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Lactobionic acid

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Lactobionic acid
Names

IUPAC name (2R,3R,4R)-2,3,5,6-Tetrahydroxy-4-[ [(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]hexanoic acid
Other names Galactosylgluconic acid
Identifiers
CAS Number	96-82-2^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:55481
ChEMBL	ChEMBL3039602
ChemSpider	7040^N
DrugBank	DB16621
ECHA InfoCard	100.002.309
EC Number	202-538-3
E number	E399 (antioxidants, ...)
KEGG	C22921
PubChem CID	7314
UNII	65R938S4DV^Y
CompTox Dashboard (EPA)	DTXSID3048861
InChI InChI=1S/C12H22O12/c13-1-3(15)10(7(18)8(19)11(21)22)24-12-9(20)6(17)5(16)4(2-14)23-12/h3-10,12-20H,1-2H2,(H,21,22)/t3-,4-,5+,6+,7-,8-,9-,10-,12+/m1/s1 Key: JYTUSYBCFIZPBE-AMTLMPIISA-N
SMILES O[C@@H]1[C@H](O)[C@@H](O)[C@H](O[C@@]([C@H](O)CO)([H])[C@H](O)[C@@H](O)C(O)=O)O[C@@H]1CO
Properties
Chemical formula	C₁₂H₂₂O₁₂
Molar mass	358.296 g·mol⁻¹
Appearance	Syrup^[1]
Solubility in water	Freely soluble^[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references

Lactobionic acid (4-O-β-galactopyranosyl-D-gluconic acid) is a sugar acid. It is a disaccharide formed from gluconic acid and galactose. It can be formed by oxidation of lactose. The carboxylate anion of lactobionic acid is known as lactobionate.

As an acid, lactobionic acid can form salts with mineral cations such as calcium, potassium, sodium and zinc. Calcium lactobionate is a food additive used as a stabilizer. Potassium lactobionate is added to organ preservation solutions such as Viaspan or CoStorSol to provide osmotic support and prevent cell swelling. Mineral salts of lactobionic acid are also used for mineral supplementation.

Lactobionic acid is also used in the cosmetics industry as an antioxidant^[2] and in the pharmaceutical industry as an excipient for formulation. For example, the antibiotic erythromycin is used as the salt erythromycin lactobionate when intravenously delivered.

References

[edit]

^ ^a ^b Merck Index, 11th Edition, 5219
^ Tasic-Kostov, M.; Pavlovic, D.; Lukic, M.; Jaksic, I.; Arsic, I.; Savic, S. (2012-10-12). "Lactobionic acid as antioxidant and moisturizing active in alkyl polyglucoside-based topical emulsions: the colloidal structure, stability and efficacy evaluation". International Journal of Cosmetic Science. 34 (5): 424–434. doi:10.1111/j.1468-2494.2012.00732.x. ISSN 1468-2494. PMID 22691034. S2CID 2854711.

