In vitro toxicity evaluation of caffeine imprinted polymer (CAF-MIP) for decaffeination method on normal chang liver cells

F. Hashim, F. S. Mehamod, Naizatul Akmal Nawi
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Abstract

Over consuming of caffeine is one of the factors to a few health problems such as insomnia, hypertensi on and cardiovascular disease. This preliminary study was conduc te to evaluate the Caffeine-Imprinted Polymer (CAF -MIP) toxicity that was synthesized for a new alternative method f or ecaffeination. It is crucial to evaluate the to xicity of CAF-MIPas this product is potential to be used as complimenta ry with any drinks containing caffeine. In this stu dy, the CAF-MIP toxicity potential was confirmed on Normal Chang Li ver cell (NCLC) based on its IC 50 value andacridine orange and propidium iodide (AO/PI) staining for mode of cell death observation.Proliferation assay was also cond ucte after 24, 48 and 72 hours at 30 μg/ml on NCLC and it showed t hat CAF-MIP promote NCLC growth as shown by at vari ous concentrationof CAF-MIPincrease the percentage of N CLC viability. Observation under light microscopes on NCLC incubated wit CAF-MIP and NIP showed the normal, v iable cell morphology, cuboidal and monolayer cell morphology and this can be seen with green fluorescence when v iew under fluorescence microscope. In conclusion, f rom this study, it is proved that the CAF-MIP does not initiate tox icity effects on human liver cells, meanwhile induc tion of cell proliferation was observed.
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咖啡因印迹聚合物(cafmip)脱咖啡因法对正常肝细胞的体外毒性评价
过量摄入咖啡因是导致失眠、高血压和心血管疾病等健康问题的因素之一。本文对合成的咖啡因印迹聚合物(caff -MIP)的毒性进行了初步研究。评估cafa - mipa的毒性是至关重要的,该产品有潜力作为任何含咖啡因饮料的补充剂。本研究通过对CAF-MIP的ic50值和吖啶橙和碘化丙啶(AO/PI)染色观察细胞死亡模式,证实了CAF-MIP对正常昌利肝细胞(NCLC)的毒性作用。在30 μg/ml浓度下,对NCLC进行24、48和72 h的增殖实验,结果表明,不同浓度的cafm - mip均能提高N - CLC的存活率,从而促进NCLC的生长。在光镜下观察,cafm - mip和NIP孵育的NCLC细胞形态为正常、可变、立方体和单层细胞形态,荧光显微镜下可见绿色荧光。综上所述,本研究证明了CAF-MIP对人肝细胞不产生毒性作用,同时观察到对细胞增殖的诱导作用。
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