Objective: To improve the treatment of H. pylori infection, by achieving the required bactericidal concentrations of antibiotics in the stomach, by delivering the antibiotics to the mucus layer and release the drug at the site of infection for a prolonged period would be significantly more effective than conventional dosage forms. Methods: The experimental method of the research was designed to prepare Levofloxacin floating by using Hydroxypropyl Methylcellulose (HPMC K4M), Hydroxypropyl Methylcellulose (HPMC K100M) and Xanthan gum by Three-level Box–Behnken design optimization method. The prepared tablets were evaluated for Thickness, Hardness, Friability, Weight variation, Swelling index (SI), Floating lag time (FLT) and Time required to ...
Floating microspheres of Levofloxacin were prepared using Eudtagit RSPO and HPMC K15M. The nature of...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
The objective of the present work was to develop Gastro retentive dosage forms which would remain in...
Objective: To improve the treatment of H. pylori infection, by achieving the required bactericidal c...
AbstractGastroretentive levofloxacin (LVF) floating mini-tablets for the eradication of Helicobacter...
Objective: The present investigation concerns the design and evaluation of floating tablets of Levof...
Objective: The present investigation concerns the design and evaluation of floating tablets of Levof...
AbstractGastroretentive levofloxacin (LVF) floating mini-tablets for the eradication of Helicobacter...
The objective of the present work was to develop Gastro retentive dosage forms which would remain in...
H. pylori colonize the gastric mucosa leading to gastritis, gastric ulcer, and gastric carcinoma. To...
In this study levofloxacin hemihydrate mucoadhesive microcapsules were prepared by ion gelation met...
The aim of the present research work was to formulate and evaluate mucoadhesive microspheres of lev...
Objective: The present investigation concerns the design and evaluation of floating tablets of Levof...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
Floating microspheres of Levofloxacin were prepared using Eudtagit RSPO and HPMC K15M. The nature of...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
The objective of the present work was to develop Gastro retentive dosage forms which would remain in...
Objective: To improve the treatment of H. pylori infection, by achieving the required bactericidal c...
AbstractGastroretentive levofloxacin (LVF) floating mini-tablets for the eradication of Helicobacter...
Objective: The present investigation concerns the design and evaluation of floating tablets of Levof...
Objective: The present investigation concerns the design and evaluation of floating tablets of Levof...
AbstractGastroretentive levofloxacin (LVF) floating mini-tablets for the eradication of Helicobacter...
The objective of the present work was to develop Gastro retentive dosage forms which would remain in...
H. pylori colonize the gastric mucosa leading to gastritis, gastric ulcer, and gastric carcinoma. To...
In this study levofloxacin hemihydrate mucoadhesive microcapsules were prepared by ion gelation met...
The aim of the present research work was to formulate and evaluate mucoadhesive microspheres of lev...
Objective: The present investigation concerns the design and evaluation of floating tablets of Levof...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
Floating microspheres of Levofloxacin were prepared using Eudtagit RSPO and HPMC K15M. The nature of...
The rationale of the present investigation is to develop a new oral drug delivery system utilizing b...
The objective of the present work was to develop Gastro retentive dosage forms which would remain in...