Palsson B O, Shen B Q, Meyerhoff M E, Trojanowicz M
Department of Chemical Engineering, University of Michigan, Ann Arbor 48109-040.
Analyst. 1993 Nov;118(11):1361-5. doi: 10.1039/an9931801361.
A novel split stream flow injection (FI) system suitable for the simultaneous determination of L-glutamine and ammonia nitrogen (ammonia-N) in cell culture media is described. Potentiometric detection of ammonia-N in one portion of the manifold is achieved using a commercial ammonia gas-sensing electrode fitted with a wall-jet cap. L-Glutamine is quantified in the other part of the split sample by potentiometric detection of ammonium ions (by an ammonium-selective polymer membrane electrode), liberated from the hydrolysis of glutamine after the sample flows through a glass bead reactor containing immobilized glutaminase. Endogenous ammonia-N and potassium ions that would normally interfere with the glutamine measurement are removed upstream using a unique tubular cation-exchange unit. Using 50 microliters sample volumes and mixed solutions of ammonium chloride and L-glutamine in Iscove's Modified Dulbecco's Medium to calibrate the FI measuring system, values for ammonia-N and L-glutamine determined for 22 media samples obtained from a bioreactor growing retroviral producer cells correlate well with those measured with commercial, manual enzymic-spectrophotometric assay kits.
本文描述了一种新型分流流动注射(FI)系统,该系统适用于同时测定细胞培养基中的L-谷氨酰胺和氨氮(氨-N)。在流路的一部分中,使用配备壁流帽的商用氨气敏电极对氨-N进行电位检测。在分流样品的另一部分中,通过对样品流经装有固定化谷氨酰胺酶的玻璃珠反应器后谷氨酰胺水解产生的铵离子(通过铵选择性聚合物膜电极)进行电位检测,对L-谷氨酰胺进行定量。使用独特的管状阳离子交换单元在样品上游去除通常会干扰谷氨酰胺测量的内源性氨-N和钾离子。使用50微升的样品体积以及在伊斯科夫改良杜尔贝科培养基中的氯化铵和L-谷氨酰胺混合溶液来校准FI测量系统,从培养逆转录病毒生产细胞的生物反应器中获得的22个培养基样品中测定的氨-N和L-谷氨酰胺值与使用商用手动酶促分光光度测定试剂盒测量的值相关性良好。