Dynamic Disulfide Research Articles

Sustainable and Recyclable Acrylate Resins for Liquid-Crystal Display 3D Printing Based on Lipoic Acid.

The development of renewable vinyl-based photopolymer resins offers a promising solution to reducing the environmental impact associated with 3D printed materials. This study introduces a bifunctional lipoate cross-linker containing a dynamic disulfide bond, which is combined with acrylic monomers (n-butyl acrylate) and conventional photoinitiators to develop photopolymer resins that are compatible with commercial stereolithography 3D printing. The incorporation of disulfide bonds within the polymer network's backbone imparts the 3D printed objects with self-healing capabilities and complete degradability. Remarkably, the degraded resin can be fully recycled and reused for high-resolution reprinting of complex structures while preserving mechanical properties that are comparable to the original material. This proof-of-concept study not only presents a sustainable strategy for advancing acrylate-based 3D printing materials, but also introduces a novel approach for fabricating fully recyclable 3D-printed structures. This method paves the way for reducing the environmental impact while enhancing material reusability, offering significant potential for the development of eco-friendly additive manufacturing.

Self-healable epoxy/graphene oxide vitrimers and their recyclable glass fiber reinforced composites

Glass fiber-reinforced polymers (GFRPs) made from thermoset polymers have been widely used across various industries. However, these composites have significant drawbacks, including poor interfacial adhesion between the fiber and matrix, as well as a substantial contribution to waste and environmental pollution due to the challenges in recycling, reprocessing, and reuse. Herein, firstly graphene oxide (GO) was incorporated in vitrimer matrix to fabricate recyclable vitrimer nanocomposites with improved interfacial interaction, high thermal stability, low dielectric constant, fast stress relaxation as well as rapid self-healing ability. The nanocomposite with 0.2 wt% GO is optimized to achieve excellent remoulding (89% of flexural strength) and self-healing (60 min for a 48 μm scratch) properties due to dynamic disulfide bond exchange mechanism. Furthermore, epoxy/GO matrix was used to develop glass fiber reinforced composites via vacuum assisted resin infusion molding process (VARIM). The developed composites demonstrate tremendous mechanical strength (250 MPa), shape-memory, weldability, and degradable properties. Due to the rapid chemical degradation of epoxy vitrimer under mild conditions in the thiol (2-mercaptoethanol and 1-otanethiol), facilitated by thiol disulfide exchange reaction, glass fibers (GFs) can be effectively recycled. The performance of recycled glass fibers closely matches that of original fibers, exhibiting nearly identical woven structure and mechanical properties. The single yarn of recycled glass fibers can achieve tensile strength of 85% (1-octanethiol) and 72% (2-mercaptoethanol) of the original glass fibers, thus, the recycling of glass fibers would be highly advantageous in terms of achieving the sustainability goals.

SO2F2 mediated click chemistry enables modular disulfide formation in diverse reaction media

The dynamic disulfide linkage plays a vital role in various biological processes as well as drugs and biomaterials. The conversion of thiols to their corresponding disulfides is a hallmark of sulfur chemistry, but notoriously difficult to control. Achieving optimal reactivity and selectivity continues to pose significant challenges. Here, we describe a click chemistry for disulfide formation from thiols in both batch and flow-mode using SO2F2, which display exceptional selectivity toward disulfide formation through an effective nucleophilic substitution cascade. This reaction’s unique characteristics satisfy the stringent click-criteria with its high thermodynamic driving force, straightforward conditions, wide scope, quantitative yields, exceptional chemoselectivity, and non-chromatographic purification process. The modular synthesis of symmetrical, unsymmetrical, cyclic and polydisulfides is demonstrated, along with the formation of disulfide cross-linked hydrogels.

Unlocking Auxetic Behavior in Recyclable Thermosetting Foams Enabled by Dynamic Disulfide Cross‐linking Strategy

