Ascorbic acid (H₂A) is an important antioxidant that displays a redox couple (ascorbic acid (H₂A)/dehydroascorbic (A)) useful in hydroxylation reactions in the body [18], the reduction reaction of several compounds such as reactive oxygen species [19], and protecting cells against oxidative stress caused by infections [20]. Owing to these properties, ascorbic acid plays an important role in the treatment of several respiratory infections such as bronchitis, pneumonia [20], and influenza, and recently, there have been several trials for the treatment of SARS-CoV-2 [21,22,23].

On the other hand, uric acid is a product of purine metabolism present in diverse human fluids such as blood serum or urine, where its concentration range is 0.24–0.50 and 0.214–4.40 mM, respectively. High levels of UA may cause many urinary tract diseases and renal failure.

Ascorbic acid and uric acid sensors have interesting applicability in medical sciences. The examples of these sensors fabricated with coordination compounds are scarce; however, interesting results have been obtained by using diverse composites of porphyrin complexes based on Mn³⁺, Fe²⁺, and Zn²⁺ that display a redox pair M²⁺ ⇆ M³⁺, which mimics the active site of several enzymes, and it is useful for oxidation and reduction of diverse kind of biomolecules [24]. The selective oxidation of ascorbic acid or uric acid on the electrode’s surface depends on the metallic center and other components on the electrode. Interesting results were obtained with composites of [Zn²⁺(Pro)³⁺R(Cl)] and tetraoctilammonium bromide (TOAB) for the electroanalytical sensing of ascorbic acid at pH 7.0 [25,26]. In the composites, the tetraoctylammonium bromide aids in the oxidation of ascorbic acid through an irreversible oxidation process, while the dye only works as an electron-transfer mediator. An analysis conducted by CV indicated that Zn(II) metalloporphyrins showed four redox process (in an anodic and cathodic sense) between 0.5–1.2 V related to the oxidation and reduction of the porphyrin ligand and the Zn²⁺ ion. Based on these results, it was proposed that the key role of the dye follows the next mechanism:

The anion (A⁻) produced in Reaction (1) is coordinated in the complex [Zn²⁺(Pro)³⁺R(X)] in Reaction (2) to create a coordination bond with A-; then, in Reaction (3), the electrons are captured by the complex to produce its reduced form [Zn(Pro)³⁺R(X)] and dehydro-L-ascorbic acid; finally, in Reaction (4), the complex [Zn²⁺(Pro)³⁺R(X)] is regenerated again. The oxidation of H₂A is carried out by TOAB present in the composite.

For the selective oxidation of uric acid, it is only reported the use of a manganese (III) porphyrin complex (MnNH₂TPP) composite [27]. The interesting part of this work is the proposed oxidation mechanism, which suggests that UA is coordinated to the complex, and uric acid is then oxidized in several electron transfer steps as shown in Figure 5, where, after the coordination of UA molecules, these are rearranged to produce carbocations that undergo a dehydrogenation reaction to yield allantoin as the final product.

On the other hand, in some specific cases, metalloporphyrins catalyze the oxidation of both substrates (ascorbic acid and uric acid). This property was presented on iron (III) porphyrin complexes [24]. The simultaneous oxidation for ascorbic acid and uric acid gives dehydroascorbic acid and allantoin, respectively, as former oxidation products. During the oxidation process, Fe³⁺ center is reduced to Fe²⁺ during the oxidation of the analytes at diverse potentials. The final oxidation products obtained from the analytes are represented in Figure 6. The process is highly pH-dependent (pH = 4.0), and the results obtained with these electrodes displayed very low detection limits in the micromolar order and a wide linear range (from micromolar to millimolar). These results demonstrate the potential applicability of MP or MPc as multi-analyte electrochemical sensors; nonetheless, because the application of complexes to electroanalytical chemistry is new, few reports can be found in the literature.

As part of this work, we summarized the recent examples of electrodes modified with porphyrin complexes for the electroanalytical sensing of ascorbic acid (Table 1) and uric acid (Table 2), including the potentials of work, limits of detection, and other analytic parameters.

