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Lifestyle

​Illuminating Health: The Remarkable Benefits of Red and Near-Infrared Light Therapy

12/31/2023

1 Comment

 
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In the realm of emerging wellness technologies, red and near-infrared light therapy stands out as a beacon of potential health benefits. This non-invasive treatment, also known as photobiomodulation, has gained attention for its positive effects on various aspects of health, particularly in skin and muscle recovery. Let's delve into the illuminating world of red and near-infrared light therapy and explore how it can enhance your well-being.

Photobiomodulation (PBM)

Photobiomodulation, often referred to as PBM therapy, is a non-invasive and non-thermal treatment that utilizes light to stimulate various cellular processes. This therapeutic approach harnesses the power of specific wavelengths of light to enhance cellular function, promote tissue repair, and reduce inflammation. Among the key contributors to PBM are red and near-infrared (NIR) light.

The Sun: the Original Photobiomodulator

The Sun emits energy in various forms, each associated with specific ranges of the electromagnetic spectrum. Here's a breakdown of the forms of energy emitted by the Sun:

1. Visible Light: This is the portion of solar radiation that is visible to the human eye, creating the spectrum of colors we perceive.                  
  • Percentage: Approximately 42%
  • Wavelength Range: 380 to 750 nanometers
2. Infrared (IR) Radiation: Infrared radiation is not visible to the human eye but is felt as heat. It can be categorized into near, mid, and far infrared based on its wavelength.
  • Percentage: Approximately 49%
  • Wavelength Range: Greater than 750 nanometers
  • Further Breakdown:
    • Near-Infrared (NIR): 0.75 to 1.5 micrometers
    • Mid-Infrared (MIR): 1.5 to 4 micrometers
    • Far-Infrared (FIR): 4 to 1000 micrometers (1 millimeter)
3. Ultraviolet (UV) Radiation: UV radiation is beyond the violet end of the visible spectrum. UVA and UVB reach the Earth's surface, playing a role in processes like vitamin D synthesis and causing sunburn.
  • Percentage: Approximately 9%
  • Wavelength Range:
    • UVA: 320 to 400 nanometers
    • UVB: 280 to 320 nanometers
    • UVC: 100 to 280 nanometers (mostly absorbed by Earth's atmosphere)
Each form of energy serves different functions and has distinct interactions with the Earth's atmosphere and surface. While visible light is the most familiar, infrared and ultraviolet radiation also play crucial roles in various natural processes. Most of the energy emitted from the sun in in the form of infrared light, so using infrared technology is approximating exposure to the sun, without the harm of UV light.
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Red and Near-Infrared Light Therapy

Red and near-infrared (NIR) light therapy involves exposing the body to light in the red (600-700 nanometers) and NIR (700-1100 nanometers) spectrums. These wavelengths are known to penetrate the skin and underlying tissues, interacting with cellular structures and triggering beneficial responses.

Skin Layers and Light Penetration: ​

The human skin consists of several layers, each with distinct properties and functions. Understanding how red and NIR light navigate through these layers provides insight into their therapeutic reach.
  1. Epidermis: The outermost layer of the skin is the epidermis, primarily composed of dead skin cells. Red light is adept at penetrating this layer, influencing various surface-level processes such as collagen production and inflammation.
  2. Dermis: Deeper within lies the dermis, home to blood vessels, hair follicles, and connective tissues. Both red and NIR light penetrate the dermal layer, impacting blood flow, promoting wound healing, and influencing cellular activities that contribute to skin health.
  3. Subcutaneous Tissue: The subcutaneous layer, rich in fat cells and larger blood vessels, poses a greater challenge for light penetration. While red light can reach this layer to a certain extent, NIR light excels in penetrating deeper, influencing cellular and metabolic processes within the subcutaneous tissues.
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As red and NIR light journey through the skin layers, they engage with chromophores—molecules that absorb specific wavelengths of light. Key chromophores include cytochrome c oxidase, found in mitochondria, and various light-absorbing proteins and enzymes. These interactions trigger a cascade of cellular events, such as enhanced ATP production, increased circulation, and modulation of inflammatory responses.
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Understanding the depth of light penetration is crucial for tailoring red and NIR therapy to specific therapeutic goals. While red light may be more suitable for surface-level applications like skin rejuvenation, NIR light's ability to reach deeper tissues makes it a preferred choice for addressing musculoskeletal conditions and promoting systemic benefits.

Mechanisms of Action

  1. Mitochondrial Stimulation: Red and NIR light are absorbed by mitochondria, the cellular powerhouses responsible for energy production (ATP). This stimulation enhances mitochondrial function, optimizing cellular energy metabolism. Red and NIR light stimulates cytochrome C oxidase inside the complex four of the mitochondrial electron transport chain which promotes ATP synthesis.
  2. Increased Blood Flow: Light therapy promotes vasodilation, leading to improved blood circulation. Enhanced blood flow carries more oxygen and nutrients to tissues, aiding in the healing process.
  3. Reduction of Inflammation: PBM has anti-inflammatory effects by modulating immune responses. It reduces pro-inflammatory markers and promotes a balanced immune reaction.
  4. Cellular Repair and Regeneration: Light therapy supports the synthesis of DNA and proteins, facilitating cellular repair and regeneration. This is particularly valuable for tissues undergoing healing or recovery.
  5. Neuroprotective Effects: PBM exhibits neuroprotective properties, promoting the survival of neurons and potentially mitigating the impact of neurodegenerative conditions
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Influence of NIR on Water

