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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Analysis of human luteinizing hormone and human chorionic gonadotropin preparations of different origins by reversed-phase high-performance liquid chromatography

Texto completo
Autor(es):
Almeida, B. E. [1] ; Oliveira, J. E. [1] ; Carvalho, C. M. [1] ; Dalmora, S. L. [2] ; Bartolini, P. [1] ; Ribela, M. T. C. P. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] IPEN CNEN, Dept Biotechnol, BR-05508900 Sao Paulo - Brazil
[2] Univ Fed Santa Maria, Dept Ind Pharm, BR-97119900 Santa Maria, RS - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Journal of Pharmaceutical and Biomedical Analysis; v. 53, n. 1, p. 90-97, SEP 21 2010.
Citações Web of Science: 9
Resumo

Specific reversed-phase high-performance liquid chromatography conditions are reported for the analysis of recombinant and native human luteinizing hormone (hLH) and human chorionic gonadotropin (hCG) preparations. Heterodimeric hLH, hCG and their alpha- and beta-subunits migrated with significantly different retention times (t(R)) in the following order of increasing hydrophobicity: alpha-hCG < alpha-hLH < hCG < hLH < beta-hCG < beta-hLH. Under these conditions, the main peak of three hCG preparations ran about 4% faster than the average t(R) (38.35 +/- 0.42 min; RSD = 1.1%) of four hLH preparations. Four heterogeneous urinary products were also analyzed, hLH, hFSH and hCG peaks being identified. Quantitative analysis was validated for the homogeneous preparations and a highly linear dose-response curve (r = 0.99998; p < 0.0001; n = 20) used to assess the accuracy, precision and sensitivity of the analysis. Quantification of the different gonadotropins in the heterogeneous preparations was also carried out, but with limitations in accuracy. (C) 2010 Elsevier B.V. All rights reserved. (AU)

Processo FAPESP: 07/56094-2 - Sintese de tireotrofina humana (r-htsh) em celulas cho "humanizadas", capazes de introduzir a ligacao alfa-2,6 entre o acido sialico e a galactose.
Beneficiário:Maria Teresa de Carvalho Pinto Ribela
Modalidade de apoio: Auxílio à Pesquisa - Regular