메뉴 건너뛰기




Volumn 33, Issue 6, 2016, Pages 1456-1471

Characterization of Solid Dispersion of Itraconazole Prepared by Solubilization in Concentrated Aqueous Solutions of Weak Organic Acids and Drying

Author keywords

acid base interaction; amorphous solid dispersion; Itraconazole; solubilization; stabilization; weak organic acid

Indexed keywords

CARBOXYLIC ACID; CITRIC ACID; GLUTARIC ACID; HYDROGEN; ITRACONAZOLE; MALIC ACID; NANOPARTICLE; TARTARIC ACID; WATER; ANTIFUNGAL AGENT; DICARBOXYLIC ACID; GLUTARIC ACID DERIVATIVE; HYDROCHLORIC ACID; MALIC ACID DERIVATIVE; TARTARIC ACID DERIVATIVE;

EID: 84960110225     PISSN: 07248741     EISSN: 1573904X     Source Type: Journal    
DOI: 10.1007/s11095-016-1890-8     Document Type: Article
Times cited : (46)

References (56)
  • 1
    • 0034461768 scopus 로고    scopus 로고
    • Drug-like properties and the causes of poor solubility and poor permeability
    • COI: 1:CAS:528:DC%2BD3MXitF2ksrc%3D, PID: 11274893
    • Lipinski CA. Drug-like properties and the causes of poor solubility and poor permeability. J Pharmacol Toxicol Methods. 2000;44(1):235–49.
    • (2000) J Pharmacol Toxicol Methods , vol.44 , Issue.1 , pp. 235-249
    • Lipinski, C.A.1
  • 2
    • 1042264121 scopus 로고    scopus 로고
    • Impact of solid state properties on developability assessment of drug candidates
    • COI: 1:CAS:528:DC%2BD2cXhtV2nu7Y%3D, PID: 14962584
    • Huang LF, Tong WQ. Impact of solid state properties on developability assessment of drug candidates. Adv Drug Deliv Rev. 2004;56(3):321–34.
    • (2004) Adv Drug Deliv Rev , vol.56 , Issue.3 , pp. 321-334
    • Huang, L.F.1    Tong, W.Q.2
  • 3
    • 84915758373 scopus 로고    scopus 로고
    • The biopharmaceutics risk assessment roadmap for optimizing clinical drug product performance
    • COI: 1:CAS:528:DC%2BC2cXhslOkurvE, PID: 25256402
    • Selen A, Dickinson PA, Müllertz A, Crison JR, Mistry HB, Cruañes MT, et al. The biopharmaceutics risk assessment roadmap for optimizing clinical drug product performance. J Pharm Sci. 2014;103(11):3377–97.
    • (2014) J Pharm Sci , vol.103 , Issue.11 , pp. 3377-3397
    • Selen, A.1    Dickinson, P.A.2    Müllertz, A.3    Crison, J.R.4    Mistry, H.B.5    Cruañes, M.T.6
  • 4
    • 77953290060 scopus 로고    scopus 로고
    • Influence of preparation methods on solid state supersaturation of amorphous SD: a case study with itraconazole and Eudragit E 100
    • COI: 1:CAS:528:DC%2BC3cXis1ertLk%3D, PID: 20195707
    • Janssens S, De Zeure A, Paudel A, Van Humbeeck J, Rombaut P, Van den Mooter G. Influence of preparation methods on solid state supersaturation of amorphous SD: a case study with itraconazole and Eudragit E 100. Pharm Res. 2010;27:775–85.
    • (2010) Pharm Res , vol.27 , pp. 775-785
    • Janssens, S.1    De Zeure, A.2    Paudel, A.3    Van Humbeeck, J.4    Rombaut, P.5    Van den Mooter, G.6
  • 6
    • 84864223415 scopus 로고    scopus 로고
    • O’Neil M.J. (ed.). The Merck index - an encyclopedia of chemicals, drugs, and biologicals. Whitehouse station, NJ: , 2006., p. 907
    • O’Neil M.J. (ed.). The Merck index - an encyclopedia of chemicals, drugs, and biologicals. Whitehouse station, NJ: Merck and Co., Inc., 2006., p. 907
    • (2006) Merck and Co., Inc.
