Works matching DE "DRUG solubility testing"
Results: 115
Dissolution Test: Causes of Understated Results and their Elimination (Review).
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 8, p. 821, doi. 10.1007/s11094-021-02501-1
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Comparative in vitro dissolution testing of trimetazidine prolonged-release tablets.
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- Pharmaceutical Chemistry Journal, 2009, v. 43, n. 12, p. 677, doi. 10.1007/s11094-010-0379-8
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Gastroretentive sustained release acyclovir tablets based on synergistically interacting polysaccharides.
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- Pharmaceutical Chemistry Journal, 2007, v. 41, n. 12, p. 656, doi. 10.1007/s11094-008-0038-5
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Optimization of the Composition and Technology of Diazoline Tablets.
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- Pharmaceutical Chemistry Journal, 2005, v. 39, n. 8, p. 437, doi. 10.1007/s11094-005-0176-y
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Using the Drug Dissolution Test for the Characterization of Generics: Ofloxacin Tablets.
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- Pharmaceutical Chemistry Journal, 2004, v. 38, n. 5, p. 264, doi. 10.1023/B:PHAC.0000042092.05652.bc
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Determining the Effective Surfactant Concentration for the Drug Dissolution Test.
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- Pharmaceutical Chemistry Journal, 2004, v. 38, n. 5, p. 267, doi. 10.1023/B:PHAC.0000042093.32672.db
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The Problem of Device Calibration for the Pharmacopoeial Drug Dissolution Test.
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 10, p. 550, doi. 10.1023/B:PHAC.0000014863.86593.b3
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A Comparative Analysis of Requirements to the Pharmacopoeial Drug Dissolution Test.
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 1, p. 37, doi. 10.1023/A:1023655230101
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Solubility enhancement of mefenamic acid by inclusion complex with β-cyclodextrin: in silico modelling, formulation, characterisation, and in vitro studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 605, doi. 10.1080/14756366.2020.1869225
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A new approach to determining the performance of superdisintegrants.
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- Journal of Bioactive & Compatible Polymers, 2015, v. 30, n. 1, p. 3, doi. 10.1177/0883911514558370
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3D printing of carvedilol oral dosage forms using selective laser sintering technique.
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- Macedonian Pharmaceutical Bulletin / Makedonsko Farmacevtski Bilten, 2023, v. 69, p. 169, doi. 10.33320/maced.pharm.bull.2023.69.03.083
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Development and characterization of ivermectin loaded liposomes prepared by lipid film hydration and ethanol injection method.
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- Macedonian Pharmaceutical Bulletin / Makedonsko Farmacevtski Bilten, 2023, v. 69, p. 71, doi. 10.33320/maced.pharm.bull.2023.69.03.035
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Dissolution enhancement of chlorzoxazone using cogrinding technique.
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- International Journal of Pharmaceutical Investigation, 2015, v. 5, n. 4, p. 247, doi. 10.4103/2230-973X.167689
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FORMULATION AND EVALUATION OF FAST DISSOLVING FILM OF FORMULATION AND EVALUATION OF FAST DISSOLVING FILM OF METHYLCOBALAMIN.
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- Pharma Science Monitor, 2015, v. 6, n. 4, p. 50
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Physicochemical Equivalence Studies of Two Amlodipine Tablet Formulations.
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- Scripta Medica, 2018, v. 49, n. 1, p. 18, doi. 10.18575/msrs.sm.e.18.03
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A Novel Domperidone Hydrogel: Preparation, Characterization, Pharmacokinetic, and Pharmacodynamic Properties.
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- Journal of Drug Delivery, 2011, p. 1, doi. 10.1155/2011/841054
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Preparation and Evaluation of Sustained Release Matrix Tablets of Tramadol Hydrochloride Using Glyceryl Palmitostearate.
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- Tropical Journal of Pharmaceutical Research, 2010, v. 9, n. 3, p. 275
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Formulation of Sustained-Release Diltiazem Matrix Tablets Using Hydrophilic Gum Blends.
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- Tropical Journal of Pharmaceutical Research, 2010, v. 9, n. 3, p. 283, doi. 10.4314/tjpr.v9i3.56291
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Biodegradable Microcapsules from D,L–PLA/PCL as Controlled Nifedipine Drug Delivery Carrier.
