Comparison of Amorphous Solid Dispersions of Spironolactone Prepared by Spray Drying and Electrospinning: The Influence of the Preparation Method on the Dissolution Properties

被引:17
|
作者
Szabo, Edina [1 ]
Zahonyi, Petra [1 ]
Brecska, Daniel [1 ]
Galata, Dorian L. [1 ]
Meszaros, Lilla A. [1 ]
Madarasz, Lajos [1 ]
Csorba, Kristof [2 ]
Vass, Panna [1 ]
Hirsch, Edit [1 ]
Szafraniec-Szczesny, Joanna [3 ]
Csontos, Istvan [1 ]
Farkas, Attila [1 ]
Van denMooter, Guy [4 ]
Nagy, Zsombor K. [1 ]
Marosi, Gyorgy [1 ]
机构
[1] Budapest Univ Technol & Econ BME, Dept Organ Chem & Technol, H-1111 Budapest, Hungary
[2] Budapest Univ Technol & Econ BME, Dept Automat & Appl Informat, H-1111 Budapest, Hungary
[3] Jagellonian Univ, Fac Pharm, Dept Pharmaceut Technol & Biopharmaceut, Med Coll, PL-30688 Krakow, Poland
[4] Katholieke Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Drug Delivery & Disposit, B-3000 Leuven, Belgium
关键词
amorphous solid dispersion; spray drying; electrospinning; scale-up; dissolution; WATER-SOLUBLE DRUGS; FORMULATION; DELIVERY; STATE; BIOAVAILABILITY; SOLUBILITY; ITRACONAZOLE; TECHNOLOGY; NANOFIBERS; RELEASE;
D O I
10.1021/acs.molpharmaceut.0c00965
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This research aimed to compare two solvent-based methods for the preparation of amorphous solid dispersions (ASDs) made up of poorly soluble spironolactone and poly(vinylpyrrolidone-co-vinyl acetate). The same apparatus was used to produce, in continuous mode, drug-loaded electrospun (ES) and spray-dried (SD) materials from dichloromethane and ethanol-containing solutions. The main differences between the two preparation methods were the concentration of the solution and application of high voltage. During electrospinning, a solution with a higher concentration and high voltage was used to form a fibrous product. In contrast, a dilute solution and no electrostatic force were applied during spray drying. Both ASD products showed an amorphous structure according to differential scanning calorimetry and X-ray powder diffraction results. However, the dissolution of the SD sample was not complete, while the ES sample exhibited close to 100% dissolution. The polarized microscopy images and Raman microscopy mapping of the samples highlighted that the SD particles contained crystalline traces, which can initiate precipitation during dissolution. Investigation of the dissolution media with a borescope made the precipitated particles visible while Raman spectroscopy measurements confirmed the appearance of the crystalline active pharmaceutical ingredient. To explain the micro-morphological differences, the shape and size of the prepared samples, the evaporation rate of residual solvents, and the influence of the electrostatic field during the preparation of ASDs had to be considered. This study demonstrated that the investigated factors have a great influence on the dissolution of the ASDs. Consequently, it is worth focusing on the selection of the appropriate ASD preparation method to avoid the deterioration of dissolution properties due to the presence of crystalline traces.
引用
收藏
页码:317 / 327
页数:11
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