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Volumn 70, Issue 3, 2008, Pages 819-827

Inclusion complexes of tadalafil with natural and chemically modified β-cyclodextrins. I: Preparation and in-vitro evaluation

Author keywords

Chemically modified cyclodextrin; Cyclodextrin; In vitro dissolution; Inclusion complexes; Physicochemical characterization; Tadalafil

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; BETA CYCLODEXTRIN; HEPTAKIS(2,6 O DIMETHYL) BETA CYCLODEXTRIN; TADALAFIL;

EID: 54949135704     PISSN: 09396411     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejpb.2008.06.024     Document Type: Article
Times cited : (144)

References (38)
  • 2
    • 0038353576 scopus 로고    scopus 로고
    • Efficacy of tadalafil for the treatment of erectile dysfunction at 24 and 36 hours after dosing: a randomized controlled trial
    • Porst H., Padma-Nathan H., Giuliano F., Anglin G., Varanese L., and Rosen R. Efficacy of tadalafil for the treatment of erectile dysfunction at 24 and 36 hours after dosing: a randomized controlled trial. Urology 62 (2003) 121-126
    • (2003) Urology , vol.62 , pp. 121-126
    • Porst, H.1    Padma-Nathan, H.2    Giuliano, F.3    Anglin, G.4    Varanese, L.5    Rosen, R.6
  • 3
    • 0242411904 scopus 로고    scopus 로고
    • Efficacy and tolerability of tadalafil, a novel phosphodiesterase 5 inhibitor, in treatment of erectile dysfunction
    • Padma-Nathan H. Efficacy and tolerability of tadalafil, a novel phosphodiesterase 5 inhibitor, in treatment of erectile dysfunction. Am. J. Cardiol. 92 (2003) 19M-25M
    • (2003) Am. J. Cardiol. , vol.92
    • Padma-Nathan, H.1
  • 4
    • 54949156498 scopus 로고    scopus 로고
    • .
    • .
  • 5
    • 0036172264 scopus 로고    scopus 로고
    • Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds
    • Fernandes C.M., Teresa V.M., and Veiga F.J. Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds. Eur. J. Pharm. Sci. 15 (2002) 79-88
    • (2002) Eur. J. Pharm. Sci. , vol.15 , pp. 79-88
    • Fernandes, C.M.1    Teresa, V.M.2    Veiga, F.J.3
  • 6
    • 14644446047 scopus 로고    scopus 로고
    • Celecoxib-cyclodextrin systems: characterization and evaluation of in vitro and in vivo advantage
    • Nagarsenker M.S., and Joshi M.S. Celecoxib-cyclodextrin systems: characterization and evaluation of in vitro and in vivo advantage. Drug Dev. Ind. Pharm. 31 (2005) 169-178
    • (2005) Drug Dev. Ind. Pharm. , vol.31 , pp. 169-178
    • Nagarsenker, M.S.1    Joshi, M.S.2
  • 7
    • 17444420664 scopus 로고    scopus 로고
    • Cyclodextrin complexes of valdecoxib: properties and anti-inflammatory activity in rat
    • Rajendrakumar K., Madhusudan S., and Pralhad T. Cyclodextrin complexes of valdecoxib: properties and anti-inflammatory activity in rat. Eur. J. Pharm. Biopharm. 60 (2005) 39-46
    • (2005) Eur. J. Pharm. Biopharm. , vol.60 , pp. 39-46
    • Rajendrakumar, K.1    Madhusudan, S.2    Pralhad, T.3
  • 8
    • 34248561935 scopus 로고    scopus 로고
    • Preparation and characterization of simvastatin/hydroxypropyl-β-cyclodextrin inclusion complex using supercritical antisolvent (SAS) process