  • 7
    • 34047093239 scopus 로고    scopus 로고
    • Solubilization of itraconazole as a function of cyclodextrin structural space
    • COI: 1:CAS:528:DC%2BD2sXjs12lur4%3D
    • Brewster M, Neekens P, Peeters J. Solubilization of itraconazole as a function of cyclodextrin structural space. J Incl Phenom Macrocycl Chem. 2007;57:561–6.
    • (2007) J Incl Phenom Macrocycl Chem , vol.57 , pp. 561-566
    • Brewster, M.1    Neekens, P.2    Peeters, J.3
  • 8
    • 84979569954 scopus 로고    scopus 로고
    • (last accessed: 20 July 2015)
    • Sporanox capsule product information. https://www.janssen.com.au/files/Products/SPORANOX_CAPSULES_PI.pdf (last accessed: 20 July 2015)
    • (2015) Sporanox capsule product information.
  • 9
    • 0030003444 scopus 로고    scopus 로고
    • Itraconazole: pharmacology, clinical experience and future development
    • PID: 18611706
    • Beule K. Itraconazole: pharmacology, clinical experience and future development. Int J Antimicrob Agents. 1996;6:175–81.
    • (1996) Int J Antimicrob Agents , vol.6 , pp. 175-181
    • Beule, K.1
  • 10
    • 84979535414 scopus 로고    scopus 로고
    • (last accessed: 20 July 2015)
    • Sporanox oral solution product information. https://www.janssen.com.au/files/Products/SPORANOX_SOLUTION_PI.pdf (last accessed: 20 July 2015)
    • (2015) Sporanox oral solution product information.
  • 11
    • 58249102205 scopus 로고    scopus 로고
    • Preparation and evaluation of itraconazole dihydrochloride for the solubility and dissolution rate enhancement
    • COI: 1:CAS:528:DC%2BD1MXpsF2gsA%3D%3D, PID: 18930795
    • Tao T, Zhao Y, Wu J, Zhou B. Preparation and evaluation of itraconazole dihydrochloride for the solubility and dissolution rate enhancement. Int J Pharm. 2009;367:109–14.
    • (2009) Int J Pharm , vol.367 , pp. 109-114
    • Tao, T.1    Zhao, Y.2    Wu, J.3    Zhou, B.4
  • 13
    • 0038713880 scopus 로고    scopus 로고
    • Crystal engineering of novel cocrystals of a triazole drug with 1,4- dicarboxylic acids
    • COI: 1:CAS:528:DC%2BD3sXksl2htbc%3D, PID: 12848550
    • Remenar J, Morissette S, Peterson M, Moulton B, MacPhee JM, Guzmán HR, et al. Crystal engineering of novel cocrystals of a triazole drug with 1,4- dicarboxylic acids. J Am Chem Soc. 2003;125:8456–7.
    • (2003) J Am Chem Soc , vol.125 , pp. 8456-8457
    • Remenar, J.1    Morissette, S.2    Peterson, M.3    Moulton, B.4    MacPhee, J.M.5    Guzmán, H.R.6
  • 14
    • 84979514019 scopus 로고    scopus 로고
    • Nanoization of itraconazole by high pressure homogenization: stabilizer optimization and effect of particle size on oral absorption
    • Wei S, Mao S, Shi Y, Li L, Fang L. Nanoization of itraconazole by high pressure homogenization: stabilizer optimization and effect of particle size on oral absorption. J Pharm Sci. 2011;24:297–303.
    • (2011) J Pharm Sci , vol.24 , pp. 297-303
    • Wei, S.1    Mao, S.2    Shi, Y.3    Li, L.4    Fang, L.5
  • 15
    • 79958005215 scopus 로고    scopus 로고
    • Potent dried drug nanosuspensions for oral bioavailability enhancement of poorly soluble drugs with pH-dependent solubility
    • COI: 1:CAS:528:DC%2BC3MXmvFOiu7s%3D, PID: 21540090
    • Mou D, Chen H, Wan J, Xu H, Yang X. Potent dried drug nanosuspensions for oral bioavailability enhancement of poorly soluble drugs with pH-dependent solubility. Int J Pharm. 2011;413:237–44.
