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Volumn 33, Issue 7, 2007, Pages 783-789

Part II: Bioavailability in beagle dogs of nimodipine solid dispersions prepared by hot-melt extrusion

Author keywords

Bioavailability; Dissolution; Hot melt extrusion; Nimodipine; Solid dispersion

Indexed keywords

ACRYLIC ACID ETHYL ESTER; AMINE; COPOLYMER; EUDRAGIT; HYDROXYPROPYLMETHYLCELLULOSE; METHYLCELLULOSE; NIMODIPINE; POLY(METHYL METHACRYLATE); POLYMER; POVIDONE; VINYL ACETATE;

EID: 34547143790     PISSN: 03639045     EISSN: 15205762     Source Type: Journal    
DOI: 10.1080/03639040601050205     Document Type: Article
Times cited : (33)

References (22)
  • 1
    • 1842865536 scopus 로고    scopus 로고
    • Melt extrusion: From process to drug delivery technology
    • Breitenbach, J. (2002). Melt extrusion: from process to drug delivery technology. Eur. J. Pharm. Biopharm., 54(2), 107-117.
    • (2002) Eur. J. Pharm. Biopharm , vol.54 , Issue.2 , pp. 107-117
    • Breitenbach, J.1
  • 2
    • 0037074108 scopus 로고    scopus 로고
    • The mechanisms of drug release from solid dispersions in water-soluble polymers
    • Craig, D. Q. M. (2002) The mechanisms of drug release from solid dispersions in water-soluble polymers. Int. J. Pharm., 231(2), 131-144.
    • (2002) Int. J. Pharm , vol.231 , Issue.2 , pp. 131-144
    • Craig, D.Q.M.1
  • 3
    • 0036025238 scopus 로고    scopus 로고
    • Improving the dissolution and bioavailability of nifedipine using solid dispersions and solubilizers
    • Emara, L. H., Badr, R. M., & Elbary, A. A. (2002). Improving the dissolution and bioavailability of nifedipine using solid dispersions and solubilizers. Drug Dev. Ind. Pharm., 28(7), 795-807.
    • (2002) Drug Dev. Ind. Pharm , vol.28 , Issue.7 , pp. 795-807
    • Emara, L.H.1    Badr, R.M.2    Elbary, A.A.3
  • 4
    • 0035095847 scopus 로고    scopus 로고
    • Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with hydrophilic amorphous polymers
    • Forster, A., Hempenstall, J., & Rades, T. (2001a). Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with hydrophilic amorphous polymers. J. Pharm. Pharmacol., 53(3), 303-315.
    • (2001) J. Pharm. Pharmacol , vol.53 , Issue.3 , pp. 303-315
    • Forster, A.1    Hempenstall, J.2    Rades, T.3
  • 5
    • 0035845751 scopus 로고    scopus 로고
    • Selection of excipients for melt extrusion with two poorly water-soluble drugs by solubility parameter calculation and thermal analysis
    • Forster, A., Hempenstall, J., Tucker, I., & Rades, T. (2001b). Selection of excipients for melt extrusion with two poorly water-soluble drugs by solubility parameter calculation and thermal analysis. Int. J. Pharm., 226(1-2), 147-161.
    • (2001) Int. J. Pharm , vol.226 , Issue.1-2 , pp. 147-161
    • Forster, A.1    Hempenstall, J.2    Tucker, I.3    Rades, T.4
  • 6
    • 0028941436 scopus 로고
    • Polymorphism in binary mixtures, as exemplified by nimodipine
    • Grunenberg, A., Keil, B., & Henck, J. O. (1995). Polymorphism in binary mixtures, as exemplified by nimodipine. Int. J. Pharm., 118(1), 11-21.
    • (1995) Int. J. Pharm , vol.118 , Issue.1 , pp. 11-21
    • Grunenberg, A.1    Keil, B.2    Henck, J.O.3
  • 7
    • 0025860978 scopus 로고
    • Oxidation of dihydropyridine calcium channel blockers and analogues by human liver cytochrom P-450 3A4
    • Guengerich, F. P., Brian, W. R., Iwasaki, M., Sari, M. A., Baarnhielm, C., & Berntssom, P. (1991). Oxidation of dihydropyridine calcium channel blockers and analogues by human liver cytochrom P-450 3A4. J. Med. Chem., 34(6) 1834-1844.
    • (1991) J. Med. Chem , vol.34 , Issue.6 , pp. 1834-1844
    • Guengerich, F.P.1    Brian, W.R.2    Iwasaki, M.3    Sari, M.A.4    Baarnhielm, C.5    Berntssom, P.6
  • 8
    • 1442333455 scopus 로고    scopus 로고
    • Development of a dissolution medium for nimodipine tablets based on bioavailability evaluation
    • He, Z., Zhong, D., Chen, X., Liu, X., Tang, X., & Zhao, L. (2004). Development of a dissolution medium for nimodipine tablets based on bioavailability evaluation. Eur. J. Pharm. Sci., 21(4), 487-491.
    • (2004) Eur. J. Pharm. Sci , vol.21 , Issue.4 , pp. 487-491
    • He, Z.1    Zhong, D.2    Chen, X.3    Liu, X.4    Tang, X.5    Zhao, L.6
  • 9
    • 0035013531 scopus 로고    scopus 로고
    • Stability of extruded 17 beta-estradiol solid dispersions
    • Hulsmann, S., Backensfeld, T., & Bodmeier, R. (2001). Stability of extruded 17 beta-estradiol solid dispersions. Pharm. Dev. Technol., 6(2), 223-229.
    • (2001) Pharm. Dev. Technol , vol.6 , Issue.2 , pp. 223-229
    • Hulsmann, S.1    Backensfeld, T.2    Bodmeier, R.3
