The effects of polymer carrier, hot melt extrusion process and downstream processing parameters on the moisture sorption properties of amorphous solid dispersions

被引:37
|
作者
Feng, Xin [1 ]
Vo, Anh [1 ]
Patil, Hemlata [1 ]
Tiwari, Roshan V. [1 ]
Alshetaili, Abdullah S. [1 ]
Pimparade, Manjeet B. [1 ]
Repka, Michael A. [1 ,2 ]
机构
[1] Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
[2] Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USA
关键词
amorphous; hot melt extrusion; moisture; polymer carrier; solid dispersion; PHARMACEUTICAL APPLICATIONS; STATE CHARACTERIZATION; POLY(ETHYLENE OXIDE); SORBED WATER; DISSOLUTION; FELODIPINE; STABILITY; DRUGS; FILMS; SYSTEMS;
D O I
10.1111/jphp.12488
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective The aim of this study was to evaluate the effect of polymer carrier, hot melt extrusion and downstream processing parameters on the water uptake properties of amorphous solid dispersions. Methods Three polymers and a model drug were used to prepare amorphous solid dispersions utilizing the hot melt extrusion technology. The sorption-desorption isotherms of solid dispersions and their physical mixtures were measured by the dynamic vapour sorption system, and the effects of polymer hydrophobicity, hygroscopicity, molecular weight and the hot melt extrusion process were investigated. Fourier transform infrared (FTIR) imaging was performed to understand the phase separation driven by the moisture. Key findings Solid dispersions with polymeric carriers with lower hydrophilicity, hygroscopicity and higher molecular weight could sorb less moisture under the high relative humidity (RH) conditions. The water uptake ability of polymer-drug solid dispersion systems were decreased compared with the physical mixture after hot melt extrusion, which might be due to the decreased surface area and porosity. The FTIR imaging indicated that the homogeneity of the drug molecularly dispersed within the polymer matrix was changed after exposure to high RH. Conclusion Understanding the effect of formulation and processing on the moisture sorption properties of solid dispersions is essential for the development of drug products with desired physical and chemical stability.
引用
收藏
页码:692 / 704
页数:13
相关论文
共 50 条
  • [21] Stability and recrystallization of amorphous solid dispersions prepared by hot-melt extrusion and spray drying
    Martynek, Dominik
    Ridvan, Ludek
    Siven, Mia
    Soos, Miroslav
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2025, 672
  • [22] Stable amorphous solid dispersions of fenofibrate using hot melt extrusion technology: Effect of formulation and process parameters for a low glass transition temperature drug
    Kallakunta, Venkata Raman
    Sarabu, Sandeep
    Bandari, Suresh
    Batra, Amol
    Bi, Vivian
    Durig, Thomas
    Repka, Michael A.
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2020, 58
  • [23] Molecularly designed lipid microdomains for solid dispersions using a polymer/inorganic carrier matrix produced by hot-melt extrusion
    Adler, Camille
    Schoenenberger, Monica
    Teleki, Alexandra
    Kuentz, Martin
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2016, 499 (1-2) : 90 - 100
  • [24] Hypromellose acetate succinate based amorphous solid dispersions via hot melt extrusion: Effect of drug physicochemical properties
    Sarabu, Sandeep
    Kallakunta, Venkata Raman
    Bandari, Suresh
    Batra, Amol
    Bi, Vivian
    Durig, Thomas
    Zhang, Feng
    Repka, Michael A.
    CARBOHYDRATE POLYMERS, 2020, 233
  • [25] A comparative study of the effect of spray drying and hot-melt extrusion on the properties of amorphous solid dispersions containing felodipine
    Mahmah, Osama
    Tabbakh, Rami
    Kelly, Adrian
    Paradkar, Anant
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2014, 66 (02) : 275 - 284
  • [26] The application of temperature-composition phase diagrams for hot melt extrusion processing of amorphous solid dispersions to prevent residual crystallinity
    Moseson, Dana E.
    Taylor, Lynne S.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 553 (1-2) : 454 - 466
  • [27] Downstream processing of polymer-based amorphous solid dispersions to generate tablet formulations
    Demuth, B.
    Nagy, Z. K.
    Balogh, A.
    Vigh, T.
    Marosi, G.
    Verreck, G.
    Van Assche, I.
    Brewster, M. E.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 486 (1-2) : 268 - 286
  • [28] Downstream processing of a ternary amorphous solid dispersion: The impacts of spray drying and hot melt extrusion on powder flow, compression and dissolution
    Davis, Mark T.
    Potter, Catherine B.
    Walker, Gavin M.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 544 (01) : 242 - 253
  • [29] An innovative carrier for the formulation of amorphous solid dispersion by hot-melt extrusion with no further downstream processes: a case study with indomethacin.
    Lacerda, S. P.
    Del Confetto, S.
    Haurie, L.
    Bernard, M.
    Faget, S.
    Re, M., I
    PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2024, 29 (02) : 131 - 142
  • [30] Effects of the Preparation Process on the Properties of Amorphous Solid Dispersions
    Siyuan Huang
    Robert O. Williams
    AAPS PharmSciTech, 2018, 19 : 1971 - 1984