AbstractAuxetic foams with a negative Poisson's ratio (NPR) have attracted considerable attention in material engineering due to their outstanding performance in seismic and energy absorption. Nevertheless, thermoplastic auxetic foams are compromised by weak non‐covalent crosslinking that diminishes the mechanical strength and durability of foams. Conversely, thermosetting foams with chemical crosslinking, although mechanically robust, face challenges in elaborating auxetic structure and in achieving recyclability. Herein, an alternative approach is proposed to tackle this dilemma by incorporating dynamic disulfide bonds into the polymer network for preparing a thermosetting polyurethane foam with covalent adaptable network. By leveraging the unidirectional multi‐effect compression technique, the topological network reorganization of foam is induced, transforming the initial circular open‐cell structure into a re‐entrant cell structure. This structural transformation endows the foam with stable NPR capability, achieving a minimum Poisson's ratio value of −0.4 within 30% compressive strain. Benefiting from its reinforced network structure, the foam also demonstrates high compressive strength (6.47 MPa) and tensile strength (1.67 MPa). Furthermore, it is recyclable and can be recompressed into thermosetting films. This work offers a straightforward approach to making auxetic thermosetting foams with good mechanical and recyclable properties, which is interesting for the development of high‐performance auxetic materials.

Rapid photo‐responsive dynamic disulfide strategy for accessing self‐healing, reconfigurable shape of high‐strength shape memory polyurethane

Rapid photo‐responsive dynamic disulfide strategy for accessing self‐healing, reconfigurable shape of high‐strength shape memory polyurethane

Multiscale study on fatigue healing performance and molecular healing behavior of self-healing SBS modified bitumen

Self-healing polymer modified bitumen based on dynamic chemical bonds is a potential approach to improve the durability of bitumen pavement and save fossil energy. Herein, a novel self-healing SBS modified bitumen on the basis of dynamic disulfide bonds and hydrogen bonds was prepared. Firstly, an aliphatic disulfide (A-ALD) with disulfide bonds and hydrogen bonds was synthesized. Then A-ALD/SBS modified bitumen (A-ALD/SMB) was prepared by blending A-ALD and SBS modified bitumen. The chemical structure and microstructure of A-ALD/SMB were evaluated. In addition, the self-healing performance of A-ALD/SMB at the macroscopic scale and the self-healing behavior at the molecular scale were investigated by a combination of fatigue healing test and molecular dynamics (MD) simulation. The chemical structure analysis showed the formation of disulfide bonds and hydrogen bonds in A-ALD, and A-ALD was successfully attached to the CC bonds in SBS. Fluorescent images revealed that a better network structure appeared in A-ALD/SMB and formed a two-phase continuous morphology. The optimal dosage of A-ALD in SBS modified bitumen was 0.6 %. The fatigue healing test results indicated that A-ALD markedly enhanced the self-healing ability of SBS modified bitumen, and prolonging resting time and raising healing temperature can increase the self-healing performance of A-ALD/SMB. When the damage degree, healing temperature, and resting time were 30 %, 30 °C, and 60 min, respectively, the healing rate of A-ALD/SMB was 98.5 %, which was 30.2 % higher than SMB. The MD simulation results showed that the A-ALD enhanced the molecular diffusion capacity of SBS modified bitumen, and crack healing time of A-ALD/SMB was earlier than that of SMB under the same conditions. When the healing temperature was 40 °C, the time for the A-ALD/SMB and SMB molecular chain segments to start contacting and healing was 27 ps and 49 ps, respectively, which was improved by 44.9 % for A-ALD/SMB compared to SMB. Furthermore, the self-healing behavior of A-ALD/SMB at the molecular scale was consistent with the self-healing performance at the macroscopic scale under different healing temperatures and damage degrees. This study provided a theoretical basis for exploring the self-healing mechanism of SBS modified bitumen.

Study on Anticorrosion and Wear Resistance of Self-Healing Coating Based on Functional MXene and Dynamic Disulfide Bond

Study on Anticorrosion and Wear Resistance of Self-Healing Coating Based on Functional MXene and Dynamic Disulfide Bond

Polyfunctional and Multisensory Bio-Ionoelastomers Enabled by Covalent Adaptive Networks With Hierarchically Dynamic Bonding.

Developing versatile ionoelastomers, the alternatives to hydrogels and ionogels, will boost the advancement of high-performance ionotronic devices. However, meeting the requirements of bio-derivation, high toughness, high stretchability, autonomous self-healing ability, high ionic conductivity, reprocessing, and favorable recyclability in a single ionoelastomer remains a challenging endeavor. Herein, a dynamic covalent and supramolecular design, lipoic acid (LA)-based dynamic covalent ionoelastomer (DCIE), is proposed via melt building covalent adaptive networks with hierarchically dynamic bonding (CAN-HDB), wherein lithium bonds aid in the dissociation of ions and the integration of dynamic disulfide metathesis, lithium bonds, and binary hydrogen bonds enhances the mechanical performances, self-healing capability, reprocessing, and recyclability. Therefore, the trade-off among mechanical versatility, ionic conductivity, self-healing capability, reprocessing, and recyclability is successfully handled. The obtained DCIE demonstrates remarkable stretchability (1011.7%), high toughness (3877kJm-3), high ionic conductivity (3.94×10-4Sm-1), outstanding self-healing capability, reprocessing for 3D printing, and desirable recyclability. Significantly, the selective ion transport endows the DCIE with multisensory feature capable of generating continuous electrical signals for high-quality sensations towards temperature, humidity, and strain. Coupled with the straightforward methodology, abundant availability of LA and HPC, as well as multifunction, the DCIEs present new concept of advanced ionic conductors for developing soft ionotronics.

