Indexing powder patterns in physical form screening: Instrumentation and data quality

被引:70
作者
Florence, AJ [1 ]
Baumgartner, B
Weston, C
Shankland, N
Kennedy, AR
Shankland, K
David, WIF
机构
[1] Univ Strathclyde, Dept Pharmaceut Sci, Glasgow G4 0NR, Lanark, Scotland
[2] Stoe & Cie GmbH, D-64213 Darmstadt, Germany
[3] Bruker AXS Ltd, Congelton CW12 1DN, Cheshire, England
[4] CrystallografX Ltd, Glasgow G1 3DX, Lanark, Scotland
[5] Univ Strathclyde, Dept Pure & Appl Chem, Glasgow G1 1XL, Lanark, Scotland
[6] Rutherford Appleton Lab, ISIS Facil, Chilton OX11 0QX, Oxon, England
基金
英国工程与自然科学研究理事会;
关键词
high-throughput technologies; physical form screen; physical characterization; crystallography; X-ray powder diffractometry; powder pattern indexing; crystal structure; DICVOL-91; DASH;
D O I
10.1002/jps.10459
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two multisample laboratory powder diffractometers have been evaluated for the purpose of pattern indexing in the context of physical form screening. Both diffractometers utilise foil transmission geometry, primary monochromated radiation, and a position-sensitive detector. Data collected from six compounds (sotalol hydrochloride, hydroflumethiazide, verapamil hydrochloride, captopril, clomipramine hydrochloride, and famotidine) showed good angular resolution (FWHM as small as ca. 0.06degrees) and lattice parameters were easily obtained using the indexing program DICVOL-91. The extent of preferred orientation in each pattern was estimated using the DASH implementation of the March-Dollase function and is most evident with clomipramine hydrochloride and famotidine. Otherwise, the data compare favorably with reference capillary data sets. In conclusion, where there is a requirement to analyze 20-30 samples per day, with an emphasis on obtaining the high-quality data that are important in pattern recognition and imperative in indexing, the combination of foil transmission geometry, primary monochromated radiation, plus a position-sensitive detector is highly effective. The data also afford opportunities for crystal structure determination. (C) 2003 Wiley-Liss, Inc. and the American Pharmacists Association.
引用
收藏
页码:1930 / 1938
页数:9
相关论文
共 10 条
[1]   The Cambridge Structural Database: a quarter of a million crystal structures and rising [J].
Allen, FH .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2002, 58 (3 PART 1) :380-388
[2]   INDEXING OF POWDER DIFFRACTION PATTERNS FOR LOW-SYMMETRY LATTICES BY THE SUCCESSIVE DICHOTOMY METHOD [J].
BOULTIF, A ;
LOUER, D .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1991, 24 (pt 6) :987-993
[3]  
DAVID WIF, 2001, DASH USER MANUAL
[4]   CORRECTION OF INTENSITIES FOR PREFERRED ORIENTATION IN POWDER DIFFRACTOMETRY - APPLICATION OF THE MARCH MODEL [J].
DOLLASE, WA .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1986, 19 (pt 4) :267-272
[5]   The powder diffraction file: present and future [J].
Faber, J ;
Fawcett, T .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2002, 58 (3 PART 1) :325-332
[6]  
Klug H. P., 1974, XRAY DIFFRACTION PRO, P354
[7]  
LOUER D, 2002, IUCR MONOGRAPHS CRYS, V13, P29
[8]   Molecular, crystallographic and algorithmic factors in structure determination from powder diffraction data by simulated annealing [J].
Shankland, K ;
McBride, L ;
David, WIF ;
Shankland, N ;
Steele, G .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2002, 35 :443-454
[9]  
STUDIENGESELLSCHAFT, 2000, Patent No. 29919861