Polyethylene Glycol Oligomers Research Articles

Physical-Entanglements-Supported Polymeric Form Stable Phase Change Materials with Ultrahigh Melting Enthalpy.

With the rapid development of new energy and the upgrading of electronic devices, structurally stable phase change materials (PCMs) have attracted widespread attentions from both academia and industries. Traditional cross-linking, composites, or microencapsulation methods for preparation of form stable PCMs usually sacrifice part of the phase change enthalpy and recyclability. Based on the basic polymer viscoelasticity and crystallization theories, here, a kind of novel recyclable polymeric PCM is developed by simple solution mixing ultrahigh molecular weight of polyethylene oxide (UHMWPEO) with its chemical identical oligomer polyethylene glycol (PEG). Rheological and leakage-proof experiments confirm that, even containing 90% of phase change fraction PEG oligomers, long-term of structure stability of PCMs can be achieved when the molecular weight of UHMWPEO is higher than 7000kg mol-1 due to their ultralong terminal relaxation time and large number of entanglements per chain. Furthermore, because of the reduced overall entanglement concentration, phase change enthalpy of PCMs can be greatly promoted, even reaching to ≈185 J g-1, which is larger than any PEG-based form stable PCMs in literatures. This work provides a new strategy and mechanism for designing physical-entanglements-supported form stable PCMs with ultrahigh phase change enthalpies.

Hydration sphere structure of architectural molecules: Polyethylene glycol and polyoxymethylene oligomers

Non-toxic, chemically inert, organic polymers as polyethylene glycol (PEG) and polyoxymethylene (POM) have versatile applications in basic research, industry and pharmacy. In this work, we aim to characterize the hydration structure of PEG and POM oligomers by exploring how the solute disturbs the water structure compared to the bulk solvent and how the solute chain interacts with the solvent. We explore the effect of (i) the C–C–O (PEG) versus C-O (POM) constitution of the chain and (ii) chain length. To this end, MD simulations followed by clustering and topological analysis of the hydration network, as well as quantum mechanical calculations of atomic charges are used.We show that the hydration varies with chain conformation and length. The degree of folding of the chain impacts its degree of solvation, which is measurable by different parameters as for example the number of water molecules in the first solvation shell and the solvent accessible surface. Atomic charges calculated on the oligomers in gas phase are stable throughout conformation and chain length and seem not to determine solvation. Hydration however induces charge transfer from the solute molecule to the solvent, which depends on the degree of hydration.

Solid-Adsorbed Polymer-Electrolyte Interphases for Stabilizing Metal Anodes in Aqueous Zn and Non-Aqueous Li Batteries.

Polymers are known to adsorb spontaneously from liquid solutions in contact with high-energy substrates to form configurationally complex, but robust phases that often exhibit higher durability than might be expected from the individual physical bonds formed with the substrate. Rational control of the physical, chemical, and transport properties of such interphases has emerged as a fundamental opportunity for scientific and technological advances in energy storage technology but requires in-depth understanding of the conformation states and electrochemical effect of the adsorbed polymers. Here, we analyze the interfacial adsorption of oligomeric polyethylene glycol (PEG) chains of moderate sizes dissolved in protic and aprotic liquid electrolytes and find that there is an optimum polymer molecular weight of approximately 400 Da at which the highest columbic efficiency is achieved for both Zn and Li deposition. These findings point to a simple, versatile approach for extending the lifetime of batteries.

Solid‐Adsorbed Polymer‐Electrolyte Interphases for Stabilizing Metal Anodes in Aqueous Zn and Non‐Aqueous Li Batteries

AbstractPolymers are known to adsorb spontaneously from liquid solutions in contact with high‐energy substrates to form configurationally complex, but robust phases that often exhibit higher durability than might be expected from the individual physical bonds formed with the substrate. Rational control of the physical, chemical, and transport properties of such interphases has emerged as a fundamental opportunity for scientific and technological advances in energy storage technology but requires in‐depth understanding of the conformation states and electrochemical effect of the adsorbed polymers. Here, we analyze the interfacial adsorption of oligomeric polyethylene glycol (PEG) chains of moderate sizes dissolved in protic and aprotic liquid electrolytes and find that there is an optimum polymer molecular weight of approximately 400 Da at which the highest columbic efficiency is achieved for both Zn and Li deposition. These findings point to a simple, versatile approach for extending the lifetime of batteries.