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- Macromolecular Symposia, 2020, v. 391, n. 1, p. 1, doi. 10.1002/masy.201900132
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Cocrystal habit engineering to improve drug dissolution and alter derived powder properties.
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- Journal of Pharmacy & Pharmacology, 2016, v. 68, n. 5, p. 665, doi. 10.1111/jphp.12476
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Optimization of self-microemulsifying drug delivery system for telmisartan using Box- Behnken design and desirability function.
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- Journal of Pharmacy & Pharmacology, 2013, v. 65, n. 10, p. 1440, doi. 10.1111/jphp.12115
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Formulation and Evaluation of Fast Dissolving Tablets of Oxcarbazepine Using Liquisolid Technology.
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- Indian Journal of Pharmaceutical Education & Research, 2024, v. 58, p. S880, doi. 10.5530/ijper.58.3s.89
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Modeling of non‐Fickian diffusion and dissolution from a thin polymeric coating: An application to drug‐eluting stents.
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- International Journal for Numerical Methods in Engineering, 2018, v. 114, n. 3, p. 292, doi. 10.1002/nme.5744
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In vitro quantitative and qualitative analysis of anti-hypertensive tablets and comparison between their generic versus branded formulations.
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- National Journal of Physiology, Pharmacy & Pharmacology, 2024, v. 14, n. 7, p. 1459, doi. 10.5455/njppp.2024.14.04181202429052024
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Model predictive in vitro dissolution testing in pharmaceutical continuous manufacturing: An equivalence study.
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- AIChE Journal, 2023, v. 69, n. 9, p. 1, doi. 10.1002/aic.18124
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Design and Optimization of Floating Drug Delivery System of Acyclovir.
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- Indian Journal of Pharmaceutical Sciences, 2010, v. 72, n. 5, p. 599, doi. 10.4103/0250-474X.78527
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Comparative Bioavailability Studies of Indomethacin from Two-Controlled Release Formulations in Healthy Albino Sheep.
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- Indian Journal of Pharmaceutical Sciences, 2006, v. 68, n. 6, p. 760, doi. 10.4103/0250-474X.31010
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Compatibility study of hydroxychloroquine sulfate with pharmaceutical excipients using thermal and nonthermal techniques for the development of hard capsules.
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- Journal of Thermal Analysis & Calorimetry, 2020, v. 140, n. 5, p. 2283, doi. 10.1007/s10973-019-08953-8
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Pluronic F127 as a suitable carrier for preparing the imatinib base solid dispersions and its potential in development of a modified release dosage forms.
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- Journal of Thermal Analysis & Calorimetry, 2017, v. 130, n. 1, p. 383, doi. 10.1007/s10973-017-6139-1
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Design of microcrystalline cellulose-free alginate spheroids by extrusion-spheronization technique.
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- Chemical Engineering Research & Design: Transactions of the Institution of Chemical Engineers Part A, 2013, v. 91, n. 12, p. 2437, doi. 10.1016/j.cherd.2013.04.017
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Formulation and evaluation of anti-rheumatic dexibuprofen transdermal patches: a quality-by-design approach.
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- Journal of Drug Targeting, 2016, v. 24, n. 7, p. 603, doi. 10.3109/1061186X.2015.1116538
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Dissolution Testing and Potentiometric Assay of Sertraline Hydrochloride in Batch and FIA Conditions.
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- Analytical Letters, 2011, v. 44, n. 9, p. 1713, doi. 10.1080/00032719.2010.520397
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SYNTHESIS AND ANALYSIS OF NANOFIBERS CONTAINING KETOPROFEN-BETACYCLODEXTRIN COMPLEXES AND POLYVINYL ALCOHOL FOR MEDICAL APPLICATIONS.
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- International Journal of Medical Dentistry, 2020, v. 24, n. 2, p. 282
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EVALUACIÓN DEL RIESGO ACUÁTICO DE SIETE PRODUCTOS FARMACÉUTICOS SOBRE Daphnia magna.
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- Ecologia Aplicada, 2009, v. 8, n. 1/2, p. 71, doi. 10.21704/rea.v8i1-2.384
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Ulcerative Colitis as a Novel Cause of Increased Need for Levothyroxine.