Preparation and properties of solvent induced biodegradable thermosetting poly (siloxane urethane)

AbstractIt is difficult to recycle classic thermosetting plastics. Although some of them can be reprocessed, the mechanical properties decline linearly after processing. In addition, most thermosetting plastics are not environmentally friendly and difficult to degrade, resulting in a lot of pollution and limiting their practical application potential. In this paper, the prepolymer is synthesized by using castor oil (CO), hydroxyl terminated polydimethylsiloxane (PDMS‐OH), and toluene diisocyanate (TDI). Using 4,4'‐diaminodiphenyl disulfide (ODD) as a chain extender with dynamic disulfide bond and aniline (An) as a blocking agent, polysiloxane‐aminoester (SiCPUO) with recyclable function under DMF induction was prepared. The effect of the amount of rigid chain extender (ODD) containing disulfide bond on the properties of SiCPUO was studied, its heat resistance will first increase and then decrease with the increase of ODD content, especially the mechanical properties are more obvious, this trend has never been reported before; the mechanical properties and recyclability of SiCPUO are tested, and the comprehensive performance of SiCPUO2 is the best, the tensile strength is 0.84 MPa and the elongation at break was 65.81%; the solubility test of different solvents showed that it has recyclability, recovery rate is 95%;the material has self‐healing function, the repair efficiency is up to 95%.

Ultra-short running-in period and robust lubricity constructed by dynamic disulfide and hydrogen bonds from ionic liquid polyethylene glycol lubrication

Polyethylene glycol (PEG) system behave the characteristics of non-toxic, non-irritating and good compatibility with various substances, so the improvement and stability of lubrication property and comprehensive performance is vital for PEG system under harsh working conditions. Here, highly reactive ionic liquids (ILs) are designed and introduced with a specifically designed molecular structure, the ultra-short running-in period and robust lubricity can be obtained by dynamic disulfide and hydrogen bonds from the constructed IL-PEG200 lubrication system. Combined with analytical techniques (XPS, FIB-TEM, Nanoindentation, Raman, TOF-SIMS), their interaction was explored to further clarify the interfacial self-assembly behavior. The superior bearing capacity is mainly ascribed to the synergistic effect of carbon-like film, dynamic disulfide bond, hydrogen bonding and interfacial tribochemical reaction.

UV-Mediated Facile Fabrication of a Robust, Fully Renewable and Controllably Biodegradable Poly(lactic acid)-Based Covalent Adaptable Network.

A robust and fully biobased covalent adaptable network (CAN) that allows recyclability, biocompatibility, and controlled biodegradability is reported. The CAN was fabricated through a simple photo-cross-linking method, wherein low-molecular-weight poly(lactic acid) (∼3 kDa) was modified with end 1,2-dithiolane rings through a one-step Steglich esterification reaction with thioctic acid (TA). These incorporated 1,2-dithiolane rings undergo photoinduced ring-opening polymerization, thus enabling the cross-linking of poly(lactic acid) with abundant dynamic disulfide bonds. The resultant CAN demonstrates excellent transparency, effective UV-blocking capabilities below 320 nm, robust tensile strength (∼39 MPa), and superior dimensional stability at 80 °C, alongside attractive biocompatibility. Moreover, owing to the dynamic exchange and redox-responsiveness of disulfide bonds, the material can be recycled by hot-pressing and a reduction-oxidation process while also being capable of controllably biodegrading at the end of its lifecycle. Furthermore, it exhibits reconfigurable shape memory properties with fast recovery. This study elucidates a straightforward approach to fabricating multifunctional and sustainable polymer materials with potential applications in diverse fields such as packaging, coating, and biomedicine.