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Lactobionic acid is a polyhydroxy acid (PHA) and aldobionic acid derived from the oxidation of lactose, consisting of a β-D-galactose unit linked via a glycosidic bond to a D-gluconic acid unit, with the chemical formula C₁₂H₂₂O₁₂ and systematic name 4-O-β-D-galactopyranosyl-D-gluconic acid.^[1]^[2]^[3] First produced through bacterial oxidation in the late 1940s,^[4] it is a white, crystalline, hygroscopic powder with a molecular weight of approximately 358 Da and a pKa of 3.8, featuring eight hydroxyl groups that confer strong humectant properties and the ability to form gel matrices with water.^[3]^[2] Key properties of lactobionic acid include its antioxidant activity, achieved by chelating metal ions like Fe(II) to inhibit hydroxyl radical production and lipid peroxidation, as well as its chelating, moisturizing, gelling, and emulsifying capabilities.^[5]^[3]^[2] It also exhibits antimicrobial effects by disrupting bacterial cell membrane integrity, inhibiting DNA and protein synthesis, and inducing oxidative stress, with minimum inhibitory concentrations (MICs) ranging from 10–18.75 mg/mL against pathogens such as Staphylococcus aureus, MRSA, and Listeria monocytogenes.^[2] Production of lactobionic acid primarily involves the selective oxidation of the aldehyde group in the glucose moiety of lactose to a carboxylic acid, using methods such as microbial fermentation (e.g., with Pseudomonas taetrolens or Acetobacter orientalis, achieving high yields from dairy by-products like whey), enzymatic synthesis with glucose-fructose oxidoreductase, or chemical oxidation (though less preferred due to toxic catalysts).^[5]^[2]^[6] Microbial and enzymatic approaches are favored for sustainability, with recent advances enabling conversion rates up to 95% using waste streams.^[5]^[7] In applications, lactobionic acid serves as a food additive and preservative, reducing microbial growth in dairy products by 2–2.3 log₁₀ CFU/mL and extending shelf life, while acting as a prebiotic fermented by gut bacteria like Bifidobacterium.^[2] In cosmetics, it functions as a gentle exfoliant that enhances cell turnover, inhibits matrix metalloproteinases to reduce photodamage, and soothes inflamed skin post-procedures.^[3]^[5] In medicine, it is used in organ preservation solutions (e.g., 100 mmol/L in University of Wisconsin solution) as an antioxidant and impermeant to prevent cell swelling, and in drug delivery systems and tissue engineering matrices.^[3]^[5] The calcium salt is FDA-approved as a food additive, including as a stabilizer.^[2]

Chemical properties

Structure and formula

Lactobionic acid is a sugar acid classified as a disaccharide, consisting of β-D-galactose linked to D-gluconic acid via a β-1,4-glycosidic bond.^[8] This structure positions it as an oligoaldonic acid, featuring eight hydroxyl groups and a carboxylic acid group at the anomeric carbon of the gluconic acid moiety.^[8] The molecular formula of lactobionic acid is

\ce{C12H22O12}

, with a molecular weight of 358.30 Da.^[1] It arises as an oxidation product of lactose, in which the aldehyde group at the C1 position of the glucose unit is selectively oxidized to a carboxylic acid, yielding a polyhydroxy acid that combines aldose features from the intact galactose unit and aldonic acid properties from the modified glucose-derived unit.^[8] Lactobionic acid exhibits defined stereochemistry across its nine chiral centers, including the β-D configuration at the anomeric carbon of the galactose (C1') and the D-series configuration of the gluconic acid chain, with the glycosidic oxygen bridging the C4 position of the gluconic acid to the C1' of galactose.^[9] The full systematic IUPAC name is (2R,3R,4R,5R)-2,3,5,6-tetrahydroxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanoic acid, commonly abbreviated as 4-O-(β-D-galactopyranosyl)-D-gluconic acid.^[9]^[8]

Physical characteristics

Lactobionic acid is typically observed as a white to off-white crystalline powder under standard conditions.^[10]^[11] This form reflects its solid-state structure, which is stable at room temperature and often supplied in this manner for industrial and laboratory use. The compound exhibits high solubility in water, reported values ranging from 5–20 g/100 mL at 20°C, owing to its polar nature and multiple hydroxyl groups.^[11]^[12]^[10] It is slightly soluble in ethanol and practically insoluble in non-polar solvents such as ether and acetone.^[13] This solubility profile facilitates its dissolution in aqueous media for various applications while limiting compatibility with hydrophobic systems. Lactobionic acid has a melting point of 113–118 °C.^[10] Its pKa value of 3.8 characterizes it as a weak acid, influencing its behavior in mildly acidic environments.^[14] The specific optical rotation is approximately [α]_D²⁰ +25° (c = 10 in water), confirming its chiral properties derived from the constituent sugars.^[10] Due to its eight hydroxyl groups, lactobionic acid is hygroscopic, readily absorbing moisture from the atmosphere to form gels containing about 14% water.^[8] This property contributes to its exceptional water retention capacity, making it effective as a humectant in formulations requiring hydration stability.^[14]

