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1.435.216.7370

Neurofeedback Centers of Utah
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Methylene Blue

The History of Methylene Blue

Methylene blue was first synthesized in 1876 by German chemist Heinrich Caro as a textile dye.
Its transition to medicine began in 1891 when Paul Guttmann and Paul Ehrlich pioneered its use for treating malaria, based on the idea that dyes could selectively stain and target pathogens. This marked it as the first fully synthetic drug used in medicine. During World War II, it continued to be employed for malaria, though it was unpopular among soldiers due to side effects like turning urine blue.  In 1933, biologist Matilda Brooks discovered its role as an antidote for carbon monoxide and cyanide poisoning.  It served as a lead compound for developing other drugs, including antimalarials like chloroquine, antihistamines, and antipsychotics such as chlorpromazine. Over time, its applications expanded into neuropsychiatry and other fields, and it remains on the World Health Organization's List of Essential Medicines today.

Methylene Blue Clinical Trials, Reviews and Human Studies

We asked artificial intelligence program "Grok" to analyze every study and clinical trial concerning methylene blue and provide a summary of it's accepted and potential uses.  

Here's the result.


Based on clinical trials, systematic reviews, and human studies, methylene blue has demonstrated therapeutic potential for various conditions. While it is FDA-approved primarily for methemoglobinemia, research indicates improvements in other areas, often as an adjunct or investigational therapy. Note that many uses are off-label or emerging, with varying levels of evidence, and side effects (e.g., chromaturia, nausea, or tissue necrosis) have been reported in some cases. Below is a summarized list of conditions, grouped by category for clarity, with key improvements observed in studies.


Established and Approved Uses

  • Methemoglobinemia: Acts as a reducing agent to convert ferric iron in hemoglobin back to its ferrous state, enabling oxygen transport. Studies show rapid resolution of symptoms at doses of 1-2 mg/kg IV, making it a first-line treatment for congenital or acquired cases. 


Infectious Diseases

  • Malaria (Falciparum Malaria): Eliminates Plasmodium falciparum parasites, enhances efficacy of antimalarials like artemisinin or chloroquine, and reduces transmission. Clinical trials report effective parasite clearance and prevention of resistance at doses of 36-72 mg/kg over 3 days, with good tolerability in combinations. 
  • COVID-19: Improves respiratory function, shortens hospital stays, and reduces mortality. Trials show a 10.1-fold higher improvement rate in respiration by day 3 at 1 mg/kg every 8 hours, with antiviral effects inhibiting viral titers and reducing nasal viral loads via photodynamic therapy (PDT). 
  • Methicillin-Resistant Staphylococcus Aureus (MRSA) Infections (e.g., in Wounds): Kills bacteria via PDT combined with light, effective for superficial and deep wounds. 
  • Viral Infections (e.g., HIV-1, Hepatitis C): Inactivates viral nucleic acids through PDT, showing potential for plasma sterilization and reducing infectivity. 


Cardiovascular and Shock-Related Conditions

  • Septic Shock: Increases mean arterial pressure (MAP), systemic vascular resistance (SVR), and cardiac function while reducing vasopressor needs. Studies report hemodynamic stabilization at 1-3 mg/kg IV, with safety in refractory cases, though no impact on mortality in some subgroups like cirrhotic. 
  • Vasoplegic Syndrome: Inhibits nitric oxide effects, raising MAP and addressing hypotension/tachycardia post-surgery (e.g., cardiopulmonary bypass). Trials show reduced incidence and severity at 2 mg/kg IV, with lower mortality compared to placebo or norepinephrine. 
  • Hepatopulmonary Syndrome (in Cirrhosis): Reduces pulmonary vasodilatation and cGMP levels, increasing partial pressure of oxygen (PaO2) and alleviating hypoxia in all treated patients. 


Neurological and Psychiatric Conditions

  • Alzheimer's Disease: Attenuates amyloid plaques and neurofibrillary tangles, repairs mitochondrial function, and enhances cognitive performance. RCTs show benefits on ADAS-cog scores at 138 mg/day for up to 50 weeks in mild/moderate cases, with reduced beta-amyloid buildup using modified forms like LMTM. 
  • Bipolar Disorder (Cognitive Dysfunction and Residual Depression/Anxiety): Reduces symptoms on scales like Montgomery-Åsberg and Hamilton Depression Rating Scales. Studies report meaningful improvements at 195 mg/day oral, with mild side effects. 
  • Post-Traumatic Stress Disorder (PTSD): Enhances imaginal exposure therapy, improving working memory retention, learning, and quality of life at 260-290 mg oral, with mild side effects. 
  • Ifosfamide-Induced Neurotoxicity (Encephalopathy): Prevents and reverses symptoms by inhibiting toxic metabolites and NADH effects on gluconeogenesis. 
  • Postoperative Delirium and Cognitive Dysfunction (in Elderly Surgical Patients): Significantly reduces incidence after major noncardiac surgery at 2 mg/kg IV intraoperatively, with no major adverse events. 


Pain Management

  • Chronic Discogenic Low Back Pain: Denervates nociceptive fibers and reduces inflammation via nitric oxide inhibition, serving as an effective alternative, though transient side effects like increased pain or dizziness occur. 
  • Refractory Neuropathic Pain: Inhibits nitric oxide synthase and cGMP accumulation, showing promise at 2 mg/kg bolus, with side effects like abdominal pain. 
  • Postoperative Pain (After Hemorrhoidectomy, Lumbar Discectomy, or Thoracolumbar Fixation): Temporarily ablates nerve endings, reducing pain levels at 0.5% (1 mL) doses, with no significant adverse effects. 


Oncology and Dermatology

  • Cancer (e.g., Breast Cancer Imaging and Photodynamic Therapy): Aids intraoperative tumor identification via fluorescence at 1 mg/kg IV, though with risks like necrosis. PDT supports killing cancer cells in various types, per systematic reviews. 
  • Resistant Plaque Psoriasis: Treats via PDT, showing effectiveness in resistant cases. 


Methylene Blue is not safe for everyone.  Some conditions, supplements and medications do not allow for the safe use of Methylene Blue.  As with all supplements, consult your doctor before using Methylene Blue.


Troscription's Methylene Blue

We searched far and wide to find, what we feel, is the highest quality Methylene Blue coupled with the most reliable delivery system.  Enter Troscription. They are dedicated to promoting health and wellness through their products and services with the goal of helping you achieve optimal physical and mental well-being.  Live your best life! Explore and learn more about their products and how they can help you on your journey to better health.

Video

 Troscriptions' very own Dr. Scott Sherr answers the internet’s most pressing questions about methylene blue.  

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