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Journal Abstract Search

513 related items for PubMed ID: 29496456

  • 1. Formulation of a poorly water-soluble drug in sustained-release hollow granules with a high viscosity water-soluble polymer using a fluidized bed rotor granulator.
    Asada T, Yoshihara N, Ochiai Y, Kimura SI, Iwao Y, Itai S.
    Int J Pharm; 2018 Apr 25; 541(1-2):246-252. PubMed ID: 29496456
    [Abstract] [Full Text] [Related]

  • 2. An innovative method for the preparation of high API-loaded hollow spherical granules for use in controlled-release formulation.
    Asada T, Kobiki M, Ochiai Y, Iwao Y, Itai S.
    Int J Pharm; 2017 May 15; 523(1):167-175. PubMed ID: 28323098
    [Abstract] [Full Text] [Related]

  • 3. Influence of drug load on dissolution behavior of tablets containing a poorly water-soluble drug: estimation of the percolation threshold.
    Wenzel T, Stillhart C, Kleinebudde P, Szepes A.
    Drug Dev Ind Pharm; 2017 Aug 15; 43(8):1265-1275. PubMed ID: 28398095
    [Abstract] [Full Text] [Related]

  • 4. Mechanism of the formation of hollow spherical granules using a high shear granulator.
    Asada T, Nishikawa M, Ochiai Y, Noguchi S, Kimura SI, Iwao Y, Itai S.
    Eur J Pharm Sci; 2018 May 30; 117():371-378. PubMed ID: 29524593
    [Abstract] [Full Text] [Related]

  • 5. Development of a controlled release formulation by continuous twin screw granulation: Influence of process and formulation parameters.
    Vanhoorne V, Vanbillemont B, Vercruysse J, De Leersnyder F, Gomes P, Beer TD, Remon JP, Vervaet C.
    Int J Pharm; 2016 May 30; 505(1-2):61-8. PubMed ID: 27041123
    [Abstract] [Full Text] [Related]

  • 6. Preparation and characterization of Compritol 888 ATO matrix tablets for the sustained release of diclofenac sodium.
    Roberts M, Pulcini L, Mostafa S, Cuppok-Rosiaux Y, Marchaud D.
    Pharm Dev Technol; 2015 Jun 30; 20(4):507-12. PubMed ID: 24354893
    [Abstract] [Full Text] [Related]

  • 7. Development and characterisation of sustained release solid dispersion oral tablets containing the poorly water soluble drug disulfiram.
    Shergill M, Patel M, Khan S, Bashir A, McConville C.
    Int J Pharm; 2016 Jan 30; 497(1-2):3-11. PubMed ID: 26608620
    [Abstract] [Full Text] [Related]

  • 8. The impact of the injection mold temperature upon polymer crystallization and resulting drug release from immediate and sustained release tablets.
    Van Renterghem J, Dhondt H, Verstraete G, De Bruyne M, Vervaet C, De Beer T.
    Int J Pharm; 2018 Apr 25; 541(1-2):108-116. PubMed ID: 29409747
    [Abstract] [Full Text] [Related]

  • 9. Application of fluidized hot-melt granulation (FHMG) for the preparation of granules for tableting; properties of granules and tablets prepared by FHMG.
    Kidokoro M, Haramiishi Y, Sagasaki S, Shimizu T, Yamamoto Y.
    Drug Dev Ind Pharm; 2002 Jan 25; 28(1):67-76. PubMed ID: 11858526
    [Abstract] [Full Text] [Related]

  • 10. The effects of formulation factors on the moist granulation technique for controlled-release tablets.
    Railkar AM, Schwartz JB.
    Drug Dev Ind Pharm; 2001 Oct 25; 27(9):893-8. PubMed ID: 11763466
    [Abstract] [Full Text] [Related]

  • 11. Oral controlled release formulations of rifampicin. Part II: Effect of formulation variables and process parameters on in vitro release.
    Hiremath PS, Saha RN.
    Drug Deliv; 2008 Oct 25; 15(3):159-68. PubMed ID: 18379928
    [Abstract] [Full Text] [Related]

  • 12. Does the performance of wet granulation and tablet hardness affect the drug dissolution profile of carvedilol in matrix tablets?
    Košir D, Ojsteršek T, Vrečer F.
    Drug Dev Ind Pharm; 2018 Sep 25; 44(9):1543-1550. PubMed ID: 29848075
    [Abstract] [Full Text] [Related]

  • 13. Chitosan and sodium sulfate as excipients in the preparation of prolonged release theophylline tablets.
    Alsarra IA, El-Bagory I, Bayomi MA.
    Drug Dev Ind Pharm; 2005 May 25; 31(4-5):385-95. PubMed ID: 16093204
    [Abstract] [Full Text] [Related]

  • 14. Simplified formulations with high drug loads for continuous twin-screw granulation.
    Meier R, Thommes M, Rasenack N, Krumme M, Moll KP, Kleinebudde P.
    Int J Pharm; 2015 Dec 30; 496(1):12-23. PubMed ID: 26024821
    [Abstract] [Full Text] [Related]

  • 15. Two- and three-layer tablet drug delivery systems for oral sustained release of soluble and poorly soluble drugs.
    Efentakis M, Naseef H, Vlachou M.
    Drug Dev Ind Pharm; 2010 Aug 30; 36(8):903-16. PubMed ID: 20196641
    [Abstract] [Full Text] [Related]

  • 16. Influence of granulation temperature on particle size distribution of granules in twin-screw granulation (TSG).
    Ito A, Kleinebudde P.
    Pharm Dev Technol; 2019 Sep 30; 24(7):874-882. PubMed ID: 31169439
    [Abstract] [Full Text] [Related]

  • 17. Use of Drug Release Testing to Evaluate the Retention of Abuse-Deterrent Properties of Polyethylene Oxide Matrix Tablets.
    Meruva S, Rezaei L, Thool P, Donovan MD.
    AAPS PharmSciTech; 2020 Oct 06; 21(7):270. PubMed ID: 33025237
    [Abstract] [Full Text] [Related]

  • 18. Study of standard tablet formulation based on fluidized-bed granulation.
    Sunada H, Hasegawa M, Makino T, Sakamoto H, Fujita K, Tanino T, Kokubo H, Kawaguchi T.
    Drug Dev Ind Pharm; 1998 Mar 06; 24(3):225-33. PubMed ID: 9876579
    [Abstract] [Full Text] [Related]

  • 19. Tableting of hot-melt coated paracetamol granules: Material tableting properties and quality characteristics of the obtained tablets.
    Milanovic A, Aleksic I, Ibric S, Parojcic J, Cvijic S.
    Eur J Pharm Sci; 2020 Jan 15; 142():105121. PubMed ID: 31669762
    [Abstract] [Full Text] [Related]

  • 20. A new deferiprone controlled release system obtained by ultrasound-assisted compression.
    Aguilar-De-Leyva A, Gonçalves-Araujo T, Daza V, Caraballo I.
    Pharm Dev Technol; 2014 Sep 15; 19(6):728-34. PubMed ID: 23984972
    [Abstract] [Full Text] [Related]

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