Graphene/dodecanol floating solidification microextraction for the preconcentration of trace levels of cinnamic acid derivatives in traditional Chinese medicines
Abstract:A novel graphene/dodecanol floating solidification microextraction followed by HPLC with diode-array detection has been developed to extract trace levels of four cinnamic acid derivatives in traditional Chinese medicines. Several parameters affecting the performance were investigated and optimized. Also, possible microextraction mechanism was analyzed and discussed. Under the optimum conditions (amount of graphene in dodecanol: 0.25 mg/mL; volume of extraction phase: 70 μL; pH of sample phase: 3; extraction ti… Show more
“…The normality assumption was satisfied as to the residuals in the plot distributed along a straight line ( (Przyjazny, 2019). 1-dodecanol is a good extraction solvent owing to its hydrophobic end and hydroxyl group that can extract target analytes by hydrophobic or hydrogen bond effect (Hu et al, 2017).…”
A rapid and straightforward method based on effervescent-assisted dispersive liquid-liquid microextraction combined with high-performance liquid chromatography-ultraviolet (HPLC-UV) detection for preconcentration of ketoprofen in water samples was developed. The extraction efficiency of ketoprofen drug was investigated using 23 central composite design. The values of optimum extraction condition were set as 300 µL volume of 1-dodecanol, three pieces of tablets, and 30°C extraction temperature. The runtime was conducted in less than 6 min using a non-polar C18 column and an isocratic mobile phase (acetonitrile: water of 40:60 (v/v)) at a controlled flow rate of 1 mL min-1. A good linear response was achieved in the range of 0.01–0.50 µg mL-1 (R2 > 0.990). Detection and quantification limits were calculated at 0.001 and 0.004 µg mL-1, respectively. The average recoveries at three spiking concentration levels were within the range of 85%–108% with RSD < 10% (n = 3). Real sample analysis was fortified using gel and standard solutions, and the calculated values were close to the actual values at 0.059 µg mL-1 (KET gel, initial concentration 0.075 µg mL-1) and 4.49 µg mL-1 (standard solution, initial concentration 5 µg mL-1), respectively.
“…The normality assumption was satisfied as to the residuals in the plot distributed along a straight line ( (Przyjazny, 2019). 1-dodecanol is a good extraction solvent owing to its hydrophobic end and hydroxyl group that can extract target analytes by hydrophobic or hydrogen bond effect (Hu et al, 2017).…”
A rapid and straightforward method based on effervescent-assisted dispersive liquid-liquid microextraction combined with high-performance liquid chromatography-ultraviolet (HPLC-UV) detection for preconcentration of ketoprofen in water samples was developed. The extraction efficiency of ketoprofen drug was investigated using 23 central composite design. The values of optimum extraction condition were set as 300 µL volume of 1-dodecanol, three pieces of tablets, and 30°C extraction temperature. The runtime was conducted in less than 6 min using a non-polar C18 column and an isocratic mobile phase (acetonitrile: water of 40:60 (v/v)) at a controlled flow rate of 1 mL min-1. A good linear response was achieved in the range of 0.01–0.50 µg mL-1 (R2 > 0.990). Detection and quantification limits were calculated at 0.001 and 0.004 µg mL-1, respectively. The average recoveries at three spiking concentration levels were within the range of 85%–108% with RSD < 10% (n = 3). Real sample analysis was fortified using gel and standard solutions, and the calculated values were close to the actual values at 0.059 µg mL-1 (KET gel, initial concentration 0.075 µg mL-1) and 4.49 µg mL-1 (standard solution, initial concentration 5 µg mL-1), respectively.
“…Atmaram Upare et al synthesized cinnamic acid derivatives (10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26) (Figure 4) in which the carboxyl group was replaced with bioisostere 1,2,4-oxadiazole followed by substituting the phenyl ring of the cinnamic acid resulting in a series of novel styryl oxadiazoles. The compounds were tested in vitro at day 8 for their anti-tubercular activity against H37Ra strain of Mycobacterium tuberculosis (Table 2).…”
Section: Lunatus Aniger P Ostreatusmentioning
confidence: 99%
“…Apart from them being intermediates in producing other compounds like stilbenes and styrenes, cinnamic acid derivatives exhibit antibacterial, antifungal, anti-inflammatory [10], neuroprotective [11], anticancer [12] and antidiabetic activities [13]. Cinnamic acid derivatives that have been reported by researchers include ferulic acid, curcumin [11], caffeic acid, p-hydroxycinnamic acid [14] coumaric and chlorogenic acids [15], etc. These cinnamic acid analogues are differentiated by the presence of hydroxyl groups on the phenyl ring that are either free or methoxylated [15].…”
The role played by cinnamic acid derivatives in treating cancer, bacterial infections, diabetes and neurological disorders, among many, has been reported. Cinnamic acid is obtained from cinnamon bark. Its structure is composed of a benzene ring, an alkene double bond and an acrylic acid functional group making it possible to modify the aforementioned functionalities with a variety of compounds resulting in bioactive agents with enhanced efficacy. The nature of the substituents incorporated into cinnamic acid has been found to play a huge role in either enhancing or decreasing the biological efficacy of the synthesized cinnamic acid derivatives. Some of the derivatives have been reported to be more effective when compared to the standard drugs used to treat chronic or infectious diseases in vitro, thus making them very promising therapeutic agents. Compound 20 displayed potent anti-TB activity, compound 27 exhibited significant antibacterial activity on S. aureus strain of bacteria and compounds with potent antimalarial activity are 35a, 35g, 35i, 36i, and 36b. Furthermore, compounds 43d, 44o, 55g–55p, 59e, 59g displayed potent anticancer activity and compounds 86f–h were active against both hAChE and hBuChE. This review will expound on the recent advances on cinnamic acid derivatives and their biological efficacy.
“…LPME can be mainly classified into single‐drop microextraction (SDME), dispersive liquid‐liquid microextraction (DLLME), and hollow fiber liquid‐phase microextraction (HF‐LPME) . So far, various types of LPME methods have been developed and applied for the analysis of cinnamic acids in complex‐matrix samples, including carbon nanotube reinforced hollow fiber solid/liquid phase microextraction , ionic liquid DLLME , DLLME based on amine‐functionalized Fe 3 O 4 nanoparticles , simultaneous two‐phase/three‐phase HF‐LPME , graphene/dodecanol floating solidification microextraction , and in‐syringe binary‐solvent LPME .…”
A novel three‐phase hollow fiber liquid‐phase microextraction was developed based on reverse micelle as extraction solvent and acceptor phase, and compared with conventional two‐phase hollow fiber liquid‐phase microextraction. Both procedures were used in the extraction and concentration of four cinnamic acids (caffeic acid, p‐hydroxycinnamic acid, ferulic acid, and cinnamic acid) in traditional Chinese medicines prior to high‐performance liquid chromatography analysis. Parameters affecting the two procedures were investigated and optimized to obtain the optimum enrichment factors. The mechanism of the developed procedure was explored and elucidated by comparison with conventional two‐phase hollow fiber liquid‐phase microextraction. Under the optimized conditions, the analytes’ enrichment factors were between 50 and 118 for the proposed procedure, and 31–96 for conventional two‐phase mode. Satisfactory linear ranges (r2 ≥ 0.99), detection limits (0.1–0.6 ng/mL), precisions (<9.2%), and accuracies (recoveries: 80–123.1%) were observed for the two procedures. The results showed that the enrichment capacity of the proposed procedure for the cinnamic acids is better than that of conventional two‐phase procedure, and both are eco‐friendly, simple, and effective for the enrichment and detection of cinnamic acids in traditional Chinese medicines.
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