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      KCI등재 SCOPUS SCIE

      Oral lipid based multiparticulate pastilles: design and effect of pore former

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      https://www.riss.kr/link?id=A104980107

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      다국어 초록 (Multilingual Abstract)

      The purpose of this research work was todesign and develop droplet solidification apparatus for lipidbased pastilles. Oral lipid based multiparticulate pastillesof solid lipid glycerol monostearate were formulated tocontrol the release of highly water...

      The purpose of this research work was todesign and develop droplet solidification apparatus for lipidbased pastilles. Oral lipid based multiparticulate pastillesof solid lipid glycerol monostearate were formulated tocontrol the release of highly water soluble drug metoprololsuccinate. The apparatus was optimized at 14G needle sizeand metallic surface base plate cooled at 4 ˚C. Pastilleswere evaluated for their size, shape, contact angle, density,flow properties, friability, crushing strength, drug content,thermal properties, in vitro and in vivo drug release. Pastilleswere hemispherical in shape of size 3.1–4.3 mm.
      Contact angle was found to be more than 120˚. Drugrelease was controlled for 8 h. Scanning electron microscopystudy revealed the smooth external surface with poresto ingress dissolution media to enhance the drug releaserate. Increased quantity of pore former enhanced the dissolutionrate. Other operating variables like contact angleand height of needle from base plate were found to affectthe size of pastilles. The dissolution of optimized batch ofpastilles was best fitted to first order kinetic model. In vivopharmacokinetic study showed correlation with in vitrodrug release profile.

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      참고문헌 (Reference)

      1 Windbergs M, "Understanding the solid-state behaviour of triglyceride solid lipid extrudates and its influence on dissolution" 71 : 80-87, 2009

      2 Cespi M, "Stress relaxation test for the characterization of the viscoelasticity of pellets" 67 : 476-484, 2007

      3 Almeida PS, "Starch–dextrin mixtures as base excipients for extrusion–spheronization pellets" 59 : 511-521, 2005

      4 Reitz C, "Solid lipid extrusion of sustained release dosage forms" 67 : 440-448, 2007

      5 Young C, "Production of spherical pellets by a hot-melt extrusion and spheronization process" 242 : 87-92, 2002

      6 Djuris J, "Preparation of carbamazepine–soluplus solid dispersions by hotmelt extrusion and prediction of drug–polymer miscibility by thermodynamic model fitting" 84 : 228-237, 2013

      7 Grassi M, "Preparation and evaluation of a melt pelletised paracetamol/stearic acid sustained release delivery system" 88 : 381-391, 2003

      8 Kim J, "Prediction of degree of deformation and crystallization time of molten droplets in pastillation process" 257 : 205-215, 2003

      9 Novoa G, "Physical solid-state properties and dissolution of sustained-release matrices of polyvinylacetate" 59 : 343-350, 2005

      10 Nandi U, "Pharmacokinetics, pharmacodynamics and toxicity of a combination of metoprolol succinate and telmisartan in Wistar albino rats: safety profiling" 65 : 68-78, 2013

      1 Windbergs M, "Understanding the solid-state behaviour of triglyceride solid lipid extrudates and its influence on dissolution" 71 : 80-87, 2009

      2 Cespi M, "Stress relaxation test for the characterization of the viscoelasticity of pellets" 67 : 476-484, 2007

      3 Almeida PS, "Starch–dextrin mixtures as base excipients for extrusion–spheronization pellets" 59 : 511-521, 2005

      4 Reitz C, "Solid lipid extrusion of sustained release dosage forms" 67 : 440-448, 2007

      5 Young C, "Production of spherical pellets by a hot-melt extrusion and spheronization process" 242 : 87-92, 2002

      6 Djuris J, "Preparation of carbamazepine–soluplus solid dispersions by hotmelt extrusion and prediction of drug–polymer miscibility by thermodynamic model fitting" 84 : 228-237, 2013

      7 Grassi M, "Preparation and evaluation of a melt pelletised paracetamol/stearic acid sustained release delivery system" 88 : 381-391, 2003

      8 Kim J, "Prediction of degree of deformation and crystallization time of molten droplets in pastillation process" 257 : 205-215, 2003

      9 Novoa G, "Physical solid-state properties and dissolution of sustained-release matrices of polyvinylacetate" 59 : 343-350, 2005

      10 Nandi U, "Pharmacokinetics, pharmacodynamics and toxicity of a combination of metoprolol succinate and telmisartan in Wistar albino rats: safety profiling" 65 : 68-78, 2013

      11 Rubinstein M, "Pharmaceutics: the science of dosage form design" Churchill Livingstone 305-, 2000

      12 Dali Shukla, "Pastillation: A novel technology for development of oral lipid based multiparticulate controlled release formulation" Elsevier BV 209 (209): 65-72, 2011

      13 Prabhu S, "Novel lipid-based formulations enhancing the in vitro dissolution and permeability characteristics of a poorly water-soluble model drug, piroxicam" 301 : 209-216, 2005

      14 Ochoa L, "Novel extended-release formulation of lovastatin by one-step melt granulation : in vitro and in vivo evaluation" 77 : 306-312, 2011

      15 Chakraborty S, "Lipid-an emerging platform for oral delivery of drugs with poor bioavailability" 73 : 1-15, 2009

      16 Porter CJ, "In vitro assessment of oral lipid based formulations" 50 : S127-S147, 2001

      17 Shukla D, "In vitro and in vivo evaluation of multilayered pastilles for chronotherapeutic management of nocturnal asthma" 9 : 9-18, 2012

      18 Mathur V, "Formulation and evaluation of controlled release antibiotic biodegradable implants for post operative site delivery" 60 : 111-117, 2010

      19 Pandit AP, "Formulation and development of twocompartment HPMC capsule for concurrent administration of drugs" 2 (2): 79-83, 2014

      20 Almeida A, "Ethylene vinyl acetate as matrix for oral sustained release dosage forms produced via hot-melt extrusion" 77 : 297-305, 2011

      21 Kumar K, "Effect of drug solubility and different excipients on floating behaviour and release from glyceryl monooleate matrices" 272 : 151-160, 2004

      22 Gures S, "Drug release from extruded solid lipid matrices : theoretical predictions and independent experiments" 80 : 122-129, 2012

      23 Kojima M, "Development of controlled release matrix pellets by annealing with micronized water-insoluble or enteric polymers" 82 : 335-343, 2002

      24 Ashlesha Pravin Pandit, "Development and in vitro evaluation of sustained release multiparticulate tablet of freely water soluble drug" FapUNIFESP (SciELO) 46 (46): 463-471, 2010

      25 Hamdani J, "Development and in vitro evaluation of a novel floating multiple unit dosage form obtained by melt pelletization" 322 : 96-103, 2006

      26 Siepmann F, "Controlled drug release from gelucire-based matrix pellets : experiment and theory" 317 : 136-143, 2006

      27 Goyanes A, "Co-processed MCC-Eudragit E excipients for extrusion–spheronization" 79 : 658-663, 2011

      28 Passerini N, "Characterization of carbamazepine-gelucire 50/13 microparticles prepared by a spray-congealing process using ultrasounds" 91 : 699-707, 2002

      29 Qi S, "An investigation into the mechanisms of drug release from taste-masking fatty acid microspheres" 97 : 3842-3854, 2008

      30 Thies C, "A supercritical fluid-based coating technology 1 : process considerations" 20 : 87-96, 2003

      31 Abdul S, "A flexible technology for modified-release drugs: multiple-unit pellet system, (MUPS)" 147 : 2-16, 2010

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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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