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Volumn 103, Issue 9, 2014, Pages 2911-2923

Physical characterization of drug:Polymer dispersion behavior in polyethylene glycol 4000 solid dispersions using a suite of complementary analytical techniques

Author keywords

crystallinity; miscibility; pair distribution function; physical characterization; polyethylene glycol (PEG); powder X ray diffraction; solid dispersions; solubility; thermal analysis

Indexed keywords

CHLORPROPAMIDE; CIMETIDINE; DRUG DERIVATIVE; GRISEOFULVIN; IBUPROFEN; INDOMETACIN; ITRACONAZOLE; KETOCONAZOLE; MACROGOL 4000; MELATONIN; NIFEDIPINE; PROPRANOLOL; QUINIDINE; SULFANILAMIDE; TERFENADINE; TOLBUTAMIDE; DRUG; MACROGOL DERIVATIVE; POLYMER; POWDER;

EID: 84906306657     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.24008     Document Type: Article
Times cited : (21)

References (50)
  • 1
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Leuner C, Dressman J,. 2000. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 50: 47-60.
    • (2000) Eur J Pharm Biopharm , vol.50 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 2
    • 0032885450 scopus 로고    scopus 로고
    • Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
    • Serajuddin A,. 1999. Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs. J Pharm Sci 88: 1058-1066.
    • (1999) J Pharm Sci , vol.88 , pp. 1058-1066
    • Serajuddin, A.1
  • 3
    • 63949088026 scopus 로고    scopus 로고
    • Aqueous solubility enhancement through engineering of binary solid composites: Pharmaceutical applications
    • Moore MD, Wildfong PLD,. 2009. Aqueous solubility enhancement through engineering of binary solid composites: Pharmaceutical applications. J Pharm Innov 4: 36-49.
    • (2009) J Pharm Innov , vol.4 , pp. 36-49
    • Moore, M.D.1    Wildfong, P.L.D.2
  • 4
    • 36549042006 scopus 로고    scopus 로고
    • Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
    • Vasconcelos T, Sarmento B, Costa P,. 2007. Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov Today 12: 1068-1075.
    • (2007) Drug Discov Today , vol.12 , pp. 1068-1075
    • Vasconcelos, T.1    Sarmento, B.2    Costa, P.3
  • 5
    • 0015124656 scopus 로고
    • Pharmaceutical applications of solid dispersion systems
    • Chiou WL, Riegelman S,. 1971. Pharmaceutical applications of solid dispersion systems. J Pharm Sci 60: 1281-1302.
    • (1971) J Pharm Sci , vol.60 , pp. 1281-1302
    • Chiou, W.L.1    Riegelman, S.2
  • 6
    • 41549150839 scopus 로고    scopus 로고
    • Formulation and characterization of ternary solid dispersions made up of Itraconazole and two excipients, TPGS 1000 and PVPVA 64, that were selected based on a supersaturation screening study
    • Janssens S, Nagels S, Armas HNd, D'Autry W, Van Schepdael A, Van den Mooter G,. 2008. Formulation and characterization of ternary solid dispersions made up of Itraconazole and two excipients, TPGS 1000 and PVPVA 64, that were selected based on a supersaturation screening study. Eur J Pharm Biopharm 69: 158-166.
    • (2008) Eur J Pharm Biopharm , vol.69 , pp. 158-166
    • Janssens, S.1    Nagels, S.2    Hnd, A.3    D'Autry, W.4    Van Schepdael, A.5    Den Mooter, G.V.6
  • 7
    • 1442348833 scopus 로고    scopus 로고
    • Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods
    • Sethia S, Squillante E,. 2004. Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods. Int J Pharm 272: 1-10.
    • (2004) Int J Pharm , vol.272 , pp. 1-10
    • Sethia, S.1    Squillante, E.2
  • 8
    • 37349024249 scopus 로고    scopus 로고
    • Unexpected differences in dissolution behavior of tablets prepared from solid dispersions with a surfactant physically mixed or incorporated
    • De Waard H, Hinrichs W, Visser M, Bologna C, Frijlink H,. 2008. Unexpected differences in dissolution behavior of tablets prepared from solid dispersions with a surfactant physically mixed or incorporated. Int J Pharm 349: 66-73.
    • (2008) Int J Pharm , vol.349 , pp. 66-73
    • Waard, H.D.1    Hinrichs, W.2    Visser, M.3    Bologna, C.4    Frijlink, H.5
  • 9
    • 85111386879 scopus 로고    scopus 로고
    • Hot-melt extrusion technique: A review
    • Chokshi R, Zia H,. 2010. Hot-melt extrusion technique: A review. Iran J Pharm Res 3: 3-16.
