Hybrid Nanosystem Research Articles

An enzyme-responsive and NIR-triggered lipid-polymer hybrid nanoplatform for synergistic photothermal/chemo cancer therapy.

A combination of photothermal therapy (PTT) and chemotherapy is an emerging therapeutic strategy with promising clinical prospects in cancer treatment. Despite the huge progress achieved in the past years, a number of obstacles still hamper the therapeutic efficacy of this synergistic modality such as uneven heat distribution, lack of targetability of anti-cancer agents and dosage-related side effects. Thus, developing a nanoplatform for targeted drug delivery against cancer is of great necessity. Herein, a lipid-polymer hybrid nanosystem (LP/ID) based on polyethyleneimine (PEI)-lecithin-polyethylene glycol (PEG) was fabricated to co-load indocyanine green (ICG) and dichloroacetate (DCA) for combined photothermal/chemotherapy. DCA and ICG were linked to the PEI backbone to form a dense hydrophobic core through amide bonds and electrostatic interactions, which increased the payload of DCA and ICG as well as achieved enzyme-responsive drug release because of the overexpressed amidase in tumor cells. Lecithin and DSPE-PEG2000 self-assembled around the hydrophobic complexes to obtain prolonged blood circulation and attenuated systemic toxicity of the hybrid nanosystem. The prepared LP/ID exhibited favourable stability in a physiological environment, good tumor imaging properties, and satisfactory photothermal/chemotherapeutic performance. Moreover, LP/ID could also enhance the cellular uptake and tumor retention capacity in comparison with free drug administration. Notably, by co-loading two therapeutic agents with different anti-cancer mechanisms, an obvious inhibitory effect on tumor growth was observed with negligible damage to normal tissues and organs because of the synergistic photothermal/chemotherapy effect, indicating the great potential of LP/ID as a robust nanoplatform for cancer treatment.

Predicting the structure configuration and Raman analysis of caffeine molecules encapsulated into single-walled carbon nanotubes: Evidence for charge transfer

A new hybrid nano-system constituted of a single-walled carbon nanotube (SWNT) filled by caffeine (Caff) molecule(s) is proposed as a potential candidate for organic solar cells. The stability of this hybrid system with either a single or two Caff molecule(s) encapsulated into SWNTs has been investigated. In particular, the optimal SWNT diameter is discussed for each configuration. Raman spectra have been calculated using an approach combining the density functional theory, molecular mechanics, bond polarizability model and the spectral moment’s method. We have analyzed the influence of the nanoconfinement on the Raman-active modes of Caff molecule and those of SWNT. The analysis of the nanoconfinement effect on the Raman active modes of Caff molecules and those of SWNTs (radial breathing mode (RBM) and tangential mode (TM)) confirm the structural stability and indicate an evidence for a charge transfer between the Caff molecules and the nanotubes.

Luminescence transformation mechanisms of indocyanine green dye in the presence of gold nanorods

Spectral-luminescent manifestations of the plasmon-exciton interaction between gold nanorods (Au NRs) with average length and diameter of 35± 5 nm and 9± 2 nm, passivated by molecules of cetyltrimethylammonium bromide (CTAB) and the indocyanine green dye (ICG) molecules are found. Extinguishing of the ICG luminescence near Au NRs and its buildup are detected at spacial separation of hybrid nanosystem components achieved by a spherical shell of SiO2 with an average thickness of 26±5 nm formed on the Au NRs. The amplification of the luminescence with growth of the dielectric shell is provided due to blocking of steric transformations of ICG polymethine chain when the interaction emerges between the dye and the silicious shell, and the Purcell effect. Keywords: luminescence, indocyanine green, gold nanorods, Purcell effect.

Plasmonic enhancement of the antibacterial photodynamic efficiency of a zinc tetraphenylporphyrin photosensitizer/dextran graft polyacrylamide anionic copolymer/Au nanoparticles hybrid nanosystem.

