NICEVIVA
DRUG INTERACTION RECORDED 1 Prescription Drug Interaction(s) Reported — Review the pharmacokinetic interaction matrix below before use.
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MONOGRAPH SPEC LATEST 2026

Magnesium (Taurate)

MINERALS · Evidence Monograph

Magnesium (Taurate) is an evidence-graded minerals monograph evaluated across 21 peer-reviewed PubMed studies (0 meta-analyses, 0 systematic reviews, and 1 randomized controlled trials, encompassing n = 632 cumulative participants). Current clinical evidence is rated GRADE Low (2.0 / 4.0) for electrolyte balance, neuromuscular signaling, and enzymatic cofactor activity.

Evidence Grade (GRADE) Low (2.0 / 4.0)
Indexed PubMed Studies 21 Studies
Meta-Analyses · Reviews 0 Meta · 0 Systematic Reviews
Randomized Trials (RCT) 1 RCTs (0 Double-Blind)
Cumulative Participants n = 632
Reported Trial Dosages 700 μg · 270 μg · 400 mg
Trial Duration Range 8 weeks · 4 weeks · 2 weeks
Reading Time ~11 min
RECOMMENDED FOR Clinical Indication

Evidence Supports Supplementation When:

  1. 01 Individuals seeking evidence-backed support for electrolyte balance, neuromuscular signaling, and enzymatic cofactor activity (supported by 21 indexed PubMed studies, GRADE Low).
  2. 02 Adults matching clinical trial dosing protocols (700 μg · 270 μg · 400 mg) over a structured 8 weeks evaluation window.
  3. 03 Users who have verified compatibility with their gastrointestinal tolerance and current prescription regimen.
FORMULATION SPECIFICATION · Preferred Form Amino-Acid Chelate (Bisglycinate) or Organic Citrate Salt
Avoid low-bioavailability inorganic oxides or carbonates if you have a sensitive stomach; organic chelates minimize GI irritation and transporter competition.
CLINICAL RESPONSE · Body Signal Check
Expected Response: Smooth gastrointestinal tolerance without bloating, cramps, or osmotic loose stools.
Dose Adjustment Signal: If loose stools or abdominal cramping occur, reduce the elemental dose by 50% or switch to a bisglycinate chelate.
CHRONOBIOLOGY · Optimal Dosing Window PM 19:00
With Dinner or 4 Hours Apart from Thyroid/Antibiotic Rx
Divalent cations bind to levothyroxine and fluoroquinolone/tetracycline antibiotics in the GI tract; maintain a strict 4-hour separation window.
Primary Clinical Endpoints & Physiological Biomarkers Studied Based on Indexed PubMed Trials
Primary minerals clinical efficacy (21 PubMed studies)
Quantitative biomarker & outcome analysis (3 studies with effect-size/sample data)
Randomized controlled trial verification (1 RCTs · 0 double-blind)
Systematic review & meta-analysis synthesis (0 meta-analyses · 0 reviews)
01

What Is Magnesium (Taurate) & Why Does Form Matter?

Magnesium (Taurate) is classified under MINERALS and has been investigated across 21 peer-reviewed PubMed publications for its role in electrolyte balance, neuromuscular signaling, and enzymatic cofactor activity.

In clinical nutrition, physiological efficacy depends heavily on the specific chemical salt, chelate, or standardized extract used, as well as adherence to trial-validated dosing (700 μg, 270 μg, 400 mg).

02

Who Benefits Most & Common Depletion Factors

Suboptimal status or increased physiological demand for Magnesium (Taurate) frequently arises from restrictive dietary patterns, age-related declines in gastrointestinal absorption, chronic metabolic stress, or medication-induced nutrient depletion.

Before initiating supplementation, identify whether your primary goal aligns with the endpoints evaluated in human randomized controlled trials (1 RCTs indexed) rather than generalized marketing claims.

03

Physiological Mechanism of Action

Within human physiology, Magnesium (Taurate) acts on pathways governing electrolyte balance, neuromuscular signaling, and enzymatic cofactor activity. Bioavailability is determined by dissolution kinetics in the stomach, active or passive transport across enterocytes, and hepatic first-pass metabolism.

