Microcapsule Core Research Articles

Smart temperature-adaptive thermal regulation textiles integrating passive radiative cooling and reversible heat storage

Passive radiative cooling (PRC) textiles have garnered significant interest in next-generation wearable technology. However, current PRC textiles often fail to regulate temperature effectively throughout the day due to unnecessary cooling at nighttime. Herein, a smart temperature-adaptive thermal regulation (STATR) textile seamlessly integrating PRC technology and phase-change heat storing/releasing strategy is developed on a bilayered configuration. Highly temperature-sensitive heat-storing microparticles constructed by phase change microcapsule (PCM) core and tightly incorporated BN nanoparticle shell are designed, which is homogeneously encapsulated in ultra-stretchable nonwoven microfibers for thermal energy storage in hot daytime and heat release in cold nighttime. Moreover, TiO2 microparticle-embedded PRC fibers with high emissivity (maximum emissivity>97 %) and reflective porosity (sunlight reflectivity>90 %) are assembled on the heat-storing layer, obtaining the bilayered STATR textile with a remarkable passive cooling effect during the day (10.6°C and 4.2°C compared to pristine textile and PRC textile) and a long-term heating performance at nighttime (2.1°C above pristine textile). Concurrently, the collaboration of asymmetric porosity and wettability in the bilayered STATR textile simultaneously facilitates efficient perspiration, thereby also ensuring lengthy wet comfort on human skin. Therefore, this STATR textile opens a promising avenue for zero-energy and all-weather thermal regulation technology.

Evaluation of gum arabic and gelatine coacervated microcapsule morphology and core oil encapsulation efficiency by combining the spreading coefficient and two component surface energy theory

Microcapsules containing various flavour/fragrance oils with different properties were fabricated using gelatine and gum arabic by complex coacervation. The surface properties (surface polarity and the spreading coefficients) of core oils were investigated in order to evaluate their effects on the capsule morphology and encapsulation efficiency based on a spreading coefficient and two component surface energy theory. Contact angles, interfacial tensions, and surface polarities were measured, and results were discussed with respect to the internal structure as well as encapsulation efficiency of different oil microcapsules. The thermodynamic spreading coefficients theory did not give an exactly accurate prediction of capsule morphology using high molecular weight biopolymer as the wall material in this work. Notwithstanding, the morphology predictions for different oil microcapsules are holistically consistent with the values of their encapsulation efficiency. Also, it has been found that the encapsulation efficiency increased with the decreasing surface polarity of the core oil holistically.

Coenzyme Q10-loaded microcapsules stabilized by glyceryl monostearate and soy protein isolates-flaxseed gum: Characterization, in vitro release and digestive behavior

This study aimed to stabilize microcapsules with core materials of glyceryl monostearate (GMS) and octyl and decyl glycerate, and wall materials of soy protein isolates (SPI) and flaxseed gum (FG) by complex coacervation method to overcome the drawbacks of coenzyme Q10 (CoQ10). It was demonstrated by the study that the obtained microcapsules were irregular aggregates. Differential scanning calorimetry and x-ray diffraction patterns indicated that CoQ10 was entrapped inside the disordered semisolid cores of microcapsules. The CoQ10 loading and encapsulation efficiency analysis revealed that GMS and FG helped CoQ10 better encapsulated inside the microcapsules. The in vitro release curve showed a “burst” release of CoQ10 absorbed on the surface of microcapsules for the first 180 min, followed by a sustained release of the encapsulated CoQ10. GMS and FG contributed to the sustained release and the release mechanism of the microcapsules was Fickian diffusion. The in vitro simulated digestion demonstrated that the constructed microcapsules improved the bio-accessibility of CoQ10. Finally, due to the protection of GMS and FG, microcapsules had good storage stability. In conclusion, this study emphasized the potential of using new microcapsules to deliver and protect lipophilic ingredients, providing valuable information for developing functional foods with higher bioavailability.

