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Scientia Chromatographica最新文献

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O papel da cromatografia no controle de qualidade, conformidade e na rastreabilidade das aguardentes 色谱法在白酒质量控制、合规性和可追溯性方面的作用
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.002
Felipe Augusto Thobias Serafim
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引用次数: 0
Enantioseparation of underivatized amino acids by capillary liquid chromatography. 2. (N, S-dioctyl-(D)-penicillamine) ligand exchange chiral stationary phase 毛细管液相色谱法分离欠活化氨基酸对映体。2. (N, s -二辛基-(D)-青霉胺)配体交换手性固定相
Pub Date : 1900-01-01 DOI: 10.5935/sc.2020.002
Fernanda A. Daher, N. G. P. Santos, E. Maciel, F. Lanças
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引用次数: 0
A novel coffee oil extraction procedure employing pressurized solvents 一种采用加压溶剂的新型咖啡油提取方法
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.006
Jair Sebastião da Silva Pinto, S. Nixdorf, Marcela Jordan Sinisterrra, F. Lanças
In the present work, roasted coffee bean oil was obtained using two extraction methods, a pressurized solvent extraction system (PSE) and a method endorsed by the AOAC (Association of Official Analytical Chemists) INTERNATIONAL, using a Soxhlet extraction system. The yields (% w/w) obtained in each of them were similar, which allowed the conditions of each method to be compared, demonstrating that in the PSE the solvent consumption (20 mL) and the extraction time (20 min) is less at the volume used in the Soxhlet system (200mL) and the analysis time used (480 min). This makes PSE a promising extraction method for use in industry.
在本工作中,烘焙咖啡豆油采用两种萃取方法,一种是加压溶剂萃取系统(PSE),另一种是由AOAC(官方分析化学家协会)国际认可的索氏萃取系统。两种方法获得的产率(% w/w)相似,这使得两种方法的条件可以进行比较,表明在PSE中,在索氏体系中使用的体积(200mL)和分析时间(480 min)下,溶剂消耗(20 mL)和提取时间(20 min)更少。这使PSE成为一种很有前景的工业提取方法。
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引用次数: 3
Novas perspectivas em técnicas de microextração estática 静态微萃取技术的新视角
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.012
Alessandra Honjo Ide, J. M. Nogueira
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引用次数: 0
GC-MS/MS versus LC-MS/MS for unambiguous identification of a and ß-trenbolone in bovine urine GC-MS/MS与LC-MS/MS对牛尿液中a和ß-trenbolone的明确鉴别
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.013
A. L. Silveira, A. Faria
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引用次数: 0
Clean, Safe And Fast Method By Hplc For Quantification Of Rifaximin-Based Samples 清洁、安全、快速的高效液相色谱法定量利福昔明样品
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.009
A. Kogawa, L. Peltonen, H. R. Salgado, Marlus Chorillis
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引用次数: 1
Avaliação comparativa teórica entre métodos farmacopeicos para análise do dinitrato de isossorbida em comprimidos sublinguais 舌下片剂硝酸异山梨酯药典分析方法的理论比较评价
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.011
Valdinéa Santos Dias, Amanda dos Santos Teles Cardoso, Aylla Nunes Conceição, Edith Cristina Laignier Cazedey
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引用次数: 0
Capillary electrochromatography (CEC): recent materials for capillary column preparation, applications, and future perspectives 毛细管电色谱(CEC):毛细管柱制备的新材料、应用和未来展望
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.004
Bruno H. Fumes, João Victor Basolli Borsatto Fernando Mauro Lanças
Capillary electrochromatography (CEC) is a variation of the electrophoresis technique that employs a capillary column filled with a stationary phase. Similarly, as liquid chromatography, the development of new columns started to receive attention from scientists interested in instrumentation, and some materials have been tested in open tubular (OT) and monolithic columns. Among the materials that have received particular attention in CEC column fabrication, are highlighted: graphene oxide (GO)/graphene, ionic liquids (ILs) and molecularly imprinted polymer (MIP). The present review discusses some historical aspects of CEC, column technologies, and new materials (GO/graphene, ILs, and MIP) in column preparation focusing on their synthesis. Additionally, properties and applications in pharmaceutical, proteomic, environmental, and food analysis covering the period of 2012-2020.
