CN116496290B - 一种基于吡喃-香豆素染料的肼荧光探针的制备和应用 - Google Patents

一种基于吡喃-香豆素染料的肼荧光探针的制备和应用 Download PDF

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CN116496290B
CN116496290B CN202310305291.4A CN202310305291A CN116496290B CN 116496290 B CN116496290 B CN 116496290B CN 202310305291 A CN202310305291 A CN 202310305291A CN 116496290 B CN116496290 B CN 116496290B
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李春艳
张会
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Abstract

本发明涉及了一种基于吡喃‑香豆素的肼(N2H4)荧光探针的制备和应用,该荧光探针的结构式为:本发明提供了以3‑乙酰基‑7‑羟基香豆素、4‑二乙氨基‑2‑羟基‑苯甲酰苯甲酸、乙酰丙酸等为原料合成该荧光探针的制备方法;首先,该荧光探针对N2H4表现出较高的灵敏度,探针与N2H4反应之后荧光显著增强;其次,该荧光探针对N2H4表现出很高的选择性,不受其他活性氧,活性硫,生物硫醇,氨基酸,有机胺的干扰;并且,该荧光探针与N2H4作用迅速,响应时间在15分钟以内;此外,该荧光探针可应用于实际水样中N2H4的检测。

Description

一种基于吡喃-香豆素染料的肼荧光探针的制备和应用
技术领域
本发明属于荧光探针技术领域,具体涉及一种基于吡喃-香豆素染料的肼荧光探针的制备和应用。
背景技术
肼(N2H4)是一种具有强还原性和亲核性的试剂,并广泛用于光敏剂、药物、农药、染料及其他化学品的制造(S.D.Zelnick,D.R.Mattie,P.C.Stepaniak,Aviat.Space.Environ.Med.,2003,74,1285-1291;U.Ragnarsson,Chem.Soc.Rev.,2001,30,205-213;K.Yamada,K.Yasuda,N.Fujiwara,Z.Siroma,H.Tanaka,Y.Miyazaki,T.Kobayashi,Electrochem.Commun.,2003,5,892-896)。肼可以广泛运用在不同领域,由于具有良好的水溶性,极容易通过皮肤和口腔被人体所吸收。作为一种神经毒素,若人体过量接触肼,可能导致肝、肺、肾和神经***严重损伤(S.Garrod,M.E.Bollard,A.W.Nicholls,S.C.Connor,J.Connelly,J.K.Nicholson,E.Holmes,Chem.Res.Toxicol.,2005,18,115-122;K.Kucukoglu,H.I.Gul,P.Taslimi,I.Gulcin,C.T.Supuran,Bioorg.Chem.,2019,86,316-321)。据报道,N2H4已被美国环境保护署(EPA)列为可能致癌物质,并建议将10ppb列为阈值。因此,需要寻求一种既简便又高效的检测手段来检测肼。
荧光方法具有灵敏度高、操作简单和响应速度快等优点而显示出很大的应用潜力(Y.Q.Tan,J.C.Yu,J.K.Gao,Y.J.Cui,Y.Yang,G.D.Qian,Dyes Pigment,2013,99,966-971;L.Q.Yan,S.Q.Zhang,Y.Xie,X.Y.Mu,J.B.Zhu,Crit.Rev.Anal.Chem.,2022,52,210-229)。