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  1. Sohn Y, Lee SY, Lee GH, Na YJ, Kim SY, Seong I, Lee BJ, Kuh HJ, Lee J.
    Development of self-microemulsifying bilayer tablets for pH-independent fast release of candesartan cilexetil. Pharmazie. 2012; 67:917-24.

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  2. Cha KH, Cho KJ, Kim MS, Kim JS, Park HJ, Park J, Cho W, Park JS, Hwang SJ.
    Enhancement of the dissolution rate and bioavailability of fenofibrate by a melt-adsorption method using supercritical carbon dioxide.
    Int J Nanomedicine. 2012; 7:5565-75.

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  3. Beg S, Swain S, Singh HP, Patra ChN, Rao MB.
    Development, optimization, and characterization of solid self-nanoemulsifying drug delivery systems of valsartan using porous carriers.
    AAPS PharmSciTech. 2012; 13:1416-27.

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  4. Alam MA, Ali R, Al-Jenoobi FI, Al-Mohizea AM.
    Solid dispersions: a strategy for poorly aqueous soluble drugs and technology updates.
    Expert Opin Drug Deliv. 2012; 9:1419-40.

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  5. Janga KY, Jukanti R, Sunkavalli S, Velpula A, Bandari S, Kandadi P, Veerareddy PR.
    In situ absorption and relative bioavailability studies of zaleplon loaded self-nanoemulsifying powders.
    J Microencapsul. 2012.

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  6. Kallakunta VR, Bandari S, Jukanti R, Veerareddy PR.
    Oral self emulsifying powder of lercanidipine hydrochloride: Formulation and evaluation.
    Powder Technology. 2012; 221:375-82.

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  7. Kanuganti S, Jukanti R, Veerareddy PR, Bandari S.
    Paliperidone-Loaded Self-Emulsifying Drug Delivery Systems (SEDDS) for Improved Oral Delivery.
    J Disp Sci Tech. 2012; 33:506-15.

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  8. Hentzschel CM, Alnaief M, Smirnova I, Sakmann A, Leopold CS.
    Enhancement of griseofulvin release from liquisolid compacts.
    Eur J Pharm Biopharm. 2012; 80:130-5.

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  9. Mura P, Valleri M, Cirri M, Mennini N.
    New solid self-microemulsifying systems to enhance dissolution rate of poorly water soluble drugs.
    Pharm Dev Technol. 2012; 17:277-84.

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  10. Hentzschel CM, Sakmann A, Leopold CS.
    Suitability of various excipients as carrier and coating materials for liquisolid compacts.
    Drug Dev Ind Pharm. 2011; 37:1200-7.

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  11. Maclean J, Medina C, Daurio D, Alvarez-Nunez F, Jona J, Munson E, Nagapudi K.
    Manufacturing and performance evaluation of a stable amorphous complex of an acidic drug molecule and Neusilin.
    J Pharm Sci. 2011; 100:3332-44.

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  12. Boldhane SP, Kuchekar BS. Development and optimization of metoprolol succinate gastroretentive drug delivery system.
    Acta Pharm. 2010; 60:415-25.

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  13. Chakraborty S, Shukla D, Vuddanda PR, Mishra B, Singh S. Utilization of adsorption technique in the development of oral delivery system of lipid based nanoparticles.
    Colloids Surf B Biointerfaces. 2010; 81:563-9.

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  14. Hailu SA, Bogner RH. Complex effects of drug/silicate ratio, solid-state equivalent pH, and moisture on chemical stability of amorphous quinapril hydrochloride coground with silicates.
    J Pharm Sci. 2010.

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  15. Hailu SA, Bogner RH.
    Solid-state surface acidity and pH-stability profiles of amorphous quinapril hydrochloride and silicate formulations.
    J Pharm Sci. 2010; 99:2786-99.

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  16. Krupa A, Majda D, Jachowicz R, Mozgawa W.
    Solid-state interaction of ibuprofen and Neusilin US2.
    Thermochim Acta. 2010; 509:12-7.

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  17. Sander C, Holm P.
    Porous magnesium aluminometasilicate tablets as carrier of a cyclosporine self-emulsifying formulation.
    AAPS PharmSciTech. 2009; 10:1388-95.

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  18. Vadher AH, Parikh JR, Parikh RH, Solanki AB.
    Preparation and characterization of co-grinded mixtures of aceclofenac and Neusilin US2 for dissolution enhancement of aceclofenac.
    AAPS PharmSciTech. 2009; 10:606-14.

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  19. Hailu SA, Bogner RH.
    Effect of the pH grade of silicates on chemical stability of coground amorphous quinapril hydrochloride and its stabilization using pH-modifiers.
    J Pharm Sci. 2009; 98:3358-72.

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  20. Asai Y, Nohara M, Fujioka S, Isaji K, Nagira S.
    Application of Neusilin UFL2 on manufacturing of tablets using direct compression method, Development of core tablets containing the function of small degree of decrease of hardness at the humid conditions.
    Pharm Tech Japan. 2009; 25:67-70.

  21. Asai Y, Nagira S, Owaki T.
    Application of Isomalt on manufacturing of tablets using direct compression method.
    Pharm Tech Japan. 2009; 25:79-83.

  22. Agarwal V, Siddiqui A, Ali H, Nazzal S.
    Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS).
    Int J Pharm. 2009; 366:44-52.

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  23. Ruhland T, Nielsen SD, Holm P, Christensen CH.
    Nanoporous magnesium aluminometasilicate tablets for precise, controlled, and continuous dosing of chemical reagents and catalysts: applications in parallel solution-phase synthesis.
    J Comb Chem. 2007; 9:301-5.

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  24. Bahl D, Bogner RH.
    Amorphization of indomethacin by co-grinding with Neusilin US2: amorphization kinetics, physical stability and mechanism.
    Pharm Res. 2006; 23:2317-25.

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  25. Ito Y, Arai H, Uchino K, Iwasaki K, Shibata N, Takada K.
    Effect of adsorbents on the adsorption of lansoprazole with surfactant.
    Int J Pharm. 2005; 289:69-77.

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  26. Gupta MK, Vanwert A, Bogner RH.
    Formation of physically stable amorphous drugs by milling with Neusilin.
    J Pharm Sci. 2003; 92:536-51.

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  27. Gupta MK, Tseng YC, Goldman D, Bogner RH.
    Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules.
    Pharm Res. 2002; 19:1663-72.

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  28. Gupta MK, Bogner RH, Goldman D, Tseng YC.
    Mechanism for further enhancement in drug dissolution from solid-dispersion granules upon storage.
    Pharm Dev Technol. 2002; 7:103-12.

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  29. Gupta MK, Goldman D, Bogner RH, Tseng YC.
    Enhanced drug dissolution and bulk properties of solid-dispersions granulated with a surface adsorbent.
    Pharm Dev Technol. 2001; 6:563-72.

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  30. Konno T, Kinuno K, Physical and chemical changes of medicinal in mixtures with adsorbents in the solid state. II. Application of reduced pressure treatment for the improvement of dissolution of flufenamic acid. Chem Pharm Bull (Tokyo). 1989; 37:2481-4.

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  31. Konno T, Kinuno K, Kataoka K.
    Physical and chemical changes of medicinal in mixtures with adsorbents in the solid state. I. Effect of vapor pressure of the medicinal on changes in crystalline properties.
    Chem Pharm Bull (Tokyo). 1986; 34:301-7.

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