    • Jun S.W., Kim M.S., Kim J.S., Park H.J., Lee S., Woo J.S., and Hwang S.J. Preparation and characterization of simvastatin/hydroxypropyl-β-cyclodextrin inclusion complex using supercritical antisolvent (SAS) process. Eur. J. Pharm. Biopharm. 66 (2007) 413-421
    • (2007) Eur. J. Pharm. Biopharm. , vol.66 , pp. 413-421
    • Jun, S.W.1    Kim, M.S.2    Kim, J.S.3    Park, H.J.4    Lee, S.5    Woo, J.S.6    Hwang, S.J.7
  • 9
    • 0029852699 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins. 2: In vivo drug delivery
    • Rajewski R.A., and Stella V.J. Pharmaceutical applications of cyclodextrins. 2: In vivo drug delivery. J. Pharm. Sci. 85 (1996) 1142-1169
    • (1996) J. Pharm. Sci. , vol.85 , pp. 1142-1169
    • Rajewski, R.A.1    Stella, V.J.2
  • 10
    • 0013936788 scopus 로고
    • Theoretical analysis of comparative studies of complex formation
    • Connors K.A., and Mollica J.A. Theoretical analysis of comparative studies of complex formation. J. Pharm. Sci. 55 (1966) 772-780
    • (1966) J. Pharm. Sci. , vol.55 , pp. 772-780
    • Connors, K.A.1    Mollica, J.A.2
  • 12
    • 0344673395 scopus 로고    scopus 로고
    • Methods to enhance the complexation efficiency of cyclodextrin
    • Loftsson T., Masson M., and Sigurjonsdottir J.F. Methods to enhance the complexation efficiency of cyclodextrin. STP Pharma Sci. 9 (1999) 237-242
    • (1999) STP Pharma Sci. , vol.9 , pp. 237-242
    • Loftsson, T.1    Masson, M.2    Sigurjonsdottir, J.F.3
  • 13
    • 0031704894 scopus 로고    scopus 로고
    • Dissolution profiles of flurbiprofen in phospholipids solid dispersions
    • Habib M.J., Phan M.T., and Owusu-Ababio G. Dissolution profiles of flurbiprofen in phospholipids solid dispersions. Drug Dev. Ind. Pharm. 24 (1998) 1077-1082
    • (1998) Drug Dev. Ind. Pharm. , vol.24 , pp. 1077-1082
    • Habib, M.J.1    Phan, M.T.2    Owusu-Ababio, G.3
  • 14
    • 0015411388 scopus 로고
    • Effect of compaction pressure on the dissolution efficiency of direct compression systems
    • Khan K.A., and Rhodes C.T. Effect of compaction pressure on the dissolution efficiency of direct compression systems. Pharm. Acta Helv. 47 (1972) 594-607
    • (1972) Pharm. Acta Helv. , vol.47 , pp. 594-607
    • Khan, K.A.1    Rhodes, C.T.2
  • 16
    • 34147173855 scopus 로고    scopus 로고
    • UV-vis and FTIR-ATR spectroscopic techniques to study the inclusion complexes of genistein with β-cyclodextrins
    • Crupi V., Ficarra R., Guardo M., Majolino D., Stancanelli R., and Venuti V. UV-vis and FTIR-ATR spectroscopic techniques to study the inclusion complexes of genistein with β-cyclodextrins. J. Pharm. Biomed. Anal. 4 (2007) 110-117
    • (2007) J. Pharm. Biomed. Anal. , vol.4 , pp. 110-117
    • Crupi, V.1    Ficarra, R.2    Guardo, M.3    Majolino, D.4    Stancanelli, R.5    Venuti, V.6
  • 17
    • 1942434694 scopus 로고    scopus 로고
    • Self association of cyclodextrin and cyclodextrin complexes
    • Loftsson T., Masson M., and Brewster M.E. Self association of cyclodextrin and cyclodextrin complexes. J. Pharm. Sci. 93 (2004) 1091-1099
