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Volumn 45, Issue 6, 2000, Pages 1001-1006

X-ray powder diffraction data for 12 drugs in current use

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; CHLORINE COMPOUNDS; CRYSTAL LATTICES; CRYSTALLINE MATERIALS; MOLECULAR STRUCTURE; RHEOLOGY; SULFUR COMPOUNDS; SUSPENSIONS (FLUIDS); X RAY POWDER DIFFRACTION;

EID: 0034319571     PISSN: 00219568     EISSN: None     Source Type: Journal    
DOI: 10.1021/je0001025     Document Type: Article
Times cited : (6)

References (15)
  • 1
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    • Identification of crystalline materials - Classification and use of x-ray diffraction patterns
    • Hanawalt, J. D.; Rinn, H. W. Identification of Crystalline Materials - Classification and Use of X-ray Diffraction Patterns. Powder Diffr. 1986, 1, 2-6.
    • (1986) Powder Diffr. , vol.1 , pp. 2-6
    • Hanawalt, J.D.1    Rinn, H.W.2
  • 4
    • 0030955457 scopus 로고    scopus 로고
    • Identification of drugs in pharmaceutical dosage forms by x-ray powder defraction
    • Phadnis, N. V.; Caratur, R. K.; Suryanarayanan, R. Identification of drugs in pharmaceutical dosage forms by X-ray powder defraction. J. Pharm. Biomed. Anal. 1997, 15, 929-943.
    • (1997) J. Pharm. Biomed. Anal. , vol.15 , pp. 929-943
    • Phadnis, N.V.1    Caratur, R.K.2    Suryanarayanan, R.3
  • 5
    • 0022628687 scopus 로고
    • Determination of α-impurities in the β-polymorph of inosine using infrared spectroscopy and x-ray powder diffraction
    • Doff, D. H.; Brownen, F. L.; Corrigan, O. I. Determination of α-Impurities in the β-Polymorph of Inosine Using Infrared Spectroscopy and X-ray Powder Diffraction. Analyst 1986, 111, 179-182.
    • (1986) Analyst , vol.111 , pp. 179-182
    • Doff, D.H.1    Brownen, F.L.2    Corrigan, O.I.3
  • 7
    • 0032949724 scopus 로고    scopus 로고
    • Solid-state characterization of candesartan cilexetil (TCV-116): Crystal structure and molecular mobility
    • Matsunage, H.; Eguchi, T.; Nishijima, K.; Enomoto, T.; Sasaoki, K.; Nakamura, N. Solid-state characterization of candesartan cilexetil (TCV-116): Crystal structure and molecular mobility. Chem. Pharm. Bull. 1999, 47 (2), 182-186.
    • (1999) Chem. Pharm. Bull. , vol.47 , Issue.2 , pp. 182-186
    • Matsunage, H.1    Eguchi, T.2    Nishijima, K.3    Enomoto, T.4    Sasaoki, K.5    Nakamura, N.6
  • 8
    • 0343488605 scopus 로고    scopus 로고
    • Preparation and characterization of a new polymorphic form and a solvate of glibenclamide
    • 1007
    • Hassan, M. A.; Sheikh-Salem, M.; Sallam, E.; Al-Hindawi, M. K. Preparation and characterization of a new polymorphic form and a solvate of glibenclamide. Acta Pharm. Hung. 1007, 67, 81-88.
    • Acta Pharm. Hung. , vol.67 , pp. 81-88
    • Hassan, M.A.1    Sheikh-Salem, M.2    Sallam, E.3    Al-Hindawi, M.K.4
  • 9
    • 0031808764 scopus 로고    scopus 로고
    • Physicochemical characterization of the orthorhombic polymorph of paracetamol crystallized from solution
    • Nichols, G.; Frampton, C. S. Physicochemical Characterization of the orthorhombic polymorph of paracetamol crystallized from solution. J. Pharm. Sci. 1998, 87, 684-693.
    • (1998) J. Pharm. Sci. , vol.87 , pp. 684-693
    • Nichols, G.1    Frampton, C.S.2
  • 11
    • 0032834712 scopus 로고    scopus 로고
    • The effect of polymorphism comparison and dissolution properties of chemically equivalent oxytetracycline hydrochloride powders
    • Liebenberg, W.; de Villiers, M. M.; Wurster, D. E.; Swanepoel, E.; Dekker, T. G.; Lotter, A. P. The effect of polymorphism comparison and dissolution properties of chemically equivalent oxytetracycline hydrochloride powders. Drug Dev. Ind. Pharm. 1999, 25 (9), 1027-1033.
    • (1999) Drug Dev. Ind. Pharm. , vol.25 , Issue.9 , pp. 1027-1033
    • Liebenberg, W.1    De Villiers, M.M.2    Wurster, D.E.3    Swanepoel, E.4    Dekker, T.G.5    Lotter, A.P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.