International audienceDeveloping amorphous pharmaceuticals can be desirable due to advantageous biopharmaceutical properties. Low glass transition temperature (Tg) amorphous drugs can be protected from crystallisation by mixing with high Tg excipients, such as polymers, or with salt forms. However, both polymers and salts can enhance the water uptake. The aim of this study was to formulate physico-chemically stable amorphous materials, by co-processing different proportions of sulfathiazole and its sodium salt to produce an optimum ratio, characterised by the best physical stability and lowest hygroscopicity. Both sulfathiazole and salt amorphised upon spray drying. At room temperature, sulfathiazole crystallised within 1 h at <5% relative ...
Spray drying is widely used in enhancing the aqueous solubility of poorly soluble compounds. In this...
Amorphous formulations provide a general approach to improving the solubility and bioavailability of...
Poorly water-soluble drugs pose a significant challenge to developability due to poor oral absorptio...
International audienceDeveloping amorphous pharmaceuticals can be desirable due to advantageous biop...
The coprocessing of active pharmaceutical ingredient (API) with an excipient which has a high glass ...
The coprocessing of active pharmaceutical ingredient (API) with an excipient which has a high glass ...
An attractive, yet challenging approach to overcome poor water solubility is to convert a crystallin...
In recent years among various formulation strategies, amorphous solid dispersions (ASDs) has gained ...
The coprocessing of active pharmaceutical ingredient (API) with an excipient which has a high glass ...
Interest in amorphous pharmaceutical systems is steadily growing over the last 10 years. The amorph...
Amorphous solid dispersions are known to improve the oral bioavailability of poorly water-soluble dr...
The aim of this thesis was to increase our knowledge of the glassy state and the glass transition ph...
Delivery of drugs with low aqueous solubility in the amorphous form can be exploited as a strategy t...
Solid-state characterisation of a drug following pharmaceutical processing and upon storage is funda...
Amorphous materials play an important role in pharmaceutical formulations due to their ability to ge...
Spray drying is widely used in enhancing the aqueous solubility of poorly soluble compounds. In this...
Amorphous formulations provide a general approach to improving the solubility and bioavailability of...
Poorly water-soluble drugs pose a significant challenge to developability due to poor oral absorptio...
International audienceDeveloping amorphous pharmaceuticals can be desirable due to advantageous biop...
The coprocessing of active pharmaceutical ingredient (API) with an excipient which has a high glass ...
The coprocessing of active pharmaceutical ingredient (API) with an excipient which has a high glass ...
An attractive, yet challenging approach to overcome poor water solubility is to convert a crystallin...
In recent years among various formulation strategies, amorphous solid dispersions (ASDs) has gained ...
The coprocessing of active pharmaceutical ingredient (API) with an excipient which has a high glass ...
Interest in amorphous pharmaceutical systems is steadily growing over the last 10 years. The amorph...
Amorphous solid dispersions are known to improve the oral bioavailability of poorly water-soluble dr...
The aim of this thesis was to increase our knowledge of the glassy state and the glass transition ph...
Delivery of drugs with low aqueous solubility in the amorphous form can be exploited as a strategy t...
Solid-state characterisation of a drug following pharmaceutical processing and upon storage is funda...
Amorphous materials play an important role in pharmaceutical formulations due to their ability to ge...
Spray drying is widely used in enhancing the aqueous solubility of poorly soluble compounds. In this...
Amorphous formulations provide a general approach to improving the solubility and bioavailability of...
Poorly water-soluble drugs pose a significant challenge to developability due to poor oral absorptio...