  • 10
    • 0342804284 scopus 로고    scopus 로고
    • Melt extrusion - An alternative method for enhancing the dissolution rate of 17β-estradiol hemihydrate
    • Hulsmann, S., Backensfeld, T., Keitel, S., & Bodmeier, R. (2000). Melt extrusion - An alternative method for enhancing the dissolution rate of 17β-estradiol hemihydrate. Eur. J. Pharm. Biopharm., 49(3), 237-242.
    • (2000) Eur. J. Pharm. Biopharm , vol.49 , Issue.3 , pp. 237-242
    • Hulsmann, S.1    Backensfeld, T.2    Keitel, S.3    Bodmeier, R.4
  • 11
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Leuner, C., & Dressman, J. (2000). Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm., 50(1), 47-60.
    • (2000) Eur. J. Pharm. Biopharm , vol.50 , Issue.1 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 12
    • 0022370696 scopus 로고
    • Nimodipine
    • Manhold, R. (1985).Nimodipine. Drugs Today., 21(7) 533-536.
    • (1985) Drugs Today , vol.21 , Issue.7 , pp. 533-536
    • Manhold, R.1
  • 13
    • 0028183348 scopus 로고
    • Bioanalytics of nimodipine - An overview of methods
    • Muck, W., & Bode, H. (1994). Bioanalytics of nimodipine - An overview of methods. Pharmazie, 49(2-3), 130-139.
    • (1994) Pharmazie , vol.49 , Issue.2-3 , pp. 130-139
    • Muck, W.1    Bode, H.2
  • 14
    • 0141653582 scopus 로고    scopus 로고
    • In vivo evaluation of modified gum karaya as a carrier for improving the oral bioavailability of a poorly water-soluble drug, nimodipine
    • Murali Mohan Babu, G. V., Kumar, N. R., Sankar, K. H., Ram, B. J., Kumar, N. K., & Murthy, K. V. (2002a). In vivo evaluation of modified gum karaya as a carrier for improving the oral bioavailability of a poorly water-soluble drug, nimodipine. AAPS Pharm. Sci., Tech., 3(2), E12.
    • (2002) AAPS Pharm. Sci., Tech , vol.3 , Issue.2
    • Murali Mohan Babu, G.V.1    Kumar, N.R.2    Sankar, K.H.3    Ram, B.J.4    Kumar, N.K.5    Murthy, K.V.6
  • 15
    • 0037006604 scopus 로고    scopus 로고
    • Murali Mohan Babu, G. V., Prasad Ch, D., & Ramana Murthy, K. V. (2002b). Evaluation of modified gum karaya as carrier for the dissolution enhancement of poorly water-soluble drug nimodipine. Int. J. Pharm. 234 (1-2), 1-17.
    • Murali Mohan Babu, G. V., Prasad Ch, D., & Ramana Murthy, K. V. (2002b). Evaluation of modified gum karaya as carrier for the dissolution enhancement of poorly water-soluble drug nimodipine. Int. J. Pharm. 234 (1-2), 1-17.
  • 16
    • 0021884711 scopus 로고
    • Overview on pharmacokinetics of nimodipine in healthy volunteer and in patients with subarachnoid hemorrhage
    • Ramsch, K. D., Ahr, G., Tettenborn, D., & Auer, L. M. (1985). Overview on pharmacokinetics of nimodipine in healthy volunteer and in patients with subarachnoid hemorrhage. Neurochirurgia, 28(sp1) 74-78.
    • (1985) Neurochirurgia, 28(sp1) , pp. 74-78
    • Ramsch, K.D.1    Ahr, G.2    Tettenborn, D.3    Auer, L.M.4
  • 17
    • 0027309055 scopus 로고
    • Pglycoprotein-mediated transcellular transport of MDRreversing agents
    • Saeki, T., Ueda, K., Tanigawara, Y., Hori, R., & Komano, T. (1993). Pglycoprotein-mediated transcellular transport of MDRreversing agents. FEBS Lett., 324(1) 99-102.
    • (1993) FEBS Lett , vol.324 , Issue.1 , pp. 99-102
    • Saeki, T.1    Ueda, K.2    Tanigawara, Y.3    Hori, R.4    Komano, T.5
  • 21
    • 0037258305 scopus 로고    scopus 로고
    • Identification of phase separation in solid dispersions of itraconazole and Eudragit E100 using microthermal analysis
    • Six, K., Murphy, J., Weuts, I., Craig, D. Q., Verreck, G., Peeters, J., Brewster, M., & Van den Mooter, G. 2003b. Identification of phase separation in solid dispersions of itraconazole and Eudragit E100 using microthermal analysis. Pharm. Res., 20 (1), 135-138.
    • (2003) Pharm. Res , vol.20 , Issue.1 , pp. 135-138
    • Six, K.1    Murphy, J.2    Weuts, I.3    Craig, D.Q.4    Verreck, G.5    Peeters, J.6    Brewster, M.7    Van den Mooter, G.8
  • 22
    • 12244283119 scopus 로고    scopus 로고
    • Characterization of solid dispersions of itraconazole and hydroxypropylmethylcellulose prepared by melt extrusion - Part I
    • Verreck, G., Six, K., Van den Mooter, G., Baert, L., Peeters, J., Brewster, M. E. (2003). Characterization of solid dispersions of itraconazole and hydroxypropylmethylcellulose prepared by melt extrusion - Part I. Int. J. Pharm., 251(1-2), 165-174.
    • (2003) Int. J. Pharm , vol.251 , Issue.1-2 , pp. 165-174
    • Verreck, G.1    Six, K.2    Van den Mooter, G.3    Baert, L.4    Peeters, J.5    Brewster, M.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.