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      KCI등재 SCOPUS SCIE

      The feasibility study of transdermal drug delivery systems for antidepressants possessing hydrophilicity or hydrophobicity

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      https://www.riss.kr/link?id=A104993102

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      다국어 초록 (Multilingual Abstract)

      The feasibility studies on the transdermal drug delivery systems have been performed to avoid the systemic side-effects and gastric disorders that could be occurred due to the transient high blood concentration after oral administration of antidepressants such as venlafaxine HCl and citalopram. When surfactants of tween 80® and plasticizer of diethyl phthalate were combined with citalopram–ethylene vinyl acetate (EVA) matrix, the permeation of citalopram showed the best enhancement. As well as, venlafaxine HCl gels were prepared using carbomer, oleic acid and/or propylene glycol to enhance the skin permeation of venlafaxine HCl. The citalopram-EVA matrix containing tween 80® and diethyl phthalate as permeation enhancers might be a good transdermal delivery system for providing sustained plasma concentrations of citalopram. Also, venlafaxine HCl showed the possibility to be enhanced skin permeation in the formulation of gels with carbomer including penetration enhancer, oleic acid and/or propylene glycol.
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      The feasibility studies on the transdermal drug delivery systems have been performed to avoid the systemic side-effects and gastric disorders that could be occurred due to the transient high blood concentration after oral administration of antidepress...

      The feasibility studies on the transdermal drug delivery systems have been performed to avoid the systemic side-effects and gastric disorders that could be occurred due to the transient high blood concentration after oral administration of antidepressants such as venlafaxine HCl and citalopram. When surfactants of tween 80® and plasticizer of diethyl phthalate were combined with citalopram–ethylene vinyl acetate (EVA) matrix, the permeation of citalopram showed the best enhancement. As well as, venlafaxine HCl gels were prepared using carbomer, oleic acid and/or propylene glycol to enhance the skin permeation of venlafaxine HCl. The citalopram-EVA matrix containing tween 80® and diethyl phthalate as permeation enhancers might be a good transdermal delivery system for providing sustained plasma concentrations of citalopram. Also, venlafaxine HCl showed the possibility to be enhanced skin permeation in the formulation of gels with carbomer including penetration enhancer, oleic acid and/or propylene glycol.

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      참고문헌 (Reference)

      1 Wilson AD, "Venlafaxine ingestion isassociated with rhabdomyolysis in adults: a case series" 32 : 97-101, 2007

      2 Sampson SM, "Treating depression with selective serotoninreuptake inhibitors: a practical approach" 76 : 739-744, 2001

      3 Troy SM, "Thepharmacokinetics of venlafaxine when given in a twice dailyregimen" 35 : 404-409, 1995

      4 Singh G, "Screeningof venlafaxine hydrochloride for transdermal delivery: passivediffusion and iontophoresis" 9 : 791-797, 2008

      5 Kent JM, "SNaRIs, NaSSAs, and NaRIs: new agents for thetreatment of depression" 355 : 911-918, 2000

      6 Stahl SM, "SNRIs: theirpharmacology, clinical efficacy and tolerability in comparisonwith other classes of antidepressants" 10 : 732-747, 2005

      7 Wille SM, "Relevantissues in the monitoring and the toxicology of antidepressants" 45 : 25-89, 2008

      8 Kilts CD, "Potential new drug delivery system for antidepressants:an overview" 64 : 31-33, 2003

      9 Hiemke C, "Pharmacokinetics of selective serotoninreuptake inhibitors" 85 : 11-28, 2000

      10 Kognan A, "Microemulsions as transdermal drugdelivery vehicles" 123 : 369-385, 2006

      1 Wilson AD, "Venlafaxine ingestion isassociated with rhabdomyolysis in adults: a case series" 32 : 97-101, 2007

      2 Sampson SM, "Treating depression with selective serotoninreuptake inhibitors: a practical approach" 76 : 739-744, 2001

      3 Troy SM, "Thepharmacokinetics of venlafaxine when given in a twice dailyregimen" 35 : 404-409, 1995

      4 Singh G, "Screeningof venlafaxine hydrochloride for transdermal delivery: passivediffusion and iontophoresis" 9 : 791-797, 2008

      5 Kent JM, "SNaRIs, NaSSAs, and NaRIs: new agents for thetreatment of depression" 355 : 911-918, 2000

      6 Stahl SM, "SNRIs: theirpharmacology, clinical efficacy and tolerability in comparisonwith other classes of antidepressants" 10 : 732-747, 2005

      7 Wille SM, "Relevantissues in the monitoring and the toxicology of antidepressants" 45 : 25-89, 2008

      8 Kilts CD, "Potential new drug delivery system for antidepressants:an overview" 64 : 31-33, 2003

      9 Hiemke C, "Pharmacokinetics of selective serotoninreuptake inhibitors" 85 : 11-28, 2000

      10 Kognan A, "Microemulsions as transdermal drugdelivery vehicles" 123 : 369-385, 2006

      11 Sweetman SC, "Martindale: the complete drug reference, 34thedn" PhP Pharmaceutical 321-323, 2005

      12 Pacher P, "Current trends inthe development of new antidepressants" 8 : 89-100, 2001

      13 Bezchlibnyk-Butler K, "Citalopram—areview of pharmacological and clinical effects" 25 : 241-256, 2000

      14 Uges DRA, "ADs and antipsychotics, In Forensic science" Elsevier 229-256, 2000

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      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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      학술지 인용정보

      학술지 인용정보
      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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