Calcium Carbonate Research Articles

Preparation of aragonite from calcium carbonate via wet carbonation to improve properties of steel slag building materials

Smelting in steel mills emitted large amounts of CO2 and produced the waste product steel slag (SS). Therefore, the use of SS to fix CO2 and produce value-added products could treat waste with waste and promote the effective use of resources. In this study, aragonite-type calcium carbonate was prepared by wet carbonation of SS, and the aragonite-rich SS (ASS) was pressed and moulded in the raw material of SS for semi-dry carbonation to obtain SS products. Through a series of experiments, the optimal conditions for the modulation and the formation mechanism of aragonite whiskers were investigated, and the effects of aragonite as a crystal seed on the properties and the degree of carbonation of SS products were also explored. In this experiment, the carbonation products were characterised microscopically by XRD, TGA, FT-IR and SEM, and the strength was tested by press machine. The results showed that aragonite phase was produced by wet carbonation of SS suspension containing 0.1M/L MgCl2 at 120 °C for 2h. The compressive strength, flexural strength, and secondary carbonation degree of the prepared SS products were increased when 5% ASS was added.

Cooperative stabilization of calcium carbonate powder, blast furnace slag, and white cement in composite concrete: Volume variation and hydration behavior

Volume stability was an important property of white concrete in long-term service. The purpose of this research is that volume stability of composite concrete was advanced by synergy of calcium carbonate powder and blast furnace slag, and its related hydration behavior was revealed. The results manifested that the early shrinkage, dry shrinkage, and creep of calcium carbonate powder-blast furnace slag-based white concrete (C20) were the lowest as content of calcium carbonate powder and blast furnace slag were 20 % and 10 %. Furthermore, early shrinkage, dry shrinkage, creep, and 120-days compressive strength of C20 were 52.49 %, 24.83 %, 22.47 %, and 82 MPa respectively, which superior to those of others white concrete. These results indicated that the long-term volume stability and strength of C20 was optimal. Information of hydration heat showed that accumulate hydration heat about C20 was minimum (226.91 J/g). This find proved that the effects of thermal expansion and cooling shrinkage on the volume of C20 were ameliorated efficiently. The results of microstructure, mineral phase, and pore structure demonstrated that dense degree of white concrete was boosted by flocculation gel product and rod ettringite. Therefore, the volume stability of white composite concrete could be enhanced by synergy of calcium carbonate powder, blast furnace slag, and white cement.

Integrating Digital Tools Optimizes Scale Management

_ This article, written by JPT Technology Editor Chris Carpenter, contains highlights of paper SPE 218700, “Integrating Digital Tools to Optimize Scale Management: Case Studies,” by Hugh M. Bourne, SPE, Shaun Hosein, and Garry Keilty, BP, et al. The paper has not been peer reviewed. _ The complete paper describes the suite of cloud-based digital-twin tools developed by the operator that provides online, real-time calculation of scale risk and barrier health on a well-by-well basis. The paper presents field case studies in which the suite of tools, integrated into a dashboard, have been implemented. Introduction Several case histories are shared in the complete paper, highlighting the challenges of updating evolving scale risk and monitoring the health of deployed barriers, which drove the decision to create the digital tools to further optimize scale management. Case Study 1 A mature asset with subsea wells had been operated for many years without any history of scaling. The wells were operated under pressure depletion with no water-injection support, but lift gas injection was initiated approximately 10 years ago to maintain production. When a decision was made to increase production from one of the wells by further opening the choke, the potential effect of this change on scale risk was not immediately assessed. Further opening the choke reduced the wellhead pressure by approximately 30 bar, and the well flowed faster, increasing wellhead temperature by as much as approximately 10°C. After an initial increase in production, a decline was observed. A light intervention vessel encountered a hard restriction below the wellhead. When solids were recovered to surface, the tool became stuck in the well and the intervention was stopped while a rig was mobilized to recover the stuck tool. In the intervening period, the recovered solids were analyzed, confirming that the restriction was calcium carbonate scale. Scale predictions were updated with the new operating conditions, confirming that the higher wellhead temperature, coupled with the lower wellhead pressure in the presence of lift gas, had pushed the fluids into a calcite scaling regime. The scale restriction was remediated using acid washing and a preventative scale squeeze treatment. The intervention, in total, cost the operation more than $50 million. Since the scaling event, wells have been routinely squeezed to protect production at a typical cost of around $5 million per well per treatment. Case Study 2 A subsea field is being developed as a tieback to a mature facility. Production from the new tieback has the potential to deposit halite in the wells and flowline at various stages of field life. A multistage wash-water-injection strategy has been proposed to allow a standard tree design. Additional wash water will be injected at the wellhead to protect the flowline from halite deposition as the fluids cool and to ensure that the produced-water chloride concentration is sufficiently reduced. This will create produced water with an almost 1:1 mix of formation water and wash water. Further wash-water injection is planned at the slug catcher. However, the host facility has produced water-handling limitations that restrict the amount of water it can process. Optimizing the amount of additional wash water while managing the halite-deposition risk, ensuring effective corrosion inhibition, and meeting export specification will be essential to minimize deferrals, thereby maximizing production.