到目前为止,已经开发了一些检测肼的荧光探针,用于实时检测环境和细胞的浓度(X.Dai,Z.Y.Wang,Z.F.Du,J.Y.Miao,B.X.Zhao,Sens.Actuators B Chem.,2016,232,369-374;R.Chen,G.J.Shi,J.J.Wang,H.F.Qin,Q.Zhang,S.J.Chen,Y.G.Wen,J.B.Guo,K.P.Wang,Z.Q.Wang,Y.Wang,Spectrochim.Acta A Mol.Biomol.Spectrosc.,2021,252,119510;X.L.Xue,Q.Zhang,K.P.Wang,S.J.Chen,L.S.Tang,Z.Q.Hu,Spectrochim.Acta AMol.Biomol.Spectrosc.,2022,279,121406)。但是,这些探针存在一些问题:(1)荧光探针的灵敏度较差;(2)这些荧光探针具有相对较长的响应时间,反应时间在30分钟以上。因此,设计和合成具有灵敏度高和响应速度快的荧光探针是十分迫切的。
吡喃-香豆素染料是目前荧光探针领域中应用比较广泛的一类染料,它具有摩尔吸光系数大、荧光量子产率高等优势。据报道,利用吡喃-香豆素荧光探针已经检测了许多目标物,如:Cys,HClO,H2O2和Hg2+等(J.Liu,Y.Q.Sun,P.Wang,J.Zhang,W.Guo,Analyst,2013,138,2654-2660;H.Lv,X.F.Yang,Y.Zhong,Y.Guo,Z.Li,H.Li,Anal.Chem.,2014,86,1800-1807;S.Ding,Q.Zhang,S.Xue,G.Feng,Analyst,2015,140,4687-4693;B.Dong,X.Song,X.Kong,C.Wang,Y.Tang,Y.Liu,W.Lin,Adv.Mater.,2016,28,8755-8759)。但是,到现在为止,还没有以吡喃-香豆素为染料,乙酰丙酸为识别基团的荧光探针来灵敏且快速检测N2H4。因此,设计和合成一种基于吡喃-香豆素染料的荧光探针来检测N2H4是非常有必要的。
发明内容
根据所提出的要求,本发明人对此进行了深入研究,在付出了大量创造性劳动后,提供了一种基于吡喃-香豆素染料的肼荧光探针。
本发明的技术方案是,一种基于吡喃-香豆素染料的肼荧光探针,其结构式如下:
一种基于吡喃-香豆素染料的肼荧光探针的制备方法。步骤如下:
在100mL的圆底烧瓶中,将1当量的化合物CP-OH,3~5当量的乙酰丙酸、1.5当量的4-二甲氨基吡啶和1.5当量1-乙基-3-(3-二甲基氨基丙基)碳二亚胺溶解到15~25mL二氯甲烷中,反应混合物室温下搅拌8~12h,停止反应,通过减压蒸馏除去溶剂,粗产品用体积比为100/1~100/3的CH2Cl2/CH3OH作洗脱剂进行柱层析,得到紫色固体产物,即为所述的荧光探针CPN。
本发明的有益效果是,一种基于吡喃-香豆素染料的肼荧光探针的良好的光谱响应性能。首先,研究该探针的荧光光谱性质。探针本身在676nm处没有明显的荧光发射;加入N2H4后,在676nm处出现了明显的发射。并且,随着N2H4浓度的增大,探针近红外荧光不断增强。当加入20μM的N2H4时,荧光强度增强4倍。该探针的检测范围从2μM到20μM,检测限为0.67μM,这说明该探针可以高灵敏的检测N2H4。接着,研究探针的紫外吸收光谱。探针本身在620nm附近无吸收带,加入N2H4后,620nm附近出现新吸收峰。然后,研究探针的选择性。考察了探针与无机离子(Na+、Mg2+、K+、Cu2+、Zn2+、NH4 +、Cl-、Br-、I-、HCO3 -、NO3 -、SO4 2-),活性氧(H2O2、ClO-),活性硫(HS-、HSO3 -),生物硫醇(Cys、GSH),氨基酸(Leu、Thr、Trp、Lys、Phe、Met、Val、Ile),有机胺(二甲胺、对硝基苯胺)以及检测物肼(N2H4)的荧光响应情况。结果发现,只有N2H4引起荧光光谱的改变,其他检测物对探针的荧光光谱没有明显的影响。最后,研究了pH值对荧光探针测定N2H4的影响,当pH值在7.0到8.0之间时,不影响荧光探针对N2H4的测定。此外,该荧光探针响应比较迅速,响应时间在15分钟以内。
一种基于吡喃-香豆素染料的肼荧光探针的应用。N2H4一般存在于水中,湖水和自来水被用来评估荧光探针在实际样品中的应用。为了确保实验的准确性,将取得的湖水和自来水样本先静置2小时,然后将两者pH调至7.4备用。接着,配制成含有不同浓度的N2H4样品,进行荧光测试,在湖水中获得了98.81%~106.35%的回收率,在自来水中获得了95.00%~106.75%的回收率。这些结果说明,探针能够检测实际样品中的N2H4,为监测水中的N2H4提供了一种可靠的手段。
