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      KCI등재 SCIE SCOPUS

      Application of Mixture Experimental Design in the Formulation and Optimization of Matrix Tablets Containing Carbomer and Hydroxypropylmethylcellulose

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      https://www.riss.kr/link?id=A104667685

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Using mixture experimental design, the effect of carbomer (Carbopol® 971P NF) and hydroxypropylmethylcellulose (Methocel® K100M or Methocel® K4M) combination on the release profile and on the mechanism of drug liberation from matrix tablet was investigated. The numerical optimization procedure was also applied to establish and obtain formulation with desired drug release. The amount of TP released, release rate and mechanism varied with carbomer
      ratio in total matrix and HPMC viscosity. Increasing carbomer fractions led to a
      decrease in drug release. Anomalous diffusion was found in all matrices containing carbomer, while Case - II transport was predominant for tablet based on HPMC only. The predicted and obtained profiles for optimized formulations showed similarity. Those results indicate that Simplex Lattice Mixture experimental design and numerical optimization procedure can be
      applied during development to obtain sustained release matrix formulation with desired release profile.
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      Using mixture experimental design, the effect of carbomer (Carbopol® 971P NF) and hydroxypropylmethylcellulose (Methocel® K100M or Methocel® K4M) combination on the release profile and on the mechanism of drug liberation from matrix tablet was inve...

      Using mixture experimental design, the effect of carbomer (Carbopol® 971P NF) and hydroxypropylmethylcellulose (Methocel® K100M or Methocel® K4M) combination on the release profile and on the mechanism of drug liberation from matrix tablet was investigated. The numerical optimization procedure was also applied to establish and obtain formulation with desired drug release. The amount of TP released, release rate and mechanism varied with carbomer
      ratio in total matrix and HPMC viscosity. Increasing carbomer fractions led to a
      decrease in drug release. Anomalous diffusion was found in all matrices containing carbomer, while Case - II transport was predominant for tablet based on HPMC only. The predicted and obtained profiles for optimized formulations showed similarity. Those results indicate that Simplex Lattice Mixture experimental design and numerical optimization procedure can be
      applied during development to obtain sustained release matrix formulation with desired release profile.

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      참고문헌 (Reference)

      1 Petrovic, A., "Theophylline release from aminophylline matrix tablets containing HPMC and Carbopol®" 2006

      2 Furlanetto, S., "Study of formulation variables influencing the drug release rate from matrix tablets by experimental design" 62 : 77-84, 2006

      3 Khan, G. M., "Studies on Drug Release Kinetics from Ibuprofen-carbomer hydrophilic matrix tablets: Influence of co-excipients on release rate of the drug" 57 : 197-203, 1999

      4 Perez-Marcos, B., "Release of propranolol hydrochloride from matrix tablets containing hydroxypropyl methylcellulose K4M and Carbopol 974" 111 : 251-259, 1994

      5 Zuleger, S., "Polymer particle erosion controlling drug release. II, in: Swelling investigations to clarify the release mechanism" 247 : 23-37, 2002

      6 Zuleger, S., "Polymer particle erosion controlling drug release. I. in: Factors influencing drug release and characterization of the release mechanism" 217 : 139-152, 2001

      7 Lubrizol, "Pharmaceutical Polymers for Controlled Release Tablets and Capsules" 30 : 2008a

      8 Huang, Y. B., "Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology" 289 : 87-95, 2005

      9 Huang, Y. B., "Once-daily propranolol extended-release tablet dosage form: formulation design and in vitro/in vivo investigation" 58 : 607-614, 2004

      10 Khanna, R., "Muco-adhesive buccal tablets of clotrimazole for oral candidiasis" 23 : 831-837, 1997

      1 Petrovic, A., "Theophylline release from aminophylline matrix tablets containing HPMC and Carbopol®" 2006

      2 Furlanetto, S., "Study of formulation variables influencing the drug release rate from matrix tablets by experimental design" 62 : 77-84, 2006

      3 Khan, G. M., "Studies on Drug Release Kinetics from Ibuprofen-carbomer hydrophilic matrix tablets: Influence of co-excipients on release rate of the drug" 57 : 197-203, 1999

      4 Perez-Marcos, B., "Release of propranolol hydrochloride from matrix tablets containing hydroxypropyl methylcellulose K4M and Carbopol 974" 111 : 251-259, 1994

      5 Zuleger, S., "Polymer particle erosion controlling drug release. II, in: Swelling investigations to clarify the release mechanism" 247 : 23-37, 2002

      6 Zuleger, S., "Polymer particle erosion controlling drug release. I. in: Factors influencing drug release and characterization of the release mechanism" 217 : 139-152, 2001

      7 Lubrizol, "Pharmaceutical Polymers for Controlled Release Tablets and Capsules" 30 : 2008a

      8 Huang, Y. B., "Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology" 289 : 87-95, 2005

      9 Huang, Y. B., "Once-daily propranolol extended-release tablet dosage form: formulation design and in vitro/in vivo investigation" 58 : 607-614, 2004

      10 Khanna, R., "Muco-adhesive buccal tablets of clotrimazole for oral candidiasis" 23 : 831-837, 1997

      11 Siepman, J., "Modeling of drug release from delivery systems based on hydroxypropylmethylcellulose (HPMC)" 48 : 139-157, 2001

      12 Costa, P., "Modeling and comparison of dissolution profiles" 13 : 123-133, 2001

      13 Narasimhan, B., "Mathematical models describing polymer dissolution: Consequences for drug delivery" 48 : 195-210, 2001

      14 Perez-Marcos, B., "Influence of the pH on the release of propranolol hydrochloride from matrices containing hydroxypropyl methylcellulose K4M and Carbopol 974" 85 : 330-334, 1996

      15 Hayashi, T., "Formulation study and drug release mechanism of a new theophylline sustained-release preparation" 304 : 91-101, 2005

      16 Lubrizol, "Formulating Controlled Release Tablets and Capsules with Carbopol® Polymers" 31 : 2008b

      17 Streubel, A., "Floating matrix tablets based on low density foam powder: effects of formulation and processing parameters on drug release" 18 : 37-45, 2003

      18 Li, S., "Effect of HPMC and Carbopol on the release and floating properties of Gastric floating Drug Delivery System using factorial design" 253 : 13-22, 2003

      19 Draganoiu, E., "Effect of Carbomer and hydroxypropyl methylcellulose combination on drug release from matrix tablets" 25 (25): S222-S223, 2005

      20 Kiortsis, S., "Drug release from tableted wet granulations comprising cellulosic (HPMC or HPC) and hydrophobic component" 59 : 73-83, 2005

      21 Das, N. G., "Development of mucoadhesive dosage forms of buprenophine for sublingual drug delivery" 11 : 89-95, 2004

      22 Yuksel, A., "Comparison of in vitro dissolution profiles by Anova based model dependent and independent methods" 209 : 57-67, 2000

      23 Varshosaz, J., "Biopharmaceutical characterization of oral theophylline and aminophylline tablets. Quantitative correlation between dissolution and bioavailability studies" 50 : 301-306, 2000

      24 Parojcic, J., "An investigation into the factors influencing drug release from hydrophilic matrix tablets based on novel carbomer polymers" 11 : 59-65, 2004

      25 Prudat-Christiaens, C., "Aminophylline bioadhesive tablets attempted by wet granulation" 141 : 109-116, 1996

      26 Ritger, P. L., "A simple equation for disposition of solute release II: Fickian and anomalous release from swellable devices" 5 : 37-42, 1987

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      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) 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
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      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.96 0.2 1.44
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.07 0.87 0.439 0.05
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