• 제목/요약/키워드: Polyethylene glycol-400

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Streptomyces lincolnensis에 의한 Lincomycin 생산에 소포제의 영향

  • 이유리;이미자;정연호;전계택;정용섭
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2000년도 춘계학술발표대회
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    • pp.279-282
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    • 2000
  • S. lincolnensis 배양시 나타나는 거품의 문제를 해결하기위해 UP-1과 OP-1배지에 소포제 종류를 PPG, PEG 및 CA-110을 첨가하여 실험하였다. OP-1배지를 이용한 플라스크 배양의 경우 PPG와 PEG 각각 402 mg/L, 394 mg/L로 높은 Lincomycin 생산농도를 나타내었으나, UP-1배지의 경우 대조구에 비해 Lincomycin 생산농도는 큰 차이가 없었다. 두 가지 배지에서 소포제 농도의 변화에 대한 Lincomycin생산을 통계처리한 결과는 실험한 농도 범위에서 큰 차이를 나타내지 않았다. 충분한 산소공급은 Lincomycin 생산에 필수적이고, rpm의 변화에 따른 실험 결과 300 rpm의 경우 가장 효과적이었다. 발효조에서 PPG 농도 5, 1, 0.5 g/L를 첨가하여 발효한 결과 상당한 차이를 나타내었다. Lincomycin 생산을 위한 소포제로서 PPG가 가장 좋았으며 농도는 0.5 g/L가 적절하였다.

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메칠메타크릴레이트-부틸메타크릴레이트 공중합체 필름의 평가 및 니트로푸라존 방출의 속도론적 연구 (Evaluation of Methyl Methacrylate-Butyl Methacrylate Copolymer Films and Kinetics of Nitrofurazone Release)

  • 전인구
    • Journal of Pharmaceutical Investigation
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    • 제17권3호
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    • pp.111-126
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    • 1987
  • Methyl methacrylate-butyl methacrylate copolymer (MMBM)-dibutyl phthalate (DBP) films were investigated as a potential topical drug delivery system for the controlled release of nitrofurazone. The kinetic analysis of release data indicated that drug release followed a diffusion-controlled granular matrix model, where the quantity released per unit area is proportional to the square root of time. DBP of several hydrophobic plasticizers selected was found to give the highest release of nitrofurazone. However, hydrophilic plasticizers such as propylene glycol and polyethylene glycol 400 had no controlled release properties and acceptable film formation. The effects of changes in film composition, drug concentration, film thickness, pH of release medium, and temperature on the in vitro release of nitrofurazone were analyzed both theoretically and experimentally. The release rate constant (k') was found to be proportional to DBP content, pH, and the temperature of release medium, but independent of film thickness, and drug concentration in a range of 0.1-0.4% by weight. The linear relationship was found to exist between the log k' and DBP content. The release of nitrofurazone from MMBM-DBP (8:2) films was found to be an energy-linked process. Two energy terms were calculated ; the activation energy for matrix diffusion was 13.45 kcal/mole, and the heat of drug crystal solvation was 27.26-29.34 kcal/mole. Observation of scanning electron micrographs and microscopic photographs showed that the incorporation of DBP in films increased markedly the particle size of nitrofurazone dispersed in the film matrix, comparing with the fine dispersion of nitrofurazone in pure MMBM film alone.

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Preparation of Buccal Patch Composed of Carbopol, Poloxamer and Hydroxypropyl Methylcellulose