Evaluation of carbonated fossil bone consolidation by induction of calcium hydroxide nanoparticles in a Miocene Cheirogaster richardi specimen

In this research, calcium hydroxide nanoparticles, as a carbonate consolidation method, have been evaluated on carbonated fossil bone samples from decontextualized Cheirogaster richardi specimens’ fragments.The main objective was to assess whether the treatment improved fossil bone surface cohesion and mechanical strength by creating a consolidated carbonate matrix in fossil substrate. Treatment penetration capacity and chemical compatibility without causing observable alterations in substrate porosity and external appearance were considered as significant questions to be assessed. Samples were analysed both before and after treatment using scanning electron microscopy, spectrophotometry, weight measurement control, water absorption assessment, conductivity and pH measurement, Vickers microindentation and tape testing. During analysis and evaluation, changes in fossil bone after treatment compared to its original condition have been taken into account.Results point out that hardness and cohesion increased significantly after treatment, bonding together disaggregated particles via a calcium carbonate micrometric layer, with almost negligible changes in surface topography and colour. In addition, calcium hydroxide nanoparticles penetration depth was remarkable. Conductivity, pH and weight hardly changed and porosity reduction was observed without complete pore blockage. To sum up, the treatment was effective and suitable for carbonate fossil bones having a highly compatibility with carbonate fossil bones substrates.

Mechanism of organic additives-induced carbonation activators on affecting cement mortars

In this study, we investigated the impact of introducing an in-situ activator, produced by carbonating cement particles in an aqueous solution, on the properties of cement mortars through secondary mixing. Two organic additives, ethylenediaminetetraacetic acid (EDTA) and glutamic acid (GLTA), were employed to enhance the leaching of calcium ions during carbonation, thereby improving the carbonation efficiency. A suite of characterization techniques revealed that the presence of organic additives could refine the carbonated particles and influence the morphology. The carbonated activators generated by this process were rich in silica gel and various polymorphic forms of calcium carbonate. These components, serving as fillers and nucleation for cement hydration, significantly accelerated the hydration process of cement mortar and promoted the formation of carboaluminate in the secondary mixing process. This approach effectively decreased the porosity of the cement mortar, refined the pore structure, and enhanced the mechanical strength.

Stabilization of Metastable Calcium Carbonate Polymorphs on the Surface of Recycled Cement Paste Particles: A Two-Step Carbonation Approach without Chemical Additives

Stabilization of Metastable Calcium Carbonate Polymorphs on the Surface of Recycled Cement Paste Particles: A Two-Step Carbonation Approach without Chemical Additives

Paleo-ecological quality status induced by natural and anthropogenic impacts in the last 2000 years: a multidisciplinary approach in the outer region of Sepetiba Bay (SE Brazil)

