메뉴 건너뛰기




Volumn 14, Issue 2, 2013, Pages 854-860

Formulation and in vivo evaluation of orally disintegrating tablets of clozapine/hydroxypropyl-β-cyclodextrin inclusion complexes

Author keywords

bioavailability; clozapine; hydroxypropyl cyclodextrin; inclusion complexes; orally disintegrating tablets

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; CLOZAPINE;

EID: 84879112536     PISSN: None     EISSN: 15309932     Source Type: Journal    
DOI: 10.1208/s12249-013-9973-x     Document Type: Article
Times cited : (25)

References (27)
  • 2
    • 3843097202 scopus 로고    scopus 로고
    • Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system
    • 10.1016/j.ejpb.2004.03.001
    • Lindenberg M, Kopp S, Dressman JB. Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system. Eur J Pharm Biopharm. 2004;58:265-78.
    • (2004) Eur J Pharm Biopharm , vol.58 , pp. 265-278
    • Lindenberg, M.1    Kopp, S.2    Dressman, J.B.3
  • 3
    • 0003700389 scopus 로고    scopus 로고
    • American Society of Health-System Pharmacists Press Bethesda
    • Gerald KM. AHFS drug information. Bethesda: American Society of Health-System Pharmacists Press; 2004. p. 2273-85.
    • (2004) AHFS Drug Information , pp. 2273-2285
    • Gerald, K.M.1
  • 4
    • 0031958859 scopus 로고    scopus 로고
    • Drug delivery products and the Zydis fast dissolving dosage forms
    • 10.1111/j.2042-7158.1998.tb06876.x 1:CAS:528:DyaK1cXjsVyls7c%3D
    • Seager H. Drug delivery products and the Zydis fast dissolving dosage forms. J Pharm Pharmacol. 1998;50:375-82.
    • (1998) J Pharm Pharmacol , vol.50 , pp. 375-382
    • Seager, H.1
  • 5
    • 79959426405 scopus 로고    scopus 로고
    • The technologies used for developing orally disintegrating tablets: A review
    • 10.2478/v10007-011-0020-8 1:CAS:528:DC%2BC3MXptFKntrw%3D
    • Badgujar BP, Mundada AS. The technologies used for developing orally disintegrating tablets: a review. Acta Pharm. 2011;61:117-39.
    • (2011) Acta Pharm , vol.61 , pp. 117-139
    • Badgujar, B.P.1    Mundada, A.S.2
  • 6
    • 58049198455 scopus 로고    scopus 로고
    • Orally disintegrating systems: Innovations in formulation and technology
    • 10.2174/187221108786241660 1:CAS:528:DC%2BD1cXhtlWnsr7P
    • Goel H, Rai P, Rana V, Tiwary AK. Orally disintegrating systems: innovations in formulation and technology. Recent Pat Drug Deliv Formul. 2008;2:258-74.
    • (2008) Recent Pat Drug Deliv Formul , vol.2 , pp. 258-274
    • Goel, H.1    Rai, P.2    Rana, V.3    Tiwary, A.K.4
  • 7
    • 0346461917 scopus 로고    scopus 로고
    • Introduction and general overview of cyclodextrin chemistry
    • 10.1021/cr970022c 1:CAS:528:DyaK1cXksV2itrw%3D
    • Szejtli J. Introduction and general overview of cyclodextrin chemistry. Chem Rev. 1998;98:1743-54.
    • (1998) Chem Rev , vol.98 , pp. 1743-1754
    • Szejtli, J.1
  • 8
    • 0032119526 scopus 로고    scopus 로고
    • Cyclodextrin drug carrier systems
    • 10.1021/cr970025p 1:CAS:528:DyaK1cXksV2itr0%3D
    • Uekama K, Hirayama F, Irie T. Cyclodextrin drug carrier systems. Chem Rev. 1998;98:2045-76.
    • (1998) Chem Rev , vol.98 , pp. 2045-2076
    • Uekama, K.1    Hirayama, F.2    Irie, T.3
  • 9
    • 67349198514 scopus 로고    scopus 로고
    • Investigation of inclusion complex of trazodone hydrochloride with hydroxypropyl-β-cyclodextrin
    • 10.1016/j.carbpol.2009.01.033 1:CAS:528:DC%2BD1MXmtVeqsbo%3D
    • Misiuk W, Zalewska M. Investigation of inclusion complex of trazodone hydrochloride with hydroxypropyl-β-cyclodextrin. Carbohydr Polym. 2009;77:482-8.
    • (2009) Carbohydr Polym , vol.77 , pp. 482-488
