New nano radio medicine for tumor long term study and early diagnosis of tuomr
محل انتشار: سومین سمپوزیوم بین المللی سرطان نسترن
سال انتشار: 1396
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 551
نسخه کامل این مقاله ارائه نشده است و در دسترس نمی باشد
- صدور گواهی نمایه سازی
- من نویسنده این مقاله هستم
این مقاله در بخشهای موضوعی زیر دسته بندی شده است:
استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
NASTARANCANSER03_036
تاریخ نمایه سازی: 7 اسفند 1396
چکیده مقاله:
The purpose of this study is to develop an appropriate radiopharmaceutical agent in long-term imaging for improved diagnosis and evaluation of tumors (and also,in inflammation and infectious foci), whichis an important goal in nuclear medicine. Liposomes, as pharmaceutical nanocarriers, have been extensively studied in pharmaceutical industry and depending on their structural characteristics can bedisposed in various pathological sites in the body. PEGylated liposomes have smaller volume of distribution and decreased clearance, consequently, due to their more prolonged presence in bloodstream and maintaining their stability during this period, these liposomes can be applied for imaging blood vessel and identifying hemorrhagic ,infectious and tumoral sites. In this study, liposomal formulations encapsulating albumin is synthesized by solvent evaporation method along with homogenization, and their characteristics including size, zeta potential and encapsulation efficiency were assessed. Then these liposomes labeled by Philips method and the rate of stability of labeled liposomes in serum and ultimately the rate of biodistribution and gamma scintigraphy in C26-colon carcinoma tumor-bearing mice were studied. The result of the study of liposomal characteristics displayed that synthesized liposomes have a size of about 130 nanometers, and capable of accumulating in tumor sites based of EPR phenomenon. these liposomes also have high stability for maintaining encapsulated albumin in a long time. In the study of biodistribution of these liposomes in mice, they accumulated more in the kidney, liver, spleen and tumor sites, which even after clearing formulations in the bloodstream, they existed in high levels in these organs up to 96 hours. In gamma scintigraphy also, organs with high activity accumulation from early hours up to 96 hours, were visible in the form of hot spots. In sum, concluded that PEGylated liposomal formulation encapsulating albumin can be labeled with In-Oxine , and obtained stabilized formulation for long-term imaging of organs, which compared to In-IgG and In-Liposome, that have more favorable conditions for the evaluation of tumors and it will cause early diagnosis of tumors
کلیدواژه ها:
نویسندگان
Mohamad Ahrari
Department Of Biology, Facalty of Sciences Mashhad Branch, Islamic Azad University, Mashhad Iran
Mahmoud Raza Jafari
Department Of Medicine, Mashhad University Of Medical Sciences, Mashhad, Iran
Keyvan Sadri
Department Of Medicine, Mashhad University Of Medical Sciences, Mashhad, Iran
Jafar Rahnama
Department Of Medicine, Mashhad University Of Medical Sciences, Mashhad, Iran