Coarse-Grained Force Field for Polyethylene Oxide and Polyethylene Glycol Aqueous Solutions Based on a Polarizable Water Model

A new, accurate and transferable coarse-grained (CG) force field (FF) for polyethylene oxide (PEO) and polyethylene glycol (PEG) aqueous solutions based on a polarizable CG water (PCGW) model is developed in this work. A PCGW bead, which represents four water molecules, is modeled as two charged dummy particles connected by two constrained bonds to a central neutral particle; a PEO or PEG oligomer is modeled as a chain with repeated middle beads (PEOM) representing diether groups and two terminal beads (PEOT or PEGT) of a different type compared to PEOM. To describe nonbonded van der Waals interactions, a piecewise Morse potential with four tunable parameters is used. The force parameters are automatically and rigorously optimized by a meta-multilinear interpolation parameterization (meta-MIP) algorithm to simultaneously match multiple thermodynamic properties, including the density, heat of vaporization, vapor-liquid interfacial tension, and solvation free energy of the pure PEO or PEG oligomer bulk system as well as the mixing density and hydration free energy of the oligomer/water binary mixture. Additional thermodynamic and structural properties for longer PEO and PEG polymer aqueous solutions, such as the self-diffusion coefficient, radius of gyration, and end-to-end distance, are predicted to test the accuracy and transferability of this new CG FF. Based on the PCGW model, the presented FF optimization algorithm and strategy can be extended to more complex polyelectrolytes and surfactants.

Peptide functionalized actively targeted MoS2 nanospheres for fluorescence imaging-guided controllable pH-responsive drug delivery and collaborative chemo/photodynamic therapy

The combination of imaging and different therapeutic strategies into one single nanoplatform often demonstrates improved efficacy over monotherapy in cancer treatments. Herein, a multifunctional nanoplatform (labelled as MPRD) based on molybdenum disulfide quantum dots (MoS2 QDs) is developed to achieve enhanced antitumor efficiency by integrating fluorescence imaging, tumor-targeting and synergistic chemo/photodynamic therapy (PDT) into one system. First, polyethylene glycol (PEG)ylated MoS2 QDs (MP) with desirable stability are synthesized via a hydrothermal process using MoS2 QDs and carboxyamino-terminated oligomeric PEG as raw materials. Then, MP were conjugated with arginine-glycine-aspartic acid (RGD) peptide via amidation to form a novel nanocarrier (MPR), which possesses strong blue fluorescence, good biocompatibility and ανβ3 receptor-mediated targeting ability. More importantly, MPR generated reactive oxygen species under 808 nm laser activation to realize targeted antitumor PDT. Further doxorubicin (DOX) was loaded onto MPR, which endows MPRD with localized chemotherapy and pH-responsive drug release. The MPRD exhibits improved chemotherapy performance on HepG2 cells (overexpressing integrin ανβ3) owing to enhanced cellular uptake mediated by ανβ3 receptor and effective drug release triggered by intracellular pH. Notably, MPRD with efficient tumor targeting ability and high chemo/PDT efficacy under NIR laser irradiation is capable of inhibiting HepG2 tumor cell growth both in vitro and in vivo, which is significantly superior to each individual therapy. These findings demonstrate that MPRD holds great potential in effective cancer therapy.

Enabling Solution Processable COFs through Suppression of Precipitation during Solvothermal Synthesis.

Covalent organic frameworks (COFs) are crystalline, nanoporous materials of interest for various applications, but current COF synthetic routes lead to insoluble aggregates which precludes processing for practical implementation. Here, we report a COF synthesis method that produces a stable, homogeneous suspension of crystalline COF nanoparticles that enables the preparation of COF monoliths, membranes, and films using conventional solution-processing techniques. Our approach involves the use of a polar solvent, diacid catalyst, and slow reagent mixing procedure at elevated temperatures which altogether enable access to crystalline COF nanoparticle suspension that does not aggregate or precipitate when kept at elevated temperatures. On cooling, the suspension undergoes a thermoreversible gelation transition to produce crystalline and highly porous COF materials. We further show that the modified synthesis approach is compatible with various COF chemistries, including both large- and small-pore imine COFs, hydrazone-linked COFs, and COFs with rhombic and hexagonal topologies, and in each case, we demonstrate that the final product has excellent crystallinity and porosity. The final materials contain both micro- and macropores, and the total porosity can be tuned through variation of sample annealing. Dynamic light scattering measurements reveal the presence of COF nanoparticles that grow with time at room temperature, transitioning from a homogeneous suspension to a gel. Finally, we prepare imine COF membranes and measure their rejection of polyethylene glycol (PEG) polymers and oligomers, and these measurements exhibit size-dependent rejection and adsorption of PEG solutes. This work demonstrates a versatile processing strategy to create crystalline and porous COF materials using solution-processing techniques and will greatly advance the development of COFs for various applications.