Abstract Purpose Some marine organisms can be used as Biological Quality Elements to estimate the degree of environmental impact and to monitor the health of benthic habitats. Organisms with mineralized protections, such as benthic foraminifera, can provide helpful information on the evolution of the coastal system over a long period and determine the Paleo-Ecological Quality Status (Paleo-EcoQS). This work aims at reconstructing the Paleo-EcoQS in the heavily anthropized Sepetiba Bay (SB; Rio de Janeiro State, SE Brazil). Materials and methods This work is based on a multiproxy approach, including textural, geochemical, and foraminiferal data along the core SP11 retrieved near the Pico da Marambaia (a mountain on the tip of the Marambaia Barrier Island). Geochemical analyses encompassing total organic carbon (TOC), total sulfur (S), total nitrogen (N), calcium carbonate (CaCO3), stable isotopes in organic matter (OMδ13C, and OMδ15N) and elemental concentrations as well as 201Pb, 137Cs, and radiocarbon dating were performed to characterize the Paleo-EcoQS in the bay. Results The values of the Paleo-EcoQS.st (standardized Paleo-EcoQS) index in core SP11 indicate that the paleoenvironmental quality varied from moderate to good between ≈50 AD and ≈1500 AD and from good to high between the ~ 1920s and ~ 1990s. Since the 1990s, the Paleo-EcoQS.st has deteriorated considerably, probably due to the deposition of contaminated dredging material in nearby areas. Ballast water discharge may have introduced alien species, such as Ammonia buzasi, into the SB. Conclusions The results obtained in core SP11, compared to those of another core (i.e., SP8) from a nearby area, suggest that the reference level of maximum environmental quality is not always reached in a period before industrialization in coastal ecosystems with significant interaction with the ocean; natural factors, related, for example, to sedimentary dynamic processes or geomorphological changes, can lead to unexpected results.

Improving the Productivity and Physiological Characteristics of Lettuce Plants Using Spraying Calcium as a Nanofertilizer

Implementing nanofertilizers in cultivation to enhance food security is important and gaining great significance, as they have good properties to improve plant production, phytochemicals, and nutrient efficiency and thereby meet the demands of the increasing world population for food. This work demonstrated the impact of calcium carbonate nanoparticles (Ca-NPs) and Ca bulk at three concentrations (0, 100, and 200 mg L−1) on growth, productivity, photosynthetic pigments, phytochemical content, antioxidant activity enzymes, minerals, toxicity, and genomic DNA of lettuce plants. In this regard, Ca-NPs at a concentration of 200 mg L−1 reinforced the vegetative growth characteristics of lettuce plants, increasing head length by 15.7 and 19.2%, head diameter by 20.3 and 19.9%, head fresh weight by 54.4 and 52.9%, and production per hectare by 54.7 and 52.8% as compared to the control during the two growing seasons. Furthermore, the percentages of total chlorophyll (62.6 and 59.5%), carotenoids (48.4 and 56.5%), total phenolics (63.6 and 65.7%), total indoles (39.4 and 36.4%), vitamin C (39.7 and 39.6%), antioxidant activity (57.8 and 53.7%), nitrogen (70.5 and 67.5%), phosphorus (120 and 110.5%), potassium (33.0 and 33.2%), and calcium (67.14 and 63.2%) were also increased compared with the control during two consecutive growing seasons. Additionally, Ca-NPs and Ca bulk had an impact on the plants’ genomic DNA compared to the control. In addition, lettuce plants treated with Ca-NPs were proven to be nontoxic and safe for humans by using the Microtox 500 analyzer.

Evaluation of Material Characteristics and Durability of Mixture of Carbon-Eating Concrete and Electric Arc Furnace Slag via Optimal Carbon Dioxide Curing

This study evaluates the material characteristics and durability of a mixture of carbon-eating concrete (CEC) and electric arc furnace slag. Due to the high C<sub>3</sub>A content present in the electric arc furnace reducing slag binder used in the CEC mix, the initial and final setting times of CEC are observed to be 18.8% and 7.0% faster than those of ordinary Portland cement (OPC), respectively. The optimal carbon dioxide curing condition is determined by varying the pressure and temperature variables within the scope of this study. The 3-day compressive strength of CEC under optimal carbon dioxide curing conditions is observed to exceed the 28-day compressive strength of OPC. The formation of calcium carbonate, which contributes to early strength, is confirmed via scanning electron microscopy and thermogravimetric analysis. Additionally, CEC exhibits significantly higher improvements in abrasion resistivity and chloride-ion penetration resistivity when subjected to carbon dioxide curing compared to OPC.

In Vitro Study on Combined Effect of Drugs for Hyperphosphatemia on Phosphorus Adsorption Capacity.

