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Volumn 285, Issue , 2015, Pages 2-15

Amorphous formulations for dissolution and bioavailability enhancement of poorly soluble APIs

Author keywords

Amorphous formulation; Dissolution enhancement; Solid dispersion

Indexed keywords

BIOCHEMISTRY; CRYSTALLINE MATERIALS; DRUG DOSAGE; DRUG PRODUCTS; ENERGY UTILIZATION; MELT SPINNING; STABILIZATION;

EID: 84942197969     PISSN: 00325910     EISSN: 1873328X     Source Type: Journal    
DOI: 10.1016/j.powtec.2015.05.012     Document Type: Review
Times cited : (146)

References (102)
  • 1
    • 36549010477 scopus 로고    scopus 로고
    • Unfinished business: target-based drug discovery
    • Brown D. Unfinished business: target-based drug discovery. Drug Discov. Today 2007, 12:1007-1012.
    • (2007) Drug Discov. Today , vol.12 , pp. 1007-1012
    • Brown, D.1
  • 2
    • 0036742053 scopus 로고    scopus 로고
    • Poor aqueous solubility-an industry wide problem in drug discovery
    • Lipinski C. Poor aqueous solubility-an industry wide problem in drug discovery. Am. Pharm. Rev. 2002, 5:82-85.
    • (2002) Am. Pharm. Rev. , vol.5 , pp. 82-85
    • Lipinski, C.1
  • 3
    • 33947487639 scopus 로고
    • The rate of dissolution of solid substances in their own solutions
    • Noyes A., Whitney W.R. The rate of dissolution of solid substances in their own solutions. J. Am. Chem. Soc. 1897, 19:930-934.
    • (1897) J. Am. Chem. Soc. , vol.19 , pp. 930-934
    • Noyes, A.1    Whitney, W.R.2
  • 5
    • 4544383493 scopus 로고    scopus 로고
    • Nanosuspensions in drug delivery
    • Rabinow B.E. Nanosuspensions in drug delivery. Nat. Rev. Drug Discov. 2004, 3:785-796.
    • (2004) Nat. Rev. Drug Discov. , vol.3 , pp. 785-796
    • Rabinow, B.E.1
  • 6
    • 34548032742 scopus 로고    scopus 로고
    • Salt formation to improve drug solubility
    • Serajuddin A.T. Salt formation to improve drug solubility. Adv. Drug Deliv. Rev. 2007, 59:603-616.
    • (2007) Adv. Drug Deliv. Rev. , vol.59 , pp. 603-616
    • Serajuddin, A.T.1
  • 7
    • 84929089524 scopus 로고    scopus 로고
    • Formulation of solid self-nanoemulsifying drug delivery systems using N-methyl pyrrolidone as cosolvent
    • Agrawal A.G., Kumar A., Gide P.S. Formulation of solid self-nanoemulsifying drug delivery systems using N-methyl pyrrolidone as cosolvent. Drug Dev. Ind. Pharm. 2015, 41:594-604.
    • (2015) Drug Dev. Ind. Pharm. , vol.41 , pp. 594-604
    • Agrawal, A.G.1    Kumar, A.2    Gide, P.S.3
  • 8
    • 0029908157 scopus 로고    scopus 로고
    • Hydrotropic solubilization-mechanistic studies
    • Coffman R., Kildsig E.D.O. Hydrotropic solubilization-mechanistic studies. Pharm. Res. 1996, 13:1460-1463.
    • (1996) Pharm. Res. , vol.13 , pp. 1460-1463
    • Coffman, R.1    Kildsig, E.D.O.2
  • 9
    • 0029819323 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
    • Loftsson T., Brewster M.E. Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. J. Pharm. Sci. 1996, 85:1017-1025.
    • (1996) J. Pharm. Sci. , vol.85 , pp. 1017-1025
    • Loftsson, T.1    Brewster, M.E.2
  • 10
    • 33847394968 scopus 로고    scopus 로고
    • Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs
    • Porter C.J., Trevaskis N.L., Charman W.N. Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs. Nat. Rev. Drug Discov. 2007, 6:231-248.
    • (2007) Nat. Rev. Drug Discov. , vol.6 , pp. 231-248
    • Porter, C.J.1    Trevaskis, N.L.2    Charman, W.N.3
  • 11
    • 0032885450 scopus 로고    scopus 로고
    • Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs
    • Serajuddin A.T. Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J. Pharm. Sci. 1999, 88:1058-1066.
    • (1999) J. Pharm. Sci. , vol.88 , pp. 1058-1066
    • Serajuddin, A.T.1
  • 13
    • 0030638567 scopus 로고    scopus 로고
    • Characteristics and significance of the amorphous state in pharmaceutical systems
    • Hancock B.C., Zografi G. Characteristics and significance of the amorphous state in pharmaceutical systems. J. Pharm. Sci. 1997, 86:1-12.
    • (1997) J. Pharm. Sci. , vol.86 , pp. 1-12
    • Hancock, B.C.1    Zografi, G.2
  • 15
    • 84881251428 scopus 로고    scopus 로고
    • Physical stability of pharmaceutical formulations: solid-state characterization of amorphous dispersions
    • Guo Y., Shalaev E., Smith S. Physical stability of pharmaceutical formulations: solid-state characterization of amorphous dispersions. TrAC, Trends Anal. Chem. 2013, 49:137-144.
