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Dissolution Performance sentence examples within Vitro Dissolution Performance



Comparative in vitro dissolution studies of fixed-dose combination formulations: analgesic tablets of acetaminophen/caffeine



RAPID AND SIMPLE DETERMINATION OF IBUPROFEN AND CAFFEINE IN FIXED-DOSE COMBINATION FORMULATIONS: APPLICATION TO DISSOLUTION STUDIES


Dissolution Performance sentence examples within Drug Dissolution Performance



Effect of Storage Humidity on Physical Stability of Spray-Dried Naproxen Amorphous Solid Dispersions with Polyvinylpyrrolidone: Two Fluid Nozzle vs. Three Fluid Nozzle



Multicomponent solid dispersion as a formulation strategy to improve drug permeation: A case study on the anti-colorectal cancer irinotecan


Dissolution Performance sentence examples within Enhanced Dissolution Performance



Hydrochlorothiazide Nanocrystals Stabilization by Silk Sericin



Facile Tuning of the Photoluminescence and Dissolution Properties of Phloretin through Cocrystallization




Dissolution Performance sentence examples within Excellent Dissolution Performance



Spray dried nanoemulsions loaded with curcumin, resveratrol, and borage seed oil: The role of two different modified starches as encapsulating materials.



A reservoir-damage-free encapsulated acid dually controlled by hydrogen ion concentration and temperature


Dissolution Performance sentence examples within Better Dissolution Performance



Preparation and Characterization of Instant Casein Phosphopeptide by Supercritical Fluid Assisted Atomization



A New Ferulic Acid-Nicotinamide Cocrystal With Improved Solubility and Dissolution Performance.


Dissolution Performance sentence examples within Scale Dissolution Performance



Development of a Unique Organic Acid Solution for Removing Composite Field Scales



Increasing ESP Lifetime by Employing Novel Non-Corrosive Acid System for Scales Removal


Dissolution Performance sentence examples within Poor Dissolution Performance



Potential application of low molecular weight excipients for amorphization and dissolution enhancement of carvedilol.



Feasibility of Dissolution of U–Zr Alloy in an Acid-Saturated Amide Ligand



Comparative in vitro dissolution studies of fixed-dose combination formulations: analgesic tablets of acetaminophen/caffeine


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10.1016/j.ijpharm.2021.121025

Dry powder inhaler formulation comparison: study of the role of particle deposition pattern and dissolution.


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10.1016/j.carbpol.2021.118399

Sodium alginate and alginic acid as pharmaceutical excipients for tablet formulation: Structure-function relationship.



Can Fused Deposition Modelling Enable the Manufacture of Uniform and Precise Dose Tablets?



Influence of Particle Size and Drug Load on Amorphous Solid Dispersions Containing pH-Dependent Soluble Polymers and the Weak Base Ketoconazole



Automated PET-RAFT Polymerization Towards Pharmaceutical Amorphous Solid Dispersion Development.



Influence of high pressure compaction on solubility and intrinsic dissolution of ibuprofen binary mixtures employing standard excipients



Preparation and Characterization of Instant Casein Phosphopeptide by Supercritical Fluid Assisted Atomization



Study on the mechanism of reactive acid transport in fractured two-mineral carbonate rocks


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10.3390/pharmaceutics13070994

Studying the Complex Formation of Sulfonatocalix[4]naphthalene and Meloxicam towards Enhancing Its Solubility and Dissolution Performance


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10.22159/IJAP.2021V13I3.40975

RAPID AND SIMPLE DETERMINATION OF IBUPROFEN AND CAFFEINE IN FIXED-DOSE COMBINATION FORMULATIONS: APPLICATION TO DISSOLUTION STUDIES


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10.3390/pharmaceutics13071074

Effect of Storage Humidity on Physical Stability of Spray-Dried Naproxen Amorphous Solid Dispersions with Polyvinylpyrrolidone: Two Fluid Nozzle vs. Three Fluid Nozzle


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10.1021/acs.molpharmaceut.1c00325

Effect of Counterions on Dissolution of Amorphous Solid Dispersions Studied by Surface Area Normalized Dissolution.


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10.3390/pharmaceutics13050735

Exploring the Role of Surfactants in Enhancing Drug Release from Amorphous Solid Dispersions at Higher Drug Loadings



Development and Validation of a Discriminatory Dissolution Model for an Immediately Release Dosage Form by DOE and Statistical Approaches.


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10.1016/j.ijpharm.2021.120239

Direct Compression Tablet Formulation of Celecoxib Enabled with a Pharmaceutical Solvate.



Metal-Based Ionic Liquids in Oxidative Desulfurization: A Critical Review.


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10.1016/J.BIORTECH.2020.124219

An integrated insight into bioleaching performance of chalcopyrite mediated by microbial factors: Functional types and biodiversity.



