메뉴 건너뛰기




Volumn 63, Issue 1, 2011, Pages 19-25

Fast-dissolving sublingual solid dispersion and cyclodextrin complex increase the absorption of perphenazine in rabbits

Author keywords

absorption; cyclodextrin complex; solid dispersion; sublingual administration

Indexed keywords

BETA CYCLODEXTRIN; MACROGOL 8000; PERPHENAZINE;

EID: 78650371506     PISSN: 00223573     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.2042-7158.2010.01173.x     Document Type: Article
Times cited : (20)

References (27)
  • 2
    • 73949133650 scopus 로고    scopus 로고
    • Non-invasive systemic drug delivery: Developability considerations for alternate routes of administration
    • Mathias NR, Hussain MA,. Non-invasive systemic drug delivery: developability considerations for alternate routes of administration. J Pharm Sci 2009; 99: 1-20.
    • (2009) J Pharm Sci , vol.99 , pp. 1-20
    • Mathias, N.R.1    Hussain, M.A.2
  • 3
    • 5144234094 scopus 로고    scopus 로고
    • Mucosal drug delivery: Membranes, methodologies, and applications
    • Song Y, et al. Mucosal drug delivery: membranes, methodologies, and applications. Crit Rev Ther Drug Carrier Syst 2004; 21: 195-256.
    • (2004) Crit Rev Ther Drug Carrier Syst , vol.21 , pp. 195-256
    • Song, Y.1
  • 4
    • 18944386737 scopus 로고    scopus 로고
    • Perphenazine for schizophrenia
    • CD003443. DOI: 10.1002/14651858.CD003443.pub2
    • Hartung B, et al. Perphenazine for schizophrenia. Cochrane Database Syst Rev 2005; 1: CD003443. DOI: 10.1002/14651858.CD003443.pub2
    • (2005) Cochrane Database Syst Rev , vol.1
    • Hartung, B.1
  • 5
    • 59649094986 scopus 로고    scopus 로고
    • Intraorally fast-dissolving particles of a poorly soluble drug: Preparation and in vitro characterization
    • Laitinen R, et al. Intraorally fast-dissolving particles of a poorly soluble drug: preparation and in vitro characterization. Eur J Pharm Biopharm 2009; 71: 271-281.
    • (2009) Eur J Pharm Biopharm , vol.71 , pp. 271-281
    • Laitinen, R.1
  • 6
    • 34548134519 scopus 로고    scopus 로고
    • Cyclodextrins as pharmaceutical solubilizers
    • Brewster ME, Loftsson T,. Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv Rev 2007; 59: 645-666.
    • (2007) Adv Drug Deliv Rev , vol.59 , pp. 645-666
    • Brewster, M.E.1    Loftsson, T.2
  • 7
    • 49849086012 scopus 로고    scopus 로고
    • Enhanced solubility and dissolution rate of lamotrigine by inclusion complexation and solid dispersion technique
    • Shinde VR, et al. Enhanced solubility and dissolution rate of lamotrigine by inclusion complexation and solid dispersion technique. J Pharm Pharmacol 2008; 60: 1121-1129.
    • (2008) J Pharm Pharmacol , vol.60 , pp. 1121-1129
    • Shinde, V.R.1
  • 8
    • 1442309058 scopus 로고    scopus 로고
    • Solid dispersions based on inulin for the stabilisation and formulation of Δ9-tetrahydrocannabinol
    • van Drooge DJ, et al. Solid dispersions based on inulin for the stabilisation and formulation of Δ9-tetrahydrocannabinol. Eur J Pharm Sci 2004; 21: 511-518.
    • (2004) Eur J Pharm Sci , vol.21 , pp. 511-518
    • Van Drooge, D.J.1
  • 9
    • 85047686260 scopus 로고    scopus 로고
    • Cefuroxime axetil solid dispersion with polyglycolized glycerides for improved stability and bioavailability
    • Dhumal RS, et al. Cefuroxime axetil solid dispersion with polyglycolized glycerides for improved stability and bioavailability. J Pharm Pharmacol 2009; 61: 743-751.
