Changes of salivary biomarkers under different storage conditions: effects of temperature and length of storage

Author:

Barranco Tomás1,Tvarijonaviciute Asta1,Escribano Damián2,Tecles Fernando1,Cerón José J1,Cugat Ramón3,Lamy Elsa4,Damia Elena5,Rubio Mónica5,P Rubio Camila1

Affiliation:

1. Interdisciplinary Laboratory of Clinical Analysis (Interlab-UMU), Campus of Excellence Mare Nostrum, University of Murcia, Murcia, Spain

2. Department of Animal and Food Science, Faculty of Veterinary Medicine, Autonomous University of Barcelona, Barcelona, Spain

3. Arthroscopy and Traumatology Unit of the Quirón Hospital, Barcelona, Spain

4. Institute of Mediterranean Agricultural and Environmental Sciences (ICAAM), University of Évora, Évora, Portugal

5. Department of Animal Medicine and Surgery, University CEU Cardenal Herrera, Valencia, Spain

Abstract

Introduction: In this report, we aimed to examine the stability of various analytes in saliva under different storage conditions. Materials and methods: Alpha-amylase (AMY), cholinesterase (CHE), lipase (Lip), total esterase (TEA), creatine kinase (CK), aspartate aminotransferase (AST), lactate dehydrogenase (LD), lactate (Lact), adenosine deaminase (ADA), Trolox equivalent antioxidant capacity (TEAC), ferric reducing ability (FRAS), cupric reducing antioxidant capacity (CUPRAC), uric acid (UA), catalase (CAT), advanced oxidation protein products (AOPP) and hydrogen peroxide (H2O2) were colorimetrically measured in saliva obtained by passive drool from 12 healthy voluntary donors at baseline and after 3, 6, 24, 72 hours, 7 and 14 days at room temperature (RT) and 4 ºC, and after 14 days, 1, 3 and 6 months at – 20 ºC and – 80 ºC. Results: At RT, changes appeared at 6 hours for TEA and H2O2; 24 hours for Lip, CK, ADA and CUPRAC; and 72 hours for LD, Lact, FRAS, UA and AOPP. At 4 ºC changes were observed after 6 hours for TEA and H2O2; 24 hours for Lip and CUPRAC; 72 hours for CK; and 7 days for LD, FRAS and UA. At – 20 ºC changes appeared after 14 days for AST, Lip, CK and LD; and 3 months for TEA and H2O2. At – 80 ºC observed changes were after 3 months for TEA and H2O2. Conclusions: In short-term storage, the analytes were more stable at 4 ºC than at room temperature, whereas in long-term storage they were more stable at - 80 ºC than at – 20 ºC.

Publisher

Croatian Society for Medical Biochemistry and Laboratory Medicine

Subject

Biochemistry, medical,Clinical Biochemistry

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