    • (2011) Int J Pharm , vol.413 , pp. 237-244
    • Mou, D.1    Chen, H.2    Wan, J.3    Xu, H.4    Yang, X.5
  • 16
    • 78650680019 scopus 로고    scopus 로고
    • Development of solid dispersions for poorly water-soluble drug
    • Liu R, (ed), Informa healthcare, New York
    • Vasanthavada M, Tong WQ, Serajuddin ATM. Development of solid dispersions for poorly water-soluble drug. In: Liu R, editor. Water-insoluble drug formulations. 2nd ed. New York: Informa healthcare; 2008. p. 149–84.
    • (2008) Water-insoluble drug formulations , pp. 149-184
    • Vasanthavada, M.1    Tong, W.Q.2    Serajuddin, A.T.M.3
  • 17
    • 48149085297 scopus 로고    scopus 로고
    • Characterization of ternary solid dispersions of itraconazole in polyethylene glycol 6000/ polyvidone- vinylacetate 64 blends
    • Janssens S, de Armas HN, D’ Autry W, Van Schepdael A, Van den Mooter G. Characterization of ternary solid dispersions of itraconazole in polyethylene glycol 6000/ polyvidone- vinylacetate 64 blends. Eur J Pharm Biopharm. 2008;69:1114–20.
    • (2008) Eur J Pharm Biopharm , vol.69 , pp. 1114-1120
    • Janssens, S.1    de Armas, H.N.2    D’ Autry, W.3    Van Schepdael, A.4    Van den Mooter, G.5
  • 18
    • 85026975223 scopus 로고    scopus 로고
    • Solid mixtures of cyclodextrins prepared via melt extrusion. Patent no
    • Baert L, Peeters J, Verreck G. Solid mixtures of cyclodextrins prepared via melt extrusion. Patent no. US 6,365,188 B1, 2002.
    • (2002) US 6,365 , vol.188 , pp. B1
    • Baert, L.1    Peeters, J.2    Verreck, G.3
  • 19
    • 41549142680 scopus 로고    scopus 로고
    • Increasing the oral bioavailability of the poorly water soluble drug itraconazole with ordered mesoporous silica
    • COI: 1:CAS:528:DC%2BD1cXktlGltLg%3D, PID: 18164930
    • Mellaerts R, Mole R, Jammaer J, Aerts CA, Paudel A, Van Humbeeck J, et al. Increasing the oral bioavailability of the poorly water soluble drug itraconazole with ordered mesoporous silica. Eur J Pharm Biopharm. 2008;69:223–30.
    • (2008) Eur J Pharm Biopharm , vol.69 , pp. 223-230
    • Mellaerts, R.1    Mole, R.2    Jammaer, J.3    Aerts, C.A.4    Paudel, A.5    Van Humbeeck, J.6
  • 20
    • 49449093730 scopus 로고    scopus 로고
    • Enhanced in vivo absorption of itraconazole via stabilization of supersaturation following acidic to neutral pH transition
    • COI: 1:CAS:528:DC%2BD1cXptlaitLo%3D, PID: 18608468
    • Miller D, DiNunzio J, Yang W, McGinity J, Williams R. Enhanced in vivo absorption of itraconazole via stabilization of supersaturation following acidic to neutral pH transition. Drug Dev Ind Pharm. 2008;34:890–902.
    • (2008) Drug Dev Ind Pharm , vol.34 , pp. 890-902
    • Miller, D.1    DiNunzio, J.2    Yang, W.3    McGinity, J.4    Williams, R.5
  • 21
    • 84873373553 scopus 로고    scopus 로고
    • Correlation between molecular mobility and physical stability of amorphous itraconazole
    • COI: 1:CAS:528:DC%2BC38XhslKhs7nL, PID: 23198856
    • Bhardwaj S, Arora K, Kwong E, Templeton A, Clas S, Suryanarayanan R. Correlation between molecular mobility and physical stability of amorphous itraconazole. Mol Pharm. 2013;10:694–700.
