|本期目录/Table of Contents|

[1]李华锟,廖永芳,刘阳平.基于芴母核的新型水溶性弱酸性荧光pH指示剂[J].天津医科大学学报,2019,25(05):531-535+539.
 LI Hua-kun,LIAO Yong-fang,LIU Yang-ping.A water soluable fluorene core pH indicator in weak acidic environments[J].Journal of Tianjin Medical University,2019,25(05):531-535+539.
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
25卷
期数:
2019年05期
页码:
531-535+539
栏目:
技术分析
出版日期:
2019-09-20

文章信息/Info

Title:
A water soluable fluorene core pH indicator in weak acidic environments
文章编号:
1006-8147(2019)05-0531-05
作者:
李华锟廖永芳刘阳平
(天津医科大学药学院药物化学教研室,天津市临床药物关键技术重点实验室,天津300070)
Author(s):
LI Hua-kun LIAO Yong-fang LIU Yang-ping
(Department of Pharmacochemistry, School of Pharmacy, Tianjin Medical University, Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics, Tianjin 300070, China)
关键词:
弱酸性荧光pH指示剂
Keywords:
weak acid fluorescence pHindicatorfluorine
分类号:
R914
DOI:
-
文献标志码:
A
摘要:
目的:设计并合成可以检测弱酸性环境的pH荧光探针,为检测溶酶体 (pH =4~5)和内涵体(pH=5~6)中的酸性环境提供科学的方法依据。方法:以2,7-二溴芴为荧光母核,分别与电子给体二乙胺基和电子受体苯并噻唑相连,构建供体-π-受体体系,并在芴的亚甲基上引入能够改善水溶性的二乙二醇甲醚乙基得到目标化合物5,并对其进行核磁表征确定结构,采用紫外分光光度计法和荧光光谱法研究目标化合物5对pH值的响应性,计算pKa。结果:核磁数据与化合物结构相吻合,化合物5紫外吸光度与荧光强度变化具有pH依赖性,通过非线性回归显示pKa为5.88。结论:基于芴母核结构设计并合成了探针化合物5,紫外和荧光结果表明是一个弱酸性pH荧光指示剂,在弱酸性环境的检测方面应该具有很好的应用前景。
Abstract:
Objective: To design and synthesizethe pH-sensitive fluorescent probes that could detect weak acidic conditions, which would provide a scientific basis fordetecting the acidic environments of lysosomes (pH=4~5) and endosomes (pH=5~6). Methods:Based on a fluorescent core 2,7-dibromofluorene, a donor- -acceptor system was developed via conjugation with the electron donor diethylamine and the electron acceptor benzothiazole. The diethylene glycol methyl ether ethyl group was introduced to the methylene position of fluorene to improve the solubility and finally compound 5 was obtained. The compound 5 was characterized by NMR.UV-Vis and fluorescence spectroscopies were used to study itspH-responsive properties andthe pKa was calculated. Results:The NMR spectradata were well agreement withthe compound 5 as well as the intermediates. The changes of UV-vis absorbance and fluorescence intensity of compound 5 were pH-dependent. The pKa was calculated to be 5.88 by nonlinear regression analysis. Conclusion: The compound 5 can be designed and synthesized based on thefluorine core. The results from UV-Vis and fluorescence experiments indicate that it may be a weak acidic fluorescent pH indicator, showingagreatpromise in the detection of weak acidic environment.

参考文献/References:

[1] Haugland R P, Spence M T Z, Johnson I, et al. The Molecular ProbesTM Handbook: A Guide to Fluorescent Probes and Labeling Technologies.10th ed[M]. Carlsbad: Molecular Probes, Invitrogen Detection Technologies, 2011: 1276
[2] Thomas J A, Buchsbaum R N, Zimniak, et al. Intracellular pH measurements in Ehrlich ascites tumor cells utilizing spectroscopic probes generated in situ[J]. Biochem, 1979, 18(11): 2210
[3] Belt J A, Thomas J A, Buchsbaum R N, et al. Inhibition of lactate transport and glycolysis in Ehrlich ascites tumor cells by bioflavonoids[J]. Biochem, 1979, 18(16): 3506
[4] El-Shishtawy R M, Almeida P. A new Vilsmeier-type reaction for one-pot synthesis of pH sensitive fluorescent cyanine dyes[J]. Tetrahedron, 2006, 62(33): 7793
[5] Bizzarri R, Arcangeli C, Arosio D, et al. Development of a novel GFP-based ratiometric excitation and emission pH indicator for intracellular studies[J]. Biophys J, 2006, 90(9): 3300
[6] Zhang Z, Achilefu S. Design,synthesis and evaluation of near-infrared fluorescent pH indicators in a physiologically relevant range[J]. Chem Commun(Camb), 2005(47): 5887
[7] Valuk V F, Duportail G, Pivovarenko V G. A wide-range fluorescent pH-indicator based on 3-hydroxyflavone structure[J]. Photochem Photobiol, 2005, 175(2/3): 226
[8] Baruah M, Qin W, Basaric N D, et al. BODIPY-based hydroxyaryl derivatives as fluorescent pH probes[J]. J Org Chem, 2005, 70(10): 4152
[9] Ertekin K, Cinar S, Aydemir T, et al. Glucose sensing employing fluorescent pH indicator: 4-[(pN.N-dimethylamino)benzylidene]-2-phenyloxazole-5-one[J]. Dyes Pigments, 2005, 67(2): 133
[10] Dong S, Ma H, Li X, et al. Synthesis of a New Water-Soluble Polymeric Probe and its Fluorescent Properties for Ratiometric Measurement of Near-Neutral pH[J]. Anal Lett, 2004, 37(14): 2937
[11] Diwu Z, Chen C S, Zhang C, et al. A novel acidotropic pH indicator and its potential application in labeling acidic organelles of live cells[J]. Chem Biol, 1999, 6(7): 411
[12] Belfield K D, Bondar M V, Przhonska O V, et al. Photostability of a series of two-photon absorbing fluorene derivatives[J]. J Photochem Photobiol A Chem, 2004, 162(2/3): 489
[13] Corredor C C, Belfield K D, Bondar M V, et al. One- and two-photon photochemical stability of linear and branched fluorene derivatives[J]. J Photochem Photobiol A Chem, 2006, 184(1/2):105
[14] Belfield K D, Schafer K J, Mourad W, et al. Synthesis of new two-photon absorbing fluorene derivatives via Cu-mediated Ullmann condensations[J]. J Org Chem, 2000, 65(15): 4475
[15] Belfield K D, Morales A R, Hales J M, et al. Linear and two-photon photophysical properties of a series of symmetrical diphenylaminofluorenes[J]. Chem Mater, 2004, 16(11): 2267
[16] Belfield K D, Morales A R, Kang B S, et al. Synthesis, characterization, and optical properties of new two-photon-absorbing fluorene derivatives[J]. Chem Mater, 2004, 16(23): 4634
[17] Morales A R, Belfield K D, Hales J M, et al. Synthesis of two-photon absorbing unsymmetrical fluorenyl-based chromophores[J]. Chem Mater, 2006, 18(20): 4972
[18] Yao S, Belfield K D. Synthesis of two-photon absorbing unsymmetrical branched chromophores through direct tris (bromomethylation) of fluorine[J]. J Org Chem, 2005, 70(13): 5126

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备注/Memo

备注/Memo:
作者简介 李华锟(1985-),男,硕士在读,研究方向:药物化学;通信作者:刘阳平,E-mail:liuyangping@tmu.edu.cn。
更新日期/Last Update: 2019-10-11