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Connection

Chang Sun to Tablets

This is a "connection" page, showing publications Chang Sun has written about Tablets.
Connection Strength

26.123
  1. Cocrystallization improves the tabletability of ligustrazine despite a reduction in plasticity. Int J Pharm. 2024 Apr 10; 654:123939.
    View in: PubMed
    Score: 0.860
  2. Air entrapment during tablet compression - Diagnosis, impact on tableting performance, and mitigation strategies. Int J Pharm. 2022 Mar 05; 615:121514.
    View in: PubMed
    Score: 0.743
  3. Tabletability Flip - Role of Bonding Area and Bonding Strength Interplay. J Pharm Sci. 2020 12; 109(12):3569-3573.
    View in: PubMed
    Score: 0.676
  4. 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.
    View in: PubMed
    Score: 0.670
  5. A microcrystalline cellulose based drug-composite formulation strategy for developing low dose drug tablets. Int J Pharm. 2020 Jul 30; 585:119517.
    View in: PubMed
    Score: 0.664
  6. Toward a Molecular Understanding of the Impact of Crystal Size and Shape on Punch Sticking. Mol Pharm. 2020 04 06; 17(4):1148-1158.
    View in: PubMed
    Score: 0.652
  7. Minimum Interfacial Bonding Strength for Bilayer Tablets Determined Using a Survival Test. Pharm Res. 2019 Jul 29; 36(10):139.
    View in: PubMed
    Score: 0.626
  8. Relationship between hydrate stability and accuracy of true density measured by helium pycnometry. Int J Pharm. 2019 Aug 15; 567:118444.
    View in: PubMed
    Score: 0.620
  9. 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.
    View in: PubMed
    Score: 0.614
  10. Mechanism for the Reduced Dissolution of Ritonavir Tablets by Sodium Lauryl Sulfate. J Pharm Sci. 2019 Jan; 108(1):516-524.
    View in: PubMed
    Score: 0.594
  11. Modulating Sticking Propensity of Pharmaceuticals Through Excipient Selection in a Direct Compression Tablet Formulation. Pharm Res. 2018 Mar 30; 35(6):113.
    View in: PubMed
    Score: 0.570
  12. A mesoporous silica based platform to enable tablet formulations of low dose drugs by direct compression. Int J Pharm. 2018 Mar 25; 539(1-2):184-189.
    View in: PubMed
    Score: 0.564
  13. Crystal and Particle Engineering Strategies for Improving Powder Compression and Flow Properties to Enable Continuous Tablet Manufacturing by Direct Compression. J Pharm Sci. 2018 04; 107(4):968-974.
    View in: PubMed
    Score: 0.559
  14. Dependence of Friability on Tablet Mechanical Properties and a Predictive Approach for Binary Mixtures. Pharm Res. 2017 Dec; 34(12):2901-2909.
    View in: PubMed
    Score: 0.552
  15. 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.
    View in: PubMed
    Score: 0.547
  16. Dependence of Punch Sticking on Compaction Pressure-Roles of Particle Deformability and Tablet Tensile Strength. J Pharm Sci. 2017 08; 106(8):2060-2067.
    View in: PubMed
    Score: 0.536
  17. Gaining insight into tablet capping tendency from compaction simulation. Int J Pharm. 2017 May 30; 524(1-2):111-120.
    View in: PubMed
    Score: 0.532
  18. 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.
    View in: PubMed
    Score: 0.531
  19. Tensile and shear methods for measuring strength of bilayer tablets. Int J Pharm. 2017 May 15; 523(1):121-126.
    View in: PubMed
    Score: 0.530
  20. Powder properties and compaction parameters that influence punch sticking propensity of pharmaceuticals. Int J Pharm. 2017 Apr 15; 521(1-2):374-383.
    View in: PubMed
    Score: 0.529
  21. Mechanism and Kinetics of Punch Sticking of Pharmaceuticals. J Pharm Sci. 2017 01; 106(1):151-158.
    View in: PubMed
    Score: 0.513
  22. Microstructure of Tablet-Pharmaceutical Significance, Assessment, and Engineering. Pharm Res. 2017 05; 34(5):918-928.
    View in: PubMed
    Score: 0.506
  23. Mini review: Mechanisms to the loss of tabletability by dry granulation. Eur J Pharm Biopharm. 2016 Sep; 106:9-14.
    View in: PubMed
    Score: 0.497
  24. A critical Examination of the Phenomenon of Bonding Area - Bonding Strength Interplay in Powder Tableting. Pharm Res. 2016 May; 33(5):1126-32.
