Page 5 - Shimadzu i-Series Method Transfer System
P. 5

ACTO Function Achieves Higher Reproducibility






                                                                                                    ™
               The newly developed Analytical Condition Transfer and Optimization (ACTO) function incorporated in LabSolutions
               allows users to transfer injection timings matched to differences in system volumes between instruments, without
               editing the concentration gradient programs in existing methods.



                 More Optimal Method Transfer with a Simple Operation



               Reproducing analysis results is difficult even when the same columns and the same mobile phase conditions are used,
               because the gradient analysis start times differ due to differences in internal volumes between LC systems. With the
               ACTO function, differences in internal volume can be fine-tuned to heighten data reproducibility between different
               systems and streamline method transfer.



                           Sulfa Drug Analysis

                                   No ACTO Correction                After ACTO Correction
                            mAU                                mAU
                          40.0                               40.0                           Peaks
                          35.0                 Vendor A      35.0                 Vendor A  1. Sulfadiazine
                                               i-Series MT system                 i-Series MT system  2. Sulfamerazine
                          30.0                               30.0   1                      3. Sulfadimidine
                                 1
                          25.0     2                         25.0     2  3 4               4. Sulfamethoxypyridazine
                                                                                           5. Sulfamonomethoxine
                          20.0       3 4                     20.0                          6. Sulfamethoxazole
                                        5  6                               5  6  7         7. Sulfisoxazole
                          15.0              7    8 9         15.0                   8 9    8. Sulfadimethoxine
                          10.0                               10.0                          9. Sulfaquinoxaline Sodium
                           5.0                                5.0
                           0.0                                0.0
                          −5.0                               −5.0
                            0.0  2.5  5.0  7.5  10.0  12.5  15.0  17.5  20.0  22.5  min  0.0  2.5  5.0  7.5  10.0  12.5  15.0  17.5  20.0  22.5  min
                                                  0.486 min                                0.043 min







                           Ultraviolet Absorber Analysis


                                   No ACTO Correction                After ACTO Correction
                            mAU                                mAU
                           60                                 60                            Peaks
                                   2       4      Vendor B           2        4      Vendor B
                                      3           i-Series              3            i-Series   1. 2-Hydroxy-4-
                           50                                 50                            Methoxybenzophenone-
                                                  MT system                          MT system  5-Sulfonic Acid
                                                                                           2. 2,2’,4,4’-
                           40    1                 5          40    1                 5     Tetrahydroxybenzophenone
                                                                                           3. Ethyl p-Aminobenzoate
                           30                                 30                           4. 2,4-Dihydroxybenzophenone
                                                                                           5. 2,2’-Dihydroxy-4,4’-
                                                                                            Dimethoxybenzophenone
                           20                                 20
                           10                                 10
                           0                                  0
                            0.0  2.5  5.0  7.5  10.0  12.5  15.0  17.5  min  0.0  2.5  5.0  7.5  10.0  12.5  15.0  17.5  min
                                                  0.252 min                                 0.009 min







                                                                                                                   5
   1   2   3   4   5   6   7   8