Methemoglobin Activity Explains Rapid Increase in Oxygen Saturation Among COVID-19 Patients Healed with Chlorine Dioxide Gas in Solution

1. Introduction

Chlorine dioxide (ClO₂) is a water-soluble mineral gas, discovered in 1811, that is used as antiviral and antibiotic agent [1], allowing also its use for obtaining drinkable water. Thus, the US Environmental Protection Agency recommends 0.8 mg/L of ClO2 to obtain drinkable water [2]. In an analysis of its toxicity, it has been shown that a human being of 70 K can take until 210 mg of ClO₂/day without risk [3]. Below this dose, it has been hypothesized that the obtained ClO₂- would act as an antioxidant and above that threshold it becomes an oxidant agent [4], a biochemical property called hormesis, evoked in some molecules having anticancer activity [5,6]. Thus, medical use of this gas has started in different clinical cases. For instance the dermic use of ClO₂ has allowed wound healing in complicated cases of comorbidity (including diabetics) and/or patients risking feet amputation [7,8]. The pharmacokinetics and pharmacodynamics analysis of ClO₂ [9] reveals some properties that support anti-inflammatory and even anticarcinogenic activity [10,11,12].

Besides fighting covid-19 testing ClO₂ in hospitals spaces [1] it was also used on patients that accepted to be treated by this molecule during the world pandemics, particularly in Ecuador [13]. and Mexico [14]. In the Mexican case, patients were monitored by medical doctors and nurses to track their daily Oxygen saturation (SpO₂). In this short report of such study cases, we transcribe some of their methodology, the results concerning SpO₂ and we discuss a revised biochemical explanation about the way this fast blood Oxygen increase was obtained for the COVID-19 patients, all treated with ClO₂ during 2020/2021 pandemic years, in the city of Querétaro, in Mexico [14].

2. Materials and Methods Section Transcribed from Part of the Protocol Used with COVID-19 Patients in the Mexican Case [Reference [14]]

From May 30, 2020 to January 15, 2021 the clinical records of 1,136 positive/suspected COVID-19 patients (treated by the same physician) who voluntarily requested therapeutic management at home in Mexico were reviewed. The inclusion criteria for the clinical records were as follows: 1) Patients that were diagnosed by molecular tests (Real-Time Reverse Transcriptase (RT)-PCR to SARSCoV- 2, antigen detection, specific Immunoglobulin M (IgM) and Immunoglobulin G (IgG) antibodies against SARS-CoV-2, computed assisted tomography of the lungs, chest radiographies, or a combination of clinical manifestations such as headache, fever, cough, throat pain, dyspnea, malaise, and fatigue; 2) patients that were informed of the benefits and possible side effects of ClO₂ consumption before starting treatment and that they had signed un informed consent form. The collected medical records were: sex, age, comorbidities, previous medications, date of onset, date of discharge or date of death, secondary effects posterior to a CDS consumption, milliliters of ClO₂ consumed per day , partial Oxygen saturation (SpO₂), Oxygen supplementation (O₂ L/min) and COVID- 19-like symptoms. These parameters allowed classifying the patients among three groups according to COVID severity and partial Oxygen saturation: Mild (>95% SpO₂), Moderate (90-95% SpO₂) and Severe (<90% SpO₂), Table 1. Thus, we report here the results of previous case studies where ClO₂ was given to the Mexican patients [14], but we focus mainly on the Oxygen saturation of patients. Afterwards we give the biochemical bases of the observed results.

According to severity, the patients were given different protocols of ClO₂ intake. Two groups of patients were analyzed: 1) Multidrug patients: persons consuming drugs usually used for treating COVID-19 (Azytromicine, Dexamethasone, Ivermectin and Hydroxychloroquine) plus ClO₂, and 2) Exclusively ClO₂ patients: people treated only with a the gas solution. All patients were treated at home by their relatives or nurses following the indications of the treating physician. Two types of oral aqueous solutions made with ClO₂ at 3000 ppm (3 mg/ml) were used for treating COVID-19: Protocol C (ClO₂ in 1000 ml of water, divided in ten intakes of 100 ml that were administered orally every hour, per day) and Protocol F (ClO₂ in 500 ml of water, divided in ten intakes of 50 ml that were administered orally every 15 minutes, 1 to 5 times a day). For intravenous use, Protocol Y (ClO₂ in 500 ml of 0.9% sterile saline solution plus 5 ml of 10% calcium gluconate and 10 ml of 7.5% sodium bicarbonate, administered at a mean rate of 70 ml per hour). All patients started treatment with Protocol F and, depending on the severity of the disease, were placed on Protocols C, F or Y until the symptoms were resolved. After the disappearance of symptoms, they continued with Protocol C as maintenance until the treatment ended (14-21 days depending on the severity of the disease).

The ClO2 used by patients for oral use was made by oxidation of 28% sodium chlorite (NaClO₂) and 4% Hydrochloric Acid (HCl) as an activator [14]. For intravenous use, ClO₂ was produced with the membrane electrolysis method [14]. As per the instructions given to each patient, the ClO₂ solution was kept in a closed bottle, protected from direct sunlight and maintained below 11°C [14].