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- Frontiers in Endocrinology, 2019, p. N.PAG, doi. 10.3389/fendo.2019.00233
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Dissolution Rate Enhancement of Clarithromycin Using Ternary Ground Mixtures: Nanocrystal Formation.
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- Iranian Journal of Pharmaceutical Research, 2013, v. 12, n. 4, p. 587
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Update on Safety Issues in the Treatment of Rheumatic Diseases.
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- MD Conference Express, 2012, p. 7, doi. 10.1177/155989771219002
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Simple and Reliable HPLC Method of Abacavir Determination in Pharmaceuticals, Human Serum and Drug Dissolution Studies from Tablets.
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- Journal of Liquid Chromatography & Related Technologies, 2005, v. 28, n. 3, p. 423, doi. 10.1081/JLC-200044523
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Development and Validation of an RP-HPLC Method for the Dissolution Studies of Bisoprolol in Pharmaceutical Dosage Forms.
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- Journal of Liquid Chromatography & Related Technologies, 2005, v. 28, n. 3, p. 477, doi. 10.1081/JLC-200044531
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Development and Validation of an RP-HPLC Method for the Determination of Valacyclovir in Tablets and Human Serum and Its Application to Drug Dissolution Studies#.
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- Journal of Liquid Chromatography & Related Technologies, 2003, v. 26, n. 11, p. 1747, doi. 10.1081/JLC-120021283
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HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC ASSAY AND DRUG DISSOLUTION STUDIES OF FLUOXETINE HYDROCHLORIDE IN CAPSULE FORMULATIONS.
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- Journal of Liquid Chromatography & Related Technologies, 2000, v. 23, n. 11, p. 1699, doi. 10.1081/JLC-100100446
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IN VITRO DISSOLUTION METHODOLOGY AND ESTIMATED CONSEQUENCES OF BIOWAIVER EXTENSION FOR IMMEDIATE RELEASE SOLID ORAL DOSAGE FORMS WITH METFORMIN HYDROCHLORIDE.
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- Farmacia, 2018, v. 66, n. 1, p. 18
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Human whole blood assay for rapid and routine testing of non-steroidal anti-inflammatory drugs (NSAIDs) on cyclo-oxygenase-2 activity.
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- Inflammopharmacology, 2008, v. 16, n. 4, p. 155, doi. 10.1007/s10787-008-8007-x
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Development of Fast Dissolving Tablets of Nisoldipine by Solid Dispersion Technology using Poloxamer 407 and Poloxamer 188.
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- Journal of Young Pharmacists, 2016, v. 8, n. 4, p. 341, doi. 10.5530/jyp.2016.4.9
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Improvement in the dissolution profile of diacerein using a surfactant-based solid dispersion technique.
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- Drug Discoveries & Therapeutics, 2010, v. 4, n. 6, p. 435
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Evaluating drug delivery of solid dose tablets by isothermal mechanical analysis.
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- Journal of Thermal Analysis & Calorimetry, 2012, v. 108, n. 3, p. 1287, doi. 10.1007/s10973-011-1477-x
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Drug Solubility Prediction: A Comparative Analysis of GNN, MLP, and Traditional Machine Learning Algorithms.
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- Gazi Üniversitesi Fen Bilimleri Dergisi Part C: Tasarım ve Teknoloji, 2024, v. 21, n. 1, p. 164, doi. 10.29109/gujsc.1371519
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Influence of water uptake, gel network, and disintegration time on prednisone release from encapsulated solid dispersions.
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- Pharmaceutical Development & Technology, 2010, v. 15, n. 2, p. 184, doi. 10.3109/10837450903085434
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Design, Development and Optimization of a Novel Time and pH-Dependent Colon Targeted Drug Delivery System.
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- Pharmaceutical Development & Technology, 2009, v. 14, n. 1, p. 62, doi. 10.1080/10837450802409412
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Characterization and Physical Stability of Tolfenamic Acid-PVP K30 Solid Dispersions.
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- Pharmaceutical Development & Technology, 2007, v. 12, n. 1, p. 43, doi. 10.1080/10837450601166577
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