附图说明
图1为荧光探针的合成路线。
图2为荧光探针与不同浓度的N2H4作用后的荧光光谱图。
横坐标为波长,纵坐标为荧光强度。荧光探针的浓度为10.0μM,N2H4的浓度分别为:0,2.0,4.0,6.0,8.0,10.0,12.0,14.0,16.0,18.0,20.0μM。发射波长范围为640-740nm,对应的激发波长为620nm。
图3为荧光探针对不同N2H4浓度的荧光线性响应图。
图4为荧光探针及荧光探针与N2H4作用后的紫外可见吸收光谱图。
横坐标为波长,纵坐标为吸光度。荧光探针的浓度为10.0μM,N2H4浓度为20.0μM。
图5为荧光探针的选择性图。
荧光探针的浓度为10.0μM,N2H4浓度为20.0μM,其它分析物浓度均为20.0μM。
图6为pH对荧光探针的影响图。
图7为荧光探针与N2H4作用后荧光强度随时间变化的曲线图,N2H4浓度为10.0,15.0,20.0μM。
具体实施方式
下面结合附图和具体实施例对本发明进行详细说明,但不限于此。
实施例1:
荧光探针的合成
合成路线如图1。在100mL的圆底烧瓶中,将1当量的化合物CP-OH,3当量的乙酰丙酸、1.5当量的4-二甲氨基吡啶和1.5当量的1-乙基-3-(3-二甲基氨基丙基)碳二亚胺溶解到25mL二氯甲烷中,反应混合物室温下搅拌2h,停止反应,通过减压蒸馏除去溶剂,粗产品用体积比为100/1~100/3的CH2Cl2/CH3OH作洗脱剂进行柱层析,得到紫色固体产物(产率为40%),即为所述的荧光探针。1H NMR(400MHz,CDCl3,δ,ppm)δ7.96(d,J=7.5Hz,1H),7.63(d,J=7.5Hz,1H),7.24(s,2H),7.11(t,J=3.9Hz,2H),6.76(s,2H),6.50(s,1H),6.31(s,2H),5.4(s,1H),3.34(q,J=12.0Hz,4H),2.88–2.83(t,J=8.0Hz,4H),2.23(s,3H),1.18(t,J=8.0Hz,6H).13C NMR(101MHz,CDCl3,δ,ppm)δ206.80,171.28,170.20,158.05,154.32,154.17,153.87,153.01,149.83,146.26,139.82,135.00,131.39,130.15,129.91,128.97,126.98,125.50,124.41,119.27,118.65,117.01,110.18,109.71,105.18,104.11,97.74,44.90,38.30,30.14,28.08,13.00.MS(TOF):579.19
实施例2:
荧光探针和N2H4溶液配制
称取一定量荧光探针CPN固体溶解在DMSO中来制备1.0×10-3mol·L-1的CPN备用溶液。N2H4溶液的配制:将一定量的N2H4溶解在二次蒸馏水中,转移到10mL的容量瓶中,加水至刻度线,得到浓度为1.0×10-2mol·L-1的N2H4。将50μL CPN备用溶液,1.2mL DMSO和不同体积的N2H4备用溶液加入5mL的容量瓶,最终通过HEPES缓冲溶液来定容,得到浓度为1.0×10-5mol·L-1的荧光探针和2.0×10-6~2.0×10-5mol·L-1的N2H4混合待测溶液。
实施例3:
荧光探针与N2H4作用的荧光光谱的测定
图2为荧光探针与N2H4作用的荧光光谱,荧光探针的浓度为10μM,N2H4的浓度依次为0,2.0,4.0,6.0,8.0,10.0,12.0,14.0,16.0,18.0,20.0μM。实验所用激发波长为620nm,发射波长范围为640~740nm。狭缝宽度为10.0nm/10.0nm,所用的荧光测定仪器为日立F4600荧光分光光度计。从图2可以看出,加入N2H4之前,由于乙酰丙酯基团的淬灭作用,探针本身几乎没有发射峰;随着N2H4的加入,在676nm处发射峰增强。并且,随着N2H4浓度的增大,探针的荧光强度不断增强。图3为探针对不同N2H4浓度的线性响应图。荧光强度跟N2H4的浓度呈现线性关系,该探针的检测范围从2.0μM到20.0μM,检测限为0.67μM。这说明该探针可以高灵敏的检测N2H4