  • Chun, Myung-Kwan;Kwak, Byoung-Tae;Choi, Hoo-Kyun
    • Archives of Pharmacal Research
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    • 제26권11호
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    • pp.973-978
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    • 2003
  • A polymeric film composed of Carbopol, Poloxamer and hydroxypropyl methylcellulose was prepared to develop a buccal patch and the effects of composition of the film on adhesion time, swelling ratio, and dissolution of the film were studied. The effects of plasticizers or penetration enhancers on the release of triamcinolone acetonide (TAA) were also studied. The hydrogen bonding between Carbopol and Poloxamer played important role in reducing swelling ratio and dissolution rate of polymer film and increasing adhesion time. The swelling ratio of the composite film was significantly reduced and the adhesion time was increased when compared with Carbopol film. As the ratio of Poloxamer to hydroxypropyl methylcellulose increased from 0/66 to 33/33, the release rate of TAA decreased. However, no further significant decrease of release rate was observed beyond the ratio of 33/33. The release rate of TAA in the polymeric film containing polyethylene glycol 400, a plasticizer, showed the highest release rate followed by triethyl citrate, and castor oil. The release rate of TAA from the polymeric film containing permeation enhancers was slower than that from the control without enhancers. Therefore, these observations indicated that a preparation of a buccal patch is feasible with the polymeric film composed of Cabopol, Poloxamer and hydropropyl methylcellulose.

테마제팜 연질캅셀제의 제조와 가토에 있어서 생체이용율 (Preparation of Temazepam Soft Elastic Gelatin Capsule (Softgel) and Bioavailability in Rabbits)

  • 박기배;정의차;조정기;이광표
    • Journal of Pharmaceutical Investigation
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    • 제22권1호
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    • pp.49-54
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    • 1992
  • This study was carried out for the purpose of developing an effective temazepam soft elastic gelatin capsule (softgel) which exhibits an excellent bioavailability and of comparing the rate and extent of absorption of temazepam from the marked elixir and prepared softgel using hydrophilic liquid such as polyethylene glycol 400 as a suspending agent by rotary die method. Both softgel and elixir containing 3 mg of temazepam were given to 7 healthy male New Zealand White rabbits in a single oral dose cross-over study. Plasma temazepam concentrations were measured by HPLC. The mean peak concentrations of temazepam following a single oral dosing as softgel and elixir dosage form were 13.84 and 13.25 ng/ml, respectively. And the mean time to peak concentration was 1.29 hr for the softgel and 1.07 hr for the elixir. There was no significant difference in the extent of drug absorption (AUC) for the two different dosage froms (p>0.05). While the softgel exhibited mean lag time of 0.63 hr, the elixir did not show any lag time. Statistical moment parameters such as the mean residence time and variance of the mean residence time did not differ significantly for the two formulations.

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비페닐디메칠디카르복실레이트의 비수성 경구 액상제제의 설계 및 위장관 투과성 (Design and Gastrointestinal Permeation of Non-aqueous Biphenyl Dimethyl Dicarboxylate Oral Liquid Preparations)

  • 김혜진;전인구
    • Journal of Pharmaceutical Investigation
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    • 제30권2호
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    • pp.119-125
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    • 2000
  • In an attempt to develop a non-aqueous liquid formulation of practically insoluble biphenyl dimethyl dicarboxylate (DDB), dissolution and permeation studies were performed. Various non-aqueous DDB solutions were formulated and filled into empty hard capsules. Dissolution rates of a new formulation were compared with those of commercially available DDB preparations using one and eight dose units. Dissolution rates after 2 hr of DDB tablets (DDB 25 mg), hard capsules (DDB 7.5 mg) and soft capsules (DDB 7.5 mg) on market and new formulation (DDB 7.5 mg) were 6.3, 15.0, 84.5 and 98.0%, respectively. Higher doses (8 units) resulted in a supersaturation within one hr of dissolution, and dissolved amounts were reduced markedly. Due to the saturation and precipitation, a directly proportional dose-dissolution relationship was not observed. The addition of copolyvidone and/or glycyrrhizic acid ammonium salt to DDB solution in polyethylene glycol 300 and 400 inhibited the formation of precipitates during dissolution and markedly enhanced the rabbit duodenal permeation of DDB. From the site-specific gastrointestinal permeation studies, it was found that permeation rates of DDB after mixing of non-aqueous DDB solutions with aqueous buffered solutions were faster in the order of $rectal\;<\;colonic\;{\risingdotseq}\;ileal\;{\risingdotseq}\;duodenal\;<\;jejunal\;<\;gastric$.

