메뉴 건너뛰기




Volumn 100, Issue 6, 2011, Pages 2333-2342

Surface-active derivative of inulin (Inutec® SP1) is a superior carrier for solid dispersions with a high drug load

Author keywords

Amorphous; Dissolution; Inulin; Inulin derivative; Inutec SP1; Polyvinylpyrrolidone; Preformulation; Solid dispersion; Spray freeze drying; Surfactants

Indexed keywords

DIAZEPAM; DRUG CARRIER; EFAVIRENZ; FENOFIBRATE; INULIN; INULIN DERIVATIVE; INUTEC SP1; POVIDONE; RITONAVIR; SURFACTANT; UNCLASSIFIED DRUG;

EID: 79954585108     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.22471     Document Type: Article
Times cited : (29)

References (28)
  • 1
    • 0344052670 scopus 로고    scopus 로고
    • Micronization of drugs using supercritical carbon dioxide
    • Kerc J, Srcic S, Knez Z, Sencar-Bozic P. 1999. Micronization of drugs using supercritical carbon dioxide. Int J Pharm 182:33-39.
    • (1999) Int J Pharm , vol.182 , pp. 33-39
    • Kerc, J.1    Srcic, S.2    Knez, Z.3    Sencar-Bozic, P.4
  • 2
    • 0042845922 scopus 로고    scopus 로고
    • Scale-up and optimization of an evaporative drying process applied to aqueous dispersions of solid lipid nanoparticles
    • Marengo E, Cavalli R, Rovero G, Gasco MR. 2003. Scale-up and optimization of an evaporative drying process applied to aqueous dispersions of solid lipid nanoparticles. Pharm Dev Technol 8:299-309.
    • (2003) Pharm Dev Technol , vol.8 , pp. 299-309
    • Marengo, E.1    Cavalli, R.2    Rovero, G.3    Gasco, M.R.4
  • 4
    • 52949135898 scopus 로고    scopus 로고
    • Surface composition and contact angle relationships for differently prepared solid dispersions
    • Dahlberg C, Millqvist-Fureby A, Schuleit M. 2008. Surface composition and contact angle relationships for differently prepared solid dispersions. Eur J Pharm Biopharm 70:478-485.
    • (2008) Eur J Pharm Biopharm , vol.70 , pp. 478-485
    • Dahlberg, C.1    Millqvist-Fureby, A.2    Schuleit, M.3
  • 6
    • 68349157666 scopus 로고    scopus 로고
    • Strongly enhanced dissolution rate of fenofibrate solid dispersion tablets by incorporation of superdisintegrants
    • Srinarong P, Faber JH, Visser MR, Hinrichs WLJ, Frijlink HW. 2009. Strongly enhanced dissolution rate of fenofibrate solid dispersion tablets by incorporation of superdisintegrants. Eur J Pharm Biopharm 73:154-161.
    • (2009) Eur J Pharm Biopharm , vol.73 , pp. 154-161
    • Srinarong, P.1    Faber, J.H.2    Visser, M.R.3    Hinrichs, W.L.J.4    Frijlink, H.W.5
  • 7
    • 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 AN, Vemavarapu C, Lodaya M. 2006. Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: Stability testing of selected solid dispersions. Pharm Res 23:1928-1936.
    • (2006) Pharm Res , vol.23 , pp. 1928-1936
    • Ghebremeskel, A.N.1    Vemavarapu, C.2    Lodaya, M.3
  • 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
    • de Waard H, Hinrichs WLJ, Visser MR, Bologna C, Frijlink HW. 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.1    Hinrichs, W.L.J.2    Visser, M.R.3    Bologna, C.4    Frijlink, H.W.5
  • 9
    • 3042549390 scopus 로고    scopus 로고
    • Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions
    • van Drooge DJ, Hinrichs WLJ, Frijlink HW. 2004. Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions. J Control Release 97:441-452.
    • (2004) J Control Release , vol.97 , pp. 441-452
    • van Drooge, D.J.1    Hinrichs, W.L.J.2    Frijlink, H.W.3
  • 11
    • 33646799460 scopus 로고    scopus 로고
    • Evaluation of Inutec SP1 as a new carrier in the formulation of solid dispersions for poorly soluble drugs
    • Van Den Mooter G, Weuts I, De Ridder T, Blaton N. 2006. Evaluation of Inutec SP1 as a new carrier in the formulation of solid dispersions for poorly soluble drugs. Int J Pharm 316:1-6.