    • (2004) J. Pharm. Sci. , vol.93 , pp. 1091-1099
    • Loftsson, T.1    Masson, M.2    Brewster, M.E.3
  • 18
    • 0034988419 scopus 로고    scopus 로고
    • Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats
    • Arima H., Yunomae K., Miyake K., Irie T., Hirayama F., and Uekama K. Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats. J. Pharm. Sci. 90 (2001) 690-701
    • (2001) J. Pharm. Sci. , vol.90 , pp. 690-701
    • Arima, H.1    Yunomae, K.2    Miyake, K.3    Irie, T.4    Hirayama, F.5    Uekama, K.6
  • 20
    • 0035024266 scopus 로고    scopus 로고
    • Comparison of impact of the different hydrophilic carriers on the properties of piperazine-containing drug
    • Ahmed M.O. Comparison of impact of the different hydrophilic carriers on the properties of piperazine-containing drug. Eur. J. Pharm. Biopharm. 51 (2001) 221-226
    • (2001) Eur. J. Pharm. Biopharm. , vol.51 , pp. 221-226
    • Ahmed, M.O.1
  • 21
    • 0032975725 scopus 로고    scopus 로고
    • Effects of the host cavity size and the preparation method on the physicochemical properties of ibuproxam-cyclodextrin systems
    • Mura P., Adragna E., Rabasco A.M., Moyano J.R., Pérez-Marti{dotless}̀nez J.I., Arias M.J., and Ginés J.M. Effects of the host cavity size and the preparation method on the physicochemical properties of ibuproxam-cyclodextrin systems. Drug Dev. Ind. Pharm. 25 (1999) 279-287
    • (1999) Drug Dev. Ind. Pharm. , vol.25 , pp. 279-287
    • Mura, P.1    Adragna, E.2    Rabasco, A.M.3    Moyano, J.R.4    Pérez-Martìnez, J.I.5    Arias, M.J.6    Ginés, J.M.7
  • 22
    • 33645022281 scopus 로고    scopus 로고
    • Preparation, characterization and in vivo evaluation of formulation of baicalein with hydroxypropyl-β-cyclodextrin
    • Liu J., Qui L., Gao J., and Jin Y. Preparation, characterization and in vivo evaluation of formulation of baicalein with hydroxypropyl-β-cyclodextrin. Int. J. Pharm. 312 (2006) 137-143
    • (2006) Int. J. Pharm. , vol.312 , pp. 137-143
    • Liu, J.1    Qui, L.2    Gao, J.3    Jin, Y.4
  • 23
    • 0037189991 scopus 로고    scopus 로고
    • Effect of inclusion complexation with cyclodextrins on photostability of nifedipine in solid state
    • Bayomi M.A., Abanumany K.A., and Al-Angary A.A. Effect of inclusion complexation with cyclodextrins on photostability of nifedipine in solid state. Int. J. Pharm. 243 (2002) 107-117
    • (2002) Int. J. Pharm. , vol.243 , pp. 107-117
    • Bayomi, M.A.1    Abanumany, K.A.2    Al-Angary, A.A.3
  • 24
    • 15044343112 scopus 로고    scopus 로고
    • Enhancement of the release of azaleic acid through the synthetic membranes by inclusion complex formation with hydroxypropyl-β-cyclodextrin
    • Manosroi J., Apriyani M.G., Foe K., and Manosroi A. Enhancement of the release of azaleic acid through the synthetic membranes by inclusion complex formation with hydroxypropyl-β-cyclodextrin. Int. J. Pharm. 293 (2005) 235-240
    • (2005) Int. J. Pharm. , vol.293 , pp. 235-240
    • Manosroi, J.1    Apriyani, M.G.2    Foe, K.3    Manosroi, A.4
  • 25
    • 0242334093 scopus 로고    scopus 로고