    • (2013) TrAC, Trends Anal. Chem. , vol.49 , pp. 137-144
    • Guo, Y.1    Shalaev, E.2    Smith, S.3
  • 16
    • 0037043106 scopus 로고    scopus 로고
    • Comparison of the mechanical properties of the crystalline and amorphous forms of a drug substance
    • Hancock B.C., Carlson G.T., Ladipo D.D., Langdon B.A., Mullarney M.P. Comparison of the mechanical properties of the crystalline and amorphous forms of a drug substance. Int. J. Pharm. 2002, 241:73-85.
    • (2002) Int. J. Pharm. , vol.241 , pp. 73-85
    • Hancock, B.C.1    Carlson, G.T.2    Ladipo, D.D.3    Langdon, B.A.4    Mullarney, M.P.5
  • 17
    • 0001522674 scopus 로고
    • Studies on glass II: the transition between the glassy and liquid states in the case of glucose
    • Parks G.S., Huffman H.M., Cattor F.R. Studies on glass II: the transition between the glassy and liquid states in the case of glucose. J. Phys. Chem. 1928, 32:1366-1379.
    • (1928) J. Phys. Chem. , vol.32 , pp. 1366-1379
    • Parks, G.S.1    Huffman, H.M.2    Cattor, F.R.3
  • 18
    • 1142303337 scopus 로고    scopus 로고
    • What is the true solubility advantage for amorphous pharmaceuticals?
    • Hancock B.C., Parks M. What is the true solubility advantage for amorphous pharmaceuticals?. Pharm. Res. 2000, 17:397-404.
    • (2000) Pharm. Res. , vol.17 , pp. 397-404
    • Hancock, B.C.1    Parks, M.2
  • 19
    • 78651288987 scopus 로고    scopus 로고
    • Solubility advantage of amorphous pharmaceuticals: II. Application of quantitative thermodynamic relationships for prediction of solubility enhancement in structurally diverse insoluble pharmaceuticals
    • Murdande S.B., Pikal M.J., Shanker R.M., Bogner R.H. Solubility advantage of amorphous pharmaceuticals: II. Application of quantitative thermodynamic relationships for prediction of solubility enhancement in structurally diverse insoluble pharmaceuticals. Pharm. Res. 2010, 27:2704-2714.
    • (2010) Pharm. Res. , vol.27 , pp. 2704-2714
    • Murdande, S.B.1    Pikal, M.J.2    Shanker, R.M.3    Bogner, R.H.4
  • 20
    • 85008071016 scopus 로고
    • Studies on absorption of eutectic mixture. I. A comparison of the behavior of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man
    • Sekiguchi K., Obi N. Studies on absorption of eutectic mixture. I. A comparison of the behavior of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man. Chem. Pharm. Bull. 1961, 9:866-872.
    • (1961) Chem. Pharm. Bull. , vol.9 , pp. 866-872
    • Sekiguchi, K.1    Obi, N.2
  • 21
    • 36549042006 scopus 로고    scopus 로고
    • Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
    • Vasconcelos T., Sarmento B., Costa P. Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov. Today 2007, 12:1068-1075.
    • (2007) Drug Discov. Today , vol.12 , pp. 1068-1075
    • Vasconcelos, T.1    Sarmento, B.2    Costa, P.3
  • 22
    • 0014515660 scopus 로고
    • Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates
    • Simonelli A., Mehta S.C., Higuchi W.I. Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates. J. Pharm. Sci. 1969, 58:538-549.
    • (1969) J. Pharm. Sci. , vol.58 , pp. 538-549
    • Simonelli, A.1    Mehta, S.C.2    Higuchi, W.I.3
  • 23
    • 33344473894 scopus 로고    scopus 로고
    • Characterization of the molecular distribution of drugs in glassy solid dispersions at the nano-meter scale, using differential scanning calorimetry and gravimetric water vapour sorption techniques
    • Van Drooge D.J., Hinrichs W.L., Visser M.R., Frijlink H.W. Characterization of the molecular distribution of drugs in glassy solid dispersions at the nano-meter scale, using differential scanning calorimetry and gravimetric water vapour sorption techniques. Int. J. Pharm. 2006, 310:220-229.
    • (2006) Int. J. Pharm. , vol.310 , pp. 220-229
    • Van Drooge, D.J.1    Hinrichs, W.L.2    Visser, M.R.3    Frijlink, H.W.4
  • 24
    • 0015124656 scopus 로고
    • Pharmaceutical applications of solid dispersion systems
    • Chiou W.L., Riegelman S. Pharmaceutical applications of solid dispersion systems. J. Pharm. Sci. 1971, 60:1281-1302.
    • (1971) J. Pharm. Sci. , vol.60 , pp. 1281-1302
    • Chiou, W.L.1    Riegelman, S.2
  • 25
    • 84887359212 scopus 로고    scopus 로고
    • Evolution of supersaturation of amorphous pharmaceuticals: the effect of rate of supersaturation generation
    • Sun D.D., Lee P.I. Evolution of supersaturation of amorphous pharmaceuticals: the effect of rate of supersaturation generation. Mol. Pharm. 2013, 10:4330-4346.
    • (2013) Mol. Pharm. , vol.10 , pp. 4330-4346
    • Sun, D.D.1    Lee, P.I.2
  • 26
    • 84866732706 scopus 로고    scopus 로고
    • Amorphous solid dispersion enhances permeation of poorly soluble ABT-102: true supersaturation vs. apparent solubility enhancement
    • Frank K.J., Rosenblatt K.M., Westedt U., Holig P., Rosenberg J., Magerlein M., Fricker G., Brandl M. Amorphous solid dispersion enhances permeation of poorly soluble ABT-102: true supersaturation vs. apparent solubility enhancement. Int. J. Pharm. 2012, 437:288-293.
