Solid-state characterization of a novel chemotherapeutic drug

被引:4
|
作者
Marini, A
Berbenni, V
Bruni, G
Maggioni, A
Cofrancesco, P
Sinistri, C
Orlandi, A
Villa, M
机构
[1] Univ Pavia, CSGI, Dipartimento Chim Fis, I-27100 Pavia, Italy
[2] Novuspharma SpA, I-20091 Bresso, MI, Italy
[3] Univ Bergamo, Dipartimento Ingn, Bergamo, Italy
[4] INFM, Unita Pavia, Pavia, Italy
关键词
solid state; polymorphism; dehydration; chemotherapeutic drug;
D O I
10.1002/jps.10315
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We present the results of a thermal, spectroscopic, diffractometric, and microscopic study of a novel DNA intercalator synthesized by Novuspharma S.p.A. (code name BRR 2778, purity by high-performance liquid chromatography: 99.4%). We found that the form that is stable at room temperature contains 1.5 water molecules per unit of formula (or about 4.7% in mass): this water is reversibly lost in two stages below 80degrees and 90degreesC in dry and wet nitrogen atmosphere, respectively. The hydrated compound is a pseudo-polymorph and dehydration is accompanied by a structural change that modifies the diffraction pattern without changing the shape of the microcrystals. Annealing above 150degreesC causes decomposition of the anhydrous form and (above 190degreesC) amorphization of the solid residue occurs. (C) 2003 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 92:577-584, 2003.
引用
收藏
页码:577 / 584
页数:8
相关论文
共 50 条
  • [1] Solid-state characterization of AG337 (Thymitaq), a novel antitumor drug
    Dash, AK
    Tyle, P
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (10) : 1123 - 1127
  • [2] SOLID-STATE STUDIES ON STIRIPENTOL - A NOVEL ANTICONVULSANT DRUG
    CEOLIN, R
    DUGUE, J
    ROULAND, JC
    RALAMBOSOA, C
    LEPAGE, F
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 74 (01) : 77 - 82
  • [3] Solid-state characterization and solubility enhancement of apremilast drug-drug cocrystals
    Wang, Feng-Yuan
    Zhang, Qi
    Zhang, Zaiyong
    Gong, Xiaoyi
    Wang, Jian-Rong
    Mei, Xuefeng
    CRYSTENGCOMM, 2018, 20 (39): : 5945 - 5948
  • [4] SOLID-STATE CHARACTERIZATION OF ZANOTERONE
    ROCCO, WL
    MORPHET, C
    LAUGHLIN, SM
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 122 (1-2) : 17 - 25
  • [5] SOLID-STATE CHARACTERIZATION OF DEHYDROEPIANDROSTERONE
    CHANG, LC
    CAIRA, MR
    GUILLORY, JK
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (10) : 1169 - 1179
  • [6] SOLID-STATE CHARACTERIZATION OF STANOZOLOL
    ROCCO, WL
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (11) : 1831 - 1849
  • [7] Solid-state characterization of fluconazole
    Alkhamis, KA
    Obaidat, AA
    Nuseirat, AF
    PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2002, 7 (04) : 491 - 503
  • [8] Solid-state characterization of paclitaxel
    Liggins, RT
    Hunter, WL
    Burt, HM
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (12) : 1458 - 1463
  • [9] Solid-State Characterization of Nevirapine
    Sarkar, Mahua
    Perumal, O. P.
    Panchagnula, R.
    INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 70 (05) : 619 - 630
  • [10] Preparation and Solid-State Characterization of Dapsone Drug-Drug Co-Crystals
    Jiang, Linglei
    Huang, Ying
    Zhang, Qi
    He, Hongyan
    Xu, Yun
    Mei, Xuefeng
    CRYSTAL GROWTH & DESIGN, 2014, 14 (09) : 4562 - 4573