3. Results Transcription, Concerning the Observed Oxygen Saturation in Patients of the Mexican Case [Reference [14]]

Patients receiving ClO₂ treatments were healed by 99.07 % of cases (1,057 of 1,067 patients survived). 59 (5.19%) abandoned the treatment after 11.43 days (95% CI: 7.98-14.88 days), and 10 (0.93%) were hospitalized after 8.6 days (95% CI: 2.08-15.11 days) of treatment, where they died. Of the total of patients, 77 (6.78%) reported mild-sporadic secondary effects posterior to ClO₂ intake: headache (2.20%), diarrhea (1.58%), gastritis (1.32%), dizziness (1.14%), nausea (1.05%), vomit (0.44%), rash (0.44%), throat pain (0.26%), myalgia (0.18%), colitis (0.18%), tachycardia (0.09%), and chills (0.09%). Six hundred sixty-six patients (58.63%) were treated exclusively with a CDS, and 470 patients (41.37%) were treated against COVID-19 with five or more drugs in addition to the CDS (Details in Ref. 4). The duration of symptoms in those patients treated solely with a CDS was less compared with those treated with various drugs (95% CI: 2.77- 3.75 days vs. 7.33-8.97 days, respectively; Wilcoxon Rank Sum Test, P<0.001).

Respect to the response on Oxygen saturation rate, patients began the treatment with a mean SpO₂ of 86.05% (95% CI: 85.12-87.17%), increasing the blood oxygen each day of treatment. In total, 126 patients (of which 101/251 [40.24%] with severe symptoms, 21/109 [19.27%] with moderate symptoms and 4/776 [0.51%] with mild symptoms) used supplementary oxygen (mean: 5.77 Liters per minute [95% CI: 5.18-6.36 L/min] for 4.32 days [95% CI: 3.37-5.27 days]). Between days 7-8 after the start of treatment, 90% of the patients reported an hyperbolic increase in SpO₂ above 90% and a week later above 95%, at a rate of SpO₂=3.58*ln(duration of treatment) (Figure 1, modified from Ref. 14)

4. Discussion Aimed to Give Better Understanding of the Oxygen Saturation Observed in Patients of the Mexican Case

The review of the literature allow us to interpret the surprising results of the observed patients’ increased Oxygen saturation as it follows: Chlorine dioxide (ClO₂), as an oxidant agent, once in contact with electron donors (i.e. organic matter) is transformed in chlorite anion (ClO₂-) a quite different molecule. The Chlorite anion has known properties allowing interesting biochemical functions in living systems, including the human body. This anion passes through intestinal or other tissues and reaches the blood stream. (or directly by intravenous administration). In the blood stream the anion is metabolized by a reductase activity of blood methemoglobin; which is 1% of total blood Hemoglobin [15]. The final step of this reduction is the production of the Chlorure anion (Cl-) and Oxygen (O₂). This reductase activity of the methemoglobin is similar to the bacterial enzyme Chlorite Dismutase (CD), which has a Heme (Fe+++) core or allosteric site, just like methemoglobin. In fact, in some bacteria, it is this CD enzyme that dissociates ClO₂ into Cl- and O₂ [4,16,17]. More precisely, once in contact with ClO₂-, the methemoglobin, containing a Ferric cation (Fe+++) and having a higher affinity for the Oxygen then the hemoglobin, takes one atom of Oxygen of the Chlorite anion (ClO₂-)and releases an intermediary anion (OCl-). Then, thanks to this Oxygen atom capture, the methemoglobin allosteric site passes by an intermediary reactive Heme molecule, Ferryl (Fe=O). This highly reactive molecule, in turn, attracts again the just released anion OCl-, releasing the Chlorure anion (Cl-) and diatomic Oxygen (O₂) [4,15]. This reductase activity could at least partially explain the increase in Oxygen saturation in medically surveyed COVID 19 patients healed after consumption of chlorine dioxide during the compassionate treatments applied in Mexico in 2020/21 [14] and also in Equator [13]. The antiviral effect of ClO₂- anion helps to reduce the viral reproduction, reducing lung inflammation and thus restoring Oxygen absorption by its normal lung CO₂/O₂ gas exchange, which also contributes to the increased Oxygen saturation.

This Chlorite anion-mediated blood Oxygen-increase, may explain other physiological observations in patients using Chlorine Dioxide. For instance, the anti-tumor activity through the ability of pro-oxidants to capture excess electrons around mitochondria, as it is the case also for other molecules such as Methylene Blue [18], thus restoring other RedOx disorders (i.e. ferroptosis) that characterizes cancer cells [19]. Oxygen is also important in Hyperbaric Oxygen treatments (HBOT) for cancer [20] and also for healing difficult wounds, by using Chlorite anion [7,8,21] or HBOT [22].

5. Conclusions

We conclude that Oxygen can be obtained in blood stream by means of an appropriate use of Chlorine Dioxide (ClO₂) in solution, thanks to its rapid conversion to Chlorite anion (ClO₂-) and the reductase activity of the heme group (Fe+++) of the methempoglobin, by the intermediay Ferryl (Fe=O) molecule. The only caution is to keep a concentration of Chlorine Dioxide equal or below to 3 mg/K/day, so that methemoglobin will not increase over 1-2% in the blood stream and thus be efficient to increase Oxygen saturation.