Study on the mechanical behavior of microcapsules during the mixing process of asphalt mixture

To enhance the survival rate of microcapsules during the mixing process of asphalt mixture, the mechanical behavior of microcapsules during this process was investigated through simulation. Initially, the asphalt mixture containing microcapsules was divided into mesoscopic and microscopic scales. Utilizing composite material models, the stepwise inclusion method and high-temperature tensile tests, the equivalent mechanical parameters for the microcapsules, asphalt mastic and asphalt mortar at mixing temperature were estimated. Following this, the mixing process of the asphalt mixture incorporating microcapsules was simulated employing the discrete element method (DEM) coupled with multi-body dynamics (MBD). This simulation was instrumental in identifying optimal mixing parameters and enabled the analysis of force chain transmission across the multi-scale model. Furthermore, the finite element method (FEM) was employed to develop a monomer model of the microcapsules, facilitating the assessment of their mechanical behavior under optimal mixing conditions. Finally, a detailed sensitivity analysis was performed to investigate the influence of various parameters on the mechanical behavior of microcapsules. The results indicated that, at the mixing temperature, the equivalent Young’s modulus and Poisson's ratio for urea-formaldehyde (UF) resin microcapsules, asphalt mastic, and asphalt mortar were determined to be 0.22 GPa and 0.478, 19.87 GPa and 0.4986, and 88.77 GPa and 0.468, respectively. The optimal mixing parameters for AC-16 asphalt mixture including mixing speed, filling rate and mixing duration were identified as 49 rpm, 50 % and 53 s, under which the most adverse load on the microcapsule is 80 mN. Under the most adverse load, microcapsules might rupture from the inside out, and their survival rate was not less than 68.9 %. Increasing the particle size of microcapsules and reducing the relative radius of the microcapsule core could potentially enhance the crack resistance of microcapsules during mixing.

Study on the Repair Effect of Self-Healing Cementitious Material with Urea-Formaldehyde Resin/Epoxy Resin Microcapsule

Recent studies on microencapsulated self-healing cementitious materials have primarily focused on the particle size and preparation methods of the microcapsules. However, there has been limited attention paid to the microscopic aspects, such as the selection of curing agents and the curing duration of these materials. In this study, urea-formaldehyde resin/epoxy resin E-51 microcapsules were synthesized through in situ polymerization. This research investigates the feasibility of self-healing from a molecular mechanism perspective and evaluates the repair performance of microencapsulated self-healing cement mortar with varying microcapsule concentrations, curing agent types, and curing ages. The findings demonstrate that the microcapsule shells bond effectively with the cementitious matrix, with radial distribution function peaks all located within 3.5 Å. The incorporation of microcapsules enhanced the tensile strength of the modified cement mortar by 116.83% and increased the failure strain by 110%, indicating improved adhesion and mechanical properties. The restorative agent released from the microcapsule core provided greater strength after curing compared to the uncured state. Although the overall strength of the microencapsulated self-healing cement mortar decreased with higher microcapsule concentrations, the repair efficiency improved. The strength recovery rate of 28-day aged modified cement mortar had a significant improvement with the addition of X and Y curing agents, respectively.

Postmodification with Polycations Enhances Key Properties of Alginate-Based Multicomponent Microcapsules.

Postmodification of alginate-based microspheres with polyelectrolytes (PEs) is commonly used in the cell encapsulation field to control microsphere stability and permeability. However, little is known about how different applied PEs shape the microsphere morphology and properties, particularly in vivo. Here, we addressed this question using model multicomponent alginate-based microcapsules postmodified with PEs of different charge and structure. We found that the postmodification can enhance or impair the mechanical resistance and biocompatibility of microcapsules implanted into a mouse model, with polycations surprisingly providing the best results. Confocal Raman microscopy and confocal laser scanning microscopy (CLSM) analyses revealed stable interpolyelectrolyte complex layers within the parent microcapsule, hindering the access of higher molar weight PEs into the microcapsule core. All microcapsules showed negative surface zeta potential, indicating that the postmodification PEs get hidden within the microcapsule membrane, which agrees with CLSM data. Human whole blood assay revealed complex behavior of microcapsules regarding their inflammatory and coagulation potential. Importantly, most of the postmodification PEs, including polycations, were found to be benign toward the encapsulated model cells.