    • (2012) Int. J. Pharm. , vol.437 , pp. 288-293
    • Frank, K.J.1    Rosenblatt, K.M.2    Westedt, U.3    Holig, P.4    Rosenberg, J.5    Magerlein, M.6    Fricker, G.7    Brandl, M.8
  • 27
    • 0024218073 scopus 로고
    • Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersions
    • Serajuddin A.T., Sheen P.C., Mufson D., Bernstein D.F., Augustine M.A. Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersions. J. Pharm. Sci. 1988, 77:414-417.
    • (1988) J. Pharm. Sci. , vol.77 , pp. 414-417
    • Serajuddin, A.T.1    Sheen, P.C.2    Mufson, D.3    Bernstein, D.F.4    Augustine, M.A.5
  • 28
    • 0029816137 scopus 로고    scopus 로고
    • Solidification studies of polyethylene glycols, gelucire 44/14 or their dispersions with triamterene or temazepam
    • Dordunoo S.K., Ford J.L., Rubinstein M.H. Solidification studies of polyethylene glycols, gelucire 44/14 or their dispersions with triamterene or temazepam. J. Pharm. Pharmacol. 1996, 48:782-789.
    • (1996) J. Pharm. Pharmacol. , vol.48 , pp. 782-789
    • Dordunoo, S.K.1    Ford, J.L.2    Rubinstein, M.H.3
  • 29
    • 84909986317 scopus 로고    scopus 로고
    • Solid self-emulsifying drug delivery system (S-SEDDS) for improved dissolution rate of fenofibrate
    • Kanaujia P., Ng W.K., Tan R.B. Solid self-emulsifying drug delivery system (S-SEDDS) for improved dissolution rate of fenofibrate. J. Microencapsul. 2014, 31:293-298.
    • (2014) J. Microencapsul. , vol.31 , pp. 293-298
    • Kanaujia, P.1    Ng, W.K.2    Tan, R.B.3
  • 30
    • 33746889126 scopus 로고    scopus 로고
    • Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: stability testing of selected solid dispersions
    • Ghebremeskel A.N., Vemavarapu C., Lodaya M. Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: stability testing of selected solid dispersions. Pharm. Res. 2006, 23:1928-1936.
    • (2006) Pharm. Res. , vol.23 , pp. 1928-1936
    • Ghebremeskel, A.N.1    Vemavarapu, C.2    Lodaya, M.3
  • 32
    • 0025030273 scopus 로고
    • Physical and chemical changes of medicinals in mixtures with adsorbents in the solid state. IV. Study on reduced-pressure mixing for practical use of amorphous mixtures of flufenamic acid
    • Konno T. Physical and chemical changes of medicinals in mixtures with adsorbents in the solid state. IV. Study on reduced-pressure mixing for practical use of amorphous mixtures of flufenamic acid. Chem. Pharm. Bull. 1990, 38:2003-2007.
    • (1990) Chem. Pharm. Bull. , vol.38 , pp. 2003-2007
    • Konno, T.1
  • 35
    • 0036844753 scopus 로고    scopus 로고
    • Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules
    • Gupta M.K., Tseng Y.C., Goldman D., Bogner R.H. Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules. Pharm. Res. 2002, 19:1663-1672.
    • (2002) Pharm. Res. , vol.19 , pp. 1663-1672
    • Gupta, M.K.1    Tseng, Y.C.2    Goldman, D.3    Bogner, R.H.4
  • 36
    • 0037369754 scopus 로고    scopus 로고
    • Formation of physically stable amorphous drugs by milling with Neusilin
    • Gupta M.K., Vanwert A., Bogner R.H. Formation of physically stable amorphous drugs by milling with Neusilin. J. Pharm. Sci. 2003, 92:536-551.
    • (2003) J. Pharm. Sci. , vol.92 , pp. 536-551
    • Gupta, M.K.1    Vanwert, A.2    Bogner, R.H.3
  • 37
    • 0026931265 scopus 로고
    • Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism
    • Kresge C.T., Leonowicz M.E., Roth W.J., Vartuli J.C., Beck J.S. Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism. Nature 1992, 359:710-712.
    • (1992) Nature , vol.359 , pp. 710-712
    • Kresge, C.T.1    Leonowicz, M.E.2    Roth, W.J.3    Vartuli, J.C.4    Beck, J.S.5
  • 38
    • 0031801728 scopus 로고    scopus 로고
    • Nonionic triblock and star siblock copolymer and oligomeric surfactant syntheses of highly ordered, hydrothermally stable, mesoporous silica structures
    • Zhao D., Huo Q., Feng J., Chmelka B.F., Stucky G.D. Nonionic triblock and star siblock copolymer and oligomeric surfactant syntheses of highly ordered, hydrothermally stable, mesoporous silica structures. J. Am. Chem. Soc. 1998, 120:6024-6036.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6024-6036
    • Zhao, D.1    Huo, Q.2    Feng, J.3    Chmelka, B.F.4    Stucky, G.D.5
  • 39
    • 34347371246 scopus 로고    scopus 로고
    • Submicron particles of SBA-15 modified with MgO as carriers for controlled drug delivery
    • Shen S., Chow P.S., Chen F., Tan R.B. Submicron particles of SBA-15 modified with MgO as carriers for controlled drug delivery. Chem. Pharm. Bull. 2007, 55:985-991.