Experimental determination of the velocity distribution in USP Apparatus 1 (basket apparatus) using Particle Image Velocimetry (PIV)


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10.1080/03639045.2021.1934863

Shellac- a natural carrier for colon targeting of indomethacin using hot melt extrusion



Development of a Unique Organic Acid Solution for Removing Composite Field Scales



Immediate-Release Formulations Produced via Twin-Screw Melt Granulation: Systematic Evaluation of the Addition of Disintegrants


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10.1021/acs.molpharmaceut.1c00119

Effect of Excipients on Salt Disproportionation during Dissolution: A Novel Application of In Situ Raman Imaging.



Study of Steel Electro-dissolution Behavior in Presence of Some Surfactants. Electrochemical Investigation and Surface Active Properties Determination



Formulation of Gelucire®-Based Solid Dispersions of Atorvastatin Calcium: In Vitro Dissolution and In Vivo Bioavailability Study.



Influence of maskless electrochemical micromachining process parameters during microtexturing


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10.1016/j.ijbiomac.2021.07.076

Spray dried nanoemulsions loaded with curcumin, resveratrol, and borage seed oil: The role of two different modified starches as encapsulating materials.


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10.1016/j.ijpharm.2021.121033

Potential application of low molecular weight excipients for amorphization and dissolution enhancement of carvedilol.


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10.1016/J.MOLLIQ.2021.115762

Experimental and theoretical studies of chitosan dissolution in ionic liquids: Contribution ratio effect of cations and anions


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10.3390/pharmaceutics13030389

Co-Amorphous Drug Formulations in Numbers: Recent Advances in Co-Amorphous Drug Formulations with Focus on Co-Formability, Molar Ratio, Preparation Methods, Physical Stability, In Vitro and In Vivo Performance, and New Formulation Strategies



Impact of binary/ternary solid dispersion utilizing poloxamer 188 and TPGS to improve pharmaceutical attributes of bedaquiline fumarate



Feasibility of Dissolution of U–Zr Alloy in an Acid-Saturated Amide Ligand


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10.1021/acs.molpharmaceut.1c00419

Impact of Drug-Polymer Intermolecular Interactions on Dissolution Performance of Copovidone-Based Amorphous Solid Dispersions.



Increasing ESP Lifetime by Employing Novel Non-Corrosive Acid System for Scales Removal



Towards virtual bioequivalence studies for oral dosage forms containing poorly water-soluble drugs: a physiologically based biopharmaceutics modeling (PBBM) approach.



Amorphous Solid Dispersions Containing Residual Crystallinity: Competition Between Dissolution and Matrix Crystallization.


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10.1016/j.ijpharm.2021.120221

Exploring the Performance-Controlling Tablet Disintegration Mechanisms for Direct Compression Formulations.



A Novel Use of Nanocrystalline Suspensions to Develop Sub-Microgram Dose Micro-Tablets.


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10.1016/j.ijpharm.2021.121157

Investigation into the role of the polymer in enhancing microwave-induced in situ amorphization.



Investigation of Solubility Behavior of Canagliflozin Hydrate Crystals Combining Crystallographic and Hirshfeld Surface Calculations



Orphan Formulations in Pediatric Schistosomiasis Treatment: Development and Characterization of Praziquantel Nanoparticle-Loaded Powders for Reconstitution.



Prediction of the Long-Term Dissolution Performance of an Immediate-Release Tablet Using Accelerated Stability Studies.



Development of Diallylimidazolium Methoxyacetate/DMSO (DMF/DMA) Solvents for Improving Cellulose Dissolution and Fabricating Porous Material


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10.1016/j.ijpharm.2019.01.038

Hot‐melt extrusion process impact on polymer choice of glyburide solid dispersions: The effect of wettability and dissolution



The Influence of Dimethyl Sulfoxide as Electrolyte Additive on Anodic Dissolution of Alkaline Zinc-Air Flow Battery



Exploring the use of spray congealing to produce solid dispersions with enhanced indomethacin bioavailability: In vitro characterization and in vivo study


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10.1016/j.ijpharm.2019.05.062

Amorphous solid dispersions of ketoprofen and poly-vinyl polymers prepared via electrospraying and spray drying: A comparison of particle characteristics and performance.


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10.22159/IJAP.2019V11I4.33174

IN VITRO EQUIVALENCE STUDY OF DIFFERENT DOSES OF CARBAMAZEPINE REFERENCE TABLETS USING USP APPARATUSES 2 AND 4


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10.1021/ACS.ENERGYFUELS.9B00673

Innovative Encapsulating Acid with Release Dually Controlled by the Concentration of Hydrogen Ions and Temperature



Utility of Films to Anticipate Effect of Drug Load and Polymer on Dissolution Performance from Tablets of Amorphous Itraconazole Spray-Dried Dispersions



Ethinyl estradiol cocrystals assembled by chain structures: improvement in stability and solubility


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10.1080/03639045.2018.1529784

Stability investigation of FCC-based tablets for oral suspension with caffeine and oxantel pamoate as model drugs



Hydrochlorothiazide Nanocrystals Stabilization by Silk Sericin



The role of solid state properties on the dissolution performance of flufenamic acid.