    • (2006) Int J Pharm , vol.316 , pp. 1-6
    • Van Den Mooter, G.1    Weuts, I.2    De Ridder, T.3    Blaton, N.4
  • 12
    • 27144512688 scopus 로고    scopus 로고
    • Role of molecular interaction in stability of celecoxib-PVP amorphous systems
    • Gupta P, Thilagavathi R, Chakraborti AK, Bansal AK. 2005. Role of molecular interaction in stability of celecoxib-PVP amorphous systems. Mol Pharm 2:384-391.
    • (2005) Mol Pharm , vol.2 , pp. 384-391
    • Gupta, P.1    Thilagavathi, R.2    Chakraborti, A.K.3    Bansal, A.K.4
  • 13
    • 24644474682 scopus 로고    scopus 로고
    • Miscibility behavior and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions
    • Karavas E, Ktistis G, Xenakis A, Georgarakis E. 2005. Miscibility behavior and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions. Drug Dev Ind Pharm 31:473-489.
    • (2005) Drug Dev Ind Pharm , vol.31 , pp. 473-489
    • Karavas, E.1    Ktistis, G.2    Xenakis, A.3    Georgarakis, E.4
  • 15
    • 85030573605 scopus 로고    scopus 로고
    • US Pharmacopeia 29.. Rockville, Maryland: US Pharmacopeial Convention
    • US Pharmacopeia 29. 2006. General official monograph/diazepam. Rockville, Maryland: US Pharmacopeial Convention; pp 673-674.
    • (2006) General official monograph/diazepam , pp. 673-674
  • 16
    • 27544498867 scopus 로고    scopus 로고
    • Dissolution and solubility behavior of fenofibrate in sodium lauryl sulfate solutions
    • Granero GE, Ramachandran C, Amidon GL. 2005. Dissolution and solubility behavior of fenofibrate in sodium lauryl sulfate solutions. Drug Dev Ind Pharm 31:917-922.
    • (2005) Drug Dev Ind Pharm , vol.31 , pp. 917-922
    • Granero, G.E.1    Ramachandran, C.2    Amidon, G.L.3
  • 17
    • 77953365631 scopus 로고    scopus 로고
    • Validated stability indicating LC-PDA-MS method to investigate pH rate profile and degradation kinetics of efavirenz and identification of hydrolysis product by LCMS
    • Gadkari T, Chandrachood P, Ruikar A, Tele S, Deshpande D, Salvekar J, Sonawane S. 2010. Validated stability indicating LC-PDA-MS method to investigate pH rate profile and degradation kinetics of efavirenz and identification of hydrolysis product by LCMS. Int J Pharm Pharm Sci 2:169-176.
    • (2010) Int J Pharm Pharm Sci , vol.2 , pp. 169-176
    • Gadkari, T.1    Chandrachood, P.2    Ruikar, A.3    Tele, S.4    Deshpande, D.5    Salvekar, J.6    Sonawane, S.7
  • 18
    • 33646584517 scopus 로고    scopus 로고
    • LC method for studies on the stability of lopinavir and ritonavir in soft gelatin capsules
    • Donato E, Dias C, Rossi R, Valente R, Fröehlich P, Bergold A. 2006. LC method for studies on the stability of lopinavir and ritonavir in soft gelatin capsules. Chromatographia 63:437-443.
    • (2006) Chromatographia , vol.63 , pp. 437-443
    • Donato, E.1    Dias, C.2    Rossi, R.3    Valente, R.4    Fröehlich, P.5    Bergold, A.6
  • 19
    • 1442334238 scopus 로고    scopus 로고
    • Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent
    • van Drooge DJ, Hinrichs WLJ, Frijlink HW. 2004. Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent. J Pharm Sci 93:713-725.
    • (2004) J Pharm Sci , vol.93 , pp. 713-725
    • van Drooge, D.J.1    Hinrichs, W.L.J.2    Frijlink, H.W.3
  • 20
    • 0030298896 scopus 로고    scopus 로고
    • Determination of the pKa and pH-solubility behavior of an ionizable cyclic carbamate, (S)-6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-4- (trifluoromethyl)-2H-3,1-benzoxazin-2-one (DMP 266)
    • Rabel SR, Maurin MB, Rowe SM, Hussain M. 1996. Determination of the pKa and pH-solubility behavior of an ionizable cyclic carbamate, (S)-6-chloro-4-(cyclopropylethynyl)-1, 4-dihydro-4- (trifluoromethyl)-2H-3, 1-benzoxazin-2-one (DMP 266). Pharm Dev Technol 1:91-95.
