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1.
Transfus Clin Biol ; 24(1): 9-14, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-27865608

RESUMO

OBJECTIVES: The benefits of plasmapheresis (PA) for neurologic autoimmune diseases have been widely demonstrated. Little is known about the long-term neurologic prognosis and course after PA and immunosuppressive (IS) and/or intravenous immunoglobulin (IVIG) treatment. We aimed to analyse features associated with short-term response and long-term outcome and prognosis (neurologic status and mortality) of peripheral polyneuropathy (PP) and central nervous system acute inflammatory disease (CNSAID) treated with PA. PATIENTS AND METHODS: A descriptive, retrospective single-centre study from January 2005 to December 2012. RESULTS: There were 26 episodes, which included 16 CNSAID and 10 PP cases. First line therapy included PA (n=4), IS drugs (n=15), and IVIG (n=7). Responses were achieved in 80% and 50% of PP and CNSAID cases, respectively. For PP, first line treatment with IVIG and no IS treatment prior to or during PA were variables associated with short-term response (P=0.067), good or stable neurologic status at the end of follow-up (P=0.008), and lower mortality rate (P=0.008). For CNSAID, initial EDSS score≥7 (P=0.019) was related to long-term good or stable neurologic status. During the study period, 177 sessions were conducted; 3.4% had technical complications and 8.5% clinical complications. However, these incidents were all minor and no PA session had to be discontinued. CONCLUSION: The response rates achieved in our patients were similar to those of other research. PA has a safe profile but double-blind, controlled studies are needed to evaluate the synergy of sequential treatment with IGIV followed by PA and the possible benefit for long-term outcome.


Assuntos
Imunoglobulinas Intravenosas/uso terapêutico , Plasmaferese , Polineuropatias/terapia , Adolescente , Adulto , Idoso , Doenças do Sistema Nervoso Central/mortalidade , Doenças do Sistema Nervoso Central/terapia , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Polineuropatias/mortalidade , Estudos Retrospectivos , Índice de Gravidade de Doença , Resultado do Tratamento , Adulto Jovem
2.
J Chromatogr A ; 871(1-2): 207-15, 2000 Feb 25.
Artigo em Inglês | MEDLINE | ID: mdl-10735301

RESUMO

In this work development, optimization and validation of a cyclodextrin-modified micellar electrokinetic chromatography (CD-modified MEKC) method is proposed to resolve separation of the sertraline hydrochloride and synthesis-related substances. Sertraline hydrochloride, the cis-(1S,4S) enantiomer form, is used as an antidepressant therapeutic agent. A buffer concentration composed of 20 mM sodium borate, pH 9.0 with 50 mM sodium cholate, 15 mM sulfated beta-cyclodextrin and 5 mM hydroxypropyl-beta-cyclodextrin was found to be the most suitable background electrolyte. Quantitation of the impurities at levels of 0.1% in different samples of the bulk drug was determined. A comparison of the results with those obtained by HPLC methodology was also accomplished. The method proved appropriate for testing the purity of sertraline hydrochloride in bulk drug.


Assuntos
Cromatografia Capilar Eletrocinética Micelar/métodos , Inibidores Seletivos de Recaptação de Serotonina/análise , Sertralina/análise , Ciclodextrinas/química , Isomerismo , Reprodutibilidade dos Testes , Inibidores Seletivos de Recaptação de Serotonina/química , Sertralina/química
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