Chang Sun to Solubility
This is a "connection" page, showing publications Chang Sun has written about Solubility.
Connection Strength
7.348
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Impact of route of particle engineering on dissolution performance of posaconazole. Int J Pharm. 2025 Jan 25; 669:125025.
Score: 0.839
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Relative Bioavailability Assessment of Solid Forms by An Artificial Stomach and Duodenum Apparatus. J Pharm Sci. 2024 08; 113(8):2506-2512.
Score: 0.808
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Mechanism for the Reduced Dissolution of Ritonavir Tablets by Sodium Lauryl Sulfate. J Pharm Sci. 2019 Jan; 108(1):516-524.
Score: 0.550
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Direct compression tablet formulation of trimetazidine through systematic screening of oxalate salts. Int J Pharm. 2025 Feb 25; 671:125255.
Score: 0.212
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Advancing the Harmonization of Biopredictive Methodologies through the Product Quality Research Institute (PQRI) Consortium: Biopredictive Dissolution of Dipyridamole Tablets. Mol Pharm. 2024 Oct 07; 21(10):5315-5325.
Score: 0.207
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Efficient determination of critical water activity and classification of hydrate-anhydrate stability relationship. J Pharm Sci. 2025 Jan; 114(1):127-135.
Score: 0.203
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Delaying the first nucleation event of amorphous solid dispersions above the polymer overlap concentration (c*): PVP and PVPVA in posaconazole. J Pharm Sci. 2025 Jan; 114(1):98-104.
Score: 0.201
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Modulating Pharmaceutical Properties of Berberine Chloride through Cocrystallization with Benzendiol Isomers. Pharm Res. 2023 Dec; 40(12):2791-2800.
Score: 0.189
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Profound effects of gastric secretion rate variations on the precipitation of erlotinib in duodenum - An in vitro investigation. Int J Pharm. 2022 May 10; 619:121722.
Score: 0.174
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Complexation with aromatic carboxylic acids expands the solid-state landscape of berberine. Int J Pharm. 2022 Apr 05; 617:121587.
Score: 0.173
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Simultaneous improvement of physical stability, dissolution, bioavailability, and antithrombus efficacy of Aspirin and Ligustrazine through cocrystallization. Int J Pharm. 2022 Mar 25; 616:121541.
Score: 0.172
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Formulation strategies for mitigating dissolution reduction of p-aminobenzoic acid by sodium lauryl sulfate through diffusion layer modulation. Int J Pharm. 2022 Jan 05; 611:121310.
Score: 0.170
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Pharmaceutical Lauryl Sulfate Salts: Prevalence, Formation Rules, and Formulation Implications. Mol Pharm. 2022 02 07; 19(2):432-439.
Score: 0.169
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Efficient development of sorafenib tablets with improved oral bioavailability enabled by coprecipitated amorphous solid dispersion. Int J Pharm. 2021 Dec 15; 610:121216.
Score: 0.169
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Novel Salt-Cocrystals of Berberine Hydrochloride with Aliphatic Dicarboxylic Acids: Odd-Even Alternation in Physicochemical Properties. Mol Pharm. 2021 04 05; 18(4):1758-1767.
Score: 0.162
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Development of piroxicam mini-tablets enabled by spherical cocrystallization. Int J Pharm. 2020 Nov 30; 590:119953.
Score: 0.157
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The efficient development of a sildenafil orally disintegrating tablet using a material sparing and expedited approach. Int J Pharm. 2020 Nov 15; 589:119816.
Score: 0.156
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Material-Sparing and Expedited Development of a Tablet Formulation of Carbamazepine Glutaric Acid Cocrystal- a QbD Approach. Pharm Res. 2020 Jul 23; 37(8):153.
Score: 0.155
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A microcrystalline cellulose based drug-composite formulation strategy for developing low dose drug tablets. Int J Pharm. 2020 Jul 30; 585:119517.
Score: 0.154
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Simultaneous taste-masking and oral bioavailability enhancement of Ligustrazine by forming sweet salts. Int J Pharm. 2020 Mar 15; 577:119089.
Score: 0.150
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A systematic evaluation of poloxamers as tablet lubricants. Int J Pharm. 2020 Feb 25; 576:118994.
Score: 0.149
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Crystallographic and Energetic Insights into Reduced Dissolution and Physical Stability of a Drug-Surfactant Salt: The Case of Norfloxacin Lauryl Sulfate. Mol Pharm. 2020 02 03; 17(2):579-587.
