1987

This study was attempted to investigate the dissolution rate and the bioavailability of commercially available sulfamethoxazole and trimethoprim (SMX-TM) tablets in rabbits. The dissolution test was conducted in artificial gastric juice by basket method with eight SMX-TM tablets which were chemically equivalent. According to the dissolution rate, SMX-TM tablets were divided into four groups, such as rapid, intermediate, slow and very slow groups for the bioavailability test in rabbits. The results were as follows: 1) The dissolution rate of brand A was most rapid but brand H was most slow in artificial gastric juice. 2) Area under the blood concentration curve was larger in the order of brand A > C > E > H in rabbits. 3) There was a little difference in pharmacokinetic parameters such as biological half life, absorption rate constant and $t_{max}$. 4) The relationship between the dissolution rate and relative bioavailability was significant in brand A, C, E and H. From the results of this experiment, the bioavailability of SMX-TM tablets in rabbits may be predicted from the results of dissolution rate studies.