drug content
DESIGN AND IN VITRO EVALUATION OF DICLOFENAC SODIUM MATRIX TABLETS
... for drug content uniformity, drug release profiles was compared with pure ...and content uniformity test were performed in triplicate and the results are shown as an average with standard ...
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Formulation optimization of galantamine hydrobromide loaded gel drug reservoirs in transdermal patch for Alzheimer’s disease
... gel drug reservoir was formu- lated and the compositions of this reservoir were optimized by using ...(cumulative drug release at 8 hours and permeation ...high drug content, and controlled ...
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DESIGN, DEVELOPMENT AND EVALUATION OF SELECTED ANTIFUNGAL LOADED ETHOSOMAL GEL FOR TOPICAL DRUG DELIVERY
... for drug entrapment efficiency, drug content, spreadability, viscosity, pH, homogeneity and grittiness, percentage yield and in vitro drug release ...vitro drug release studies were ...
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APPLICATION OF SOME NOVEL TECHNIQUES FOR SOLUBILITY ENHANCEMENT OF MEFENAMIC ACID, A POORLY WATER SOLUBLE DRUG
... anti-inflammatory drug (NSAID), has a low oral bioavailability due to poor aqueous solubility and insufficient ...for drug content studies, solubility studies, in vitro study and in vivo evaluation ...
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FORMULATION AND EVALUATION OF MUCOADHESIVE MICROSPHERES OF AN ANTI-MIGRAINE DRUG
... anti-migraine drug for sustained ...various drug-polymer ratios of 1:1, 1:2 and ...possible drug polymer interactions, percentage yield, micromeritic properties, particle size, drug ...
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FORMULATION, CHARACTERISATION AND IN VITRO EVALUATION OF NOVEL IONICALLY CROSS LINKED CASEIN NANOPARTICLES FOR MEMANTINE HYDRO CHLORIDE DELIVERY
... of drug, which can also overcome the problems like multidose therapy, poor patient compliance and high cost associated with conventional ...potential, drug content, entrapment efficiency and in-vitro ...
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IMPROVING THE SOLUBILITY OF ANTIHELMINTIC DRUG BY SOLID DISPERSIONS AND INCLUSION COMPLEXES
... Antihelmintic drug (BCS class 2) and poorly soluble in ...different drug-polymer ratio like 1:2, 1:4and ...FTIR, drug content, Phase solubility, percent yield and in vitro release studies ...
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Novel Preparation and Effective Delivery of Mucoadeshive Nanoparticles Containing Anti-diabetic Drug
... (anti-diabetic drug) which has contributed greatly to the understnading of molecular interatcion with the DPP-4 ...a drug at site of absorption, recent efforts have focused on development of mucoadhesive ...
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Synthesis, characterization and application of borax cross linked carboxymethyl guar gum
... Control drug delivery is the new way to treat ...as drug binder in formulation of N-(4-hydroxyphenyl)acetamide (Paracetamol) and (RS)-2-(4-(2-methylpropyl)phenyl) propanoic acid ...weight content, ...
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FORMULATION AND EVALUATION OF ETHOSOMES OF CLOBETASOL PROPIONATE
... vesicular drug delivery ...entrap drug molecule of various physicochemical characters such as hydrophilic, lipophilic or amphiphilic in ...of drug molecules to the skin and through the skin to the ...
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Journal of Applied Pharmaceutical Science
... vitro drug release. Increasing xanthan gum concentrations yielded a faster drug release due to a higher liquid uptake, swelling and erosion ...vitro drug release: increasing concentrations yielded ...
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DESIGN, PREPARE AND CHARACTERIZATION OF DONEPEZIL TRANSDERMAL PATCHES
... thickness, drug content, content uniformity, moisture absorption, weight variation, and drug permeation studies of the optimized patches were ...% drug was released within 8 ...vitro ...
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EXTRACTION, NANOFORMULATION AND EVALUATION OF CURCUMIN
... of Drug Content and Entrapment Efficiency: 100mg of Drug-loaded nanosuspension is taken and dissolved in 100 ml of suitable buffer solution of pH ...
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PREPARATION OF CONTROLLED RELEASE METFORMIN HYDROCHLORIDE LOADED CHITOSAN MICROSPHERES AND EVALAUTION OF FORMULATION PARAMETERS
... anti-diabetes drug Metformin ...of drug and polymer is analyzed by using FTIR and DSC ...size, drug entrapment efficiency, surface morphology, drug content, drug loading and in ...
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Formulation of Solid Lipid Nanoparticles of Cilnidipine for the Treatment of Hypertension
... another drug to treat ...II drug with 6 to 30 percent oral bioavailability due to first pass ...the drug from degradation and improve its dissolution, solid lipid nanoparticles were ...transmittance, ...
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Enhancement of Solubility and Dissolution Rate of Lopinavir by Solid Dispersion Technique.
... wt.% drug were prepared using solvent evaporation ...low drug load proved to be amorphous, since no crystalline Felodipine or Hesperetin drugs were detected using DSC and ...the drug was in the ...
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Formulation And Evaluation Of Transdermal Patches Containing Antidiabetic DrugFormulation And Evaluation Of Transdermal Patches Containing Antidiabetic Drug
... C (USP). The uniformity of the solution in the receptor phase was maintained by stirring at a speed of 600 rpm (approx.) using a tiny Teflon coated magnetic bead. The volume of the receptor compartment was maintained at ...
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EFFECT OF LIPID COMPOSITION ON LIPOSOMAL FORMULATION OF PRAMIPEXOLE
... to drug detachment from liposomal surface, [16,17] while the later slow release results from sustained drug release from the inner ...that drug transport out of the liposomes was driven mainly by a ...
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Formulation and In Vitro Evaluation of Pulsatile Drug Delivery System of Ketoprofen
... pulsatile drug delivery system to achieve time and site specific release of Ketoprofen, based on chronopharmaceutical ...contained drug Ketoprofen and superdisintegrant Sodium Starch Glycolate or ...
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Microencapsulation by Spray Drying of Vitamin A Palmitate from Oil to Powder and Its Application in Topical Delivery System
... in-vitro drug release and SEM ...The drug content and encapsulation efficiency (53% - 63%) of differ- ent batches were found within acceptable ...stabilized drug loaded microcapsules were ...
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