WHO Expert Committee on Specifications for Pharmaceutical Preparations - WHO Technical Report Series, No. 863 - Thirty-fourth Report
(1996; 200 pages) Voir le document au format PDF
Table des matières
Afficher le document1. Introduction
Ouvrir ce répertoire et afficher son contenu2. The international pharmacopoeia and related activities
Afficher le document3. Simple test methodology
Ouvrir ce répertoire et afficher son contenu4. Stability of dosage forms
Ouvrir ce répertoire et afficher son contenu5. Good manufacturing practices for pharmaceutical products
Ouvrir ce répertoire et afficher son contenu6. Legal and administrative aspects of the functioning of national drug regulatory authorities
Ouvrir ce répertoire et afficher son contenu7. Quality assurance in the supply system
Afficher le document8. Terminology
Afficher le documentAcknowledgements
Afficher le documentReferences
Ouvrir ce répertoire et afficher son contenuAnnex 1 - Guidelines for the graphic representation of chemical formulae
Afficher le documentAnnex 2 - List of available International Chemical Reference Substances1
Afficher le documentAnnex 3 - List of available International Infrared Reference Spectra
Fermer ce répertoireAnnex 4 - General recommendations for the preparation and use of infrared spectra in pharmaceutical analysis
Afficher le document1. Introduction
Afficher le document2. Apparatus
Afficher le document3. Method of verification of frequency scale and resolution
Afficher le document4. Environment
Afficher le document5. Use of solvents
Afficher le document6. Preparation of the substance to be examined
Afficher le document7. Identification by reference substance
Afficher le document8. Identification by reference spectrum
Afficher le document9. Reflectance techniques
Ouvrir ce répertoire et afficher son contenuAnnex 5 - Guidelines for stability testing of pharmaceutical products containing well established drug substances in conventional dosage forms
Ouvrir ce répertoire et afficher son contenuAnnex 6 - Good manufacturing practices: guidelines on the validation of manufacturing processes
Ouvrir ce répertoire et afficher son contenuAnnex 7 - Good manufacturing practices: supplementary guidelines for the manufacture of investigational pharmaceutical products for clinical trials in humans
Ouvrir ce répertoire et afficher son contenuAnnex 8 - Good manufacturing practices: supplementary guidelines for the manufacture of herbal medicinal products1
Ouvrir ce répertoire et afficher son contenuAnnex 9 - Multisource (generic) pharmaceutical products: guidelines on registration requirements to establish interchangeability
Ouvrir ce répertoire et afficher son contenuAnnex 10 - Guidelines for implementation of the WHO Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce
Ouvrir ce répertoire et afficher son contenuAnnex 11 - Guidelines for the assessment of herbal medicines1,2
Ouvrir ce répertoire et afficher son contenuAnnex 12 - Guidelines on import procedures for pharmaceutical products
Afficher le documentBack Cover
 

2. Apparatus

Conventional infrared spectrometers disperse the infrared radiation by means of either gratings or prisms. The development of computerized laboratory equipment provides the additional option of using an interferometer coupled to a computer for the reduction of the data, by performing a Fourier transformation of the interferogram, to generate an infrared spectrum. These instruments are called Fourier transform infrared spectrometers (FTIRs). Apart from small differences in the low-frequency cut-off, all of the above types of infrared instruments generate comparable data and can generally be used interchangeably for qualitative analyses. However, each instrument will possess specific signal-to-noise and resolution characteristics.

Spectrophotometers suitable for use for identification tests should normally operate in the range 4000-600 cm-1 (2.5-16.7 µm) or in some cases up to 250 cm-1 (40 µm). If the attenuated total reflectance technique is to be used, the instrument must be equipped with a suitable attachment consisting of a single or multireflecting element. The attachment and a suitable mounting should permit its alignment in the spectrophotometer for maximum transmission.

vers la section précédente vers la section suivante
 

Dernière mise à jour: le 3 mai 2013