Freeze-Drying Process Optimisation for a Small Molecule - Pharmaceutical Technology

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PharmTech Europe

Freeze-Drying Process Optimisation for a Small Molecule


Pharmaceutical Technology Europe
Volume 24, Issue 6

Compared with biopharmaceuticals, most freeze-dried small-molecule drugs are relatively inexpensive. To make their manufacture profitable, a high throughput without compromising the final quality is indispensable. The best approach to an optimised freeze-drying cycle is the reduction of primary drying time because this phase is commonly the most time-consuming part (1, 2). To follow this approach, an accurate and representative measurement of the critical formulation temperature (CFT) is required, which poses the upper boundary for the product temperature at the sublimation interface (Tp) during primary drying (2,3). With regard to process time and product-quality attributes, such as elegantcake appearance, low residual moisture, quick and complete reconstitution and drug activity, the product temperature over time profile during primary drying should be close to but below the CFT (2–4). In some cases, however, drying in the microcollapse regime is possible without severe structural loss, as reported for protein formulations, and could also be a promising approach to further process optimisation for small molecule drugs (5–7). In this study, the thermal properties of gentamicin sulphate as a small-molecule model substance were characterised by means of freeze-dry microscopy (FDM) and differential scanning calorimetry (DSC) to determine the CFT at different concentrations and to investigate the potential for further freeze-drying cycle optimisation.

Materials and methods

The pure gentamicin sulphate drug substance used for the thermal characterisation was provided by Merck KGaA. Gentamicin sulphate solutions of 2, 5, 10, 20 and 30% (w/v) were prepared with deionised water.

DSC. The glass-transition temperature of the maximally freezeconcentrated solute (Tg') for the 5% (w/v) gentamicin sulphate solution was determined using a differential scanning calorimeter (DSC822e, Mettler Toledo). Data analysis was conducted with software (STARe Software V 9.01, Mettler Toledo) and values were provided as "onset" and "midpoint" (i.e., half height) of the transition. 30 L of sample solution were hermetically sealed in a 40-L aluminum pan, cooled down to -80 C at a cooling rate of 5 C/min, equilibrated for 10 min and reheated at 10, 3, and 1 C/min. For one sample measured with a heating rate of 3 C/min, an annealing step was implemented for 90 min at -20C. Nitrogen was used to purge the measuring cell throughout the experiment.

FDM. Collapse temperatures (Tc) for the 2, 5, 10, 20 and 30% (w/v) sample solutions were investigated directly after preparation and after one week of storage at room temperature. Validation of the temperature sensor and classification of collapse behaviour were conducted according to the literature and results are reported as an average of four measurements (8). The FDM equipment consisted of a microscope (Zeiss Imager.A1 microscope, Zeiss) with a polariser, a lambda disk and a freeze-drying stage (FDCS 196, Linkam Scientific Instruments). For each measurement, a sample volume of 2 L was pipetted onto a cover glass lying on the silver block oven of the stage. A smaller cover glass was placed on top of this drop. Constant layer thickness was assured by using custom-made metal pieces (i.e., 25 m) as spacers. To improve thermal contact between the bottom cover glass and the oven, a droplet of silicon oil was added. The sample droplet was frozen at a rate of 1.0 C/min and equilibrated at -45C for 10–13 min depending on the velocity of the sublimation interface. After 8 min of equilibration, the vacuum pump was switched on and sublimation could subsequently be observed. The sample was heated at a rate of 1.0 C/min following the equilibration step. The magnification used during the experiments was 200-fold. Pictures were captured by the software in 1-second intervals using a digital camera (Pixelink, 1.3 MP) and analysed with the LinkSys 32 software (Linkam Scientific Instruments). The stage was purged with dry nitrogen during freezing and heating. Pressure was measured using a calibrated Pirani gauge (Linkam Scientific Instruments) The maximum achievable vacuum (< 0.03 mbar) was kept constant throughout the measurement.


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