Spectrophotometry photodiode array

The scope of ultraviolet and visible spectrophotometry can be further extended when combined with a chromatographic separation step such as HPLC. The development of rapid-scanning detectors based on the linear photodiode array permits spectra to be acquired during the elution of peaks. Computer-aided manipulation of these spectra has led to new strategies for the examination of chromatographic peak homogeneity, based on classical techniques in spectroscopy. The use of microcomputers enables the development of archive retrieval methods for spectral characterisation (A. F. Fell etal, J. Chromat., 1984, 316, 423-440). 

Fortunately, automated fiber-optic probe-based dissolution systems have begun to appear for these solid dosage-form applications. One such system uses dip-type UV transflectance fiber-optic probes, each coupled to a miniature photodiode array (PDA) spectrophotometer to measure drug release in real time. This fiber-optic dissolution system can analyze immediate- and controlled-release formulations. The system is more accurate and precise than conventional dissolution test systems, and it is easier to set up than conventional manual sampling or automated sipper-sampling systems with analysis by spectrophotometry or HPLC. 

Complete MCP s can be stacked to provide even higher gains. For response in the vacuum ultra-violet spectral region (50-200 nm) a SSANACON, self-scanned anode array with microchannel plate electron multiplier, has been used (36). This involves photoelectron multiplication through two MOP S, collection of the electrons directly on aluminum anodes and readout with standard diode array circuitry. In cases where analyte concentrations are well above conventional detection limits, multi-element analysis with multi-channel detectors by atomic emission has been demonstrated to be quite feasible (37). Spectral source profiling has also been done with photodiode arrays (27.29.31). In molecular spectrometry, imaging type detectors have been used in spectrophotometry, spectrofluometry and chemiluminescence (23.24.26.33). These detectors are often employed to monitor the output from an HPLC or GC (13.38.39.40). 

SPD) and draw comparisons to PMT arrays as used in classical pol-ychromators. To a lesser extent, some comparisons are drawn with silicon intensified target vidicons (SIT) and intensified selfcanning photodiode array detectors (ISPD). A similar evaluation of the SPD for spectrophotometry and spectrofluorometry was recently published elsewhere (41). 

Y. Talmi, Spectrophotometry and spectrofluorometry with the self-scanned photodiode array, Appl. Spectrosc. 36 (1982) 1. 

Charge coupled detectors These devices are not yet commonly available in commercial instrumentation for analytical spectrophotometry although they are used in applications in inductively coupled plasma atomic emission spectrometry. However, they have found extensive application in imaging and astronomical applications. Essentially they are two-dimensional photodiode arrays which allow many spectra to be acquired in one readout. A typical array sensor is shown in Figure 9. 

Photodiode detectors have already been cited in this chapter in relation to near-IR fluorescence measurements on singlet oxygen,(8 16 18) in decay-time temperature sensing,(50) in liquid chromatography,(62) the study of proteins labelled with Nile Red,(64) and diode laser spectrometry,(67) Photodiodes are also conveniently packaged for many applications in an array form enabling rapid data acquisition e.g., in spectrophotometry, (35)... 

Classical transducers such as the photomultiplier tube and the photodiode have been used in most the flow systems [96,97], Since the 1980s, the tendency to use diode array spectrophotometers has increased, mainly for simultaneous determinations [98] and/or for implementing dual wavelength spectrophotometry [99], the latter being more exploited in segmented flow analysis. 

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