The combination of a chiral-selective separation mode with polarimetric detection was investigated in terms of its ability to quantitate enantiomeric mixtures of the dansylated derivatives of phenylalanine, threonine, and valine under conditions of poor chromatographic resolution. Using the difference between two Gaussian functions to model the bimodal response obtained using polarimetric detection and incomplete chiral resolution, correlation coefficients as high as 0.999 were obtained when actual enantiomeric fractions were plotted against observed enantiomeric fractions calculated from the fitting procedure. The methodology was evaluated at different levels of chromatographic resolution, and as a function of the sign and magnitude of the specific rotation of the model compounds. Limits of quantitation calculated at different levels of enantiomeric excess demonstrate the potential of the method to quantitate enantiomeric mixtures even under conditions of poor chromatographic resolution. Minimum measurable quantities (MMQ) at, or below the 1.0% enantiomeric excess (ee) level were obtained for the three amino acid derivatives tested under various conditions of chromatographic resolution when the polarimetric data were fit to the bimodal response model. Even under the lowest resolution conditions tested, the MMQ was determined to be at the 5% ee level.
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http://dx.doi.org/10.1016/s0039-9140(97)00329-9 | DOI Listing |
Methods Mol Biol
January 2025
School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
The isolation of pure compounds from complex extracts is a crucial step in natural products (NPs) research. Historically, this process has been recognized to be slow and laborious. However, significant advancements have been made in isolation methods.
View Article and Find Full Text PDFAnal Chem
January 2025
Synthetic Molecule Design and Development, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana 46285, United States.
Single-stranded guide RNAs (sgRNAs) are important therapeutic modalities that facilitate selective genome editing by the CRISPR/Cas9 system. While these therapeutic modalities are synthesized through solid phase oligonucleotide synthesis similar to small interfering RNA (siRNAs) and antisense oligonucleotide (ASOs) therapeutics, their sequence length and complex secondary and tertiary structure hinder analytical characterization. The resulting current sgRNA methodologies have limited chromatographic selectivity near the FLP and limited MS compatibility.
View Article and Find Full Text PDFChemosphere
January 2025
Empa, Swiss Federal Laboratories for Materials Testing and Research, Laboratory for Advanced Analytical Technologies, Überlandstrasse 129, CH-8600, Dübendorf, Switzerland. Electronic address:
The universe of possible chloro-paraffin (CP) structures is a complex one. Even the world of short-chain CPs (SCCPs) is large, containing thousands of constitutional isomers and stereoisomers. We investigated a technical SCCP mixture (Hordalub 80, Vantage Leuna, m = 56%) and found 33 CP-homologues in this material with carbon- (n) and chlorine-numbers (n) varying from 10 to 13 and 4-12, respectively.
View Article and Find Full Text PDFJ Anal Toxicol
January 2025
Center for Forensic Science Research and Education, Fredric Rieders Family Foundation, Horsham, PA.
Identification of N,N-dimethylpentylone (DMP) in counterfeit "Ecstasy" and "Molly" tablets poses risk to public health due to its adverse effects. Little information is available regarding the pharmacological activity or relevant blood or tissue concentrations of DMP, and even less is known about other structurally related beta-keto methylenedioxyamphetamine analogues on recreational drug markets, such as N-propyl butylone. Here, a novel toxicological assay utilizing liquid chromatography-tandem quadrupole mass spectrometry (LC-QQQ-MS) was developed and validated for the quantitation of DMP and five related synthetic cathinones (eutylone, pentylone, N-ethyl pentylone (NEP), N-propyl butylone, and N-cyclohexyl butylone), with chromatographic resolution from isomeric variants and quantitation performed by standard addition.
View Article and Find Full Text PDFJ Chromatogr A
January 2025
Laboratório Bioquímica e Biofísica, Instituto Butantan, São Paulo, Av. Vital Brasil 1500, São Paulo, SP 05503-900, Brazil. Electronic address:
Although proteins in snake venoms have been extensively studied and characterized, low-mass molecules remain relatively unexplored, mainly due to their low abundance, secondary role in envenomation, and some analytical technique limitations. However, these small molecules can provide new important data related to venom toxins' molecular structure, functions, and evolutionary relationships. This research aimed to characterize molecules below 10 kDa in the venoms of snakes from the Viperidae families (Bothrops, Agkistrodon, and Bitis) and compare two chromatographic approaches: reverse-phase chromatography (RP), a classic technique, and hydrophilic interaction liquid chromatography (HILIC), an alternative technique, both coupled with high-resolution mass spectrometry (HRMS).
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