As a commonly used organic iron supplement, ferrous gluconate offers advantages over inorganic iron (e.g., ferrous sulfate) such as lower irritation and higher bioavailability. However, the ferrous ion (Fe²⁺) in its molecular structure is prone to oxidation into ferric ion (Fe³⁺), leading to reduced activity, darkening of color (e.g., from pale yellow to brown), and even the development of off-odors. Temperature and light are the core environmental factors affecting its decomposition and oxidation. Below is an analysis of the specific impacts of these two factors on the stability of ferrous gluconate, covering mechanisms of action, influence patterns, and implications for practical application.

I. Impact of Temperature on the Decomposition of Ferrous Gluconate: Accelerating Oxidation and Molecular Motion

Temperature accelerates the decomposition of ferrous gluconate primarily by increasing molecular kinetic energy and promoting the rate of oxidation reactions. Its influence can be examined from two perspectives: "oxidation kinetics" and "system stability."

From the perspective of reaction mechanism, the decomposition of ferrous gluconate essentially involves the oxidation of Fe²⁺ (Fe²⁺ → Fe³⁺), a reaction that requires energy absorption to overcome the activation energy barrier. When temperature rises, the kinetic energy of molecules in the system (including ferrous gluconate molecules, oxygen molecules, and water molecules) increases significantly. On one hand, this makes Fe²⁺ more likely to lose electrons and undergo oxidation; on the other hand, it accelerates the diffusion rate of oxygen in the system, increasing the collision frequency between Fe²⁺ and oxygen and directly driving the oxidation reaction forward. At the same time, high temperatures disrupt the coordination bonding between carboxyl groups and Fe²⁺ in ferrous gluconate molecules, causing Fe²⁺ to dissociate more easily from the molecular structure and be exposed to the environment for oxidation. This process is more pronounced in liquid systems (e.g., ferrous gluconate oral solutions), as molecular movement is more free in liquid environments, and high temperatures exert a stronger destructive effect on coordination bonds.

In terms of practical influence patterns, the higher the temperature and the longer the exposure time, the more significant the decomposition of ferrous gluconate. For example, when stored at room temperature (25°C), the oxidation rate of ferrous gluconate solid powder is usually low, with an activity retention rate of over 90% within one month. In high-temperature environments (e.g., 40°C, 50°C), however, the color of the solid powder gradually darkens, and the Fe³⁺ content can increase by 20%–30% after one month, leading to a noticeable decline in activity. At temperatures above 60°C (e.g., in summer transportation vehicles or unshaded warehouses), not only does the oxidation rate increase sharply, but slight degradation of gluconate may also occur, producing small amounts of organic acids that further lower the system’s pH value. The increased acidity, in turn, promotes the oxidation of Fe²⁺ (oxygen has stronger oxidizing capacity in acidic environments), forming a vicious cycle of "temperature rise → accelerated oxidation → pH decrease → further accelerated oxidation." For liquid formulations, the impact of high temperatures is more severe: for instance, the shelf life of a ferrous gluconate oral solution can reach 12 months at 25°C, but at 37°C (simulating tropical climates or improper storage), the Fe²⁺ content may drop below the lower limit of the standard in just 3 months, accompanied by obvious brown precipitates, rendering the product unusable.

II. Impact of Light on the Decomposition of Ferrous Gluconate: Photooxidation and Bond Breakage

The effect of light (especially ultraviolet rays and short-wave components of visible light) on the decomposition of ferrous gluconate is a form of "photooxidation," which primarily involves exciting molecular activity through photon energy to directly or indirectly trigger the oxidation of Fe²⁺. This process can be categorized into two mechanisms: "direct photolysis" and "indirect photosensitized oxidation."

In terms of direct photolysis, Fe²⁺ in ferrous gluconate molecules exhibits certain light absorption properties. When irradiated with ultraviolet light (wavelength 200–400 nm) or blue light (wavelength 400–500 nm), Fe²⁺ absorbs photon energy and transitions from the ground state to an excited state (Fe²⁺*). Excited Fe²⁺ is extremely unstable and tends to transfer excess energy to surrounding oxygen molecules, converting oxygen into reactive oxygen species (ROS) such as singlet oxygen (¹O₂) and superoxide anions (O₂⁻). ROS have much stronger oxidizing capacity than ordinary oxygen and can quickly capture electrons from Fe²⁺, oxidizing it to Fe³⁺. Meanwhile, photon energy may also directly break the coordination bonds between gluconate and Fe²⁺, causing Fe²⁺ dissociation and further increasing the probability of oxidation.