Phosphorus binders are often used in combination to produce synergistic effects. However, the synergistic effect may be affected by the change in pH or concomitant drugs. Nonetheless, the data on the adsorption capacities of these binders when used in combination with other binders are limited. In this study, we evaluated the adsorption capacity of phosphorus binders when used in combination. Precipitated calcium carbonate (CC), ferric citrate hydrate (FC), lanthanum carbonate hydrate (LC), and sucroferric oxyhydroxide (SO) were used as phosphorus binders. SO showed high adsorption capacity in the 1st and 2nd fluid, and the adsorption capacity of SO in combination with other binders was stable. In contrast, the adsorption capacities of CC + FC and FC + LC decreased in the 1st and 2nd fluid compared with that when used alone because of the release of citrate ions that chelate calcium or lanthanum ions. These results suggest that SO is less affected by interactions with other phosphorus binders and changes in pH and may be suitable for patients receiving concomitant drugs.

Calcium Carbonate as an Ionic Molecular Lock for Ultrastrong Fluorescence of Single Organic Molecules

Locking molecular conformation are widely applied in molecular engineering for improved performance. However, locking via organic functional groups often changes the original molecular properties. Following the rigidity and stability of ionic interaction in ionic compounds, we suggested the use of a molecular‐scale ionic compound, calcium carbonate oligomer, as a robust molecular segment to functionalize organic molecules. The rigid structure of the ionic molecular segments locked the organic molecules, which could remarkably limit the intramolecular motion and intermolecular interactions. This ensured a stable and ultrastrong fluorescence of the single organic molecule while preserving its original maximum emission wavelength. The locking strategy was general and extendable to multiple organic molecules. Additionally, the ultrastrong single‐molecular fluorescence can be maintained in inorganic solids with even higher quantum yields and almost unchanged maximum emission wavelength. The highest quantum yield of the investigated molecules reached 99.9%, superior to all reported organic‒inorganic fluorescent composite under air conditions. This work demonstrates a general strategy to restrict intramolecular motion and intermolecular interactions by using ionic oligomers as molecular locks, providing an alternative method for realizing ultraemissive molecules. This further demonstrates a fascinating example of molecular engineering in the presence of inorganic ionic molecules.

Calcium Carbonate as an Ionic Molecular Lock for Ultrastrong Fluorescence of Single Organic Molecules.

Locking molecular conformation are widely applied in molecular engineering for improved performance. However, locking via organic functional groups often changes the original molecular properties. Following the rigidity and stability of ionic interaction in ionic compounds, we suggested the use of a molecular-scale ionic compound, calcium carbonate oligomer, as a robust molecular segment to functionalize organic molecules. The rigid structure of the ionic molecular segments locked the organic molecules, which could remarkably limit the intramolecular motion and intermolecular interactions. This ensured a stable and ultrastrong fluorescence of the single organic molecule while preserving its original maximum emission wavelength. The locking strategy was general and extendable to multiple organic molecules. Additionally, the ultrastrong single-molecular fluorescence can be maintained in inorganic solids with even higher quantum yields and almost unchanged maximum emission wavelength. The highest quantum yield of the investigated molecules reached 99.9%, superior to all reported organic‒inorganic fluorescent composite under air conditions. This work demonstrates a general strategy to restrict intramolecular motion and intermolecular interactions by using ionic oligomers as molecular locks, providing an alternative method for realizing ultraemissive molecules. This further demonstrates a fascinating example of molecular engineering in the presence of inorganic ionic molecules.

An anomalous otolith of Engraulis australis (Clupeiformes, Engraulidae) from the food of the Australasian gannet Morus serrator, New Zealand

ABSTRACT Saccular otoliths are hearing and balance structures in teleost fish and usually consist of the aragonite form of calcium carbonate but may contain varying amounts of the vaterite polymorph in abnormal cases. Environmental impacts, nutritional problems, pollution, stress, and changes in water parameters, or a combination of these factors, may cause deformities in saccular otoliths. In this study, we examined the morphologies and calcium carbonate polymorphs within abnormal and normal saccular otoliths in the anchovies Engraulis australis, retrieved from regurgitated stomach contents of the Australasian gannet Morus serrator, Hauraki Gulf, New Zealand. Scanning electron microscopy (SEM) and Raman microscopy revealed several prominences in numerous areas on the surfaces of abnormal otoliths. This is the first study to report on the morphology and compositional differences in abnormal otoliths retrieved from the food of a piscivorous bird in New Zealand. Abnormalities in the structure and composition of otoliths may impact balance and hearing functions in fish and have implications on their fitness. Further studies should explore whether such fish are preferentially targeted by their avian predators.