    • (2013) Mol Pharm , vol.10 , pp. 694-700
    • Bhardwaj, S.1    Arora, K.2    Kwong, E.3    Templeton, A.4    Clas, S.5    Suryanarayanan, R.6
  • 22
    • 84888347219 scopus 로고    scopus 로고
    • Hot melt extrusion for amorphous solid dispersions: temperature and moisture activated drug – polymer interactions for enhanced stability
    • COI: 1:CAS:528:DC%2BC3sXht12htbfM, PID: 23961978
    • Sarode A, Sandhu H, Shah N, Malick W, Zia H. Hot melt extrusion for amorphous solid dispersions: temperature and moisture activated drug – polymer interactions for enhanced stability. Mol Pharm. 2013;10:3665–75.
    • (2013) Mol Pharm , vol.10 , pp. 3665-3675
    • Sarode, A.1    Sandhu, H.2    Shah, N.3    Malick, W.4    Zia, H.5
  • 23
    • 34447543016 scopus 로고    scopus 로고
    • Influence of preparation method on itraconazole oral solutions using cyclodextrins as complexing agents
    • COI: 1:CAS:528:DC%2BD2sXnvFCksb4%3D, PID: 17718191
    • Holvoet C, Vander Heyden Y, Plaizier-Vercammen J. Influence of preparation method on itraconazole oral solutions using cyclodextrins as complexing agents. Die Pharmazie. 2007;62(7):510–4.
    • (2007) Die Pharmazie , vol.62 , Issue.7 , pp. 510-514
    • Holvoet, C.1    Vander Heyden, Y.2    Plaizier-Vercammen, J.3
  • 24
    • 84877789049 scopus 로고    scopus 로고
    • Supersolubilization and amorphization of a model basic drug, haloperidol, by interaction with weak acids
    • COI: 1:CAS:528:DC%2BC3sXivFekurY%3D, PID: 23430485
    • Singh S, Parikh T, Sandhu HK, Shah NH, Malick AW, Singhal D, et al. Supersolubilization and amorphization of a model basic drug, haloperidol, by interaction with weak acids. Pharm Res. 2013;30(6):1561–73.
    • (2013) Pharm Res , vol.30 , Issue.6 , pp. 1561-1573
    • Singh, S.1    Parikh, T.2    Sandhu, H.K.3    Shah, N.H.4    Malick, A.W.5    Singhal, D.6
  • 25
    • 18044381309 scopus 로고    scopus 로고
    • Investigation of solubility and dissolution of a free base and two different salt forms as a function of pH
    • COI: 1:CAS:528:DC%2BD2MXjsFahtbY%3D, PID: 15846471
    • Li S, Wong S, Sethia S, Almoazen H, Joshi YM, Serajuddin ATM. Investigation of solubility and dissolution of a free base and two different salt forms as a function of pH. Pharm Res. 2005;22(4):628–35.
    • (2005) Pharm Res , vol.22 , Issue.4 , pp. 628-635
    • Li, S.1    Wong, S.2    Sethia, S.3    Almoazen, H.4    Joshi, Y.M.5    Serajuddin, A.T.M.6
  • 26
    • 23844475290 scopus 로고    scopus 로고
    • Effect of chloride ion on dissolution of different salt forms of haloperidol, a model basic drug
    • COI: 1:CAS:528:DC%2BD2MXhtVOrurvL, PID: 16136556
    • Li S, Doyle P, Metz S, Royce AE, Serajuddin ATM. Effect of chloride ion on dissolution of different salt forms of haloperidol, a model basic drug. J Pharm Sci. 2005;94(10):2224–31.
    • (2005) J Pharm Sci , vol.94 , Issue.10 , pp. 2224-2231
    • Li, S.1    Doyle, P.2    Metz, S.3    Royce, A.E.4    Serajuddin, A.T.M.5
  • 27
    • 84934331945 scopus 로고    scopus 로고
    • Supersolubilization by using nonsalt-forming acid–base interaction
    • Shah N, Sandhu H, Choi D, Chokshi H, Malick AW, (eds), Springer-Verlag, New York
    • Shah A, Serajuddin ATM. Supersolubilization by using nonsalt-forming acid–base interaction. In: Shah N, Sandhu H, Choi D, Chokshi H, Malick AW, editors. Amorphous solid dispersions theory and practice. New York: Springer-Verlag; 2014. p. 595–611.