In indirect photosensitized oxidation, if trace impurities (e.g., residual pigments, metal ions from the production process) or excipients (e.g., certain vitamins, sweeteners) are present in the ferrous gluconate system, these substances may act as "photosensitizers." After absorbing light, photosensitizers enter an excited state and then transfer energy to oxygen and ferrous gluconate, indirectly triggering the oxidation of Fe²⁺. For example, if vitamin C is added to an oral solution (though it can act as an antioxidant, it may also function as a photosensitizer at high concentrations), it may accelerate the oxidation of ferrous gluconate under light exposure. In solid formulations, trace iron ion impurities can also catalyze the oxidation of Fe²⁺ under light.

Regarding influence patterns, the stronger the light intensity and the longer the irradiation time, the more severe the decomposition of ferrous gluconate, with significant differences in impact among light of different wavelengths: ultraviolet light has the strongest destructive effect (highest photon energy), followed by blue and green light, while red and infrared light have weaker effects. For example, when ferrous gluconate solid powder is placed in a transparent glass bottle and exposed to natural light (containing ultraviolet rays) for one week, the Fe³⁺ content can increase by 15%–25%, and the color turns light brown. If irradiated under an ultraviolet lamp (254 nm, 30 W) for 48 hours, the Fe³⁺ content may even exceed 50%, completely losing its iron-supplementing activity. In contrast, when stored in light-proof conditions (e.g., brown glass bottles, aluminum-plastic packaging), even in the same temperature environment, the increase in Fe³⁺ content is less than 5% within one month, and stability is significantly improved. For liquid formulations, the impact of light is more prominent—since liquids have higher light transmittance, photons are more likely to interact with ferrous gluconate molecules. For example, an oral solution in transparent packaging may show obvious darkening and a 10%–15% decrease in Fe²⁺ content after 24 hours of exposure to sunlight.

III. Research Implications: Recommendations for Stabilized Storage and Application of Ferrous Gluconate

Based on the patterns of how temperature and light affect the decomposition of ferrous gluconate, targeted stabilization measures should be adopted in practical production, storage, and use:

Temperature control: Both solid formulations (e.g., tablets, capsules) and liquid formulations (e.g., oral solutions, syrups) should be stored at low or room temperature, away from high-temperature environments (e.g., stoves, radiators, windowsills exposed to direct sunlight). During production, the temperature for preparing liquid formulations should be controlled below 40°C to prevent premature oxidation of Fe²⁺ due to high temperatures. For transportation, cold chain or thermal insulation packaging should be used to avoid damage to the product from high temperatures inside the vehicle in summer.

Light protection: Packaging materials should be highly light-shielding. For example, solid formulations can use aluminum-plastic blister packaging (aluminum foil can completely block light), and liquid formulations can use brown glass bottles or opaque plastic bottles (e.g., high-density polyethylene bottles). Products should be stored in a cool, light-proof place, avoiding prolonged exposure to natural light or artificial light (especially ultraviolet lamps). After opening, the product should be used as soon as possible to minimize light exposure time.

Synergistic stabilization: In formulation production, appropriate antioxidants (e.g., vitamin E, sodium sulfite, in compliance with food additive or pharmaceutical standards) or chelating agents (e.g., citric acid, EDTA) can be added to enhance the stability of ferrous gluconate by inhibiting the oxidation of Fe²⁺ or stabilizing its coordination structure. Meanwhile, the pH value of the system should be controlled within a neutral or weakly acidic range (avoiding strong acidity or alkalinity) to reduce the promotion of Fe²⁺ oxidation by the environment.

Temperature affects the stability of ferrous gluconate by accelerating molecular motion and oxidation reaction rates, while light triggers decomposition through photooxidation and bond breakage—both factors lead to reduced activity of ferrous gluconate. In practical applications, by storing the product at low temperatures and away from light, optimizing packaging, and adding stabilizers, the decomposition of ferrous gluconate can be effectively delayed, ensuring the product’s quality and effectiveness.