Reactivity and stability

Lactobionic acid possesses a carboxylic acid functional group that imparts acidity with a pKa of 3.8, enabling protonation/deprotonation behavior that influences its solubility and reactivity in solution.^[14] The molecule also contains multiple hydroxyl groups, which promote hydrogen bonding and coordinate with metal ions for chelation, such as with divalent (e.g., Ca²⁺) and trivalent (e.g., Fe³⁺) metals, primarily through the carboxylic oxygen and adjacent α-hydroxyl oxygens.^[15] This chelating ability is exemplified by the formation of stable complexes, as in the general reaction:

\text{LBA} + \text{M}^{2+} \to [\text{LBA} \cdot \text{M}]^{n+}

where LBA denotes lactobionic acid and M²⁺ a metal ion, with binding sites involving the polyol chain for enhanced stability.^[16] In terms of reactivity, lactobionic acid exhibits antioxidant properties through free radical scavenging and inhibition of hydroxyl radical formation, primarily via iron chelation that prevents Fenton-type reactions.^[3] Under acidic conditions, it undergoes intramolecular cyclization to form the δ-lactone, a process favored at low pH where the open-chain carboxylic acid dehydrates with a nearby hydroxyl group.^[17] This pH-dependent equilibrium shifts toward the lactone form in acidic media and the open-chain acid in neutral or basic environments, affecting its overall reactivity and solubility.^[18] Regarding stability, lactobionic acid remains intact in neutral to slightly acidic aqueous solutions and demonstrates resilience against forced degradation in both acidic and alkaline pH conditions, as well as at elevated temperatures up to 80°C and under oxidative stress.^[19] However, it undergoes thermal decomposition at temperatures exceeding 100°C, with multiple endothermic events observed during differential scanning calorimetry, leading to breakdown products including carbon oxides.^[20] The glycosidic bond linking the galactose and gluconic acid moieties is susceptible to acid-catalyzed hydrolysis, yielding galactose and gluconic acid, though enzymatic cleavage occurs more slowly.^[21]

Synthesis and production

Chemical methods

Lactobionic acid was first synthesized in 1889 by Emil Fischer and Gustav Meyer through the oxidation of lactose using bromine water, marking the initial chemical route for its production.^[8] This method selectively targets the aldehyde group of the glucose moiety in lactose, converting it to a carboxylic acid while preserving the galactosyl linkage.^[22] The primary chemical method remains hypohalite oxidation, typically employing bromine or hypobromite generated in situ from bromine in aqueous solution. In this process, lactose reacts with Br₂ in water under mildly acidic to neutral conditions, yielding lactobionic acid and hydrobromic acid, as represented by the simplified reaction:

\text{Lactose} + \text{Br}_2 / \text{H}_2\text{O} \rightarrow \text{Lactobionic acid} + \text{HBr}