    View in: PubMed
    Score: 0.490
  25. 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.
    View in: PubMed
    Score: 0.481
  26. Dependence of tablet brittleness on tensile strength and porosity. Int J Pharm. 2015 Sep 30; 493(1-2):208-13.
    View in: PubMed
    Score: 0.474
  27. Tabletability Modulation Through Surface Engineering. J Pharm Sci. 2015 Aug; 104(8):2645-8.
    View in: PubMed
    Score: 0.469
  28. Validation and applications of an expedited tablet friability method. Int J Pharm. 2015 Apr 30; 484(1-2):146-55.
    View in: PubMed
    Score: 0.460
  29. A formulation strategy for solving the overgranulation problem in high shear wet granulation. J Pharm Sci. 2014 Aug; 103(8):2434-40.
    View in: PubMed
    Score: 0.440
  30. A pitfall in analyzing powder compactibility data using nonlinear regression. J Pharm Sci. 2013 Mar; 102(3):1135-6.
    View in: PubMed
    Score: 0.398
  31. Overcoming poor tabletability of pharmaceutical crystals by surface modification. Pharm Res. 2011 Dec; 28(12):3248-55.
    View in: PubMed
    Score: 0.357
  32. Initial moisture content in raw material can profoundly influence high shear wet granulation process. Int J Pharm. 2011 Sep 15; 416(1):43-8.
    View in: PubMed
    Score: 0.357
  33. 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.
    View in: PubMed
    Score: 0.301
  34. On the mechanism of reduced tabletability of granules prepared by roller compaction. Int J Pharm. 2008 Jan 22; 347(1-2):171-2; author reply 173-4.
    View in: PubMed
    Score: 0.276
  35. Reduced tabletability of roller compacted granules as a result of granule size enlargement. J Pharm Sci. 2006 Jan; 95(1):200-6.
    View in: PubMed
    Score: 0.244
  36. Quantifying errors in tableting data analysis using the Ryshkewitch equation due to inaccurate true density. J Pharm Sci. 2005 Sep; 94(9):2061-8.
    View in: PubMed
    Score: 0.239
  37. A new insight into the mechanism of the tabletability flip phenomenon. Int J Pharm. 2024 Apr 10; 654:123956.
    View in: PubMed
    Score: 0.215
  38. Worsened punch sticking by external lubrication with magnesium stearate. Int J Pharm. 2024 Jan 05; 649:123636.
    View in: PubMed
    Score: 0.211
  39. The ubiquity of the tabletability flip phenomenon. Int J Pharm. 2023 Aug 25; 643:123262.
    View in: PubMed
    Score: 0.206
  40. Understanding the role of magnesium stearate in lowering punch sticking propensity of drugs during compression. Int J Pharm. 2023 Jun 10; 640:123016.
    View in: PubMed
    Score: 0.203
  41. An approach for predicting the true density of powders based on in-die compression data. Int J Pharm. 2023 Apr 25; 637:122875.
    View in: PubMed
    Score: 0.201
  42. An extended macroindentation method for determining the hardness of poorly compressible materials. Int J Pharm. 2022 Aug 25; 624:122054.
    View in: PubMed
    Score: 0.192
  43. Effect of deaeration on processability of poorly flowing powders by roller compaction. Int J Pharm. 2022 Jun 10; 621:121803.
    View in: PubMed
    Score: 0.189
  44. Complexation with aromatic carboxylic acids expands the solid-state landscape of berberine. Int J Pharm. 2022 Apr 05; 617:121587.
    View in: PubMed
    Score: 0.187
  45. Efficient development of sorafenib tablets with improved oral bioavailability enabled by coprecipitated amorphous solid dispersion. Int J Pharm. 2021 Dec 15; 610:121216.
    View in: PubMed
    Score: 0.183
  46. Direct compression tablet formulation of celecoxib enabled with a pharmaceutical solvate. Int J Pharm. 2021 Mar 01; 596:120239.
    View in: PubMed
    Score: 0.173
  47. Modulation of the powder properties of lamotrigine by crystal forms. Int J Pharm. 2021 Feb 15; 595:120274.
    View in: PubMed
    Score: 0.173
  48. Development of piroxicam mini-tablets enabled by spherical cocrystallization. Int J Pharm. 2020 Nov 30; 590:119953.
    View in: PubMed
    Score: 0.170
  49. Profound tabletability deterioration of microcrystalline cellulose by magnesium stearate. Int J Pharm. 2020 Nov 30; 590:119927.
    View in: PubMed
    Score: 0.170
  50. The efficient development of a sildenafil orally disintegrating tablet using a material sparing and expedited approach. Int J Pharm. 2020 Nov 15; 589:119816.
