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1.
J Chromatogr Sci ; 59(1): 30-39, 2021 Jan 01.
Article in English | MEDLINE | ID: mdl-33107906

ABSTRACT

One of the highest incidences of illegal drug products is related to phosphodiesterase-5 inhibitors, used in treatment of erectile dysfunction, including those containing sildenafil citrate and tadalafil. In this context, comprehensive evaluation of the quality of genuine and illegal medicines was performed. A simple and rapid ultra-high performance liquid chromatography (UHPLC-UV) method to quantify sildenafil and tadalafil in the presence of six degradation products was developed and validated. Sildenafil and tadalafil were submitted to forced degradation. The separation was carried out on a Kinetex C18 (50 × 2.1 mm; 1.7 µm) column with mobile phase composed of acetonitrile and aqueous triethylamine solution. The calibration curves were linear in the range of 14-126 µg mL-1 for sildenafil citrate and 4-36 µg mL-1 for tadalafil and the method proved to be selective, precise, accurate and robust. Sildenafil degraded in oxidative media, whereas tadalafil degraded in acidic, alkaline and oxidative environment. The chemical structures and the mechanisms for the formation of the main degradation products were proposed by UHPLC coupled to tandem mass spectrometry. The UHPLC-UV method was applied in the pharmaceutical analysis of genuine and seized medicines. Some of them did not meet quality standards, mainly due to contents below specifications and the large variation on contents between units within a batch.


Subject(s)
Chromatography, High Pressure Liquid/methods , Illicit Drugs , Sildenafil Citrate , Tadalafil , Counterfeit Drugs , Illicit Drugs/analysis , Illicit Drugs/chemistry , Limit of Detection , Linear Models , Reproducibility of Results , Sildenafil Citrate/analysis , Sildenafil Citrate/chemistry , Sildenafil Citrate/standards , Tadalafil/analysis , Tadalafil/chemistry , Tadalafil/standards , Tandem Mass Spectrometry
2.
J Pharm Biomed Anal ; 185: 113222, 2020 Jun 05.
Article in English | MEDLINE | ID: mdl-32145539

ABSTRACT

During routine screening of illegal adulterants in health supplements, a novel sildenafil analogue was discovered, and subsequently isolated by recrystallization. Its structure was elucidated by extensive analyses of high resolution mass spectrometry (HRMS), one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR) data. The analogue was finally determined as hydroxycarbodenafil, featuring a hydroxyethyl group instead of an ethyl group on piperazine ring in comparison with carbodenafil.


Subject(s)
Dietary Supplements/analysis , Drug Contamination/prevention & control , Sildenafil Citrate/analysis , Dietary Supplements/standards , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Structure , Sildenafil Citrate/analogs & derivatives , Sildenafil Citrate/standards
3.
J Pharm Biomed Anal ; 166: 304-309, 2019 Mar 20.
Article in English | MEDLINE | ID: mdl-30685655

ABSTRACT

Erectile dysfunction medicines such as Cialis and Viagra are very popular worldwide and are between the most prevalent counterfeit medicines in Brazil. A range of analytical methods has been used to analyze Cialis and Viagra, such as ATR-FTIR, GCMS and UPLC-MS. Until now, there are no data available of DSC methods for analysis of counterfeit medicines of Cialis and Viagra. DSC is a thermal analysis that provides useful information of physico-chemical events, and however is almost not used for forensic purposes. In this study, thermal analysis of 25 counterfeit Viagra and Cialis seized by Brazilian Federal Police were performed by DSC and compared to their authentic medicines and analytical standards, along with chemometric tools. Authentic samples of Viagra displayed a similar thermal profile with the API, while Cialis were different with additional endothermic peaks, that could be related to excipients interference. Thermograms of Viagra counterfeit samples were similar to authentic samples, while Cialis showed an enlargement and displacement of endothermic peaks. Also, some Cialis counterfeit samples showed melting peaks attributed to sildenafil, the API of Viagra, instead tadalafil, confirming previous results obtained by UPLC-MS. Multivariate analysis with application of Hierarchical Cluster Analysis classified different groups of samples, including a cluster with counterfeit Cialis and Viagra, indicating the use of same API for both counterfeit medicines and possibly the same illicit production; and a cluster with authentic Viagra and counterfeit Cialis, confirming the addition of sildenafil instead tadalafil to Cialis counterfeit samples. Here for the first time we described the use of DSC for chemical profiling of Cialis and Viagra and showed that even when applied to a small group of samples, DSC along with chemometric tools can be considered as a good auxiliary method in forensic casework samples. DSC provided useful data to perform the identification of counterfeit and authentic medicines, with low cost and a simple method.


