医药前沿
醫藥前沿
의약전연
YIAYAO QIANYAN
2014年
14期
117-118,119
,共3页
陈雷%刘铖%朱良兴%李贺然
陳雷%劉鋮%硃良興%李賀然
진뢰%류성%주량흥%리하연
头孢克洛%AfPGA%工艺%分离纯化
頭孢剋洛%AfPGA%工藝%分離純化
두포극락%AfPGA%공예%분리순화
cefaclor%AfPGA. Process%Separation and purification
目的:本文通过实验考察了AfPGA催化合成头孢克洛的工艺及其产物的分离纯化方法,最终确定最优反应条件为:pH(7.0);温度(25℃);缓冲体系(磷酸钠);酶投入量(3U/mL);底物浓度(7-ACCA60mmol/L,苯甘氨酸甲酯120mmol/L)。在此条件下底物转化率将达到85%以上,产物纯度可超过99.5%,杂质含量低于0.5%。
目的:本文通過實驗攷察瞭AfPGA催化閤成頭孢剋洛的工藝及其產物的分離純化方法,最終確定最優反應條件為:pH(7.0);溫度(25℃);緩遲體繫(燐痠鈉);酶投入量(3U/mL);底物濃度(7-ACCA60mmol/L,苯甘氨痠甲酯120mmol/L)。在此條件下底物轉化率將達到85%以上,產物純度可超過99.5%,雜質含量低于0.5%。
목적:본문통과실험고찰료AfPGA최화합성두포극락적공예급기산물적분리순화방법,최종학정최우반응조건위:pH(7.0);온도(25℃);완충체계(린산납);매투입량(3U/mL);저물농도(7-ACCA60mmol/L,분감안산갑지120mmol/L)。재차조건하저물전화솔장체도85%이상,산물순도가초과99.5%,잡질함량저우0.5%。
this article through the experiment investigates the AfPGA catalytic synthesis of cefaclor process and product separation and purification method, final y the optimal reaction conditions were determined as: pH (7.0); Temperature (25℃); (sodium phosphate buffer system); Enzyme mass (3u/mL); The substrate concentration (7-ACCA60mmol/L, methyl phenyl glycine tendency for 120/L). Under the condition of the substrate conversion rate wil reach more than 85%, product purity over 99.5%, impurity content lower than 0.5%.