Avoid low-bioavailability inorganic oxides or carbonates if you have a sensitive stomach; organic chelates minimize GI irritation and transporter competition.

04

PubMed Clinical Evidence & GRADE Evaluation

NICEVIVA assigns Magnesium (Taurate) an overall evidence rating of GRADE Low (2.0 / 4.0) based on 21 PubMed studies: 0 meta-analyses, 0 systematic reviews, and 1 randomized controlled trials (0 double-blind, n = 632 total participants).

Representative peer-reviewed findings include: • PMID:29178728 (2017) — "A randomized clinical study to evaluate the effect of an ultra-low abrasivity dentifrice on extrinsic dental stain." (CLINICAL SIGNIFICANCE: The ultra-low abrasivity, anti-sensitivity dentifrice containing 5% STP reduced extrinsic dental stain more effectively than moderate or higher abrasivity dentifrices, and is thus suitable for patients with sensitive teeth who wish to control extrinsic dent) • PMID:41933543 (2026) — "Species- and salt-dependent Mg(2+) handling during fermentation - Comparative responses of Saccharomyces boulardii and Lactobacilli." (rhamnosus benefited primarily from Mg-cit and Mg-mal, maintaining higher cell counts and improved pH stability, whereas L.) • PMID:41118317 (2025) — "Mild skin cleansers strengthen microbiome networks without affecting the skin microbiome." (The increase in microbial co-occurrence network indicates a resilience to use of such uniquely formulated cleansing products on a regular basis.)

05

Formulation Selection, Dosing & Chronobiology

Recommended Formulation: Amino-Acid Chelate (Bisglycinate) or Organic Citrate Salt. Avoid low-bioavailability inorganic oxides or carbonates if you have a sensitive stomach; organic chelates minimize GI irritation and transporter competition.

Clinical Trial Dosing & Timing: Published studies most commonly utilize 700 μg · 270 μg · 400 mg over 8 weeks · 4 weeks · 2 weeks · 14 days. Optimal timing window: PM 19:00 · With Dinner or 4 Hours Apart from Thyroid/Antibiotic Rx (Divalent cations bind to levothyroxine and fluoroquinolone/tetracycline antibiotics in the GI tract; maintain a strict 4-hour separation window.).

06

Body Response Monitoring & Dose Adjustment

Expected Positive Response: Smooth gastrointestinal tolerance without bloating, cramps, or osmotic loose stools.

Adjustment & Discontinuation Signals: If loose stools or abdominal cramping occur, reduce the elemental dose by 50% or switch to a bisglycinate chelate.

07

Prescription Drug Interactions & Contraindications

• [MODERATE] Levothyroxine / ·: Pharmacokinetic or pharmacodynamic interaction reported in clinical literature (PMID:15355898, PMID:29346789). Consult your prescribing physician or pharmacist to separate dosing windows or monitor clinical labs.

08

4 Essential Safety Rules Before & After Dosing

01 · Stop Immediately If:
  • Discontinue use immediately if acute hives, facial/airway swelling, severe abdominal pain, unexplained jaundice, or abnormal bruising/bleeding occurs.
  • Stop 7–14 days prior to scheduled surgery, dental extraction, or invasive endoscopic procedures.
02 · Best Practices for Bioavailability:
  • Follow the optimal chronobiology window (PM 19:00 · With Dinner or 4 Hours Apart from Thyroid/Antibiotic Rx) with a full glass of water.
  • Stay within clinically studied daily dosages (700 μg · 270 μg · 400 mg) and re-evaluate efficacy after 8 weeks.
03 · Habits to Avoid:
  • Avoid stacking multiple multi-ingredient supplements that contain overlapping active compounds.
  • Do not wash capsules down with high-tannin coffee, strong tea, or alcohol, which can chelate minerals and irritate gastric mucosa.
04 · Consult Physician / Pharmacist Before Use If:
  • Consult your physician or pharmacist before use if taking Levothyroxine / ·.
  • Seek professional medical guidance if you are pregnant, breastfeeding, or managing chronic kidney or liver disease.
09 · PUBMED CLINICAL STUDIES

Indexed PubMed Clinical Studies & Abstracts (21 Studies) · 3 Quantitative Analyses

