Determination Of Ascorbic Acid Research Articles

Low-cost digital colorimetric sensor for rapid on-site determination of ascorbic acid in vegetable- and fruit-based purees and juices

Ascorbic acid is essential for human health due to its potent antioxidant properties; however, excessive intake can lead to adverse effects. This has created a high demand for simple and cost-effective analytical techniques to determine this analyte outside of laboratory settings for food quality control. In this study, a portable colorimetric sensor was developed for the quantitative on-site determination of ascorbic acid. The technique is based on the reduction of phosphorus heteropoly acid by ascorbic acid, resulting in the formation of a blue-colored product. The heteropoly acid was immobilized on a polymer template in the sensor's indicator zone with menthol used as an environmentally friendly extractant to enhance the device’s stability and extend its shelf life. The colorimetric sensor demonstrated reliable detection with a low limit of detection of 5mgkg-1, calculated based on a blank test using 3σ. Under optimized conditions, the linear detection range was 15-150mgkg-1. The disposable sensors were applied to determine ascorbic acid in fruit and vegetable juices and purees for baby food, with recovery rates between 88 and 110%. This easy-to-produce and ready-to-use technique presents significant potential for mass on-site screening of ascorbic acid in food samples.

A colorimetric platform using highly active Prussian blue composite nanocubes for the rapid determination of ascorbic acid and acid phosphatase.

Cobalt-doped Prussian blue composite nanocubes (Co-PB NCs) were synthesized, which can quickly convert O2 to O2•- and 1O2. Due to the presence of cobalt and iron transition metal redox electron pairs, Co-PB NCs with high oxidase mimetic activity can rapidly oxidize the substrate 3,3',5,5'-tetramethylbenzidine (TMB) to produce blue products (ox-TMB) without the assistance of unstable H2O2. Using ascorbic acid-2-phosphate trisodium salt (AAP) as a substrate, it can be converted to reduced ascorbic acid (AA) under acid phosphatase (ACP) hydrolysis, resulting in suppression of TMB oxidation. Therefore, an enzyme cascade signal amplification strategy for rapid colorimetric detection of AA/ACP was developed based on the high-efficiency oxidase-like activity of Co-PB NCs combined with the hydrolysis effect of ACP. The color changes at low concentrations of AA and ACP could be observed by the naked eye, and the detection limits of AA and ACP were 1.67μM and 0.0266 U/L, respectively. The developed colorimetric method was applied to the determination of AA in beverages and ACP in human serum, and the RSDs were less than 3%, showing good reproducibility. This work provides a promising strategy for the use of metal-doped Prussian blue composite material for the construction of rapid colorimetric sensing platforms that avoid the use of unstable hydrogen peroxide.

Carbon cloth surface engineering for simultaneous detection of ascorbic acid, dopamine, and uric acid in fetal bovine serum

Carbon cloth (CC) was electrochemically activated using three electrochemical methods in different electrolytes. The gases released during the activation process etched the surface of the CC, thereby increasing its surface area of the activated CC (FCC). Moreover, functional groups such as oxygen-containing groups and N-doping have been introduced. The quantity and type of functional groups introduced during the activation process were related to the anions in the solution. FCC electrodes were used to construct electrochemical sensors for the simultaneous determination of ascorbic acid (AA), dopamine (DA), and uric acid (UA). The PFCC electrode activated by advanced cyclic voltammetry in (NH4)2HPO4 showed linear ranges for AA, DA, and UA concentrations of 0.1 to 2.1 mM, 0.5 to 11 µM, and 0.5 to 11 µM, respectively. The detection limits are 72.93, 0.22, and 0.42 µM, respectively. The good flexibility the PFCC electrode made it suitable for the preparation of flexible sensors. The simultaneous determination of AA, DA, and UA in fetal bovine serum showed a reliable recovery ratio. This study provides a simple and green approach for activating carbon cloth and constructing flexible electrochemical sensors with the potential to simultaneously detect AA, DA, and UA.

Hydrogen-Bonded Organic Framework Enhanced Antifouling Property for Efficient In Situ Electrochemical Assay of Cerebral Ascorbic Acid.