    • (2009) J Pharm Pharmacol , vol.61 , pp. 743-751
    • Dhumal, R.S.1
  • 10
    • 34548023425 scopus 로고    scopus 로고
    • Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates
    • Blagden N, et al. Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates. Adv Drug Deliv Rev 2007; 59: 617-630.
    • (2007) Adv Drug Deliv Rev , vol.59 , pp. 617-630
    • Blagden, N.1
  • 11
    • 1342281182 scopus 로고    scopus 로고
    • Micron-size drug particles: Common and novel micronization techniques
    • Rasenack N, Muller BW,. Micron-size drug particles: common and novel micronization techniques. Pharm Dev Technol 2004; 9: 1-13.
    • (2004) Pharm Dev Technol , vol.9 , pp. 1-13
    • Rasenack, N.1    Muller, B.W.2
  • 12
    • 37849030370 scopus 로고    scopus 로고
    • Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: Comparison with commercial preparations
    • Vogt M, et al. Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: comparison with commercial preparations. Eur J Pharm Biopharm 2008; 68: 283-288.
    • (2008) Eur J Pharm Biopharm , vol.68 , pp. 283-288
    • Vogt, M.1
  • 13
    • 0030573061 scopus 로고    scopus 로고
    • Bioavailability of danazol-hydroxypropyl-β-cyclodextrin complex by different routes of administration
    • Badawy SIF, et al. Bioavailability of danazol-hydroxypropyl-β- cyclodextrin complex by different routes of administration. Int J Pharm 1996; 145: 137-143.
    • (1996) Int J Pharm , vol.145 , pp. 137-143
    • Badawy, S.I.F.1
  • 14
    • 0035998952 scopus 로고    scopus 로고
    • Development and in vivo evaluation of buccal tablets prepared using danazol-sulfobutylether 7 β-cyclodextrin (SBE 7) complexes
    • Jain AC, et al. Development and in vivo evaluation of buccal tablets prepared using danazol-sulfobutylether 7 β-cyclodextrin (SBE 7) complexes. J Pharm Sci 2002; 91: 1659-1668.
    • (2002) J Pharm Sci , vol.91 , pp. 1659-1668
    • Jain, A.C.1
  • 15
    • 23244451187 scopus 로고    scopus 로고
    • Effects of RM-β-CD on sublingual bioavailability of Δ9-tetrahydrocannabinol in rabbits
    • Mannila J, et al. Effects of RM-β-CD on sublingual bioavailability of Δ9-tetrahydrocannabinol in rabbits. Eur J Pharm Sci 2005; 26: 71-77.
    • (2005) Eur J Pharm Sci , vol.26 , pp. 71-77
    • Mannila, J.1
  • 16
    • 0345580769 scopus 로고    scopus 로고
    • Increased bioavailability of clomipramine after sublingual administration in rats
    • Yoo SD, et al. Increased bioavailability of clomipramine after sublingual administration in rats. J Pharm Sci 1999; 88: 1119-1121.
    • (1999) J Pharm Sci , vol.88 , pp. 1119-1121
    • Yoo, S.D.1
  • 17
    • 52949134415 scopus 로고    scopus 로고
    • Formulation and evaluation of primaquine phosphate taste-masked rapidly disintegrating tablet
    • Shah PP, Mashru RC,. Formulation and evaluation of primaquine phosphate taste-masked rapidly disintegrating tablet. J Pharm Pharmacol 2008; 60: 1279-1285.
    • (2008) J Pharm Pharmacol , vol.60 , pp. 1279-1285
    • Shah, P.P.1    Mashru, R.C.2
  • 18
    • 33745516475 scopus 로고    scopus 로고
    • Formulation and optimization of mouth dissolve tablets containing rofecoxib solid dispersion
    • Sammour OA, et al. Formulation and optimization of mouth dissolve tablets containing rofecoxib solid dispersion. AAPS PharmSciTech 2006; 7: E55.
    • (2006) AAPS PharmSciTech , vol.7