Yields from this approach typically range from 70% to 80%, though it requires careful control to minimize over-oxidation or side products like lactone formation.^[22] Hypochlorite oxidation has also been explored as a variant, using sodium hypochlorite in buffered media for similar selective conversion, but it is less commonly applied due to potential chlorination byproducts.^[23] Electrochemical oxidation represents another established chemical route, utilizing platinum electrodes in an alkaline medium to achieve selective oxidation of lactose at the anode. This method operates under controlled potential, often in carbonate buffers, to favor lactobionic acid formation with minimal degradation of the disaccharide structure, achieving selectivities over 90% under optimized conditions.^[24] The process avoids stoichiometric oxidants, reducing waste, but demands significant electrical energy input. Catalytic oxidation with molecular oxygen over noble metal catalysts has gained prominence for industrial scalability. Palladium (Pd) or gold (Au) nanoparticles, supported on materials like alumina or carbon, facilitate the reaction in alkaline aqueous solutions at moderate temperatures (40–60°C) and pressures (1–10 bar O₂). For instance, Au/Al₂O₃ catalysts exhibit high activity and selectivity (>95%) toward lactobionic acid, with turnover frequencies exceeding 1000 h⁻¹. A notable early advancement is the 1927 patent by Stoll and Kussmaul, describing a calcium chloride-mediated process that enhances crystallization of the intermediate calcium lactobionate during oxidation.^[25]^[26] Purification of lactobionic acid from reaction mixtures commonly involves ion-exchange chromatography to remove inorganic salts and convert salts to the free acid form, followed by crystallization of the calcium lactobionate salt for isolation, and subsequent acidification with sulfuric or hydrochloric acid to yield the pure acid. This sequence ensures high purity (>98%) but adds processing steps.^[27] While chemical methods provide high-purity lactobionic acid suitable for pharmaceutical and food applications, they are disadvantaged by energy intensity, particularly in electrochemical and catalytic processes requiring heating and pressurization, as well as the use of harsh reagents like halogens that generate corrosive byproducts. Yields are generally moderate (70–80% for traditional oxidations), limiting economic viability compared to emerging alternatives.^[6]

Biotechnological methods

Biotechnological methods for producing lactobionic acid leverage enzymes and microorganisms to oxidize lactose selectively, offering sustainable alternatives to chemical synthesis by utilizing renewable feedstocks like whey permeate. These approaches emphasize high specificity and environmental compatibility, converting lactose to lactobionic acid through oxidation of its aldehyde group. Enzymatic synthesis primarily employs cellobiose dehydrogenase (CDH) from fungi such as Sclerotium rolfsii or Phanerochaete chrysosporium, often coupled with laccase for cofactor regeneration. The reaction proceeds as lactose + O₂ → lactobionic acid + H₂O₂, where CDH oxidizes lactose and laccase reduces the electron acceptor, such as 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), enabling continuous catalysis. Glucose-fructose oxidoreductase (GFOR) from Zymomonas mobilis, expressed in recombinant Escherichia coli, provides an alternative, catalyzing lactose oxidation in a coupled system with gluconolactonase to yield lactobionic acid and sorbitol from lactose/fructose substrates. Yields reach up to 42.6% conversion (21.28 mM lactobionic acid from 50 mM lactose) in multi-enzymatic CDH/laccase systems at 50°C with ABTS mediation.^[28]^[29]^[30] Microbial fermentation, first discovered in 1947 by Stodola and Lockwood using Pseudomonas species, remains a cornerstone method. Strains such as Pseudomonas fragi NL20W or Pseudomonas taetrolens efficiently convert whey-derived lactose, achieving over 90% molar yield through aerobic oxidation via glucose dehydrogenase, with titers up to 300 g/L. Engineered E. coli overexpressing GFOR from Z. mobilis supports production from whey permeate, though with lower titers compared to Pseudomonas strains.^[31]^[32]^[33]^[29] Processes typically involve aerobic batch or submerged fermentation at 25–30°C and pH 6–7, with initial lactose concentrations of 200–300 g/L supplemented by CaCO₃ for pH control and aeration at 1 vvm. Optimal conditions yield productivities up to 6.38 g/L/h in flasks and 3.09 g/L/h in 3-L bioreactors, with maximum titers of 37–300 g/L depending on strain and substrate. Downstream processing includes centrifugation or filtration to remove cells, followed by ion exchange for purification and evaporation for concentration.^[32]^[33] Recent advances include immobilization of CDH and laccase on carriers like functionalized beads for repeated use, improving stability and reducing costs, and whole-cell biocatalysts with engineered Pseudomonas putida expressing novel dehydrogenases, boosting yields by up to 486%. These methods enable green catalysis, though scale-up requires sterile conditions to prevent contamination.^[34]^[32] Biotechnological routes offer eco-friendly benefits, including high regioselectivity and utilization of dairy waste, contrasting with harsher chemical methods, but face challenges in maintaining enzyme stability and achieving economic viability at industrial scales without optimization.^[6]