Accurate determination of cerebral ascorbic acid (AA) is crucial for understanding ischemic stroke (IS) related pathological events. Carbon fiber microelectrodes (CFEs) have proven to be robust tools with high sensitivity toward AA, however, they face ongoing challenges for in situ measurement due to the non-specific adsorption of proteins in brain tissue. In this study, the hydrogen-bonded organic framework PFC-71 is synthesized and modified on CFEs through π-π stacking interactions with carboxylated carbon nanotubes (CNT-COOH). It is found that the gating effect and hydrophilicity of PFC-71 provided the CFE with excellent antibiofouling properties. As a result, AA exhibited a low oxidation potential of -30mV on the CFE/CNT-COOH/PFC-71, even in the presence of 20mgmL-1 bovine serum albumin. Given the structural advantages of CFE/CNT-COOH/PFC-71, a ratiometric electrochemical strategy for AA is established, enabling the in situ assay of cerebral AA in a middle cerebral artery occlusion (MCAO) model with high accuracy and stability.

Fluorescence and colorimetric rapiddual-signal "on-off-on" switching detection of ascorbic acidbased on TSPP/DCIP.

Afluorescence and colorimetric dual-signal sensing system for the determination of ascorbic acid (AA) in complex media was developed by using 5,10,15, 20-tetrakis(4-sulfonyl) porphyrin (TSPP) as a sensing probe and sodium 2,6-dichloroindophenol (DCIP) as a bridge. A fluorescence resonance energy transfer (FRET) effect occurred when DCIP was added to the TSPP solution, resulting in the quenching of the fluorescence signal of TSPP and a change in the color of the solution from pink to blue. The DCIP in the system reacted with AA in a redoxreaction to produce colorless phenol imine, the color of the solution changed from blue to green causing an obvious colorimetric response, and the TSPP/DCIP sensing system's fluorescence signal restored owing to AA introduced. The fluorescence method for AAshowed good linearity in the ranges 0.08mM ~ 1mM and 1mM ~ 43.6mM with a detection limit of 6.4μM. And the colorimetric method for AAshowed excellent linearity in the range 0.46mM ~ 40.2mM with a detection limit of 76.0μM. Theconstructed "dual-signal" probe in the study has been successfully applied to the detection of AA in practical samples. The method proposed has great potential for practical applications and provides new ideas for the visual inspection of portable measurements.

Unveiling the Versatile Applications of Cobalt Oxide-Embedded Nitrogen-Doped Porous Graphene for Enhanced Energy Storage and Simultaneous Determination of Ascorbic Acid, Dopamine and Uric Acid

The advancement of electrode materials is essential for addressing the energy and biomedical challenges. A multi-functional approach was employed to create a new electrode material of cobalt oxide-embedded nitrogen-doped porous graphene (Co3O4@NpG) for sensing and energy storage applications. In the present study, we have fabricated a new electrochemical sensing platform based on Co3O4@NpG. The sensing performance and selective detection capability of the demonstrated sensor was optimized and tested by determining dopamine (DA), uric acid (UA), and ascorbic acid (AA) simultaneously in analyte fortified biological samples. The sensing response is noticed to be linearly dependent upon the concentration of AA, DA, and UA in the range of 0.1–450, 0.1–502, and 0.2–396 μM, respectively. This material also showed good electrochemical energy storage performance when assessed as a supercapacitor electrode. The Co3O4@NpG electrode material showcased a remarkable specific capacitance of 314.58 Fg−1, an energy density of 10.06 Wh kg−1 at a power density of 240 Wkg−1 at 0.5 Ag−1, in a 6 M KOH electrolyte, along with excellent long-term cycling stability. Hence, the material Co3O4@NpG stands out as a promising multifunctional electrode candidate, excelling in the precise simultaneous detection of critical biomolecules besides exhibiting superior energy storage performance.

Derivative spectrophotometric method for simultaneous determination of ascorbic acid and folic acid in the pharmaceutical formulation; Comparative greenness assessment

Ascorbic acid and folic acid are frequently included together in multivitamin pharmaceutical products due to their complementary roles in maintaining human health. The quality and efficiency of supplements can vary depending on the manufacturer and the specific ingredients used, which are vital factors to consider. This research presents the development and validation of a simple, sensitive, accurate, and environmentally friendly derivative spectrophotometric technique utilizing the zero-crossing method for the simultaneous determination of ascorbic acid and folic acid, both in their pure form and in pharmaceutical formulations. The derivative spectrophotometry technique demonstrated measurable amplitude and substantial linearity for both analytes. At the zero-crossing points of folic acid (249.6 and 281 nm), ascorbic acid showed a measurable amplitude with a linear range of 0.17–12.0 μg/mL and 0.37–12 μg/mL, and detection limits of 0.057 μg/mL and 0.121 μg/mL, respectively. Conversely, folic acid displayed an observable amplitude at the zero-crossing point of ascorbic acid (265.6 nm) with a linear range from 0.26 to 15.0 μg/mL and a detection limit of 0.088 μg/mL.The greenness of the proposed derivative spectrophotometric method was evaluated using the White Analytical Chemistry (WAC) framework and the Green Analytical Procedure Index (GAPI). The method scored highly in both evaluations, confirming its minimal environmental impact and alignment with the principles of Green Analytical Chemistry. The GAPI assessment highlighted low environmental and health risks throughout the analytical process, making this method a green and sustainable choice for the simultaneous determination of ascorbic acid and folic acid. The method was successfully applied to synthetic laboratory mixtures and formulated tablets, showing excellent precision, accuracy, and recovery, while also being environmentally friendly.

