These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

349 related items for PubMed ID: 31771033

  • 1. Real-time monitoring of pharmaceutical properties of medical tablets during direct tableting process by hybrid tableting process parameter-time profiles.
    Saito S, Hattori Y, Sakamoto T, Otsuka M.
    Biomed Mater Eng; 2020; 30(5-6):509-524. PubMed ID: 31771033
    [Abstract] [Full Text] [Related]

  • 2. Evaluation of tableting and tablet properties of Kollidon SR: the influence of moisture and mixtures with theophylline monohydrate.
    Hauschild K, Picker-Freyer KM.
    Pharm Dev Technol; 2006 Feb; 11(1):125-40. PubMed ID: 16544916
    [Abstract] [Full Text] [Related]

  • 3. Prediction of tablet properties based on near infrared spectra of raw mixed powders by chemometrics: Scale-up factor of blending and tableting processes.
    Otsuka M, Yamane I.
    J Pharm Sci; 2009 Nov; 98(11):4296-305. PubMed ID: 19530073
    [Abstract] [Full Text] [Related]

  • 4. Predictive evaluation of pharmaceutical properties of direct compression tablets containing theophylline anhydrate during storage at high humidity by near-infrared spectroscopy.
    Otsuka Y, Yamamoto M, Tanaka H, Otsuka M.
    Biomed Mater Eng; 2015 Nov; 25(3):223-36. PubMed ID: 26407109
    [Abstract] [Full Text] [Related]

  • 5. Prediction of tablet hardness based on near infrared spectra of raw mixed powders by chemometrics.
    Otsuka M, Yamane I.
    J Pharm Sci; 2006 Jul; 95(7):1425-33. PubMed ID: 16721793
    [Abstract] [Full Text] [Related]

  • 6. Real-time monitoring of changes of adsorbed and crystalline water contents in tablet formulation powder containing theophylline anhydrate at various temperatures during agitated granulation by near-infrared spectroscopy.
    Otsuka M, Kanai Y, Hattori Y.
    J Pharm Sci; 2014 Sep; 103(9):2924-2936. PubMed ID: 24832393
    [Abstract] [Full Text] [Related]

  • 7. Evaluation of the effect of granule size of raw tableting materials on critical quality attributes of tablets during the continuous tablet manufacturing process using near-infrared spectroscopy.
    Otsuka M, Ogata T, Hattori Y, Sasaki T.
    Drug Dev Ind Pharm; 2023 Nov; 49(11):692-702. PubMed ID: 37847490
    [Abstract] [Full Text] [Related]

  • 8. In-line monitoring of the drug content of powder mixtures and tablets by near-infrared spectroscopy during the continuous direct compression tableting process.
    Järvinen K, Hoehe W, Järvinen M, Poutiainen S, Juuti M, Borchert S.
    Eur J Pharm Sci; 2013 Mar 12; 48(4-5):680-8. PubMed ID: 23313622
    [Abstract] [Full Text] [Related]

  • 9. Orally Disintegrating Tablet Manufacture via Direct Powder Compression Using Cellulose Nanofiber as a Functional Additive.
    Nakamura S, Fukai T, Sakamoto T.
    AAPS PharmSciTech; 2021 Dec 23; 23(1):37. PubMed ID: 34950985
    [Abstract] [Full Text] [Related]

  • 10. Optimization of Premix Powders for Tableting Use.
    Todo H, Sato K, Takayama K, Sugibayashi K.
    Chem Pharm Bull (Tokyo); 2018 Jul 01; 66(7):748-756. PubMed ID: 29743471
    [Abstract] [Full Text] [Related]

  • 11. Influence of raw material properties upon critical quality attributes of continuously produced granules and tablets.
    Fonteyne M, Wickström H, Peeters E, Vercruysse J, Ehlers H, Peters BH, Remon JP, Vervaet C, Ketolainen J, Sandler N, Rantanen J, Naelapää K, De Beer T.
    Eur J Pharm Biopharm; 2014 Jul 01; 87(2):252-63. PubMed ID: 24589422
    [Abstract] [Full Text] [Related]

  • 12. Utility of Microcrystalline Cellulose for Improving Drug Content Uniformity in Tablet Manufacturing Using Direct Powder Compression.
    Nakamura S, Tanaka C, Yuasa H, Sakamoto T.
    AAPS PharmSciTech; 2019 Mar 22; 20(4):151. PubMed ID: 30903317
    [Abstract] [Full Text] [Related]

  • 13. Comparative evaluation of powder and tableting properties of low and high degree of polymerization cellulose I and cellulose II excipients.
    de la Luz Reus Medina M, Kumar V.
    Int J Pharm; 2007 Jun 07; 337(1-2):202-9. PubMed ID: 17376616
    [Abstract] [Full Text] [Related]

  • 14. Influence of excipients, drugs, and osmotic agent in the inner core on the time-controlled disintegration of compression-coated ethylcellulose tablets.
    Lin SY, Lin KH, Li MJ.
    J Pharm Sci; 2002 Sep 07; 91(9):2040-6. PubMed ID: 12210050
    [Abstract] [Full Text] [Related]

  • 15. Radial die-wall pressure as a reliable tool for studying the effect of powder water activity on high speed tableting.
    Abdel-Hamid S, Betz G.
    Int J Pharm; 2011 Jun 15; 411(1-2):152-61. PubMed ID: 21497644
    [Abstract] [Full Text] [Related]

  • 16. Prediction of tablet characteristics from residual stress distribution estimated by the finite element method.
    Hayashi Y, Miura T, Shimada T, Onuki Y, Obata Y, Takayama K.
    J Pharm Sci; 2013 Oct 15; 102(10):3678-86. PubMed ID: 23897300
    [Abstract] [Full Text] [Related]

  • 17. Effect of disintegrants on the properties of multiparticulate tablets comprising starch pellets and excipient granules.
    Mehta S, De Beer T, Remon JP, Vervaet C.
    Int J Pharm; 2012 Jan 17; 422(1-2):310-7. PubMed ID: 22101283
    [Abstract] [Full Text] [Related]

  • 18. Effect of friction between powder and tooling on the die-wall pressure evolution during tableting: Experimental and numerical results for flat and concave punches.
    Mazel V, Diarra H, Tchoreloff P.
    Int J Pharm; 2019 Jan 10; 554():116-124. PubMed ID: 30395955
    [Abstract] [Full Text] [Related]

  • 19. Predicting the Occurrence of Sticking during Tablet Production by Shear Testing of a Pharmaceutical Powder.
    Nakamura S, Otsuka N, Yoshino Y, Sakamoto T, Yuasa H.
    Chem Pharm Bull (Tokyo); 2016 Jan 10; 64(5):512-6. PubMed ID: 27150485
    [Abstract] [Full Text] [Related]

  • 20. A quality-by-design study for an immediate-release tablet platform: examining the relative impact of active pharmaceutical ingredient properties, processing methods, and excipient variability on drug product quality attributes.
    Kushner J, Langdon BA, Hicks I, Song D, Li F, Kathiria L, Kane A, Ranade G, Agarwal K.
    J Pharm Sci; 2014 Feb 10; 103(2):527-38. PubMed ID: 24375069
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.