    • (2007) Chem. Pharm. Bull. , vol.55 , pp. 985-991
    • Shen, S.1    Chow, P.S.2    Chen, F.3    Tan, R.B.4
  • 40
    • 79955636907 scopus 로고    scopus 로고
    • Physical state and dissolution of ibuprofen formulated by co-spray drying with mesoporous silica: effect of pore and particle size
    • Shen S.C., Ng W.K., Chia L., Hu J., Tan R.B. Physical state and dissolution of ibuprofen formulated by co-spray drying with mesoporous silica: effect of pore and particle size. Int. J. Pharm. 2011, 410:188-195.
    • (2011) Int. J. Pharm. , vol.410 , pp. 188-195
    • Shen, S.C.1    Ng, W.K.2    Chia, L.3    Hu, J.4    Tan, R.B.5
  • 43
    • 79958812827 scopus 로고    scopus 로고
    • Evaluation of ordered mesoporous silica as a carrier for poorly soluble drugs: influence of pressure on the structure and drug release
    • Vialpando M., Aerts A., Persoons J., Martens J., Van Den Mooter G. Evaluation of ordered mesoporous silica as a carrier for poorly soluble drugs: influence of pressure on the structure and drug release. J. Pharm. Sci. 2011, 100:3411-3420.
    • (2011) J. Pharm. Sci. , vol.100 , pp. 3411-3420
    • Vialpando, M.1    Aerts, A.2    Persoons, J.3    Martens, J.4    Van Den Mooter, G.5
  • 44
    • 84873721895 scopus 로고    scopus 로고
    • In vitro and in vivo evaluation of paclitaxel-loaded mesoporous silica nanoparticles with three pore sizes
    • Jia L., Shen J., Li Z., Zhang D., Zhang Q., Liu G., Zheng D., Tian X. In vitro and in vivo evaluation of paclitaxel-loaded mesoporous silica nanoparticles with three pore sizes. Int. J. Pharm. 2013, 445:12-19.
    • (2013) Int. J. Pharm. , vol.445 , pp. 12-19
    • Jia, L.1    Shen, J.2    Li, Z.3    Zhang, D.4    Zhang, Q.5    Liu, G.6    Zheng, D.7    Tian, X.8
  • 46
    • 34548295850 scopus 로고    scopus 로고
    • Synthesis of sol-gel mesoporous silica materials providing a slow release of doxorubicin
    • Prokopowicz M., Przyjazny A. Synthesis of sol-gel mesoporous silica materials providing a slow release of doxorubicin. J. Microencapsul. 2007, 24:682-701.
    • (2007) J. Microencapsul. , vol.24 , pp. 682-701
    • Prokopowicz, M.1    Przyjazny, A.2
  • 47
    • 77954314846 scopus 로고    scopus 로고
    • Spherical mesoporous silica nanoparticles for loading and release of the poorly water-soluble drug telmisartan
    • Zhang Y., Zhi Z., Jiang T., Zhang J., Wang Z., Wang S. Spherical mesoporous silica nanoparticles for loading and release of the poorly water-soluble drug telmisartan. J. Control. Release 2010, 145:257-263.
    • (2010) J. Control. Release , vol.145 , pp. 257-263
    • Zhang, Y.1    Zhi, Z.2    Jiang, T.3    Zhang, J.4    Wang, Z.5    Wang, S.6
  • 49
    • 84903173189 scopus 로고    scopus 로고
    • Stabilisation of amorphous ibuprofen in Upsalite, a mesoporous magnesium carbonate, as an approach to increasing the aqueous solubility of poorly soluble drugs
    • Zhang P., Forsgren J., Stromme M. Stabilisation of amorphous ibuprofen in Upsalite, a mesoporous magnesium carbonate, as an approach to increasing the aqueous solubility of poorly soluble drugs. Int. J. Pharm. 2014, 472:185-191.
    • (2014) Int. J. Pharm. , vol.472 , pp. 185-191
    • Zhang, P.1    Forsgren, J.2    Stromme, M.3
  • 51
    • 0014982253 scopus 로고
    • Hot extruded dosage forms. I. Technology and dissolution kinetics of polymeric matrices
    • El-Egakey M.A., Soliva M., Speiser P. Hot extruded dosage forms. I. Technology and dissolution kinetics of polymeric matrices. Pharm. Acta Helv. 1971, 46:31-52.
    • (1971) Pharm. Acta Helv. , vol.46 , pp. 31-52
    • El-Egakey, M.A.1    Soliva, M.2    Speiser, P.3
  • 53
    • 77951205335 scopus 로고    scopus 로고
    • Formation of nano/micro-dispersions with improved dissolution properties upon dispersion of ritonavir melt extrudate in aqueous media
    • Tho I., Liepold B., Rosenberg J., Maegerlein M., Brandl M., Fricker G. Formation of nano/micro-dispersions with improved dissolution properties upon dispersion of ritonavir melt extrudate in aqueous media. Eur. J. Pharm. Sci. 2010, 40:25-32.
    • (2010) Eur. J. Pharm. Sci. , vol.40 , pp. 25-32
    • Tho, I.1    Liepold, B.2    Rosenberg, J.3    Maegerlein, M.4    Brandl, M.5    Fricker, G.6
  • 54
    • 84889089518 scopus 로고    scopus 로고
    • Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension
    • Zhang K., Yu H., Luo Q., Yang S., Lin X., Zhang Y., Tian B., Tang X. Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension. Eur. J. Pharm. Biopharm. 2013, 85:1285-1292.