    • Sammour, O.A.1
  • 19
    • 0035141796 scopus 로고    scopus 로고
    • Pharmacokinetic behaviour of sublingually administered 8-methoxypsoralen for PUVA therapy
    • Shephard SE, et al. Pharmacokinetic behaviour of sublingually administered 8-methoxypsoralen for PUVA therapy. Photodermatol Photoimmunol Photomed 2001; 17: 11-21.
    • (2001) Photodermatol Photoimmunol Photomed , vol.17 , pp. 11-21
    • Shephard, S.E.1
  • 20
    • 49849090604 scopus 로고    scopus 로고
    • Development and validation of a gas chromatographic-mass spectrometric method for quantitative determination of perphenazine in rabbit plasma after sublingual administration
    • Turunen E, et al. Development and validation of a gas chromatographic-mass spectrometric method for quantitative determination of perphenazine in rabbit plasma after sublingual administration. J Chromatogr B 2008; 872: 51-57.
    • (2008) J Chromatogr B , vol.872 , pp. 51-57
    • Turunen, E.1
  • 21
    • 0000817098 scopus 로고
    • Phase-solubility techniques
    • In: Reilley C.N., ed. New York: Interscience Publisher/John Wiley & Sons.
    • Higuchi T, Connors KA,. Phase-solubility techniques. In:, Reilley CN, ed. Advances in Analytical Chemistry and Instrumentation. New York: Interscience Publisher/John Wiley & Sons, 1965: 117-212.
    • (1965) Advances in Analytical Chemistry and Instrumentation , pp. 117-212
    • Higuchi, T.1    Connors, K.A.2
  • 22
    • 33847607136 scopus 로고    scopus 로고
    • Precipitation complexation method produces cannabidiol/β- cyclodextrin inclusion complex suitable for sublingual administration of cannabidiol
    • Mannila J, et al. Precipitation complexation method produces cannabidiol/β-cyclodextrin inclusion complex suitable for sublingual administration of cannabidiol. J Pharm Sci 2007; 96: 312-319.
    • (2007) J Pharm Sci , vol.96 , pp. 312-319
    • Mannila, J.1
  • 24
    • 33645237337 scopus 로고    scopus 로고
    • A rabbit model for sublingual drug delivery: Comparison with human pharmacokinetic studies of propranolol, verapamil and captopril
    • Dali MM, et al. A rabbit model for sublingual drug delivery: comparison with human pharmacokinetic studies of propranolol, verapamil and captopril. J Pharm Sci 2006; 95: 37-44.
    • (2006) J Pharm Sci , vol.95 , pp. 37-44
    • Dali, M.M.1
  • 25
    • 0345643336 scopus 로고    scopus 로고
    • Pharmacokinetics of midazolam: Comparison of sublingual and intravenous routes in rabbit
    • Odou P, et al. Pharmacokinetics of midazolam: comparison of sublingual and intravenous routes in rabbit. Eur J Drug Metab Pharmacokinet 1999; 24: 1-7.
    • (1999) Eur J Drug Metab Pharmacokinet , vol.24 , pp. 1-7
    • Odou, P.1
  • 26
    • 0033106029 scopus 로고    scopus 로고
    • Mechanisms of drug release from cyclodextrin complexes
    • Stella VJ, et al. Mechanisms of drug release from cyclodextrin complexes. Adv Drug Deliv Rev 1999; 36: 3-16.
    • (1999) Adv Drug Deliv Rev , vol.36 , pp. 3-16
    • Stella, V.J.1
  • 27
    • 0028957759 scopus 로고
    • The use of amorphous model substances to study mechanically activated materials in the solid state
    • Elamin AA, et al. The use of amorphous model substances to study mechanically activated materials in the solid state. Int J Pharm 1995; 119: 25-36.
    • (1995) Int J Pharm , vol.119 , pp. 25-36
    • Elamin, A.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.