Unmatched resilience and fatigue resistance in a novel cellulose-derived ionic gel with hierarchical superstructured synergy for advanced human-computer interaction

Unlike traditional hydrogels, solvent-free ionic gels eliminate leakage and solvent volatilization, making them suitable for applications in electronic skin, sensing, and other fields due to their excellent conductivity and flexibility. However, designing solvent-free ionic gels with exceptional fatigue resistance, high ionic conductivity, and toughness remains a significant challenge. We address this challenge by employing small molecule/polymer heating self-assembly to regulate the synergistic effects of various components on the hierarchical superstructure. A multi-stage network was formed through the free radical polymerization of 3-Ethyl-1-vinyl-1H-imidazol-3-ium bromide ([C2VIm]Br), lipoic acid (LA), acrylic acid (AA), and hydroxypropyl cellulose (HPC), stabilized by dense hydrogen bonding and polymer chain entanglement. The resulting HPC/LA/AA/iLs (HLAI) ionic gel exhibits exceptional properties: excellent flexibility (with an elongation at break of 4222 %), toughness (1.03 MJ/m3), high ionic conductivity (3.29 × 10−2 S/m), and outstanding fatigue resistance (with a resilience of 91.9 % after 1000 load-unloading cycles at 50 % strain). Additionally, it shows low sensitivity to crack propagation (50 % notched sample can be stretched to 9 times without breaking) and good environmental stability, demonstrating excellent sensing sensitivity and stability (GF=3.23). The conductive ionic gel features a sophisticated hierarchical superstructure that synergistically enhances its properties at the molecular level. The integration of dynamic disulfide bonds, achieved through the polymerization of Lipoic acid, imparts remarkable self-healing capabilities and superior fatigue resistance. Additionally, the incorporation of a rigid HPC structure with dense cross-linking points bolsters elasticity, fracture resistance, and resilience. The gel’s ionic conductivity and sensing sensitivity are significantly enhanced by the inclusion of ionic liquids with polymerizable double bonds, making it an ideal material for applications requiring both flexibility and conductivity. This work presents a novel strategy for designing high-performance multi-stage network solvent-free ionic gels, opening up exciting possibilities for biomimetic electronic skin applications.

Biomass-derived dynamic polyurethanes: Enhanced self-healing and recyclability through reversible cross-linking

Chemically cross-linked polyurethanes (CCPUs), renowned for their superior solvent resistance, high strength, and exceptional thermostability, have emerged as extensively used polymeric materials. Despite their advantages, CCPUs face a significant limitation that their stable cross-linked structures can preclude healing and recycling once damaged. This limitation underscores the urgent need for a new CCPUs variant that offers self-healing and recyclability to extend service life. In this work, a new type of cross-linked polyurethanes (CPUs) was designed and synthesized by incorporating the biomass-derived castor oil (CO) as a cross-linking agent and dynamic disulfide bond into a traditional polyurethane without using any catalysts. These newly developed CPUs exhibit superior mechanical performance with an impressive tensile strength of 29.37 MPa and a remarkable maximum elongation at break of 769.9 %. Notably, our recycled CPU-2 can retain a tensile strength of 22.40 MPa and an elongation at break above 604.8 % even after four thermal recycling cycles. Furthermore, the addition of conductive carbon black (CB) into this CPU matrix imparts remarkable self-healing properties to the polyurethanes/carbon black composite (CPU-2/CB), activated solely by near-infrared light. This inventive approach effectively enhances the functionality of traditional CCPUs, broadening their application potential.

Synthesis of a copolymer with a dynamic disulfide network and its application to a lithium-ion capacitor polymer electrolyte

Polymer electrolytes are being actively researched in energy storage applications because of their large operating potential range and cycle stability. Among them, poly(ethylene glycol) (PEG) is most commonly used to take advantage of the high ionic conductivity generated by polar functional groups in the structure. However, the polar functional group in the PEG structure has limitations that not only interfere with the movement of ions through interchain interaction, but also prevent the penetration of the polymer structure into the electrode material. In this paper, a copolymer into which a dynamic disulfide bonding network was introduced based on PEG was synthesized to control the polar functional effect of the polymer chain. The copolymer was then applied as a lithium-ion hybrid capacitor electrolyte. Due to the disconnection of the dynamic disulfide bond, the viscosity of the polymer electrolyte was reduced, allowing smooth penetration into the electrode material. The copolymer-based polymer electrolyte showed better energy storage performance and shorter relaxation time than a commercial PEG-based device (225 F g−1/5.18 × 10−5 s for copolymer and 166 F g−1/7.96 × 10−3 s for PEG). In addition, the copolymer not only preserved excellent ionic conductivity of PEG at a certain level (from 6.3 × 10−4 S cm−1 to 3.73 × 10−4 S cm−1) but also decreased the polarity of the material due to the presence of the nonpolar disulfide chain, thereby reducing crystallinity and dielectric permittivity (from 1460 to 246).

