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Production and stability study of a hospital parenteral nutrition solution for neonates
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作者 Anne-Laure Yailian Céline Serre +7 位作者 Justine Fayard Marina Faucon Patrick Thomaré Samira Filali Christine Pivot Florence Vételé Fabrice Pirot Emmanuelle Olivier 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2019年第2期83-90,共8页
Standard parenteral nutrition solutions are mixtures comprising interacting components that may degrade themselves over time. The objective of this study was to investigate the physicochemical and microbiological stab... Standard parenteral nutrition solutions are mixtures comprising interacting components that may degrade themselves over time. The objective of this study was to investigate the physicochemical and microbiological stability of a hospital preparation for parenteral nutrition in neonatology. The analyses were performed throughout the storage of the preparations at 2–8 °C(up to 4 months). The extent of stability was based on the determination of amino acids dosage, visual and physicochemical properties(glucose and electrolytes concentrations, pH and osmolality measurements, particle counting) and microbiological analysis(sterility test). A thermal degradation of ascorbic acid was conducted to evaluate the antioxidant properties of the parenteral mixture. Physicochemical and microbiological controls were found to comply with the specifications. Amino acids showed a good stability throughout the 4 months storage except for cysteine, which was progressively degraded to cystine, conferring a yellow coloration to parenteral solutions. Parenteral nutrition standards solutions remain stable for 4 months at 2–8 °C,ensuring safe administration in preterm infants. 展开更多
关键词 STABILITY-INDICATING method study PARENTERAL nutrition NEONATOLOGY Amino ACIDS high-performance liquid chromatographic
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Research of Quality Standards for Stachydrine Hydrochloride in Chinese Medicine TJF Granule
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作者 Yao Lu Wei Yu +2 位作者 Pingniang Shen T. J. Khoo C. Wiart 《Pharmacology & Pharmacy》 2013年第3期277-282,共6页
A high-performance liquid chromatographic method was applied to the determination of stachydrine hydrochloride concentration in TJF granule (Chinese name: Tiao-Jing-Fang), using a mobile phase of methanol-acetonitrile... A high-performance liquid chromatographic method was applied to the determination of stachydrine hydrochloride concentration in TJF granule (Chinese name: Tiao-Jing-Fang), using a mobile phase of methanol-acetonitrile (50:50, v/v) by the Agilent Kromasi NH2 column (250 mm × 4.6 mm, 5 μm, S/N: 22N25110). Detection wavelength was 201 nm. The result revealed good linearity of stachydrine hydrochloride and was obtained within the range of 0.20 - 1.98 μg/mL (R = 0.9995). The average recovery was 97.01%;the relative standard deviation (RSD) was 0.19%. To the best of our knowledge, this is the first report dedicated to the determination of stachydrine hydrochloride by the evaporative light scattering detector-high-performance liquid chromatographic (ELSD-HPLC) method. 展开更多
关键词 TJF GRANULE Quality Standards Traditional Chinese Medicine EVAPORATIVE Light Scattering Detector (ELSD) high-performance liquid chromatographic (HPLC) method Stachydrine HYDROCHLORIDE PHARMACEUTICAL Analysis Determination
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