Influence of some hydrophilic polymers on dissolution characteristics of furosemide through solid dispersion: An unsatisfied attempt for immediate release formulation

Abstract

Influence of some hydrophilic polymers on dissolution characteristics of furosemide through solid dispersion: An unsatisfied attempt for immediate release formulationFurosemide (FRMD) is 5-(aminosulfonyl)-4-chloro-Background: The objective of the present investigation was to enhance dissolution characteristics of water insoluble drug, furosemide (FRMD), by solid dispersion in various hydrophilic carriers. Materials and Methods: The solid dispersions were prepared by solvent evaporation technique using urea and Hydroxy Propyl Methyl Cellulose (HPMC E50 LV). Physical mixtures of drug with above-mentioned polymers were also prepared. Phase solubility studies were performed for drug in the presence of excipients in different ratios. The formulations were evaluated for drug content, in vitro dissolution, Fourier transform infrared (FT-IR) and differential scanning calorimetry (DSC). Similarity factor (f2) was calculated for comparison between dissolution of pure drug and drug-polymer physical mixtures with solid dispersions. Results: Phase solubility studies indicated linear increase in the drug solubility with increase in carrier concentration. In vitro release studies revealed that dissolution characteristic of FRMD was improved by solid dispersion technique. All the preparations of FRMD exhibited significant improvement in its dissolution profiles. Solid dispersion of FRMD with HPMC E50 LV exhibited the highest rate and extent of dissolution. Optimized batches of solid dispersions of both the carriers were characterized by FT-IR and DSC analysis, which indicated absence of major interactions between FRMD and carriers. Conclusion: Solid dispersion technique is one of the finest techniques to improve dissolution of poorly soluble drugs. AbstractAccess this article online Quick Response Code: Website:www.pnrjournal.com

Unsuccessful Delivery of Tetrandrine From Colon-Targeted Dosage Forms Comprising Alginate/Hydroxypropyl Methylcellulose and Alginate–chitosan Beads

“…We performed FTIR spectroscopy (Shimadzu FTIR 8400S, Japan) to investigate interactions between the components in prepared formulations [20]. Samples of alginate, HPMC, chitosan, their composite beads, and loaded beads were crushed with dry potassium bromide, and analyses were performed at 400-4000 cm −1 .…”

Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch

“…At 1 hour, around 70% and 35% drug released from solid dispersions: API to HPMC E50 LV and urea were 1:2 and 1:5 respectively. Dosage forms equal to 10 mg drug was tested in 900 ml SGF (pH 1.2) [133].…”