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  <controlfield tag="001">UP-1685675941131387418</controlfield>
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   <subfield code="a">LG 993.5 2023 P5</subfield>
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   <subfield code="a">Aldeguer, Thea Chariz B.</subfield>
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   <subfield code="a">Simultaneous determination and stability profiling of diphenhydramine and diazepam in human urine using a validated RP-HPLC-QTOF-MS method</subfield>
   <subfield code="c">Thea Chariz B. Aldeguer,  Rosalina A. Areola,  Vincent Morlie R. Tolentino ; adviser, Joanna V. Toralba,.</subfield>
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   <subfield code="a">Manila</subfield>
   <subfield code="b">Department of Pharmacy, College of Pharmacy, University of the Philippines Manila</subfield>
   <subfield code="c">2023</subfield>
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   <subfield code="a">xv, 158 leaves</subfield>
   <subfield code="c">23 cm.</subfield>
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   <subfield code="a">Thesis (Bachelor of Science in Pharmaceutical Sciences)--University of the Philippines Manila, June 2023</subfield>
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   <subfield code="a">Available to the public.</subfield>
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   <subfield code="a">Determination of the stability of drug analytes in biological samples and the development of reliable analytical methods for their detection are crucial for accurate analyses. For this research, diphenhydramine (DPH) and diazepam (DZP) stability profiles were investigated following the revalidation of a developed reversed-phase high performance liquid chromatography coupled with high resolution quadrupole time-of-flight mass spectrometry (RP-HPLC-QTOF-MS) method for their simultaneous determination. The method was specific for both drugs and showed acceptable degrees of linearity and accuracy. Intra-day and inter-day precision were satisfactory. The determined range was 15.625-250 ng/mL for DPH and 15.625-200 ng/mL for DZP. No significant matrix effect and carryover effect were obseved for both drugs. Autosampler stability under 4°C showed both drugs were stable for up to 72 hours. For benchtop stability studies, the drugs were only stable up to 1 hour at 20 to 26°C. Freeze-thaw stability studies revealed that both drugs were only stable up to one freeze-thaw cycle. Further qualitative analysis exhibited new fragments and peaks more polar than their parent compounds in both unstable samples of DPH and DZP. In conclusion, the study provides a validated RP-HPLC-QTOF-MS method that can simultaneously quantify DPH and DZP in human urine samples. Findings of the study significantly contribute to a better understanding of the stability of DPH and DZP in human urine. Moreover, it emphasizes the importance of immediate processing of samples and minimizing their exposure to high temperatures to ultimately preserve analyte stability and produce accurate test results and interpretations.</subfield>
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   <subfield code="a">Diphenhydramine.</subfield>
   <subfield code="x">Analysis.</subfield>
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   <subfield code="a">Diazepam</subfield>
   <subfield code="x">Analysis.</subfield>
   <subfield code="x">High performance liquid chromatography.</subfield>
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   <subfield code="a">Drug Stability</subfield>
   <subfield code="x">High-performance liquid chromatography.</subfield>
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   <subfield code="a">Areola, Rosalina A.  </subfield>
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   <subfield code="a">Tolentino, Vincent Morlie R. </subfield>
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   <subfield code="a">Toralba, Joanna V. </subfield>
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