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Volumn 6, Issue 3, 2007, Pages 159-165

Enhancing dissolution rate of carbamazepine via cogrinding with crospovidone and hydroxypropylmethylcellulose

Author keywords

Carbamazepine; Cogrinding; Crospovidone; Dissolution rate; HPMC; Solid dispersion

Indexed keywords

CARBAMAZEPINE; CROSPOVIDONE; HYDROXYPROPYLMETHYLCELLULOSE; KOLLIDON CL M; UNCLASSIFIED DRUG;

EID: 68349132588     PISSN: 17350328     EISSN: 17266890     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (30)

References (21)
  • 1
    • 0343527392 scopus 로고    scopus 로고
    • Modern bioavailability, bioequivalence and biopharmaceutics classification system; new scientific approaches to international regulatory standards
    • Löbenberg R and Amidon GL. Modern bioavailability, bioequivalence and biopharmaceutics classification system; new scientific approaches to international regulatory standards. Eur. J. Pharm. Biopharm. (2000) 50: 3-12
    • (2000) Eur. J. Pharm. Biopharm , vol.50 , pp. 3-12
    • Löbenberg, R.1    Amidon, G.L.2
  • 2
    • 0348107338 scopus 로고    scopus 로고
    • Quantitative biopharmaceutics classification system: The central role of dose/solubility ratio
    • Rinaki E, Valsami G and Macheras P. Quantitative biopharmaceutics classification system: The central role of dose/solubility ratio. Pharm. Res. (2003) 20: 1917-1925
    • (2003) Pharm. Res , vol.20 , pp. 1917-1925
    • Rinaki, E.1    Valsami, G.2    Macheras, P.3
  • 3
    • 0032988257 scopus 로고    scopus 로고
    • In vitro/in vivo correlations of dissolution data of carbamazepine immediate release tablets with pharmacokinetic data obtained in healthy volunteers
    • Lake OA, Olling M and Barends DM. In vitro/in vivo correlations of dissolution data of carbamazepine immediate release tablets with pharmacokinetic data obtained in healthy volunteers. Eur. J. Pharm. Biopharm. (1999) 48: 9-13
    • (1999) Eur. J. Pharm. Biopharm , vol.48 , pp. 9-13
    • Lake, O.A.1    Olling, M.2    Barends, D.M.3
  • 4
    • 0035964465 scopus 로고    scopus 로고
    • In vitro and in vivo evaluation of carbamazepine-PFG 6000 solid dispersions
    • Zerrouk N, Chemtob C, Arnaud P, Toscani S and Dugue J. In vitro and in vivo evaluation of carbamazepine-PFG 6000 solid dispersions. Int J. Pharm. (2001) 225: 49-62
    • (2001) Int J. Pharm , vol.225 , pp. 49-62
    • Zerrouk, N.1    Chemtob, C.2    Arnaud, P.3    Toscani, S.4    Dugue, J.5
  • 5
    • 0035800251 scopus 로고    scopus 로고
    • Processing of carbamazepine-PEG 4000 solid dispersions with supercritical carbon dioxide: Preparation, characterization, and in vitro dissolution
    • Moneghini M, Kikic I, Voinovich D, Perissutti B and Filipovic G. Processing of carbamazepine-PEG 4000 solid dispersions with supercritical carbon dioxide: Preparation, characterization, and in vitro dissolution. Int. J. Pharm. (2001) 222: 129-138
    • (2001) Int. J. Pharm , vol.222 , pp. 129-138
    • Moneghini, M.1    Kikic, I.2    Voinovich, D.3    Perissutti, B.4    Filipovic, G.5
  • 7
    • 0036771080 scopus 로고    scopus 로고
    • Physicochemical characterization of solid dispersions of carbamazepine formulated by supercritical carbon dioxide and conventional solvent evaporation method
    • Sethia S and Squilante E. Physicochemical characterization of solid dispersions of carbamazepine formulated by supercritical carbon dioxide and conventional solvent evaporation method. J. Pharm. Sci. (2002) 91: 1948-1957
    • (2002) J. Pharm. Sci , vol.91 , pp. 1948-1957