Applications

Food and beverage industry

Lactobionic acid serves as a versatile functional ingredient in the food and beverage industry, primarily due to its antioxidant, stabilizing, and antimicrobial properties derived from its chelating ability to bind metal ions like iron and copper, which prevents oxidative reactions in food systems.^[35] This chelation also contributes to its role in preservation by inhibiting microbial growth through pH lowering and metal sequestration, making it effective against bacteria and fungi in acidic environments.^[35] Additionally, it acts as a stabilizer and gelling agent, enhancing texture and water retention in various products without introducing off-flavors.^[36] In dairy processing, lactobionic acid functions as an acidifier in cheese and yogurt production, reducing fermentation time by 20-30% at concentrations of 1-10% and improving gel firmness compared to alternatives like glucono-delta-lactone.^[35] It is also used in milk powders to replace skimmed milk components in ice cream formulations, promoting non-melting textures during storage.^[35] For beverages and fruit juices, it enables calcium fortification via calcium lactobionate complexes at 50-90% incorporation levels, extending shelf life in acidic drinks while maintaining stability.^[35] In desserts, jams, and meat products, it serves as a gelling agent and stabilizer, reducing water loss in meats by up to 15% and enhancing gelation in dairy-based desserts at 0.5-2.7% concentrations.^[36] These applications leverage its antimicrobial synergy, such as with nisin against Listeria monocytogenes in milk, further supporting preservation in whey-derived products.^[35] Sensory-wise, lactobionic acid imparts a mild sweet taste (about 15-30% as sweet as sucrose) and improves mouthfeel in fruit preparations and fermented milks without altering overall flavor profiles, as demonstrated in studies on yogurt and juice fortification.^[35] Its integration into production often involves valorizing cheese whey, a dairy byproduct generating approximately 190 million tons annually worldwide (as of 2023 estimates), through microbial oxidation yielding up to 42.4 g/L of food-grade lactobionic acid with near-100% lactose conversion using bacteria like Pseudomonas taetrolens.^[35]^[36]^[37] This approach reduces waste and supports sustainable manufacturing of additives for beverages and dairy.^[38] Regulatory approval for its use in food comes via the calcium salt form, approved by the FDA as a food additive under 21 CFR 172.720 for use as a firming agent in various products, with no specified upper limits beyond good manufacturing practices. This status underscores its safety for direct addition in milk powders, juices, and other acidic foods to enhance shelf life and nutritional value.^[36]^[39]

Cosmetics and personal care

Lactobionic acid serves as a polyhydroxy acid (PHA) in cosmetic formulations, functioning as a gentle exfoliant due to its larger molecular size compared to alpha hydroxy acids (AHAs), which allows it to penetrate the skin more slowly and reduce irritation while effectively removing dead skin cells and promoting hydration.^[40] This makes it particularly advantageous for individuals with sensitive or compromised skin, as it exfoliates without the stinging or redness often associated with stronger acids.^[3] In addition to exfoliation, lactobionic acid acts as a humectant that attracts and retains water in the skin, enhancing moisturization and supporting the skin's barrier function to soothe inflammation and prevent moisture loss.^[41] Its antioxidant properties neutralize free radicals, contributing to anti-aging effects by improving skin elasticity, smoothing texture, and reducing signs of photoaging, such as fine lines, without compromising skin integrity.^[40] These multifaceted benefits position it as a versatile ingredient suitable for daily use in skincare routines. Lactobionic acid is commonly incorporated into creams, serums, and chemical peels at concentrations typically ranging from 1% to 5%, where it also serves as a chelating agent to stabilize emulsions by binding metal ions and preventing oxidation.^[3] This formulation flexibility allows for targeted applications, such as overnight treatments or gentle peels, enhancing product efficacy while maintaining a low irritation profile.^[42] Since the early 2000s, lactobionic acid has seen increasing adoption in "clean beauty" products, driven by consumer demand for natural-derived, multifunctional ingredients that align with sustainable and gentle skincare trends.^[43] Its biocompatibility and eco-friendly profile have fueled market growth, with the global lactobionic acid market valued at USD 245 million in 2024 and projected to reach USD 483 million by 2033 (CAGR 8.2%), particularly in the cosmetics sector.^[44]

