Mirtazapine is a tetracyclic anti-depressant with poor water solubility. The aim of this study was to improve the dissolution rate of mirtazapine by delivering the drug as a liquisolid compact.
Faiza Naureen +12 more
doaj +1 more source
DESIGN, FORMULATION AND EVALUATION OF CELECOXIB SOLID DISPERSIONS PREPARED BY THE SOLVENT- EVAPORATION TECHNIQUE [PDF]
The aim of the present study was to improve dissolution of poorly water-soluble Celecoxib by solid dispersion technique using water soluble carriers. Solid dispersions of Celecoxib were prepared with different polymers or carriers such as Hydroxy Propyl ...
Yasmin Mortagi
doaj +1 more source
Impact of the manufacturing technique on the dissolution-enhancement functionality of PEG4000 in Cilostazol tablets [PDF]
Cilostazol was selected as poorly-soluble model drug to investigate the impact of the manufacturing method on the excipient functionality of PEG4000 at various levels.
Obada Sawafta +4 more
doaj +3 more sources
Spontaneous In Situ Formation of Liposomes from Inert Porous Microparticles for Oral Drug Delivery
Despite the wide-spread use of liposomal drug delivery systems, application of these systems for oral purposes is limited due to their large-scale formulation and storage issues.
Maryam Farzan +6 more
doaj +1 more source
Lignin enhances cellulose dissolution in cold alkali
Aqueous sodium hydroxide solutions are extensively used as solvents for lignin in kraft pulping. These are also appealing systems for cellulose dissolution due to their inexpensiveness, ease to recycle and low toxicity. Cellulose dissolution occurs in a narrow concentration region and at low temperatures.
Costa, Carolina +6 more
openaire +6 more sources
Preparation and characterization of fenofibrate-loaded zeolitic imidazolate frameworks and their evaluation in dissolution enhancement of the formulation [PDF]
The purpose of this study was to develop zeolitic imidazolate frameworks (ZIFs) incorporated with poorly water-soluble drug fenofibrate (FEN), belonging to Biopharmaceutical Classification System (BCS) class II, to improve drug dissolution, intended to ...
Aziz maleki +5 more
doaj +1 more source
ENHANCEMENT OF DISSOLUTION OF CANDESARTAN CILEXETIL
Objective: The main aim of our investigation was to enhance the dissolution of Candesartan Cilexetil (CC), a prodrug of Candesartan, used in the treatment of hypertension. CC bioavailability is dissolution rate limited. The drug was formulated using various excipients such as surfactants, and liquid lipids to improve solubility, dissolution, and hence ...
APARNA C, ANUSHA M, MANISHA B
openaire +1 more source
Dissolution Enhancement of Artemisinin with .BETA.-Cyclodextrin
The main objective of this research is to improve the dissolution rate of artemisinin (ART) by fabrication with β-cyclodextrin (β-CD) as a hydrophilic carrier. Artemisinin nanoparticles and ART/β-CD complexes were successfully fabricated by means of evaporative precipitation of nanosuspension.
Kakran, Mitali +3 more
openaire +3 more sources
Engineering Cocrystals of Poorly Water-Soluble Drugs to Enhance Dissolution in Aqueous Medium
Biopharmaceutics Classification System (BCS) Class II and IV drugs suffer from poor aqueous solubility and hence low bioavailability. Most of these drugs are hydrophobic and cannot be developed into a pharmaceutical formulation due to their poor aqueous ...
Indumathi Sathisaran +1 more
doaj +1 more source
Dissolution enhancement of chlorzoxazone using cogrinding technique.
The aim of the present work was to improve rate of dissolution and processing parameters of BCS class II drug, chlorzoxazone using cogrinding technique in the presence of different excipients as a carrier.The drug was coground with various carriers like polyethylene glycol (PEG 4000), hydroxypropyl methylcellulose (HPMC) E50LV, polyvinylpyrrolidone ...
Raval MK, Patel JM, Parikh RK, Sheth NR.
europepmc +4 more sources

