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  • Detection, identification and quantification by 1H NMR of adulterants in 150 herbal dietary supplements marketed for improving sexual performance.

Detection, identification and quantification by 1H NMR of adulterants in 150 herbal dietary supplements marketed for improving sexual performance.

Journal of pharmaceutical and biomedical analysis (2014-12-03)
Véronique Gilard, Stéphane Balayssac, Aurélie Tinaugus, Nathalie Martins, Robert Martino, Myriam Malet-Martino
ABSTRACT

One hundred and fifty dietary supplements (DS) marketed to increase sexual performance were analyzed. All these formulations were claimed to contain only natural compounds, plant extracts and/or vitamins. (1)H NMR spectroscopy was used for detecting the presence of adulterants and for their identification and quantification. Mass spectrometry was used as a complementary method for confirming the chemical structures. 61% of DS were adulterated with phosphodiesterase-5 inhibitors (PDE-5i) (27% with the PDE-5i medicines sildenafil, tadalafil and vardenafil, and 34% with their structurally modified analogues). Among them, 64% contained only one PDE-5i and 36% mixtures of two, three and even four. The amounts of PDE-5i medicines were higher than the maximum recommended dose in 25% of DS tainted with these drugs. Additional 5.5% DS included other drugs for the treatment of sexual dysfunction (yohimbine, flibanserin, phentolamine, dehydroepiandrosterone or testosterone). Some DS (2.5%) contained products (osthole, icariin) extracted from plants known to improve sexual performance. Only 31% of the samples could be considered as true herbal/natural products. A follow-up over time of several DS revealed that manufacturers make changes in the chemical composition of the formulations. Lack of quality or consistent manufacture (contamination possibly due to inadequate cleaning of the manufacturing chain, presence of impurities or degradation products, various compositions of a given DS with the same batch number, inadequate labelling) indicated poor manufacturing practices. In conclusion, this paper demonstrates the power of (1)H NMR spectroscopy as a first-line method for the detection of adulterated herbal/natural DS and the need for more effective quality control of purported herbal DS.

MATERIALS
Product Number
Brand
Product Description

Supelco
Testosterone solution, 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®
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Acetaminophen, analytical standard
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Caffeine, BioXtra
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D-(−)-Salicin, ≥99% (GC)
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Caffeine, powder, ReagentPlus®
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Caffeine, meets USP testing specifications, anhydrous
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Caffeine, Sigma Reference Standard, vial of 250 mg
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trans-Dehydroandrosterone, ≥99%
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Acetaminophen, meets USP testing specifications, 98.0-102.0%, powder
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Testosterone, ≥98%
Supelco
Testosterone, VETRANAL®, analytical standard
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Caffeine, anhydrous, tested according to Ph. Eur.
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Methanesulfonic acid solution, 4 M (with 0.2% (w/v) tryptamine)
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Mettler-Toledo Calibration substance ME 18872, Caffeine, traceable to primary standards (LGC)
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Caffeine, anhydrous, 99%, FCC, FG
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Methanesulfonic acid, ≥99.0%
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Methanesulfonic acid concentrate, 0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
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Methanesulfonic acid solution, 70 wt. % in H2O
Caffeine, European Pharmacopoeia (EP) Reference Standard
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D-(−)-Salicin, analytical standard
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Methanesulfonic acid, suitable for HPLC, LiChropur, ≥99.5% (T)
Supelco
Acetaminophen, Pharmaceutical Secondary Standard; Certified Reference Material
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Caffeine Melting Point Standard, Pharmaceutical Secondary Standard; Certified Reference Material
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Caffeine, Pharmaceutical Secondary Standard; Certified Reference Material
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Caffeine, SAJ special grade, ≥98.5%
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Acetaminophen solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
USP
Caffeine, United States Pharmacopeia (USP) Reference Standard