Pharmaceuticals and medicine

Lactobionic acid (LBA) is employed in pharmaceutical applications primarily for its ability to facilitate targeted drug delivery to hepatocytes through conjugation with nanocarriers. The galactose moiety in LBA's structure enables specific binding to asialoglycoprotein receptors (ASGPR) overexpressed on liver cells, enhancing uptake and minimizing off-target effects.^[45] This property has been leveraged in dendrimer-based systems for delivering anticancer agents like sorafenib to hepatocellular carcinoma cells, demonstrating improved efficacy in preclinical models.^[46] Similarly, LBA-modified nanoparticles, such as selenium or gold-based ones, have shown enhanced liver accumulation and therapeutic potential against hepatic tumors.^[47]^[48] In wound care, LBA serves as a biocompatible component in hydrogel formulations that promote healing by maintaining a moist environment and exhibiting antimicrobial activity. LBA-modified chitosan hydrogels have been developed for endoscopic submucosal dissection, where they provide lesion elevation while accelerating tissue repair through reduced inflammation and enhanced cell proliferation.^[49] Its antimicrobial effects stem from disrupting bacterial cell walls and membranes, effective against pathogens like Pseudomonas fluorescens and methicillin-resistant Staphylococcus aureus, which supports its role in preventing wound infections. These properties make LBA hydrogels suitable for advanced wound dressings that balance hydration and infection control.^[2] Beyond targeting and wound management, LBA functions as a stabilizer in biologic formulations, aiding in the preservation of protein-based therapeutics due to its chelating and buffering capabilities.^[50] In tissue engineering, LBA-functionalized scaffolds, such as polyethersulfone membranes, support hepatocyte adhesion and spheroid formation for liver tissue regeneration.^[51] LBA's antioxidant properties contribute to its use in therapies aimed at mitigating oxidative stress, as it chelates metals like iron to inhibit reactive oxygen species formation.^[52] Emerging research explores LBA in ocular formulations, such as eye drops combined with hyaluronic acid, which alleviate dry eye symptoms by improving tear film stability and reducing ocular surface damage.^[53]

Safety and environmental aspects

Health and toxicity profile

Lactobionic acid exhibits low acute toxicity, with an oral LD50 greater than 5,000 mg/kg in rats and a dermal LD50 greater than 2,000 mg/kg in rats, indicating it is not acutely hazardous at typical exposure levels.^[54] It is non-irritating to skin and eyes at concentrations used in cosmetics and personal care products, though mild irritation may occur with undiluted exposure in animal tests.^[54] The compound is not genotoxic, as evidenced by negative results in the Ames test, and shows no evidence of carcinogenicity according to classifications by IARC, NTP, and OSHA.^[54] Lactobionic acid is approved by the U.S. Food and Drug Administration (FDA) as a direct food additive under 21 CFR 172.720 for firming and stabilizing purposes, with no limitation other than current good manufacturing practice. At high oral doses, such as 24 g/day, it may exert a mild laxative effect due to its osmotic activity in the gut, leading to symptoms like bloating and flatulence similar to those in lactose intolerance.^[35] No significant adverse health effects are reported at lower dietary levels, and it demonstrates prebiotic potential by supporting beneficial gut bacteria without systemic toxicity.^[35] In terms of metabolism, lactobionic acid is resistant to human digestive enzymes and poorly absorbed in the small intestine, allowing it to reach the colon largely intact where it is partially fermented by gut microbiota into short-chain fatty acids and other metabolites.^[55] The unfermented portion is excreted primarily in feces, with minimal urinary elimination of unchanged compound.^[35] Allergenicity is rare, but individuals with lactose intolerance may experience gastrointestinal discomfort from trace lactose impurities in some preparations, though purified forms pose low risk.^[35] Primary exposure routes include oral ingestion via food and supplements, dermal contact in cosmetics, and potential inhalation of powders, the latter presenting low risk due to poor volatility and non-respiratory irritancy at ambient levels.^[54]

