Role of water in the physical stability of solid dosage formulations

被引:85
作者
Airaksinen, S [1 ]
Karjalainen, M
Shevchenko, A
Westermarck, S
Leppänen, E
Rantanen, J
Yliruusi, J
机构
[1] Univ Helsinki, Fac Pharm, Pahrmaceut Technol Div, FIN-00014 Helsinki, Finland
[2] Orion Pharma, Espoo, Finland
[3] Univ Helsinki, Viikki FDrug Discovery Technol Ctr, DDTC, FIN-00014 Helsinki, Finland
关键词
dynamic vapor sorption; excipients; near-infrared (NIR) spectroscopy; phase transition; sorption isotherms; X-ray powder diffraction;
D O I
10.1002/jps.20411
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The interaction of moisture with pharmaceutical solids is highly crucial to an understanding of water-based processes, for example, manufacturing processes or prediction of solid dosage form stability and shelf life. Both the active pharmaceutical ingredient (API) and excipients in the formulation have different moisture sorption properties that can result in unexpected processing-induced phase transitions and they can affect solid-state phase transitions in the final dosage forms. The character of excipient effects on the stability of formulation. Phase transformations in formulations can lead to instability in physicochemical, biopharmaceutical, and processing properties of products. The aim of the present study was to investigate the water sorption properties of different excipients, model the sorption isotherms, examine the phase transitions, and identify differences of excipients in solid dosage form stability using dynamic vapor sorption analysis, near-infrared spectroscopy, and X-ray diffraction methods. The thermal processing was carried out with a variable temperature X-ray powder diffractometer to compare the dehydration behavior of wet excipients and evaluate solid-state properties during heating. These results showed that despite some limitations, moisture sorption isotherms of excipients are useful in predicting solid-state stability, interactions at early stages of formulation development, and effects of moisture on physicochemical properties of the final dosage forms. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:2147 / 2165
页数:19
相关论文
共 47 条
  • [1] THE MOLECULAR-BASIS OF MOISTURE EFFECTS ON THE PHYSICAL AND CHEMICAL-STABILITY OF DRUGS IN THE SOLID-STATE
    AHLNECK, C
    ZOGRAFI, G
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1990, 62 (2-3) : 87 - 95
  • [2] Effects of excipients on hydrate formation in wet masses containing theophylline
    Airaksinen, S
    Luukkonen, P
    Jorgensen, A
    Karjalainen, M
    Rantanen, J
    Yliruusi, J
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (03) : 516 - 528
  • [3] Water sorption isotherms of starch powders - Part 1: mathematical description of experimental data
    Al-Muhtaseb, AH
    McMinn, WAM
    Magee, TRA
    [J]. JOURNAL OF FOOD ENGINEERING, 2004, 61 (03) : 297 - 307
  • [4] MODIFICATIONS OF THE BRUNAUER, EMMETT AND TELLER EQUATION
    ANDERSON, RB
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1946, 68 (04) : 686 - 691
  • [5] BELL LN, 2000, MOISTURE SORPTION PR, P14
  • [6] CRYSTAL STRUCTURES OF ALPHA' AND BETA FORMS OF D-MANNITOL
    BERMAN, HM
    JEFFREY, GA
    ROSENSTEIN, RD
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL CRYSTALLOGRAPHY AND CRYSTAL CHEMISTRY, 1968, B 24 : 442 - +
  • [7] Moisture sorption isotherms for crystalline, amorphous and predominantly crystalline lactose powders
    Bronlund, J
    Paterson, T
    [J]. INTERNATIONAL DAIRY JOURNAL, 2004, 14 (03) : 247 - 254
  • [8] Adsorption of gases in multimolecular layers
    Brunauer, S
    Emmett, PH
    Teller, E
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 : 309 - 319
  • [9] Burger A, 2000, J PHARM SCI-US, V89, P457, DOI 10.1002/(SICI)1520-6017(200004)89:4<457::AID-JPS3>3.0.CO
  • [10] 2-G