Spectrofluorometric determination of ascorbic acid in the plasma matrix: Exploring correlation with autism spectrum disorder

Ascorbic acid (Vitamin C) is crucial for bodily functions, including collagen synthesis, immune system support and antioxidant defense. Despite autism spectrum disorder's multifactorial nature involving genetic, environmental and neurological factors, robust evidence exploring the association between ascorbic acid and this disorder is notably lacking. This study introduces an innovative spectrofluorometric method to quantify ascorbic acid in the plasma of healthy children and those with autism spectrum disorder. The method relies on the interaction of ascorbic acid with the fluorescent dye propidium iodide. In acidic conditions, propidium iodide undergoes protonation and selectively binds to the negatively charged ascorbic acid forming an ion-pair complex. This complex alters the molecular structure of propidium iodide inducing chemical fluorescence quenching, that can be utilized for ascorbic acid quantification. The developed method undergoes rigorous validation following ICH guidelines, demonstrating a linear relationship within a concentration range of 4–40 μg/mL, with high precision and accuracy metrics. Analysis of real plasma samples from autistic and healthy children reveals clinically and statistically elevated levels of ascorbic acid in those with autism spectrum disorder.

Nickel Doped Hydroxyapatite Nanocomposite via Salt Melting Approach: A Colorimetric Sensing Platform for the Determination of Ascorbic Acid

Abnormal levels of ascorbic acid in the human body can induce various diseases. We reported a nickel-doped hydroxyapatite (Ni-HAp)-based biosensor for ascorbic acid and confirmed it through various spectroscopic techniques. Ni-HAp demonstrated peroxidase-like activity that was detected through the chromogenic substrate. The analyte produces a color change from blue-green to colorless. The optimized sensor has a correlation coefficient of 0.997, a limit of detection of 0.11 µM, a limit of quantification value of 0.36 µM, and a linear range from 2 to 47 µM for ascorbic acid. The synthesized sensor was used to determine ascorbic acid in spiked physiological solutions.

Amperometric sensor based on carbon nanotube, ionic liquid, and polyaspartic acid for ascorbic acid determination

AbstractAn amperometric sensor for ascorbic acid determination has been developed by modifying the surface of a glassy carbon electrode (GCE) with polyaspartic acid (PolyAsp), carboxylated multi‐walled carbon nanotube (c‐MWCNT), and ionic liquid (IL, 1‐butyl‐3‐methylimidazolium hexafluorophosphate). The amount of each modification material on the surface was optimized in order to achieve good analytical performance. The operating conditions of c‐MWCNT−IL/PolyAsp/GCE were optimized. The performance characteristics of c‐MWCNT−IL/PolyAsp/GCE were investigated at optimum pH (8.0) and optimum potential (+0.20 V), and the sensor responded linearly to ascorbic acid between 5.3–2766.3 μM with a sensitivity of 19.64 μA mM−1 and detection limit of 3.0 μM. Determination of ascorbic acid in vitamin C tablet, vitamin C injection solution, and orange juice was successfully performed with the presented sensor and the recovery values were found between 98.9% and 101.6%.