    • (2014) Amorphous solid dispersions theory and practice , pp. 595-611
    • Shah, A.1    Serajuddin, A.T.M.2
  • 28
    • 84923928603 scopus 로고    scopus 로고
    • Conversion of solid dispersion prepared by acid–base interaction into free-flowing and tabletable powder by using Neusilin® US2
    • COI: 1:CAS:528:DC%2BC2MXjtlWgsLk%3D, PID: 25724137
    • Shah A, Serajuddin ATM. Conversion of solid dispersion prepared by acid–base interaction into free-flowing and tabletable powder by using Neusilin® US2. Int J Pharm. 2015;484(1–2):172–80.
    • (2015) Int J Pharm , vol.484 , Issue.1-2 , pp. 172-180
    • Shah, A.1    Serajuddin, A.T.M.2
  • 30
    • 34548032742 scopus 로고    scopus 로고
    • Salt formation to improve drug solubility
    • COI: 1:CAS:528:DC%2BD2sXpsFGksrc%3D
    • Serajuddin ATM. Salt formation to improve drug solubility. Adv Drug Del Rev. 2007;59(7):603–16.
    • (2007) Adv Drug Del Rev , vol.59 , Issue.7 , pp. 603-616
    • Serajuddin, A.T.M.1
  • 31
    • 8844275016 scopus 로고    scopus 로고
    • Crystal and co-crystal
    • COI: 1:CAS:528:DC%2BD2cXhtlamur0%3D
    • Desiraju GR. Crystal and co-crystal. Cryst Eng Comm. 2003;5:466–7.
    • (2003) Cryst Eng Comm , vol.5 , pp. 466-467
    • Desiraju, G.R.1
  • 32
    • 33745660776 scopus 로고    scopus 로고
    • Solid-state acid–base interactions in complexes of heterocyclic bases with dicarboxylic acids: crystallography, hydrogen bond analysis, and 15 N NMR spectroscopy
    • COI: 1:CAS:528:DC%2BD28XltlCitrc%3D, PID: 16787084
    • Li ZJ, Abramov Y, Bordner J, Leonard J, Medek A, Trask AV. Solid-state acid–base interactions in complexes of heterocyclic bases with dicarboxylic acids: crystallography, hydrogen bond analysis, and 15 N NMR spectroscopy. J Am Chem Soc. 2006;128(25):8199–210.
    • (2006) J Am Chem Soc , vol.128 , Issue.25 , pp. 8199-8210
    • Li, Z.J.1    Abramov, Y.2    Bordner, J.3    Leonard, J.4    Medek, A.5    Trask, A.V.6
  • 33
    • 0141627908 scopus 로고    scopus 로고
    • Molecular complexes of homologous alkanedicarboxylic acids with isonicotinamide: X-ray crystal structures, hydrogen bond synthons, and melting point alternation
    • COI: 1:CAS:528:DC%2BD3sXks12nu7g%3D
    • Vishweshwar P, Nangia A, Lynch VM. Molecular complexes of homologous alkanedicarboxylic acids with isonicotinamide: X-ray crystal structures, hydrogen bond synthons, and melting point alternation. Cryst Growth Des. 2003;3:783–90.
    • (2003) Cryst Growth Des , vol.3 , pp. 783-790
    • Vishweshwar, P.1    Nangia, A.2    Lynch, V.M.3
  • 35
    • 33846138330 scopus 로고    scopus 로고
    • Supramolecular heterocatemers and their role in cocrystal design
    • COI: 1:CAS:528:DC%2BD28XhtFOjsL7K
    • Bis JA, McLaughlin OL, Vishweshwar P, Zaworotko MJ. Supramolecular heterocatemers and their role in cocrystal design. Cryst Growth Des. 2006;6:2648–50.
