高效液相色譜法
高效液相色譜法測定與Shimadzu模型進行了
LC-6A高效液相色譜儀配置Reodyne模型
7125手冊和20-μl噴油器循環(huán).這個探測器
紫外分光計SPD-6A Shimadzu模型.這個熱分離
產(chǎn)品積分模型被用來四千四百藻數(shù)據(jù)采集
和記錄.使用前,eluents少了
μm.0.45過濾(生產(chǎn))和degassed真空.這個
ODS柱(150×反Hypersil 46毫米;分詞
5μm大小.)(Supelco ODS柱Hypersil護衛(wèi)股份有限公司).
分析了啤酒樣品為生物胺根據(jù)
修正法[d]蓋.其中的教材
一個漸變系統(tǒng)與下列溶劑:(一)0.005).
醋酸銨緩沖溶液調(diào)節(jié)pH 4.3和冰川
醋酸;(2)甲醇.裝船后,分析了樣本
用甲醇(B)梯度的緩沖液,由65%的80%
然后用20術(shù):目標(biāo)可以隱形等靜洗脫100%甲醇
10分鐘.最后,equilibrated柱與等靜
65%的甲醇緩沖液為10分鐘.
流量是1毫升/分鐘.dansylamines的eluted
通過監(jiān)測紫外吸光度檢測在340海里.
結(jié)果
27個樣本進行拋光啤酒流行
采用高效液相色譜法測定方法.8生物胺:monoamines
他PHM,給出TRP(,)、二胺、鐘、計算機輔助設(shè)計(CAD),(把
摘要多胺(SPD,以及polyamine-derived次要的
代謝物(PRP,PIR)進行了啤酒
樣品.梯度洗脫甲醇在銨
醋酸緩沖區(qū)允許洗脫所有的胺在更少
超過30分鐘.在測試范圍的生物胺濃度
從0.2到10.0毫克/升)的相關(guān)系數(shù)
峰面積與濃度之間的標(biāo)準(zhǔn)
三聚氰胺是高于0.99每標(biāo)準(zhǔn)
曲線.平均回收率的銨
104.1% 81.6%,以最低的價值為spermine和
為spermidine最高.量化的極限
從建立了新葉asranged毫克/升),為spermidine遺傳毫克/升)for2-phenylethylamine 3倍的檢測限和介于新葉毫克/升),為spermidine遺傳毫克/升)
2-phenylethylamine.
英語翻譯
英語翻譯
High performance liquid chromatography
HPLC determination was performed with a Shimadzu Model
LC-6A liquid chromatograph supplied with a Reodyne Model
7125 manual injector with a 20-μl loop.The detector was
Shimadzu Model SPD-6A UV spectrometer.The Thermo Separation
Products integrator Model SP 4400 was used for data acquisition
and recording.Prior to use,the eluents were filtrated through
0.45 μm.filters (Sartorius) and degassed under the vacuum.The
column was reversed-phase Hypersil ODS (150×4.6 mm; participle
size 5 μm.) with a Hypersil ODS guard column (Supelco Inc.).
The beer samples were analysed for biogenic amines according to
the modified Geiger method [18].The elution program consisted
of a gradient system with the following solvents:(A) 0.005 M.
ammonium acetate buffer solution adjusted to pH 4.3 with glacial
acetic acid; (B) methanol.After loading the sample,analysis started
with a methanol (B) gradient in buffer A from 65% to 80% for
20 min.and then with isocratic elution of 100% methanol for
10 min.Finally,the column was equilibrated with an isocratic elution
of 65% methanol in buffer A for 10 min.
The flow rate was 1 mL/min.The eluted dansylamines were
detected by monitoring the UV absorbency at 340 nm.
Results
Twenty-seven samples of popular Polish beers were tested
by HPLC method.Eight biogenic amines:monoamines
(TRP,PHM,HIS,TYR),diamines (PUT,CAD),
polyamines (SPD,SPM) and polyamine-derived secondary
metabolites (PRP,PIR) were investigated in the beer
samples.The gradient elution of methanol in ammonium
acetate buffer allowed elution of all the amines in less
than 30 min.In the tested range of biogenic amine concentration
from 0.2 to 10.0 mg/L the correlation coefficient
between peak area and concentration of each standard
amine was higher than 0.99 for every standard
curve.The average recoveries of the amines ranged from
81.6% to 104.1% with the lowest value for spermine and
the highest for spermidine.The quantification limits
were established asranged from 0.19 mg/L for spermidine to 0.49 mg/L for2-phenylethylamine three times the detection limit and
and后再加一句ranged from 0.19 mg/L for spermidine to 0.49 mg/L for
2-phenylethylamine.
High performance liquid chromatography
HPLC determination was performed with a Shimadzu Model
LC-6A liquid chromatograph supplied with a Reodyne Model
7125 manual injector with a 20-μl loop.The detector was
Shimadzu Model SPD-6A UV spectrometer.The Thermo Separation
Products integrator Model SP 4400 was used for data acquisition
and recording.Prior to use,the eluents were filtrated through
0.45 μm.filters (Sartorius) and degassed under the vacuum.The
column was reversed-phase Hypersil ODS (150×4.6 mm; participle
size 5 μm.) with a Hypersil ODS guard column (Supelco Inc.).
The beer samples were analysed for biogenic amines according to
the modified Geiger method [18].The elution program consisted
of a gradient system with the following solvents:(A) 0.005 M.
ammonium acetate buffer solution adjusted to pH 4.3 with glacial
acetic acid; (B) methanol.After loading the sample,analysis started
with a methanol (B) gradient in buffer A from 65% to 80% for
20 min.and then with isocratic elution of 100% methanol for
10 min.Finally,the column was equilibrated with an isocratic elution
of 65% methanol in buffer A for 10 min.
The flow rate was 1 mL/min.The eluted dansylamines were
detected by monitoring the UV absorbency at 340 nm.
Results
Twenty-seven samples of popular Polish beers were tested
by HPLC method.Eight biogenic amines:monoamines
(TRP,PHM,HIS,TYR),diamines (PUT,CAD),
polyamines (SPD,SPM) and polyamine-derived secondary
metabolites (PRP,PIR) were investigated in the beer
samples.The gradient elution of methanol in ammonium
acetate buffer allowed elution of all the amines in less
than 30 min.In the tested range of biogenic amine concentration
from 0.2 to 10.0 mg/L the correlation coefficient
between peak area and concentration of each standard
amine was higher than 0.99 for every standard
curve.The average recoveries of the amines ranged from
81.6% to 104.1% with the lowest value for spermine and
the highest for spermidine.The quantification limits
were established asranged from 0.19 mg/L for spermidine to 0.49 mg/L for2-phenylethylamine three times the detection limit and
and后再加一句ranged from 0.19 mg/L for spermidine to 0.49 mg/L for
2-phenylethylamine.
英語人氣:342 ℃時間:2020-06-27 08:25:25
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