Exploring structure and dynamics of the polylactic‐co‐glycolic acid–polyethylene glycol copolymer and its homopolymer constituents in various solvents using all‐atom molecular dynamics

AbstractPolylactic‐co‐glycolic acid (PLGA)‐basedpolymers are synthetic materials that are prominent in drug delivery. PLGA homopolymer is biodegradable, biocompatible and is often polymerized to polyethylene glycol (PEG) to form a block copolymer used to form core‐shell nanoparticles. PEG is known for reducing blood clearance and opsonization, in addition to imparting “stealth” properties to various drugs and biomaterials. Current formulation methodologies for PLGA–PEG copolymer nanoparticles can be tuned to control key parameters for improved therapeutic delivery; however, molecular‐level understanding of copolymer‐solvent interactions during nanoparticle formulation is lacking. Therefore, three different PLGA–PEG/solvent pairs are examined, in comparison to their homopolymer constituents, to better understand copolymerization effects and its impact on nanoparticle formulation. Results show that at room temperature PLGA–PEG oligomers in dimethyl sulfoxide are the most rigid in good solvent conditions (Flory exponent >0.5) and have the largest end‐to‐end relaxation times when compared to acetone and water. PEG has a Flory exponent of ~0.5 in both water and acetone, showing that the molecular dynamic model that is employed can reproduce its amphiphilic nature in solution. Knowledge of PLGA–PEG structure and dynamics can be used in the design of novel biomedical technologies that improve drug efficacy and reduce cost of treatment.

PVT properties of binary systems of diisopropylethylammonium octanoate ionic liquid with oligomeric polyethylene glycol or polypropylene glycol at elevated pressures

The densities were measured for two binary systems of protic ammonium-based ionic liquid, diisopropylethylammonium octanoate ([DIPEA][C7COO]), with oligomeric polyethylene glycol (PEG-200) or polypropylene glycol (PPG-425) at temperatures from 298.2 K to 348.2 K and pressures up to 50 MPa. Tait equation was used to represent the pressure-dependence of the liquid densities and then applied to estimate the isothermal compressibilities. The excess molar volumes of [DIPEA][C7COO] + PEG-200 are negative over the entire composition range, while those of [DIPEA][C7COO] + PPG-425 varying with the mole fraction of the ionic liquid are S-shape changing from positive to negative. While the excess volumes were fitted to a modified Redlich-Kister equation, the density data were correlated with a generalized equation and with the Flory-Orwoll-Vrij (FOV) and the Schotte equations of state.

Synthesis of cross-linked triple shape memory polyurethane with self-healing functionalities

A series of shape memory polymers (SMPs) comprising poly (10-hydroxydecanoate) (PHDA) and polyethylene glycol (PEG) oligomer were facilely prepared. The effect of PEG content on the thermal dynamic properties of the cross-linking network were studied by differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA). The obtained polyurethane has two separated melting temperatures (Tm), which make the material a triple SMP. The shaped specimen only needs 8 s to get a 98.5% the shape recovery. Furthermore, disulfide bonds were introduced into the polyurethane to give the triple SMP self-healing ability. The synthetic polymer exhibited a self-healing efficiency of 78.3%. The healed samples could lift a weight of 100 g, which is 150 times of its own weight, without tearing. This polyurethane exhibits impressive triple-shape memory ability and a high potential for biomedical applications.