Subject(s)
Calorimetry, Differential Scanning , Counterfeit Drugs/analysis , Phosphodiesterase 5 Inhibitors/analysis , Sildenafil Citrate/analysis , Tadalafil/analysis , Brazil , Cluster Analysis , Erectile Dysfunction/drug therapy , Excipients/chemistry , Humans , Male , Phosphodiesterase 5 Inhibitors/standards , Principal Component Analysis , Sildenafil Citrate/standards , Tadalafil/standards
4.
Anal Chem ; 90(18): 10765-10770, 2018 09 18.
Article in English | MEDLINE | ID: mdl-30148354

ABSTRACT

A novel "Prediction and Confirmation" (PC) strategy was proposed for characterizing phosphodiesterase-5 inhibitor (PDE-5) derivatives in botanical dietary supplements (BDSs) for on-site detection. Discovery Studio (DS) and density functional theory (DFT) calculations were used for the "Prediction" step in order to estimate PDE-5 derivative structures and theoretical Raman shifts without synthesizing the derivatives. After 11 potentially bioactive sildenafil derivatives were acquired through DS, 32 common calculated Raman shifts were obtained through DFT. The mean absolute wavenumber deviation (δ, peak range) of the major bands and the minimum number (τ) of Raman spectral peaks matching the calculated common shifts were optimized, so that a positive result of an unknown sample could be reasonably produced. In this study, δ was set at ±10 cm-1 and the corresponding τ was set at 4-5 after optimization. Surface plasmon resonance (SPR) biosensor and surface-enhanced Raman scattering (SERS) detection were the "Confirmation" step to validate the reliability and accuracy of DS and DFT in the "Prediction" step, respectively. The optimized δ and τ criteria were used as indexes for on-site SERS detection after thin-layer chromatographic (TLC) separation of six real-world samples, one of which was preliminarily identified as "suspected positive samples." This strategy allows for a quick determination of the BDSs adulterated with sildenafil or its derivatives, independent of any standard materials.


Subject(s)
Dietary Supplements/analysis , Models, Theoretical , Phosphodiesterase 5 Inhibitors/analysis , Plant Extracts/chemistry , Sildenafil Citrate/analysis , Biosensing Techniques , Chromatography, Thin Layer , Density Functional Theory , Molecular Docking Simulation , Phosphodiesterase 5 Inhibitors/standards , Reference Standards , Sildenafil Citrate/standards , Spectrum Analysis, Raman , Surface Plasmon Resonance/methods
5.
J Pharm Biomed Anal ; 135: 199-205, 2017 Feb 20.
Article in English | MEDLINE | ID: mdl-28040654

ABSTRACT

1H spin-lattice Nuclear Magnetic Resonance (NMR) relaxometry, vibrational spectroscopy and Atomic Force Microscopy (AFM) have been applied to differentiate between original and counterfeit Viagra®. The relaxation studies have been performed in a frequency range covering four orders of magnitude, from 4kHz to 40MHz. It has been shown that for the counterfeit product the relaxation is bi-exponential in the whole frequency range, while for the original Viagra® the relaxation process is always single exponential. Thus, even a qualitative analysis of the relaxation data makes it possible to identify the falsified medicine. Moreover, it has been demonstrated that vibrational spectroscopy does not allow for differentiating between the products, while AFM studies are likely to lead one to deceptive conclusions regarding the originality of the medicine. Furthermore, a quantitative analysis of the relaxation data has been performed to describe in detail the relaxation properties of the original and falsified products.


Subject(s)
Counterfeit Drugs/chemistry , Magnetic Resonance Spectroscopy/methods , Phosphodiesterase 5 Inhibitors/adverse effects , Sildenafil Citrate/analysis , Phosphodiesterase 5 Inhibitors/standards , Sildenafil Citrate/standards , Spectroscopy, Fourier Transform Infrared/methods
6.
J Pharm Biomed Anal ; 131: 133-139, 2016 Nov 30.
Article in English | MEDLINE | ID: mdl-27589030

ABSTRACT

There must be a large market for active pharmaceutical ingredients of illegal source to support the huge and lucrative business of trade in illegal medicines. The active substances found in illegal pharmaceuticals may differ from their legal counterparts concerning purity and associated risks for the health of the user. In this study we show two examples in which the active substance sildenafil, used in erectile dysfunction products, was not of European Pharmacopeia quality. In one case milligram-scale amounts of a 2-mercaptobenzothiazole contamination were found, in another case the mesylate salt rather than the monograph based citrate was used. For the user of products containing these active substances, the risks of side effects increase through the inherent properties of the impurity and the chance of overdosing. The fact that the users are most likely not aware of the poor quality of the products adds up to the health risk of using prescription medication without consulting medical professionals.


Subject(s)
Counterfeit Drugs/analysis , Sildenafil Citrate/analysis , Sildenafil Citrate/standards , Erectile Dysfunction/drug therapy , Humans , Male , Sildenafil Citrate/therapeutic use , Spectroscopy, Fourier Transform Infrared/methods , Tandem Mass Spectrometry/methods
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