    • (2010) Iran J Pharm Res , vol.3 , pp. 3-16
    • Chokshi, R.1    Zia, H.2
  • 10
    • 77951270694 scopus 로고    scopus 로고
    • Influence of excipients in comilling on mitigating milling-induced amorphization or structural disorder of crystalline pharmaceutical actives
    • Balani PN, Ng WK, Tan RB, Chan SY,. 2010. Influence of excipients in comilling on mitigating milling-induced amorphization or structural disorder of crystalline pharmaceutical actives. J Pharm Sci 99: 2462-2474.
    • (2010) J Pharm Sci , vol.99 , pp. 2462-2474
    • Balani, P.N.1    Ng, W.K.2    Tan, R.B.3    Chan, S.Y.4
  • 11
    • 0037413412 scopus 로고    scopus 로고
    • Comparison between polyvinylpyrrolidone and silica nanoparticles as carriers for indomethacin in a solid state dispersion
    • Watanabe T, Hasegawa S, Wakiyama N, Kusai A, Senna M,. 2003. Comparison between polyvinylpyrrolidone and silica nanoparticles as carriers for indomethacin in a solid state dispersion. Int J Pharm 250: 283-286.
    • (2003) Int J Pharm , vol.250 , pp. 283-286
    • Watanabe, T.1    Hasegawa, S.2    Wakiyama, N.3    Kusai, A.4    Senna, M.5
  • 12
    • 1142303337 scopus 로고    scopus 로고
    • What is the true solubility advantage for amorphous pharmaceuticals?
    • Hancock BC, Parks M,. 2000. What is the true solubility advantage for amorphous pharmaceuticals? Pharm Res 17: 397-404.
    • (2000) Pharm Res , vol.17 , pp. 397-404
    • Hancock, B.C.1    Parks, M.2
  • 13
    • 38349182320 scopus 로고    scopus 로고
    • Drug-polymer interaction and its significance on the physical stability of nifedipine amorphous dispersion in microparticles of an ammonio methacrylate copolymer and ethylcellulose binary blend
    • Huang J, Wigent RJ, Schwartz JB,. 2008. Drug-polymer interaction and its significance on the physical stability of nifedipine amorphous dispersion in microparticles of an ammonio methacrylate copolymer and ethylcellulose binary blend. J Pharm Sci 97: 251-262.
    • (2008) J Pharm Sci , vol.97 , pp. 251-262
    • Huang, J.1    Wigent, R.J.2    Schwartz, J.B.3
  • 14
    • 0031423468 scopus 로고    scopus 로고
    • Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions
    • Taylor LS, Zografi G,. 1997. Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. Pharm Res 14: 1691-1698.
    • (1997) Pharm Res , vol.14 , pp. 1691-1698
    • Taylor, L.S.1    Zografi, G.2
  • 16
    • 33749442356 scopus 로고    scopus 로고
    • Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility
    • Marsac PJ, Shamblin SL, Taylor LS,. 2006. Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility. Pharm Res 23: 2417-2426.
    • (2006) Pharm Res , vol.23 , pp. 2417-2426
    • Marsac, P.J.1    Shamblin, S.L.2    Taylor, L.S.3
  • 17
    • 80052961698 scopus 로고    scopus 로고
    • Informatics calibration of a molecular descriptors database to predict solid dispersion potential of small molecule organic solids
    • Moore MD, Wildfong PLD,. 2011. Informatics calibration of a molecular descriptors database to predict solid dispersion potential of small molecule organic solids. Int J Pharm 418: 217-226.
    • (2011) Int J Pharm , vol.418 , pp. 217-226
    • Moore, M.D.1    Wildfong, P.L.D.2
  • 18
    • 71649107836 scopus 로고    scopus 로고
    • Miscibility/stability considerations in binary solid dispersion systems composed of functional excipients towards the design of multi-component amorphous systems
    • Yoo S, Krill SL, Wang Z, Telang C,. 2009. Miscibility/stability considerations in binary solid dispersion systems composed of functional excipients towards the design of multi-component amorphous systems. J Pharm Sci 98: 4711-4723.
    • (2009) J Pharm Sci , vol.98 , pp. 4711-4723
    • Yoo, S.1    Krill, S.L.2    Wang, Z.3    Telang, C.4
  • 19
    • 64649100465 scopus 로고    scopus 로고
    • Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: An overview
    • Friesen DT, Shanker R, Crew M, Smithey DT, Curatolo W, Nightingale J,. 2008. Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: An overview. Mol Pharm 5: 1003-1019.