A multifunctional nanoplatform based on graphitic carbon nitride quantum dots for imaging-guided and tumor-targeted chemo-photodynamic combination therapy

Graphitic carbon nitride quantum dots (g-CNQDs) have shown great potential in imaging, drug delivery and photodynamic therapy (PDT). However, relevant research on g-CNQDs for PDT or drug delivery has been conducted separately. Herein, we develop a g-CNQDs-based nanoplatform (g-CPFD) to achieve simultaneously imaging and chemo-photodynamic combination therapy in one system. A g-CNQDs-based nanocarrier (g-CPF) is first prepared by successively introducing carboxyamino-terminated oligomeric polyethylene glycol and folic acid onto the surface of g-CNQDs via two-step amidation. The resultant g-CPF possesses good physiological stability, strong blue fluorescence, desirable biocompatibility, and visible light-stimulated reactive oxygen species generating ability. Further non-covalently loaded doxorubicin enables the system with chemotherapy function. Compared with free doxorubicin, g-CPFD expresses more efficient chemotherapy to HeLa cells due to improved folate receptor-mediated cellular uptake and intracellular pH-triggered drug release. Furthermore, g-CPFD under visible light irradiation shows enhanced inhibition on the growth of cancer cells compared to sole chemotherapy or PDT. Thus, g-CPFD exhibits exceptional anti-tumor efficiency due to folate receptor-mediated targeting ability, intracellular pH-triggered drug release and a combined treatment effect arising from PDT and chemotherapy. Moreover, this nanoplatform benefits imaging-guided drug delivery because of inherent fluorescent properties of doxorubicin and g-CPF, hence achieving the goal of imaging-guided chemo-photodynamic combination treatments.

Construction of ion conducting channels by embedding hydrophilic oligomers in piperidine functionalized poly(2, 6-dimethyl-1, 4-phenylene oxide) membranes

A suitable microphase separation morphology has been demonstrated to be an efficient strategy to achieve high ionic conductivity with reasonable durability to anion exchange membranes (AEMs). Herein, hydrophilic oligomers of polyethylene glycols (PEGs) with different molecular weights were blended, separately, with poly(2,6-dimethyl-1,4-phenylene oxide) modified by 4,4-diethoxybutan-1-amine and 1-methylpiperidine (20PDM). The presence of hydrophilic PEGs facilitates the formation of the interconnected nano-channels in the AEMs for ion conduction according to the analysis results by both transmission electron microscopy (TEM) and small angle X-ray scattering (SAXS). The membrane containing 2 wt% PEGs with a molecular weight of 2 kDa reaches a hydroxide conductivity of 97.2 mS cm−1 at 80 °C, which is 25 mS cm−1 higher than that the pristine 20PDM membrane possessing the same ion exchange capacity. A peak power density of 328 mW cm−2 is attained at 60 °C by the proposed membrane based single fuel cell fueling with humidified H2 and O2 with 0.1 MPa of back pressure. The chemical structure, water uptake and swelling as well as resistance to hot alkali solutions of the prepared membranes were investigated.

How Intramolecular Vibrational Energy Transport Changes with Rigidity and Polarity of the Environment?

Vibrational energy transport through oligomeric polyethylene glycol (PEG) chains can occur ballistically via optical vibrational chain bands, showing fast and constant transport speed and high efficiency of the transport, thus offering means to transfer significant quanta of energy, exceeding 1000 cm–1, to large distances exceeding 60 A. We report how the intramolecular energy transport time, through-chain transport speed, and end-group cooling rate depend on the rigidity and polarity of the environment. The experiments were performed with end-group labeled PEG oligomers using two-dimensional infrared (2DIR) spectroscopy. The ballistic energy transport was initiated at one end of the chain by exciting an azido moiety at ca. 2100 cm–1 and recorded at another end of the chain by probing the carbonyl stretching mode of succinimide ester. We found that the rigidity of the environment, polystyrene (PS) matrix vs. a solution of similar polarity, did not change the energy transport times much, nor the through-chain transport speed. These results suggest that in mildly polar media, dynamic fluctuations, occurring in solution but largely frozen in a solid matrix, are not the dominant cause of the dephasing of the chain states, despite the presence of fast relaxation components in the solution. The similarity of the transport times in different media suggests that the secondary chain structure does not affect much the transport in PEG chains. The solvent polarity affected the intramolecular transport significantly: the transport efficiency in polar DMSO is ca. 1.6 fold smaller than that in nonpolar CCl4 or PS. The cooling time of the succinimide ester end group is reduced in more polar solvents affecting the waiting time dependence shape and thus the energy arrival time to the reporter. The analysis of different ways of extracting the energy arrival time from the data is presented. The observed dependences of the through-chain transport time on the solvent polarity suggests the presence of multiple wavepackets propagating in the PEG chain with different group velocities.

Extractive desulfurization of liquid fuel using diamine-terminated polyethylene glycol as a very low vapour pressure and green molecular solvent.

