Insight into the solubility and dissolution behavior of piroxicam anhydrate and monohydrate forms

被引:35
|
作者
Paaver, Urve [1 ]
Lust, Andres [1 ]
Mirza, Sabiruddin [2 ]
Rantanen, Jukka [3 ]
Veski, Peep [1 ]
Heinamaki, Jyrki [1 ]
Kogermann, Karin [1 ]
机构
[1] Univ Tartu, Dept Pharm, Fac Med, EE-50411 Tartu, Estonia
[2] Univ Helsinki, Div Pharmaceut Technol, FIN-00014 Helsinki, Finland
[3] Univ Copenhagen, Dept Pharm, Fac Hlth & Med Sci, DK-2100 Copenhagen, Denmark
关键词
Piroxicam; Dissolution; Hydrate formation; Solubility; Supersaturation; Nucleation; SODIUM LAURYL SULFATE; SOLID-STATE FORMS; PHASE-TRANSFORMATIONS; SPECTROSCOPIC METHODS; HYDRATE FORMATION; CRYSTAL-GROWTH; CARBAMAZEPINE; SURFACTANTS; KINETICS; CLASSIFICATION;
D O I
10.1016/j.ijpharm.2012.04.042
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the present study was two-fold: (1) to investigate the effect of pH and presence of surfactant sodium lauryl sulphate (SLS) on the solubility and dissolution rate of two solid-state forms of piroxicam (PRX), anhydrate (PRXAH) and monohydrate (PRXMH), and (2) to quantitatively assess the solid-phase transformation of PRXAH to PRXMH in slurry with a special interest to the impact on the solubility and dissolution behavior of the drug. X-ray powder diffractometry (XRPD), Raman spectroscopy and scanning electron microscopy (SEM) were used for characterization of the solid-state forms. Phase transformation was monitored in slurry by means of in-line Raman spectroscopy, and the partial least squares (PLS) regression model was used for predicting the amount of PRXMH. The results showed that the solubility and dissolution rate of PRXAH were higher compared to PRXMH at different pHs. The pH and presence of SLS together affected the solubility and dissolution rate of different PRX forms. The lowest solubility values and dissolution rates for PRX forms were observed in distilled water (pH 5.6) at 37 degrees C. The changes in the dissolution rate could be explained by the hydrate formation during solubility testing. The rate of hydrate formation was also dependent on the pH of the dissolution medium. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:111 / 119
页数:9
相关论文
共 50 条
  • [1] PHYSICOCHEMICAL PROPERTIES OF NITROFURANTOIN ANHYDRATE AND MONOHYDRATE AND THEIR DISSOLUTION
    OTSUKA, M
    TERAOKA, R
    MATSUDA, Y
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1991, 39 (10) : 2667 - 2670
  • [2] Mechanistic Insight of Polymer Effects on the Kinetic of Solution-Mediated Phase Transformation of Nitrofurantoin Anhydrate to Monohydrate
    Wang, Xiyan
    Ji, Xiaohong
    Cai, Ting
    Guo, Minshan
    PHARMACEUTICAL RESEARCH, 2023, 40 (06) : 1587 - 1598
  • [3] Lyophilization monophase solution technique for improvement of the solubility and dissolution of piroxicam
    Dixit, M.
    Kulkarni, P. K.
    RESEARCH IN PHARMACEUTICAL SCIENCES, 2012, 7 (01) : 13 - 21
  • [4] ROTATING-DISK DISSOLUTION KINETICS OF NITROFURANTOIN ANHYDRATE AND MONOHYDRATE AT VARIOUS TEMPERATURES
    OTSUKA, M
    TERAOKA, R
    MATSUDA, Y
    PHARMACEUTICAL RESEARCH, 1992, 9 (03) : 307 - 311
  • [5] Enhancement of solubility, dissolution release profile and reduction in ulcerogenicity of piroxicam by inclusion complex with skimmed milk
    Sanka, Krishna
    Munjulury, Venkata Saidheeraj
    Mohd, Abdul Bari
    Diwan, Prakash V.
    DRUG DELIVERY, 2014, 21 (07) : 560 - 570
  • [6] Structure, Solubility and Stability of Orbifloxacin Crystal Forms: Hemihydrate versus Anhydrate
    Martins Santos, Olimpia Maria
    Jacon Freitas, Jennifer Tavares
    Laignier Cazedey, Edith Cristina
    de Araujo, Magali Benjamim
    Doriguetto, Antonio Carlos
    MOLECULES, 2016, 21 (03)
  • [7] Studies on the Crystal Forms of Istradefylline: Structure, Solubility, and Dissolution Profile
    Wang, Yiyun
    Xu, Youwei
    Zheng, Zhonghui
    Xue, Min
    Meng, Zihui
    Xu, Zhibin
    Li, Jiarong
    Lin, Qing
    CRYSTALS, 2022, 12 (07)
  • [8] Solid-State Carbon NMR Characterization and Investigation of Intrinsic Dissolution Behavior of Fluconazole Polymorphs, Anhydrate Forms I and II
    Park, Hee Jun
    Kim, Min-Soo
    Kim, Jeong-Soo
    Cho, Wonkyung
    Park, Junsung
    Cha, Kwang-Ho
    Kang, Young-Shin
    Hwang, Sung-Joo
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2010, 58 (09) : 1243 - 1247
  • [9] Non-Sink Dissolution Behavior and Solubility Limit of Commercial Tacrolimus Amorphous Formulations
    Trasi, Niraj S.
    Purohit, Hitesh S.
    Wen, Hong
    Sun, Dajun D.
    Taylor, Lynne S.
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 106 (01) : 264 - 272
  • [10] Insight into the dissolution behavior of valsartan (form E) in twelve pure solvents: Solubility, modelling and molecular simulation
    Zhang, Huixiang
    Zhang, Yang
    Chen, Hui
    Gao, Zhenguo
    Du, Shichao
    Wang, Yan
    JOURNAL OF MOLECULAR LIQUIDS, 2024, 402