    • Physicochemical investigation of the effects of water-soluble polymers on vinpocetine complexation with β-cyclodextrin and its sulfobutyl ether derivative in solution and solid state
    • Ribeiro L.S.S., Ferreira D.C., and Veiga F.J.B. Physicochemical investigation of the effects of water-soluble polymers on vinpocetine complexation with β-cyclodextrin and its sulfobutyl ether derivative in solution and solid state. Eur. J. Pharm. Sci. 20 (2003) 253-266
    • (2003) Eur. J. Pharm. Sci. , vol.20 , pp. 253-266
    • Ribeiro, L.S.S.1    Ferreira, D.C.2    Veiga, F.J.B.3
  • 26
    • 0031853979 scopus 로고    scopus 로고
    • Interactions of griseofulvin with cyclodextrins in solid binary systems
    • Veiga M.D., Di{dotless}̀az P.J., and Ahsan F. Interactions of griseofulvin with cyclodextrins in solid binary systems. J. Pharm. Sci. 87 (1998) 891-900
    • (1998) J. Pharm. Sci. , vol.87 , pp. 891-900
    • Veiga, M.D.1    Dìaz, P.J.2    Ahsan, F.3
  • 27
    • 0032215146 scopus 로고    scopus 로고
    • Characterization of a inclusion complex of cholesterol and hydroxypropyl-β-cyclodextrin
    • Williams R.O., Mahaguna V., and Sriwongjanya M. Characterization of a inclusion complex of cholesterol and hydroxypropyl-β-cyclodextrin. Eur. J. Pharm. Biopharm. 46 (1998) 355-360
    • (1998) Eur. J. Pharm. Biopharm. , vol.46 , pp. 355-360
    • Williams, R.O.1    Mahaguna, V.2    Sriwongjanya, M.3
  • 28
    • 0029923106 scopus 로고    scopus 로고
    • A study on the differentiation between amorphous piroxicam:β-cyclodextrin complex and a mixture of the two amorphous components
    • Redenti E., Peveri T., Zanol M., Ventura P., Gnappi G., and Montenero A. A study on the differentiation between amorphous piroxicam:β-cyclodextrin complex and a mixture of the two amorphous components. Int. J. Pharm. 129 (1996) 289-294
    • (1996) Int. J. Pharm. , vol.129 , pp. 289-294
    • Redenti, E.1    Peveri, T.2    Zanol, M.3    Ventura, P.4    Gnappi, G.5    Montenero, A.6
  • 29
    • 0036389390 scopus 로고    scopus 로고
    • An effective anticonvulsant prepared following a host-guest strategy that uses hydroxypropyl-β-cyclodextrin and benzaldehyde semicarbazone
    • Beraldo H., Sinisterra R.D., Teixeira L.R., Vieira R.P., and Doretto M.C. An effective anticonvulsant prepared following a host-guest strategy that uses hydroxypropyl-β-cyclodextrin and benzaldehyde semicarbazone. Biochem. Biophys. Res. Commun. 296 (2002) 241-246
    • (2002) Biochem. Biophys. Res. Commun. , vol.296 , pp. 241-246
    • Beraldo, H.1    Sinisterra, R.D.2    Teixeira, L.R.3    Vieira, R.P.4    Doretto, M.C.5
  • 31
    • 0028924778 scopus 로고
    • Study of the dissolution characteristics of oxazepam via complexation with β-cyclodextrin
    • Moyano J.R., Ginés J.M., Arias M.J., and Rabasco A.M. Study of the dissolution characteristics of oxazepam via complexation with β-cyclodextrin. Int. J. Pharm. 114 (1995) 95-102
    • (1995) Int. J. Pharm. , vol.114 , pp. 95-102
    • Moyano, J.R.1    Ginés, J.M.2    Arias, M.J.3    Rabasco, A.M.4
  • 32
    • 0032845315 scopus 로고    scopus 로고