Dopamine (DA) is an important catecholaminergic neurotransmitter that plays an essential role as a chemical messenger in the central nervous system and cardiovascular system. The normal level of dopamine in the brain is around 0.01–1.0 µM [30], and the decrease of this level may cause severe affectations such as Parkinson’s disease or schizophrenia [31]. The development of novel sensors for detecting DA is an important topic in electrochemistry; however, the coexistence of ascorbic acid and uric acid in real samples interferes with the accurate quantification of DA because both molecules are oxidized at the same potential as DA, and electrodes are unable to separate their electroanalytical signals. As a result, there is intensive research on new materials with the capability of selective sensing of DA at low potentials. The biological compatibility of porphyrins and phthalocyanine complexes make them attractive for their use as active materials on electrodes for the electroanalytical sensing of DA. For these purposes, composite-based Co²⁺, Cu²⁺, or Zn²⁺ complexes and carbon nanomaterials have been used in the selective oxidation of dopamine on amperometric sensors, displaying the limits of detection in the micromolar/nanomolar order and low oxidation potentials (under 0.3 V). When these electrodes are in the presence of diverse concentrations of DA, a linear increase of the anodic current is observed, indicating the great sensitivity of the electrodes fabricated with MP and MPc. Additionally, it is reported that the electroanalytical response increases in the presence of diverse scan rates, which suggests that the oxidation of dopamine is a diffusion-controlled mass process [32]. The electro-oxidation of dopamine is carried out by the redox pair M²⁺/M³⁺ present in the complexes, where the formation of M³⁺OOH plays an essential role as a redox catalyst. In an anodic sense, the complex is forced to be oxidized by the potential applied, and as result, unstable and highly oxidant M³⁺ species are obtained in the electrode surface and reduced to the M²⁺ due to the electron gain during the oxidation process. As illustrated in Figure 7, the reaction has a loss of two protons and is carried out via two-electron oxidation to yield dopamine-o-quinine as the final oxidation product.

The obtaining of M³⁺ species and the electro-oxidation process are dependent on the pH, and better results have been obtained at pH 6–7. At this pH range, the changes in the coordination environment can be clearly seen by cyclic voltammetry. In other cases, the addition of hydrogen peroxide was a fundamental step to obtain the high valence M³⁺ species [31,32]. In this case, H₂O₂ activates the complex to obtain the M³⁺OOH active layer on the electrode’s surface. For now, the results obtained with these electrochemical sensors are promising. These features can be assigned to the conductivity properties of the nanomaterials employed on the composites and the redox properties of complexes. At present, only a few examples of dopamine sensors elaborated with MPc or MP are reported. We expect that in the future, the application of these kinds of complexes will attract the attention of electroanalytical chemistry; nonetheless, it is necessary to evaluate new complexes (such as those based on Ni²⁺) and enhance their solubility or conductivity to obtain better electrochemical signals. As part of this work, we have summarized in Table 3 the recent electrochemical sensors based on MP or MPc for dopamine quantification.

Today, glucose amperometric sensors are one of the most critical topics in electroanalytical chemistry. The demand for more reliable and exact analytical devices is based on the constant increment of diabetic patients around the world [34]. There are several proposals of innovative and promising wearable devices based on enzymes for detecting glucose in fluids such as sweat [35], saliva [36,37,38], or urine [39,40,41]; however, the use of enzymes is challenging, and several problems are faced during their immobilization on the electrode’s surface. Moreover, the electron transference between the enzyme redox center and the electrode surface is slow, and the glucose oxidation requires elevated positive overpotentials. In this regard, several types of electroactive materials such as metallophthalocyanines and metalloporphyrins are being employed on integrated biosensors as electron-transfer mediators and co-immobilizers of enzymes, helping to enhance the electroanalytical signal.

There is a growing interest in designing bio-amperometric sensors (second generation), based on the use of nanocomposites of cobalt (II) phthalocyanine, and currently, diverse examples can be found in the literature [8,42,43,44]. This particular interest is due to their versatility, biocompatibility, and the redox-active activity of metals in the complex, which present a redox pair (Co²⁺/Co³⁺) in presence of alkaline media that is useful in electrocatalytic processes [43] and the electron-transfer capability of the nanomaterials employed to fabricate the nanocomposite.

