THE PREPARATION OF A NEW PROTEIN BASED HPLC COLUMN PACKING MATERIAL AND ENANTIOMERIC RESOLUTION OF SOME PHARMACEUTICAL RELATED COMPOUNDS VIA THIS COLUMN
Chromatographic parameters such as Rs and α were calculated for each resoluted compounds.
📌 3 Maddede Bu Makale
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Amaç & Hipotez:In this study, BSA was bounded to 3-chloropropyl functionalized silica gel via ethylenediamine and glutaric dialdehyde.
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Temel Bulgular & Veri:The prepared CSP was packed into 150X4.6mm HPLC column according to slurry method.
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Sonuç & Katkı:Chromatographic parameters such as Rs and α were calculated for each resoluted compounds.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Enantiomeric separation · hplc · bovine serum albumin
Abstract
In this study, BSA was bounded to 3-chloropropyl functionalized silica gel via ethylenediamine and glutaric dialdehyde. The prepared CSP was packed into 150X4.6mm HPLC column according to slurry method. The enantiomeric resolution of some pharmaceutical related compounds such as rac-mandelic acid, rac-methyl mandelate, rac-epinephrine, rac-propranolol, rac-α-phenylethylamine and rac-3-hydroxybutyric acid was employed in 1mL/rpm, 1,5mL/rpm, 2mL/rpm, 2,5mL/rpm, 3mL/rpm flow rate in various pHs such pH=6, pH=7, pH=8 0,1M phosphate buffer. Chromatographic parameters such as Rs and α were calculated for each resoluted compounds.
ERDOĞAN, Ö., TOPAL, G., ÇAKMAK, R., SÜNKÜR, M., CANPOLAT, M. (2016). THE PREPARATION OF A NEW PROTEIN BASED HPLC COLUMN PACKING MATERIAL AND ENANTIOMERIC RESOLUTION OF SOME PHARMACEUTICAL RELATED COMPOUNDS VIA THIS COLUMN. Middle East Journal of Science, Cilt: 2 - Sayı: 1, 77–92. https://ajindex.com/articles/691592
Aboul-Enein, H. Y., & Ali, I. (2003). Chiral separations by liquid chromatography and related technologies (Vol. 90): CRC Press
Altria, K. D. (1996). Capillary electrophoresis guidebook: principles, operation, and applications (Vol. 52): Springer
Armstrong, D. W., Chang, C.-d., & Haing Lee, S. (1991). (R)-and (S)-Naphthylethylcarbamate-substituted β-cyclo-dextrin bonded stationary phases for the reversed-phase liquid chromatographic separation of enantiomers. Journal of Chromatography A, 539, 83-90
Bencini, A., Benelli, C., & Gatteschi, D. (1984). The angular overlap model for the description of the paramagnetic properties of transition metal complexes. Coordination chemistry reviews, 60, 131-169
Berthod, A., Chen, X., Kullman, J. P., Armstrong, D. W., Gasparrini, F., D'Acquaric, I., Villani, C., & Carotti, A. (2000). Role of the carbohydrate moieties in chiral recognition on teicoplanin-based LC stationary phases. Analytical chemistry, 72, 1767-1780
Bezhan Chankvetadze. (2012). Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers. Journal of Chromatography A, 1269, 26-51 [7] Bojarski, J., Aboul-Enein, H. Y., & Ghanem, A. (2005). What's new in chromatographic enantioseparations. Current Analytical Chemistry, 1, 59-77
Cabrera, K. (2004). Applications of silica‐based monolithic HPLC columns. Journal of separation science, 27, 843-852
Cakmak, R. (2008). PirkLe -tip kiral kolon kromotografisi yöntemiyle biyolojik öneme sahip kiral aminlerden (±)-β-metilfeniletilamin’in rezolüsyonu. Yüksek Lisans Tezi, Harran Üniversitesi
Caude, M., Tambuté, A., & Siret, L. (1991). Chiral stationary phases derived from tyrosine. Journal of Chromatography A, 550, 357-382
Cavazzini, A., Pasti, L., Massi, A., Marchetti, N., & Dondi, F. (2011). Recent applications in chiral high performance liquid chromatography: A review. Analytica Chimica Acta, 706, 205-222
Chankvetadze, B., Chankvetadze, L., Sidamonidze, S., Kasashima, E., Yashima, E., & Okamoto, Y. (1997). 3-Fluoro-, 3-chloro- and 3-bromo-5-methylphenylcarbamates of cellulose and amylose as chiral stationary phases for high-performance liquid chromatographic enantioseparation. Journal of Chromatography A, 787, 67-77
Chen, Z., Fuyumuro, T., Watabe, K., & Hobo, T. (2004). Influence of spacers and organic modifiers on chromatographic behaviors on chiral diamide stationary phase with N-(3, 5-dimethylbenzoyl)-D-p