Porous reduced graphene oxide modified electrodes for the analysis of protein aggregation. Part 2: Application to the analysis of calcitonin containing pharmaceutical formulation. (10th March 2018)

• Record Type: Journal Article
• Authors: Vasilescu, Alina; Ye, Ran; Boulahneche, Samia; Lamraoui, Sabrina; Jijie, Roxana; Medjram, Mohamed Salah; Gáspár, Szilveszter; Singh, Santosh K.; Kurungot, Sreekumar; Melinte, Sorin; Boukherroub, Rabah; Szunerits, Sabine
• Is Part Of: Electrochimica acta. Volume 266(2018)
• Page Start: 364
• Page End: 372
• Publication Date: 2018-03-10
• Subjects: Protein aggregation -- Calcitonin -- Porous reduced graphene oxide -- Electrochemistry -- Disposable electrodes; Electrochemistry -- Periodicals; Electrochemistry, Industrial -- Periodicals; 541.37
• DOI: 10.1016/j.electacta.2018.02.038
• Languages: English
• ISSNs: 0013-4686

Abstract

Abstract: In part 1 (A. Vasilescu et al., Porous reduced graphene oxide modified electrodes for the analysis of protein aggregation. Part 1: Lysozyme aggregation at pH 2 and 7.4 Electrochem. Acta, 254 (2017) 375–383) we proposed porous reduced graphene oxide coated glassy carbon electrode (GC/prGO) in combination with differential pulse voltammetry as a new analytical tool for aggregation studies of proteins. Lysozyme was used as a model to follow its aggregation by electrochemical means at pH 2 and pH 7.4, leading to the formation of amyloid and amorphous aggregates, respectively. Part 2 of this work widens the scope of this approach by investigating a biopharmaceutical product, as the aggregation of peptide based drugs affects their therapeutic activity and can induce allergic reactions in patients. The salmon polypeptide calcitonin (sCT) was chosen as an example of a bioactive peptide with limited pharmaceutical potential due to a tendency to form cytotoxic aggregates and amyloid fibrils. For practical applications, screen printed electrodes (SPE) and flexible electrodes (FE) modified with polydiallyldimethylammonium (PDDA) and prGO by using the layer-by-layer deposition technique have been developed for the detection of sCT. The results indicate that these electrodes can differentiate between formation of amyloid aggregates of calcitonin (2 mg mL −1 ) in citrate buffer to no aggregation in acetate buffer. It was further demonstrated that these electrodes are able to analyze a pharmaceutical drug product of low potency, Miacalcic (8.3 μg mL −1 ), where no aggregation was observed.