NIR light can affect the structure of water molecules through a process known as photodissociation or photolysis. This process involves breaking molecular bonds using light energy. While NIR light does not directly ionize water molecules, it can influence their structure in several ways:
  1. Vibrational Resonance: Water molecules have natural vibrational frequencies, and NIR light is capable of resonating with these frequencies. When NIR light interacts with water molecules, it can enhance the vibrational motion of the water molecules. This increased vibrational energy may lead to changes in the structure and properties of the water.
  2. Cluster Formation: Water molecules can form clusters due to hydrogen bonding. NIR light has been suggested to influence the clustering of water molecules, potentially leading to alterations in the arrangement and properties of water clusters.
  3. Temperature Effects: NIR light can induce heating in water molecules by increasing their kinetic energy. The temperature rise associated with NIR exposure may contribute to changes in water structure and dynamics.
  4. Hydrogen Bonding: NIR light can influence the strength and dynamics of hydrogen bonds between water molecules. Changes in hydrogen bonding patterns may affect the overall structure and properties of water.

​The concept of NIR light influencing the structuring of water into exclusion zone (EZ) water, also known as the fourth phase of water, is associated with the work of Dr. Gerald Pollack. According to Pollack's research, EZ water differs in its molecular arrangement from ordinary water, showing a structured pattern that extends beyond the traditional liquid structure.
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Formation of Exclusion Zone (EZ) Water:
  1. Light Absorption: Near-Infrared light is thought to be absorbed by certain molecules, particularly chromophores, present in water. This absorption may trigger changes in the molecular arrangement of water molecules, leading to the formation of structured zones known as exclusion zones.
  2. Structured Water Molecules: EZ water is characterized by a more ordered structure, where water molecules align in a way that creates a distinct phase with unique properties. This structured water has been suggested to have enhanced stability and a higher viscosity compared to regular water.
Influence on Mitochondrial Function:
  1. Increased Cellular Energy Production: Mitochondria, often referred to as the powerhouse of the cell, play a crucial role in energy production through processes like oxidative phosphorylation. Some theories propose that EZ water, with its structured nature, may have properties that enhance mitochondrial function.
  2. Improved Cellular Communication: Structured water may influence intercellular communication, potentially enhancing signaling pathways vital for cellular processes. Improved communication between cells could contribute to better overall cellular function, including mitochondrial activities.
  3. Reduced Oxidative Stress: The structured nature of EZ water has been associated with potential antioxidant-like properties. Mitochondria are susceptible to oxidative stress, and if EZ water indeed possesses antioxidant characteristics, it may contribute to a more favorable cellular environment.

It's important to note that the exact mechanisms and effects of NIR light on water structure are complex and may vary depending on factors such as the wavelength of the light, intensity, and exposure duration. The idea of NIR light structuring water has gained attention in various fields, including alternative health practices, and environmental research. The field of water structuring and its potential implications for cellular biology is still an area of active investigation within scientific communities.

Harnessing the Power of Hormetic Stress: The Biphased Dose Response of Red Light Therapy

Red light therapy emerges not only as a therapeutic modality but as a potent hormetic stressor, operating on a biphasic dose-response principle. In the realm of hormesis, a phenomenon where exposure to low doses of stressors triggers adaptive responses, red light therapy takes center stage by demonstrating a nuanced and beneficial relationship with the body's stress response.

Hormesis, in its essence, is the body's ability to adapt and respond positively to low doses of stress. Red light therapy, with its application of low levels of red and NIR light, acts as a hormetic stressor, initiating adaptive responses that strengthen cellular resilience and overall well-being.

The biphasic dose response of red light therapy implies that its effects on the body follow a distinctive pattern. At lower doses, red light elicits a positive response, triggering cellular repair, mitochondrial enhancement, and anti-inflammatory effects. As the dose increases, the beneficial effects continue, but there's a point where diminishing returns occur. Understanding this biphasic response allows for optimized use of red light therapy for maximum benefit.
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Learn more about Hormesis
Understanding the biphasic dose response of red light therapy allows for a personalized and optimal application. Tailoring the dose to individual needs ensures that the therapy remains within the hormetic zone, where the benefits are maximized without reaching a point of diminishing returns.

Incorporating red light therapy into your wellness routine becomes a strategic choice for embracing hormetic stress. The biphasic dose response unfolds a journey of cellular resilience, mitochondrial optimization, and enhanced well-being, showcasing red light therapy as a dynamic and adaptive ally in the pursuit of holistic health.

Applications: The Science Behind Red and Near-Infrared Light Therapy

  1. Cellular Energy Boost: Red and NIR light wavelengths penetrate the skin, reaching the cells' mitochondria – the powerhouse of the cell. This interaction stimulates the production of adenosine triphosphate (ATP), the primary source of cellular energy. Increased ATP levels contribute to improved cellular function and overall energy production.
  2. Wound Healing: Red and NIR light therapy accelerates wound healing by promoting cellular proliferation and tissue repair. Studies reveal red light therapy accelerates closure and healing of wounds, including diabetic ulcers
  3. Muscle Recovery: Athletes use PBM to alleviate muscle soreness, enhance recovery, and improve performance. Red light reduces inflammation and damage in muscles while enhancing performance and growth by increasing microcirculation and tissue oxygenation. It’s been shown to help muscles heal after exercise and injury.
  4. Joint Health: Light therapy may help manage joint disorders by reducing inflammation and supporting cartilage health.
  5. Skin Conditions: PBM is employed for various dermatological concerns, including acne, rosacea, psoriasis, and skin aging. Researchers have observed that red light therapy visibly reduces wrinkles, fine lines, skin roughness and boosts collagen synthesis and density by stimulating fibroblast activity. It triggers specialized skin cells to regenerate and repair themselves. 
  6. Pain Management: Light therapy can contribute to pain relief in conditions like arthritis or musculoskeletal injuries. Red light is proven to successfully reduce nerve, back and other chronic pain.
  7. Improves Brain Function: Applying red light to the scalp can boost cognition and memory in people with dementia and other brain disorders by reducing inflammation and oxidative stress. It may also lift mood and reduce anxiety by stimulating nerve cell growth.
  8. Regrows Hair: In those with androgenic alopecia, red light grows new, thicker, denser hair by stimulating follicles.