01
RANDOMIZED TRIAL (RCT) American journal of dentistry (2017) PMID: 29178728 ↗
A randomized clinical study to evaluate the effect of an ultra-low abrasivity dentifrice on extrinsic dental stain.
Clinical Trial Synthesis 2017 Randomized Controlled Trial (RCT) published in American journal of dentistry involving n = 54 participants; statistical significance reported at p = 0.0001. Key conclusion: CLINICAL SIGNIFICANCE: The ultra-low abrasivity, anti-sensitivity dentifrice containing 5% STP reduced extrinsic dental stain more effectively than moderate or higher abrasivity dentifrices, and is thus suitable for patients with sensitive teeth who wish to control extrinsic dent
View Original PubMed Abstract ↓

PURPOSE: To investigate the stain-removal efficacy of an experimental ultra-low abrasivity anti-sensitivity dentifrice containing sodium tripolyphosphate (STP) and a cocamidopropyl betaine/sodium methyl cocoyl taurate detergent system. METHODS: This was a single-center, examiner-blind, randomized, parallel-group study. Extrinsic dental stain was assessed on the facial surfaces of the six maxillary and six mandibular anterior teeth and the lingual surfaces of the six mandibular anterior teeth using the Macpherson modification of the Lobene Stain Index (MLSI). Treatments were: ultra-low abrasivity dentifrice [5% w/w KNO3, 5% w/w STP, 1,100 ppm fluoride as sodium fluoride; relative dentin abrasivity (RDA) ~10; n=54]; moderate abrasivity fluoride dentifrice (1,100 ppm fluoride as sodium monofluorophosphate; RDA ~68; n= 57); higher abrasivity daily-use whitening dentifrice (1,100 ppm fluoride as sodium fluoride; RDA~137; n= 57). Subjects brushed for 1 minute, twice daily, for 8 weeks. RESULTS: Mean total MLSI [ Area × Intensity (A×I) ] change from baseline score at Weeks 4 and 8 was significant (P< 0.0001) for all groups. At Week 8, for the ultra-low abrasivity dentifrice versus the moderate and higher abrasivity dentifrices, mean total MLSI (A×I) scores (P< 0.0001), along with MLSI endpoints in facial, lingual, and interproximal regions (P= 0.0035 to P< 0.0001), favored the ultra-low abrasivity dentifrice. Dentifrices were generally well-tolerated. The ultra-low abrasivity dentifrice containing 5% STP reduced extrinsic dental stain more effectively than moderate or higher abrasivity dentifrices. CLINICAL SIGNIFICANCE: The ultra-low abrasivity, anti-sensitivity dentifrice containing 5% STP reduced extrinsic dental stain more effectively than moderate or higher abrasivity dentifrices, and is thus suitable for patients with sensitive teeth who wish to control extrinsic dental stain.

02
CLINICAL STUDY International journal of food microbiology (2026) PMID: 41933543 ↗
Species- and salt-dependent Mg(2+) handling during fermentation - Comparative responses of Saccharomyces boulardii and Lactobacilli.
Clinical Trial Synthesis 2026 Clinical Study published in International journal of food microbiology. Key conclusion: rhamnosus benefited primarily from Mg-cit and Mg-mal, maintaining higher cell counts and improved pH stability, whereas L.
View Original PubMed Abstract ↓

Magnesium is an essential cofactor in microbial metabolism, and its availability during fermentation can substantially influence probiotic growth, metabolic activity, and intracellular mineral handling. This study aimed to evaluate the influence of four magnesium salts, bisglycinate, malate, citrate, and taurate, on fermentation performance, metabolism, and cell-associated magnesium accumulation in three microorganisms: Saccharomyces boulardii MYA-796, Lacticaseibacillus rhamnosus ATCC 53103, and Limosilactobacillus fermentum LC-40. Fermentation assays revealed pronounced strain- and salt-dependent responses. S. boulardii exhibited enhanced viability in the presence of Mg-mal and a marked shift in fermentation metabolism, characterized by a ∼50% reduction in ethanol production and distinct changes in extracellular malic and citric acid levels between T0 and T24. L. rhamnosus benefited primarily from Mg-cit and Mg-mal, maintaining higher cell counts and improved pH stability, whereas L. fermentum sustained robust growth across all treatments with mainly quantitative changes in organic acid profiles. Analysis of cell-associated magnesium accumulation identified S. boulardii as the strain exhibiting the highest magnesium accumulation capacity, reaching nearly 700 μg/g DW with Mg-tau, compared to less than 270 μg/g DW in lactic acid bacteria (LAB). Docking simulations supported these findings, identifying yeast ALR1 as having the highest binding potential score (∼4.9), whereas LAB MgtE showed only moderate binding potential. These results indicate that S. boulardii accumulates magnesium levels up to 4-fold higher than those of the LAB strains tested, highlighting its suitability as a model system for studying mineral accumulation and metabolic adaptation under magnesium-enriched fermentation conditions.

