• Title/Summary/Keyword: preparations

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Determination of Selenium in Dried Yeast Preparations (셀레늄 함유 건조효모제제 중 셀레늄 분석방법에 관한 연구)

  • Oh, Sea-Jong;Oh, Young-Taek;Yoon, Won-Yong;Park, Sung-Bae
    • Journal of Pharmaceutical Investigation
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    • v.24 no.1
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    • pp.29-32
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    • 1994
  • In order to improve the sensitivity of the current assay methods of selenium in dried-yeast preparations, atomic absorption spectrophotometry (AAS), high performance liquid chromatography (HPLC) and UV-Vis spectrophotometry were employed. The sample was prepared with the digestion by acid mixture of hydrochloric acid, nitric acid and perchloric acid after elimination of ether-soluble substances. The range of quantitation of selenium was $1.0{\sim}6.0\;{\mu}g/ml$ by UV-Vis spectrophotometry, $5.0{\sim}20.0\;{\mu}g/ml$ by HPLC and $0.03{\sim}0.10\;{\mu}g/ml$ by AAS.

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Studies on Pollen Preparations as a Health Food(I) (건강(健康) 식품(食品)으로서 화분(花粉) 제제(製劑)에 관한 연구(硏究)(제1보)(第1報))

  • Kim, Jung-Woo;Shin, Sang-Chul;Kim, Byong-Kak
    • Korean Journal of Pharmacognosy
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    • v.15 no.3
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    • pp.147-149
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    • 1984
  • To examine pollen preparations which are being sold as a health food, one of these pollen tablets and one of the capsules were selected and investigated by microscopy. It was shown that the pollen coat which can act as a potent allergen was not removed and that the tablets contained other impurities. The results suggest that they are not safe as a food and that they may cause systemic allergy to certain persons. On the contrary, the pollens of the capsule preparation did not have the pollen coat and, therefore, have a less risk of causing allergy.

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Determination of ${\beta}$-sitosterol in Unsaponifiable Fraction of Zea mays and Related Drug Preparations by HPLC (HPLC에 의한 Zea mays 불검화추출물과 그의 함유제제 중 ${\beta}$-시토스테롤의 정량)

  • Kim, Kyeong-Ho;Park, Woo-Sun;Shim, Chang-Gu
    • YAKHAK HOEJI
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    • v.40 no.2
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    • pp.149-154
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    • 1996
  • A high-performance liquid chromatographic method for the determination of ${\beta}$-sitosterol in the unsaponifiable fraction of Zea mays L. and its related drug preparations using a cholesterol as an internal standard was investigated. They were saponified with 20% methanolic KOH solution. Phytosterols in the reaction mixture were extracted with diethyl ether and separated on silica gel TLC plate with n-hexane-diethyl ether(40:60) as the solvent and then were scraped off. They were separated by reversed phase high perfomance liquid chromatography on Inertsil ODS-2 column with detection at 205nm. Cholesterol and ${\beta}$-sitosterol were resolved from interferences by adjusting the acetonitrile content in the MeOH-tetrahydrofuran-$H_2O$ eluent. The detection limit of ${\beta$-sitosterol was 0.43${\mu}$g.

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Determination of Aloesin in Aloe Preparations by HPLC (고속액체크로마토그래피에 의한 알로에 제제 중의 알로에신의 정량)

  • Kim, Kyeong-Ho;Kim, Hyun-Ju;Park, Jeong-Hill;Shin, Young-Geun
    • YAKHAK HOEJI
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    • v.40 no.2
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    • pp.177-182
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    • 1996
  • The contents of aloesin in aloe preparations were determined by HPLC. Aloesin was extracted 3 times with ethanol for 30 minutes. The ethanol extract was concentrated and suspend ed in saturated NaCl aqueous solution and successively partitioned with dichloromethane, n-butanol. Prepared samples were analyzed by HPLC on a reverse column(Inertsil ODS-2). In assay, internal standard was a puerarin and regression of calibration curve was 0.998. Recoveries of aloesin added to aloe preparation were 98~123(%).

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Study on the Stability of Ascorbic acid in several Antacid Preparations (분말성제제(粉末性製劑)의 안정성(安定性)에 관(關)한 연구(硏究) -수종제산제중(數種制酸劑中)의 Ascorbic acid의 안정성(安定性)에 관(關)한 연구(硏究)-)

  • Shin, Sang-Chul;Lee, Min-Hwa;Woo, Chong-Hak
    • Journal of Pharmaceutical Investigation
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    • v.3 no.1_2
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    • pp.34-50
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    • 1973
  • There are many reports on the stability of drugs in powders and tablets. The stabilities of ascorbic acid in the antacid preparations, such as calcium carbonate, magnesium carbonate, magnesium trisilicate, magnesium alumino silicate, and dried aluminum hydroxide gel under various humidities were examined. From the result of the experiment, it was assumed that the concentration of ascorbic acid, the amount of water-vapor sorption, and the physical character of the antacid ingredients were the main factors, influencing the degradation of ascorbic acid. The ascorbic acid, mixed with carbonates, such as calcium carbonate, was degradaded rapidly, while the preparation with dried aluminum hydroxide gel was slightly degraded after 10 days. A 2% ascorbic acid in the prepation was rapidly degraded than 10% ascorbic acid in the preparation.

