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Journal Abstract Search

568 related items for PubMed ID: 24880992

  • 1. Towards a real time release approach for manufacturing tablets using NIR spectroscopy.
    Pestieau A, Krier F, Thoorens G, Dupont A, Chavez PF, Ziemons E, Hubert P, Evrard B.
    J Pharm Biomed Anal; 2014 Sep; 98():60-7. PubMed ID: 24880992
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  • 7. Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets.
    Shah RB, Tawakkul MA, Khan MA.
    J Pharm Sci; 2007 May; 96(5):1356-65. PubMed ID: 17455359
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  • 11. Process analytical technology for continuous manufacturing tableting processing: A case study.
    Pauli V, Roggo Y, Pellegatti L, Nguyen Trung NQ, Elbaz F, Ensslin S, Kleinebudde P, Krumme M.
    J Pharm Biomed Anal; 2019 Jan 05; 162():101-111. PubMed ID: 30227355
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  • 12. A "Large-N" Content Uniformity Process Analytical Technology (PAT) Method for Phenytoin Sodium Tablets.
    Pawar P, Talwar S, Reddy D, Bandi CK, Wu H, Sowrirajan K, Friedman R, Drazer G, Drennen JK, Muzzio FJ.
    J Pharm Sci; 2019 Jan 05; 108(1):494-505. PubMed ID: 30009795
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  • 13. Near-infrared spectroscopic analysis of the breaking force of extended-release matrix tablets prepared by roller-compaction: influence of plasticizer levels and sintering temperature.
    Dave VS, Fahmy RM, Hoag SW.
    Drug Dev Ind Pharm; 2015 Jun 05; 41(6):898-905. PubMed ID: 24785574
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  • 16. Content uniformity determination of pharmaceutical tablets using five near-infrared reflectance spectrometers: a process analytical technology (PAT) approach using robust multivariate calibration transfer algorithms.
    Sulub Y, LoBrutto R, Vivilecchia R, Wabuyele BW.
    Anal Chim Acta; 2008 Mar 24; 611(2):143-50. PubMed ID: 18328314
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  • 17. Quantitation of drug content in a low dosage formulation by transmission near infrared spectroscopy.
    Meza CP, Santos MA, Romañach RJ.
    AAPS PharmSciTech; 2006 Mar 24; 7(1):E29. PubMed ID: 16584160
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