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References Dept of Pharmaceutics, JSSCP, Mysore 228 1. Nkansah P, Antipas A, Lu Y, Varma M, Rotter C, Rago B, El-Kattan A, Taylor G, Rubio M, Litchfield J. Development and evaluation of novel solid nanodispersion system for oral delivery of poorly water-soluble drugs. J Control Release. 2013;169:150-61. 2. Elder DP, Holm R, Diego HLD. Use of pharmaceutical salts and cocrystals to address the issue of poor solubility. Int J Pharm. 2013;453:88-100. 3. Shayanfar A, Zeynali KA, Jouyban A. Solubility and dissolution rate of a carbamazepine-cinnamic acid cocrystal. J Mol Liquids. 2013;187:171-6. 4. Kawakami K. Modification of physicochemical characteristics of active pharmaceutical ingredients and application of supersaturatable dosage forms for improving bioavailability of poorly absorbed drugs. Adv Drug Deliv Rev. 2012;64:480-95. 5. Liversidge EM, Liversidge GG. Nanosizing for oral and parenteral drug delivery: A perspective on formulating poorly-water soluble compounds using wet media milling technology. Adv Drug Deliv Rev. 2011;63:427-40. 6. Baird JA, Taylor LS. Evaluation of amorphous solid dispersion properties using thermal analysis techniques. Adv Drug Deliv Rev. 2012;64:396-421. 7. Aqil F, Munagala R, Jeyabalan J, Vadhanam MV. Bioavailability of phytochemicals and its enhancement by drug delivery systems. Cancer Letters 2013;334:133-41. 8. Elder D, Holm R. Aqueous solubility: Simple predictive methods (in silico, in vitro and bio-relevant approaches). Int J Pharm. 2013;453(1):3-11.

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References

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1. Nkansah P, Antipas A, Lu Y, Varma M, Rotter C, Rago B, El-Kattan A,

Taylor G, Rubio M, Litchfield J. Development and evaluation of novel solid

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