Bioanalytical method development and validation for the simultaneous estimation of Olanzapine and Samidorphan in rabbit plasma by using HPLC-MS/MS and application to pharmacokinetic study

被引:1
作者
Kantipudi, Rambabu [1 ]
Pavuluri, Sugandha Kumar [1 ]
机构
[1] RVR&JC Coll Engn, Dept Chem, Guntur 522019, AP, India
关键词
Development; HPLC-MS/MS; Olanzapine; Samidorphan; Validation; Rabbit plasma; ORTHOSTATIC HYPOTENSION;
D O I
10.1186/s43094-023-00570-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundSamidorphan is an opioid antagonist while Olanzapine is an effective medication for schizophrenia and bipolar disorder. A unique and accurate MS/HPLC approach due to simultaneous measurement of Olanzapine and Samidorphan is, therefore, more urgently required. Simultaneous quantification of Olanzapine and Samidorphan in rabbit plasma using HPLC-MS. Using a buffer composed of 1 mL of formic acid in 1 L of water and a mixture of two components, buffer and acetonitrile in a ratio of 50:50 and a flow rate of 1 mL/min at room temperature, we separated compounds on an Inertsil ODS column (250 x 4.6 mm, 5 m).ResultsAnalysis was performed within 8 min over a satisfactory linear concentration range of 2-40 ng/mL for Olanzapine (r2 = 0.99901 0.024) and 2-40 ng/mL for Samidorphan (r2 = 0.99927 0.012). The matrix effect recoveries of Olanzapine and Samidorphan at various QC concentration levels were 104.5, 100.51% and 110.36, 99.25%, respectively. The precision and recovery study outcomes fall within the acceptable range. An electrospray ionization source was used to analysis of Olanzapine and Samidorphan at m/z 313.40 -> 192.54, m/z 371.45 -> 220.61 for Olanzapine and Samidorphan, m/z 316.40 -> 237.58, m/z 374.41 -> 223.61 for D3 Olanzapine and D3 Samidorphan that were ion pairs of mass analysis.ConclusionsLiquid-liquid extraction was used to remove Olanzapine (0.17 mg/kg) and its reference standard (D3-Olanzapine) from rabbit plasma. Both the active compound Samidorphan (0.17 mg/kg) and its reference, D3-samidorphan, were isolated from rabbit plasma. We conducted stability studies to ensure that the medications would remain stable in accordance with USFDA regulations.
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页数:14
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