Fast Dissolving Curcumin Cocrystals
暂无分享,去创建一个
N. Rajesh Goud | Palash Sanphui | Ashwini Nangia | A. Nangia | U. B. Rao Khandavilli | N. R. Goud | Palash Sanphui | U. Khandavilli
[1] S. Bourne,et al. New polymorphs of isonicotinamide and nicotinamide. , 2011, Chemical communications.
[2] K. Balasubramanian. Molecular orbital basis for yellow curry spice curcumin's prevention of Alzheimer's disease. , 2006, Journal of agricultural and food chemistry.
[3] Abu T M Serajuddin,et al. Trends in solubility of polymorphs. , 2005, Journal of pharmaceutical sciences.
[4] J. Crison,et al. A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability , 1995, Pharmaceutical Research.
[5] N. Sugimoto,et al. Synthesis of water-soluble porphyrin and the corresponding highly planar benzoporphyrin without meso-substituents , 2005 .
[6] Jen-kun Lin,et al. Stability of curcumin in buffer solutions and characterization of its degradation products. , 1997, Journal of pharmaceutical and biomedical analysis.
[7] William Jones,et al. Solvent-drop grinding: green polymorph control of cocrystallisation. , 2004, Chemical communications.
[8] B. Stuart. Infrared Spectroscopy , 2004, Analytical Techniques in Forensic Science.
[9] Tejender S. Thakur,et al. Co-Crystals of the Anti-HIV Drugs Lamivudine and Zidovudine , 2009 .
[10] P. Matousek,et al. Characterization of New Cocrystals by Raman Spectroscopy, Powder X-ray Diffraction, Differential Scanning Calorimetry, and Transmission Raman Spectroscopy , 2010 .
[11] R. Planalp,et al. Curcumin: From ancient medicine to current clinical trials , 2008, Cellular and Molecular Life Sciences.
[12] Matthew L Peterson,et al. Celecoxib:nicotinamide dissociation: using excipients to capture the cocrystal's potential. , 2007, Molecular pharmaceutics.
[13] Hurng-Wern Huang,et al. Pyrogallol induces G2-M arrest in human lung cancer cells and inhibits tumor growth in an animal model. , 2009, Lung cancer.
[14] N. Schultheiss,et al. Improving the Poor Aqueous Solubility of Nutraceutical Compound Pterostilbene through Cocrystal Formation , 2011 .
[15] Ashwini Nangia,et al. Solubility Advantage of Amorphous Drugs and Pharmaceutical Cocrystals , 2011 .
[16] Orn Almarsson,et al. Crystal engineering of novel cocrystals of a triazole drug with 1,4-dicarboxylic acids. , 2003, Journal of the American Chemical Society.
[17] Daniel Normolle,et al. Dose escalation of a curcuminoid formulation , 2006, BMC complementary and alternative medicine.
[18] I. Kola,et al. Can the pharmaceutical industry reduce attrition rates? , 2004, Nature Reviews Drug Discovery.
[19] Peddy Vishweshwar,et al. Pharmaceutical co-crystals. , 2006, Journal of pharmaceutical sciences.
[20] L. Fábián,et al. New solid forms of artemisinin obtained through cocrystallisation , 2010 .
[21] G. P. Stahly,et al. A Survey of Cocrystals Reported Prior to 2000 , 2009 .
[22] Robert A Newman,et al. Bioavailability of curcumin: problems and promises. , 2007, Molecular pharmaceutics.
[23] Aeri Park,et al. Use of a Glutaric Acid Cocrystal to Improve Oral Bioavailability of a Low Solubility API , 2006, Pharmaceutical Research.
[24] W. Jordan,et al. Curcumin--a natural herb with anti-HIV activity. , 1996, Journal of the National Medical Association.
[25] P. Russo,et al. A novel solubility-enhanced curcumin formulation showing stability and maintenance of anticancer activity. , 2011, Journal of pharmaceutical sciences.
[26] N. Schultheiss,et al. Nutraceutical cocrystals: utilizing pterostilbene as a cocrystal former , 2010 .
