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Volumn 39, Issue 4, 2010, Pages 248-255

Crystallization and polymorphic transitions of chlorpropamide in aqueous 2-hydroxybutyl-β-cyclodextrin solution

Author keywords

2 Hydroxybutyl cyclodextrin; Chlorpropamide; Crystallization; Polymorph; Solution mediated polymorphic transition

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; CHLORPROPAMIDE;

EID: 75149115652     PISSN: 09280987     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejps.2009.12.008     Document Type: Article
Times cited : (26)

References (24)
  • 1
    • 0006034482 scopus 로고
    • Polymorphism in sulphonylurea hypoglycaemic agents. II. Chlorpropamide
    • Al-Saieq S.S., and Riley G.S. Polymorphism in sulphonylurea hypoglycaemic agents. II. Chlorpropamide. Pharm. Acta Helv. 57 (1982) 8-11
    • (1982) Pharm. Acta Helv. , vol.57 , pp. 8-11
    • Al-Saieq, S.S.1    Riley, G.S.2
  • 4
    • 0004284003 scopus 로고    scopus 로고
    • Brittain H.G. (Ed), Marcel Dekker, New York
    • In: Brittain H.G. (Ed). Polymorphism of Pharmaceutical Solids (2009), Marcel Dekker, New York
    • (2009) Polymorphism of Pharmaceutical Solids
  • 5
    • 0016716639 scopus 로고
    • Zur polymorphie oraler antidiabetika, 1: chlorpropamid
    • Burger A. Zur polymorphie oraler antidiabetika, 1: chlorpropamid. Sci. Pharm. 43 (1975) 152-161
    • (1975) Sci. Pharm. , vol.43 , pp. 152-161
    • Burger, A.1
  • 7
    • 0033025528 scopus 로고    scopus 로고
    • Isothermal interconversion of chlorpropamide polymorphs kinetically quantified by X-ray powder diffractometry, diffuse reflectance Fourier transform infrared spectroscopy and isoperibol solution calorimetry
    • De Villiers M.M., and Wurster D.E. Isothermal interconversion of chlorpropamide polymorphs kinetically quantified by X-ray powder diffractometry, diffuse reflectance Fourier transform infrared spectroscopy and isoperibol solution calorimetry. Acta Pharm. 49 (1999) 79-88
    • (1999) Acta Pharm. , vol.49 , pp. 79-88
    • De Villiers, M.M.1    Wurster, D.E.2
  • 10
    • 40849085495 scopus 로고    scopus 로고
    • Preparation of amorphous indomethacin from aqueous 2,6-di-O-methyl-β-cyclodextrin solution
    • Iohara D., Hirayama F., Ishiguro T., Arima H., and Uekama K. Preparation of amorphous indomethacin from aqueous 2,6-di-O-methyl-β-cyclodextrin solution. Int. J. Pharm. 354 (2008) 70-76
    • (2008) Int. J. Pharm. , vol.354 , pp. 70-76
    • Iohara, D.1    Hirayama, F.2    Ishiguro, T.3    Arima, H.4    Uekama, K.5
  • 11
    • 51149091837 scopus 로고    scopus 로고
    • Prominent inhibitory effect of 2-hydroxybutyl-β-cyclodextrin on solution-mediated polymorphic transition of chlorpropamide
    • Ishiguro T., Hirayama F., Iohara D., and Uekama K. Prominent inhibitory effect of 2-hydroxybutyl-β-cyclodextrin on solution-mediated polymorphic transition of chlorpropamide. Chem. Lett. (2008) 816-817
    • (2008) Chem. Lett. , pp. 816-817
    • Ishiguro, T.1    Hirayama, F.2    Iohara, D.3    Uekama, K.4
  • 12
    • 0001511660 scopus 로고
    • Formation and stability of inorganic complexes in solution
    • Job P. Formation and stability of inorganic complexes in solution. Ann. Chem. 9 (1928) 113-203
    • (1928) Ann. Chem. , vol.9 , pp. 113-203
    • Job, P.1
  • 13
    • 0029819323 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrin. 1. Drug solubilization and stabilization
    • Loftsson T., and Brewster M.E. Pharmaceutical applications of cyclodextrin. 1. Drug solubilization and stabilization. J. Pharm. Sci. 85 (1996) 1017-1025
    • (1996) J. Pharm. Sci. , vol.85 , pp. 1017-1025
    • Loftsson, T.1    Brewster, M.E.2
  • 14
    • 0009354974 scopus 로고
    • Crystal growth in pharmaceutical formulation
