Green analytical chemistry: Opportunities for pharmaceutical quality control

This review article summarizes the opportunities for utilizing the green analytical chemistry (GAC) techniques and principles in the field of quality control (QC) of pharmaceuticals. Green analytical chemistry is considered a branch of the green chemistry based on the principles overlapping with the goals of sustainable development. General definitions of quality and quality control, the principles of GAC, proposals for greener sample pretreatment and greener chromatographic method of analysis applied in QC laboratories are discussed herein. The main goal is to achieve more eco-friendly analysis in QC laboratories through different strategies and techniques, replace toxic reagents, and modify or replace analytical methods and/or techniques with safer ones, making it possible to dramatically reduce the amounts of reagents consumed and waste generated.     

Green analytical chemistry approaches on environmental analysis

Green analytical chemistry is a comprehensive perspective that aims to reduce or eliminate the toxic and harmful solvents, reagents, and techniques in the preparation, pre-treatment, and determination steps of an analysis process. With the increase in environmental pollution in recent years, awareness has been increasing in terms of both the contamination analysis of environmental sources and the more environmentally friendly analysis methods. This review evaluates the solvents such as bio-based solvents and deep eutectic solvents, nanomaterials synthesized by non-toxic methods, the greener changes in the extraction methods, and chromatographic techniques considering the most recent studies. In particular, trying to make the methods used to analyze environmental samples safer and less toxic is an important point that overlaps with the green approach, which aims to minimize environmental pollution. In this context, this review provides information on green analytical chemistry-based environmental applications covering the last ten years so that the applications of this approach can be examined and understood in more detail and can be applied by other researchers.     

Green analytical chemistry as an integral part of sustainable education development

1. Download : Download high-res image (137KB)
2. Download : Download full-size image

     

Green analytical chemistry in sample preparation for determination of trace organic pollutants

The principles of green chemistry are applied to not only chemical engineering and synthesis, but also increasingly analytical chemistry. We describe environment-friendly analytical techniques applied to isolate and to enrich trace organic pollutants from solid and aqueous samples. Amounts of organic solvents used in analytical laboratories are reduced by applying solventless extraction, extraction using other types of solvent, assisted solvent extraction and miniaturized analytical systems.     

Traceability and analytical chemistry

 The basic concepts of traceability as they are defined by the Comité Consultatif pour la Cluantité de Matière are contrasted with the practical exploitation in chemical analysis. The applicability of traceability concepts are tested for their practical applicability on four different analytical methodologies, neutron activation analysis, plasma mass spectrometry, beam microscopical analysis and speciation analysis of organometallic compounds. Received: 31 March 1998 · Accepted: 6 June 1998     

1 General analytical chemistry

Abstracts

     

1 General analytical chemistry

Abstracts

1 General analytical chemistry1.1 Fundamentals, methods, apparatus, reagents, automation, data processing     

Vinylallenes—VI : Synthese de cetones de la serie de la jasmone

Dehydrojasmone 1a and nor-methyl dehydrojasmone 1b have been prepared by action of a peracid on appropriately substituted vinylallenes. Several pathways to these hydrocarbons are described.     

Long-chain alkylbenzenes: their analytical chemistry, environmental occurrence and fate

Since ca. 1950 long-chain alkylbenzenes have been produced industrially for the synthesis of alkylbenzenesulfonates, the anionic surfactants most commonly used in commercial detergents. Prior to 1965 the alkylbenzenes were generated by Frieldel-Crafts alkylation of benzene with tetrapropylene. This reaction produces a complex assemblage of phenylalkanes (TABs) having highly branched side chains. Due to their stability, the TABs proved to be environmentally troublesome and were ultimately replaced (during the mid-1960s) by the linear alkylbenzenes (LABs). The LABs consist of a mixture of secondary phenylalkanes with linear alkyl side chains ranging in length from C10 to C14. Because of their unique structures and composition, these compounds are easily identified and measured in complex environmental samples. The linear alkylbenzenes are also found in municipal wastewaters where their presence is thought to result from the use of domestic and industrial detergents. Because they are synthetic and unlikely to occur in other significant inputs to coastal marine waters, long-chain alkylbenzenes have obvious potential as waste-specific molecular tracers. The presence of long-chain alkylbenzenes in sediment trap particulates and marine sediments collected near a major waste outfall system in southern California indicates that these hydrocarbons can survive exposure to an oxygenated water column during sedimentation. Whereas changes in the isomer composition of the LABs with depth in the sediments are suggestive of microbial alteration, the vertical distribution of the TABs and LABs can be used as a geochronological tool to reconstruct waste depositional histories.