Conducting Nickel Hydroxide Thin Film on Molybdenum Disulfide – Reduced Graphene Oxide Composite Electrode for Simultaneous Detection of Uric Acid, Dopamine and Ascorbic Acid

AbstractHerein we report the fabrication of a simple electrochemical sensor based on an electrode containing reduced graphene oxide and molybdenum disulphide (RGO/MoS2) as a conducting film onto the glassy carbon electrode (GCE) via a drop dry method to form GCE‐RGO/MoS2. The surface (GCE‐RGO/MoS2) was further modified with nickel hydroxide thin film using electrodeposition method to form GCE‐RGO/MoS2/Ni(OH)2. The materials and modification steps were thoroughly characterized using microscopy and spectroscopy methods. The composite electrode, GCE‐RGO/MoS2/Ni(OH)2, showed excellent electrocatalytic potential separation for the detection of dopamine, uric acid, and ascorbic acid. The electrocatalytic oxidation peak potentials were at 3 mV, 157 mV and 303 mV for AA, DA and UA, respectively. The composite electrode was also selective towards the determination of ascorbic acid (AA), dopamine (DA), uric acid (UA), and simultaneously in mixture of analytes. The low detection limits for AA, DA and UA were 1.17 μM, 0.15 μM and 1.15 μM, respectively. The composite electrode was applied for the detection of AA, DA and UA in spiked newborn calf serum samples with high percentage recoveries ranging from 96.6–100.8 % for AA, 92.8–104.2 % for DA and 99.4–102.3 % for UA.

Highly efficient electrochemical ascorbic acid determination via a cooperative catalytic effect of dendritic Bi/Bi2O3 junctions and oxygen vacancies

This study developed an electrochemical sensor for ascorbic acid (AA) using dendritic nanostructured (DN) bismuth/bismuth oxide thin films with oxygen-deficient (SOD) surfaces (SOD-DN Bi/Bi2O3-x thin films) that were successfully fabricated through electrodeposition on fluorine-doped tin oxide (FTO) substrates. Using cyclic voltammetry and amperometry, we assessed electrocatalytic activity in neutral media. The prepared SOD-DN Bi/Bi2O3-x thin film was used, for the first time, as electrodes in a highly sensitive and selective electrochemical AA sensor. The SOD-DN Bi/Bi2O3-x thin film with optimal characteristics was shown to be ultrasensitive in AA detection in neutral conditions, whereby high detection sensitivity ∼ 2.30 µA µM-1cm−2 over a wide range of AA concentration ∼ 0.01 µM to 1.0 mM and working potential range ∼ 0.3–1.0 V vs. SCE. The results indicate that SOD-DN Bi/Bi2O3-x can provide large amounts of active reaction sites, thereby enhancing electrocatalytic activity and electrochemical sensitivity. Due to this, it is a unique electrochemical sensor able to detect AA without interference from DA, UA, or other contaminants. A further amperometric test demonstrated that this sensor was capable of detecting AA even under conditions of dopamine and uric acid. Accordingly, the proposed sensor provides a promising avenue for developing electrochemical sensing for AA determination. This strategy introduces a novel type of high-efficiency electrocatalyst for ultrasensitive detection of medical and environmental biomarkers.

Binder-free and efficient voltammetric sensor based on Zn-Ca2CuO3 nanoparticles for simultaneous determination of amlodipine, acetaminophen, and ascorbic acid in hypertension patients.

Amlodipine (AM) is a long active calcium channel blocker used to relax blood vessels by preventing calcium ion transport into the vascular walls and its supporting molecules acetaminophen (AP) and ascorbic acid (AA) are recommended for hypertension control and prevention. Considering their therapeutic importance and potential side effects due to over dosage, we have fabricated a sensor for individual and simultaneous determination of AA, AP, and AM in pharmaceuticals and human urine using novel Zn-doped Ca2CuO3 nanoparticles modified glassy carbon electrode (GCE). Optimally doped Ca2CuO3 (2.5 wt% Zn at Cu site) enhanced the detection of target molecules over much wider concentration ranges of 50 to 3130 µM for AA, 0.25 to 417 µM for AP, and 0.8 to 354 µM for AM with the corresponding lowest detection limits of 14 µM, 0.05 µM, and 0.07 µM, respectively. Furthermore, the Zn-Ca2CuO3/GCE exhibited excellent selectivity and high sensitivity even in the presence of several potential interfering agents. The usefulness of the developed electrode was tested using an amlodipine besylate tablet and urine samples of seven hypertension patients under medication. The results confirmed the presence of a significant amount of AP and AM in six patients' urine samples indicating that the personalized medication is essential and the quantum of medication need to be fixed by knowing the excess medicines excreted through urine. Thus, the Zn-Ca2CuO3/GCE with a high recovery percentage and good sensitivity shall be useful in the pharmaceutical and biomedical sectors.