    • Improvement in solubility and dissolution rate of 1,2-dithiole-3-thiones upon complexation with β-cyclodextrin and its hydroxypropyl and sulfobutyl ether-7 derivatives
    • Dollo G., Corre P., Chollet M., Chevanne F., Bertault M., Burgot J., and Verge R. Improvement in solubility and dissolution rate of 1,2-dithiole-3-thiones upon complexation with β-cyclodextrin and its hydroxypropyl and sulfobutyl ether-7 derivatives. J. Pharm. Sci. 88 (1999) 889-895
    • (1999) J. Pharm. Sci. , vol.88 , pp. 889-895
    • Dollo, G.1    Corre, P.2    Chollet, M.3    Chevanne, F.4    Bertault, M.5    Burgot, J.6    Verge, R.7
  • 33
    • 0029586490 scopus 로고
    • Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques
    • Betageri G.V., and Makarla K.R. Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques. Int. J. Pharm. 126 (1995) 155-160
    • (1995) Int. J. Pharm. , vol.126 , pp. 155-160
    • Betageri, G.V.1    Makarla, K.R.2
  • 34
    • 25144471564 scopus 로고    scopus 로고
    • Development of fast-dissolving tablets of flurbiprofen-cyclodextrin complexes
    • Cirri M., Rangoni C., Maestrelli F., Corti G., and Mura P. Development of fast-dissolving tablets of flurbiprofen-cyclodextrin complexes. Drug Dev. Ind. Pharm. 31 (2005) 697-707
    • (2005) Drug Dev. Ind. Pharm. , vol.31 , pp. 697-707
    • Cirri, M.1    Rangoni, C.2    Maestrelli, F.3    Corti, G.4    Mura, P.5
  • 35
    • 33644774329 scopus 로고    scopus 로고
    • Improving cyclodextrin complexation of a new antihepatitis drug with glacial acetic acid
    • article 18
    • Johnson J.L.H., He Y., Jain A., and Yalkowsky S.H. Improving cyclodextrin complexation of a new antihepatitis drug with glacial acetic acid. AAPS PharmSciTech 7 (2006) E1-E6 article 18
    • (2006) AAPS PharmSciTech , vol.7
    • Johnson, J.L.H.1    He, Y.2    Jain, A.3    Yalkowsky, S.H.4
  • 36
    • 1642419522 scopus 로고    scopus 로고
    • Preparation of solid drug/cyclodextrin complexes of acidic and basic drugs
    • Loftsson T., Sigurdsson H.H., Másson M., and Schipper N. Preparation of solid drug/cyclodextrin complexes of acidic and basic drugs. Pharmazie 59 (2004) 25-29
    • (2004) Pharmazie , vol.59 , pp. 25-29
    • Loftsson, T.1    Sigurdsson, H.H.2    Másson, M.3    Schipper, N.4
  • 37
    • 0036348527 scopus 로고    scopus 로고
    • Inclusion complexes of piroxicam with β-cyclodextrin derivatives in comparison with the natural β-cyclodextrin: in-vitro and in-vivo drug availability
    • Elkheshen S.A., Ahmed S.M., and Al-Quadeib B.T. Inclusion complexes of piroxicam with β-cyclodextrin derivatives in comparison with the natural β-cyclodextrin: in-vitro and in-vivo drug availability. Pharm. Ind. 64 (2002) 708-715
    • (2002) Pharm. Ind. , vol.64 , pp. 708-715
    • Elkheshen, S.A.1    Ahmed, S.M.2    Al-Quadeib, B.T.3
  • 38
    • 21844459973 scopus 로고    scopus 로고
    • 2-Hydroxypropyl-β-cyclodextrin: a toxicology review
    • Gould S., and Scott R.C. 2-Hydroxypropyl-β-cyclodextrin: a toxicology review. Food Chem. Toxicol. 43 (2005) 1451-1459
    • (2005) Food Chem. Toxicol. , vol.43 , pp. 1451-1459
    • Gould, S.1    Scott, R.C.2


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