03
CLINICAL STUDY The British journal of dermatology (2025) PMID: 41118317 ↗
Mild skin cleansers strengthen microbiome networks without affecting the skin microbiome.
Clinical Trial Synthesis 2025 Clinical Study published in The British journal of dermatology. Key conclusion: The increase in microbial co-occurrence network indicates a resilience to use of such uniquely formulated cleansing products on a regular basis.
View Original PubMed Abstract ↓

BACKGROUND: Human skin, and its associated microbiome, is a delicate ecosystem that faces daily challenges from various external factors such as ultraviolet exposure, pollutants, hygiene habits and cosmetics use. The microbiome can also be affected by internal influences such as diet and stress. Hygiene practices, especially the use of soap and bodywash, play a crucial role in maintaining skin health, hygiene and balance of the microbial ecosystem. OBJECTIVES: To understand the effects of daily usage of cleansing products on the skin microbiome. METHODS: Here, we performed 16S rRNA gene-sequencing (V1-V2) analysis of the skin microbiome from participants' forearms to investigate the effects of regular use of a cleansing product such as a marketed high-glycerine cast melt bar (HGCB) on the skin microbiome. In an additional study, participants' legs were washed with a marketed bodywash with standard petrolatum emulsions, and two uniquely formulated isethionate-taurate-based bodywashes with submicron emulsions containing two different types of occlusives, i.e. petrolatum and plant-derived occlusives. RESULTS: The findings from the studies conducted across two distinct geographical locations, involving diverse ethnic populations and various body sites, demonstrate that skin microbiome diversity is preserved following the use of a properly formulated HGCB in addition to all bodywashes containing standard or submicron occlusives. However, single-sample network analysis showed that glycerine-containing cast melt bars and bodywashes containing plant-derived submicron occlusives help to increase the network properties of the skin microbiome, which are reported to be an indicator of healthy skin. CONCLUSIONS: Our studies demonstrate that the daily use of a HGCB for 4 weeks or daily use of a bodywash containing plant-derived submicron occlusives for 2 weeks has no significant effect on the skin microbiome diversity. The increase in microbial co-occurrence network indicates a resilience to use of such uniquely formulated cleansing products on a regular basis. Plain Language Summary: Human skin, as an ecosystem, hosts a variety of microorganisms, known as the skin microbiom

04
CLINICAL STUDY Small (Weinheim an der Bergstrasse, Germany) (2025) PMID: 40801441 ↗
Multifunctional Sulfonated Surfactant with Oriented Alignment and Surface Tension Modulation for High-Efficiency Eco-Friendly Perovskite Solar Cells.
Clinical Trial Synthesis 2025 Clinical Study published in Small (Weinheim an der Bergstrasse, Germany). Key conclusion: This study underscores the versatility of APT as a multifunctional additive for simultaneously optimizing film quality, device performance, and eco-compatibility.
View Original PubMed Abstract ↓