One-step microwave-assisted synthesis of fluorescent carbon quantum dots for determination of ascorbic acid and riboflavin in vitamin supplements

The synthesis of carbon quantum dots (CQDs) using chemical precursors with different organic groups is a strategy to improve optical properties and expand applications in several fields of research such as Analytical Chemistry. Ascorbic acid and riboflavin are widely used in human food supplementation, making quality monitoring of these vitamin supplements relevant and necessary. In this work, disodium ethylenediaminetetraacetic, sodium thiosulfate and urea were applied to obtain CQDs through a single-step microwave-assisted synthesis. The CQDs were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray powder diffraction, infrared spectroscopy, zeta potential measurements, ultraviolet–visible spectroscopy and photoluminescence spectroscopy. The synthesized nanoparticles exhibited satisfactory and stable optical properties with luminescence at 430 nm, water solubility, and fluorescence quantum yield of 8.9 %. They were applied in the quantification of ascorbic acid and riboflavin in vitamin supplements. The fluorescence mechanisms observed were dynamic quenching for the CQDs/Cr(VI) sensor, followed by a return of fluorescence in the presence of ascorbic acid, and static quenching and inner filter effect in the interaction with riboflavin. Factorial designs 23 and 24 were used to optimize the analytical parameters. The CQDs/Cr(VI) sensor used in the determination of ascorbic acid, employing an on–off-on strategy, resulted in a linear range of 0.5 to 50 µg mL−1 and a limit of detection of 0.15 µg mL−1. The ratiometric fluorescence used in the determination of riboflavin resulted in a linear range of 0.1 to 7 µg mL−1 and a limit of detection of 0.09 µg mL−1. The analytical results for ascorbic acid were compared to the reference method of the Brazilian pharmacopeia, showing accuracy and precision according to the Brazilian Health Regulation Agency. Therefore, the synthesized CQDs were used to determine ascorbic acid and riboflavin in vitamin supplements, and the application of this nanomaterial can be expanded to different analytes and matrices, using simple and low-cost analysis techniques.

Multifunctional N, Fe-doped carbon dots with peroxidase-like activity for the determination of H2O2 and ascorbic acid and cell protection against oxidation.

Multifunctional N, Fe-doped carbon dots (N, Fe-CDs) were synthesized by the one-step hydrothermal method using ferric ammonium citrate and dicyandiamide as raw materials. The N, Fe-CDs exhibited peroxidase-like (POD) activity by catalyzing the oxidization of 3,3',5,5'-tetramethylbenzidine (TMB) to the green oxidation state ox-TMB in the presence of hydrogen peroxide (H2O2). Subsequently, based on the POD activity of N, Fe-CDs, an efficient and sensitive colorimetric method for the detection of H2O2 and ascorbic acid (AA) was established with a limit of detection of 0.40 µM and 2.05 µM. The proposed detection method has been successfully applied to detect AA in fruit juice, vitamin C tablets, and human serum samples and has exhibited excellent application prospects in biotechnology and food fields. Furthermore, N, Fe-CDs also showed a protective effect on the cell damage caused by H2O2 and could be used as an antioxidant agent.

The effect of salicylic acid on the content of ascorbic acid and phenolic compounds in wheat plants

Background. Salicylic acid is an important phytohormone in plants, influencing various functions such as senescence, respiration, and stress resistance. Despite extensive studies the role of salicylic acid in stress, its effects under normal conditions are less understood. This study explores the influence of salicylic acid on the biosynthesis of important biochemical compounds such as ascorbic acid, rutin, and other phenolic compounds in wheat (Triticum aestivum L.), aiming to elucidate potential applications in agriculture. Materials and Methods. Wheat variety 'Podolyanka' was treated with 0.05 mM salicylic acid and grown under controlled conditions. Biochemical analyses were studied on 7, 10 and 20 days of growth to using the spectrophotometric method for the determination of ascorbic acid, rutin, total phenolic compounds, anthocyanins, flavonoids, and xanthones. Methods included chromatography on the plate with silicagel for rutin. Results and Discussion. Salicylic acid treatment significantly increased the ascorbic acid content in wheat shoots at all studied stages. There was also a notable increase in rutin content in the early growth phase. However, the content of other phenolic compounds, such as xanthones, generally decreased under salicylic acid treatment. Intriguingly, anthocyanin content was increased, suggesting a complex interaction within the biosynthetic pathways influenced by salicylic acid. The study also revealed correlations among different phenolic compounds, indicating intertwined metabolic pathways. Conclusion. Salicylic acid enhances the biosynthesis of specific phenolic compounds like ascorbic acid and rutin in wheat, which can have implications for agricultural practices aiming at improving plant resilience and nutritional quality. The differential impact of SA on various phenolic compounds underscores the complexity of plant biochemical pathways and highlights the need for further research to fully understand these interactions and their practical applications.