    • (2008) Mol Pharm , vol.5 , pp. 1003-1019
    • Friesen, D.T.1    Shanker, R.2    Crew, M.3    Smithey, D.T.4    Curatolo, W.5    Nightingale, J.6
  • 20
    • 77953290060 scopus 로고    scopus 로고
    • Influence of preparation methods on solid state supersaturation of amorphous solid dispersions: A case study with itraconazole and eudragit e100
    • Janssens S, De Zeure A, Paudel A, Van Humbeeck J, Rombaut P, Van den Mooter G,. 2010. Influence of preparation methods on solid state supersaturation of amorphous solid dispersions: A case study with itraconazole and eudragit e100. Pharm Res 27: 775-785.
    • (2010) Pharm Res , vol.27 , pp. 775-785
    • Janssens, S.1    Zeure, A.D.2    Paudel, A.3    Van Humbeeck, J.4    Rombaut, P.5    Den Mooter, G.V.6
  • 21
    • 68949089977 scopus 로고    scopus 로고
    • Novel methods for the assessment of miscibility of amorphous drug-polymer dispersions
    • Ivanisevic I, Bates S, Chen P,. 2009. Novel methods for the assessment of miscibility of amorphous drug-polymer dispersions. J Pharm Sci 98: 3373-3386.
    • (2009) J Pharm Sci , vol.98 , pp. 3373-3386
    • Ivanisevic, I.1    Bates, S.2    Chen, P.3
  • 22
    • 24044499657 scopus 로고    scopus 로고
    • Molecular properties of ibuprofen and its solid dispersions with Eudragit RL100 studied by solid-state nuclear magnetic resonance
    • Geppi M, Guccione S, Mollica G, Pignatello R, Veracini CA,. 2005. Molecular properties of ibuprofen and its solid dispersions with Eudragit RL100 studied by solid-state nuclear magnetic resonance. Pharm Res 22: 1544-1555.
    • (2005) Pharm Res , vol.22 , pp. 1544-1555
    • Geppi, M.1    Guccione, S.2    Mollica, G.3    Pignatello, R.4    Veracini, C.A.5
  • 23
    • 55749088198 scopus 로고    scopus 로고
    • Characterization of amorphous API: Polymer mixtures using X-ray powder diffraction
    • Newman A, Engers D, Bates S, Ivanisevic I, Kelly RC, Zografi G,. 2008. Characterization of amorphous API: Polymer mixtures using X-ray powder diffraction. J Pharm Sci 97: 4840-4856.
    • (2008) J Pharm Sci , vol.97 , pp. 4840-4856
    • Newman, A.1    Engers, D.2    Bates, S.3    Ivanisevic, I.4    Kelly, R.C.5    Zografi, G.6
  • 24
    • 70350220585 scopus 로고    scopus 로고
    • Evaluation of drug-polymer miscibility in amorphous solid dispersion systems
    • Rumondor AC, Ivanisevic I, Bates S, Alonzo DE, Taylor LS,. 2009. Evaluation of drug-polymer miscibility in amorphous solid dispersion systems. Pharm Res 26: 2523-2534.
    • (2009) Pharm Res , vol.26 , pp. 2523-2534
    • Rumondor, A.C.1    Ivanisevic, I.2    Bates, S.3    Alonzo, D.E.4    Taylor, L.S.5
  • 25
    • 0037074108 scopus 로고    scopus 로고
    • The mechanisms of drug release from solid dispersions in water-soluble polymers
    • Craig DQ., 2002. The mechanisms of drug release from solid dispersions in water-soluble polymers. Int J Pharm 231: 131-144.
    • (2002) Int J Pharm , vol.231 , pp. 131-144
    • Craig, D.Q.1
  • 26
    • 0035800251 scopus 로고    scopus 로고
    • Processing of carbamazepine-PEG 4000 solid dispersions with supercritical carbon dioxide: Preparation, characterisation, and in vitro dissolution
    • Moneghini M, Kikic I, Voinovich D, Perissutti B, Filipovic̈- Grčic̈ J,. 2001. Processing of carbamazepine-PEG 4000 solid dispersions with supercritical carbon dioxide: Preparation, characterisation, and in vitro dissolution. Int J Pharm 222: 129-138.
    • (2001) Int J Pharm , vol.222 , pp. 129-138
    • Moneghini, M.1    Kikic, I.2    Voinovich, D.3    Perissutti, B.4    Filipovic̈- Grčic̈, J.5
  • 27
    • 12844253104 scopus 로고    scopus 로고
    • Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000
    • Liu C, Desai KGH, Liu C,. 2005. Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000. Drug Dev Ind Pharm 31: 1-10.
