Validation of an enzyme-linked immunosorbent assay for C-peptide analysis in Cameroon

Alahkala Asanghanwa, Farah Van Genderen, Katrijn Verhaeghen, Bart Van Der Auwera, Christiaan Van Schravendijk

Onderzoeksoutput: Article

3 Citaten (Scopus)

Samenvatting

AIMS:To validate an ELISA method for C-peptide analysis in Cameroon.

METHODS: We evaluated the linearity, detection limit, functional sensitivity, precision and accuracy, and further investigated for cross-reactivity by proinsulin, and interferences by lipids, bilirubin and hemoglobin. This method was compared with the Roche electrochemiluminescence immunoassay. C-peptide stability was assessed following a series of freeze-thaw cycles, and after storage at room temperature. The C-peptide reference range was determined by analyzing fifty plasma samples of Cameroonians without diabetes.

RESULTS: The ELISA was linear at least up to 7.09 ?g/L, and had a detection limit of 0.09 ?g/L, and a functional sensitivity of 0.32 ?g/L. The inter- and intraassay %CV were 2.9-9.9%, and 5.2-9.4%, respectively. Recoveries were 81-94% in serum, and 93-98% in buffer. Comparison with the ECLIA yielded a good correlation coefficient (R(2)=0.98). There was no cross-reactivity with proinsulin, and no interference with lipids, bilirubin and hemoglobin. C-peptide was stable at room temperature for 24 h and up to 7 freeze-thaw cycles for medium (1-6 ?g/L) and high (>6 ?g/L) levels (
CONCLUSIONS: This method is suitable for C-peptide analysis in low-income countries like Cameroon.
Originele taal-2English
Pagina's (van-tot)459-464
Aantal pagina's6
TijdschriftDiabetes Research and Clinical Practice
Volume98
Nummer van het tijdschrift3
StatusPublished - 2012

Vingerafdruk

Duik in de onderzoeksthema's van 'Validation of an enzyme-linked immunosorbent assay for C-peptide analysis in Cameroon'. Samen vormen ze een unieke vingerafdruk.

Citeer dit