Removal of sulfur compounds from liquid fuel is one of the important issues in the field of energy and environment. Among the available methods, extractive desulfurization (EDS) is of great interest due to its convenient operating conditions. In this study, EDS performance of 4,7,10-trioxatridecane-1,13-diamine (TTD), a very low vapour pressure diamine-terminated oligomeric polyethylene glycol (PEG), was studied. Effect of the influencing factors, as well as multiple extraction, mutual solubility, reusability and regeneration of TTD were investigated. Results showed that the TTD/fuel volume ratio of 0.5 could extract benzothiophene, dibenzothiophene and dimethyl dibenzothiophene with the efficiencies 67%, 74% and 53%, respectively, in less than 1 min at ambient temperature. The distribution coefficient (KN) value for removal of dibenzothiophene by TTD was 3.66 higher than that of PEG, and it is similar to KN values (approx. 4) for polyethylene glycol dimethyl ether (as a modified PEG) and Lewis acid-containing ionic liquids. It was observed that spent TTD after five cycles could be regenerated using the back-extraction method. Also, deep EDS was achievable after three times extraction using fresh TTD. Finally, the extraction mechanism was studied using 1H-NMR. These observations, as well as very low vapour pressure and insignificant dependency of TTD on the initial S-concentration of fuel and temperature, make this extractant to be introduced as a valuable option for green and effective EDS.

Crucial effect of transverse vibrations on the transport through polymer chains.

The low temperature transport of electron, or vibrational or electronic exciton toward polymer chains, turns out to be dramatically sensitive to its interaction with transverse acoustic vibrations. We show that this interaction leads to a substantial polaron effect and decoherence, which are generally stronger than those associated with longitudinal vibrations. For site-dependent interactions, transverse phonons form subohmic bath leading to the quantum phase transition accompanied by full suppression of the transport at zero temperature and fast decoherence characterized by temperature dependent rate k2 ∝ T3/4 at low temperature, while k2 ∝ T2 for site-independent interactions. The latter dependence was used to interpret recent measurements of temperature dependent vibrational energy transport in polyethylene glycol oligomers.

Elasticity and plasticity of highly concentrated noncolloidal suspensions under shear

The rheological properties (viscosity, plasticity, viscoelasticity, and elasticity) of noncolloidal suspensions with varying concentrations of a solid phase (Al powder) in oligomeric polyethylene glycol have been studied in the shear mode of deformation. All typical types of rheological behavior have been observed. In the concentration range up to approximately 30%, suspensions are Newtonian liquids, while at a certain concentration, non-Newtonian and viscoelastic effects appear. With further increases in concentration, the flow curves become a power-law type, though the yield stress can be found only for suspensions with a high solid phase content. The elasticity of the suspensions can be detected at concentrations in the order of 55%. In a narrow range of concentrations, the rheological state of the suspensions can be treated as viscoplastic, wherein they preserve fluidity and become elastic. This concentration threshold, determined by the change in various rheological characteristics including the loss tangent, corresponds to the gelation or “colloid” glass transition. The most detailed experiments were devoted to the concentration range of 60–70 vol. %, which are treated as highly concentrated suspensions (HCSs). A concentration of 70% is the upper limit, because mixtures with higher concentrations do not keep their continuity and crumble. The rheological state of HCSs corresponds to the elastoplastic type of behavior. The separation of the total deformation into plastic and elastic components showed that plastic deformations (but not the flow) in the shearing of HCSs are small. Repeated shearing in the loading-unloading mode has been performed. In this case, a decrease in the elastic deformation and a remarkable growth of the shear elastic modulus was observed. This effect is presumably explained by the orientation of the particles and shear-induced anisotropy. A stress-concentration diagram of the physical states of suspensions has been proposed. The concentration range somewhat below that of the HCS state is of special interest for the powder injection molding technology, which is limited by the domain of plasticity.

Highly luminescent un-doped carbon nano-dots driven from folic acid and passivated by polyethylene glycol

Carbon nano-dots (CDs) are considered nowadays as one of the most interesting fluorescence nanomaterials with various technological applications in almost all aspects of needs e.g., in medicine, biology and engineering. Yet, as reported in many previous works, un-doped CDs suffer from low quantum yield particularly when synthesized at relatively low temperatures. Here, we report on synthesis and characterization of a small size (4.7 nm in diameter) intentionally un-doped CDs with high fluorescence intensity, from Folic Acid as a single precursor, using hydrothermal process at relatively low temperature 200 °C. By attaching organics species of diamine-terminated oligomeric poly-ethylene glycol (PEG) to the surface of the derived CDs, a much stronger photoluminescence from the passivated dots was observed. Namely, we observe a strong enhancement of the CDs quantum yield from 44.4% to 67.5% by varying the PEG concentrations from 0 to 0.2 mM, respectively.