    • (2013) Eur. J. Pharm. Biopharm. , vol.85 , pp. 1285-1292
    • Zhang, K.1    Yu, H.2    Luo, Q.3    Yang, S.4    Lin, X.5    Zhang, Y.6    Tian, B.7    Tang, X.8
  • 55
    • 80455122887 scopus 로고    scopus 로고
    • Characterization of thermal and rheological properties of zidovudine, lamivudine and plasticizer blends with ethyl cellulose to assess their suitability for hot melt extrusion
    • Maru S.M., De Matas M., Kelly A., Paradkar A. Characterization of thermal and rheological properties of zidovudine, lamivudine and plasticizer blends with ethyl cellulose to assess their suitability for hot melt extrusion. Eur. J. Pharm. Sci. 2011, 44:471-478.
    • (2011) Eur. J. Pharm. Sci. , vol.44 , pp. 471-478
    • Maru, S.M.1    De Matas, M.2    Kelly, A.3    Paradkar, A.4
  • 56
    • 84908363115 scopus 로고    scopus 로고
    • Use of polymer combinations in the preparation of solid dispersions of a thermally unstable drug by hot-melt extrusion
    • Liu J., Cao F., Zhang C., Ping Q. Use of polymer combinations in the preparation of solid dispersions of a thermally unstable drug by hot-melt extrusion. Acta Pharmacol. Sin. B 2013, 3:263-272.
    • (2013) Acta Pharmacol. Sin. B , vol.3 , pp. 263-272
    • Liu, J.1    Cao, F.2    Zhang, C.3    Ping, Q.4
  • 57
    • 84880692410 scopus 로고    scopus 로고
    • Solubility and dissolution rate enhancement of lumefantrine using hot melt extrusion technology with physicochemical characterisation
    • Fule R., Meer T., Sav A., Amin P. Solubility and dissolution rate enhancement of lumefantrine using hot melt extrusion technology with physicochemical characterisation. J. Pharm. Investig. 2013, 43:305-321.
    • (2013) J. Pharm. Investig. , vol.43 , pp. 305-321
    • Fule, R.1    Meer, T.2    Sav, A.3    Amin, P.4
  • 58
    • 84942202444 scopus 로고    scopus 로고
    • The production of active substance compositions in the form of a solid solution of the active substance in a polymer matrix, and active substance compositions produced by this process
    • J. Rosenberg, Breitenbach, J., The production of active substance compositions in the form of a solid solution of the active substance in a polymer matrix, and active substance compositions produced by this process. US Patent 5741519 (1998).
    • (1998)
    • Rosenberg, J.1    Breitenbach, J.2
  • 59
    • 33745929028 scopus 로고    scopus 로고
    • Melt extrusion can bring new benefits to HIV therapy: the example of Kaletra® tablets
    • Breitenbach J. Melt extrusion can bring new benefits to HIV therapy: the example of Kaletra® tablets. Am. J. Drug Deliv. 2006, 4:61-64.
    • (2006) Am. J. Drug Deliv. , vol.4 , pp. 61-64
    • Breitenbach, J.1
  • 61
    • 75449093807 scopus 로고    scopus 로고
    • Fusion production of solid dispersions containing a heat-sensitive active ingredient by hot melt extrusion and Kinetisol dispersing
    • Dinunzio J.C., Brough C., Hughey J.R., Miller D.A., Williams R.O., Mcginity J.W. Fusion production of solid dispersions containing a heat-sensitive active ingredient by hot melt extrusion and Kinetisol dispersing. Eur. J. Pharm. Biopharm. 2010, 74:340-351.
    • (2010) Eur. J. Pharm. Biopharm. , vol.74 , pp. 340-351
    • Dinunzio, J.C.1    Brough, C.2    Hughey, J.R.3    Miller, D.A.4    Williams, R.O.5    Mcginity, J.W.6
  • 62
    • 0001946453 scopus 로고    scopus 로고
    • Physics of crystal-to-glass transformations
    • Okamoto P., Lam N. Physics of crystal-to-glass transformations. Solid State Phys. 1999, 52:1-135.
    • (1999) Solid State Phys. , vol.52 , pp. 1-135
    • Okamoto, P.1    Lam, N.2
  • 63
    • 34249043919 scopus 로고    scopus 로고
    • Transformation of pharmaceutical compounds upon milling and comilling: the role of T(g)
    • Descamps M., Willart J.F., Dudognon E., Caron V. Transformation of pharmaceutical compounds upon milling and comilling: the role of T(g). J. Pharm. Sci. 2007, 96:1398-1407.
    • (2007) J. Pharm. Sci. , vol.96 , pp. 1398-1407
    • Descamps, M.1    Willart, J.F.2    Dudognon, E.3    Caron, V.4
  • 64
    • 84878593644 scopus 로고    scopus 로고
    • Amorphous solid dispersions of sulfonamide/Soluplus(R) and sulfonamide/PVP prepared by ball milling
    • Caron V., Hu Y., Tajber L., Erxleben A., Corrigan O.I., Mcardle P., Healy A.M. Amorphous solid dispersions of sulfonamide/Soluplus(R) and sulfonamide/PVP prepared by ball milling. AAPS PharmSciTech 2013, 14:464-474.
    • (2013) AAPS PharmSciTech , vol.14 , pp. 464-474
    • Caron, V.1    Hu, Y.2    Tajber, L.3    Erxleben, A.4    Corrigan, O.I.5    Mcardle, P.6    Healy, A.M.7
  • 65
    • 84942193240 scopus 로고    scopus 로고
    • Cryomilling-induced solid dispersion of poor glass forming/poorly water-soluble mefenamic acid with polyvinylpyrrolidone K12
    • Kang N., Lee J., Choi J.N., Mao C., Lee E.H. Cryomilling-induced solid dispersion of poor glass forming/poorly water-soluble mefenamic acid with polyvinylpyrrolidone K12. Drug Dev. Ind. Pharm. 2014, 1-11.