    • (2006) Cryst Growth Des , vol.6 , pp. 2648-2650
    • Bis, J.A.1    McLaughlin, O.L.2    Vishweshwar, P.3    Zaworotko, M.J.4
  • 36
    • 0006589268 scopus 로고
    • Encoding and decoding hydrogen bonds patterns of organic compounds
    • COI: 1:CAS:528:DyaK3cXhsFOgt74%3D
    • Etter MC. Encoding and decoding hydrogen bonds patterns of organic compounds. Acc Chem Res. 1990;23:120–6.
    • (1990) Acc Chem Res , vol.23 , pp. 120-126
    • Etter, M.C.1
  • 37
    • 34250891895 scopus 로고    scopus 로고
    • Hierarchy of supramolecular synthons: persistent hydroxyl…pyridine hydrogen bonds in cocrystals that contain a cyano acceptor
    • COI: 1:CAS:528:DC%2BD2sXlt1eitbs%3D, PID: 17500564
    • Bis JA, Vishweshwar P, Weyna D, Zaworotko MJ. Hierarchy of supramolecular synthons: persistent hydroxyl…pyridine hydrogen bonds in cocrystals that contain a cyano acceptor. Mol Pharm. 2007;4(3):401–16.
    • (2007) Mol Pharm , vol.4 , Issue.3 , pp. 401-416
    • Bis, J.A.1    Vishweshwar, P.2    Weyna, D.3    Zaworotko, M.J.4
  • 38
    • 61549094336 scopus 로고    scopus 로고
    • Hierarchy of supramolecular synthons: persistent carboxylic acid-pyridine hydrogen bonds in cocrystals that also contain hydroxyl moiety
    • COI: 1:CAS:528:DC%2BD1cXht1OjtLjI
    • Shattock T, Arora K, Vishweshwar P, Zaworotko M. Hierarchy of supramolecular synthons: persistent carboxylic acid-pyridine hydrogen bonds in cocrystals that also contain hydroxyl moiety. Cryst Growth Des. 2008;8(12):4533–45.
    • (2008) Cryst Growth Des , vol.8 , Issue.12 , pp. 4533-4545
    • Shattock, T.1    Arora, K.2    Vishweshwar, P.3    Zaworotko, M.4
  • 40
    • 58849104102 scopus 로고    scopus 로고
    • Freeze-drying of proteins in glass solids formed by basic amino acids and dicarboxylic acids
    • COI: 1:CAS:528:DC%2BD1MXmsVGltrw%3D, PID: 19122314
    • Izutsu KI, Kadoya S, Yomota C, Kawanishi T, Yonemochi E, Terada K. Freeze-drying of proteins in glass solids formed by basic amino acids and dicarboxylic acids. Chem Pharm Bull. 2009;57(1):43–8.
    • (2009) Chem Pharm Bull , vol.57 , Issue.1 , pp. 43-48
    • Izutsu, K.I.1    Kadoya, S.2    Yomota, C.3    Kawanishi, T.4    Yonemochi, E.5    Terada, K.6
  • 41
    • 84904310486 scopus 로고    scopus 로고
    • Improving co-amorphous drug formulations by the addition of the highly water soluble amino acid proline
    • COI: 1:CAS:528:DC%2BC2cXhslensLbK, PID: 25025400
    • Jensen KT, Löbmann K, Rades T, Grohganz H. Improving co-amorphous drug formulations by the addition of the highly water soluble amino acid proline. Pharmaceutics. 2014;6(3):416–35.
    • (2014) Pharmaceutics , vol.6 , Issue.3 , pp. 416-435
    • Jensen, K.T.1    Löbmann, K.2    Rades, T.3    Grohganz, H.4
  • 42
    • 80053505508 scopus 로고    scopus 로고
    • Coamorphous drug systems: enhanced physical stability and dissolution rate of indomethacin and naproxen
    • COI: 1:CAS:528:DC%2BC3MXhtVWhurfI, PID: 21815614
    • Lobmann K, Laitinen R, Grohganz H, Strachan C, Rades T, Gordon K. Coamorphous drug systems: enhanced physical stability and dissolution rate of indomethacin and naproxen. Mol Pharm. 2011;8(5):1919–28.