实施例4:
荧光探针与N2H4作用的紫外可见吸收光谱的测定
图4为荧光探针与N2H4作用后的紫外可见吸收光谱图,荧光探针的浓度为10.0μM,N2H4的加入量为20.0μM。紫外可见吸收光谱测定用的仪器为安捷伦Cary60紫外可见分光光度计。从图4中可以看出,探针本身在620nm处无吸收带;加入N2H4之后,620nm处的出现新的吸收峰。
实施例5:
荧光探针对N2H4测定的选择性
图5为荧光探针对N2H4测定的选择性图。考察在浓度为10.0μM的荧光探针中加入N2H4(20.0μM)以及无机离子(Na+、Mg2+、K+、Cu2+、Zn2+、NH4 +、Cl-、Br-、I-、HCO3 -、NO3 -、SO4 2-),活性氧(ClO-、H2O2),氨基酸(Leu、Thr、Trp、Lys、Phe、Met、Val、Lle)),活性硫(HS-、HSO3 -),生物硫醇(Cys、GSH),有机胺(p-Nitroaniline、Dimethylamine)的荧光响应情况。从图5可以看出,只有N2H4能引起荧光光谱的明显增强,其他检测物对探针的荧光光谱没有明显的影响。这些结果表明,荧光探针对N2H4有良好的选择性。
实施例6:
溶液pH值对荧光探针测定N2H4的荧光性质的影响
考察pH值对荧光探针测定N2H4的荧光光谱的影响,其结果如图6。我们研究的pH范围为6.0-9.5,荧光探针的浓度为10.0μM,N2H4的浓度为20.0μM。从图中可以看出,荧光探针随着pH的变化,荧光强度基本不变,说明pH对探针本身没有影响。然而,加入N2H4之后,在pH在7.0~8.0范围内,荧光强度比值显著增强。综上所述,当pH值在7.0到8.0之间时,不影响荧光探针对N2H4的测定,是比较合适的pH值范围,这非常有利于该探针用于实际样品中N2H4的测定。
实施例7:
荧光探针与N2H4作用的响应时间的测定
我们研究了荧光探针对N2H4的响应时间,其结果如图7。从图中可以看出,该探针对N2H4的响应时间为15min,这能够满足在实际样品中进行监测的要求。从图7还可以看出,荧光强度达到最大值后,在之后的时间里,荧光强度不再发生变化,这表明此荧光探针光稳定性较好。
实施例8:
荧光探针应用于湖水样品的检测
湖水样本取自湘潭大学画眉潭,样品静置2小时,将静置后的湖水pH调至7.4。由于湖水样本不含有N2H4,因此需要外加N2H4配制成待测混合溶液,然后进行荧光检测,结果列于表1。从表中可以看出,探针对湖水中N2H4的回收率为98.81%~106.35%。
表1湖水中N2H4加标回收率的测定
实施例9:
荧光探针应用于自来水样品的检测
湖水样本取自湘潭大学化学化工大楼自来水水龙头,将自来水的pH调至7.4。由于自来水样本不含有N2H4,因此需要外加N2H4配制成待测混合溶液,然后进行荧光检测,结果列于表2。从表中可以看出,探针对自来水中N2H4的回收率为95.00%~106.75%。
表2自来水中N2H4加标回收率的测定

Claims (3)

1.一种基于吡喃-香豆素染料的肼荧光探针,即CPN,其特征在于,结构如下:
2.根据权利要求1所述的一种基于吡喃-香豆素染料的肼荧光探针的制备方法,其特征在于,反应步骤如下:
在100mL的圆底烧瓶中,将1当量的化合物CP-OH,3~5当量的乙酰丙酸、1.5当量的4-二甲氨基吡啶和1.5当量1-乙基-3-(3-二甲基氨基丙基)碳二亚胺溶解到15~25mL二氯甲烷中,反应混合物室温下搅拌1~2h,停止反应,通过减压蒸馏除去溶剂,粗产品用体积比为100/1~100/3的CH2Cl2/CH3OH作洗脱剂进行柱层析,得到紫色固体产物,即为所述的荧光探针CPN,其中,CP-OH的结构如下:
3.根据权利要求1所述的一种基于吡喃-香豆素染料的肼荧光探针的应用,其特征在于,所述荧光探针可应用于实际水样中肼含量的检测。
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