Photothermal Transduction Efficiency Research Articles

Epigallocatechin-3-gallate adsorbed on core–shell gold nanorod@mesoporous silica nanoparticles, an antioxidant nanomaterial with photothermal properties

Epigallocatechin-3-gallate (EGCG) exhibits several pharmacological activities with potential benefits for human health, however, it has low oral bioavailability. A promising approach is to transport EGCG in a nanostructured system to protect it until it reaches the site of action and also allow combining chemotherapy with phototherapy to improve its therapeutic efficiency. The aim of this work was to synthesize GNR@mSiO2-NH2/EGCG and characterize the adsorption process, its antioxidant activity, properties and photothermal stability, for its potential use in chemo-photothermal therapy. The nanosystem presented good encapsulation efficiency (19.2 %) and EGCG loading capacity (6.0 %). The DPPH• free radical scavenging capacity (RSA) and chelating activity of the nanosystem was 60.7 ± 6.9 % and 71.0 ± 6.4 % at an EGCG equivalent concentration of 1 µg/mL and 30 µg/mL, respectively. The core–shell NPs presented a good photothermal transduction efficiency of 17 %. EGCG free, as well as its RSA and chelating activity, remained stable after NIR irradiation (808 nm, 7 W/cm2). The morphology of GNR@mSiO2 remained intact after being irradiated with NIR, however, ultrasmall gold NPs could be observed, probably a product of photocracking of GNR. In summary, the nanosystem has good antioxidant activity, photothermal stability, and photothermal transduction ability making it potentially useful for chemo-photothermal therapy.

Three-dimensional Au-MnO2 nanostructure as an agent of synergistic cancer therapy: chemo-/photodynamic and photothermal approaches.

The design of multimodal cancer therapy was focused on reaching an efficient process and minimizing harmful effects on patients. In the present study, the Au-MnO2 nanostructures have been successfully constructed and produced as novel multipurpose photosensitive agents simultaneously for photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT). The prepared AuNPs were conjugated with MnO2 NPs by its participation in the thermal decomposition process of KMnO4 confirmed by X-ray diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared (FTIR) spectroscopy (FT-IR). The 16.5 nm Au-MnO2 nanostructure exhibited an absorbance at 438 nm, which is beneficial for application in light induction therapy due to the NIR band, as well as its properties of generating reactive oxygen species (ROS) associated with the 808 nm laser light for PDT. The photothermal transduction efficiency was calculated and compared with that of the non-irradiated nanostructure, in which it was found that the 808 nm laser induced a high efficiency of 83%, 41.5%, and 37.5% for PDT, PTT, and CDT, respectively. The results of DPBF and TMB assays showed that the efficiency of PDT and PTT was higher than that of CDT. The nanostructure also confirmed the time-dependent peroxidase properties at different H2O2, TMB, and H2TMB concentrations, promising good potency in applying nanomedicine in clinical cancer therapy.

Synthesis and Photothermal Properties of UV-Plasmonic Group IV Transition Metal Carbide Nanoparticles

Refractory nanostructures can be low-cost and chemically and thermally robust alternatives to metal-based plasmonic materials. While transition metal nitrides have received much attention recently, there has been less emphasis on their closely related non-layered carbide counterparts. In this work, plasmonic group IV transition metal carbide (TiC, ZrC, and HfC) nanostructures were prepared using a facile magnesiothermic reduction method, which yielded a phase pure product. TiC, ZrC, and HfC with rock salt crystal structures and an average particle size of 24, 31, and 42 nm, respectively, were obtained by reacting corresponding metal oxide, magnesium, and biochar in the solid state. Calculations performed using a finite element method predicted these group IV carbide nanostructures to have localized surface plasmon resonance in the UV region between 150 and 175 nm. The photothermal transduction efficiency of each carbide was explored to further verify the plasmonic behavior. HfC was found to have the highest photothermal transduction efficiency of 73%, followed by ZrC (69%), and then TiC (60%) at 365 nm.

Real-time SERS monitoring anticancer drug release along with SERS/MR imaging for pH-sensitive chemo-phototherapy.

In situ and real-time monitoring of responsive drug release is critical for the assessment of pharmacodynamics in chemotherapy. In this study, a novel pH-responsive nanosystem is proposed for real-time monitoring of drug release and chemo-phototherapy by surface-enhanced Raman spectroscopy (SERS). The Fe3O4@Au@Ag nanoparticles (NPs) deposited graphene oxide (GO) nanocomposites with a high SERS activity and stability are synthesized and labeled with a Raman reporter 4-mercaptophenylboronic acid (4-MPBA) to form SERS probes (GO-Fe3O4@Au@Ag-MPBA). Furthermore, doxorubicin (DOX) is attached to SERS probes through a pH-responsive linker boronic ester (GO-Fe3O4@Au@Ag-MPBA-DOX), accompanying the 4-MPBA signal change in SERS. After the entry into tumor, the breakage of boronic ester in the acidic environment gives rise to the release of DOX and the recovery of 4-MPBA SERS signal. Thus, the DOX dynamic release can be monitored by the real-time changes of 4-MPBA SERS spectra. Additionally, the strong T2 magnetic resonance (MR) signal and NIR photothermal transduction efficiency of the nanocomposites make it available for MR imaging and photothermal therapy (PTT). Altogether, this GO-Fe3O4@Au@Ag-MPBA-DOX can simultaneously fulfill the synergistic combination of cancer cell targeting, pH-sensitive drug release, SERS-traceable detection and MR imaging, endowing it great potential for SERS/MR imaging-guided efficient chemo-phototherapy on cancer treatment.

