A COMPUTER-PROGRAM FOR THE ANALYSIS OF CHROMATOGRAMS USED IN PHARMACOKINETIC STUDIES
Citation
Y. Yoshikawa et al., A COMPUTER-PROGRAM FOR THE ANALYSIS OF CHROMATOGRAMS USED IN PHARMACOKINETIC STUDIES, International journal of bio-medical computing, 38(3), 1995, pp. 269-276
Categorie Soggetti
Mathematical Methods, Biology & Medicine","Engineering, Biomedical","Computer Science Interdisciplinary Applications","Computer Science Theory & Methods
SICI code
0020-7101(1995)38:3<269:ACFTAO>2.0.ZU;2-5
Abstract
An analog/digital (A/D) converter and software written in BASIC langua
ge have been developed for the analysis of chromatographic data which
are needed for pharmacokinetic (PK) studies in humans and in experimen
tal animals such as dogs and rats. Using an A/D converter, widely sold
personal computers produced by NEC or EPSON are applicable to both hi
gh-performance liquid-chromatography (HPLC) data analysis and PK analy
sis. When chromatographic data is taken up by the computer and treated
as a variable, a maximum of 12 000 data points are saved by the compu
ter. As 10 digital data points are taken up by the computer per second
through the A/D converter, the maximum run time of a chromatogram is
20 min. For the purpose of HPLC analysis, however, five digital data p
oints per second are usually enough for routine analysis. In this soft
ware, the program is written to take and save five digital data points
/s. Therefore, the maximum run time of this software increased to 40 m
in per chromatogram. All the digital data through the A/D converter ar
e saved into the data file on a floppy disk or hard disk. For the chro
matogram analysis, both automatic peak identification and manual peak
identification, which must be selected with the use of the mouse drive
r, are available. All the data, peak area, peak height, etc. are also
saved into the data file. After a calibration curve is produced, follo
wing the input of peak analysis data of known spiked samples, the drug
concentration for each sample is estimated. These concentration-time
data are also saved into the data file. The plasma drug concentration-
time curve is plotted on the CRT display in semi-logarithmic scale, by
reading the saved plasma concentration-time data from the data file.
The drug concentration-time data finally obtained are saved into the d
ata disk, which then may be used for PK analysis. This system does not
require re-input of the data for PK analysis and thus significantly d
ecreases the work of re-input.