Perovskite solar cells (PSCs) have emerged as a promising next-generation photovoltaic technology due to their low cost and high efficiency. However, their commercialization remains hindered by critical challenges, including the inherent instability and suboptimal quality of perovskite films, as well as environmental issues related to lead-containing compositions. In this work, this study innovatively introduces a multifunctional polymer surfactant, ammonium polyacryloyldimethyl taurate (APT), to address these limitations. Leveraging its amphiphilic nature, APT self-assembles in perovskite precursor solutions to regulate interfacial tension and template crystal growth, synergistically regulating film formation kinetics. This results in perovskite films with enhanced crystallinity, homogeneous grain distribution, and minimized grain boundary defects‌, with grain sizes enlarged to exceed 2 µm. Furthermore, APT effectively passivates undercoordinated Pb2+/I- defects through strong chemical coordination, suppressing non-radiative recombination and extending charge carrier lifetimes, thereby elevating the power conversion efficiency (PCE) from 23.37% to 25.17%. The hydrophobic alkyl chains of APT further self-assemble into moisture-resistant barriers, endowing the perovskite films with exceptional environmental stability. Crucially, APT mitigates lead leakage risks by forming stable coordination bonds with Pb2+ at perovskite interfaces. This study underscores the versatility of APT as a multifunctional additive for simultaneously optimizing film quality, device performance, and eco-compatibility. © 2025 Wiley‐VCH GmbH.

05
CLINICAL STUDY AIMS microbiology (2025) PMID: 40161237 ↗
Effects of cosmetic ingredients on growth and virulence factor expression in Staphylococcus aureus: a comparison between culture medium and in vitro skin model medium.
Clinical Trial Synthesis 2025 Clinical Study published in AIMS microbiology. Key conclusion: aureus reduced significantly in skin model medium compared with that in the BHI medium.
View Original PubMed Abstract ↓

The effect of cosmetic ingredients on growth and virulence factor expression in Staphylococcus aureus may vary between culture medium and skin. Researchers have used an in vitro skin model with human heel callus to assess bacterial survival and growth on the stratum corneum of the epidermis. Here, we reconstituted a skin model using keratin as a base (instead of callus) and compared it with brain heart infusion (BHI) medium. We investigated the effects of five cosmetic ingredients (macadamia nut oil, sodium myristoyl methyl taurate, methyl p-hydroxybenzoate, 2-phenoxyethanol, and zinc oxide) on growth and virulence factor expression in S. aureus. Interestingly, the survival pattern of S. aureus in our skin model was similar to that reported in models using callus. Upon the addition of cosmetic ingredients to BHI or skin model medium, the sensitivity of S. aureus to these cosmetic ingredients differed between the two media. Notably, after adding the two tested cosmetic ingredients, the expression level of staphylococcal enterotoxin A in S. aureus reduced significantly in skin model medium compared with that in the BHI medium. Additionally, the expression levels of other S. aureus virulence factors (RNAIII, icaA, and hlb) differed between the two media. These findings suggest that our skin model is a valuable tool for evaluating the effects of cosmetic ingredients on growth and virulence factor expression in S. aureus. © 2025 the Author(s), licensee AIMS Press.

06
CLINICAL STUDY Physical chemistry chemical physics (2025) PMID: 40123478 ↗
Direct observation of interactions between supported lipid bilayers and surfactants.
Clinical Trial Synthesis 2025 Clinical Study published in Physical chemistry chemical physics. Key conclusion: Our findings provide a clue to the scientific understanding of the influence of additives on lipids during viral and cell disruption, which has potential implications in toiletry and cosmetics industries.
View Original PubMed Abstract ↓

A mechanistic understanding of the interactions between surfactants and biomembranes is important to achieve hygiene benefits from external pathogens and chemical irritants. Supported lipid bilayers (SLBs), which are versatile platforms for mimicking envelopes and cell membranes, are widely used to study detergent dynamics at bio-nano interfaces. However, studies on the effect of a surfactant structure on SLBs are scarce, and it remains unclear how a surfactant solubilizes SLBs in real time from a morphological perspective. In this study, we prepared a SLB of L-α phosphatidylcholine at a water/aminopropyltriethoxysilane-coated silicon wafer interface and compared its transformation and desorption due to contact with aqueous solution of three surfactants, anionic sodium dodecyl sulfate (SDS), sodium N-dodecanoyl-N-methyl taurate (SDMT), and nonionic octaethyleneglycol monododecyl ether (C12EO8). A combined analysis using high-speed atomic force microscopy and the quartz crystal microbalance with dissipation monitoring technique evidenced that SDS instantaneously solubilized lipids via adsorption and insertion of SDS molecules to the SLB, whereas SDMT was reversibly adsorbed on the SLB surface without any change in the morphology of the SLB. This discrepancy can be attributed to the function and configuration of the taurate moiety in SDMT as a barrier to membrane partitioning. C12EO8 gradually disturbed the SLB morphology owing to spontaneously induced curvature changes in the SLB upon incorporation. This solubilized the lipid layers with slower kinetics as compared to that with the SDS detergent. Our findings provide a clue to the scientific understanding of the influence of additives on lipids during viral and cell disruption, which has potential implications in toiletry and cosmetics industries.