A zinc tetraphenylporphyrin photosensitizer/dextran graft polyacrylamide anionic copolymer/Au nanoparticles (ZnTPP/D-g-PAAan/AuNPs) triple hybrid nanosystem was synthesized in water-based solution as a nanodrug for potential photodynamic therapy applications. Dynamic light scattering studies showed that the nanosystem is stable against aggregation and sedimentation for several days after preparation. The dependence of the ZnTPP fluorescence intensity on the gold concentration in the ZnTPP/D-g-PAAan/AuNPs nanosystem has been revealed to be non-monotonic, with a maximum 2.5-fold enhancement at a concentration of 0.008 g L−1. The non-monotonic dependence was explained to be caused by two competing processes, namely plasmonic enhancement and FRET, indicating the existence of an optimal concentration of Au NPs that can provide the highest plasmonic enhancement of the electronic processes involving the ZnTPP photosensitizer. A 2.6-fold enhancement of singlet oxygen photogeneration under excitation resonant with the localized surface plasmon resonance of the Au NPs has been detected for ZnTPP/D-g-PAAan/AuNPs, proving the plasmonic origin of this phenomenon. The high bactericidal efficiency of ZnTPP/D-g-PAAan/AuNPs water-based solution under 420 nm and 530 nm light irradiation was revealed against wild strains of Staphylococcus aureus. Therefore, the ZnTPP/D-g-PAAan/AuNPs nanosystem can potentially be used in photodynamic therapy for the prevention and treatment of the bacterial contamination of open wounds.

A plasmon-enhanced fluorescent gold coated novel lipo-polymeric hybrid nanosystem: synthesis, characterization and application for imaging and photothermal therapy of breast cancer.

This study reports a hybrid lipo-polymeric nanosystem (PDPC NPs) synthesized by a modified hydrogel-isolation technique. The ability of the nanosystem to encapsulate hydrophilic and hydrophobic molecules has been demonstrated, and their enhanced cellular uptake has been observed in vitro. The PDPC NPs, surface coated with gold by in situ reduction of chloroauric acid (PDPC-Au NPs), showed a photothermal transduction efficacy of ∼65%. The PDPC-Au NPs demonstrated an increase in intracellular ROS, triggered DNA damage and resulted in apoptotic cell death when tested against breast cancer cells (MCF-7). The disintegration of PDPC-Au NPs into smaller nanoparticles with near-infrared (NIR) laser irradiation was understood using transmission electron microscopy imaging. The lipo-polymeric hybrid nanosystem exhibited plasmon-enhanced fluorescence when loaded with IR780 (a NIR dye), followed by surface coating with gold (PDPC-IR-Au NPs). This paper is one of the first reports on the plasmon-enhanced fluorescence within a nanosystem by simple surface coating of Au, to the best of our knowledge. This plasmon-enhanced fluorescence was unique to the lipo-polymeric hybrid system, as the same was not observed with a liposomal nanosystem. The plasmon-enhanced fluorescence of PDPC-IR-Au NPs, when applied for imaging cancer cells and zebrafish embryos, showed a strong fluorescence signal at minimal concentrations of the dye. The PDPC-IR-Au NPs were also applied for photothermal therapy of breast cancer in vitro and in vivo, and the results depicted significant therapeutic benefits.

Glucose-Targeted Hydroxyapatite/Indocyanine Green Hybrid Nanoparticles for Collaborative Tumor Therapy.

Nanoscale hydroxyapatite (nHA) is considered as a promising drug carrier or therapeutic agent against malignant tumors. But the strong agglomeration tendency and lack of active groups seriously hamper their usage in vivo. To address these issues, we fabricated an organic-inorganic hybrid nanosystem composed of poly(acrylic acid) (PAA), nHA, and indocyanine green (ICG), and further modified with glucose to give a targeting nanosystem (GA@HAP/ICG-NPs). These hybrid nanoparticles (∼90 nm) showed excellent storage and physiological stability assisted by PAA and had a sustained drug release in an acidic tumor environment. In vitro cell experiments confirmed that glucose-attached particles significantly promoted cellular uptake and increased intracellular ICG and Ca2+ concentrations by glucose transporter 1 (GLUT1)-mediated endocytosis. Subsequently, the excessive Ca2+ induced cell or organelle damage and ICG triggered photothermal and photodynamic effects (PTT/PDT) under laser irradiation, resulting in enhanced cell toxicity and apoptosis. In vivo tests revealed that the hybrid nanosystem possessed good hemocompatibility and biosafety, facilitating in vivo circulation and usage. NIR imaging further showed that tumor tissues had more drug accumulation, resulting in the highest tumor growth inhibition (87.89%). Overall, the glucose-targeted hybrid nanosystem was an effective platform for collaborative therapy and expected to be further used in clinical trials.