    • (2011) Mol Pharm , vol.8 , Issue.5 , pp. 1919-1928
    • Lobmann, K.1    Laitinen, R.2    Grohganz, H.3    Strachan, C.4    Rades, T.5    Gordon, K.6
  • 44
    • 84871650627 scopus 로고    scopus 로고
    • Formation of itraconazole-succinic acid cocrystals by gas antisolvent cocrystallization
    • COI: 1:CAS:528:DC%2BC38XhvVSms7jK, PID: 23054991
    • Ober C, Gupta R. Formation of itraconazole-succinic acid cocrystals by gas antisolvent cocrystallization. AAPS PharmSciTech. 2012;13(4):1396–406.
    • (2012) AAPS PharmSciTech , vol.13 , Issue.4 , pp. 1396-1406
    • Ober, C.1    Gupta, R.2
  • 45
    • 0042471543 scopus 로고    scopus 로고
    • Nucleation in solutions revisited
    • COI: 1:CAS:528:DC%2BD3sXmtF2rsrk%3D
    • Kashchiev D, Van Rosmalen G. Nucleation in solutions revisited. Cryst Res Technol. 2003;38:555–74.
    • (2003) Cryst Res Technol , vol.38 , pp. 555-574
    • Kashchiev, D.1    Van Rosmalen, G.2
  • 46
    • 82955163290 scopus 로고    scopus 로고
    • Prenucleation clusters and non-classical nucleation
    • COI: 1:CAS:528:DC%2BC3MXhs1Sqt73M
    • Gebauer D, Coelfen H. Prenucleation clusters and non-classical nucleation. Nano Today. 2011;6:564–84.
    • (2011) Nano Today , vol.6 , pp. 564-584
    • Gebauer, D.1    Coelfen, H.2
  • 47
    • 78649974915 scopus 로고    scopus 로고
    • Nucleation
    • COI: 1:CAS:528:DC%2BC3cXhsVaisrnO, PID: 21132117
    • Vekilov PG. Nucleation. Cryst Growth Des. 2010;10:5007–19.
    • (2010) Cryst Growth Des , vol.10 , pp. 5007-5019
    • Vekilov, P.G.1
  • 48
    • 66249101601 scopus 로고    scopus 로고
    • Solubility advantage of pharmaceutical cocrystals
    • COI: 1:CAS:528:DC%2BD1MXjsVKkurs%3D
    • Good D, Rodriguez-Hornedo N. Solubility advantage of pharmaceutical cocrystals. Cryst Growth Des. 2009;9:2252–64.
    • (2009) Cryst Growth Des , vol.9 , pp. 2252-2264
    • Good, D.1    Rodriguez-Hornedo, N.2
  • 49
    • 84884142576 scopus 로고    scopus 로고
    • Pharmaceutical cocrystals and poorly soluble drugs
    • COI: 1:CAS:528:DC%2BC3sXitlent7c%3D, PID: 23207015
    • Thakuria R, Delori A, Jones W, Lipert M, Roy L, Rodriguez N. Pharmaceutical cocrystals and poorly soluble drugs. Int J Pharm. 2013;453(1):101–25.
    • (2013) Int J Pharm , vol.453 , Issue.1 , pp. 101-125
    • Thakuria, R.1    Delori, A.2    Jones, W.3    Lipert, M.4    Roy, L.5    Rodriguez, N.6
  • 50
    • 84865291348 scopus 로고    scopus 로고
    • A new cocrystal and salts of itraconazole: comparison of solid-state properties, stability and dissolution behavior
    • COI: 1:CAS:528:DC%2BC38Xht12jsL3L, PID: 22750429
    • Shevchenko A, Bimbo LM, Miroshnyk I, Haarala J, Jelínková K, Syrjänen K, et al. A new cocrystal and salts of itraconazole: comparison of solid-state properties, stability and dissolution behavior. Int J Pharm. 2012;436(1):403–9.
