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      자가미세유화를 이용한 이부프로펜 액상제제의 제조와 특성 = Preparation and Characterization of Liquefied Ibuprofen Using Self-Microemulsion Drug Delivery System (SMEDDS)

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      https://www.riss.kr/link?id=A40102077

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      다국어 초록 (Multilingual Abstract)

      Ibuprofen (IBU), is a non-steroidal anti-inflammatory drug, used to treat rheumatoid arthritis, removal of fever and mild to moderate pain. Because of small dosage and very low accumulation in the body, IBU has been used to heal children`s fever. However, IBU was very low solubility in a low pH and water (in water 0.03∼2.5 ㎎/ml). A nanoemulsion containing IBU by means of self-micromulsion drug delivery system (SMEDDS) was prepared in order to enhance the solubility of IBU. The SMEDDS was composed of cosurfactant, oil and surfactant. The solubility of IBU in various components such as cosurfactant, oil and surfactant was examined. Carbitol^(??) (389.99±20.5 ㎎/ml) as a cosurfctant, Labrafil^(??) M1944CS (90.16±1.60 ㎎/ml) as an oil and Cremopher^(??) RH-40(239.01±2.8 ㎎/ml) as a surfactant were used in this study for preparing SMEDDS. Optimized formulation of SMEDDS was obtained by phase diagram which express the section of nanoemulsion formation. The SMEDDS containing IBU had higher dissolution rate than conventional IBU sirups. Thus the SMEDDS was a potential candidate of stable conventional and effective oral dosage form for IBU.
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      Ibuprofen (IBU), is a non-steroidal anti-inflammatory drug, used to treat rheumatoid arthritis, removal of fever and mild to moderate pain. Because of small dosage and very low accumulation in the body, IBU has been used to heal children`s fever. Howe...

      Ibuprofen (IBU), is a non-steroidal anti-inflammatory drug, used to treat rheumatoid arthritis, removal of fever and mild to moderate pain. Because of small dosage and very low accumulation in the body, IBU has been used to heal children`s fever. However, IBU was very low solubility in a low pH and water (in water 0.03∼2.5 ㎎/ml). A nanoemulsion containing IBU by means of self-micromulsion drug delivery system (SMEDDS) was prepared in order to enhance the solubility of IBU. The SMEDDS was composed of cosurfactant, oil and surfactant. The solubility of IBU in various components such as cosurfactant, oil and surfactant was examined. Carbitol^(??) (389.99±20.5 ㎎/ml) as a cosurfctant, Labrafil^(??) M1944CS (90.16±1.60 ㎎/ml) as an oil and Cremopher^(??) RH-40(239.01±2.8 ㎎/ml) as a surfactant were used in this study for preparing SMEDDS. Optimized formulation of SMEDDS was obtained by phase diagram which express the section of nanoemulsion formation. The SMEDDS containing IBU had higher dissolution rate than conventional IBU sirups. Thus the SMEDDS was a potential candidate of stable conventional and effective oral dosage form for IBU.

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      참고문헌 (Reference)

      1 "pressurised aerosols formulated as solutions" 3 : 33-40, 1992

      2 "alkanediol" int. j. pharm. : 111-, 63-72

      3 "The mechanochemical preperation of solid disperse system of ibuprofen-polyethylene glycol" 130 : 25-32, 1996

      4 "Synthesis of NiS nanoparticles using a sugar-ester nonionic water-in-oil microemulsion" 58 : 762-767, 2004

      5 "Synthesis and characterization of novel dipeptide ester prodrugs of acyclovir" 59 : 2033-2039, 2003

      6 "Stereoselective pharmacokinetics of ibuprofen and its lysinate from suppsitiories in rabbits" 199 : 159-166, 2000

      7 "Spectrofluorimetric study of the b-cyclodextrin-ibuprofen complex and determination of ibuprofen in phamaceutical preperation and serum" 60 : 235-246, 2003

      8 "Solubilization of ibuprofen in aqueous solution" 27 : 279-286, 1997

      9 "Self-emulsifying drug delivery system:Assessment of the efficiency of emulsification" 27 : 335-348, 1985

      10 "Preparation of solid dosage form containing SMEDDS of simvastatin by microencapsulation," 33 : 121-127, 2003