Incorporating Light Therapy into Your Routine

  1. Choose the Right Device: Invest in a reputable red or NIR light therapy device designed for your specific needs. The evidence suggests the maximum benefits come the exposure to specific wavelengths: 690-900 nm. Devices come in various forms, including handheld devices, panels, and full-body systems.
  2. Consistency is Key: To reap the maximum benefits, consistency is crucial. Incorporate light therapy sessions into your routine, and adhere to the recommended usage guidelines for your specific device.
  3. Consult with Professionals:​ Before starting any light therapy regimen, it's advisable to consult with healthcare professionals, especially if you have pre-existing health conditions.

Experience Revolutionary Healing with Boncharge Red Light Therapy Devices

Unlock the potential of cutting-edge healing with Boncharge Red Light Therapy devices, designed to redefine your wellness journey. These state-of-the-art devices boast a range of features aimed at maximizing therapeutic benefits while prioritizing your safety and comfort.
​
  1. Low EMF Levels: Boncharge sets the gold standard with impressively low EMF (Electromagnetic Field) levels ranging from 0.1 to 0.05 microtesla. This places Boncharge at the forefront of the market, ensuring that your exposure to electromagnetic fields during therapy sessions is minimized, fostering a safer and more effective healing environment.
  2. Flicker-Free LEDs for Enhanced Sleep: Bid farewell to restless nights! Boncharge Red Light Therapy devices incorporate flicker-free LEDs, a feature known to contribute to improved sleep quality. By eliminating the flickering effect associated with some light sources, Boncharge prioritizes your well-being, providing a seamless and relaxing experience.
  3. Built-in Timer for Convenience: Effortlessly integrate red light therapy into your routine with Boncharge's built-in timer feature. This user-friendly functionality allows you to tailor your sessions to your schedule, ensuring that you receive the optimal dosage of therapeutic light without any hassle.
  4. Dual or Independent Sessions: Enjoy versatility in your therapy approach with Boncharge's unique capability to deliver sessions with both NIR and red light simultaneously or independently. This flexibility enables you to customize your sessions based on your specific wellness goals, providing a personalized and targeted experience.
  5. Evidence-Based Design: Boncharge Red Light Therapy devices are grounded in evidence-based design, incorporating the latest research and technological advancements in the field. This commitment to scientific rigor ensures that you receive a therapy experience backed by credible data and designed to deliver tangible benefits to your overall well-being.
Save 15% with the code JOE15
For as little as 10 minutes per day (ideally in the morning), you can incorporate Boncharge Red Light Therapy devices into your wellness routine and embark on a journey of transformative healing. Elevate your experience with the assurance of low EMF, flicker-free LEDs, convenient built-in timers, and the flexibility to customize your sessions. Boncharge is not just a device; it's a commitment to evidence-based wellness, empowering you to thrive with the power of red light therapy.

Safety and Considerations

Red and NIR light therapy is generally considered safe with minimal side effects. However, appropriate device selection, treatment duration, and wavelength specificity are crucial for optimizing therapeutic outcomes.

It is very important to do a photosensitivity test prior to long sessions with your red light therapy device. To perform the test, turn on both the red and NIR functions on your red light therapy device and shine the light on an exposed part of your forearm, about 3 inches to 1 foot away, for 4 minutes. If you experience any discomfort or redness on your skin it is encouraged to not use your red light therapy device until you have sought professional advice from your doctor or healthcare provider.

Illuminating cellular healing

In conclusion, red and NIR light therapy, within the realm of PBM, represents a promising avenue for promoting cellular healing and overall well-being. As research continues, the applications and benefits of this non-invasive therapy are expected to expand.

​Red and NIR light therapy presents a compelling avenue for enhancing skin health and muscle recovery. As this technology continues to be explored, its potential applications in various fields, from sports medicine to dermatology, are expanding. By harnessing the power of light, individuals can embark on a journey toward improved vitality, resilience, and overall well-being. As with any wellness practice, informed decisions and professional guidance contribute to a holistic approach to health.

references

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  3. Barolet, D., Roberge, C. J., & Auger, F. A. (2009). Regulation of skin collagen metabolism in vitro using a pulsed 660 nm LED light source: clinical correlation with a single-blinded study. Journal of Investigative Dermatology. https://doi.org/10.1038/jid.2009.97
  4. Liebert, A. D., Bicknell, B. T., Adamskaya, N., & Adamskaya, N. (2006). Pulsed LED light therapy increases collagen production in skin fibroblasts in vitro. Lasers in Surgery and Medicine. https://doi.org/10.1002/lsm.20279
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  7. Klepeis, N. E., Nelson, W. C., Ott, W. R., Robinson, J. P., Tsang, A. M., Switzer, P., ... & Engelmann, W. H. (2001). The National Human Activity Pattern Survey (NHAPS): a resource for assessing exposure to environmental pollutants. Journal of Exposure Science & Environmental Epidemiology, 11(3), 231-252.
  8. Wunsch, A., & Matuschka, K. (2014). A controlled trial to determine the efficacy of red and near-infrared light treatment in patient satisfaction, reduction of fine lines, wrinkles, skin roughness, and intradermal collagen density increase. Photomedicine and laser surgery, 32(2), 93-100.
  9. Avci, P., Gupta, A., Sadasivam, M., Vecchio, D., Pam, Z., Pam, N., & Hamblin, M. R. (2013). Low-level laser (light) therapy (LLLT) in skin: stimulating, healing, restoring. Seminars in Cutaneous Medicine and Surgery, 32(1), 41-52.
  10. De Marchi, T., Leal Junior, E. C., Bortoli, C., Tomazoni, S. S., Lopes-Martins, R. Á. B., & Salvador, M. (2017). Low-level laser therapy (LLLT) in human progressive-intensity running: effects on exercise performance, skeletal muscle status, and oxidative stress. Lasers in medical science, 32(9), 1939-1948.
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  16. Alfieri, D. F., de Jesus Guirro, R. R., de Cássia Registro Fonseca, M., dos Santos Tomazoni, S., da Silva, N. S. A., Tacani, R. E., ... & Leal-Junior, E. C. (2021). Immediate effects of photobiomodulation therapy on latent trigger points in the upper trapezius muscle: A randomized, double-blinded, sham-controlled trial. Lasers in Medical Science, 36(1), 105-114.
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Selecting non-toxic Baby wipes