A smart insulation material achieving self-reporting and autonomous repairing against electrical and mechanical damages based on targeted controllable microcapsules

Under the long-term action of electrical and mechanical stresses, irreversible micro-damages, such as electrical trees and cracks tend to occur inside solid insulation materials, leading to insulation failures, which have no effective countermeasures. This study develops a multi-responsive, target-controlled microcapsule to endow the epoxy resin with dual functions of self-reporting and autonomous repair against internal damage even under strong electric fields without human intervention. A turn-on mechanism for self-reporting signals is designed, to be applicable to electrical tree damage inside an epoxy matrix. In situ UV emissions generated by the partial discharge during electrical treeing are employed to automatically cure the microcapsule core material released into the damaged channel. This triggers aggregation-induced emission (AIE) signals and simultaneously repairs the damaged matrix. The polyurethane hybrid shell filled with magnetic particles endows the microcapsules with magnetic response characteristics. Under the control of a directional magnetic field, the microcapsule is concentrated around the vulnerable areas, obtaining high fluorescence emission intensity under low doping content without affecting the matrix performance. This method enables the autonomous inspection and maintenance of electric equipment and electronic devices under live working and provides new insight into the bionic intelligence of electrical and electronic insulation materials.

Micro-scale study of microcapsule cracking performance based on XFEM and fluid cavity model

Microcapsule self-healing has become popular for microcrack repairing in resin mineral composites, and the cracking performance of microcapsule directly affect their repair efficiency on the matrix material. In this study, the problem of how the volume of microcapsule core affects the cracking performance of microcapsule is addressed. Based on the extended finite element method, the representative volume element (RVE) considering the volume of microcapsule core is established by combining the cohesive zone model and the fluid cavity model. On this basis, a numerical simulation study of the cracking performance of RVE with different volumes of microcapsule core under dynamic loading is conducted to investigate the triggered cracking process of the fully filled and incompletely filled microcapsules besides their cracking behavior, respectively. This study provides a reference for the preparation of microcapsules and the numerical simulation of microcapsule mechanical properties.

Anti‐solvent method synthesized phosphorylated microcapsules with flame retardancy and self‐healing analysis

AbstractIn this study, an anti‐solvent method is employed to encapsulate linseed oil (LO) into phosphorylated ethyl cellulose (P‐EC), successfully preparing microcapsules (LO@P‐EC). Scanning electron microscopy and Fourier transform infrared spectroscopy experimental results indicate the introduction of phosphoric groups into P‐EC, and the successful encapsulation of LO within the microcapsules, which are spherical with an average diameter of 145 μm. Hartmann tests reveal that the introduction of phosphate groups reduces the microcapsule flame propagation height by 43.75% and the average flame propagation speed by 55.67%. Thermodynamic analyses based on the Coats‐Redfern equation are performed to determine the changes in activation energy during thermal degradation. Furthermore, fitting analysis shows that the apparent activation energy of microcapsules with shell material of P‐EC significantly increases, confirming the evident thermodynamic inhibition of microcapsule deflagration by P‐EC. This is mainly attributed to the formation of a char structure by the P‐EC shell during combustion, which hinders the progress of the combustion reaction. When immersed in 3.5 wt% NaCl corrosive solution for 15 days, the microcapsule‐filled epoxy resin (LO@P‐EC/EP) coating exhibits excellent corrosion resistance, which is mainly attributed to the excellent self‐healing properties of the microcapsule core LO.

Controlling the Synthesis of Polyurea Microcapsules and the Encapsulation of Active Diisocyanate Compounds.

The encapsulation of active components is currently used as common methodology for the insertion of additional functions like self-healing properties on a polymeric matrix. Among the different approaches, polyurea microcapsules are used in different applications. The design of polyurea microcapsules (MCs) containing active diisocyanate compounds, namely isophorone diisocyanate (IPDI) or hexamethylene diisocyanate (HDI), is explored in the present work. The polyurea shell of MCs is formed through the interfacial polymerization of oil-in-water emulsions between the highly active methylene diphenyl diisocyanate (MDI) and diethylenetriamine (DETA), while the cores of MCs contain, apart from IPDI or HDI, a liquid Novolac resin. The hydroxyl functionalities of the resin were either unprotected (Novolac resin), partially protected (Benzyl Novolac resin) or fully protected (Acetyl Novolac resin). It has been found that the formation of MCs is controlled by the MDI/DETA ratio, while the shape and size of MCs depends on the homogenization rate applied for emulsification. The encapsulated active compound, as determined through the titration of isocyanate (NCO) groups, was found to decrease with the hydroxyl functionality content of the Novolac resin used, indicating a reaction between NCO and the hydroxyl groups. Through the thorough investigation of the organic phase, the rapid reaction (within a few minutes) of MDI with the unprotected Novolac resin was revealed, while a gradual decrease in the NCO groups (within two months) has been observed through the evolution of the Attenuated Total Reflectance-Fourier-Transform Infrared (ATR-FTIR) spectroscopy and titration, due to the reaction of these groups with the hydroxyl functionalities of unprotected and partially protected Novolac resin. Over longer times (above two months), the reaction of the remaining NCO groups with humidity was evidenced, especially when the fully protected Acetyl Novolac resin was used. HDI was found to be more susceptible to reactions, as compared with IPDI.

