pharmaceutical impurity analysis solutions - Lcms-connect.com
pharmaceutical impurity analysis solutions - Lcms-connect.com
pharmaceutical impurity analysis solutions - Lcms-connect.com
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AmAU40Chlorhexidine, spiked with 1 ppm PGIsDAD 260 nm30201002 3 4 5 6 7min1PGI 5, 166.1>130.0 (80.4%)010×10 -21PGI 4, 163.1>120.0 (98.3%)PGI 6, 150.1>108.0 (3.8%, coelution with API)B2000PGI 5, 166.1>130.00×10 -110×10 -110PGI 7, 129.1>93.0 (79.1%)PGI 3, 136.1>121.0 (101.7%)100010002000PGI 4, 163.1>120.0PGI 6, 150.1>108.0PGI 3, 136.1>121.0×10 21PGI 8, 128.1>93.0 (Present in API, > 20 ppm)500PGI 7, 129.1>93.00×10 -21PGI 2, 126.1>111.0 (96.0%)1000PGI 8, 128.1>93.00×10 -110PGI 9, 122.1>105.1 (98.5%)100500PGI 2, 126.1>111.0PGI 9, 122.1>105.1×10 -210PGI 1, 119.1>92.0 (89.6%)2 3 4 5 6 7Counts (%) vs. Acquisition Time (min)250PGI 1, 119.1>92.00.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4Counts vs. Acquisition Time (min)Figure 15. DAD result and quantifier MRM transitions for the <strong>analysis</strong> of a chlorohexidine sample spiked with PGIs. A <strong>com</strong>parison is shown between results achievedwith 150 mm column (A) and 50 mm column (B) Agilent ZORBAX Eclipse Plus C18 RRHD (2.1 mm id, 1.8 μm) columns. Transitions and calculated recoveries are alsoindicated. See Agilent publication 5990-5732EN.22