12/13/2023

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Whether baby wipes are toxic or not depends on the ingredients. Some popular brands, such as Huggies or Pampers, that are known for their baby scent use an astounding amount of chemicals to achieve that scent.
​
These chemicals are toxic for both babies and the environment. Baby wipes using natural and organic ingredients typically do not contain these additional chemicals, making them wonderful non-toxic baby wipes. 

Common baby wipe ingredients to avoid

Many moms are well-intended to select the common brands of baby wipes. Afterall, baby wipes are packed with chemicals to make them efficient, a little more durable than toilet paper, and smell beautiful. However, some of those chemicals are not good for your baby.
​
It is in the best interest of the consumer, the mom and baby, to make sure to read the package before you purchase a pack of disposable baby wipes. Here are some ingredients to look out for:

fragrance

The fragrance is a general term that is used to encompass several different ingredients. If an ingredient contributes to making the wipes smell good, it can be labeled as “fragrance.”
Many of these fragrances are petro-chemicals and are therefore toxic, and some of them are just not good for your little one’s skin. Instead, opt for fragrance-free wipes. Babies naturally smell adorable!

If you do wind up buying baby wipes that are scented, double-check the ingredient list. Companies can use the term fragrance to encompass harmful ingredients. They are not required to list the ingredients or chemicals that are used to make their baby wipes smell the way that they do because this is considered a trade secret. This means that if the fragrance is created using parabens, for example, the company does not have to tell you because it is in the “fragrance” category.

Fragrances have been linked to all sorts of health conditions, from autoimmune issues including contact dermatitis, and migraines and respiratory issues.

Formaldehyde

Make no mistake - you read that right. Formaldehyde has made headlines in recent years as it’s been found in baby wipes. This chemical is a known carcinogen, meaning that it can cause cancer.
It’s also a known irritant causing allergic reactions in babies. Additionally, formaldehyde is known to be:
  • Genotoxic: damage the genetic information within a cell causing mutations, which may lead to cancer
  • ​Inflammatory
  • Neurotoxic: damage to the brain and nerve cells
  • Hepatotoxic: damage to the liver and liver cells
  • Oxidant: damage cells by starting chemical chain reactions such as lipid peroxidation, or by oxidizing DNA or proteins
  • Teratogenic: cause congenital disorders in a developing embryo or fetus

Researchers have observed over half of the popular baby wipe brands that were tested released formaldehyde during a study. What is even scarier is that none of the wipes listed formaldehyde as an ingredient. 

A current examination of the scientific data collected on the exposure to formaldehyde is associated with the following health conditions and abnormal physiologic events:
​Oxidative Stress
​Alzheimer's Disease
Testicular Injury
Cancers
​Lung Inflammation
​Vaccine-induced Toxicity
​Air Pollution Linked Toxicity
​Chemically-Induced Liver Damage
​Asthma
DNA damage
​Brain Damage
​Cognitive Decline & Dysfunction
Infertility: Male
​Inflammation
​Dermatitis: Contact

Triclosan

This antibacterial ingredient found in soaps and other products has been linked to allergies, endocrine disruption, weight gain and inflammatory responses, and may aggravate the growth of liver and kidney tumors. It’s also used commonly as a preservative.

However, Triclosan was recently removed from antibacterial hand soaps because it can pass through the skin, which will lead to it having an effect on the body. It’s known to cause an allergic reaction as well as disrupt hormones. When triclosan is broken down, it can turn into Dioxin, which is known to cause cancer. 

Here is list of the known physiologic mechanisms in which triclosan exerts it's harmful effects:
  • Anti-Fertility: an agent that is known to disrupt reproductive function
  • Neurotoxic
  • Abortive: an agent that can result in spontaneous abortion to pregnant mothers
  • Endocrine Disruptor (Thyroid): suppresses the function of the thyroid gland which is essential for normal homeostasis
  • Cardiotoxic: damages the function of the heart cells and heart function
  • Cytotoxic: damages cellular function
  • Genotoxic: property of chemical agents that damage the genetic information within a cell causing mutations, which may lead to cancer
  • Hepatotoxic
  • Sulfotransferase inhibitors: inhibits the function of the enzyme sulfotransferase, which plays a role in liver diseases

