Abstract
Determination of serum cholesterol (Chol) is important for disease diagnosis, and has attracted great attention during the last few decades. Herein, a new magnetic nanoparticle-based ligand replacement strategy has been presented for chemical luminescence detection of Chol. The detection depends on ligand replacement from ferrocene (Fc) to Chol through a β-cyclodextrin (β-CD)–based host–guest interaction, which releases Fc–Hemin as a catalyst for the luminol/hydrogen peroxide chemical luminescence system. More importantly, the luminescence signal can be captured by the camera of a smartphone, thus realizing Chol detection with less instrument dependency. The limit of detection of this method is calculated to be 0.18 μM, which is comparable to some of the developed methods. Moreover, this method has been used successfully to quantify Chol from serum samples with a simple extraction process.
Highlights
Cholesterol (Chol) is a type of biological lipid, which could be generated by the liver or from the daily intake of fat
Luminol/H2O2/horseradish peroxidase (HRP)–based chemical luminescence system has been used for various biochemical detection
Hemin-catalyzing luminol oxidation by H2O2 is normally performed under basic pH conditions without the requirement of enhancers
Summary
Cholesterol (Chol) is a type of biological lipid, which could be generated by the liver or from the daily intake of fat. It is essential for the formation of cell membranes, vitamin D, and several steroid hormones such as glucocorticoids, estrogen, and progesterone that are vital signal molecules for mammalians (Tabas, 2002). Chol can exist in blood as free molecules or be carried with lipoproteins. Multiple analyzing assays have been developed for blood Chol, which could be divided into two types, the enzyme-based methods and non–enzyme-based methods. Many subtypes of ChOx-based detection assays have been developed.
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