    • Misiuk, W.1    Zalewska, M.2
  • 10
    • 21844459973 scopus 로고    scopus 로고
    • 2-Hydroxypropyl-β-cyclodextrin (HP-β-CD): A toxicology review
    • 10.1016/j.fct.2005.03.007 1:CAS:528:DC%2BD2MXmt1eiu78%3D
    • Gould S, Scott RC. 2-Hydroxypropyl-β-cyclodextrin (HP-β-CD): a toxicology review. Food Chem Toxicol. 2005;43:1451-9.
    • (2005) Food Chem Toxicol , vol.43 , pp. 1451-1459
    • Gould, S.1    Scott, R.C.2
  • 11
    • 0000817098 scopus 로고
    • Phase solubility techniques
    • 1:CAS:528:DyaF2MXktlGitrg%3D
    • Higuchi T, Connors KA. Phase solubility techniques. Adv Anal Chem Instrum. 1965;4:117-212.
    • (1965) Adv Anal Chem Instrum , vol.4 , pp. 117-212
    • Higuchi, T.1    Connors, K.A.2
  • 12
    • 70449520196 scopus 로고    scopus 로고
    • Effect of cyclodextrin complexation of curcumin on its solubility and antiangiogenic and anti-inflammatory activity in rat colitis model
    • 10.1208/s12249-009-9264-8 1:CAS:528:DC%2BC3cXosVansL8%3D
    • Yadav VR, Suresh S, Devi K, Yadav S. Effect of cyclodextrin complexation of curcumin on its solubility and antiangiogenic and anti-inflammatory activity in rat colitis model. AAPS PharmSciTech. 2009;10:752-62.
    • (2009) AAPS PharmSciTech , vol.10 , pp. 752-762
    • Yadav, V.R.1    Suresh, S.2    Devi, K.3    Yadav, S.4
  • 13
    • 77955368629 scopus 로고    scopus 로고
    • Development and in vitro evaluation of ibuprofen mouth dissolving tablets using solid dispersion technique
    • 10.1248/cpb.58.1037 1:CAS:528:DC%2BC3cXht1aht73L
    • Jain SK, Shukla M, Shrivastava V. Development and in vitro evaluation of ibuprofen mouth dissolving tablets using solid dispersion technique. Chem Pharm Bull. 2010;58:1037-42.
    • (2010) Chem Pharm Bull , vol.58 , pp. 1037-1042
    • Jain, S.K.1    Shukla, M.2    Shrivastava, V.3
  • 15
    • 0000488030 scopus 로고
    • In vivo bioequivalence guidances
    • US Food and Drug Administration
    • US Food and Drug Administration. In vivo bioequivalence guidances. Pharmacopeial Forum. 1993;19:6501-8.
    • (1993) Pharmacopeial Forum , vol.19 , pp. 6501-6508
  • 16
    • 0029819323 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
    • 10.1021/js950534b 1:CAS:528:DyaK28XlsFSrsr4%3D
    • Loftsson T, Brewster ME. Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. J Pharm Sci. 1996;85:1017-25.
    • (1996) J Pharm Sci , vol.85 , pp. 1017-1025
    • Loftsson, T.1    Brewster, M.E.2
  • 17
    • 0032528439 scopus 로고    scopus 로고
    • Inclusion complexation of glisentide with α-, β- And γ-cyclodextrins
    • 10.1016/S0378-5173(98)00124-0 1:CAS:528:DyaK1cXkslGns7w%3D
    • Zornoza A, Martín C, Sánchez M, Vélaz I, Piquer A. Inclusion complexation of glisentide with α-, β- and γ-cyclodextrins. Int J Pharm. 1998;169:239-44.
    • (1998) Int J Pharm , vol.169 , pp. 239-244
    • Zornoza, A.1    Martín, C.2    Sánchez, M.3    Vélaz, I.4    Piquer, A.5
  • 18
    • 0036172264 scopus 로고    scopus 로고
    • Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds
    • 10.1016/S0928-0987(01)00208-1 1:CAS:528:DC%2BD38Xms1Glsg%3D%3D
    • Fernandes CM, Teresa Vieira M, Veiga FJ. Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds. Eur J Pharm Sci. 2002;15:79-88.
    • (2002) Eur J Pharm Sci , vol.15 , pp. 79-88
    • Fernandes, C.M.1    Teresa Vieira, M.2    Veiga, F.J.3
  • 19
    • 35248822616 scopus 로고    scopus 로고
    • The utility of cyclodextrins for enhancing oral bioavailability
    • 10.1016/j.jconrel.2007.07.018 1:CAS:528:DC%2BD2sXhtFyku7fI