Regulatory approvals

Lactobionic acid is approved by the U.S. Food and Drug Administration (FDA) for use as an excipient in pharmaceutical formulations, appearing on the Inactive Ingredient Database for applications such as injections and topicals, with no specific daily intake limits established due to its low toxicity profile. Its calcium salt, calcium lactobionate, is permitted as a direct food additive under 21 CFR 172.720 for firming and stabilizing purposes at levels not exceeding 0.1% in baked goods, fillings, and dairy products.^[56] Lactobionic acid, as a polyhydroxy acid, is considered safe in cosmetics when formulated to be non-irritating, with typical use concentrations up to 10% in leave-on products at pH above 3.5. In the European Union, lactobionic acid lacks approval as a food additive and has no assigned E-number, limiting its direct use in foodstuffs despite interest in its preservative properties.^[35] It complies with the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) regulation as a registered substance for industrial and cosmetic applications, ensuring safety data on handling and environmental release. For cosmetics, it falls under general EU cosmetic regulation (EC) No 1223/2009, where it must be assessed for safety in formulations, often used at low concentrations as a mild exfoliant. Health Canada permits lactobionic acid in cosmetics but restricts it as part of alpha-hydroxy acids on the Cosmetic Ingredient Hotlist, requiring concentrations not exceeding 18% total alpha hydroxy acid equivalents in leave-on consumer skin care products and a pH ≥ 3.5, with mandatory warnings for sun protection if used in exfoliating formulations.^[57] In Japan, it is approved for food use without specific quantitative limits, notably in dairy products like Caspian Sea yogurt as a prebiotic and stabilizer.^[35] The Joint FAO/WHO Expert Committee on Food Additives (JECFA) has not established an acceptable daily intake (ADI) for lactobionic acid, reflecting its evaluation primarily through national frameworks due to low anticipated exposure. Regulatory limits emphasize its safety at typical use levels, with no ADI set globally owing to negligible toxicity, and food uses (via salts) remain below 0.1%.^[58] Labeling requirements mandate disclosure as "lactobionic acid" in ingredient lists for cosmetics and pharmaceuticals under FDA and EU rules, or by function (e.g., firming agent) in foods where applicable, ensuring transparency for consumers.^[58]

Biodegradability and impact

Lactobionic acid is readily biodegradable according to OECD 301 guidelines (≥60% mineralization within 28 days). In terms of environmental impact, lactobionic acid demonstrates low toxicity to aquatic organisms, with EC50 and LC50 values exceeding 100 mg/L, posing negligible risk to ecosystems even at elevated concentrations.^[59] Its production from renewable whey substrates contributes to sustainability by valorizing dairy industry waste, thereby reducing the environmental burden of whey disposal.^[32] Biotechnological production routes enhance overall sustainability, offering a reduced carbon footprint relative to chemical oxidation methods through milder conditions and renewable feedstocks.^[6] These approaches align with green chemistry principles, enabling recyclability and lower energy demands. For waste management, lactobionic acid is non-persistent in the environment due to its rapid biodegradation and exhibits no bioaccumulation potential, as indicated by a computed log Kow of -5.67, well below the threshold of 3 for concern.^[60] Cradle-to-grave evaluations underscore its favorable eco-profile, supporting its use in environmentally conscious applications.

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