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Synthesis of taurine-fluorescein conjugate and evaluation of its retina-targeted efficiency in vitro.


ABSTRACT: In this work, retinal penetration of fluorescein was achieved in vitro by covalent attachment of taurine to fluorescein, yielding the F-Tau conjugate. Nuclear magnetic resonance (NMR) and high resolution mass spectrometry (HRMS) were used to confirm the successful synthesis of F-Tau. The cellular uptake of F-Tau in adult retinal pigment epithelial cells (ARPE-19) and human retinal microvascular endothelial cells (hRMECs) was visualized via confocal scanning microscopy. The results indicated an improvement of solubility and a reduction of logP of F-Tau compared with fluorescein. As compared with fluorescein, F-Tau showed little toxicity, and was retained longer by cells in uptake experiments. F-Tau also displayed higher transepithelial permeabilities than fluorescein in ARPE-19 and hRMECs monolayer cells (P<0.05). These results showed that taurine may be a useful ligand for targeting small-molecule hydrophobic pharmaceuticals into the retina.

SUBMITTER: Huang M 

PROVIDER: S-EPMC4629109 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature

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Synthesis of taurine-fluorescein conjugate and evaluation of its retina-targeted efficiency in vitro.

Huang Meihong M   Song Jiaqi J   Lu Bingzheng B   Huang Huizhi H   Chen Yizhen Y   Yin Wei W   Zhu Wenbo W   Su Xinwen X   Wu Chuanbin C   Hu Haiyan H  

Acta pharmaceutica Sinica. B 20141120 6


In this work, retinal penetration of fluorescein was achieved in vitro by covalent attachment of taurine to fluorescein, yielding the F-Tau conjugate. Nuclear magnetic resonance (NMR) and high resolution mass spectrometry (HRMS) were used to confirm the successful synthesis of F-Tau. The cellular uptake of F-Tau in adult retinal pigment epithelial cells (ARPE-19) and human retinal microvascular endothelial cells (hRMECs) was visualized via confocal scanning microscopy. The results indicated an i  ...[more]

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