Paracetamol powder (PAR) has poor compressibility, high cohesivity and is difficult to compress. We have prepared dispersions of PAR and 3-cyclodextrin (β-CD) in physical mixture form, kneaded solid dispersion and spray dried solid dispersion (the ratio 1:1 w/w), and spray dried solid dispersion of PAR-Ethocel-Macogol 6000 (95:2:3), as well. The Theological characteristics of this dispersions were observed. The crystalline structure, size and shape of PAR dispersion powders differed from PAR alone. Consequently, they showed improvement in packing density; reductions in cohesivity (Kawakita's cohesivity constant was the lowest with kneaded solid dispersion PAR-β-CD); good flowability and angle of repose (especially with kneded solid dispersi...
Solid dosage forms are invariably multiparticulate systems of heterogenous particle size distributio...
Abstract: Paracetamol (PCM) is poor water soluble drug which comes under Biopharmaceutical classific...
A pharmaceutical suspension is a semi-liquid dosage form suitable for patients being unable to swall...
Abstract— The effect of cyclodextrin (β‐CD) on the solubility and dissolution rate of various parace...
The compression behaviour of three powder products of Paracetamol-beta-cyclodextrin solid dispersion...
The formulation of active pharmaceutical ingredients (APIs) in amorphous solid dispersions (ASDs) is...
Monoclinic paracetamol (PA) is notorious as a poorly compactible model drug. Polyvinylpyrrolidone (P...
This work compared the compressional, mechanical and drug release properties of paracetamol tablets ...
1st International Electronic Conference on Oral Drug Delivery Abstract onlyMonoclinic paracetamol i...
A thesis submitted in partial fulfilment of the requirements of the University of Wolverhampton for ...
Evaluation of the tableting mixtures containing the paracetamolum by the parameters of the equation ...
Background: Capping and lamination are major problems encountered in tablet production and they are ...
Paracetamol (PCT) and propyphenazone (PRP) are analgesic drugs that are often combined in a single d...
β‐Cyclodextrin (β‐CD) has been applied in various fields of drug formulation. Its presence in powder...
Paracetamol solid state has three known polymorphic forms; monoclinic form (Form I), orthorhombic fo...
Solid dosage forms are invariably multiparticulate systems of heterogenous particle size distributio...
Abstract: Paracetamol (PCM) is poor water soluble drug which comes under Biopharmaceutical classific...
A pharmaceutical suspension is a semi-liquid dosage form suitable for patients being unable to swall...
Abstract— The effect of cyclodextrin (β‐CD) on the solubility and dissolution rate of various parace...
The compression behaviour of three powder products of Paracetamol-beta-cyclodextrin solid dispersion...
The formulation of active pharmaceutical ingredients (APIs) in amorphous solid dispersions (ASDs) is...
Monoclinic paracetamol (PA) is notorious as a poorly compactible model drug. Polyvinylpyrrolidone (P...
This work compared the compressional, mechanical and drug release properties of paracetamol tablets ...
1st International Electronic Conference on Oral Drug Delivery Abstract onlyMonoclinic paracetamol i...
A thesis submitted in partial fulfilment of the requirements of the University of Wolverhampton for ...
Evaluation of the tableting mixtures containing the paracetamolum by the parameters of the equation ...
Background: Capping and lamination are major problems encountered in tablet production and they are ...
Paracetamol (PCT) and propyphenazone (PRP) are analgesic drugs that are often combined in a single d...
β‐Cyclodextrin (β‐CD) has been applied in various fields of drug formulation. Its presence in powder...
Paracetamol solid state has three known polymorphic forms; monoclinic form (Form I), orthorhombic fo...
Solid dosage forms are invariably multiparticulate systems of heterogenous particle size distributio...
Abstract: Paracetamol (PCM) is poor water soluble drug which comes under Biopharmaceutical classific...
A pharmaceutical suspension is a semi-liquid dosage form suitable for patients being unable to swall...