A critical analysis of L-asparaginase activity quantification methods-colorimetric methods versus high-performance liquid chromatography

Autor(es)

Magri, Agnes ^[1] ; Soler, Matheus F. ^[1] ; Lopes, Andre M. ^[1] ; Cilli, Eduardo M. ^[2] ; Barber, Patrick S. ^[3] ; Pessoa, Jr., Adalberto ^[4] ; Pereira, Jorge F. B. ^[1]

Afiliação do(s) autor(es)

^[1] Sao Paulo State Univ UNESP, Sch Pharmaceut Sci, Dept Bioproc & Biotechnol, Rodovia Araraquara Jau Km 01, Campos Ville, BR-14800903 Araraquara, SP - Brazil

^[2] Sao Paulo State Univ UNESP, Biochem & Technol Chem Dept, Inst Chem, BR-14800900 Araraquara, SP - Brazil

^[3] Earlham Coll, Dept Chem, 801 Natl Rd West, Richmond, IN 47374 - USA

^[4] Univ Sao Paulo, Pharmaceut Biotechnol Lab, Dept Biochem Pharmaceut Technol, BR-05508000 Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: ANALYTICAL AND BIOANALYTICAL CHEMISTRY; v. 410, n. 27, p. 6985-6990, NOV 2018.
• Citações Web of Science: 4

Resumo

L-asparaginaseor ASNase (L-asparagine aminohydrolase, E.C.3.5.1.1) is an enzyme clinically accepted as an antitumor agent to treat acute lymphoblastic leukemia (ALL) and lymphosarcoma through the depletion of L-asparagine (L-Asn) resulting in cytotoxicity to leukemic cells. ASNase is also important in the food industry, preventing acrylamide formation in processed foods. Several quantification techniques have been developed and used for the measurement of the ASNase activity, but standard pharmaceutical quality control methods were hardly reported, and in general, no official quality control guidelines were defined. To overcome this lack of information and to demonstrate the advantages and limitations, this work properly compares the traditional colorimetric methods (Nessler; L-aspartic acid beta-hydroxamate (AHA); and indooxine) and the high-performance liquid chromatography (HPLC) method. A comparison of the methods using pure ASNase shows that the colorimetric methods both overestimate (Nessler) and underestimate (AHA and indooxine) the ASNase activity when compared to the values obtained with HPLC, considered the most precise method as this method monitors both substrate consumption and product formation, allowing for overall mass-balance. Correlation and critical analysis of each method relative to the HPLC method were carried out, resulting in a demonstration that it is crucial to select a proper method for the quantification of ASNase activity, allowing bioequivalence studies and individualized monitoring of different ASNase preparations. (AU)

• Processo FAPESP: 14/16424-7 - Otimização e aumento de escala do processo de extração líquido-líquido com líquidos iônicos (LIs) como ferramenta de separação sustentável do biofármaco antileucêmico L-asparaginase (ASPase)
• Beneficiário: Jorge Pereira
• Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores