Chang Sun to Chemistry, Pharmaceutical
This is a "connection" page, showing publications Chang Sun has written about Chemistry, Pharmaceutical.
Connection Strength
11.203
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Direct compression tablet formulation of celecoxib enabled with a pharmaceutical solvate. Int J Pharm. 2021 Mar 01; 596:120239.
Score: 0.656
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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: 0.628
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Interfacial bonding in formulated bilayer tablets. Eur J Pharm Biopharm. 2020 Feb; 147:69-75.
Score: 0.608
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Relationship between hydrate stability and accuracy of true density measured by helium pycnometry. Int J Pharm. 2019 Aug 15; 567:118444.
Score: 0.587
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Computational Techniques for Predicting Mechanical Properties of Organic Crystals: A Systematic Evaluation. Mol Pharm. 2019 04 01; 16(4):1732-1741.
Score: 0.577
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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: 0.562
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Gaining insight into tablet capping tendency from compaction simulation. Int J Pharm. 2017 May 30; 524(1-2):111-120.
Score: 0.503
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Enabling the Tablet Product Development of 5-Fluorocytosine by Conjugate Acid Base Cocrystals. J Pharm Sci. 2016 06; 105(6):1960-1966.
Score: 0.475
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Macroindentation hardness measurement-Modernization and applications. Int J Pharm. 2016 Jun 15; 506(1-2):262-7.
Score: 0.472
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Mini review: Mechanisms to the loss of tabletability by dry granulation. Eur J Pharm Biopharm. 2016 Sep; 106:9-14.
Score: 0.470
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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: 0.435
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Cocrystallization for successful drug delivery. Expert Opin Drug Deliv. 2013 Feb; 10(2):201-13.
Score: 0.374
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Roles of granule size in over-granulation during high shear wet granulation. J Pharm Sci. 2010 Aug; 99(8):3322-5.
Score: 0.317
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On the identification of slip planes in organic crystals based on attachment energy calculation. J Pharm Sci. 2008 Aug; 97(8):3456-61.
Score: 0.276
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A material-sparing method for simultaneous determination of true density and powder compaction properties--aspartame as an example. Int J Pharm. 2006 Dec 01; 326(1-2):94-9.
Score: 0.240
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Predicting the tabletability of binary powder mixtures from that of individual components. Eur J Pharm Sci. 2025 Aug 01; 211:107151.
Score: 0.222
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Elucidating critical factors driving the tabletability flip phenomenon. Int J Pharm. 2025 Mar 15; 672:125337.
Score: 0.217
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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: 0.216
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Some properties and applications of the tabletability equation. Int J Pharm. 2025 Feb 25; 671:125246.
Score: 0.216
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Impact of route of particle engineering on dissolution performance of posaconazole. Int J Pharm. 2025 Jan 25; 669:125025.
Score: 0.214
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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: 0.206
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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: 0.165
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Recent Advances in Co-processed APIs and Proposals for Enabling Commercialization of These Transformative Technologies. Mol Pharm. 2020 07 06; 17(7):2232-2244.
Score: 0.157
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Toward a Molecular Understanding of the Impact of Crystal Size and Shape on Punch Sticking. Mol Pharm. 2020 04 06; 17(4):1148-1158.
Score: 0.154
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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: 0.152
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Tableting performance of various mannitol and lactose grades assessed by compaction simulation and chemometrical analysis. Int J Pharm. 2019 Jul 20; 566:24-31.
Score: 0.146
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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: 0.143
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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: 0.140
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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: 0.133
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Dependence of Friability on Tablet Mechanical Properties and a Predictive Approach for Binary Mixtures. Pharm Res. 2017 Dec; 34(12):2901-2909.
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: 0.130
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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: 0.129
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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: 0.114
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A new tablet brittleness index. Eur J Pharm Biopharm. 2015 Jun; 93:260-6.
Score: 0.110
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[Research about improving flowability of powder of Chinese herbs extracts by surface modification technology]. Zhongguo Zhong Yao Za Zhi. 2014 Dec; 39(23):4590-5.
Score: 0.107
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Massing in high shear wet granulation can simultaneously improve powder flow and deteriorate powder compaction: a double-edged sword. Eur J Pharm Sci. 2011 May 18; 43(1-2):50-6.
Score: 0.083
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Materials science tetrahedron--a useful tool for pharmaceutical research and development. J Pharm Sci. 2009 May; 98(5):1671-87.
Score: 0.073
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Improving powder flow properties of citric acid by crystal hydration. J Pharm Sci. 2009 May; 98(5):1744-9.
Score: 0.073
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Development of a high drug load tablet formulation based on assessment of powder manufacturability: moving towards quality by design. J Pharm Sci. 2009 Jan; 98(1):239-47.
Score: 0.071
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Influence of crystal structure on the tableting properties of n-alkyl 4-hydroxybenzoate esters (parabens). J Pharm Sci. 2007 Dec; 96(12):3324-33.
Score: 0.066
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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: 0.059
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True density of microcrystalline cellulose. J Pharm Sci. 2005 Oct; 94(10):2132-4.
Score: 0.057
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Quantifying errors in tableting data analysis using the Ryshkewitch equation due to inaccurate true density. J Pharm Sci. 2005 Sep; 94(9):2061-8.
Score: 0.056
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Simultaneously improving tabletability and solubility of diclofenac by cocrystallization with picolinamide. Int J Pharm. 2025 Feb 10; 670:125172.
Score: 0.054
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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: 0.053
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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: 0.051
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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: 0.041
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Resveratrol cocrystals with enhanced solubility and tabletability. Int J Pharm. 2016 Jul 25; 509(1-2):391-399.
Score: 0.030
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Development of highly stabilized curcumin nanoparticles by flash nanoprecipitation and lyophilization. Eur J Pharm Biopharm. 2015 Aug; 94:436-49.
Score: 0.028
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Near-infrared chemical imaging (NIR-CI) as a process monitoring solution for a production line of roll compaction and tableting. Eur J Pharm Biopharm. 2015 Jun; 93:293-302.
Score: 0.028