SERS Quantification of Galunisertib Delivery in Colorectal Cancer Cells by Plasmonic-Assisted Diatomite Nanoparticles.

The small molecule Galunisertib (LY2157299, LY) shows multiple anticancer activities blocking the transforming growth factor-β1 receptor, responsible for the epithelial-to-mesenchymal transition (EMT) by which colorectal cancer (CRC) cells acquire migratory and metastatic capacities. However, frequent dosing of LY can produce highly toxic metabolites. Alternative strategies to reduce drug side effects can rely on nanoscale drug delivery systems that have led to a medical revolution in the treatment of cancer, improving drug efficacy and lowering drug toxicity. Here, a hybrid nanosystem (DNP-AuNPs-LY@Gel) made of a porous diatomite nanoparticle decorated with plasmonic gold nanoparticles, in which LY is retained by a gelatin shell, is proposed. The multifunctional capability of the nanosystem is demonstrated by investigating the efficient LY delivery, the enhanced EMT reversion in CRCs and the intracellular quantification of drug release with a sub-femtogram resolution by surface-enhanced Raman spectroscopy (SERS). The LY release trigger is the pH sensitivity of the gelatin shell to the CRC acidic microenvironment. The drug release is real-time monitored at single-cell level by analyzing the SERS signals of LY in CRC cells. The higher efficiency of LY delivered by the DNP-AuNPs-LY@Gel complex paves the way to an alternative strategy for lowering drug dosing and consequent side effects.

Chirality Nanosensor with Direct Electric Readout by Coupling of Nanofloret Localized Plasmons with Electronic Transport.

The detection of enantiopurity for small sample quantities is crucial, particularly in the pharmaceutical industry; however, existing methodologies rely on specific chiral recognition elements, or complex optical systems, limiting its utility. A nanoscale chirality sensor, for continuously monitoring molecular chirality using an electric circuit readout, is presented. This device design represents an alternative real-time scalable approach for chiral recognition of small quantity samples (less than 103 adsorbed molecules). The active device component relies on a gold nanofloret hybrid structure, i.e., a high aspect ratio semiconductor-metal hybrid nanosystem in which a SiGe nanowire tip is selectively decorated with a gold metallic cap. The tip mechanically touches a counter electrode to generate a nanojunction, and upon exposure to molecules, a metal-molecule-metal junction is formed. Adsorption of chiral molecules at the gold tip induces chirality in the localized plasmonic resonance at the electrode-tip junction and manifests in an enantiospecific current response.

MOF-enzyme hybrid nanosystem decorated 3D hollow fiber membranes for in-situ blood separation and biosensing array

Modified metal–organic frameworks (MOFs) doping with enzymes exhibit high enzyme stability and catalytic performance, which is a research hotspot in the field of enzyme-based sensing. Although the MOF-enzyme constitutes a 3D structure in the nanoscale, the macroscopic assembly configuration still stays in 1D or 2D structures, limiting sensing applications towards complex biological targets. Herein, the MOF-enzyme hybrid nanosystem was assembled into 3D porous conductive supports via a controllable physical embedding method, displaying high enzymatic loading, stability and cascade catalytic performance. The modified MOFs combing with enzymes served as a sensing reaction system, and the conductive hollow fiber membranes (HFMs) served as a functional platform. The multifunctional device integrates pumpless hydrodynamic transport, interconnected conductive polymer, and blood separation modules, showing fast capillary fluid flow, trace sampling (3 μL), high selectivity and accuracy. The linear sensing range was in 2–24 mM glucose, 0.05–6 mM lactic acid, and 0.1–10 mM cholesterol, respectively, with sensitivities of 24.2, 150, 73.6 nA mM−1. Furthermore, this strategy of modular assembly of biosensing array can easily implement multiplex metabolites detection simultaneously.

Dark bridge at the interface of hybrid nanosystem: Lanthanide-triplet NIR photosensitization

"Dark" organic triplet states typically require visible light to activate via singlet-triplet intersystem crossing. In this issue of <i>Chem</i>, Deng and co-workers report a new near-infrared photosensitization strategy using lanthanide-doped nanoparticles to directly activate the dark triplet states of organic photosensitizers, significantly reducing the power requirement of irradiance.