[27] S. Byrn. Solid state chemistry of drugs , 1982 .
[28] Sheng Jiang,et al. Pyrogallol-based molecules as potent inhibitors of the antiapoptotic Bcl-2 proteins. , 2007, Journal of medicinal chemistry.
[29] R. M. Fisher,et al. An accurate reappraisal of the elemental form factors and charge density of copper , 1990 .
[30] M. Dinger,et al. Extended Structures Built on a Triphenoxymethane Platform − C3‐Symmetric, Conformational Mimics of Calix[n]arenes , 2000 .
[31] A. Shah,et al. Toxicity studies on Alpinia galanga and Curcuma longa. , 1992, Planta medica.
[32] G. Kuttan,et al. Anti-tumour and antioxidant activity of natural curcuminoids. , 1995, Cancer letters.
[33] B. Moulton,et al. Supramolecular medicinal chemistry: mixed-ligand coordination complexes. , 2007, Molecular pharmaceutics.
[34] G. Mahady,et al. Turmeric (Curcuma longa) and curcumin inhibit the growth of Helicobacter pylori, a group 1 carcinogen. , 2002, Anticancer research.
[35] G. G. Stokes. "J." , 1890, The New Yale Book of Quotations.
[36] Pui Shan Chow,et al. Trimorphs of a pharmaceutical cocrystal involving two active pharmaceutical ingredients: potential relevance to combination drugs , 2009 .
[37] Anthony L. Spek,et al. Journal of , 1993 .
[38] Tejender S. Thakur,et al. Polymorphs, Pseudopolymorphs, and Co-Crystals of Orcinol: Exploring the Structural Landscape with High Throughput Crystallography , 2011 .
[39] A. Newman,et al. Pharmaceutical Cocrystals and Their Physicochemical Properties , 2009, Crystal growth & design.
[40] Ranjit Thakuria,et al. Highly soluble olanzapinium maleate crystalline salts , 2011 .
[41] Raymond E. Davis,et al. Patterns in Hydrogen Bonding: Functionality and Graph Set Analysis in Crystals , 1995 .
[42] F. Vogt,et al. Solid-State NMR Analysis of Organic Cocrystals and Complexes , 2009 .
[43] S. Byrn,et al. Solid-state nuclear magnetic resonance spectroscopy--pharmaceutical applications. , 2003, Journal of pharmaceutical sciences.
[44] Bruno C. Hancock,et al. What is the True Solubility Advantage for Amorphous Pharmaceuticals? , 2000, Pharmaceutical Research.
[45] A. Bak,et al. Drug Substance and Former Structure Property Relationships in 15 Diverse Pharmaceutical Co-Crystals , 2009 .
[46] Sreenu Bhanoth,et al. New polymorphs of curcumin. , 2011, Chemical communications.
[47] Paolo Righi,et al. Crystal forms of rifaximin and their effect on pharmaceutical properties , 2008 .
[48] V. Dixit,et al. Bioavailability enhancement of curcumin by complexation with phosphatidyl choline. , 2011, Journal of pharmaceutical sciences.
[49] Na Sun,et al. Dissolution rate and apparent solubility of poorly soluble drugs in biorelevant dissolution media. , 2010, Molecular pharmaceutics.
[50] F. Krebs,et al. Crystal structures of 2,3,6,7,10,11-oxytriphenylenes. Implications for columnar discotic mesophases , 2000 .
[51] M. Otsuka,et al. Physicochemical Properties of Nitrofuratoin Anhydrate and Monohydrate and Their Dissolution , 1991 .
[52] S. Yalkowsky. Techniques of solubilization of drugs , 1981 .
[53] A. Glomme,et al. Comparison of a miniaturized shake-flask solubility method with automated potentiometric acid/base titrations and calculated solubilities. , 2005, Journal of pharmaceutical sciences.
[54] T. Osawa,et al. Involvement of the beta-diketone moiety in the antioxidative mechanism of tetrahydrocurcumin. , 1996, Biochemical pharmacology.
[55] Richard J. Gildea,et al. OLEX2: a complete structure solution, refinement and analysis program , 2009 .