Exposure to, and the consumption of triclosan is associated with the following health conditions and abnormal physiologic events: 
​Infertility: Male
​Fetal Origin of Adult Disease
​Oxidative Stress
Prenatal Chemical Exposure
​Bisphenol-A Toxicity
​Gestational Diabetes
​Miscarriage
​Phthalate Toxicity
​Breast Cancer
​Hypothyroidism
Infertility
​Chemically-Induced Liver Damage
​Cancer Metastasis
Estrogen Dominance
​Food Allergies
​Hormonal Disorders: Children
Hormone Imbalances
​Infants: Low Birth Weight
Liver Disease
Sexual Dysfunction
​Thyroid Diseases
​Allergic Airway Diseases
​Autoimmune Thyroiditis
Cancers: All
​Cardiovascular Diseases
Impaired 
detoxification 
Hypersensitivity
Hyperthyroidism
​Lung Cancer
​Neurodevelopmental Disorders
Obesity
Value

Propylene Glycol

Propylene glycol, also known as propane-1,2-diol, is compound used for various cosmetic, pharmaceutical and industrial applications, including as a solvent, humectant, preservative, and surfactant.

Propylene glycol consumption results in kidney, liver, and neurologic toxicity, and it is certainly not recommended for pregnant women. Propylene glycol is a skin irritant, it may increase the absorption of other harmful excipients, and disrupts permeability of the blood brain barrier.

When used in products like baby wipes, propylene glycol is intended to increase skin absorption of any ingredients more effectively, and at a quicker rate. This results in the body absorbing all of the toxic ingredients that are found in baby wipes, so it’s best to avoid this ingredient entirely. 

Polyethylene Glycol 

​Polyethylene Glycol (PEG), otherwise known as Macrogol, Carbowax and many other derivatives when combined with other substances. PEG is a synthetic chemical compound derived from petroleum that is widely used for a variety of uses, including as a moisture carrier, solvent, preservative, thickener, and much more. 

PEG 
is another chemical that will help the skin absorb the ingredients of the baby wipes. Even though it’s a different chemical that is used, it still does the same thing as propylene glycol, which helps your little one absorb chemicals which may include carcinogens, including ethylene oxide, and potentially dioxane depending on the manufacturer. 

PEG is classified as biologically inert by our FDA. It is the “Gold Standard” for use in many medications to increase the blood clearance time, or in other words, the time it remains in one’s system, thereby enhancing drug effect. It is also used in drug manufacturing as an excipient for long term stabilization, bulking, and other therapeutic enhancements. It is used as a coating to prevent bacterial adhesion on orthopedic screws and sutures. In addition to medical uses, PEG is also used in cosmetics, foods, industrial applications, and other health and beauty products such as soaps, shampoos, toothpastes. It is also used as an e-cigarette liquid. PEG is everywhere in our environment, which is what many have surmised has led to a high percentage of the US population developing anti-PEG antibodies. This, of course, presents a significant challenge to those who rely on this substance in their manufacturing.
​
Scientific studies to quantify the seriousness of the problem estimate that approximately 72% of the US population has acquired anti PEG antibodies. The referenced study used blood samples taken from 1990-1999 and earlier, showing a steady increase over time in the percentage of those with antibodies to PEG, making it conservative to estimate, after two decades, that the incidence is closer to 80% today. This circumstance has concerned the medical and pharmaceutical communities as an equally effective alternative has escaped identification, although several have been suggested, and because the great cost of shifting to such an alternative.

Not only is PEG a “stealth” medicinal additive, delaying blood clearance due to its properties, but it is a stealth allergen, the vast majority of the population never having heard of it and many in the healthcare industry being unaware of its antigenic properties. A physician survey found:

“Although 91% of respondents were aware of antidrug antibodies in general, only 22% were aware of APA (Anti-PEG Antibody) responses. Further, there was limited awareness (35%) of PEG’s inclusion in prescribed PEGylated therapeutics.”
"Scientific studies to quantify the seriousness of the problem estimate that approximately 72% of the US population has acquired anti PEG antibodies."

sodium benzoate

Sodium benzoate is also used as a preservative, to extend the shelf-life of products, and is actually the sodium salt of benzoic acid. 

The substance is an odorless, crystalline powder made by combining benzoic acid and sodium hydroxide, per a December 2015 article in ​Biotechnology and Health Sciences​.

Chemical exposure and consumption of sodium benzoate is linked with a variety of health conditions and abnormal physiologic events, including but not limited to:
​
​Attention Deficit Hyperactivity Disorder
​Food Allergies
​Cancers: All
​DNA damage
Inflammation
​Neurotoxicity
​Ammonia: Elevated
​​Genotoxicity

safe Baby wipes

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purchase: amazon
Terra biodegradable wipes are durable and extra moist, with an easy dispensing flip-top lid. They are cross-woven for a soft cloth-like texture that is non-irritating while cleaning baby's delicate skin. Terra provides transparency with their ingredients:
  • CLOTH: 100% Biodegradable FSC Certified Bamboo Fiber (NOT Bamboo Viscose); 0% Plastic.
  • LIQUID: 99.5% Pure NZ Purified Water, Hydrolyzed Soy Protein, Aloe Vera Extract, Organic NZ Manuka Honey, Tocopherol (Vitamin E)​
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references

Liou, Yujie Linda, et al. “Formaldehyde Release from Baby Wipes: Analysis Using the Chromotropic Acid Method.” Dermatitis, vol. 30, no. 3, May 2019, pp. 207–212, https://doi.org/10.1097/der.0000000000000478. 

Steinemann, Anne. “Health and Societal Effects from Exposure to Fragranced Consumer Products.” Preventive Medicine Reports, vol. 5, Mar. 2017, pp. 45–47, https://doi.org/10.1016/j.pmedr.2016.11.011.