On nanocomposites of phthalocyanine complexes, graphene is commonly used, because it improves the conductivity problems related to the semiconductor behavior of the complexes. The key role of cobalt (II) phthalocyanine in the nanocomposite is to act as a peroxidase, mediating the electro-oxidation of H₂O₂ produced during the glucose oxidation with the GOx enzyme. This electro-catalytic process is carried out by the redox pair (Co²⁺/Co³⁺) presented on the complex, as illustrated in the reaction in Figure 8, and is directly used to measure the glucose concentration in the function of the amount of hydrogen peroxide produced during the enzymatic reaction. As a result, these electrodes have the capability of sensing glucose or hydrogen peroxide at neutral pH.

As shown in Table 4, the few examples of biosensors elaborated with cobalt phthalocyanine [8,42,43,44] or other kinds of porphyrins derivative complexes [45] have displayed good detection limits (around 1.6–63 µM), although in the presence of real samples of human serum blood or drinks. Despite the low sensitivity and accurate detection limits (in the micromolar order) obtained with these electrodes, the use of expensive enzymes as principal active materials limits the commercial production and applications [46]. As a result, porphyrin and phthalocyanine complexes are being explored as a direct redox-catalyst for glucose oxidation in non-enzymatic electrochemical sensors. It is demonstrated that materials based on specific transition metals such as Co²⁺, Ni²⁺, and Cu²⁺, have redox catalysis activity toward glucose [47]. In this respect, coordination compounds such as MOFs based on these ions are being mainly used as active materials for the selective oxidation of glucose in alkaline media, presenting extraordinary results [13]. Regarding metal porphyrins, films of diverse types of nickel and cobalt porphyrins have been explored on glucose electro-oxidation in alkaline media, and they have displayed high stability in aqueous solutions, low detection limits, low oxidative potentials, and wide linear response. To explain the mechanism of glucose electro-oxidation, the most accepted hypothesis suggests that M³⁺OOH species obtained in alkaline media from M²⁺ complexes act as a redox mediator for the electro-oxidation of glucose to obtain gluconolactone as former oxidation product [8,10,13,16,48], according to the following mechanism:

In Reaction (5), the M²⁺ is oxidized to M³⁺ and produces MOOH, which generates an increase of the anodic peak current in cyclic voltammetry; then, in Reaction (6), MOOH oxidizes glucose (C₆H₁₂O₆) to gluconolactone (C₆H₁₂O₇), enhancing the height of the anodic peak. This oxidation process is easily observable by CV for nickel complexes in comparison with the cobalt complex.

For example, Maia and coworkers [49] reported the modification of a GCE with tetra{bis(2,2-bipyridyl)chlororuthenium(II)}{5,10,15,20-tetra(4-pyridyl)porphynatonickel(II)}(Ni-TRP) for electro-oxidation of glucose in alkaline media. In the absence of glucose, the CV experiments displayed the characteristic Ni²⁺/Ni³⁺ redox pair between 0.4–0.6 V (Figure 9a). In the presence of glucose (0.95 mM), there was an increment of 20 µA in the anodic peak current at 0.58 V, which increases at diverse glucose concentrations (Figure 9b). The evaluation as an electrochemical sensor was carried out by cyclic voltammetry in a linear range of 0.019–1.8 mM, obtaining a LOD of 6.1 µM.

The use of cobalt phthalocyanines complexes is more common due to its high electro-catalytic activity toward biomolecules. As presented before, cobalt phthalocyanines were used in conjunction with enzymes to obtain novel enzymatic electrodes, and diverse examples have demonstrated the capability of cobalt phthalocyanine composites as redox mediators on glucose detection without enzymes, presenting lower detection limits (0.14–0.6 µM) than enzyme-based electrodes. Furthermore, the linear range is over 20 mM, which is very important for glucose detection in real samples. As shown in Table 5, the analytical parameters of non-enzymatic electrodes surpass those reported for enzyme-based electrodes in Table 4. Nonetheless, the research on porphyrins derivative complexes for non-enzymatic glucose sensors is losing ground and is being replaced with other metal-coordinated materials such as MOFs.