Self‐Healing Waterborne Polyurethanes as a Sustainable Gel Electrolyte for Flexible Electrochromic Devices

Self‐healing polymers are promising for diverse applications in wearable technology and electronic skin. Polyurethanes are versatile polymers that can incorporate various monomer structures. Waterborne polyurethanes (WPUs) emerge as an environmentally conscious choice due to water usage instead of organic solvents, thereby minimizing the generation of volatile organic compounds. This study introduces a novel approach to enhance the self‐healing properties of WPUs by integrating disulfide bonds. These dynamic disulfide bonds undergo exchange reactions upon heating, facilitating the renewal of cross‐links on damaged film surfaces. Self‐healing WPUs with a low glass transition temperature achieve excellent self‐healing efficiency under mild conditions. Self‐healing adhesives applied to various flexible substrates retain stable peel strength, which confirms their potential as self‐healing solutions. Furthermore, the WPU hydrogel electrolyte is prepared with dihydroxyhexyl viologen (DHHV), and the prepared electrochromic gel exhibits good ionic conductivity while maintaining high transparency. The flexible electrochromic device exhibited excellent performances, including low coloration voltage, high coloration efficiency, and long‐term stability. The transmittance difference is exceptional, with over 99%, and no decay after repeated bending cycles is observed. The current results demonstrate the feasibility of self‐healing WPUs in improving the operation and durability of high‐performance flexible electrochromic devices.

Hybrid Self‐Repairing Polymer Composites Based on a Mixture of Intrinsic and Extrinsic Self‐Healing

AbstractThe development of high‐strength and multiple self‐healing polymer materials remains a major challenge. In this study, a hybrid self‐healable polymer using the combination of intrinsic and extrinsic self‐healing is demonstrated. The epoxy resin microcapsules with dynamic disulfide bonded shells are successfully prepared through an interfacial polymerization method, which are then added into the intrinsically self‐healable epoxy resin substrate also containing disulfide bonds. The unique combination structure enables the polymer composites to exhibit high mechanical strength and excellent multiple self‐healing efficiency. On the one hand, the Young's modulus and tensile strength of the material are enhanced due to the reinforcement effect of the fillers. On the other hand, the extrinsic self‐healing strategy of the microcapsules, which released repair agents, can support the intrinsic repairing substrate to improve the self‐healing ability of the material. More interestingly, the design of the disulfide bond structure of the microcapsule shell contributes to the high self‐healing capability of the material during multiple self‐healing processes.

Evaluation of oxidative stress and inflammation in patients with polycystic ovary syndrome.

Polycystic ovary syndrome (PCOS) is a heterogeneous endocrine and metabolic disorder characterized by hyperandrogenism, hyperinsulinemia, and insulin resistance. The prevalence of PCOS is increasing worldwide. Although the etiology of this disease is currently unknown, it is thought to be closely related to inflammation and oxidative stress. Our study aimed to compare patients have PCOS to healthy volunteers and assess the changes in oxidative stress and inflammatory parameters in these patients. Thirty patients between the ages of 18-45 diagnosed with PCOS and 30 healthy volunteers with the same demographic characteristics were included in this study. Clinical parameters were measured using immunoassays. Oxidative stress biomarkers, total oxidant (TOS), total antioxidant (TAS), total thiol (TT), and native thiol (NT) levels were measured using photometric methods according to Erel's method. The dynamic disulfide level (DIS) and oxidative stress index (OSI) were calculated using mathematical equations. Among the inflammatory parameters, values for interleukin (IL)-1β, IL-6, and tumor necrosis factor-α (TNF-α) were measured photometrically using commercially purchased kits. Moreover, TT and NT levels were lower in patients with PCOS compared to those in the healthy group statistically significantly (P<0.001). In addition, TAS, TOS, OSI, DIS, IL-1β, IL-6, and TNF-α levels were identified to be significantly higher in the patients with PCOS than those in the healthy group (P<0.001). Evaluation of oxidative stress and clinical parameters used in the follow-up may be beneficial for the disease.