Evaluation of Rutting, Cracking, and Fatigue Characteristics of Unmodified and ABS-Modified HMA Mixtures Involving Calcium Carbonate and Blowdown Fillers

Evaluation of Rutting, Cracking, and Fatigue Characteristics of Unmodified and ABS-Modified HMA Mixtures Involving Calcium Carbonate and Blowdown Fillers

Influence of Magnetic Field on Calcium Carbonate Precipitation: A Critical Review

This review reports a critical study on the effect of magnetic fields on the precipitation process of calcium carbonate scale from hard water. Indeed, the harmful consequences of the water scaling phenomenon urged researchers to find effective solutions. One of the interesting antiscaling processes is the magnetic treatment of water, which triggers a reduction in the precipitation of calcium carbonate on the walls when in contact with hard water. In the present review, we discuss selected examples related to this process in a combined analysis of the latest advances and the mechanism of action of the magnetic field. Despite the diversity of studies investigating this phenomenon, the effectiveness of this treatment remains a controversial issue, and it is not possible to obtain a clear explanation of the phenomenon. This review proposes, finally, interesting hypotheses which can effectively explain the effect of magnetic treatment on the behavior of hard waters and the precipitation of calcium carbonate, which include magnetohydrodynamics and the hydration effect.

Evaluation of encapsulated Bacillus subtilis bio-mortars for use under acidic conditions

This research aimed to examine the effects of an acidic environment on the mechanical properties and durability of bio-mortar (BM) encapsulated with Bacillus subtilis bacteria, in comparison to normal mortar (NM). The results at 28 days indicated that both 3% and 6% HCl significantly increased the compressive strength of the BM by 25% and 50%, respectively, compared with that of the NM. However, when 11% HCl was introduced, the compressive strength of the BM decreased to 50% lower than that of the NM. Furthermore, the water absorption rate of the BM was 33% lower than that of the NM. The mass loss for both 3% and 6% HCl was comparable, whereas at 11% HCl, BM experienced a mass loss that was 68% greater than that of NM. These findings suggest that with 3% and 6% HCl, the microbially induced calcium carbonate precipitation (MICP) process effectively generated CaCO3, which filled the pores and enhanced the structural integrity of the BM, leading to improved compressive strength and durability. Conversely, at 11% HCl, the MICP benefits in BM were diminished due to adverse environmental conditions that negatively affected the bacterial cells, highlighting the limitations of the HCl concentration for optimizing MICP efficiency in mortar.

A molecular view of peptoid-induced acceleration of calcite growth

The extensive deposits of calcium carbonate (CaCO 3 ) generated by marine organisms constitute the largest and oldest carbon dioxide (CO 2 ) reservoir. These organisms utilize macromolecules like peptides and proteins to facilitate the nucleation and growth of carbonate minerals, serving as an effective method for CO 2 sequestration. However, the precise mechanisms behind this process remain elusive. In this study, we report the use of sequence-defined peptoids, a class of peptidomimetics, to achieve the accelerated calcite step growth kinetics with the molecular level mechanistic understanding. By designing peptoids with hydrophilic and hydrophobic blocks, we systematically investigated the acceleration in step growth rate of calcite crystals using in situ atomic force microscopy (AFM), varying peptoid sequences and concentrations, CaCO 3 supersaturations, and the ratio of Ca 2+ / HCO 3 − . Mechanistic studies using NMR, three-dimensional fast force mapping (3D FFM), and isothermal titration calorimetry (ITC) were conducted to reveal the interactions of peptoids with Ca 2+ and HCO 3 − ions in solution, as well as the effect of peptoids on solvation and energetics of calcite crystal surface. Our results indicate the multiple roles of peptoid in facilitating HCO 3 − deprotonation, Ca 2+ desolvation, and the disruption of interfacial hydration layers of the calcite surface, which collectively contribute to a peptoid-induced acceleration of calcite growth. These findings provide guidelines for future design of sequence-specific biomimetic polymers as crystallization promoters, offering potential applications in environmental remediation (such as CO 2 sequestration), biomedical engineering, and energy storage where fast crystallization is preferred.

Modulation of biomineralization morphology by phosphorylated collagen peptides: insights into osteogenesis imperfecta pathophysiology.

