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      KCI등재 SCOPUS SCIE

      온도감응성 키토산 중성용액을 이용한 약물송달시스템 = Temperature-Sensitive Drug Delivery System of Acetaminophen Using Neutral Chitosan Solution

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      https://www.riss.kr/link?id=A104997992

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      다국어 초록 (Multilingual Abstract)

      In the present study, chitosan-glycerophosphate sodium salt solution as a thermosensitive system (TSS) was used to formulate a temperature-sensitive drug delivery system (TSDDS) containing acetaminophen (AAP). The optimized
      TSS was prepared by measuring gelation temperature, gelation time and rheological properties of TSS. The optimized gelation temperature and time of TSS were 36oC and 100 seconds, respectively. The viscosity of TSS was also suitable for maintaining gel structure at 37.2oC. The release profiles of TSDDS in PBS/pH 7.4 with various apparatuses and mass loss of TSDDS were investigated. The time required to release 50% of AAP from TSDDS (t50%) was 120 min with the formation of pore on the surfaces, which was 2 times longer than that from AAP-chitosan gel. In addition, TSDDS was degraded approximately 80% within 4 hr and then degraded slowly for 20 hrs. In conclusion, AAP-TSS (TSDDS) formulated in this study might be suitable for some specific uses such as subcutaneous injection and rectal formulation.
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      In the present study, chitosan-glycerophosphate sodium salt solution as a thermosensitive system (TSS) was used to formulate a temperature-sensitive drug delivery system (TSDDS) containing acetaminophen (AAP). The optimized TSS was prepared by measuri...

      In the present study, chitosan-glycerophosphate sodium salt solution as a thermosensitive system (TSS) was used to formulate a temperature-sensitive drug delivery system (TSDDS) containing acetaminophen (AAP). The optimized
      TSS was prepared by measuring gelation temperature, gelation time and rheological properties of TSS. The optimized gelation temperature and time of TSS were 36oC and 100 seconds, respectively. The viscosity of TSS was also suitable for maintaining gel structure at 37.2oC. The release profiles of TSDDS in PBS/pH 7.4 with various apparatuses and mass loss of TSDDS were investigated. The time required to release 50% of AAP from TSDDS (t50%) was 120 min with the formation of pore on the surfaces, which was 2 times longer than that from AAP-chitosan gel. In addition, TSDDS was degraded approximately 80% within 4 hr and then degraded slowly for 20 hrs. In conclusion, AAP-TSS (TSDDS) formulated in this study might be suitable for some specific uses such as subcutaneous injection and rectal formulation.

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      참고문헌 (Reference)

      1 J. Wu, "Thermo-and pH-sensitive hydrogel composed of quaternized chitosan/glycerophosphate" 315 : 1-11, 2006

      2 M. Malmsten, "Self-assembly in aqueous block copolymer solutions" 25 : 5440-5445, 1992

      3 K. Edsman, "Rheological evaluation of poloxamer as an in situ gel for opthalmic use" 6 : 105-112, 1998

      4 A. Chenite, "Rheological characterisation of thermogelling chitosan/glycerol-phosphate solutions" 46 : 39-47, 2001

      5 "Pharmaceutical Technical Procedures in European Pharmacopeia 3rd ed. Supplement"

      6 A. Chenite, "Novel injectable neutral solutions of chitosan form biodegradable gels in situ." 21 : 2155-2161, 2000

      7 N. Avoyagi, "Inter-laboratory reproducibility of release tests for suppositories" 21 : 176-183, 1996

      8 R. Baker, "In: Controlled Release of Bioactive Materials" Academic 15-, 1986

      9 H. Tomida, "In vitro release characteristics of diclofenac and hydrocortisone from Pluronic F-127 gels" 24 : 263-272, 1987

      10 P. He, "In vitro evaluation of mucoadhesive properties of chitosan microspheres" 145 : 231-240, 1992

      1 J. Wu, "Thermo-and pH-sensitive hydrogel composed of quaternized chitosan/glycerophosphate" 315 : 1-11, 2006

      2 M. Malmsten, "Self-assembly in aqueous block copolymer solutions" 25 : 5440-5445, 1992

      3 K. Edsman, "Rheological evaluation of poloxamer as an in situ gel for opthalmic use" 6 : 105-112, 1998

      4 A. Chenite, "Rheological characterisation of thermogelling chitosan/glycerol-phosphate solutions" 46 : 39-47, 2001

      5 "Pharmaceutical Technical Procedures in European Pharmacopeia 3rd ed. Supplement"

      6 A. Chenite, "Novel injectable neutral solutions of chitosan form biodegradable gels in situ." 21 : 2155-2161, 2000

      7 N. Avoyagi, "Inter-laboratory reproducibility of release tests for suppositories" 21 : 176-183, 1996

      8 R. Baker, "In: Controlled Release of Bioactive Materials" Academic 15-, 1986

      9 H. Tomida, "In vitro release characteristics of diclofenac and hydrocortisone from Pluronic F-127 gels" 24 : 263-272, 1987

      10 P. He, "In vitro evaluation of mucoadhesive properties of chitosan microspheres" 145 : 231-240, 1992

      11 A. Bilia, "In vitro evaluation of a pH-sensitive hydrogel for control of GI drug delivery from silicone-based matrices" 130 : 83-92, 1996

      12 M. Yamazaki, "Effect of temperature on the release of commercially available acetaminophen suppository" 54 : 227-231, 1994

      13 D. S. Jones, "Dynamic mechanical analysis of polymeric systems of pharmaceutical and biomedical significance" 179 : 167-178, 1999

      14 B. Jeong, "Drug release from biodegradable injectable thermosensitive hydrogel of PEGPLGA- PEG triblock copolymers" 63 : 155-163, 2000

      15 B. Jeong, "Drug release from biodegradable injectable thermosensitive hydrogel of PEGPLGA- PEG triblock copolymers" 63 : 155-163, 2000

      16 E. Ruel-Gariepy, "Characterization of thermosensitive chitosan gels for the sustained delivery of drugs" 203 : 89-98, 2000

      17 I. Henriksen, "Bioadhesion of hydrated chitosans; an in vitro study" 145 : 231-240, 1996

      18 H. Struszcyk, "Advances in chitin and chiosan" Elsevier Applied Science 580-, 1991

      19 N. V. Majeti, "A review of chitin and chitosan applications" 46 : 1-27, 2000

      20 N. V. Majeti, "A review of chitin and chitosan appliations" 46 : 1-27, 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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