    • (2014) Drug Dev. Ind. Pharm. , pp. 1-11
    • Kang, N.1    Lee, J.2    Choi, J.N.3    Mao, C.4    Lee, E.H.5
  • 66
    • 84872449300 scopus 로고    scopus 로고
    • Selection of excipient, solvent and packaging to optimize the performance of spray-dried formulations: case example fenofibrate
    • Hugo M., Kunath K., Dressman J. Selection of excipient, solvent and packaging to optimize the performance of spray-dried formulations: case example fenofibrate. Drug Dev. Ind. Pharm. 2013, 39:402-412.
    • (2013) Drug Dev. Ind. Pharm. , vol.39 , pp. 402-412
    • Hugo, M.1    Kunath, K.2    Dressman, J.3
  • 67
    • 1442348833 scopus 로고    scopus 로고
    • Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods
    • Sethia S., Squillante E. Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods. Int. J. Pharm. 2004, 272:1-10.
    • (2004) Int. J. Pharm. , vol.272 , pp. 1-10
    • Sethia, S.1    Squillante, E.2
  • 69
    • 34447334239 scopus 로고    scopus 로고
    • Physicochemical characterization of solid dispersions of three antiepileptic drugs prepared by solvent evaporation method
    • Douroumis D., Bouropoulos N., Fahr A. Physicochemical characterization of solid dispersions of three antiepileptic drugs prepared by solvent evaporation method. J. Pharm. Pharmacol. 2007, 59:645-653.
    • (2007) J. Pharm. Pharmacol. , vol.59 , pp. 645-653
    • Douroumis, D.1    Bouropoulos, N.2    Fahr, A.3
  • 70
    • 33750430305 scopus 로고    scopus 로고
    • Industrially feasible alternative approaches in the manufacture of solid dispersions: a technical report
    • Karanth H., Shenoy V.S., Murthy R.R. Industrially feasible alternative approaches in the manufacture of solid dispersions: a technical report. AAPS PharmSciTech 2006, 7:87.
    • (2006) AAPS PharmSciTech , vol.7 , pp. 87
    • Karanth, H.1    Shenoy, V.S.2    Murthy, R.R.3
  • 71
    • 84870540084 scopus 로고    scopus 로고
    • Development of fully amorphous dispersions of a low Tg drug via co-spray drying with hydrophilic polymers
    • Zhao M., Barker S.A., Belton P.S., Mcgregor C., Craig D.Q.M. Development of fully amorphous dispersions of a low Tg drug via co-spray drying with hydrophilic polymers. Eur. J. Pharm. Biopharm. 2012, 82:572-579.
    • (2012) Eur. J. Pharm. Biopharm. , vol.82 , pp. 572-579
    • Zhao, M.1    Barker, S.A.2    Belton, P.S.3    Mcgregor, C.4    Craig, D.Q.M.5
  • 72
    • 15044343842 scopus 로고    scopus 로고
    • Solid dispersion particles of amorphous indomethacin with fine porous silica particles by using spray-drying method
    • Takeuchi H., Nagira S., Yamamoto H., Kawashima Y. Solid dispersion particles of amorphous indomethacin with fine porous silica particles by using spray-drying method. Int. J. Pharm. 2005, 293:155-164.
    • (2005) Int. J. Pharm. , vol.293 , pp. 155-164
    • Takeuchi, H.1    Nagira, S.2    Yamamoto, H.3    Kawashima, Y.4
  • 73
    • 84904890958 scopus 로고    scopus 로고
    • Nano-amorphous spray dried powder to improve oral bioavailability of itraconazole
    • Kumar S., Shen J., Burgess D.J. Nano-amorphous spray dried powder to improve oral bioavailability of itraconazole. J. Control. Release 2014, 192:95-102.
    • (2014) J. Control. Release , vol.192 , pp. 95-102
    • Kumar, S.1    Shen, J.2    Burgess, D.J.3
  • 74
    • 84873678017 scopus 로고    scopus 로고
    • Design and physicochemical characterization of advanced spray-dried tacrolimus multifunctional particles for inhalation
    • Wu X., Hayes D., Zwischenberger J.B., Kuhn R.J., Mansour H.M. Design and physicochemical characterization of advanced spray-dried tacrolimus multifunctional particles for inhalation. Drug Des. Devel. Ther. 2013, 7:59.
    • (2013) Drug Des. Devel. Ther. , vol.7 , pp. 59
    • Wu, X.1    Hayes, D.2    Zwischenberger, J.B.3    Kuhn, R.J.4    Mansour, H.M.5
  • 77
    • 28444436280 scopus 로고    scopus 로고
    • Spray freezing into liquid versus spray-freeze drying: influence of atomization on protein aggregation and biological activity
    • Yu Z., Johnston K.P., Williams R.O. Spray freezing into liquid versus spray-freeze drying: influence of atomization on protein aggregation and biological activity. Eur. J. Pharm. Sci. 2006, 27:9-18.
    • (2006) Eur. J. Pharm. Sci. , vol.27 , pp. 9-18
    • Yu, Z.1    Johnston, K.P.2    Williams, R.O.3
  • 78
    • 0037333353 scopus 로고    scopus 로고
    • Enhanced aqueous dissolution of a poorly water soluble drug by novel particle engineering technology: spray-freezing into liquid with atmospheric freeze-drying
    • Rogers T.L., Nelsen A.C., Sarkari M., Young T.J., Johnston K.P., Williams R.O. Enhanced aqueous dissolution of a poorly water soluble drug by novel particle engineering technology: spray-freezing into liquid with atmospheric freeze-drying. Pharm. Res. 2003, 20:485-493.
