Analytical techniques, overview

LCEC has become a widely used analytical technique for biomedical analysis. Several reports appear each month deairibing new LCEC analyses or reporting results obtain-with LCEC. While space does not permit a complete review of all bitwhemical applications, this section will consider applications of LCEC to general classes of compounds to provide an overview of the uses of this technique. For a thorough survey of the literature, a bibliography of LCEC applications is available... 

Parkinson D-R, Dust JM (2010) Overview of the current status of sediment chemical analysis trends in analytical techniques. Environ Rev 18(NA) 37-59... 

Table 7.6 gives an overview about the analytical resolving power of various analytical techniques. 

In Table 1, the typical validation parameters required for the different types of analytical procedures are listed. For all these analytical procedures CE might be an appropriate analytical technique. In fact numerous validated CE methods for pharmaceutical analysis have been described in literature during the last decade.In Table 2, an overview is listed of the ICH validation parameters included in several reported CE validation studies. Since chiral purity determination is an important application area of CE methods, this test is listed separately as a specific analytical procedure. In addition, the determination of drug counterions has been included as a separate application. This overview illustrates that in general the required validation parameters are addressed in reported CE validation studies. It should be noted, however, that the validation parameters included in Table 2 are not necessarily evaluated exactly according ICH requirements in the reported references. Many pharmaceutical companies apply a phase-related validation approach in which the depth of validation depends on the clinical phase of development of the product involved. 

CE has been included as a distinct analytical technique in a general monograph in the Ph.Eur., JP, and USP. These monographs have been harmonized and at present only some minor differences exist between the different pharmacopoeias. They give an overview of the general principles, instrumental considerations, and the different separation modes. Also, attention is paid to quantification and system suitability aspects. 

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