Temperature-responsive microcapsule hydrogel fabricated by pickering emulsion polymerization for pheromones application

Insect pheromone is a natural effective biological pesticide. To improve the utilization efficiency of pheromone pesticides and reduce labor costs, a sustained and controlled release preparation coordinating with the circadian rhythm of insects has been proposed by our previous report. However, that preparation has some deficiencies, such as the loading capacity of pheromone and sustained time. In order to overcome the existent shortcomings, a temperature-responsive release microcapsule hydrogel loaded with myrcene (as a pheromone model) was fabricated by Pickering emulsion polymerization using modified SiO2 nanoparticles as a stabilizer of microcapsule wall, octadecane and Poly(N-isopropylacrylamide) (PNIPAM) separately as temperature responders of microcapsule core and wall in the present study. The morphological structure and thermal performance of the microcapsule hydrogel were characterized. The release behaviors of myrcene at different environmental temperatures and alternating temperature cycles were also tested. The results indicated that myrcene was successfully loaded in the Myrcene/Octadecane@SiO2-PNIPAM (MOSP) microcapsule hydrogel with encapsulation efficiency and loading capacity of 80.3 % and 13.3 %, respectively. The results of the myrcene release under simulated diurnal temperature cycles revealed that the cumulative release amount was only about 43 % during 15 cycles and release rates respectively were about 0.79 μg/h at 35 °C and 0.058 μg/h at 25 °C, which demonstrated the persistent temperature sensitivity and good temperature rhythm remained after 15 cycles. These results suggested that the MOSP microcapsule hydrogel had a good controlled release effect on myrcene and could adapt well to the circadian rhythm activity of some insects. Therefore, this study provided a promising strategy to improve the utilization efficiency of pheromones through the combination of octadecane and PNIPAM as pheromones release controllers.

Stimulus triggered release of actives from composite microcapsules based on sporopollenin from Lycopodium clavatum.

Smart drug delivery systems (SDDSs) are a paradigm shift in drug delivery, particularly in microencapsulation technology where the drug is released in response to an internal and/or external stimulus. In this study, a smart microencapsulation platform was developed using three different types of stimuli triggered release of a model active (rhodamine 6G) from sporopollenin from Lycopodium clavatum. Triggers were based on pH-, thermal- and near infrared light-sensitive polymer composition. Carbopol nanogel and methylcellulose were used as responsive aqueous polymers for pH and thermally triggered release, respectively. Methylcellulose loaded with active and gold nanoparticles was used for photothermal triggered release. The formulations were encapsulated into the empty cores of sporopollenin microcapsules using the compressed tablet technique. The pH triggered release of the active was achieved above pH 7, which was mediated by the swelling of the carbopol nanogel that forced its way out of the elastic trilite scars of the sporopollenin. Results from measuring the active fluorescent intensity and its content over time confirmed the crucial role of carbopol in the pH triggered release. For the thermo-sensitive polymer methylcellulose, it was found that the release of the active from methylcellulose loaded sporopollenin was triggered upon heating the system reaching 90% whereas it levelled out at 40% for methylcellulose-free sporopollenin. The maximum amount of active was released at around 55 °C, where the sol-gel transition of the methylcellulose starts. Photothermally triggered release using near infrared (NIR) laser revealed that the amount of active released from sporopollenin loaded with both gold nanoparticles and methylcellulose was approximately four times higher than that from sporopollenin loaded with methylcellulose/active only, confirming the key role of gold nanoparticles in the release via photothermal heating of the polymer formulation.

