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. 2013 Aug 17;86:189–197. doi: 10.1016/j.jpba.2013.08.010

Table 3.

Recoveries, matrix effects and stability of neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, 3,5-dicaffeoylquinic acid and 3,4-dicaffeoylquinic acid (n = 6).

Compound Concentration (ng ml−1) Recovery
Matrix effect
Freeze-thaw cycles
At −70 °C for 1 month
Autosampler for 24 h
Average (%) RSD (%) Average (%) RSD (%) Remain (%) RSD (%) Remain (%) RSD (%) Remain (%) RSD (%)
Neochlorogenic acid 1.50 40.09 12.4 97.9 6.2 106.8 6.7 102.6 8.3 91.4 13.8
20.0 40.6 10.4 110.2 1.3 92.9 13.4 107.3 14.1 108.2 14.1
250 42.0 8.2 110.7 11.8 100.9 4.6 85.7 13.8 88.2 9.0



Chlorogenic acid 1.00 59.9 11.5 101.9 8.7 99.2 7.5 108.7 11.0 98.5 9.9
25.0 67.7 12.7 113.3 5.5 110.6 8.5 114.9 10.5 111.8 11.8
650 60.7 4.6 111.4 2.4 98.9 6.8 90.0 11.1 87.8 11.6



Cryptochlorogenic acid 4.00 57.7 8.1 102.1 8.7 91.2 11.4 100.7 12.5 114.3 12.7
25.0 64.0 10.8 102.2 9.8 96.8 7.3 105.4 13.4 86.6 9.9
160 58.7 4.1 97.1 14.3 105.4 10.1 104.4 9.6 99.3 6.1



3,5-dicaffeoylquinic acid 1.50 75.0 14.5 98.5 6.5 92.5 7.2 111.3 12.6 104.5 5.1
20.0 82.8 8.1 103.2 10.4 87.7 11.8 85.2 12.8 90.8 13.7
250 77.3 11.7 113.6 1.0 88.4 8.6 93.3 10.8 94.4 10.2



3,4-dicaffeoylquinic acid 10.0 80.4 10.2 104.6 4.6 95.6 11.1 93.9 11.3 98.3 10.1
45.0 70.9 13.6 102.0 7.2 97.5 9.8 108.8 8.3 86.0 12.5
220 89.6 9.6 112.6 9.6 108.4 9.0 86.1 11.23 86.86 11.2