Plasmonic properties of nanohybrids made of metallic nanoring and benzene molecules

AbstractPlasmon‐molecule coupling has recently been attracted great research interest in material science and quantum optics with a multitude of potential applications. In this work, using the linear combination of atomic orbitals real‐time‐propagation rt‐time dependent density functional theory (TDDFT) technique (LCAO‐rt‐TDDFT) and transition contribution maps, we investigate the optical and plasmonic features of a hybrid nanosystem comprising an elliptical‐shaped metal nanoring (ENR) and a couple of benzene molecules (located in close proximity at both sides of the ENR short axis and/or long axis). We find that pristine ENR exhibits localized surface plasmon resonances (LSPRs) and plasmon‐molecule coupling in hybrid nanosystems is highly sensitive to the location of the molecules. More specifically, when benzene molecules are placed at both sides of the ENR short axis, the dominant peak in the photoabsorption spectrum sustains its LSPR features with a significant enhancement in intensity. On the other hand, in an alternative situation where benzene molecules are placed at both sides of the ENR long axis, the dominant peak in the photoabsorption spectrum splits into three with diminishing LSPR features.

Biodegradable/disintegrable nanohybrids for photothermal theranostics

Nanohybrids using biocompatible and biodegradable materials are explored for their photothermal mediated theranostic applications. These hybrids are so chosen that they are biocompatible and biodegradable. Gold-based different nanosystems have NIR absorption which is highly favored for PTT, but they are limited by their toxicity, stability, and clearance. To overcome these challenges, we have demonstrated thermosensitive liposome-gold hybrid nanosystem for photothermal therapy and its clearance in vivo for the first time. We have also explored the possibility of using the same hybrid as drug (curcumin) carrier for triggered delivery and were successful in using curcumin as an adjuvant to PTT. Thermoresponsive polymers coated with gold for photothermal therapy and X-ray imaging of deep seated tumors has been evaluated. Fluorescent Poly (ethylene glycol) encapsulated metal nanoparticles were also synthesized and their application for cancer theranostics has been explored. Biodegradable and biocompatible polymer (PLGA) and liposomes loaded with anticancer plant fraction and a NIR dye showed synergistic photo-chemo therapy against cancer in-vitro & in-vivo. The intracellular changes with PTT and the mechanistic action of anti-cancer agent were explored in detail.

Micro-photoluminescence of Carbon Dots Deposited on Twisted Double-Layer Graphene Grown by Chemical Vapor Deposition.

Carbon-based nanomaterials, such as carbon dots (CDs) and graphene (Gr), feature outstanding optical and electronic properties. Hence, their integration in optoelectronic and photonic devices is easier thanks to their low dimensionality and offers the possibility to reach high-quality performances. In this context, the combination of CDs and Gr into new nanocomposite materials CDs/Gr can further improve their optoelectronic properties and eventually create new ones, paving the way for the development of advanced carbon nanotechnology. In this work, we have thoroughly investigated the structural and emission properties of CDs deposited on single-layer and bilayer graphene lying on a SiO2/Si substrate. A systematic Raman analysis points out that bilayer (BL) graphene grown by chemical vapor deposition does not always respect the Bernal (AB) stacking, but it is rather a mixture of twisted bilayer (t-BL) featuring domains with different twist angles. Moreover, in-depth micro-photoluminescence measurements, combined with atomic force microscopy (AFM) morphological analysis, show that CD emission efficiency is strongly depleted by the presence of graphene and in particular is dependent on the number of layers as well as on the twist angle of BL graphene. Finally, we propose a model which explains these results on the basis of photoinduced charge-transfer processes, taking into account the energy levels of the hybrid nanosystem formed by coupling CDs with t-BL/SiO2.

Temperature Driven Plasmon-Exciton Coupling in Thermoresponsive Dextran-Graft-PNIPAM/Au Nanoparticle/CdTe Quantum Dots Hybrid Nanosystem

The temperature-driven plasmon-exciton coupling in thermoresponsive dextran-graft-PNIPAM/Au nanoparticle/CdTe quantum dot (D-g-PNIPAM/Au NPs/CdTe QDs) hybrid nanosystem was studied. A significant (0.84 eV) splitting of the absorption peak was observed in the absorption spectrum of the nanosystem, which reflects the fact of formation of plexcitons, occurring due to strong plasmon-exciton coupling. An increasing with time plasmonic enhancement of the photoluminescence of CdTe QDs was revealed, as a result of the penetration of quantum dots into the volume of the D-g-PNIPAM/Au NP hybrid nanosystem and bonding to it. The heating–cooling cycle of the aqueous solution of the studied nanosystem leads to a reversible quenching-recovery alteration of the QD photoluminescence. The quenching was rationalized as a result of an increased probability of nonradiative resonance energy transfer (RET) from CdTe QDs to Au NPs, which occurs due to shortening of the NP-QD distance, caused by shrinking of the macromolecule due to cooling-induced lower critical solution temperature phase transition. Increasing the NP-QD distance in the heating stage recovers the QD PL intensity. The observed effect opens up opportunities for the controlled reversible temperature-driven tuning of the photoluminescence intensity of D-g-PNIPAM/Au NP/CdTe QD nanosystem, which is highly important for its potential use in photonics and biomedical applications.