Preparation of thermal energy storage microcapsule with double-layer ceramic shell possessing sponge effect to improve the thermal cycling performance

In present study, thermal energy storage microcapsules with double-layer ceramic shell were fabricated and thermal cycling test was conducted. Thermal cycling test results showed that when ceramic shell constituted of dense inner layer and loose outer layer, the microcapsule had excellent thermal stability. After 3000 thermal cycles, latent heat retention ratio of the microcapsule was more than 90 % and almost no leakage of molten core. This super durability and stability attributed to “sponge effect” of loose outer layer which offered volume buffer for microcapsule core and inhibited molten core overflow during phase change. According to the Mass Conservation Law, criterion Г for describing “sponge effect” was deduced. Г was defined as a quarter of the product of the specific surface area of the microcapsule and criterion Г was derived as Г≥1ρL−1ρS. The criterion shows that when the value of Г is larger than or equal to the difference between the specific volumes of liquid and solid phase change material, microcapsule core is not overflow during phase change. Criterion Г provides theoretical guidance for the preparation of thermal energy storage microcapsules with excellent thermal cycling performance.

Photochromic performance optimization of polyurethane microcapsules by interfacial polymerization method

AbstractSpiropyran photochromic materials have been widely studied in military camouflage, optical data storage, information encryption, and fashion ornaments. The non‐photochromism and low endurance of solid spiropyran make the challenges of their application. Photochromic microcapsules with a butyl acetate solution of spiropyran as core and polyurethane as shell are synthesized via interfacial polymerization. The optimized polyurethane photochromic microcapsules are prepared with a Tween 20 concentration of 4 wt%, core–shell ratio of 16:5, and spiropyran concentration of 0.40 wt%. Polyurethane photochromic microcapsules with a mean particle diameter of 0.33 μm are obtained. The morphology shows smooth spheres, and the core–shell structure is observed. Butyl acetate in the microcapsule core does not evaporate at a temperature lower than 218.01°C as the microcapsule shell insulates heat. The polyurethane photochromic microcapsules are mixed with adhesive, thickener, and water into a paste and screen‐printed on cotton fabric. The printed fabric shows the ΔE of 17.56, 11.93, and 6.96 after 80s irradiation with the xenon lamp intensity of 102, 68, and 34 mW cm−2. The light stability of the photochromic fabric is excellent as ΔE decreases about 8.28% after 20 cycles of UV‐Vis irradiation.

The Influence of the Specifics of the Formation of the Polymer Shell of a Microcapsule with a Nitrogen-Containing Compound Core on the Durability of the Tool During Blade Cutting

Microcapsules with gelatin shells are obtained by coacervation. In the process of microcapsulation,the shells of microcapsules are treated with ozone and ozonated water is introduced into their core. Magneticsensitivity was imparted to microcapsules by introducing magnetite in their shell. The influence of the compositionand concentration of microcapsules in an aqueous emulsion on the durability of the tool during bladecutting is studied. It is shown that the lubricating and cooling technological means obtained by introducingozonated water into the core of a gelatin microcapsule is more effective for increasing the tool’s durabilityduring blade cutting.

Remote Loading: The Missing Piece for Achieving High Drug Payload and Rapid Release in Polymeric Microbubbles.

The use of drug-loaded microbubbles for targeted drug delivery, particularly in cancer treatment, has been extensively studied in recent years. However, the loading capacity of microbubbles has been limited due to their surface area. Typically, drug molecules are loaded on or within the shell, or drug-loaded nanoparticles are coated on the surfaces of microbubbles. To address this significant limitation, we have introduced a novel approach. For the first time, we employed a transmembrane ammonium sulfate and pH gradient to load doxorubicin in a crystallized form in the core of polymeric microcapsules. Subsequently, we created remotely loaded microbubbles (RLMBs) through the sublimation of the liquid core of the microcapsules. Remotely loaded microcapsules exhibited an 18-fold increase in drug payload compared with physically loaded microcapsules. Furthermore, we investigated the drug release of RLMBs when exposed to an ultrasound field. After 120 s, an impressive 82.4 ± 5.5% of the loaded doxorubicin was released, demonstrating the remarkable capability of remotely loaded microbubbles for on-demand drug release. This study is the first to report such microbubbles that enable rapid drug release from the core. This innovative technique holds great promise in enhancing drug loading capacity and advancing targeted drug delivery.

Interfacial Polymerization Depth Mediated by the Shuttle Effect Regulating the Application Performance of Pesticide-Loaded Microcapsules.