McCann, Donna, et al. “Food Additives and Hyperactive Behaviour in 3-Year-Old and 8/9-Year-Old Children in the Community: A Randomised, Double-Blinded, Placebo-Controlled Trial.” The Lancet, vol. 370, no. 9598, Nov. 2007, pp. 1560–1567, www.thelancet.com/journals/lancet/article/PIIS0140-6736(07)61306-3/fulltext, https://doi.org/10.1016/s0140-6736(07)61306-3.
​

Nair, B. “Final Report on the Safety Assessment of Benzyl Alcohol, Benzoic Acid, and Sodium Benzoate.” International Journal of Toxicology, vol. 20 Suppl 3, 2001, pp. 23–50, www.ncbi.nlm.nih.gov/pubmed/11766131, https://doi.org/10.1080/10915810152630729.

Fujitani, T. “Short-Term Effect of Sodium Benzoate in F344 Rats and B6C3F1 Mice.” Toxicology Letters, vol. 69, no. 2, 1 Aug. 1993, pp. 171–179, pubmed.ncbi.nlm.nih.gov/8212059/, https://doi.org/10.1016/0378-4274(93)90102-4.

Tsay, Huey-Jen, et al. “Treatment with Sodium Benzoate Leads to Malformation of Zebrafish Larvae.” Neurotoxicology and Teratology, vol. 29, no. 5, 1 Sept. 2007, pp. 562–569, pubmed.ncbi.nlm.nih.gov/17644306/, https://doi.org/10.1016/j.ntt.2007.05.001.

Hu, Mingqian, et al. “[Analysis of Sodium Benzoate Biotoxicity by Atomic Force Microscope].” Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology, vol. 24, no. 8, 1 Aug. 2008, pp. 1428–1432, pubmed.ncbi.nlm.nih.gov/18998546/, https://doi.org/10.1016/s1872-2075(08)60064-3.

Oyanagi, Kazuhiko, et al. “Cytotoxicities of Sodium Benzoate in Primary Culture of Hepatocytes from Adult Rat Liver.” The Tohoku Journal of Experimental Medicine, vol. 152, no. 1, 1987, pp. 47–51, www.jstage.jst.go.jp/article/tjem1920/152/1/152_1_47/_article, https://doi.org/10.1620/tjem.152.47.

Haque, Haroon, et al. “Effectiveness of Sodium Benzoate as a Freshwater Low Toxicity Antifoulant When Dispersed in Solution and Entrapped in Silicone Coatings.” Biofouling, vol. 21, no. 2, 2005, pp. 109–119, pubmed.ncbi.nlm.nih.gov/16109600/, https://doi.org/10.1080/08927010500222551. 

O’Connor, J. E., et al. “The Potentiation of Ammonia Toxicity by Sodium Benzoate Is Prevented by L-Carnitine.” Biochemical and Biophysical Research Communications, vol. 145, no. 2, 15 June 1987, pp. 817–824, pubmed.ncbi.nlm.nih.gov/3593373/, https://doi.org/10.1016/0006-291x(87)91038-2. 

Stefanidou, M., et al. “Assessing Food Additive Toxicity Using a Cell Model.” Veterinary and Human Toxicology, vol. 45, no. 2, 1 Mar. 2003, pp. 103–105, pubmed.ncbi.nlm.nih.gov/12678300/. 

Mpountoukas, P., et al. “Cytogenetic Study in Cultured Human Lymphocytes Treated with Three Commonly Used Preservatives.” Food and Chemical Toxicology, vol. 46, no. 7, July 2008, pp. 2390–2393, https://doi.org/10.1016/j.fct.2008.03.021.

Whittaker, A., et al. “Toxic Additives in Medication for Preterm Infants.” Archives of Disease in Childhood. Fetal and Neonatal Edition, vol. 94, no. 4, 1 July 2009, pp. F236-240, pubmed.ncbi.nlm.nih.gov/19158148/, https://doi.org/10.1136/adc.2008.146035. 

Zosel, Amy, et al. “Severe Lactic Acidosis after an Iatrogenic Propylene Glycol Overdose.” Pharmacotherapy, vol. 30, no. 2, Feb. 2010, pp. 219–219, https://doi.org/10.1592/phco.30.2.219. 

Bailey, David N. “Propylene Glycol as a Vehicle for Percutaneous Absorption of Therapeutic Agents.” Journal of Analytical Toxicology, vol. 16, no. 2, 1 Mar. 1992, pp. 97–98, https://doi.org/10.1093/jat/16.2.97. 

Sood, Rohit, et al. “Quantitative Evaluation of the Effect of Propylene Glycol on BBB Permeability.” Journal of Magnetic Resonance Imaging: JMRI, vol. 25, no. 1, 1 Jan. 2007, pp. 39–47, pubmed.ncbi.nlm.nih.gov/17173307/, https://doi.org/10.1002/jmri.20802. Accessed 14 Dec. 2023.

Den Hond, Elly, et al. “Human Exposure to Endocrine Disrupting Chemicals and Fertility: A Case–Control Study in Male Subfertility Patients.” Environment International, vol. 84, Nov. 2015, pp. 154–160, https://doi.org/10.1016/j.envint.2015.07.017.

​Jurewicz, Joanna, et al. “Environmental Levels of Triclosan and Male Fertility.” Environmental Science and Pollution Research, vol. 25, no. 6, 7 Dec. 2017, pp. 5484–5490, www.ncbi.nlm.nih.gov/pmc/articles/PMC5823964/, https://doi.org/10.1007/s11356-017-0866-5. 

Wang, Xiaoli, et al. “Triclosan Causes Spontaneous Abortion Accompanied by Decline of Estrogen Sulfotransferase Activity in Humans and Mice.” Scientific Reports, vol. 5, no. 1, 15 Dec. 2015, p. 18252, www.nature.com/articles/srep18252, https://doi.org/10.1038/srep18252. 