Optimized Alkali-Metal Cationization in Secondary Ion Mass Spectrometry of Polyethylene Glycol Oligomers with up to m/z 10000: Dependence on Cation Species and Concentration.

In secondary ion mass spectrometry (SIMS), the detection of large organic molecules is accomplished using cluster ion bombardment. Ion formation often proceeds via cationization, through the attachment of (alkali) metal ions to the molecule. To study this process, the emission of secondary ions sputtered from polyethylene glycol (PEG) samples with molecular weights (MW) of 1000-10000 was examined. They were mixed with alkali-metal trifluoroacetic acid (X-TFA, where X = Li, Na, K, or Cs) in a wide range of concentrations to investigate the efficiency of cationization for 10 keV Ar2000+ cluster irradiation. Typically, cationized molecular ions [M + X]+ (with repeat units n of up to ∼250, corresponding roughly to m/z 11000) and some characteristic fragment species were observed in the mass spectra. For all alkali cations, the oligomer intensities increase strongly with the molecular composition ratios X-TFA/PEG in the samples, and values of 5-10 seem to be optimal. With increasing molecular weight, the intensity of oligomer ions relative to the total number of ions decreases; as the latter remains rather constant, this implies that more fragment species are formed. The ion yields (detected ions per primary ions) of cationized [M + Na]+ oligomers sputtered from a PEG decrease very strongly with their size n: from 5.2 × 10-6 at n = 21 (MW ∼ 1000) to 4.5 × 10-10 at n ∼ 245 (MW ∼ 11000). By contrast, the total yields Ytot+ show only a small variation for these different specimens, from 1.3 × 10-5 to 3.7 × 10-5.

Tetrabromothiophene-Derived Sulfur-Containing Polymer Dots with Deep-Blue Luminescence and High Sensitivity to Fe3+

Polymer dots are extensively studied in the fields of catalysis, energy storage, light-emitting devices, biomedicine and engineering, and fluorescent sensors. In this paper, we report on synthesis of a new type of sulfur-containing polymer dots (SPDs) through an atomic transfer radical polymerization method. The SPDs exhibit a maximum photoluminescence at 378 nm under excitation wavelength of 280 nm. The deep-blue luminescence of SPDs may be attributed to self-passivation of SPDs by polyethylene glycol oligomers which create surface states between π* band and π energy level. Also, the SPDs show a highly selective sensitivity to Fe3+ in a mixed metal-ion solution containing Ag+, Cu2+, Hg2+, Cd2+, Pb2+, Cr3+, and Fe3+ with every metal-ion concentration set at 50 μmol L‒1. The detection limit of Fe3+ by SPDs is determined to be 1.7 μM at a signal-to-noise ratio of 3, lower than the maximum of Fe3+ tolerance (5.4 μM) in drinking water permitted by the U.S. Environmental Protection Agency.

PEGylated MoS2 quantum dots for traceable and pH-responsive chemotherapeutic drug delivery

Since low pH value is widely observed in most of solid tumors, pH-responsive drug delivery system (DDS) can provide a general strategy for tumor-targeting therapy. In this work, a traceable and pH-responsive DDS (MoS2-PEG-DOX) based on MoS2 quantum dots (MoS2 QDs) is successfully developed by covalently grafting MoS2 QDs with diamine-terminated oligomeric polyethylene glycol (PEG) and then loading with a fluorescent antineoplastic anthracycline drug, doxorubicin (DOX). The functionalization of MoS2 QDs with PEG imparts the nanocomposite with strong blue photoluminescence, low cytotoxicity, and excellent physiological stability. The MoS2-PEG-DOX nano-assembly can be effectively taken up by U251 cells, and an accelerated DOX release is then triggered by intracellular acid condition, which in turn diminishing unwanted side effects derived by the incorporation of DOX into healthy cells. Meanwhile, the cellular uptake of the MoS2-PEG-DOX nano-assembly, consequent DOX release and the localization of nanocarrier can be real-time monitored due to the inherent stable fluorescence of MoS2-PEG and DOX. These findings demonstrate that MoS2-PEG-DOX will be promising for high treatment efficacy with minimal side effects in future therapy.