دورية أكاديمية

Comparison of commercial 5-aminolevulinic acid (Gliolan®) and the pharmacy-compounded solution fluorescence in glioblastoma.

التفاصيل البيبلوغرافية
العنوان: Comparison of commercial 5-aminolevulinic acid (Gliolan®) and the pharmacy-compounded solution fluorescence in glioblastoma.
المؤلفون: Garfias Arjona, Santiago, Lara Almunia, Mónica, Ibáñez Domínguez, Javier Ángel, Delgado Sánchez, Olga, Villalonga, Priam, Villalonga-Planells, Ruth, Pierola Lopetegui, Javier, Bestard Escalas, Joan, Maimó Barceló, Albert, Brell Doval, Marta
المصدر: Acta Neurochirurgica; Aug2019, Vol. 161 Issue 8, p1733-1741, 9p, 2 Diagrams, 2 Charts, 3 Graphs
مصطلحات موضوعية: FLUORESCENCE, CELL lines, CONFOCAL microscopy, FLOW cytometry, AMINOLEVULINIC acid
مستخلص: Background: 5-Aminolevulinic acid (5-ALA) has become an important assistant in glioblastoma (GB) surgery. Unfortunately, its price affects its widespread use. Objective: The aim of this study was to compare commercial 5-ALA with the pharmacy-compounded solution. Methods: Using first an in vitro experimental approach, different concentrations of the pharmacy-compounded solution and commercial 5-ALA were tested in U87MG, LN229, U373, and T98G commercial glioblastoma cell lines. Fluorescence intensity was compared for each concentration by flow cytometry. Mean fluorescence of culture supernatant and lysate samples were analyzed. In a second phase, both preparations were used for surgical glioblastoma resection and tumor samples were analyzed by confocal microscopy. Mean fluorescence intensity was analyzed for each preparation and compared. Results: There was a high variability of fluorescence intensity between cell lines, but each cell line showed similar fluorescence for both preparations (compounded preparation and commercial 5-ALA). In the same way, both preparations had similar fluorescence intensity in glioblastoma samples. Conclusion: Both, compounded and commercial 5-ALA preparations produce equivalent fluorescent responses in human glioblastoma cells. Fluorescence intensity is cell line specific, but fluorescent properties of both preparations are undistinguishable. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:00016268
DOI:10.1007/s00701-019-03930-4