Geer, Laura A., et al. “Association of Birth Outcomes with Fetal Exposure to Parabens, Triclosan and Triclocarban in an Immigrant Population in Brooklyn, New York.” Journal of Hazardous Materials, vol. 323, no. Pt A, 5 Feb. 2017, pp. 177–183, pubmed.ncbi.nlm.nih.gov/27156397/, https://doi.org/10.1016/j.jhazmat.2016.03.028.

Weatherly, Lisa M., et al. “Antimicrobial Agent Triclosan Is a Proton Ionophore Uncoupler of Mitochondria in Living Rat and Human Mast Cells and in Primary Human Keratinocytes.” Journal of Applied Toxicology, vol. 36, no. 6, 23 July 2015, pp. 777–789, https://doi.org/10.1002/jat.3209. 

López-Pacheco, Itzel Y., et al. “Anthropogenic Contaminants of High Concern: Existence in Water Resources and Their Adverse Effects.” Science of the Total Environment, vol. 690, Nov. 2019, pp. 1068–1088, tec.mx/sites/default/files/2019-08/1-s2.0-S0048969719331651-main%20%281%29.pdf, https://doi.org/10.1016/j.scitotenv.2019.07.052. 

Paul, Katie B., et al. “Developmental Triclosan Exposure Decreases Maternal and Neonatal Thyroxine in Rats.” Environmental Toxicology and Chemistry, vol. 29, no. 12, 15 Oct. 2010, pp. 2840–2844, https://doi.org/10.1002/etc.339.

Huang, Wei, et al. “Lipid Metabolism Disorders Contribute to Hepatotoxicity of Triclosan in Mice.” Journal of Hazardous Materials, vol. 384, 15 Feb. 2020, p. 121310, www.sciencedirect.com/science/article/abs/pii/S0304389419312646, https://doi.org/10.1016/j.jhazmat.2019.121310. 

Rodríguez, Pablo E. A., and Mónica S. Sanchez. “Maternal Exposure to Triclosan Impairs Thyroid Homeostasis and Female Pubertal Development in Wistar Rat Offspring.” Journal of Toxicology and Environmental Health, Part A, vol. 73, no. 24, 29 Oct. 2010, pp. 1678–1688, https://doi.org/10.1080/15287394.2010.516241. 

Tobar, Steven, et al. “Triclosan Promotes Epicutaneous Sensitization to Peanut in Mice.” Clinical and Translational Allergy, vol. 6, no. 1, 5 Apr. 2016, https://doi.org/10.1186/s13601-016-0102-2. 


Park, Bo Kyung, et al. “Effects of Triclosan on Neural Stem Cell Viability and Survival.” Biomolecules & Therapeutics, vol. 24, no. 1, 1 Jan. 2016, pp. 99–107, www.biomolther.org/journal/view.html?volume=24&number=1&spage=99&year=2016, https://doi.org/10.4062/biomolther.2015.164. 

Pollock, Tyler, et al. “Triclosan Exacerbates the Presence of 14C-Bisphenol a in Tissues of Female and Male Mice.” Toxicology and Applied Pharmacology, vol. 278, no. 2, 15 July 2014, pp. 116–123, www.sciencedirect.com/science/article/pii/S0041008X14001574, https://doi.org/10.1016/j.taap.2014.04.017. 

Shim, Juyoung, et al. “Triclosan Is a Mitochondrial Uncoupler in Live Zebrafish.” Journal of Applied Toxicology, vol. 36, no. 12, 28 Mar. 2016, pp. 1662–1667, https://doi.org/10.1002/jat.3311. 

Lin, Dasong, et al. “Potential Biochemical and Genetic Toxicity of Triclosan as an Emerging Pollutant on Earthworms (Eisenia Fetida).” Chemosphere, vol. 81, no. 10, Nov. 2010, pp. 1328–1333, https://doi.org/10.1016/j.chemosphere.2010.08.027. 

Stoker, Tammy E., et al. “Triclosan Exposure Modulates Estrogen-Dependent Responses in the Female Wistar Rat.” Toxicological Sciences, vol. 117, no. 1, 1 Sept. 2010, pp. 45–53, academic.oup.com/toxsci/article-abstract/117/1/45/1682020?redirectedFrom=fulltext, https://doi.org/10.1093/toxsci/kfq180.

Pearce, Elizabeth N., and Lewis E. Braverman. “Environmental Pollutants and the Thyroid.” Best Practice & Research Clinical Endocrinology & Metabolism, vol. 23, no. 6, Dec. 2009, pp. 801–813, https://doi.org/10.1016/j.beem.2009.06.003.

Jm, Braun. “Early-Life Exposure to EDCs: Role in Childhood Obesity and Neurodevelopment.” Nature Reviews. Endocrinology, 1 Mar. 2017, pubmed.ncbi.nlm.nih.gov/27857130/.

Zeng, Liudan, et al. “LINE-1 Gene Hypomethylation and P16 Gene Hypermethylation in HepG2 Cells Induced by Low-Dose and Long-Term Triclosan Exposure: The Role of Hydroxyl Group.” Toxicology in Vitro: An International Journal Published in Association with BIBRA, vol. 34, 1 Aug. 2016, pp. 35–44, pubmed.ncbi.nlm.nih.gov/26970259/, https://doi.org/10.1016/j.tiv.2016.03.002. 

Wang, Cai-Feng, and Ying Tian. “Reproductive Endocrine-Disrupting Effects of Triclosan: Population Exposure, Present Evidence and Potential Mechanisms.” Environmental Pollution, vol. 206, Nov. 2015, pp. 195–201, https://doi.org/10.1016/j.envpol.2015.07.001.