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자외선 흡수제 처리 면직물의 소비성능 개선(제1보) - 자외선 차단성능에 관한 연구 - (A Study on the UV-cut Properties of Cotton Fabrics Treated with UV-absorber)

  • 강미정;권영아
    • 한국의류학회지
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    • 제25권5호
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    • pp.925-932
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    • 2001
  • The influence of ultraviolet(UV)-ray in sun light on human skin has been noted. Textiles can provide protection against harmful UV-radiation. Normally UV-absorbing finishes are used to get better protection. The purpose of this study is to evaluate the UV-cut properties of cotton fabrics treated with UV-absorber. 2,2-dihydroxy-4,4-dimethoxbenzophenone, as UV-absorber was applied to 100% cotton fabric. Reagents added in finishing solution were Triton X-100, polyethylene glycol 400, and $MgCl_2{\cdot}6H_2O$, and C.I. Direct Red 81. Both untreated and treated cotton fabrics were exposed to a xenon arc lamp for 20 and 80 hours. UV absorption spectra of finishing solutions and UV transmission spectra of fabrics were measured by the UV/VIS spectrophotometer. The results of this study can be summarized as follows. The results of this study can be summarized as follows. Absorption and the related transmission spectra were modified in a controlled way with UV-absorber. Absorption effect of UV-absorber was improved by adding Triton X-100, PEG 400, and $MgCl_2{\cdot}6H_2O$ in finishing solution. The UV absorption of finishing solution was in the following order: U/D/T/P/M>D/T/P/M> D/T> D/P, D>U/T/P/M>U/T>T/P/M>T. The UV transmittance of cotton fabrics was remarkably decreased by the application of UV-absorber and additives. The UV-cut properties were most improved by the application of U/D/T/P/M.

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Polyethylene Glycol의 분자량(分子量)이 목재(木材)의 치수 안정화(安定化)에 미치는 영향(影響) (Effects of Molecular Weight of Polyethylene Glycol on the Dimensional Stabilization of Wood)