Blue/yellow emissive carbon dots coupled with curcumin: a hybrid sensor toward fluorescence turn-on detection of fluoride ion

Trace detection of fluoride ion has gained increasing attention due to fluoride’s close association with biological and environmental processes. Herein, we construct a novel hybrid nanosystem consisting of carbon dots and curcumin for sensitive and selective sensing of F–. Carbon dots are synthesized by hydrothermal treatment of 2,3-diaminopyridine and selenourea in hydrochloric acid. This material is employed as the fluorescent indicator that exhibits intense blue and yellow emission with quantum yields of 12% and 33%, respectively. Curcumin, possessing an absorption peak at 532 nm, can significantly quench the yellow fluorescence of carbon dots through inner filter effect. Curcumin is also used to specifically recognize F–. When F– is added, the curcumin-F– complex generates, which leads to the hypochromatic shift of the absorption band from 532 to 430 nm. In such a case, the inner filter effect reduces, and yellow fluorescence of carbon dots recovers. Thus, a fluorescence turn-on sensor of F– is built based on the carbon dots/curcumin system. The limits of detection and quantitation are measured to be 0.39 and 1.30 μM, respectively. For real usage, the proposed method is applied to determinate F– in tap water and milk samples with relative standard deviations below 7.9%.

Supramolecular nanomedicine derived from cucurbit[7]uril-conjugated nano-graphene oxide for multi-modality cancer therapy.

Nano-graphene oxide (NGO) has attracted increasing attention as an advanced drug delivery system. However, the current surface functionalization and drug-loading of NGO either rely on π-π stacking that is limited to aromatic molecules, or covalent conjugation that requires tedious synthesis. Herein, we developed the first cucurbit[7]uril (CB[7])-conjugated NGO (NGO-CB[7]) that allows non-covalent, modular surface functionalization and drug loading via not only traditional π-π stacking interactions between the NGO surface and functional molecules, but also strong host-guest interactions between CB[7] and guest payloads or adamantane (ADA)-tagged functional molecules, for more versatile biomedical applications. To this end, chlorin e6 (Ce6, a photosensitizer), banoxantrone dihydrochloride (AQ4N, a hypoxia-responsive prodrug) and oxaliplatin (OX, a guest of CB[7]) were co-loaded onto NGO-CB[7] via π-π stacking and host-guest interactions, respectively. Subsequently, ADA-tagged hyaluronic acid (ADA-HA) wrapped NGO-CB[7] non-covalently via CB[7]-ADA host-guest interactions to improve the physiological stability and overall biocompatibility of this supramolecular nanosystem, and to enable targeted delivery into cancer cells with CD44 receptors overexpressed. Remarkably, this supramolecular nanomedicine exhibited significant antitumor efficacy via combined photothermal/photodynamic therapy (PTT/PDT) from NGO/Ce6, as well as dual chemotherapy from OX and AQ4N (activated by PDT-enhanced hypoxia), in vitro and in vivo. This study not only offers a new supramolecular inorganic/organic hybrid nanosystem for multi-modality cancer therapy, but may also provide important new insights into noncovalent functionalization of other carbon nanomaterials and inorganic nanomaterials leading to multifunctional drug delivery systems.

Preparation and study of the catalytic application in the synthesis of xanthenedione pharmaceuticals of a hybrid nano-system based on copper, zinc and iron nanoparticles

A novel efficiently mixed transition metal oxides catalytic system with high catalytic activity and heterogeneity constructed of copper and zinc oxide nanoparticles is presented. For preparation of this hybrid catalytic system, carrageenan as a natural polymeric matrix has been chosen to add biocompatibility to the heterogeneous catalyst. Then, the carrageenan textures have been magnetized through the composition with iron oxide nanoparticles. Copper and zinc metallic sites are employed as the main catalytic sites for catalyzing the synthesis of xanthenedione pharmaceutical derivatives from aldehyde and dimedone. Due to the magnetic behavior of the catalyst, the purification process is carried out with high convenience. Herein, a plausible mechanism for the catalytic process is suggested and reusability of the presented catalyst is also investigated. In this report, it has been well-proven that high reaction yields are obtained for xanthenedione derivatives under mild conditions, through applying the presented hybrid catalytic system.