    • (2003) Pharm. Res. , vol.20 , pp. 485-493
    • Rogers, T.L.1    Nelsen, A.C.2    Sarkari, M.3    Young, T.J.4    Johnston, K.P.5    Williams, R.O.6
  • 79
    • 78650678715 scopus 로고    scopus 로고
    • Spray freeze drying with polyvinylpyrrolidone and sodium caprate for improved dissolution and oral bioavailability of oleanolic acid, a BCS Class IV compound
    • Tong H.H., Du Z., Wang G.N., Chan H.M., Chang Q., Lai L.C., Chow A.H., Zheng Y. Spray freeze drying with polyvinylpyrrolidone and sodium caprate for improved dissolution and oral bioavailability of oleanolic acid, a BCS Class IV compound. Int. J. Pharm. 2011, 404:148-158.
    • (2011) Int. J. Pharm. , vol.404 , pp. 148-158
    • Tong, H.H.1    Du, Z.2    Wang, G.N.3    Chan, H.M.4    Chang, Q.5    Lai, L.C.6    Chow, A.H.7    Zheng, Y.8
  • 80
    • 84904309126 scopus 로고    scopus 로고
    • Improved oral absorption and chemical stability of everolimus via preparation of solid dispersion using solvent wetting technique
    • Jang S.W., Kang M.J. Improved oral absorption and chemical stability of everolimus via preparation of solid dispersion using solvent wetting technique. Int. J. Pharm. 2014, 473:187-193.
    • (2014) Int. J. Pharm. , vol.473 , pp. 187-193
    • Jang, S.W.1    Kang, M.J.2
  • 81
    • 77957879230 scopus 로고    scopus 로고
    • Delivering a hydrophobic anticancer drug for photodynamic therapy by amorphous formulation
    • Zhou L., Wang W., Feng Y., Wei S., Zhou J., Yu B., Shen J. Delivering a hydrophobic anticancer drug for photodynamic therapy by amorphous formulation. Bioorg. Med. Chem. Lett. 2010, 20:6172-6174.
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 6172-6174
    • Zhou, L.1    Wang, W.2    Feng, Y.3    Wei, S.4    Zhou, J.5    Yu, B.6    Shen, J.7
  • 82
    • 77949652722 scopus 로고    scopus 로고
    • Electrospinning: a fascinating fiber fabrication technique
    • Bhardwaj N., Kundu S.C. Electrospinning: a fascinating fiber fabrication technique. Biotechnol. Adv. 2010, 28:325-347.
    • (2010) Biotechnol. Adv. , vol.28 , pp. 325-347
    • Bhardwaj, N.1    Kundu, S.C.2
  • 83
    • 78549245541 scopus 로고    scopus 로고
    • Multicomponent amorphous nanofibers electrospun from hot aqueous solutions of a poorly soluble drug
    • Yu D.G., Gao L.D., White K., Branford-White C., Lu W.Y., Zhu L.M. Multicomponent amorphous nanofibers electrospun from hot aqueous solutions of a poorly soluble drug. Pharm. Res. 2010, 27:2466-2477.
    • (2010) Pharm. Res. , vol.27 , pp. 2466-2477
    • Yu, D.G.1    Gao, L.D.2    White, K.3    Branford-White, C.4    Lu, W.Y.5    Zhu, L.M.6
  • 84
    • 77954814859 scopus 로고    scopus 로고
    • Dissolution improvement of electrospun nanofiber-based solid dispersions for acetaminophen
    • Yu D.G., Branford-White C., White K., Li X.L., Zhu L.M. Dissolution improvement of electrospun nanofiber-based solid dispersions for acetaminophen. AAPS PharmSciTech 2010, 11:809-817.
    • (2010) AAPS PharmSciTech , vol.11 , pp. 809-817
    • Yu, D.G.1    Branford-White, C.2    White, K.3    Li, X.L.4    Zhu, L.M.5
  • 85
    • 0027163257 scopus 로고
    • Rapid expansion from supercritical solutions: application to pharmaceutical processes
    • Phillips E.M., Stella V.J. Rapid expansion from supercritical solutions: application to pharmaceutical processes. Int. J. Pharm. 1993, 94:1-10.
    • (1993) Int. J. Pharm. , vol.94 , pp. 1-10
    • Phillips, E.M.1    Stella, V.J.2
  • 86
    • 0030791709 scopus 로고    scopus 로고
    • Pharmaceutical processing with supercritical carbon dioxide
    • Subramaniam B., Rajewski R.A., Snavely K. Pharmaceutical processing with supercritical carbon dioxide. J. Pharm. Sci. 1997, 86:885-890.
    • (1997) J. Pharm. Sci. , vol.86 , pp. 885-890
    • Subramaniam, B.1    Rajewski, R.A.2    Snavely, K.3
  • 87
    • 0032771526 scopus 로고    scopus 로고
    • Phase behavioral effects on particle formation processes using supercritical fluids
    • Palakodaty S., York P. Phase behavioral effects on particle formation processes using supercritical fluids. Pharm. Res. 1999, 16:976-985.