Improvement of the Firocoxib Dissolution Performance Using Electrospun Fibers Obtained from Different Polymer/Surfactant Associations



Monitoring microsphere coating processes using PAT tools in a bench scale fluid bed.


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10.1021/acs.molpharmaceut.8b00593

Effect of Organic Acids on Molecular Mobility, Physical Stability, and Dissolution of Ternary Ketoconazole Spray-Dried Dispersions.



Sericin Inhibits Devitrification of Amorphous Drugs


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10.22159/IJAP.2019V11I4.33293

INFLUENCE OF DOSE AND USP DISSOLUTION APPARATUS IN THE RELEASE PERFORMANCE OF REFERENCE TABLETS: PROPRANOLOL-HCl AND RANITIDINE-HCl CASES


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10.1021/acs.molpharmaceut.9b00186

Miniaturized Measurement of Drug-Polymer Interactions via Viscosity Increase for Polymer Selection in Amorphous Solid Dispersions.


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10.1021/acs.molpharmaceut.8b01068

Fixed Dose Combination Formulations: Multilayered Platforms Designed for the Management of Cardiovascular Disease.



Characterization of Phase Transformations for Amorphous Solid Dispersions of a Weakly Basic Drug upon Dissolution in Biorelevant Media


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10.1016/j.ijpharm.2019.118917

Impact of amorphization and GI physiology on supersaturation and precipitation of poorly soluble weakly basic drugs using a small-scale in vitro transfer model.



Quality-by-Design based development and characterization of pioglitazone loaded liquisolid compact tablets with improved biopharmaceutical attributes



Facile Tuning of the Photoluminescence and Dissolution Properties of Phloretin through Cocrystallization


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10.1021/acs.molpharmaceut.9b00601

Recent Advances in Understanding the Micro- and Nanoscale Phenomena of Amorphous Solid Dispersions.


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10.3390/pharmaceutics11020067

Applying Supercritical Fluid Technology to Prepare Ibuprofen Solid Dispersions with Improved Oral Bioavailability



Effect of intra- and extragranular addition of highly porous tribasic calcium phosphate on properties of immediate release acyclovir formulation – Comparison with commercial tablets using compendial and biorelevant dissolution methods



Spherical Cocrystallization—An Enabling Technology for the Development of High Dose Direct Compression Tablets of Poorly Soluble Drugs



Optimization of Dissolution Performance for Amorphous Solid Dispersions


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10.1021/acs.molpharmaceut.8b00923

Influence of Drug-Polymer Interactions on Dissolution of Thermodynamically Highly Unstable Cocrystal.



A reservoir-damage-free encapsulated acid dually controlled by hydrogen ion concentration and temperature


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10.1021/acs.molpharmaceut.9b00955

Understanding the effects of a polymer on the surface dissolution of pharmaceutical cocrystals using combined experimental and molecular dynamics simulation approaches.


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10.1016/j.ijpharm.2019.05.022

Prediction of dissolution profiles by non-destructive NIR spectroscopy in bilayer tablets.



Multicomponent solid dispersion as a formulation strategy to improve drug permeation: A case study on the anti-colorectal cancer irinotecan


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10.1080/03639045.2019.1648502

Evaluating the bioequivalence of metronidazole tablets and analyzing the effect of in vitro dissolution on in vivo absorption based on PBPK modeling



Toward a Better Understanding of Different Dissolution Behavior of Starches in Aqueous Ionic Liquids at Room Temperature



Improve Anti-alveolar Echinococcosis Efficacy of Albendazole by a Novel Nano-crystalline Formulation with Enhanced Oral Bioavailability.


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10.1016/J.MOLLIQ.2019.111533

Chitosan dissolution with sulfopropyl imidazolium Brönsted acidic ionic liquids



Use of roller compaction and fines recycling process in the preparation of erlotinib hydrochloride tablets



Levulinate amidinium protic ionic liquids (PILs) as suitable media for the dissolution and levulination of cellulose


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10.1016/j.ijpharm.2019.01.009

Building a better particle: Leveraging physicochemical understanding of amorphous solid dispersions and a hierarchical particle approach for improved delivery at high drug loadings


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10.1016/j.ijpharm.2019.04.034

Amorphous solid dispersions of weak bases with pH-dependent soluble polymers to overcome limited bioavailability due to gastric pH variability - An in-vitro approach.


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10.1016/j.foodres.2018.10.081

Encapsulations of wild garlic (Allium ursinum L.) extract using spray congealing technology.


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10.1021/ACSSUSCHEMENG.8B05604

Metal Recovery from Spent Samarium–Cobalt Magnets Using a Trichloride Ionic Liquid



A New Ferulic Acid-Nicotinamide Cocrystal With Improved Solubility and Dissolution Performance.


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