    • (2005) Drug Dev Ind Pharm , vol.31 , pp. 1-10
    • Liu, C.1    Desai, K.G.H.2    Liu, C.3
  • 28
    • 0026783391 scopus 로고
    • Characterization of solid dispersions of piroxicam/polyethylene glycol 4000
    • Fernández M, Carmen Rodríguez I, Margarit MV, Cerezo A,. 1992. Characterization of solid dispersions of piroxicam/polyethylene glycol 4000. Int J Pharm 84: 197-202.
    • (1992) Int J Pharm , vol.84 , pp. 197-202
    • Fernández, M.1    Rodríguez, I.C.2    Margarit, M.V.3    Cerezo, A.4
  • 29
    • 0028340095 scopus 로고
    • Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000
    • Margarit MV, Rodríguez IC, Cerezo A,. 1994. Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000. Int J Pharm 108: 101-107.
    • (1994) Int J Pharm , vol.108 , pp. 101-107
    • Margarit, M.V.1    Rodríguez, I.C.2    Cerezo, A.3
  • 30
    • 0036200970 scopus 로고    scopus 로고
    • Prediction of poly (ethylene) glycol-drug eutectic compositions using an index based on the van't Hoff equation
    • Law D, Wang W, Schmitt EA, Long MA,. 2002. Prediction of poly (ethylene) glycol-drug eutectic compositions using an index based on the van't Hoff equation. Pharm Res 19: 315-321.
    • (2002) Pharm Res , vol.19 , pp. 315-321
    • Law, D.1    Wang, W.2    Schmitt, E.A.3    Long, M.A.4
  • 31
    • 70350144253 scopus 로고    scopus 로고
    • Compatibility study between chlorpropamide and excipients in their physical mixtures
    • Freire FD, Aragao CFS, de Lima e Moura TFA,. 2009. Compatibility study between chlorpropamide and excipients in their physical mixtures. J Therm Anal Calorim. 97: 355-357.
    • (2009) J Therm Anal Calorim. , vol.97 , pp. 355-357
    • Freire, F.D.1    Aragao, C.F.S.2    De Lima Moura, T.F.A.3
  • 32
    • 64649098724 scopus 로고    scopus 로고
    • Thermodynamics, molecular mobility and crystallization kinetics of amorphous griseofulvin
    • Zhou D, Zhang GGZ, Law D, Grant DJW, Schmitt EA,. 2008. Thermodynamics, molecular mobility and crystallization kinetics of amorphous griseofulvin. Mol Pharm 5 (6): 927-936.
    • (2008) Mol Pharm , vol.5 , Issue.6 , pp. 927-936
    • Zhou, D.1    Zhang, G.G.Z.2    Law, D.3    Grant, D.J.W.4    Schmitt, E.A.5
  • 34
    • 12244283119 scopus 로고    scopus 로고
    • Characterization of solid dispersions of itraconazole and hydroxypropylmethylcellulose prepared by melt extrusion - Part i
    • Verreck G, Six K, Van den Mooter G, Baert L, Peeters J, Brewster ME,. 2003. Characterization of solid dispersions of itraconazole and hydroxypropylmethylcellulose prepared by melt extrusion-Part I. Int J Pharm. 251: 165-174.
    • (2003) Int J Pharm. , vol.251 , pp. 165-174
    • Verreck, G.1    Six, K.2    Den Mooter, G.V.3    Baert, L.4    Peeters, J.5    Brewster, M.E.6
  • 35
    • 79955592721 scopus 로고    scopus 로고
    • Nanoparticle formation and growth during in vitro dissolution of ketoconazole solid dispersion
    • Kanajuia P, Lau G, Ng W, Widjaja E, Hanefeld A, Fishbach M, Maio M, Tan RBH,. 2011. Nanoparticle formation and growth during in vitro dissolution of ketoconazole solid dispersion. J Pharm Sci 100 (7): 2876-2885.
    • (2011) J Pharm Sci , vol.100 , Issue.7 , pp. 2876-2885
    • Kanajuia, P.1    Lau, G.2    Ng, W.3    Widjaja, E.4    Hanefeld, A.5    Fishbach, M.6    Maio, M.7    Tan, R.B.H.8
  • 37
    • 4243167095 scopus 로고
    • A classical thermodynamic discussion of the effect of composition on glass-transition temperatures
    • Couchman PR, Karasz FE,. 1978. A classical thermodynamic discussion of the effect of composition on glass-transition temperatures. Macromolecules 11: 117-119
    • (1978) Macromolecules , vol.11 , pp. 117-119
    • Couchman, P.R.1    Karasz, F.E.2
  • 38
    • 0025665801 scopus 로고
    • Synthesis and characterization of block copolymers from D, l -lactide and poly (ethylene glycol) with stannous chloride
    • Deng X, Xiong C, Cheng L, Xu R,. 1990. Synthesis and characterization of block copolymers from D, l -lactide and poly (ethylene glycol) with stannous chloride. J Polym Sci Part C Polym Lett 28: 411-416.