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Methods for Recording and Counting the Heart Rate of Intact Animal and Isolated Preparations (실험동물(實驗動物)의 심박계측법(心搏計測法))

  • Chang, Hwang-Nam
    • The Korean Journal of Pharmacology
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    • v.4 no.1 s.5
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    • pp.37-39
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    • 1968
  • A method for presenting the heart rate of intact animals as a kymographic record is described. A transistorized impulse generator with a dry battery power supply is used to produce pulses. The pulses are integrated and make a pen motor drived. The ability of the instrument to follow a wide range of heart rate change is demonstrated. The instrument is especially usefull to observe an acute and transitory heart rate change. A method for changing the heart beat to sound and a method for counting the heart rate of intact animal and isolated preparations by employing post office counter were also described.

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Toxicological Evaluation of Oriental Herbal Medicine Kamijadowhan Preparations

  • Park, Young-Jin;Ryu, Jae-Chun;Choi, Seung-Hun;Kwon, Oh-Seung
    • Proceedings of the PSK Conference
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    • 2002.10a
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    • pp.289.2-290
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    • 2002
  • Choi group reported that Kamijadowhan (KMD). an oriental herbal medicine, has anti-angiogenic effects and it may be a potential agent for clinical chemoprevention since it inhibits angiogenesis. Objectives of this experiment are to investigate acute, genetic and reproductive/developmental toxicities of KMD preparations. Acute toxicity was performed after single administration of KMO (200-500 mg/kg) to mice. Supravital staining micronucleus assay was conducted using peripheral reticulocytes in mice. (omitted)

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Identification of Ginger Components and Quantitative Determination of 6-Gingerol from Crude Drugs-Drink Preparations (생약복방 드링크제 중 건강성분의 확인 및 6-Gingerol의 분리 정량)

  • 고성룡;최강주
    • Journal of Ginseng Research
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    • v.14 no.3
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    • pp.442-446
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    • 1990
  • As a part of studies on the quality control of crude drug-drink preparations, ginger components were identified by TLC and 6-gingerol was determined quantitatively by HPLC. Ginger components were identified by TLC with benzene/acetone (4:1, v/v, on silica gel plate by spraying a vanillinsulfuric acid reagent. 5-Gingerol contents were determined at 280 nm by HPLC on Lichro CART RP-18 column with acetonitrile/wate(38:62, v/v). Its transfer rate in the 3 types of crude drug extract drinks was 65.4-85.1% compared to the content in the ginger extract.

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Is ginseng free from adverse effects?

  • Xie, Jing-Tian;Mehendale, Sangeeta R.;Maleckar, Spring A.;Yuan, Chun-Su
    • Advances in Traditional Medicine
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    • v.2 no.2
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    • pp.80-86
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    • 2002
  • Ginseng is a perennial herb widely used in China, Japan, and Korea. It is also one of the most commonly used herbal medicines in the U.S. Although it is generally considered safe to use, adverse effects associated with ginseng use have been reported. Inappropriate ginseng use, such as high dose administration, may cause insomnia, headaches, diarrhea, as well as cardiovascular and endocrine disorders. Other factors that may contribute to adverse effects of ginseng include the variety of ginseng species, variability in commercial ginseng preparations, and potential ginseng-drug interactions. To minimize adverse effects of ginseng, consumers should be advised to use it appropriately, and the herbal industry should try to provide standardized ginseng preparations.

The Effects of Pain Control by Electro-Anesthesia in Cavity Preparations (와동형성시의 전기마취에 의한 제통효과)

  • Jung, Gwan-Hee
    • The Journal of the Korean dental association
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    • v.11 no.11
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    • pp.745-748
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    • 1973
  • The author has studied the effects of pain control by using the Anode-S-3 electro anesthesia in cavity preparations. The electric current value had used 4~10㎂. The results were as follows. 1) The 86 tests in cases of 110 tests as much as 78% of it have showed pain control effects and the 24 of tests as much as 22% had no effects in general. 2) The cases of perfect pain control was only made to 42 tests in cases of 110 tests as much as 38% of it. 3) The pain control with a little inordinary feeilng was 33 tests in 110 of it as much as 30% 4) The slight pain were recorded 22 cases as much as 21% of the tests. 5) The severe pain were recorded 12 cases as much as 11% of the tests. 6) Meanwhlie, the case of increasing pains by using electro-anesthesia was not recorded at all.

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