    • (1999) Pharm. Res. , vol.16 , pp. 976-985
    • Palakodaty, S.1    York, P.2
  • 88
    • 79955971261 scopus 로고    scopus 로고
    • Development and in-vivo assessment of the bioavailability of oridonin solid dispersions by the gas anti-solvent technique
    • Li S., Liu Y., Liu T., Zhao L., Zhao J., Feng N. Development and in-vivo assessment of the bioavailability of oridonin solid dispersions by the gas anti-solvent technique. Int. J. Pharm. 2011, 411:172-177.
    • (2011) Int. J. Pharm. , vol.411 , pp. 172-177
    • Li, S.1    Liu, Y.2    Liu, T.3    Zhao, L.4    Zhao, J.5    Feng, N.6
  • 89
    • 77951622107 scopus 로고    scopus 로고
    • Amorphization of pharmaceutical compound by co-precipitation using supercritical anti-solvent (SAS) process (part I)
    • Lim R.T.Y., Ng W.K., Tan R.B.H. Amorphization of pharmaceutical compound by co-precipitation using supercritical anti-solvent (SAS) process (part I). J. Supercrit. Fluids 2011, 53:179-184.
    • (2011) J. Supercrit. Fluids , vol.53 , pp. 179-184
    • Lim, R.T.Y.1    Ng, W.K.2    Tan, R.B.H.3
  • 90
    • 84862631967 scopus 로고    scopus 로고
    • Enhanced bioavailability of sirolimus via preparation of solid dispersion nanoparticles using a supercritical antisolvent process
    • Kim M.S., Kim J.S., Park H.J., Cho W.K., Cha K.H., Hwang S.J. Enhanced bioavailability of sirolimus via preparation of solid dispersion nanoparticles using a supercritical antisolvent process. Int. J. Nanomedicine 2011, 6:2997-3009.
    • (2011) Int. J. Nanomedicine , vol.6 , pp. 2997-3009
    • Kim, M.S.1    Kim, J.S.2    Park, H.J.3    Cho, W.K.4    Cha, K.H.5    Hwang, S.J.6
  • 92
    • 0006165045 scopus 로고
    • Method and apparatus for the formation of particles
    • World
    • M. Hanna, P. York, Method and apparatus for the formation of particles, World patent 9 501 221 (1995).
    • (1995)
    • Hanna, M.1    York, P.2
  • 93
    • 0037448430 scopus 로고    scopus 로고
    • Evaluation of solid dispersion particles prepared with SEDS
    • Juppo A.M., Boissier C., Khoo C. Evaluation of solid dispersion particles prepared with SEDS. Int. J. Pharm. 2003, 250:385-401.
    • (2003) Int. J. Pharm. , vol.250 , pp. 385-401
    • Juppo, A.M.1    Boissier, C.2    Khoo, C.3
  • 94
    • 67650178803 scopus 로고    scopus 로고
    • Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent
    • Wu K., Li J., Wang W., Winstead D.A. Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent. J. Pharm. Sci. 2009, 98:2422-2431.
    • (2009) J. Pharm. Sci. , vol.98 , pp. 2422-2431
    • Wu, K.1    Li, J.2    Wang, W.3    Winstead, D.A.4
  • 95
    • 0037203653 scopus 로고    scopus 로고
    • Spectroscopy of polymer/drug formulations processed with supercritical fluids: in situ ATR-IR and Raman study of impregnation of ibuprofen into PVP
    • Kazarian S.G., Martirosyan G.G. Spectroscopy of polymer/drug formulations processed with supercritical fluids: in situ ATR-IR and Raman study of impregnation of ibuprofen into PVP. Int. J. Pharm. 2002, 232:81-90.
    • (2002) Int. J. Pharm. , vol.232 , pp. 81-90
    • Kazarian, S.G.1    Martirosyan, G.G.2
  • 96
    • 33749442356 scopus 로고    scopus 로고
    • Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility
    • Marsac P.J., Shamblin S.L., Taylor L.S. Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility. Pharm. Res. 2006, 23:2417-2426.
    • (2006) Pharm. Res. , vol.23 , pp. 2417-2426
    • Marsac, P.J.1    Shamblin, S.L.2    Taylor, L.S.3
  • 97
    • 77956905980 scopus 로고    scopus 로고
    • Enthalpy relaxation studies of two structurally related amorphous drugs and their binary dispersions
    • Bansal S.S., Kaushal A.M., Bansal A.K. Enthalpy relaxation studies of two structurally related amorphous drugs and their binary dispersions. Drug Dev. Ind. Pharm. 2010, 36:1271-1280.
    • (2010) Drug Dev. Ind. Pharm. , vol.36 , pp. 1271-1280
    • Bansal, S.S.1    Kaushal, A.M.2    Bansal, A.K.3
  • 99
    • 0001106314 scopus 로고
    • Ideal copolymers and the second-order transitions of synthetic rubbers. I. Non-crystalline copolymers
    • Gordon M., Taylor J.S. Ideal copolymers and the second-order transitions of synthetic rubbers. I. Non-crystalline copolymers. J. Appl. Chem. 1952, 2:493-501.
    • (1952) J. Appl. Chem. , vol.2 , pp. 493-501
    • Gordon, M.1    Taylor, J.S.2
  • 101
    • 33646850912 scopus 로고    scopus 로고
    • Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone
    • Karavas E., Ktistis G., Xenakis A., Georgarakis E. Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone. Eur. J. Pharm. Biopharm. 2006, 63:103-114.
    • (2006) Eur. J. Pharm. Biopharm. , vol.63 , pp. 103-114
    • Karavas, E.1    Ktistis, G.2    Xenakis, A.3    Georgarakis, E.4


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