    • (1990) J Polym Sci Part C Polym Lett , vol.28 , pp. 411-416
    • Deng, X.1    Xiong, C.2    Cheng, L.3    Xu, R.4
  • 39
    • 0042616238 scopus 로고
    • Mechanical relaxation in some oxide polymers
    • Read B,. 1962. Mechanical relaxation in some oxide polymers. Polymer 3: 529-542.
    • (1962) Polymer , vol.3 , pp. 529-542
    • Read, B.1
  • 40
    • 0000291805 scopus 로고
    • A review of thermal methods used for the analysis of the crystal form, solution thermodynamics and glass transition behaviour of polyethylene glycols
    • Craig DQ,. 1995. A review of thermal methods used for the analysis of the crystal form, solution thermodynamics and glass transition behaviour of polyethylene glycols. Thermochim Acta 248: 189-203.
    • (1995) Thermochim Acta , vol.248 , pp. 189-203
    • Craig, D.Q.1
  • 42
    • 0003472812 scopus 로고
    • New York: Dover Publications, Inc
    • Warren BE,. 1990. X-ray diffraction, New York: Dover Publications, Inc.
    • (1990) X-ray Diffraction
    • Warren, B.E.1
  • 44
    • 78651282639 scopus 로고    scopus 로고
    • Structural interpretation in composite systems using powder X-ray diffraction: Applications of error propagation to the pair distribution function
    • Moore MD, Shi Z, Wildfong PLD,. 2010. Structural interpretation in composite systems using powder X-ray diffraction: Applications of error propagation to the pair distribution function. Pharm Res 27: 2624-2632.
    • (2010) Pharm Res , vol.27 , pp. 2624-2632
    • Moore, M.D.1    Shi, Z.2    Wildfong, P.L.D.3
  • 45
    • 77955257620 scopus 로고    scopus 로고
    • Evaluation of the microstructure of semicrystalline solid dispersions
    • Zhu Q, Taylor LS, Harris MT,. 2010. Evaluation of the microstructure of semicrystalline solid dispersions. Mol Pharm 7: 1291-1300.
    • (2010) Mol Pharm , vol.7 , pp. 1291-1300
    • Zhu, Q.1    Taylor, L.S.2    Harris, M.T.3
  • 46
    • 0001752768 scopus 로고    scopus 로고
    • The Cambridge Structural Database: A quarter of a million crystal structure and rising
    • Allen FH,. 2002. The Cambridge Structural Database: A quarter of a million crystal structure and rising. Acta Crystallogr B 58: 380-388
    • (2002) Acta Crystallogr B , vol.58 , pp. 380-388
    • Allen, F.H.1
  • 48
    • 77956231678 scopus 로고    scopus 로고
    • Application of partial least-squares (PLS) modeling in quantifying drug crystallinity in amorphous solid dispersions
    • Rumondor AC, Taylor LS,. 2010. Application of partial least-squares (PLS) modeling in quantifying drug crystallinity in amorphous solid dispersions. Int J Pharm 398: 155-160.
    • (2010) Int J Pharm , vol.398 , pp. 155-160
    • Rumondor, A.C.1    Taylor, L.S.2
  • 49
    • 84858797264 scopus 로고    scopus 로고
    • Evaluation of amorphous solid dispersion properties using thermal analysis techniques
    • Baird JA, Taylor LS,. 2012. Evaluation of amorphous solid dispersion properties using thermal analysis techniques. Adv Drug Deliv Rev 64: 396-421.
    • (2012) Adv Drug Deliv Rev , vol.64 , pp. 396-421
    • Baird, J.A.1    Taylor, L.S.2
  • 50
    • 0001106314 scopus 로고
    • Ideal copolymers and the second-order transitions of synthetic rubbers. I. Non-crystalline copolymers
    • Gordon M, Taylor JS,. 1952. Ideal copolymers and the second-order transitions of synthetic rubbers. I. Non-crystalline copolymers. J Appl Chem 2: 493-500.
    • (1952) J Appl Chem , vol.2 , pp. 493-500
    • Gordon, M.1    Taylor, J.S.2


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