Light-induced release of the cardioprotective peptide angiotensin-(1–9) from thermosensitive liposomes with gold nanoclusters

Angiotensin-(1-9), a component of the non-canonical renin-angiotensin system, has a short half-life in blood. This peptide has shown to prevent and/or attenuate hypertension and cardiovascular remodeling. A controlled release of angiotensin-(1-9) is needed for its delivery to the heart. Our aim was to develop a drug delivery system for angiotensin-(1-9). Thermosensitive liposomes (LipoTherm) were prepared with gold nanoclusters (LipoTherm-AuNC) to increase the stability and reach a temporal and spatial control of angiotensin-(1-9) release. Encapsulation efficiencies of nearly 50% were achieved in LipoTherm, reaching a total angiotensin-(1-9) loading of around 180 μM. This angiotensin-(1–9)-loaded LipoTherm sized around 100 nm and exhibited a phase transition temperature of 43 °C. AuNC were grown on LipoTherm and the new hybrid nanosystem showed energy absorption in the near-infrared (NIR) wavelength range. By NIR laser irradiation, a controlled release of angiotensin-(1-9) was achieved from the LipoTherm-AuNC nanosystem. These nanosystems did not show any cytotoxic effect on cultured cardiomyocytes. Biological activity of angiotensin-(1-9) released from the LipoTherm-AuNC-based nanosystem was confirmed using an ex vivo Langendorff heart model.

Chitosan overlaid Fe3O4/rGO nanocomposite for targeted drug delivery, imaging, and biomedical applications

A hybrid and straightforward nanosystem that can be used simultaneously for cancer-targeted fluorescence imaging and targeted drug delivery in vitro was reported in this study. A chitosan (CS) polymer coated with reduced graphene oxide (rGO) and implanted with Fe3O4 nanoparticles was fabricated. The fundamental physicochemical properties were confirmed via FT-IR, XRD, FE-SEM, HR-TEM, XPS, and VSM analysis. The in vivo toxicity study in zebrafish showed that the nanocomposite was not toxic. The in vitro drug loading amount was 0.448 mg/mL−1 for doxorubicin, an anticancer therapeutic, in the rGO/Fe3O4/CS nanocomposite. Furthermore, the pH-regulated release was observed using folic acid. Cellular uptake and multimodal imaging revealed the benefit of the folic acid-conjugated nanocomposite as a drug carrier, which remarkably improves the doxorubicin accumulation inside the cancer cells over-express folate receptors. The rGO/Fe3O4/CS nanocomposite showed enhanced antibiofilm and antioxidant properties compared to other materials. This study's outcomes support the use of the nanocomposite in targeted chemotherapy and the potential applications in the polymer, cosmetic, biomedical, and food industries.

Highly Efficient Room-Temperature Electron-Photon Spin Conversion Using a Semiconductor Hybrid Nanosystem with Gradual Quantum Dimensionality Reduction

Improved electron-photon spin conversion efficiency is a key component of technological platforms for optospintronics integration in information processing; this concept is based on optical devices transmitting and receiving spin information superimposed on light. Semiconductor quantum dots (QDs) are the most promising materials for optospintronic devices; however, in addition to their weak room-temperature luminescence, their electron-photon spin conversion efficiencies are lower than 50%. Here, we present semiconductor QDs embedded in quantum wells (QWs) containing quasi-QDs. The proposed semiconductor hybrid nanosystem with gradual quantum dimensionality reduction demonstrates luminescence one order of magnitude stronger than that of conventional QDs and an electron-photon spin conversion efficiency of almost 80% at room temperature. Optical characterization reveals that efficient carrier capture, suppressed depolarized-spin reinjection, and quasi-three-dimensional quantum confinements in the QWs facilitate the highly efficient electron-photon spin conversion. This study constitutes a significant advance towards the realization of QD-based spin-functional optical devices for electron-spin-based quantum information platforms.