Hydrogen peroxide (H₂O₂) is a strong oxidizer industrially used for cleaning and bleaching processes. In the body, it plays an important function in the defense of the organism; however, elevated concentrations of this molecule may cause damage to cell proliferation, cancer, or Alzheimer’s disease [51]. On the other hand, H₂O₂ is a by-product generated during the oxidation of glucose-by-glucose oxidase enzymes, and it can be used for the indirect quantification of glucose by using analytical techniques such as titrimetry and spectrofluorimetry [52], and more recently, hydrogen peroxide sensors are being used for the indirect electrochemical quantification of glucose; nevertheless, this quantification implies the use of enzyme-based electrodes, which are expensive and difficult to build. At present, there is a growing interest in the design of enzyme-free sensors for the accurate detection of H₂O₂ in neutral and alkaline media [53], and materials based on transition metals are playing an important role as active materials in non-enzymatic electrodes. In this respect, composites of MP and MPc have been demonstrated to be excellent modifiers for the elaboration of innovative electrochemical sensors. Diverse electrodes modified with MP or MPc based on Mn³⁺, Fe²⁺, Co²⁺, and Zn²⁺ have been successfully applied for the selective electrocatalyst of hydrogen peroxide in neutral or alkaline media.

The electrocatalyst process of hydrogen peroxide is divided into reduction and oxidation. In both cases, the formation of a redox couple (M²⁺/M³⁺ or M³⁺/M⁴⁺) on the complex mediates the analyte’s electro-reduction or electro-oxidation. In the reduction process (Figure 10), H₂O₂ yields H₂O in a negative potential, and the metallic ions are oxidized by the effect of H₂O₂ to temporally yield a high valence state, which is reduced to its stable form. This process is observed as two peaks (anodic and cathodic) in cyclic voltammetry experiments. On the other hand, during the oxidation process, the high valence species produced on anodic potential catalyze the electro-oxidation of hydrogen peroxide to yield oxygen (O₂) as the main product. As illustrated in Figure 11, Gao and coworkers [54] proposed that during the oxidation process with Co(II) porphyrin complex, H₂O₂ is bonded to the high valence metallic center (Co³⁺) to create an intermediary product, which participates in an H₂O₂ deprotonation process to give a dioxygen intermediate. The dyoxygen is released and the Co2+ is regenerated again.

In other papers, the changes in the coordination environment are not mentioned; however, it is possible that metallic ions could be coordinated with hydroxyl ions to form an octahedral structure. This behavior was observed during the evaluation of a Co(II) porphyrin complex by cyclic voltammetry at diverse pH values, where the anodic peak displayed a negative shift when the pH increased, which indicates a strong binding of the hydroxyl ion to the Co(III) [55]. The analytical parameters of electrochemical sensors based on MP or MPc are promising, with limits of detection (LOD) from the nanomolar to micromolar order and a wide linear range. At present, the research on MP and MPc as redox-catalysts on hydrogen peroxide sensors remains active, and diverse materials such MOFs or COFs (covalent–organic frameworks) are being used in combination with MP/MPc to obtain innovative and highly selective composites for electroanalytical application. It is expected that the research on non-enzymatic sensors based on Mp and MPc could increase in the close future and completely replace enzymes. As part of this section, diverse examples of complexes-based electrodes for sensing hydrogen peroxide are summarized in Table 6.

Few examples of electrochemical sensors for the selective detection of specific analgesics, antibiotics, and phosphodiesterase inhibitors are reported in the literature. The oxidation processes with electrochemical sensors based on complexes do not require high oxidation potentials, and the detection limits obtained with these sensors are very low, similar to those presented with enzymatic sensors [63].

During the design of electrochemical sensors based on MP, functionalized MPs were used as enhanced electrocatalysts with selective properties. For example, tetraruthenated porphyrin complexes have been used as modifiers on GCE for the selective recognition of isoniazid, folic acid, acetaminophen, and tyrosine, presenting low detection limits and good sensitivities. In these cases, the peripheral Ru(II) moieties on the complexes have a strong electron-withdrawing effect on the main metallic center in the porphyrin core, which is oxidizing the catalytic properties of the main metallic center. As mentioned in the other section, the electro-catalytic process is mainly carried out by the effect of the redox couple (M²⁺/M³⁺), which is employed for the oxidation or reduction of the pharmaceuticals, while ruthenium is not involved in the catalytical process. Regarding the change in the coordination environment during the electro-catalysis, Ferreira and coworkers [64] have reported changes in the structure of the supramolecular [Ni(II)TPyP(Ru(bipy)₂Cl)]⁴⁺ complex used for folic acid electro-oxidation. In this case, there is a formation of a µ-peroxo bridge at high alkaline media in the complex structure, which promotes the redox mediation for the electrocatalytic response. On the electro-reduction of metronidazole with a glucosylated Mn(III) porphyrin complex, Gong [65] mentioned that the presence of glucopyranose groups in the complex works as a three-dimensional cage, which acts as a specific recognition site for metronidazole, and induces its coordination to the metallic center. In consequence, similar molecules such as albendazole are not able to be coordinated and recognized by the complex.