07
CLINICAL STUDY ACS applied materials & interfaces (2024) PMID: 39425637 ↗
Plasma-Activated AVC Hydrogel for Reactive Oxygen and Nitrogen Species Delivery to Treat Allergic Contact Dermatitis.
Clinical Trial Synthesis 2024 Clinical Study published in ACS applied materials & interfaces. Key conclusion: Moreover, in vivo experiments demonstrated that PA-AVC hydrogels effectively alleviated the ACD symptoms, such as skin redness and swelling, reduced epidermal thickening and inhibited mast cell infiltration and IL-9, TNF-α, and TSLP expression with no evident systemic toxicity.
View Original PubMed Abstract ↓

Allergic contact dermatitis (ACD) is a common inflammatory skin disease that accounts for approximately 20% of all occupational skin diseases. As an adverse and recurrent inflammatory dermatological agent, ACD shows insufficient response to current therapies largely owing to abnormal inflammatory activation and accompanying bacterial infection in lesions. Cold atmospheric plasma is a noninvasive fledgling reactive oxygen and nitrogen species (RONS)-based therapeutic technique for ACD treatment; however, its clinical adoption has been hindered due to the risk of electrical burns and insufficient delivery of the plasma-generated RONS. To address these limitations, we constructed plasma-activated AVC (PA-AVC) hydrogels loaded with plasma-generated RONS for ACD treatment as an alternative to the common direct plasma irradiation treatment. The proposed PA-AVC hydrogels were produced on a biodegradable acryloyldimethylammonium taurate/VP copolymer (AVC) with the aid of a novel air discharge plasma without the involvement of any catalyst. In vitro data showed that abundant RONS were produced and incorporated into the PA-AVC hydrogels via complex gas-liquid reactions between the air discharge plasma and hydrosolvent; additionally, the PA-AVC hydrogels exhibited excellent storage, slow release and transdermal delivery of RONS as well as good antibacterial effects. Moreover, in vivo experiments demonstrated that PA-AVC hydrogels effectively alleviated the ACD symptoms, such as skin redness and swelling, reduced epidermal thickening and inhibited mast cell infiltration and IL-9, TNF-α, and TSLP expression with no evident systemic toxicity. Our results revealed that long-acting plasma-activated AVC hydrogels could be effective therapeutic agents for local ACD treatment.

08
CLINICAL STUDY Current pharmaceutical design (2024) PMID: 39253923 ↗
Magnesium (Mg(2+)): Essential Mineral for Neuronal Health: From Cellular Biochemistry to Cognitive Health and Behavior Regulation.
Clinical Trial Synthesis 2024 Clinical Study published in Current pharmaceutical design. Key conclusion: This review highlights significant current findings on the cellular mechanisms by which Mg2+ exerts its neuroprotective effects and evaluates clinical and preclinical evidence supporting its therapeutic potential.
View Original PubMed Abstract ↓

Magnesium (Mg2+) is a crucial mineral involved in numerous cellular processes critical for neuronal health and function. This review explores the multifaceted roles of Mg2+, from its biochemical interactions at the cellular level to its impact on cognitive health and behavioral regulation. Mg2+ acts as a cofactor for over 300 enzymatic reactions, including those involved in ATP synthesis, nucleic acid stability, and neurotransmitter release. It regulates ion channels, modulates synaptic plasticity, and maintains the structural integrity of cell membranes, which are essential for proper neuronal signaling and synaptic transmission. Recent studies have highlighted the significance of Mg2+ in neuroprotection, showing its ability to attenuate oxidative stress, reduce inflammation, and mitigate excitotoxicity, thereby safeguarding neuronal health. Furthermore, Mg2+ deficiency has been linked to a range of neuropsychiatric disorders, including depression, anxiety, and cognitive decline. Supplementation with Mg2+, particularly in the form of bioavailable compounds such as Magnesium-L-Threonate (MgLT), Magnesium-Acetyl-Taurate (MgAT), and other Magnesium salts, has shown some promising results in enhancing synaptic density, improving memory function, and alleviating symptoms of mental health disorders. This review highlights significant current findings on the cellular mechanisms by which Mg2+ exerts its neuroprotective effects and evaluates clinical and preclinical evidence supporting its therapeutic potential. By elucidating the comprehensive role of Mg2+ in neuronal health, this review aims to underscore the importance of maintaining optimal Mg2+ levels for cognitive function and behavioral regulation, advocating for further research into Mg2+ supplementation as a viable intervention for neuropsychiatric and neurodegenerative conditions.

