Preeklampsi Hastalığının Erken Tanısına Yönelik Hedeflenmiş Metabolomik Çalışmalar İçin Gc-Ms Yöntemi Geliştirilmesi

Göster/Aç
Tarih
2022-02-25Yazar
Kuş Kale Ayse
Ambargo Süresi
Acik erisimpublications
0
supporting
0
mentioning
0
contrasting
0
0
0
0
0
Citing PublicationsSupportingMentioningContrasting
See how this article has been cited at scite.ai
scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.
Üst veri
Tüm öğe kaydını gösterÖzet
Kus Kale., Development of GC-MS Method for Targeted Metabolomic Studies for Early Diagnosis of Preeclampsia Disease. Hacettepe University Graduate School Health Sciences, Analytical Chemistry Program, Master's Thesis, Ankara, 2022. Preeclampsia is a multisystem disease specific to human pregnancy with an unknown cause. It is characterized by increased systemic vascular resistance, increased platelet aggregation, activation of the coagulation system, and abnormal vascular response to localization associated with endothelial dysfunction. Metabolomics is the broad analysis of all metabolites in a biological system and is complementary to transcriptomic and proteomic analyzes as it provides a quantitative assessment of lower molecular weight analytes (˂1800 Da) in the system. In the thesis study, 2-hydroxy butyric acid, pyroglutamic acid, glutamic acid, 4-hydroxy glutamic acid, N-acetyl L-glutamic acid and N-carbamyl L-glutmic acid, which are thought to be differential in the early diagnosis of preeclampsia, were selected. The analyzes of these metabolites are 5% diphenyl 95% dimethylpolysiloxane (30 m × 0.25 mm, 0.25 μm) with capillary column at 60 oC (1 min), at 10 oC/min at 200 oC after 30 oC/min at 320 It was made by GC-MS method using helium as mobile phase, flow rate of 0.99 mL/min and myristic acid-d27 as internal standard, in the oven temperature program at oC (5 min). Developed method was validated by parameters of stability, selectivity, linearity, sensitivity, accuracy, precision, robustness and system suitability. The mean recovery was evaluated by applying the developed and validated method to blank plasma.