  • 전철;오정수
    • 한국산림과학회지
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    • 제71권1호
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    • pp.14-21
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    • 1985
  • 본(本) 연구(硏究)는 목재(木材) 고유(固有)의 특성(特性)인 흡습성(吸濕性) 및 수축(收縮), 팽창(膨脹)의 이방성(異方性)에 의한 목재(木材) 자체(自體) 및 목제품(木製品)의 가치(價値) 저하(低下)를 방지(防止)하고 목재(木材)의 천연적(天然的)인 아름다운 무늬를 살려 더욱 목재(木材)의 효용가치(効用價値) 높이 기 위하여 비교적(比較的) 가격(價格)이 싸고 독성(毒性)이 없을 뿐만 아니라 주입처리(注入處理)가 용역(容易)한 PEG를 이용(利用)한 목재(木材)의 치수 안정화(安定化) 기술(技術)을 개발(開發)하기 위한 일환(一環)으로 PEG 분자량별(分子量別)(200, 400, 600, 1000, 1500, 2000, 4000, 6000) 및 수종별(樹種別)(Pinus densiflora S. et Z., Larix leptolepis Gordon., Cryptomeria japonica D. Don., Cornus controversa Hemsl., Quercus variabilis Blume., Prunus sargentii Rehder.)로 치수 안정화(安定化) 효과(効果)를 조사(調査)하였던 바, 다음과 같이 요약(要約)될 수 있었다. 1) PEG 주입율(注入率)은 분자량(分子量) 400일 때 137.22%(Pinus densiflora)로 최대치(最大値)를 나타내었고 그 이후(以後)는 비교적(比較的) 완만(緩慢)하게 감소(減少)하는 경향(傾向)을 보여 주었으며 비중(比重)이 낮을수록 PEG 주입량(注入量)도 증가(增加)하는 것으로 밝혀졌다. 2) 부피 팽윤율(澎潤率)은 비중(比重)에 의한 영향(影響)을 별로 받지 않았으며 굴참나무가 분자량(分子量) 400~2,000에 이르기까지 12~18%의 범위(範圍)내에 분포(分布)한 것을 제외(除外)하고는 대부분(大部分) 분자량(分子量) 600일 때 가장 높은 값을 나타내었고, 일반적(一般的)으로 활엽수재(濶葉樹材)가 침엽수재(針葉樹材)보다 높은 부피 팽윤율(澎潤率)을 보여 주었다. 3) 부피 팽윤(澎潤) 감소율(減少率)은 수종(樹種)에 따라 약간의 예외(例外)는 있었으나 대부분이 PEG 분자량(分子量) 400에서 최대치(最大値)를 나타내었고 삼나무의 경우 95.09%로서 최대치(最大値)를 나타내었으며, 산벚나무를 제외(除外)하고는 모두 80% 이상(以上)을 나타내었지만 분자량(分子量) 1,000 이상(以上)에서는 팽윤(膨潤) 감소율(減少率)이 70% 이하(以下)로 떨어졌다. 4) 치수 안정화(安定化) 효율(效率)은 비중(比重)이 큰 활엽수재(濶葉樹材)가 침엽수재(針葉樹材)보다 월등하게 높았으며 전건비중(全乾比重)이 0.89인 굴참나무는 전(全) 분자량(分子量) 범위(範圍)에 걸쳐 부피 팽윤감소율(澎潤減少率)이 1.6 이상(以上)이었는데, 일반적(一般的)으로 분자량(分子量)이 작을수록 우수(優秀)하였으나 분자량(分子量) 4,000 이상(以上)에서는 별로 차이(差異)를 나타내지 않았다. 5) 이상(以上)과 같은 결과(結果)를 종합(綜合) 분석(分析)한 바 PEG 처리(處理)에 의한 치수 안정화(安定化)는 활엽수재(濶葉樹材)의 경우, 특(特)히 효율적(效率的)이며 비록 팽윤감소율(澎潤減少率)이 분자량(分子量) 400에서 가장 높은 수치(數値)를 나타내었지만 PEG 주입율(注入率), 부피 팽윤율(澎潤率), 팽윤감소율(澎潤減少率) 및 치수 안정화(安定化) 효율(效率)을 감안할 때 분자량(分子量) 200~1,500 사이의 것을 적절(適切)한 비(比)로 혼합(混合) 사용(使用)하는 것이 바람직한 것으로 사료(思料)되며, 실용화(實用化)를 위해서는 각 분자량(分子量)의 PEG 혼합비율(混合比率)에 따른 부피 팽윤율(澎潤率), 팽윤감소율(澎潤減少率) 및 치수 안정화(安定化) 효율(效率)에 대한 보다 집중적(集中的)인 연구(硏究)가 요구(要求)된다.

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PEG 주입 침엽수 시편의 열처리 후 PEG 잔류량과 평형함수율 측정 (Measuring PEG Retentions and EMCs of PEG Impregnated Softwood Specimens after Heat-treatment)

  • 홍승현;김정호;임호묵;강호양
    • Journal of the Korean Wood Science and Technology
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    • 제41권3호
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    • pp.173-180
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    • 2013
  • PEG 주입을 통해 열처리 중 목재의 균열을 방지하기 위한 연구에 필요한 기초자료를 제공하기 위해 본 연구가 수행되었다. 국내에서 사용되는 대표적인 침엽수 세 수종의 소시편을 이용하여 PEG 분자량에 따른 침투 속도와 잔류량, 열처리 후 잔류량, 평형함수율 등을 조사하였다. PEG400의 평균 잔류량은 수종별 기본밀도에 반비례하였으며 다른 분자량 PEG에서도 비슷한 경향을 나타냈다. 한 수종 내에서는 PEG 분자량이 클수록 잔류 PEG 양이 감소하는 경향이 뚜렷하다. PEG 주입에 의해 함수율이 2% 내에서 증가하거나 감소하였으며, 시편의 평균 기본밀도는 최고 16.8%까지 증가하였다. 열처리에 의한 중량감소율은 PEG400 시편이 PEG600, PEG1000 보다 컸다. 낮은 분자량의 PEG가 더 많이 용출되었다고 볼 수 있다. 평형함수율은 상대습도가 낮을 때(32%RH) 세 수종 모두 PEG 주입 시편과 무처리 시편의 차이가 없었으나, 상대습도가 증가할수록 PEG 주입 시편이 무처리 시편보다 높게 나타났다.

