中国农学通报
中國農學通報
중국농학통보
CHINESE AGRICULTURAL SCIENCE BULLETIN
2013年
12期
164-167
,共4页
张龙涛%李昂%史怀%朱育菁%缪伏荣%冯玉兰%刘波
張龍濤%李昂%史懷%硃育菁%繆伏榮%馮玉蘭%劉波
장룡도%리앙%사부%주육정%무복영%풍옥란%류파
5-氨基乙酰丙酸%反向高效液相色谱法%柱前衍生%低浓度
5-氨基乙酰丙痠%反嚮高效液相色譜法%柱前衍生%低濃度
5-안기을선병산%반향고효액상색보법%주전연생%저농도
5-Aminolevulinic acid%reversed phase high performance liquid chromatography%precolumn derivation%low concentration
建立了一种柱前衍生反相高效液相色谱检测溶液中低浓度5-氨基乙酰丙酸的方法,填补了低浓度ALA的HPLC法检测的空白。使用Agilent SB-C18型色谱柱(250 mm×4.6 mm i.d.,5μm),以50 mM甲醇-醋酸钠缓冲溶液(pH 4.0)洗脱,流速为1 mL/min,柱温30℃,254 nm波长下检测10 min。在此条件下,5-氨基乙酰丙酸在浓度为1~1000 mg/L范围内与色谱峰面积值之间线性关系良好,回归系数均在0.9999以上。发酵液产物的加标回收率平均值为101.7%。将检测结果与分光光度法相比,符合较好。测试数据表明,此方法简单、可靠,对于低浓度的ALA测定效果良好。
建立瞭一種柱前衍生反相高效液相色譜檢測溶液中低濃度5-氨基乙酰丙痠的方法,填補瞭低濃度ALA的HPLC法檢測的空白。使用Agilent SB-C18型色譜柱(250 mm×4.6 mm i.d.,5μm),以50 mM甲醇-醋痠鈉緩遲溶液(pH 4.0)洗脫,流速為1 mL/min,柱溫30℃,254 nm波長下檢測10 min。在此條件下,5-氨基乙酰丙痠在濃度為1~1000 mg/L範圍內與色譜峰麵積值之間線性關繫良好,迴歸繫數均在0.9999以上。髮酵液產物的加標迴收率平均值為101.7%。將檢測結果與分光光度法相比,符閤較好。測試數據錶明,此方法簡單、可靠,對于低濃度的ALA測定效果良好。
건립료일충주전연생반상고효액상색보검측용액중저농도5-안기을선병산적방법,전보료저농도ALA적HPLC법검측적공백。사용Agilent SB-C18형색보주(250 mm×4.6 mm i.d.,5μm),이50 mM갑순-작산납완충용액(pH 4.0)세탈,류속위1 mL/min,주온30℃,254 nm파장하검측10 min。재차조건하,5-안기을선병산재농도위1~1000 mg/L범위내여색보봉면적치지간선성관계량호,회귀계수균재0.9999이상。발효액산물적가표회수솔평균치위101.7%。장검측결과여분광광도법상비,부합교호。측시수거표명,차방법간단、가고,대우저농도적ALA측정효과량호。
A reversed phase high performance liquid chromatography with precolumn derivation was developed for the determination of low concentration 5-aminolevulinic acid (ALA), filled the blank of low concentration of ALA detected by HPLC. An Agilent SB-C18 column (250 mm ×4.6 mm i.d., 5μm) was used for separation, and the elution was performed with methanol and 50 mmol/L sodium acetate solution (pH 4.0). The flow rate was 1 mL/min, the temperature of column was 30°C, and the detection wavelength was at 254 nm with the detection time of 10 minutes. The dynamic linear range was 1-1000 mg/L, and the correlation coefficient was above 0.9999. The average recoveries of ALA in 3 samples of fermentation were 101.7%. The results agreed well with those of spectrophotometry. So the developed method is simple and reliable for the determination of low concentration ALA.