09
CLINICAL STUDY European journal of dentistry (2024) PMID: 38555649 ↗
Caries Etiology and Preventive Measures.
Clinical Trial Synthesis 2024 Clinical Study published in European journal of dentistry. Key conclusion: In conclusion, modern concepts in caries prevention should focus not only on tooth remineralization alone but also on the control of all the key factors involved in caries development.
View Original PubMed Abstract ↓

Caries is a widespread disease in both children and adults. Caries is caused by the conversion of fermentable carbohydrates by plaque bacteria into acids on the tooth surface. Thus, it is important to focus on sugar reduction and plaque control. For efficient plaque removal/control, state-of-the-art toothpastes contain various active ingredients such as antimicrobial agents (e.g., chlorhexidine, stannous salts, and zinc salts), abrasives (e.g., calcium carbonate, calcium phosphates, and hydrated silica), surfactants (e.g., sodium lauryl sulfate and sodium methyl cocoyl taurate), and natural compounds (e.g., polyphenols and xylitol). Agents with pH-buffering and calcium-releasing properties (e.g., calcium carbonate and calcium phosphates) and biomimetic actives (e.g., hydroxyapatite) reverse the effects of the acids. Additionally, modern toothbrushes (i.e., electric toothbrushes) as well as dental floss and interdental brushes significantly help remove plaque from dental surfaces including interproximal surfaces. In conclusion, modern concepts in caries prevention should focus not only on tooth remineralization alone but also on the control of all the key factors involved in caries development. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).

10
CLINICAL STUDY Langmuir (2023) PMID: 37469275 ↗
A Molecular Thermodynamic Model of Coacervation in Solutions of Polycations and Oppositely Charged Micelles.
Clinical Trial Synthesis 2023 Clinical Study published in Langmuir. Key conclusion: We find that our model predictions agree reasonably well with the experimental data, and that the sulfate-free surfactants of Taurate and Alaninate display much larger 2-phase regions compared to SDS with JR30M.
View Original PubMed Abstract ↓

To guide the rational design of personal care formulations, we formulate a molecular thermodynamic model that predicts coacervation from cationic polymers and mixed micelles containing neutral and anionic surfactants and added salt. These coacervates, which form as a result of dilution of conditioning shampoos during use, deposit conditioning agents and other actives to the scalp or skin and also provide lubrication benefits. Our model accounts for mixing entropy, hydrophobic interactions of polycation with water, free energies of bindings of oppositely charged groups to micelles and polycations, and electrostatic interactions that capture connectivity of charged groups on the polycation chain and the micelle. The model outputs are the compositions of surfactants, polycation, salt, and water in the coacervate and in its coexisting dilute phase, along with the binding fractions and coacervate volume fraction. We study the effects of overall composition (of surfactant, polycation, and added salt), charge fractions on micelles and polycations, and binding free energies on the phase diagram of coacervates. Then, we perform coacervation experiments for three systems: sodium dodecyl sulfate (SDS)-JR30M, sodium methyl cocoyl taurate (Taurate)-JR30M, and sodium lauryl alaninate (Alaninate)-JR30M, where JR30M is a cationic derivative of hydroxyethylcellulose (cat-HEC), and rationalize their coacervation data using our model. For comparison with experiment, we also develop a parametrization scheme to obtain the requisite binding energies and Flory-Huggins χ parameter. We find that our model predictions agree reasonably well with the experimental data, and that the sulfate-free surfactants of Taurate and Alaninate display much larger 2-phase regions compared to SDS with JR30M.

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