A dual-signal optical sensing platform of CDs-MnO2 NS composites for facile detection of ascorbic acid based on a combination of Tyndall effect scattering and fluorescence.

A dual-signal optical sensing platform was successfully developed for the determination of ascorbic acid (AA) based on blue fluorescent carbon dots (CDs) and manganese dioxide nanosheets (MnO2 NSs) with strong Tyndall effect (TE) scattering and fluorescence quenching capabilities. In this nanosystem, CDs-MnO2 NS composites were employed as probes to evaluate the AA concentration. Owing to the strong reduction, the presence of the target AA could reduce the MnO2 NSs to Mn2+ and induce the degradation of the MnO2 NSs, resulting in a significant decrease in the TE scattering intensity of the MnO2 NSs and the fluorescence recovery of the CDs. Therefore, a novel optical sensor based on TE scattering and fluorescence dual detectors was developed for the sensitive determination of AA. Under optimized conditions, the limits of detection (LODs) of the two modes were 113 and 3 nM, respectively. Furthermore, the dual-signal optical sensing platform was successfully applied for the detection of AA in human serum.

Electrochemical syntheses and characterization of some polydyes and their application for the simultaneous determination of ascorbic acid and uric acid

Electrochemical syntheses and characterization of some polydyes and their application for the simultaneous determination of ascorbic acid and uric acid

Development of Response Surface Approach for Determination of Paracetamol, Chlorpheniramine Maleate, Caffeine and Ascorbic Acid by Green HPLC Method: A Desirability-Based Optimization.

Design of experiment is an efficient and cost-effective tool to optimize the chromatographic separation of a multicomponent mixture. The central composite design was conducted to develop and optimize a green high performance liquid chromatography (HPLC) method for simultaneous quantitation of a quaternary mixture of paracetamol, chlorpheniramine maleate, caffeine and ascorbic acid in their pharmaceutical dosage form as well as the determination of their dissolution profile. A five-level three-factor model was performed to investigate the effect of mobile phase composition, pH and flow rate on enhanced resolution and short run time. Analysis was performed using a Kinitex EVO C18 column and a mobile phase composed of methanol: 0.02M phosphate buffer pH3.3 (34:66, v/v) at 1.0mL/min using photodiode array detection. Optimum chromatographic separation was achieved in <6min with a desirability of 0.999. Linearity was achieved over a range of 1.00-300.00, 1.00-50.00, 2.00-50.00 and 2.00-100.00μg/mL for paracetamol, chlorpheniramine maleate, caffeine and ascorbic acid, respectively, with a limit of detection (<0.1μg/mL). The greenness profile was evaluated using the analytical eco-scale and Analytical GREEnness Metric Approach with values of 81 and 0.77, respectively.

Chemical composition and antioxidant properties of native Ecuadorian fruits: Rubus glabratus Kunth, Vaccinium floribundum Kunth, and Opuntia soederstromiana

The native berries of South America present promising marketing opportunities owing to their high antioxidant content, notably rich in anthocyanin and phenolic compounds. However, Ecuador's endemic fruits, primarily found in the wild, lack comprehensive data regarding their phytochemical composition and antioxidant capacity, underscoring the need for research in this area. Accordingly, this study evaluated the total phenolic, anthocyanin, flavonoid, resveratrol, ascorbic acid, citric acid, sugars, and antioxidant content of three native Ecuadorian fruits: mora de monte (Rubus glabratus Kunth), mortiño (Vaccinium floribundum Kunth), and tuna de monte (Opuntia soederstromiana). Determination of resveratrol, ascorbic acid, citric acid, and sugars was determined by HPLC analysis, and UPLC analysis was used to determine tentative metabolites with nutraceutical properties. Antioxidant capacity was assessed using cyclic voltammetry and the DPPH method; differential pulse voltammetry was used to evaluate antioxidant power. Analysis of results through UPLC-QTOF mass spectrometry indicated that R. glabratus Kunth and V. floribundum Kunth are important sources of various compounds with potential health-promoting functions in the body. The DPPH results showed the following antioxidant capacities for the three fruits: R. glabratus Kunth >O. soederstromiana >V. floribundum Kunth; this trend was consistent with the antioxidant capacity results determined using the electrochemical methods.