    • Macie C.M.G., and Grant D.J.W. Crystal growth in pharmaceutical formulation. Pharm. Int. 7 (1986) 233-237
    • (1986) Pharm. Int. , vol.7 , pp. 233-237
    • Macie, C.M.G.1    Grant, D.J.W.2
  • 15
    • 85007917287 scopus 로고
    • Dissolution phenomena of organic medicinals involving simultaneous phase changes
    • Nogami H., Nagai T., and Yotsuyanagi T. Dissolution phenomena of organic medicinals involving simultaneous phase changes. Chem. Pharm. Bull. 17 (1969) 499-509
    • (1969) Chem. Pharm. Bull. , vol.17 , pp. 499-509
    • Nogami, H.1    Nagai, T.2    Yotsuyanagi, T.3
  • 16
    • 0001732841 scopus 로고
    • Studien uber die Bildung und Umwandlung Fester Korper
    • Ostwald W. Studien uber die Bildung und Umwandlung Fester Korper. Z. Physik. Chem. 22 (1897) 289-302
    • (1897) Z. Physik. Chem. , vol.22 , pp. 289-302
    • Ostwald, W.1
  • 17
    • 0029852699 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrin. 2. In vivo drug delivery
    • Rajewski R.A., and Stella V.J. Pharmaceutical applications of cyclodextrin. 2. In vivo drug delivery. J. Pharm. Sci. 85 (1996) 1042-1069
    • (1996) J. Pharm. Sci. , vol.85 , pp. 1042-1069
    • Rajewski, R.A.1    Stella, V.J.2
  • 18
    • 0344603644 scopus 로고    scopus 로고
    • Significance of controlling crystallization mechanisms and kinetics in pharmaceutical systems
    • Rodriguez-Hornedo N., and Murphy D.J. Significance of controlling crystallization mechanisms and kinetics in pharmaceutical systems. J. Pharm. Sci. 88 (1999) 651-660
    • (1999) J. Pharm. Sci. , vol.88 , pp. 651-660
    • Rodriguez-Hornedo, N.1    Murphy, D.J.2
  • 20
    • 33645453611 scopus 로고    scopus 로고
    • Cyclodextrin-based isolation of Ostwald's metastable polymorphs occurring during crystallization
    • Sonoda Y., Hirayama F., Arima H., Yamaguchi Y., Saenger W., and Uekama K. Cyclodextrin-based isolation of Ostwald's metastable polymorphs occurring during crystallization. Chem. Commun. (2006) 517-519
    • (2006) Chem. Commun. , pp. 517-519
    • Sonoda, Y.1    Hirayama, F.2    Arima, H.3    Yamaguchi, Y.4    Saenger, W.5    Uekama, K.6
  • 21
    • 33744737273 scopus 로고    scopus 로고
    • Selective crystallization of metastable form IV polymorph of tolbutamide in the presence of 2,6-di-O-methyl-β-cyclodextrin in aqueous solution
    • Sonoda Y., Hirayama F., Arima H., Yamaguchi Y., Saenger W., and Uekama K. Selective crystallization of metastable form IV polymorph of tolbutamide in the presence of 2,6-di-O-methyl-β-cyclodextrin in aqueous solution. Cryst. Growth Des. 6 (2006) 1181-1185
    • (2006) Cryst. Growth Des. , vol.6 , pp. 1181-1185
    • Sonoda, Y.1    Hirayama, F.2    Arima, H.3    Yamaguchi, Y.4    Saenger, W.5    Uekama, K.6
  • 22
    • 0021364433 scopus 로고
    • Dissolution behavior of chlorpropamide polymorphs
    • Ueda H., Nambu N., and Nagai T. Dissolution behavior of chlorpropamide polymorphs. Chem. Pharm. Bull. 32 (1984) 244-250
    • (1984) Chem. Pharm. Bull. , vol.32 , pp. 244-250
    • Ueda, H.1    Nambu, N.2    Nagai, T.3
  • 23
    • 16344364096 scopus 로고    scopus 로고
    • Design and evaluation of cyclodextrin-based drug formulation
    • Uekama K. Design and evaluation of cyclodextrin-based drug formulation. Chem. Pharm. Bull. 52 (2004) 900-915
    • (2004) Chem. Pharm. Bull. , vol.52 , pp. 900-915
    • Uekama, K.1
  • 24
    • 23144436640 scopus 로고    scopus 로고
    • Crystal doping aided by rapid expansion of supercritical solutions
    • article, URL
    • Vemavarapu, C., Mollan, M.J., Needham, T.E., 2002. Crystal doping aided by rapid expansion of supercritical solutions. AAPS PharmSciTech, 3 article 29. URL: http://www.aapspharmsci.org.
    • (2002) AAPS PharmSciTech , vol.3 , pp. 29
    • Vemavarapu, C.1    Mollan, M.J.2    Needham, T.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.