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Investigation of Pharmaceutical Stability Using Dynamic Vapor
Sorption Analysis
Robert L. Hassel, Ph.D. and Nathan D. Hesse, Ph.D. TA Instruments, 109 Lukens Drive, New Castle DE 19720, USA

A variety of analytical techniques including differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) are commonly used to screen prospective
pharmaceutical active ingredients, excipients, and drug formulations. Those techniques
provide insights into characteristics such as polymorphism, amorphous / crystalline
content, and thermal stability. However, they do not indicate a material’s response to
changes in relative humidity. Dynamic vapor sorption (DVS) analysis is a technique
specifically designed to provide such information.

In a typical DVS experiment, the relative humidity (%RH) is stepped from a low initial level (either ambient or 0 %RH) to a high level (90-95 %RH), then back down to a
low level, and finally increased again to a higher level. The rate at which the material
equilibrates at each humidity level, as well as the overall shape of the resulting adsorption
/ desorption profile, provides useful information about the material’s structure and long-
term stability.

Figure 1 shows the DVS results for prednisone, which is known to exhibit low moisture absoption (<1 %) over a broad humidity range. In addition, its adsorption / desorption profile is reversible (i.e., the adsorption [increasing %RH] and desorption [decreasing %RH] profiles essentially overlap). This behavior indicates that prednisone is highly crystalline and that the moisture “picked-up” at higher humidities is adsorbed onto the surface of the material and does not affect its internal structure. Hence, prednisone should be a stable active ingredient. Figure 1. Surface Adsorption Data for Prednisone
Conversely, diphenylhydantoin exhibits significant moisture absorption with increasing humidity and also differences (hysteresis) in its adsorption and desorption profiles (Figure 2). The large moisture gain (~28 %) during the sorption profile, and the sharp weight decrease as humidity is later decreased below 30 %RH, suggests formation of a hydrate. At 5 %RH, the residual weight gain agrees well with that expected for the monohydrate form of the material. Since the hydrated form has a more open structure, its sorption profile shows more rapid uptake of moisture than the original sample. Diphenylhydantoin’s DVS behavior does not eliminate it as a potentially useful pharmaceutical, but it indicates that care must be taken during processing and storage. Figure 2. Diphenlhydantoin: Formation of Hydrates
Long-term stability of different formulations of the same active ingredient when exposed to moisture can be assessed by exposing the materials to constant humidity at higher temperature to accelerate the onset of “degradation”. Figure 3 compares the behavior of several different salts of the same base compound initially exposed to 50 %RH at 25 °C and then raised to 80 °C while maintaining 50 %RH. All three salts rapidly pick-up about 2 % moisture at 25 °C and 50 %RH. When the temperature is subsequently raised to 80 °C, the phosphate and mesylate salts retain the adsorbed water and the weight remains constant over the next 24 hours. The acetate salt, on the other hand, rapidly gives-up the water adsorbed at 25 °C when the temperature is raised to 80 °C and continues to lose weight with time, indicating that it is the least stable formulation.

Figure 3. Comparison of Formulations: Stability at 80 °C & 50 %RH
DVS can also be used to evaluate drug stability during processing. In Figure 4, the objective of the experiment is to determine proper drying parameters for a weakly hydrated material. The specific goal is to determine the lowest humidity level, which can be used at a selected drying temperature, without changing the material’s structure by removing any of the waters of hydration. These results were obtained by stepping the relative humidity from a high starting level to a lower level (right to left in the figure). The humidity, where a significant weight change (decrease) occurs, indicates loss of waters of hydration. At a 25 °C drying temperature, humidities as low as 10 %RH can be used. At 40 °C and above, the humidity must be at least 15 % to avoid issues. In this material, the impact of sample form (milled versus unmilled) has little effect on the drying properties. Figure 4. Hydrate Stability on Drying
Temperature and humidity are important factors in the processing and storage of pharmaceuticals. Dynamic Vapor Sorption provides a versatile and sensitive technique
for evaluating the stability of pharmaceutical active ingredients, excipients and
formulations under a variety of temperature / humidity combinations.

Dynamic vapor sorption, DVS, Pharmaceuticals, Temperature, Humidity TA INSTRUMENTS

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Marginal annotations on the classification of plants found in Christoph Jakob Trew’s Plantae selectae (1750-1773) [Norimbergae] [Nuremberg]: s.n., 1750 (-1773). The annotations are found in copy 1 of this work. NB. Plates 101-120 form the Supplementum to Plantae Selectae (1790) Trew’s title Annotations in copy 1 Modern name if different Cedrus foliis rigidis acumina

PATTY GHAZVINI, Pharm.D TALLAHASSEE, FLORIDA 32307 Phone: (850) 599 -3636 Fax: PATTY GHAZVINI, Pharm.D. Education:  PhD , College of Pharmacy and Pharmaceutical Sciences, Florida A and M University,  B.S., Chemistry, Florida State University,1995 Publications: 1. Mahdavian, S., Ghazvini, P., Pagan, L., Singh, A., and Woodard, T. Clinical Management of Atopi

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