The highly water-soluble nematicide fosthiazate is anticipated to undergo microencapsulation in order to enhance its retention around plant roots and mitigate leaching into groundwater. However, the underlying mechanism governing the influence of hydrophilicity of the microcapsule (MC) core on the evolution of the microcapsule shell remains unclear, posing challenges for encapsulating water-soluble core materials. This study elucidates the microlevel formation mechanism of microcapsules by investigating the impact of interfacial mass transfer on shell formation and proposes a method for regulating the structure of shells. The study reveals that enhancing the hydrophilicity of the core enhances the shuttle effect between the oil and aqueous phase, expands the region of polymerization reactions, and forms a loose and thick shell. The thickness of the microcapsule shell prepared using solvent oil 150# (MCs-SOL) measures only 264 nm, while that of the microcapsules prepared using propylene glycol diacetate and solvent oil 150# at a ratio of 2:1 (MCs-P2S1) is 5.2 times greater. The enhanced compactness of the shell reduced the release rate of microcapsules and the leaching distance of fosthiazate in soil, thereby mitigating the risk of leaching loss and facilitating the distribution of active ingredients within crop roots. The MCs-SOL had a limited leaching distance measurement of 8 cm and exhibited a satisfactory efficacy of 87.3% in controlling root galling nematodes. The thickness and compactness of the MCs shell can be regulated by manipulating the interfacial shuttle effect, providing a promising approach to enhancing utilization efficiency while mitigating potential environmental risks.

Sono-assembly of folate-decorated curcumins/alginate core-shell microcomplex and its targeted delivery and pH/reduction dual-triggered release

In this study, sodium alginate (SA), a non-toxic natural polysaccharide with good biocompatibility and biodegradability, was developed for targeted delivery of curcumin (CUR) in tumor therapy. The strategy is to sulfhydrylate the folic acid (FA) modified SA, and the CUR dissolved in ethyl acetate (EAC) phase is coated in microcapsules by a quick, efficient and environment-friendly sonochemical method. The EAC in the microcapsule core is volatile, which can be recycled and reused to reduce cost. The prepared microcapsules (FA-RSMCs@CUR) exhibited similar toxicity to free curcumin in anti-tumour evaluation in vitro. FA-RSMCs@CUR also exhibited effective antibacterial properties in the antibacterial evaluation in vitro. It is expected to become a low-cost tumor targeting vector in the future, and has the potential to be promoted in clinical application.

Development of taste-masking microcapsules containing azithromycin by fluid bed coating for powder for suspension and in vivo evaluation

This research aims to develop bitter taste-masking microcapsules containing azithromycin (AZI) by a simpler and familiar method, fluid-bed coating technology, in comparison with Zithromax®. Cores of microcapsules, AZI microparticles, were prepared by fluid-bed granulation, then taste-masking polymer was covered on by fluid-bed coating technique. Eudragit L100, Eudragit RL100, and ethyl cellulose in single and combined with Eudragit L100 and Eudragit E100 were used as taste-masking polymers. The obtained microcapsules were characterised by taste-masking ability, in vitro release, SEM, coating thickness, and coating efficiency. Combination of ethyl cellulose and Eudragit E100 (3:1) in coating thickness of 45.13 ± 2.12% w/w prevents AZI release from microcapsules below bitter taste threshold (1.78 ± 1.17 µg/ml). Bioavailability of powders containing AZI microcapsules and pH modulators (50 mg Na3PO4 and 35 mg Mg(OH)2) was not significantly different from the reference product (Zithromax®, Pfizer, New York, NY) in the rabbit model (p > 0.05). These results support the possibility of developing a generic product containing AZI.

Application of Raman spectroscopy for detecting the repairing behaviour of microcapsules in self-healing cementitious system

Evaluating the trigger mechanism of microcapsules is always an issue for self-healing cementitious materials, which could be potentially tackled by the application of Raman spectroscopy. In this paper, Raman spectroscopy was applied to tracing the repairing process in cementitious paste. Based upon the characterisation of the traditional UF/Epoxy microcapsule by Raman spectroscopy, the spectra of the microcapsule shell and core in cementitious matrix were identified and established. Furthermore, to improve the detection precision and efficiency, a newly designed microcapsule was developed in which the anatase was introduced in the microcapsule core to amplify the signal by around 90 times. Finally, the healing behaviour of the newly designed microcapsule was investigated by Raman mapping. The results clearly showed that Raman spectroscopy successfully detected the breakage of microcapsule due to the occurrence of cracking, which provides a promising approach to detecting the repairing behaviour of self-healing microcapsules in cementitious materials.