    • Carrier RL, Miller LA, Ahmed I. The utility of cyclodextrins for enhancing oral bioavailability. J Control Release. 2007;123:78-99.
    • (2007) J Control Release , vol.123 , pp. 78-99
    • Carrier, R.L.1    Miller, L.A.2    Ahmed, I.3
  • 20
    • 56749173508 scopus 로고    scopus 로고
    • Development of glyburide fast-dissolving tablets based on the combined use of cyclodextrins and polymers
    • 10.1080/03639040802192798 1:CAS:528:DC%2BD1cXhsVWjsrvE
    • Cirri M, Righi MF, Maestrelli F, Mura P, Valleri M. Development of glyburide fast-dissolving tablets based on the combined use of cyclodextrins and polymers. Drug Dev Ind Pharm. 2009;35:73-82.
    • (2009) Drug Dev Ind Pharm , vol.35 , pp. 73-82
    • Cirri, M.1    Righi, M.F.2    Maestrelli, F.3    Mura, P.4    Valleri, M.5
  • 21
    • 25144471564 scopus 로고    scopus 로고
    • Development of fast-dissolving tablets of flurbiprofen-cyclodextrin complexes
    • 10.1080/03639040500253694 1:CAS:528:DC%2BD2MXhtV2gtLfN
    • Cirri M, Rangoni C, Maestrelli F, Corti G, Mura P. Development of fast-dissolving tablets of flurbiprofen-cyclodextrin complexes. Drug Dev Ind Pharm. 2005;31:697-707.
    • (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
  • 22
    • 0032215146 scopus 로고    scopus 로고
    • Characterization of an inclusion complex of cholesterol and hydroxypropyl-beta-cyclodextrin
    • 10.1016/S0939-6411(98)00033-2 1:CAS:528:DyaK1MXks1eruw%3D%3D
    • Williams RO, Mahaguna V, Sriwongjanya M. Characterization of an inclusion complex of cholesterol and hydroxypropyl-beta-cyclodextrin. Eur J Pharm Biopharm. 1998;46:355-60.
    • (1998) Eur J Pharm Biopharm , vol.46 , pp. 355-360
    • Williams, R.O.1    Mahaguna, V.2    Sriwongjanya, M.3
  • 23
    • 0034874915 scopus 로고    scopus 로고
    • Influence of the preparation method on the physicochemical properties of tolbutamide/cyclodextrin binary systems
    • 10.1081/DDC-100105177 1:CAS:528:DC%2BD3MXmslSrsL8%3D
    • Veiga F, Fernandes C, Maincent P. Influence of the preparation method on the physicochemical properties of tolbutamide/cyclodextrin binary systems. Drug Dev Ind Pharm. 2001;27:523-32.
    • (2001) Drug Dev Ind Pharm , vol.27 , pp. 523-532
    • Veiga, F.1    Fernandes, C.2    Maincent, P.3
  • 24
    • 33645237337 scopus 로고    scopus 로고
    • A rabbit model for sublingual drug delivery: Comparison with human pharmacokinetic studies of propranolol, verapamil and captopril
    • 10.1002/jps.20312 1:CAS:528:DC%2BD28XlvVShsg%3D%3D
    • Dali MM, Moench PA, Mathias NR, Stetsko PI, Heran CL, Smith RL. 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    Moench, P.A.2    Mathias, N.R.3    Stetsko, P.I.4    Heran, C.L.5    Smith, R.L.6
  • 25
    • 0345643336 scopus 로고    scopus 로고
    • Pharmacokinetics of midazolam: Comparison of sublingual and intravenous routes in rabbit
    • 10.1007/BF03190004 1:CAS:528:DyaK1MXktlSrsLo%3D
    • Odou P, Barthelemy C, Chatelier D, Luyckx M, Brunet C, Dine T, 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    Barthelemy, C.2    Chatelier, D.3    Luyckx, M.4    Brunet, C.5    Dine, T.6
  • 26
    • 34548706619 scopus 로고    scopus 로고
    • In vitro and in vivo studies on the complexes of vinpocetine with hydroxypropyl-β-cyclodextrin
    • 10.1007/BF02993968
    • Nie S, Fan X, Peng Y, Yang X, Wang C, Pan W. In vitro and in vivo studies on the complexes of vinpocetine with hydroxypropyl-β-cyclodextrin. Arch Pharm Res. 2006;30:991-1001.
    • (2006) Arch Pharm Res , vol.30 , pp. 991-1001
    • Nie, S.1    Fan, X.2    Peng, Y.3    Yang, X.4    Wang, C.5    Pan, W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.