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首页> 外文期刊>藥學雜誌 >健康食品中に含まれる経口血糖降下薬の系統的分析法
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健康食品中に含まれる経口血糖降下薬の系統的分析法

机译:系统分析保健食品中所含的口服降糖药

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In Japan, maximum residue levels (MRL) have been set for eight pesticides (alpha-BHC, beta-BHC, gamma-BHC, delta-BHC (BHCs), p,p'-DDE, o,p'-DDT, p,p'-DDD, p,p'-DDT (DDTs)) in 14 crude drugs (below 0.2 ppm as total of BHCs, below 0.2 ppm as total of DDTs). There are fears that pesticides present in crude drugs for which MRL are set will be changed from BHCs and DDTs to other pesticides with MRL setting as the turning point. There are few surveys of pyrethroid pesticide in crude drugs distributed in Japan. The actual situation of pyrethroid pesticides in crude drugs distributed in Japan after setting MRL is not unclear and should be clarified. Although a method to analyze permethrin, cypermethrin and fenvalerate in 11 crude drugs was reported, it is not adequate because the recovery rates of permethrin, cypermethrin and fenvalerate from Cinnamomi cortex were very low and the method, including liquid-liquid partition is difficult. In this study, we developed a method using solid-phase extraction to analyze permethrin, cypermethrin and fenvalerate in Cinnamomi cortex with acceptable recovery rates. The sample solution was determined by gas chro-matography/mass spectrometry with negative chemical ionization. The recovery rates of permethrin, cypermethrin and fenvalerate from Cinnamomi cortex were between 87.9 and 90.7%. Five samples of Cinnamomi cortex were analyzed according to the proposed method. No samples contained permethrin, cypermethrin and fenvalerate over detection limits. The proposed method could analyze permethrin, cypermethrin and fenvalerate in all crude drugs for which MRL are set.
机译:在日本,已为八种农药(α-BHC,β-BHC,γ-BHC,δ-BHC(BHCs),p,p'-DDE,o,p'-DDT,p ,p'-DDD,p,p'-DDT(DDTs))(BHC总量低于0.2 ppm,DDT总量低于0.2 ppm)。有人担心,设定了最大残留限量的原料药中存在的农药会从六六六和滴滴涕变为其他以最大残留限量为转折点的农药。在日本分布的生药中,除虫菊酯类农药的调查很少。设定最大残留限量后,日本分销的粗制药物中拟除虫菊酯类农药的实际情况尚不清楚,应予以澄清。尽管已报道了一种分析11种粗制药物中氯菊酯,氯氰菊酯和氰戊菊酯的方法,但由于从肉桂皮层中回收氯菊酯,氯氰菊酯和氰戊菊酯的回收率很低并且难以进行包括液-液分配在内的方法,因此该方法尚不充分。在这项研究中,我们开发了一种使用固相萃取方法分析肉桂皮层中的氯菊酯,氯氰菊酯和氰戊菊酯的方法,回收率令人满意。通过具有负化学电离作用的气相色谱/质谱法测定样品溶液。从肉桂皮层回收苄氯菊酯,氯氰菊酯和氰戊菊酯的回收率在87.9%至90.7%之间。根据提出的方法分析了五个肉桂皮层样品。没有样品中的氯菊酯,氯氰菊酯和氰戊菊酯超过检测限。所提出的方法可以分析所有设置了最大残留限量的原料药中的氯菊酯,氯氰菊酯和氰戊菊酯。

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