毛细管电色谱法(CEC)是电泳技术的一种变体,它采用充满固定相的毛细管柱。同样,随着液相色谱法的发展,新色谱柱的开发开始受到对仪器仪表感兴趣的科学家的关注,一些材料已经在开管(OT)和整体柱上进行了测试。在CEC柱制造中受到特别关注的材料中,有:氧化石墨烯(GO)/石墨烯,离子液体(ILs)和分子印迹聚合物(MIP)。本文综述了CEC、色谱柱技术和新材料(氧化石墨烯/石墨烯、ILs和MIP)在色谱柱制备中的一些历史方面,重点讨论了它们的合成。此外,还介绍了2012-2020年期间在制药、蛋白质组学、环境和食品分析方面的特性和应用。
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引用次数: 0
Boas Práticas Para Cromatografia Líquida De Alta Eficiência: Uma Abordagem Para O Controle De Qualidade Farmacêutico 高效液相色谱的良好实践:药品质量控制的一种方法
Pub Date : 1900-01-01 DOI: 10.5935/SC.2019.010
Rodolpho Guilherme Menezes Gama, M. H. P. Chaves
The High Performance Liquid Chromatography (HPLC) is one of the most advanced techniques used in quality control laboratories in the pharmaceutical industry due to its high technical versatility. According to several regulatory agencies, it is necessary that a pharmaceutical industry has the authorization to produce and commercialize its products, by complying with Good Manufacturing Practices (GMP) standards. Given that the applicability of HPLC techniques meets the requirements of GMP, it is dazzled that these same techniques have criteria to guarantee the safety, reliability and reproducibility of the data generated, together with the maximization of the performance of the chromatographic systems in a cost- benefit analysis for the pharmaceutical industry, thus evoking the concept of Good Chromatographic Practices (GCP), present since the beginning of the development of chromatographic processes and indicated up to the present day, empirically, by the manufacturers of equipment and consumables chromatography. Identified this opportunity, the present work approaches theoretical and practical concepts of the HPLC techniques. In order to do so, it was adopted as methodology the bibliographical and documentary research in databases of scientific articles, as well as queries to documents originating from the largest manufacturers of HPLC items. Thus, through the discussion of GCP in equipment qualification processes, preparation of samples and solutions used in the tests, the cleaning of HPLC accessories and the data integrity processes generated, it is understood that these are fundamental practices for the pharmaceutical industry adding greater reliability in its processes, culminating in the reduction of costs with maintenance and in full compliance with the requirements of the regulatory agencies. It is therefore advocated that the GCP approach be a reality within the quality control laboratories of the pharmaceutical industries, following harmonized precepts and normalizing the knowledge of users, since they are justified as indispensable tools within their routines of activity.
高效液相色谱(HPLC)由于其高技术通用性,是制药工业质量控制实验室中使用的最先进的技术之一。根据一些监管机构的规定,制药行业必须通过遵守良好生产规范(GMP)标准,获得生产和商业化其产品的授权。鉴于HPLC技术的适用性符合GMP的要求,令人眼花缭乱的是,这些相同的技术有标准来保证所生成数据的安全性、可靠性和可重复性,以及在制药行业的成本效益分析中色谱系统的性能最大化,从而唤起了良好色谱规范(GCP)的概念。目前从色谱工艺的发展开始,直至今天,由色谱设备和耗材制造商经验性地表示。确定了这一机会,目前的工作接近高效液相色谱技术的理论和实践概念。为此,采用了在科学文章数据库中进行书目和文献研究以及查询来自HPLC项目最大制造商的文件作为方法。因此,通过讨论GCP在设备鉴定过程、测试中使用的样品和溶液的制备、HPLC附件的清洗和生成的数据完整性过程中的作用,可以理解,这些是制药行业的基本实践,增加了其过程的更高可靠性,最终降低了维护成本,并完全符合监管机构的要求。因此,建议在制药工业的质量控制实验室内实行GCP方法,遵循统一的规则并使用户的知识正常化,因为它们是其日常活动中不可或缺的工具。
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引用次数: 0
Extração de pesticidas em amostras de alimentos através de sorção em ponteiras descartáveis 通过吸附剂从食物样品中提取农药
Pub Date : 1900-01-01 DOI: 10.5935/sc.2019.003
Thaís Camarotto Oliveira, F. M. Lanças
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引用次数: 2
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Scientia Chromatographica
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