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العنوان
Studying the Effect of Non Thermal Plasma on Myelogenous Leukemia Cell Lines \
المؤلف
Abdel monem, Amal Elsayed Elarabi.
هيئة الاعداد
باحث / أمل السيد العربى عبد المنعم
مشرف / فاطمة مختار فوده
مشرف / جمال جابر العريجي
مشرف / عبد المنصف عبد العزيز الحضري
تاريخ النشر
2021.
عدد الصفحات
127 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
علم الحيوان والطب البيطري
تاريخ الإجازة
1/1/2021
مكان الإجازة
جامعة عين شمس - كلية البنات - علم الحيوان (علم وظائف الاعضاء)
الفهرس
Only 14 pages are availabe for public view

Abstract

Gliding Arc Discharge (GAD) non thermal plasma is one type of important new technology in the field of biomedical applications, such as skin disease, wound healing and cancer treatment. This low temperature atmospheric-pressure plasma is a multi-component system that includes biologically active agents, charged particles, reactive nitrogen and oxygen species, metastable-state molecules or atoms, and UV radiation. The main objective of this study is to investigate the effect of Gliding Arc Discharge on Acute Myelogenous leukemia cell line (AML). Different doses depends on time of exposure (40, 60 and 80 sec) applied for one time, the cells going for culture 72 hours. Two types of analysis were carried out. The first one is 3- (4, 5-dimethyl thiazol-2yl)-2,5-diphenyl tetrazolium bromide (MTT) assay where the viability of cell showed significant decrease in all treated samples, also its realised that increasing the time of exposure leads to a good treatment. the second analysis was molecular proteomics assay for two genes which are caspase-3 and cox-2 gene. It was found that, exposure for non thermal plasma gliding arc increase the level of gene transcription(protein expression)of caspase-3 gene (Apoptotic gene) which lead to more degradation of malignant cells, where the transcription of cox-2 gene (inflammatory gene) were reduced.
Conclusion: The gliding Arc non thermal plasma have a highly toxic effect on leukemia (blood cancer), and mechanism of action coming from, the chemical and physical component of the plasma on transcription of apoptotic genes and tumorgenesis genes.