Unveiling the potential of self-healing and closed-loop recyclability in bio-based non-isocyanate polyurethane

The imperative shift towards sustainable production emphasizes the need for non-isocyanate polyurethanes (NIPUs) derived from biomass as a substitute for conventional petroleum-based polyurethanes. However, challenges persist in synthesizing NIPUs from renewable resources and addressing their recyclability post-service life. In this study, we report the synthesis of bio-based and closed-loop recyclable NIPU vitrimers using carbon dioxide (CO2), a vanillin derivative, and cystamine as bio-based feedstocks. The investigation examined the effect of the structure on the mechanical, thermal, and dynamic thermomechanical properties of bio-based NIPU vitrimers. The activation energy of the synthesized NIPUs was found to be relatively low (31.37 to 72.17 kJ/mol) after the incorporation of cystamine due to the presence of dual dynamic covalent bonds (disulfide and transcarbamoylation). As a result, the prepared bio-based NIPUs exhibited rapid self-healing and exceptional reprocessing efficiency (∼100 %). The mechanical properties of the reprocessed NIPUs could be restored to 99.5 % of their original values, highlighting remarkable reprocessing capabilities. The bio-based NIPU demonstrated closed-loop recyclability thanks to the dynamic disulfide bonds present in the vitrimer structure. This work offers an approach for the synthesis of bio-based NIPUS with closed-loop recyclability within the framework of sustainable materials.

Dual Dynamic Cross-Linked Epoxy Vitrimers Used for Strong, Detachable, and Reworkable Adhesives.

Novel reprocessable thermosetting adhesives (RTAs), which combine high adhesive strength, reusability, disassembly, and recyclability features, have attracted increasing attention. However, developing RTAs with a rapidly adhesive rate while ensuring high adhesive strength and self-healing ability is still a significant challenge. Here, we prepared a novel vitrimer called DAx-DTSAy, which can be used as an RTA. First, by adjusting the ratio of rigid and flexible segments, maximum tensile strength reached 35.92 MPa. Second, the combined effect of dynamic hydroxyl ester bonds and dynamic disulfide bonds resulted in a rapid stress relaxation behavior, with a complete relaxation time 13.6 times shorter than a vitrimer only cross-linked with hydroxy ester bonds. This feature endowed its good self-healing and reprocessing capabilities. After self-healing at 180 °C, the maximum healing rate of mechanical properties was 91.8%. After three reprocesses, the maximum recovery rate of tensile strength was 120.2%. Furthermore, the combination of rigid and flexible segments and the synergistic effect of dual dynamic covalent bonds made DAx-DTSAy capable of use as a high-performance RTA. The lap shear strength of a DAx-DTSAy film on stainless steel reached 18.18 MPa after 15 min, with a recovery rate of 91.9% after 5 rebonding cycles. Additionally, DAx-DTSAy can be disassembled in chemical agents and exhibited better insulation properties compared to traditional epoxy resins. DAx-DTSAy can be employed as a novel high-performance adhesive in applications such as electronic devices and transportation, contributing to the development of thermosetting adhesives toward recyclability and sustainability.

Polyglycerol-Shelled Reduction-Sensitive Polymersome for DM1 Delivery to HER-2-Positive Breast Cancer.

Supramolecular delivery systems with the prolonged circulation, the potential for diverse functionalization, and few toxin-related limitations have been extensively studied. For the present study, we constructed a linear polyglycerol-shelled polymersome attached with the anti-HER-2-antibody trastuzumab. We then covalently loaded the anticancer drug DM1 in the polymersome via dynamic disulfide bonding. The resulted trastuzumab-polymersome-DM1 (Tra-PS-DM1) exhibits a mean size of 95.3 nm and remarkable drug loading efficiency % of 99.3%. In addition to its superior stability, we observed the rapid release of DM1 in a controlled manner under reductive conditions. Compared to the native polymersomes, Tra-PS-DM1 has shown greatly improved cellular uptake and significantly reduced IC50 up to 17-fold among HER-2-positive cancer cells. Moreover, Tra-PS-DM1 demonstrated superb growth inhibition of HER-2-positive tumoroids; specifically, BT474 tumoroids shrunk up to 62% after 12 h treatment. With exceptional stability and targetability, the PG-shelled Tra-PS-DM1 appears as an attractive approach for HER-2-positive tumor treatment.