Despite the excellent results obtained with MP and MPc, the current research on novel electrocatalysts is focused on porous materials such as MOFs, COFs, and zeolites, which present enhanced electrocatalytic properties. As part of this work, we have summarized in Table 7 diverse examples of electrochemical sensors modified with MP and their electroanalytical parameters.

The term ‘phenolic pollutants’ includes alkyl, nitro, and halophenols, which are considered important water and soil pollutants due to their slow degradation kinetics and carcinogenic effects [70]. The EPA (Environmental Protection Agency) established a permissible limit of 1 ppb for phenol in water, while toxicity levels for humans are about 9–25 mg/L [71]. As an alternative analytical tool, diverse electrochemical sensors based on coordination compounds have been developed for the identification and quantification of these pollutants in aqueous media. Cobalt (II) and iron (III) phthalocyanine or porphyrin composites are widely preferred as redox-active catalysts on this kind of electrochemical sensor due to their high efficiency in electro-oxidation reactions in acidic media, their high surface area, and the presence of high electron density on their 18 π-electron aromatic ring that make these molecules perfectly suitable for being robust electron mediators [7]. Excellent results have been obtained with these composites, presenting LOD from femtomolar to micromolar order. An interesting example of the use of these complexes is reported by Mazzota and coworkers [72]. In their work, they used a Co-porphyrin (Co(III)tetrakis(o-aminophenyl) porphyrin) as a redox mediator for the electro-mediator of 4-(2,4-dichlorophenoxy)butyric acid (2,4-DB). In this case, the complex was polymerized in the presence of 2,4-DB (used as a template) to create a molecular impressed polymer (MIP). The modified electrode was employed to recognize and quantify 2,4-DB by using chronoamperometry, presenting a LOD of 40 µM and a linear range of 200 µM–2 mM. The electro-reduction mechanism is not reported; nonetheless, it is probable that 2,4-DB is reduced to its corresponding aldehyde or alcohol, while Co(II)/Co(I) species are generated during the catalyst.

On the other hand, there is interest in the electrochemical quantification of hydrazine on wastewater and soils. This short molecule with formula N₂H₄ has wide applicability as a corrosion inhibitor or jet fuel. Despite its diverse industrial applications, hydrazine is highly toxic to humans and animals, causing carcinogenic effects; therefore, electrochemical sensors based on highly active materials with electro-oxidative properties are being explored in the direct detection of hydrazine. It is demonstrated that cobalt (II) porphyrin complexes have a strong affinity to the electro-catalysis of hydrazine in alkaline and neutral media [73,74]. The d7 electronic configuration and the presence of low-spin fields induct a coordination environment with no repulsive effects, which facilitates the electro-oxidation process of hydrazine.

Canales and coworkers [75] evaluated by CV diverse transition metal octaethylporphyrin modified GC electrodes (M = Co²⁺, Cu²⁺, Zn²⁺, Ru³⁺, Ni²⁺) in the presence of hydrazine. In their work (Figure 12), it was observed that only the Co(II)-OEP complex displayed an anodic peak assigned to the N₂H₄ oxidation, while the other complexes did not show any response.

As proposed in the following equations, it is suggested that hydrazine is coordinated to Co(II); this process generates an intermediate cation, which is rapidly oxidized to regenerate Co-OEP, forming N₂ as the final oxidation product.

Composites based on Ni²⁺, Fe³⁺, or Pt²⁺ complexes have presented incredible results, with very low detection limits (in the nanomolar order) and excellent reproducibility. Overall, the mechanism suggested for these complexes is similar to that presented by the Co-OEP complex. The decrease in the LOD is an effect caused by the presence of reduced graphene or metallic nanoparticles in the composite, which enhances the electron conductivity and the electro-oxidative properties. As a part of this section, in Table 8, we have collected diverse examples of the recent application of MPc or MP in modified electrodes with applicability in environmental sciences.