Osteogenesis imperfecta (OI) is a hereditary skeletal disorder characterized by bone fragility and deformities, primarily attributed to defects in type I collagen, the most abundant structural protein in humans. Multiple phosphorylation sites have been detected within collagen, suggesting that phosphorylation may influence mineralization processes, thereby impacting the development of OI. In this study, we investigated the modulation of biomineralization morphology by phosphorylated collagen peptides mimicking Gly-Ser mutations in osteogenesis imperfecta. A series of collagen peptide sequences, including GPO13S, GPO13pS, GPO12S, GPO12pS, GPO11S, and GPO11pS, were synthesized to explore the role of phosphorylation in peptide stability and its templating effect on biomineralization. The CD results indicated that the phosphorylation of Gly-pSer mutants reduces the stability of collagen peptides. SEM images revealed that phosphorylated peptides acted as templates, guiding the morphology of calcium carbonate into either olive-like or spherical structures, depending on their conformational state of the peptides. Non-phosphorylated peptides maintained a calcite crystal structure. The XRD patterns predominantly exhibited peaks associated with calcite and vaterite for GPO13pS-CaCO3, GPO12pS-CaCO3, and GPO11pS-CaCO3, and peaks associated with calcite for GPO13S-CaCO3, GPO12S-CaCO3, and GPO11S-CaCO3, indicating a transformation of mesocrystals influenced by peptide phosphorylation. Our findings elucidate the crucial role of phosphorylated collagen peptides in mediating biomineralization morphology and polymorph selection, offering insights into the complex pathophysiology of OI.

Investigation of Scaling and Materials’ Performance in Simulated Geothermal Brine

Geothermal energy generation faces challenges in efficiency, partly due to restrictions on reinjection temperatures caused by scaling issues. Therefore, developing strategies to prevent scaling is critical. This study aims to simulate the scaling tendencies and corrosion effects of geothermal fluids on various construction materials used in scaling reactor/retention tank systems. A range of materials, including carbon steel, austenitic stainless steel, duplex stainless steel, two proprietary two-part epoxy coatings, and thermally sprayed aluminium (TSA), were tested in a simulated geothermal brine. Experiments were conducted in a laboratory vessel designed to replicate the wall shear stress conditions expected in a scaling reactor. The tests revealed varying scaling tendencies among the materials, with minimal corrosion observed. The dominant scale formed was calcium carbonate, consistent with geochemical modelling. The findings suggest that despite the high operating temperatures, the risk of corrosion remains low due to the brine’s low chloride content, while the wettability of materials after immersion may serve as a useful indicator for selecting those that promote scaling.

Targeted Delivery of Celastrol by GA-Modified Liposomal Calcium Carbonate Nanoparticles to Enhance Antitumor Efficacy Against Breast Cancer

Background/Objectives: Breast cancer, a leading health threat affecting millions worldwide, requires effective therapeutic interventions. Celastrol (CEL), despite its antitumor potential, is limited by poor solubility and stability. This study aimed to enhance CEL’s efficacy by encapsulating it within glycyrrhizic acid (GA)-modified lipid calcium carbonate (LCC) nanoparticles for targeted breast cancer therapy. Methods: The 4T1 mouse breast cancer cells were used for the study. GA-LCC-CEL nanoparticles were prepared using a gas diffusion method and a thin-film dispersion method. GA-LCC-CEL were characterized using the zeta-potential, dynamic light scattering and transmission electron microscope (TEM). The in vitro release behavior of nanoparticles was assessed using the in vitro dialysis diffusion method. Cellular uptake was examined using flow cytometry and confocal microscopy. Intracellular ROS and Rhodamine 123 levels were observed under fluorescence microscopy. MTT and colony formation assays assessed cytotoxicity and proliferation, and apoptosis was analyzed by Annexin V-FITC/PI staining. Wound healing and transwell assays evaluated migration, and Western blotting confirmed protein expression changes related to apoptosis and migration. Results: GA-LCC-CEL nanoparticles displayed a well-defined core-shell structure with a uniform size distribution. They showed enhanced anti-proliferative and pro-apoptotic effects against 4T1 cells and significantly reduced breast cancer cell invasion and migration. Additionally, GA-LCC-CEL modulated epithelial-mesenchymal transition (EMT) protein expression, downregulating Snail and ZEB1, and upregulating E-cadherin. Conclusions: GA-LCC-CEL nanoparticles represent a promising targeted drug delivery approach for breast cancer, enhancing CEL’s antitumor efficacy and potentially inhibiting cancer progression by modulating EMT-related proteins.