ALC 블록성능의 기포콘크리트 배합설계 연구 (Foamed Concrete with a New Mixture Proportioning Method Comparable to the Quality of Conventional ALC Block)

  • 양근혁
    • 한국건축시공학회지
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    • 제15권1호
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    • pp.1-7
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    • 2015
  • 본 연구의 목적은 ALC 블록대체를 위한 고성능 기포콘크리트 배합설계를 개발하는 것이다. 대기양생 하에서 기포콘크리트의 고강도 발현(특히 초기재령에서)을 위하여 결합재 및 혼화제를 사전연구에서 다음과 같이 설계하였다. 규산3칼슘이 60% 이상인 보통포틀랜드시멘트에 무수석고 3%를 첨가하였으며, 폴리카르본산계 감수제에서 폴리알킬에테르 성분을 28%로 조절하였다. 이들 재료를 사용하여 물-결합재비와 단위결합재양을 변수로 기포콘크리트 11배합을 실험하였다. 배합된 기포콘크리트의 품질 및 실용성은 KS 규격의 ALC 블록의 요구조건 및 기존의 일반 기포콘크리트와 비교하였다. 실험결과 본 연구의 고성능 기포콘크리트는 ALC 블록의 요구조건을 만족하면서 높은 실용가능성을 보였다.

수용액중 염산카로베린의 용해성 및 안정성 (Solubility and Physicochemical Stability of Caroverine Hydrochloride in Aqueous Solution)

  • 곽혜선;이동수;전인구
    • Journal of Pharmaceutical Investigation
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    • 제28권2호
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    • pp.121-126
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    • 1998
  • The solubility and physicochemical stability of caroverine hydrochloride (CRV), an antispasmodic, in buffered aqueous solutions were studied using a reverse phase high performance liquid chromatography. The solubilty of the drug at pH 2.76-5.40 was similar at the range 31.9-36.2 mg/ml $(34^{circ}C)$, but, at the pH higher than 6.0, markedly decreased. The use of polyethylene glycol 400 as a cosolvent did not increase the solubility at any compositions examined. Moreover. increasing molar concentration of aqueous phosphate buffer from 0 to 0.5 M remarkably decreased the solubility. The degradation of CRY followed the apparent first-order kinetics. The degradation was accelerated with decreasing pH and increasing storage temperature. The half-lives for the degradation of CRY (1.0 mg/ml) at pH 1.28. 4.01 and 5.93 $(45^{\circ}C)$ were 2.8, 31.4 and 124 hr. respectively. The pHs of incubated solutions were to some extent lowered perhaps due to the formation of acidic degradation products. The addition of disodium edetate (0.01%) to the CRY solution (pH 4.95) retarded 2.5 times the degradation rate at $45^{\circ}C$, but the use of sodium bisulfite (0.1%) accelerated 2.9 times the rate. The activation energy for the CRY solution (20 mg/ml. pH 5.4) containing 0.01% EDTA was calculated to be 5.98 kcal/mole. When the solution was stored under nitrogen displacement in ampoule, there was no significant degradation even after 3 months at $40^{\circ}C$, indicating that protection from oxidation by air (oxygen) is essential for the complete stabilization of CRY solution.

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