Literature DB >> 14727870

A novel method for analyzing thick tablets by near infrared spectroscopy.

J L Ramirez1, M K Bellamy, R J Romañac.   

Abstract

A near-infrared (NIR) spectroscopic method to determine content uniformity of a large, thick tablet using an approach that could facilitate future validations has been developed. A CT ibuprofen 800-mg tablet weighs about 1150 mg and is about 18.6 mm wide and 7.6 mm thick. The FT NIR spectrometer was optimized for transmission spectra of the tablets by moving it to the sample compartment and placing it immediately behind the tablet. In spite of this dedicated setup, the transmission spectra obtained were very poor, indicating that the NIR radiation was not reaching the detector. The spectra of the tablet improved with use of a simple preparation in which a flat-face die applies pressure of 20 000 psi to the tablet; this reduced the thickness of the tablet from 7.6 mm to 3.6 mm. A calibration model was developed for tablets with drug content ranging from 70% to 130% of label. The calibration model was tested using a validation set of tablets with a drug content of 752, 800, and 848 mg. The results obtained were within 1.5% of the known drug content of the validation set tablets. Even with the sample preparation, the content uniformity results of 10 tablets could be determined using this method in less than 1 hour. The approach described in this article could also be used to validate NIR content uniformity methods for other formulations.

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Year:  2001        PMID: 14727870      PMCID: PMC2750576          DOI: 10.1208/pt020311

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  12 in total

1.  Development and validation of a method for the analysis of a pharmaceutical preparation by near-infrared diffuse reflectance spectroscopy.

Authors:  M Blanco; J Coello; A Eustaquio; H Iturriaga; S Maspoch
Journal:  J Pharm Sci       Date:  1999-05       Impact factor: 3.534

2.  Automated system for the on-line monitoring of powder blending processes using near-infrared spectroscopy. Part I. System development and control.

Authors:  P A Hailey; P Doherty; P Tapsell; T Oliver; P K Aldridge
Journal:  J Pharm Biomed Anal       Date:  1996-03       Impact factor: 3.935

3.  The use of near-infrared spectroscopy in the efficient prediction of a specification for the residual moisture content of a freeze-dried product.

Authors:  M W Derksen; P J van de Oetelaar; F A Maris
Journal:  J Pharm Biomed Anal       Date:  1998-07       Impact factor: 3.935

4.  Moisture determination in hygroscopic drug substances by near infrared spectroscopy.

Authors:  X Zhou; P Hines; M W Borer
Journal:  J Pharm Biomed Anal       Date:  1998-06       Impact factor: 3.935

5.  On-line monitoring of powder blend homogeneity by near-infrared spectroscopy.

Authors:  S S Sekulic; H W Ward; D R Brannegan; E D Stanley; C L Evans; S T Sciavolino; P A Hailey; P K Aldridge
Journal:  Anal Chem       Date:  1996-02-01       Impact factor: 6.986

6.  Near-infrared spectroscopic characterization of pharmaceutical powder blends.

Authors:  D J Wargo; J K Drennen
Journal:  J Pharm Biomed Anal       Date:  1996-08       Impact factor: 3.935

7.  Use of near-infrared spectroscopy to evaluate an active in a film coated tablet.

Authors:  B R Buchanan; M A Baxter; T S Chen; X Z Qin; P A Robinson
Journal:  Pharm Res       Date:  1996-04       Impact factor: 4.200

8.  Vibrational spectrometry for the assessment of active substance in metoprolol tablets: a comparison between transmission and diffuse reflectance near-infrared spectrometry.

Authors:  J Gottfries; H Depui; M Fransson; M Jongeneelen; M Josefson; F W Langkilde; D T Witte
Journal:  J Pharm Biomed Anal       Date:  1996-08       Impact factor: 3.935

9.  Nondestructive near-infrared analysis of intact tablets for determination of degradation products.

Authors:  J K Drennen; R A Lodder
Journal:  J Pharm Sci       Date:  1990-07       Impact factor: 3.534

10.  Assay of effervescent tablets by near-infrared spectroscopy in transmittance and reflectance mode: acetylsalicylic acid in mono and combination formulations.

Authors:  P Merckle; K A Kovar
Journal:  J Pharm Biomed Anal       Date:  1998-07       Impact factor: 3.935

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  2 in total

1.  Quantitation of drug content in a low dosage formulation by transmission near infrared spectroscopy.

Authors:  Carlos Peroza Meza; María A Santos; Rodolfo J Romañach
Journal:  AAPS PharmSciTech       Date:  2017-03-08       Impact factor: 3.246

2.  Quantitative determination of hydrate content of theophylline powder by chemometric X-ray powder diffraction analysis.

Authors:  Makoto Otsuka; Hajime Kinoshita
Journal:  AAPS PharmSciTech       Date:  2010-02-02       Impact factor: 3.246

  2 in total

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