Adequatedrug solubility in the gastrointestinal tract is essential for systemic therapyof orally administered medications. To carry out research on the solubility ofpoorly soluble drugs in vitro, simulated intestinal fluid (SIF) is usedin place of human intestinal fluid (HIF). However, typical SIF reflects averagecompositions of HIF rather than the full range of compositions previouslyreported. This study examines a new suite of SIF media (based on variabilityobserved in HIF) to explore the range of solubility of four poorly soluble drugs(Naproxen, Indomethacin, Phenytoin and Tadalafil) in the fasted state
After oral administration, a drug’s solubility in intestinal fluid is an important parameter influen...
The oral administration of solid dosage forms is the commonest method to achieve systemic therapy an...
Accurate in vivo predictions of intestinal absorption of low solubility drugs require knowing their ...
Drug solubility is a key parameter controlling oral absorption, but intestinal solubility is difficu...
Intestinal drug solubility is a key parameter controlling absorption after the administration of a s...
Solubility and dynamic light scattering (DLS) studies of three poorly soluble drugs (naproxen, indom...
Intestinal drug solubility is a key parameter controlling oral absorption but varies both intra and ...
It is widely recognised that drug solubility within the gastrointestinal tract (GIT) differs from va...
Drug solubility in intestinal fluid is a key parameter controlling absorption after the administrati...
The oral route is the preferred option for drug administration but contains the inherent issue of dr...
Upon oral administration the solubility of a drug in intestinal fluid is a key property influencing ...
The purpose of this study was to validate both existing fasted and fed state simulated intestinal fl...
After oral administration, a drug’s solubility in intestinal fluid is an important parameter influen...
The oral administration of solid dosage forms is the commonest method to achieve systemic therapy an...
Accurate in vivo predictions of intestinal absorption of low solubility drugs require knowing their ...
Drug solubility is a key parameter controlling oral absorption, but intestinal solubility is difficu...
Intestinal drug solubility is a key parameter controlling absorption after the administration of a s...
Solubility and dynamic light scattering (DLS) studies of three poorly soluble drugs (naproxen, indom...
Intestinal drug solubility is a key parameter controlling oral absorption but varies both intra and ...
It is widely recognised that drug solubility within the gastrointestinal tract (GIT) differs from va...
Drug solubility in intestinal fluid is a key parameter controlling absorption after the administrati...
The oral route is the preferred option for drug administration but contains the inherent issue of dr...
Upon oral administration the solubility of a drug in intestinal fluid is a key property influencing ...
The purpose of this study was to validate both existing fasted and fed state simulated intestinal fl...
After oral administration, a drug’s solubility in intestinal fluid is an important parameter influen...
The oral administration of solid dosage forms is the commonest method to achieve systemic therapy an...
Accurate in vivo predictions of intestinal absorption of low solubility drugs require knowing their ...