      1 "pressurised aerosols formulated as solutions" 3 : 33-40, 1992

      2 "alkanediol" int. j. pharm. : 111-, 63-72

      3 "The mechanochemical preperation of solid disperse system of ibuprofen-polyethylene glycol" 130 : 25-32, 1996

      4 "Synthesis of NiS nanoparticles using a sugar-ester nonionic water-in-oil microemulsion" 58 : 762-767, 2004

      5 "Synthesis and characterization of novel dipeptide ester prodrugs of acyclovir" 59 : 2033-2039, 2003

      6 "Stereoselective pharmacokinetics of ibuprofen and its lysinate from suppsitiories in rabbits" 199 : 159-166, 2000

      7 "Spectrofluorimetric study of the b-cyclodextrin-ibuprofen complex and determination of ibuprofen in phamaceutical preperation and serum" 60 : 235-246, 2003

      8 "Solubilization of ibuprofen in aqueous solution" 27 : 279-286, 1997

      9 "Self-emulsifying drug delivery system:Assessment of the efficiency of emulsification" 27 : 335-348, 1985

      10 "Preparation of solid dosage form containing SMEDDS of simvastatin by microencapsulation," 33 : 121-127, 2003

      11 "Preparation and characterization of microemulsion containing ibuprofen" 45 : 634-640, 2001

      12 "Preparation and characterization of ibuprofen cetyl alcohol beads by melt solidification technique:Effect of variables" 261 : 57-67, 2003

      13 "Post-iontophoresis transport of ibuprofen lysine across rabbit ear skin" 266 : 69-75, 2003

      14 "Physician's Desk Reference" Medical Economics Company 53 : 875-889, 1999

      15 "Phase studies of oil-in-water phospholipod microemulsions" 84 : 1992

      16 "Microemulsions. Colloidal aspects." 4 : 281-300, 1975

      17 "Microemulsions-interfacial aspects" 34 : 583-595, 1991

      18 "Investigations into the formation and characterization of phospholipid microemulsion IV. Pseudo-ternary phase diagrams of systems containing water-lecithin-alcohol and oil The influence of oil" 125 : 107-116, 1995

      19 "Inclusion complex of analgesic and antiinflammatory agents with cyclodextrins Enhancement of dissolution of ibuprofen by 2-hydroxypropyl-b-cyclodextrin" 11-18, 1993

      20 "Improved dissolution characteristics of ibuprofen employing self-microemulsifying drug delivery system and their bioavailability in rats" 32 : 27-33, 2002

      21 "Formulation and biopharmaceutical evaluation of an investigational lipophilic compound" 87-93, 1992

      22 "Formation of cubic structures in microemulsions containing equal volumes of water and oil" 319 : 400-, 1986

      23 "Fluorouracil prodrugs for the treatment of proliferative vitreoretinopathy: Formulation in silicone oil and in vitro release of fluorouracil" 259 : 181-192, 2003

      24 "Fast dispersible ibuprofen tablets" 15 : 295-305, 2002

      25 "Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides" 20 : 91-97, 2003

      26 "Enhancement of ibuprofen dissolution via wet granulation with beta-cyclodextrin" 6 : 305-314, 1994

      27 "Enhanced solubility of ibuprofen with poloxamer and mentol" 33 : 57-60, 2003

      28 "Effect of molecular weights and mixture ratios of polyvinylpyrrolidone on the bioavailability of ipriflavone solid dispersion" 30 : 235-239, 2000

      29 "Calorimetric study of CdS nanoparticle formation in w/o microemulsions" 23 : 1077-1081, 2003

      30 "Antipyretique activity of ibuprofen syrup in children emergency unit" 16 : 407-410, 2003

      31 "A theory of aqueous emulsion. I. Negative interfacial tension at the oil/water interface" 23 : 165-173, 1967

      32 "A study on factors influencing the droplet size in nonionic oil-in-water microemulsions" 88 : 417-422, 1992

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      학술지 이력

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      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2010-06-09 학술지명변경 한글명 : 약제학회지 -> Journal of Pharmaceutical Investigation
      외국어명 : Jorunal of Korean Pharmaceutical Sciences -> Journal of Pharmaceutical Investigation
      KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-06-16 학회명변경 영문명 : The Korean Society Of Pharmaceutics -> The Korean Society of Pharmaceutical Sciences and Technology KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.18 0.18 0.14
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.11 0.374 0.02
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