Inhibition of recrystallization of the drug substance in kinetically stabilized amorphous solid dispersions (ASDs) within and beyond shelf life is still a matter of debate. Generally, these ASD systems are considered to be prone to recrystallization, but examples of their long-term stability are emerging in the literature. Since, in some cases, the formation of crystals may impact bioavailability, recrystallization may present a relevant risk for patients as it potentially lowers the effective dose of the formulation. This study shows that such metastable formulations may indeed remain amorphous even after 15 years of storage under ambient conditions. A formulation of fenofibrate stored for 15 years was compared to a freshly prepared batch....
We seek to further addresss the questions posed by Moseson et al. regarding whether any residual cry...
The formation and physical stability of amorphous sulfathiazole obtained from polymorphic forms I an...
Poorly water-soluble drugs pose a significant challenge in developability due to poor oral absorptio...
Amorphous solid dispersions (ASDs) of a poorly water-soluble active pharmaceutical ingredient (API) ...
In formulation development, amorphous solid dispersions (ASD) are considered to improve the bioavail...
We seek to further addresss the questions posed by Moseson et al. regarding whether any residual cry...
The preparation of amorphous solid dispersions (ASDs) has enabled the development of oral dosage for...
The preparation of an amorphous solid dispersion (ASD) by dissolving a poorly water-soluble active p...
Combinatorial chemistry and high-throughput screening approaches utilized during drug discovery have...
Combinatorial chemistry and high-throughput screening approaches utilized during drug discovery have...
Amorphous materials play an important role in pharmaceutical formulations due to their ability to ge...
The formulation of amorphous solids dispersion (ASDs) is a vanguard strategy used for the improvemen...
One way to increase the slow dissolution rate and the associated low bioavailability of newly develo...
Formulation of new drug candidates is becoming increasingly difficult due to the low solubility asso...
The long term stability of amorphous solids formulated as dosage forms is a significant concern due ...
We seek to further addresss the questions posed by Moseson et al. regarding whether any residual cry...
The formation and physical stability of amorphous sulfathiazole obtained from polymorphic forms I an...
Poorly water-soluble drugs pose a significant challenge in developability due to poor oral absorptio...
Amorphous solid dispersions (ASDs) of a poorly water-soluble active pharmaceutical ingredient (API) ...
In formulation development, amorphous solid dispersions (ASD) are considered to improve the bioavail...
We seek to further addresss the questions posed by Moseson et al. regarding whether any residual cry...
The preparation of amorphous solid dispersions (ASDs) has enabled the development of oral dosage for...
The preparation of an amorphous solid dispersion (ASD) by dissolving a poorly water-soluble active p...
Combinatorial chemistry and high-throughput screening approaches utilized during drug discovery have...
Combinatorial chemistry and high-throughput screening approaches utilized during drug discovery have...
Amorphous materials play an important role in pharmaceutical formulations due to their ability to ge...
The formulation of amorphous solids dispersion (ASDs) is a vanguard strategy used for the improvemen...
One way to increase the slow dissolution rate and the associated low bioavailability of newly develo...
Formulation of new drug candidates is becoming increasingly difficult due to the low solubility asso...
The long term stability of amorphous solids formulated as dosage forms is a significant concern due ...
We seek to further addresss the questions posed by Moseson et al. regarding whether any residual cry...
The formation and physical stability of amorphous sulfathiazole obtained from polymorphic forms I an...
Poorly water-soluble drugs pose a significant challenge in developability due to poor oral absorptio...