    • (1996) Pharm Dev Technol , vol.1 , pp. 91-95
    • Rabel, S.R.1    Maurin, M.B.2    Rowe, S.M.3    Hussain, M.4
  • 21
    • 0030003789 scopus 로고    scopus 로고
    • Estimation of the increase in solubility of drugs as a function of bile salt concentration
    • Mithani SD, Bakatselou V, TenHoor CN, Dressman JB. 1996. Estimation of the increase in solubility of drugs as a function of bile salt concentration. Pharm Res 13:163-167.
    • (1996) Pharm Res , vol.13 , pp. 163-167
    • Mithani, S.D.1    Bakatselou, V.2    TenHoor, C.N.3    Dressman, J.B.4
  • 22
    • 0034886795 scopus 로고    scopus 로고
    • Physicochemical considerations in the preparation of amorphous ritonavir-poly(ethylene glycol) 8000 solid dispersions
    • Law D, Krill SL, Schmitt EA, Fort JJ, Qiu Y, Wang W, Porter WR. 2001. Physicochemical considerations in the preparation of amorphous ritonavir-poly(ethylene glycol) 8000 solid dispersions. J Pharm Sci 90:1015-1025.
    • (2001) J Pharm Sci , vol.90 , pp. 1015-1025
    • Law, D.1    Krill, S.L.2    Schmitt, E.A.3    Fort, J.J.4    Qiu, Y.5    Wang, W.6    Porter, W.R.7
  • 23
    • 33745416604 scopus 로고    scopus 로고
    • Oral absorption of poorly water-soluble drugs: Computer simulation of fraction absorbed in humans from a miniscale dissolution test
    • Takano R, Sugano K, Higashida A, Hayashi Y, Machida M, Aso Y, Yamashita S. 2006. Oral absorption of poorly water-soluble drugs: Computer simulation of fraction absorbed in humans from a miniscale dissolution test. Pharm Res 23:1144-1156.
    • (2006) Pharm Res , vol.23 , pp. 1144-1156
    • Takano, R.1    Sugano, K.2    Higashida, A.3    Hayashi, Y.4    Machida, M.5    Aso, Y.6    Yamashita, S.7
  • 24
    • 37849030370 scopus 로고    scopus 로고
    • Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: Comparison with commercial preparations
    • Vogt M, Kunath K, Dressman JB. 2008. Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: Comparison with commercial preparations. Eur J Pharm Biopharm 68:283-288.
    • (2008) Eur J Pharm Biopharm , vol.68 , pp. 283-288
    • Vogt, M.1    Kunath, K.2    Dressman, J.B.3
  • 25
    • 77952934969 scopus 로고    scopus 로고
    • On the effect of temperature on aqueous solubility of organic solids
    • Black S, Muller F. 2010. On the effect of temperature on aqueous solubility of organic solids. Org Process Res Dev 14:661-665.
    • (2010) Org Process Res Dev , vol.14 , pp. 661-665
    • Black, S.1    Muller, F.2
  • 26
    • 84876258762 scopus 로고    scopus 로고
    • Effect of hydrophilic polymer on solubilization of fenofibrate by cyclodextrin complexation
    • Patel AR, Vavia PR. 2006. Effect of hydrophilic polymer on solubilization of fenofibrate by cyclodextrin complexation. J Incl Phenom Macrocycl Chem 56:247-251.
    • (2006) J Incl Phenom Macrocycl Chem , vol.56 , pp. 247-251
    • Patel, A.R.1    Vavia, P.R.2
  • 27
    • 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 DJ, Hinrichs WLJ, Visser MR, Frijlink HW. 2006. 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 310:220-229.
    • (2006) Int J Pharm , vol.310 , pp. 220-229
    • van Drooge, D.J.1    Hinrichs, W.L.J.2    Visser, M.R.3    Frijlink, H.W.4
  • 28
    • 0036786457 scopus 로고    scopus 로고
    • Water vapor absorption into amorphous hydrophobic drug/poly(vinylpyrrolidone) dispersions
    • Crowley KJ, Zografi G. 2002. Water vapor absorption into amorphous hydrophobic drug/poly(vinylpyrrolidone) dispersions. J Pharm Sci 91:2150-2165.
    • (2002) J Pharm Sci , vol.91 , pp. 2150-2165
    • Crowley, K.J.1    Zografi, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.