Score: 0.149
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Microstructures and pharmaceutical properties of ferulic acid agglomerates prepared by different spherical crystallization methods. Int J Pharm. 2020 Jan 25; 574:118914.
Score: 0.148
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Expedited Tablet Formulation Development of a Highly Soluble Carbamazepine Cocrystal Enabled by Precipitation Inhibition in Diffusion Layer. Pharm Res. 2019 Apr 23; 36(6):90.
Score: 0.142
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Improving solid-state properties of berberine chloride through forming a salt cocrystal with citric acid. Int J Pharm. 2019 Jan 10; 554:14-20.
Score: 0.137
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Improving Dissolution Rate of Carbamazepine-Glutaric Acid Cocrystal Through Solubilization by Excess Coformer. Pharm Res. 2017 12 29; 35(1):4.
Score: 0.130
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Expedited Development of Diphenhydramine Orally Disintegrating Tablet through Integrated Crystal and Particle Engineering. Mol Pharm. 2017 10 02; 14(10):3399-3408.
Score: 0.127
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Expedited development of a high dose orally disintegrating metformin tablet enabled by sweet salt formation with acesulfame. Int J Pharm. 2017 Oct 30; 532(1):435-443.
Score: 0.127
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Particle Engineering for Enabling a Formulation Platform Suitable for Manufacturing Low-Dose Tablets by Direct Compression. J Pharm Sci. 2017 07; 106(7):1772-1777.
Score: 0.123
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Mechanical Properties and Tableting Behavior of Amorphous Solid Dispersions. J Pharm Sci. 2017 01; 106(1):217-223.
Score: 0.119
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The development of carbamazepine-succinic acid cocrystal tablet formulations with improved in vitro and in vivo performance. Drug Dev Ind Pharm. 2016; 42(6):969-76.
Score: 0.111
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Validation and applications of an expedited tablet friability method. Int J Pharm. 2015 Apr 30; 484(1-2):146-55.
Score: 0.107
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Cocrystallization for successful drug delivery. Expert Opin Drug Deliv. 2013 Feb; 10(2):201-13.
Score: 0.092
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Simultaneously improving the mechanical properties, dissolution performance, and hygroscopicity of ibuprofen and flurbiprofen by cocrystallization with nicotinamide. Pharm Res. 2012 Jul; 29(7):1854-65.
Score: 0.087
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Solid-state properties and crystallization behavior of PHA-739521 polymorphs. Int J Pharm. 2006 Aug 17; 319(1-2):114-20.
Score: 0.058
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Simultaneously improving tabletability and solubility of diclofenac by cocrystallization with picolinamide. Int J Pharm. 2025 Feb 10; 670:125172.
Score: 0.053
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Development of direct compression Acetazolamide tablet with improved bioavailability in healthy human volunteers enabled by cocrystallization with p-Aminobenzoic acid. Int J Pharm. 2024 Mar 05; 652:123793.
Score: 0.049
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Harmonizing Biopredictive Methodologies Through the Product Quality Research Institute (PQRI) Part I: Biopredictive Dissolution of Ibuprofen and Dipyridamole Tablets. AAPS J. 2023 04 21; 25(3):45.
Score: 0.047
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A Rheological Approach for Predicting Physical Stability of Amorphous Solid Dispersions. J Pharm Sci. 2023 01; 112(1):204-212.
Score: 0.045
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The impact of solid-state form, water content and surface area of magnesium stearate on lubrication efficiency, tabletability, and dissolution. Pharm Dev Technol. 2021 Feb; 26(2):150-156.
Score: 0.040
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Polymer Nanocoating of Amorphous Drugs for Improving Stability, Dissolution, Powder Flow, and Tabletability: The Case of Chitosan-Coated Indomethacin. Mol Pharm. 2019 03 04; 16(3):1305-1311.
Score: 0.035
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Dapagliflozin-citric acid cocrystal showing better solid state properties than dapagliflozin. Eur J Pharm Sci. 2017 Jun 15; 104:255-261.
Score: 0.031
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Resveratrol cocrystals with enhanced solubility and tabletability. Int J Pharm. 2016 Jul 25; 509(1-2):391-399.
Score: 0.029
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Designing micellar nanocarriers with improved drug loading and stability based on solubility parameter. Mol Pharm. 2015 Mar 02; 12(3):816-25.
Score: 0.027
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Characterization of thermal behavior of deep eutectic solvents and their potential as drug solubilization vehicles. Int J Pharm. 2009 Aug 13; 378(1-2):136-9.
Score: 0.018