    View in: PubMed
    Score: 0.169
  51. Molecular Origin of the Distinct Tabletability of Loratadine and Desloratadine: Role of the Bonding Area - Bonding Strength Interplay. Pharm Res. 2020 Jun 28; 37(7):133.
    View in: PubMed
    Score: 0.167
  52. Reduction of Punch-Sticking Propensity of Celecoxib by Spherical Crystallization via Polymer Assisted Quasi-Emulsion Solvent Diffusion. Mol Pharm. 2020 04 06; 17(4):1387-1396.
    View in: PubMed
    Score: 0.164
  53. A systematic evaluation of poloxamers as tablet lubricants. Int J Pharm. 2020 Feb 25; 576:118994.
    View in: PubMed
    Score: 0.161
  54. Interfacial bonding in formulated bilayer tablets. Eur J Pharm Biopharm. 2020 Feb; 147:69-75.
    View in: PubMed
    Score: 0.161
  55. Microstructures and pharmaceutical properties of ferulic acid agglomerates prepared by different spherical crystallization methods. Int J Pharm. 2020 Jan 25; 574:118914.
    View in: PubMed
    Score: 0.160
  56. Tableting performance of various mannitol and lactose grades assessed by compaction simulation and chemometrical analysis. Int J Pharm. 2019 Jul 20; 566:24-31.
    View in: PubMed
    Score: 0.154
  57. Effects of Water on Powder Flowability of Diverse Powders Assessed by Complimentary Techniques. J Pharm Sci. 2019 08; 108(8):2613-2620.
    View in: PubMed
    Score: 0.153
  58. Developing Biologics Tablets: The Effects of Compression on the Structure and Stability of Bovine Serum Albumin and Lysozyme. Mol Pharm. 2019 03 04; 16(3):1119-1131.
    View in: PubMed
    Score: 0.152
  59. Direct Compression Tablet Containing 99% Active Ingredient-A Tale of Spherical Crystallization. J Pharm Sci. 2019 04; 108(4):1396-1400.
    View in: PubMed
    Score: 0.149
  60. Improving solid-state properties of berberine chloride through forming a salt cocrystal with citric acid. Int J Pharm. 2019 Jan 10; 554:14-20.
    View in: PubMed
    Score: 0.148
  61. A systematic evaluation of dual functionality of sodium lauryl sulfate as a tablet lubricant and wetting enhancer. Int J Pharm. 2018 Dec 01; 552(1-2):139-147.
    View in: PubMed
    Score: 0.148
  62. Comparative analyses of flow and compaction properties of diverse mannitol and lactose grades. Int J Pharm. 2018 Jul 30; 546(1-2):39-49.
    View in: PubMed
    Score: 0.143
  63. Relating the tableting behavior of piroxicam polytypes to their crystal structures using energy-vector models. Int J Pharm. 2018 May 30; 543(1-2):46-51.
    View in: PubMed
    Score: 0.142
  64. Systematic evaluation of common lubricants for optimal use in tablet formulation. Eur J Pharm Sci. 2018 May 30; 117:118-127.
    View in: PubMed
    Score: 0.141
  65. Improving Dissolution Rate of Carbamazepine-Glutaric Acid Cocrystal Through Solubilization by Excess Coformer. Pharm Res. 2017 12 29; 35(1):4.
    View in: PubMed
    Score: 0.140
  66. Expedited Development of Diphenhydramine Orally Disintegrating Tablet through Integrated Crystal and Particle Engineering. Mol Pharm. 2017 10 02; 14(10):3399-3408.
    View in: PubMed
    Score: 0.137
  67. Tablets of multi-unit pellet system for controlled drug delivery. J Control Release. 2017 Sep 28; 262:222-231.
    View in: PubMed
    Score: 0.136
  68. Mechanical Properties and Tableting Behavior of Amorphous Solid Dispersions. J Pharm Sci. 2017 01; 106(1):217-223.
    View in: PubMed
    Score: 0.129
  69. Analytical method development for powder characterization: Visualization of the critical drug loading affecting the processability of a formulation for direct compression. J Pharm Biomed Anal. 2016 Sep 05; 128:462-468.
    View in: PubMed
    Score: 0.126
  70. Resveratrol cocrystals with enhanced solubility and tabletability. Int J Pharm. 2016 Jul 25; 509(1-2):391-399.
    View in: PubMed
    Score: 0.126
  71. Enabling the Tablet Product Development of 5-Fluorocytosine by Conjugate Acid Base Cocrystals. J Pharm Sci. 2016 06; 105(6):1960-1966.