    • (2012) Int J Pharm , vol.436 , Issue.1 , pp. 403-409
    • Shevchenko, A.1    Bimbo, L.M.2    Miroshnyk, I.3    Haarala, J.4    Jelínková, K.5    Syrjänen, K.6
  • 51
    • 0028268210 scopus 로고
    • The relationship between the glass transition temperature and the water content of amorphous pharmaceutical solids
    • COI: 1:CAS:528:DyaK2cXivVSis7k%3D, PID: 8058600
    • Hancock BC, Zografi G. The relationship between the glass transition temperature and the water content of amorphous pharmaceutical solids. Pharm Res. 1994;11:471–7.
    • (1994) Pharm Res , vol.11 , pp. 471-477
    • Hancock, B.C.1    Zografi, G.2
  • 52
    • 0033707107 scopus 로고    scopus 로고
    • Crystal nucleation and growth of indomethacin polymorphs from the amorphous state
    • COI: 1:CAS:528:DC%2BD3cXktV2ru7o%3D
    • Andronis V, Zografi G. Crystal nucleation and growth of indomethacin polymorphs from the amorphous state. J Non-cryst Sol. 2000;271:236–48.
    • (2000) J Non-cryst Sol , vol.271 , pp. 236-248
    • Andronis, V.1    Zografi, G.2
  • 53
    • 0035823327 scopus 로고    scopus 로고
    • Investigation of thermal properties of glassy itraconazole: identification of a monotropic mesophase
    • COI: 1:CAS:528:DC%2BD3MXmtFSltr8%3D
    • Six K, Verreck G, Peeters J, Binnemans K, Berghmans H, Augustijns P, et al. Investigation of thermal properties of glassy itraconazole: identification of a monotropic mesophase. Thermochim Acta. 2001;376(2):175–81.
    • (2001) Thermochim Acta , vol.376 , Issue.2 , pp. 175-181
    • Six, K.1    Verreck, G.2    Peeters, J.3    Binnemans, K.4    Berghmans, H.5    Augustijns, P.6
  • 54
    • 84934927484 scopus 로고    scopus 로고
    • Application of film casting technique to investigate drug–polymer miscibility in solid dispersion and hot melt extrudate
    • COI: 1:CAS:528:DC%2BC2MXntFCktrg%3D, PID: 25917333
    • Parikh T, Gupta SS, Meena AK, Vitez I, Mahajan N, Serajuddin ATM. Application of film casting technique to investigate drug–polymer miscibility in solid dispersion and hot melt extrudate. J Pharm Sci. 2015;104:2142–52.
    • (2015) J Pharm Sci , vol.104 , pp. 2142-2152
    • Parikh, T.1    Gupta, S.S.2    Meena, A.K.3    Vitez, I.4    Mahajan, N.5    Serajuddin, A.T.M.6
  • 55
    • 27644552573 scopus 로고    scopus 로고
    • Pharmaceutical liquid crystals: the relevance of partially ordered systems
    • COI: 1:CAS:528:DC%2BD2MXpslOgt7w%3D, PID: 16052511
    • Stevenson CL, Bennett DB, Lechuga‐Ballesteros D. Pharmaceutical liquid crystals: the relevance of partially ordered systems. J Pharm Sci. 2005;94(9):1861–80.
    • (2005) J Pharm Sci , vol.94 , Issue.9 , pp. 1861-1880
    • Stevenson, C.L.1    Bennett, D.B.2    Lechuga‐Ballesteros, D.3
  • 56
    • 80052261018 scopus 로고    scopus 로고
    • Solubility advantage of amorphous pharmaceuticals, part 3: is maximum solubility advantage experimentally attainable and sustainable?
    • COI: 1:CAS:528:DC%2BC3MXmslyms78%3D, PID: 21630280
    • Murdande S, Pikal M, Shanker R, Bogner R. Solubility advantage of amorphous pharmaceuticals, part 3: is maximum solubility advantage experimentally attainable and sustainable? J Pharm Sci. 2011;100(10):4349–56.
    • (2011) J Pharm Sci , vol.100 , Issue.10 , pp. 4349-4356
    • Murdande, S.1    Pikal, M.2    Shanker, R.3    Bogner, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.