Ginsberg, Gary L., and Sophie J. Balk. “Consumer Products as Sources of Chemical Exposures to Children.” Current Opinion in Pediatrics, vol. 28, no. 2, Apr. 2016, pp. 235–242, https://doi.org/10.1097/mop.0000000000000329. 

Buth, Jeffrey M., et al. “Dioxin Photoproducts of Triclosan and Its Chlorinated Derivatives in Sediment Cores.” Environmental Science & Technology, vol. 44, no. 12, 15 June 2010, pp. 4545–4551, sludgenews.org/resources/documents/Buth_Dioxin-Triclosan.pdf, https://doi.org/10.1021/es1001105. 

Christopher, M. M., et al. “Propylene Glycol Ingestion Causes D-Lactic Acidosis.” Laboratory Investigation; a Journal of Technical Methods and Pathology, vol. 62, no. 1, 1 Jan. 1990, pp. 114–118, pubmed.ncbi.nlm.nih.gov/2296157/. 

Yang, Qi, et al. “Analysis of Pre-Existing IgG and IgM Antibodies against Polyethylene Glycol (PEG) in the General Population.” Analytical Chemistry, vol. 88, no. 23, 16 Nov. 2016, pp. 11804–11812, https://doi.org/10.1021/acs.analchem.6b03437.
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Organic Diapers

12/6/2023

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The best organic diapers are not only safe for the environment but also safe for your baby. But, it is challenging to pick the best diaper brand when every other brand touts their diaper as the safest. Today, there are two sustainable diaper options - cloth diapers and disposable diapers. These two diapers help in two ways; reduce the buildup of diapers in landfills and protect your baby from the harsh chemicals, such as chlorine, in conventional diapers.

With the organic diapers, your baby will not suffer the chemicals' effects, and the environment will thank you for it. Cloth diapers are baby-friendly and environment-friendly, but although they might be the best natural diapers, they are not mum-friendly, which is why organic diapers rock.

When shopping for diapers, only go for a chemical-free diaper (watch out for chemicals such as parabens, phthalates, and chlorine), synthetic fragrance-free, and free of dyes. Again, ensure that all the materials used to make the diaper are natural or organic and are biodegradable.

Harmful chemicals in diapers

Besides making the environment unsightly, these disposable diapers contain chemical ingredients that could harm the environment, animals, and human beings. According to the Real Diaper Association, some components include polyethylene, petroleum, gelling material, perfume, and polypropylene. They also have non-renewable petroleum products.

Some of the disposable diapers contain chemicals that might lead to the release of dioxin into the environment. Dioxin is a toxin linked to cancer and health concerns in fetuses. ​

Health effects to Babies

  • Effects of Chlorine: Besides their negative impacts on the environment, conventional chemical-laden diapers also pose a threat to your baby's health. Most of these diapers contain chlorine, which is used to treat the core material of the diaper. Chlorine can cause skin irritations and even result in a skin rash. If you expose the baby to chlorine for a long time, they might get cancer.
  • Allergens in the Diaper: Conventional diapers also contain latex, perfumes, and dyes that might trigger an allergic reaction from the baby. Fragrances in an of them selves have been demonstrated to cause autoimmune and neurodegenerative diseases
  • Less Breathable Materials: Because these conventional diapers feature chemical-laden materials, they are less breathable. The reduced breathability raises the temperature inside the diaper. High temperatures around the groin region are not safe for male babies. It is also challenging to potty train toddlers when they are not comfortable in their diapers.
  • Increased Cost: The cost of conventional diapers and disposable organic diapers is different in the long run. On average, you will use at least $4,000 in traditional diapers in two years. It is almost the same amount you will spend with organic diapers because a piece of organic diapers can hold more liquid, some up to 17 times their weight in liquid.
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Purchase: Amazon

references

Davidson, Laurel. “The Only Way to Change Diapers Is One Baby at a Time. Real Diaper Association.” Real Diaper Association, 14 May 2015, realdiapers.org/diaper-facts.

World Health Organization. “Dioxins and Their Effects on Human Health.” Who.int, World Health Organization, 4 Oct. 2016, www.who.int/news-room/fact-sheets/detail/dioxins-and-their-effects-on-human-health.

Manikkam, Mohan, et al. “Dioxin (TCDD) Induces Epigenetic Transgenerational Inheritance of Adult Onset Disease and Sperm Epimutations.” PLoS ONE, vol. 7, no. 9, 26 Sept. 2012, p. e46249, https://doi.org/10.1371/journal.pone.0046249. Accessed 12 Mar. 2019.

“Chlorine “Allergy.”” ACAAI Public Website, 15 Jan. 2015, acaai.org/allergies/types/allergy-myths/chlorine-allergy.

Steinemann, Anne. “Fragranced Consumer Products: Exposures and Effects from Emissions.” Air Quality, Atmosphere & Health, vol. 9, no. 8, 20 Oct. 2016, pp. 861–866, https://doi.org/10.1007/s11869-016-0442-z.

Spencer, P., et al. “Neurotoxic Fragrance Produces Ceroid and Myelin Disease.” Science, vol. 204, no. 4393, 11 May 1979, pp. 633–635, https://doi.org/10.1126/science.432669. Accessed 13 Nov. 2019.

​Kazemi, Zahra, et al. “Evaluation of Pollutants in Perfumes, Colognes and Health Effects on the Consumer: A Systematic Review.” Journal of Environmental Health Science and Engineering, vol. 20, no. 1, 3 Feb. 2022, pp. 589–598, https://doi.org/10.1007/s40201-021-00783-x.
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