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Simple and ultra-fast recognition and quantitation of compounded monoclonal antibodies: Application to flow injection analysis combined to UV spectroscopy and matching method.
Jaccoulet, E; Schweitzer-Chaput, A; Toussaint, B; Prognon, P; Caudron, E.
Afiliação
  • Jaccoulet E; Hôpital européen Georges Pompidou (HEGP), Service Pharmacie (AP-HP), 75015 Paris, France. Electronic address: emmanuel.jaccoulet@aphp.fr.
  • Schweitzer-Chaput A; Hôpital européen Georges Pompidou (HEGP), Service Pharmacie (AP-HP), 75015 Paris, France.
  • Toussaint B; Hôpital européen Georges Pompidou (HEGP), Service Pharmacie (AP-HP), 75015 Paris, France.
  • Prognon P; Hôpital européen Georges Pompidou (HEGP), Service Pharmacie (AP-HP), 75015 Paris, France; Lip(Sys)(2) Chimie Analytique Pharmaceutique, Univ. Paris-Sud, Université Paris-Saclay (EA7357 Groupe de Chimie Analytique de Paris-Sud), F-92290 Châtenay-Malabry, France.
  • Caudron E; Hôpital européen Georges Pompidou (HEGP), Service Pharmacie (AP-HP), 75015 Paris, France; Lip(Sys)(2) Chimie Analytique Pharmaceutique, Univ. Paris-Sud, Université Paris-Saclay (EA7357 Groupe de Chimie Analytique de Paris-Sud), F-92290 Châtenay-Malabry, France.
Talanta ; 187: 279-286, 2018 Sep 01.
Article em En | MEDLINE | ID: mdl-29853048
ABSTRACT
Compounding of monoclonal antibody (mAbs) constantly increases in hospital. Quality control (QC) of the compounded mAbs based on quantification and identification is required to prevent potential errors and fast method is needed to manage outpatient chemotherapy administration. A simple and ultra-fast (less than 30 s) method using flow injection analysis associated to least square matching method issued from the analyzer software was performed and evaluated for the routine hospital QC of three compounded mAbs bevacizumab, infliximab and rituximab. The method was evaluated through qualitative and quantitative parameters. Preliminary analysis of the UV absorption and second derivative spectra of the mAbs allowed us to adapt analytical conditions according to the therapeutic range of the mAbs. In terms of quantitative QC, linearity, accuracy and precision were assessed as specified in ICH guidelines. Very satisfactory recovery was achieved and the RSD (%) of the intermediate precision were less than 1.1%. Qualitative analytical parameters were also evaluated in terms of specificity, sensitivity and global precision through a matrix of confusion. Results showed to be concentration and mAbs dependant and excellent (100%) specificity and sensitivity were reached within specific concentration range. Finally, routine application on "real life" samples (n = 209) from different batch of the three mAbs complied with the specifications of the quality control i.e. excellent identification (100%) and ±â€¯15% of targeting concentration belonging to the calibration range. The successful use of the combination of second derivative spectroscopy and partial least square matching method demonstrated the interest of FIA for the ultra-fast QC of mAbs after compounding using matching method.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Injeção de Fluxo / Bevacizumab / Rituximab / Infliximab / Anticorpos Monoclonais Tipo de estudo: Guideline / Qualitative_research Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Injeção de Fluxo / Bevacizumab / Rituximab / Infliximab / Anticorpos Monoclonais Tipo de estudo: Guideline / Qualitative_research Idioma: En Ano de publicação: 2018 Tipo de documento: Article