    View in: PubMed
    Score: 0.126
  72. Macroindentation hardness measurement-Modernization and applications. Int J Pharm. 2016 Jun 15; 506(1-2):262-7.
    View in: PubMed
    Score: 0.125
  73. A new tablet brittleness index. Eur J Pharm Biopharm. 2015 Jun; 93:260-6.
    View in: PubMed
    Score: 0.116
  74. Enabling tablet product development of 5-fluorocytosine through integrated crystal and particle engineering. J Pharm Sci. 2014 Apr; 103(4):1126-32.
    View in: PubMed
    Score: 0.107
  75. Evolution of structure and properties of granules containing microcrystalline cellulose and polyvinylpyrrolidone during high-shear wet granulation. J Pharm Sci. 2014 Jan; 103(1):207-15.
    View in: PubMed
    Score: 0.105
  76. 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.
    View in: PubMed
    Score: 0.093
  77. 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.
    View in: PubMed
    Score: 0.088
  78. Transforming powder mechanical properties by core/shell structure: compressible sand. J Pharm Sci. 2010 Nov; 99(11):4458-62.
    View in: PubMed
    Score: 0.085
  79. Roles of granule size in over-granulation during high shear wet granulation. J Pharm Sci. 2010 Aug; 99(8):3322-5.
    View in: PubMed
    Score: 0.084
  80. Materials science tetrahedron--a useful tool for pharmaceutical research and development. J Pharm Sci. 2009 May; 98(5):1671-87.
    View in: PubMed
    Score: 0.077
  81. Influence of crystal structure on the tableting properties of n-alkyl 4-hydroxybenzoate esters (parabens). J Pharm Sci. 2007 Dec; 96(12):3324-33.
    View in: PubMed
    Score: 0.070
  82. Mechanism of moisture induced variations in true density and compaction properties of microcrystalline cellulose. Int J Pharm. 2008 Jan 04; 346(1-2):93-101.
    View in: PubMed
    Score: 0.068
  83. 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.
    View in: PubMed
    Score: 0.063
  84. True density of microcrystalline cellulose. J Pharm Sci. 2005 Oct; 94(10):2132-4.
    View in: PubMed
    Score: 0.060
  85. Evaluation of the effects of tableting speed on the relationships between compaction pressure, tablet tensile strength, and tablet solid fraction. J Pharm Sci. 2005 Mar; 94(3):465-72.
    View in: PubMed
    Score: 0.058
  86. A novel method for deriving true density of pharmaceutical solids including hydrates and water-containing powders. J Pharm Sci. 2004 Mar; 93(3):646-53.
    View in: PubMed
    Score: 0.054
  87. Improved tableting properties of p-hydroxybenzoic acid by water of crystallization: a molecular insight. Pharm Res. 2004 Feb; 21(2):382-6.
    View in: PubMed
    Score: 0.053
  88. 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.
    View in: PubMed
    Score: 0.053
  89. 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.
    View in: PubMed
    Score: 0.051
  90. Nanomechanical testing in drug delivery: Theory, applications, and emerging trends. Adv Drug Deliv Rev. 2022 04; 183:114167.
    View in: PubMed
    Score: 0.047
  91. Effects of compaction and storage conditions on stability of intravenous immunoglobulin - Implication on developing oral tablets of biologics. Int J Pharm. 2021 Jul 15; 604:120737.
    View in: PubMed
    Score: 0.044
  92. 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.
    View in: PubMed
    Score: 0.043
  93. Effect of Hydroxypropyl Cellulose Level on Twin-Screw Melt Granulation of Acetaminophen. AAPS PharmSciTech. 2020 Aug 24; 21(7):240.
    View in: PubMed
    Score: 0.042
  94. Molecular Interpretation of the Compaction Performance and Mechanical Properties of Caffeine Cocrystals: A Polymorphic Study. Mol Pharm. 2020 01 06; 17(1):21-31.
    View in: PubMed
    Score: 0.040
  95. 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.
    View in: PubMed
    Score: 0.038
  96. Dapagliflozin-citric acid cocrystal showing better solid state properties than dapagliflozin. Eur J Pharm Sci. 2017 Jun 15; 104:255-261.
    View in: PubMed
    Score: 0.033
  97. 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.
    View in: PubMed
    Score: 0.029
  98. Understanding size enlargement and hardening of granules on tabletability of unlubricated granules prepared by dry granulation. J Pharm Sci. 2011 Feb; 100(2):758-66.
    View in: PubMed
    Score: 0.021
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.