Recently, electrospinning (ES) of fibers has been shown to be an attractive strategy for drug delivery. One of the main features of ES is that a wide variety of drugs can be loaded into the fibers to improve their bioavailability, to enhance dissolution, or to achieve controlled release. Besides, ES is a continuous technology with low energy consumption, which can make it a very economic production alternative to the widely used freeze drying and spray drying. However, the low production rate of laboratory‐scaled ES has limited the industrial application of the technology so far. This article covers the various ES technologies developed for scaled‐up fiber production with an emphasis on pharmaceutically relevant examples. The methods used for increasing the productivity are complied, which is followed by a review of specific examples from literature where these technologies are utilized to produce oral drug delivery systems. The different technologies are compared in terms of their basic principles, advantages, and limitations. Finally, the different downstream processing options to prepare tablets or capsules containing the electrospun drug are covered as well.
This article is categorized under:
Therapeutic Approaches and Drug Discovery > Emerging Technologies
Preparation and formulation of amorphous solid dispersions (ASDs) are becoming more and more popular in the pharmaceutical field because the dissolution of poorly water-soluble drugs can be effectively improved this way, which can lead to increased bioavailability in many cases. During downstream processing of ASDs, technologists need to keep in mind both traditional challenges and the newest trends. In the last decade, the pharmaceutical industry began to display considerable interest in continuous processing, which can be explained with their potential advantages such as smaller footprint, easier scale-up, and more consistent product, better quality and quality assurance. Continuous downstream processing of drug-loaded ASDs opens new ways for automatic operation. Therefore, the formulation of poorly water-soluble drugs may be more effective and safe. However, developments can be challenging due to the poor flowability and feeding properties of ASDs. Consequently, this review pays special attention to these characteristics since the feeding of the components greatly influences the content uniformity in the final dosage form. The main purpose of this paper is to summarize the most important steps of the possible ASD-based continuous downstream processes in order to give a clear overview of current course lines and future perspectives.
The pharmaceutical industry has never seen such a vast development in process analytical methods as in the last decade. The application of near-infrared (NIR) and Raman spectroscopy in monitoring production lines has also become widespread. This work aims to utilize the large amount of information collected by these methods by building an artificial neural network (ANN) model that can predict the dissolution profile of the scanned tablets. An extended release formulation containing drotaverine (DR) as a model drug was developed and tablets were produced with 37 different settings, with the variables being the DR content, the hydroxypropyl methylcellulose (HPMC) content and compression force. NIR and Raman spectra of the tablets were recorded in both the transmission and reflection method. The spectra were used to build a partial least squares prediction model for the DR and HPMC content. The ANN model used these predicted values, along with the measured compression force, as input data. It was found that models based on both NIR and Raman spectra were capable of predicting the dissolution profile of the test tablets within the acceptance limit of the f2 difference factor. The performance of these ANN models was compared to PLS models using the same data as input, and the prediction of the ANN models was found to be more accurate. The proposed method accomplishes the prediction of the dissolution profile of extended release tablets using either NIR or Raman spectra.
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.
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