Intravenous tigecycline with selected multichamber bag parenteral nutrition: A compatibility study

被引:0
|
作者
Dettlaff, Katarzyna [1 ]
Guzinska, Julia [1 ]
Klimaszewska, Marta [1 ]
Dominiak, Katarzyna [1 ]
Jelinska, Anna [1 ]
机构
[1] Poznan Univ Med Sci, Chair & Dept Pharmaceut Chem, Rokietnicka 3, PL-60806 Poznan, Poland
关键词
intravenous administration; particle size; turbidity; zeta potential; PHYSICAL COMPATIBILITY; IV DRUGS; STABILITY;
D O I
10.1002/jpen.2683
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Tigecycline is widely used to treat infections in intensive care units. Drugs often need to be delivered to critically ill patients feeding by parenteral nutrition (PN). Before two preparations are administered in the same infusion line, the safety of this combination should be established. The objective of this study was to determine the compatibility of tigecycline with selected multichamber bag PN (MCB-PN). Methods: Tigecycline was diluted in 0.9% sodium chloride solution and 5% glucose solution to obtain two 0.5 mg/ml solutions. Then the solutions were combined with selected MCB-PN in appropriate proportions. The samples were visually assessed, and pH, osmolality, turbidity, particle size, and zeta potential were measured. These measurements were made immediately after combining the solutions and after 4 h of storage at 23 degrees C +/- 1 degrees C. Results: It was determined that the pH values of the mixtures after combining with tigecycline changed by <= 0.1 unit. An increase in zeta potential was recorded, excluding one combination of tigecycline with the mixture. For all samples tested, the particle size distribution was within the acceptable range immediately after combination and after 4 h of storage. The difference in osmolality did not exceed +/- 3%, whereas the zeta potential decreased for only one combination. The turbidity of none of the samples exceeded a critical value. Conclusion: The physical compatibility of the tigecycline with five MCB-PN was proved. They can therefore be administered to patients in one infusion line using the Y-site.
引用
收藏
页码:990 / 997
页数:8
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