    • Sethia, S.1    Squilante, E.2
  • 8
    • 0037473463 scopus 로고    scopus 로고
    • Formulation design of carbamazepine fast-release tablets prepared by melt granulation technique
    • Perissutti B, Rubessa F, Moneghini M, and Voinovich D. Formulation design of carbamazepine fast-release tablets prepared by melt granulation technique. Int. J. Pharm. (2003) 256: 53-63
    • (2003) Int. J. Pharm , vol.256 , pp. 53-63
    • Perissutti, B.1    Rubessa, F.2    Moneghini, M.3    Voinovich, D.4
  • 9
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Leuner C and Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm. Biopharm. (2000) 50: 47-60
    • (2000) Eur J Pharm. Biopharm , vol.50 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 10
    • 25444501756 scopus 로고    scopus 로고
    • Solid State and Dissolution Rate Characterization of Co-Ground Mixtures of Nifedipine and Hydrophilic Carriers
    • Friedrich H, Nada A and Bodmeier R. Solid State and Dissolution Rate Characterization of Co-Ground Mixtures of Nifedipine and Hydrophilic Carriers. Drug Dev. Ind. Pharm. (2005) 31: 719-728
    • (2005) Drug Dev. Ind. Pharm , vol.31 , pp. 719-728
    • Friedrich, H.1    Nada, A.2    Bodmeier, R.3
  • 11
    • 0017178826 scopus 로고
    • Dissolution behavior and bioavailability of phenytoin from a ground mixture with microcrystalline cellulose
    • Yamamoto K, Nakano M, Arita T, Takayama Y, Nakai Y. Dissolution behavior and bioavailability of phenytoin from a ground mixture with microcrystalline cellulose. J. Pharm. Sci. (1976) 65: 1484-1488
    • (1976) J. Pharm. Sci , vol.65 , pp. 1484-1488
    • Yamamoto, K.1    Nakano, M.2    Arita, T.3    Takayama, Y.4    Nakai, Y.5
  • 12
    • 0031791549 scopus 로고    scopus 로고
    • Enhanced dissolution of furosemide by coprecipitating or cogrinding with crospovidone
    • Sang-Chul S, In-Joon O, Yong-Bok L, Hoo-Kyun C and Jun-Shik C. Enhanced dissolution of furosemide by coprecipitating or cogrinding with crospovidone. Int. J Pharm (1998) 175: 17-24
    • (1998) Int. J Pharm , vol.175 , pp. 17-24
    • Sang-Chul, S.1    In-Joon, O.2    Yong-Bok, L.3    Hoo-Kyun, C.4    Jun-Shik, C.5
  • 14
    • 0029912865 scopus 로고    scopus 로고
    • Solid dispersions of benidipine hydrochloride: I. Preparations using different solvent systems and dissolution properties
    • Suzuki H, Miyamoto N, Masada T, Hayakawa E and Ito K. Solid dispersions of benidipine hydrochloride: I. Preparations using different solvent systems and dissolution properties. Chem. Pharm. Bull. (1996) 44: 364-371
    • (1996) Chem. Pharm. Bull , vol.44 , pp. 364-371
    • Suzuki, H.1    Miyamoto, N.2    Masada, T.3    Hayakawa, E.4    Ito, K.5
  • 16
    • 85124431900 scopus 로고    scopus 로고
    • Lowes MMJ, Caira MR, Lo 'Tter AP and Vander Watt JGJ. Physicochemical properties and X-ray structural studies of the trigonal polymorph of carbamazepine. J. Pharm. Sci. (1987) 76: 744-752
    • Lowes MMJ, Caira MR, Lo 'Tter AP and Vander Watt JGJ. Physicochemical properties and X-ray structural studies of the trigonal polymorph of carbamazepine. J. Pharm. Sci. (1987) 76: 744-752
  • 19
    • 33845960792 scopus 로고    scopus 로고
    • Kinetic analysis of chlorpropamide dissolution from solid dispersions
    • Barzegar-Jalali M and Dastmalchi S. Kinetic analysis of chlorpropamide dissolution from solid dispersions. Drug. Dev. Ind. Pharm. (2007) 33: 63-70
    • (2007) Drug. Dev. Ind. Pharm , vol.33 , pp. 63-70
    • Barzegar-Jalali, M.1    Dastmalchi, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.