Microelectromechanical Microsystems-Supported Photothermal Immunoassay for Point-of-Care Testing of Aflatoxin B1 in Foodstuff.

Accurate identification of acutely toxic and low-fatality mycotoxins on a large scale in a quick and cheap manner is critical for reducing population mortality. Herein, a portable photothermal immunosensing platform supported by a microelectromechanical microsystem (MEMS) without enzyme involvement was reported for point-of-care testing of mycotoxins (in the case of aflatoxin B1, AFB1) in food based on the precise satellite structure of Au nanoparticles. The synthesized Au nanoparticles with a well-defined, graded satellite structure exhibited a significantly enhanced photothermal response and were coupled by AFB1 antibodies to form signal conversion probes by physisorption for further target-promoted competitive responses in microplates. In addition, a coin-sized miniature NIR camera device was constructed for temperature acquisition during target testing based on advanced MEMS fabrication technology to address the limitation of expensive signal acquisition components of current photothermal sensors. The proposed MEMS readout-based microphotothermal test method provides excellent AFB1 response in the range of 0.5-500 ng g-1 with detection limits as low as 0.27 ng g-1. In addition, the main reasons for the efficient photothermal transduction efficiency of Au with different graded structures were analyzed by finite element simulations, providing theoretical guidance for the development of new Au-based photothermal agents. In conclusion, the proposed portable micro-photothermal test system offers great potential for point-of-care diagnostics for residents, which will continue to facilitate immediate food safety identification in resource-limited regions.

PH‐Responsive Charge‐Convertible N‐Succinyl Chitosan‐Quercetin Coordination Polymer Nanoparticles for Effective NIR Photothermal Cancer Therapy

AbstractIn recent years, a combination of photothermal therapy (PTT) with chemotherapy has emerged as a new promising strategy to achieve synergistic cancer therapeutic efficacy. Coordination polymer nanocomposites (CPNs) are a new generation of photothermal agents (PTAs) for cancer therapy owing to their high photothermal transduction efficiency, excellent biocompatibility as well as biodegradability and bioactivity. In this study, a robust and scalable synthesis of pH‐sensitive charge convertible NSC‐Fe‐Que coordination polymer nanoparticles (CPNs) based on the coordination reaction between Fe3+, anti‐cancer prodrug quercetin (Que), and pH‐sensitive zwitterionic biopolymer N‐succinyl chitosan (NSC) is reported. The as‐prepared CPNs exhibit slightly negative zeta potential at neutral pH while positive zeta potential at pH 6.5, which ensures long blood circulation and high accumulation in the tumor region. NSC‐Fe‐Que CPNs exhibited strong absorption in NIR (500–850 nm) region and displayed a good anticancer effect against A549 cells attributing to the chemo‐photothermal synergistic effect. This study demonstrated that the NSC‐Fe‐Que CPNs hold great promise as an effective thermo‐chemotherapy agent for combination therapy against cancer.

Spatiotemporal Temperature Distribution of NIR Irradiated Polypyrrole Nanoparticles and Effects of pH.

The spatiotemporal temperature distributions of NIR irradiated polypyrrole nanoparticles (PPN) were evaluated by varying PPN concentrations and the pH of suspensions. The PPN were synthesized by oxidative chemical polymerization, resulting in a hydrodynamic diameter of 98 ± 2 nm, which is maintained in the pH range of 4.2–10; while the zeta potential is significantly affected, decreasing from 20 ± 2 mV to −5 ± 1 mV at the same pH range. The temperature profiles of PPN suspensions were obtained using a NIR laser beam (1.5 W centered at 808 nm). These results were analyzed with a three-dimensional predictive unsteady-state heat transfer model that considers heat conduction, photothermal heating from laser irradiation, and heat generation due to the water absorption. The temperature profiles of PPN under laser irradiation are concentration-dependent, while the pH increase only induces a slight reduction in the temperature profiles. The model predicts a value of photothermal transduction efficiency () of 0.68 for the PPN. Furthermore, a linear dependency was found for the overall heat transfer coefficient () and with the suspension temperature and pH, respectively. Finally, the model developed in this work could help identify the exposure time and concentration doses for different tissues and cells (pH-dependent) in photothermal applications.

Glycol chitosan stabilized bimolecular nanoparticles for chemo photothermal killing of breast cancer cells

We report a bi-molecular combination nanomedicine consisting of IR820 dye and chemotherapeutic drug lapatinib stabilized with the polyelectrolyte, glycol chitosan. The synthesized nanoformulation revealed superior photothermal transduction efficiency due to strong NIR (Near Infrared) absorbance of IR820. The in-vitro studies showed the time-dependent increase in cellular uptake of nanoparticles with significant photothermal chemotherapeutic toxicity against cancer cells. Moreover, acute toxicity assessment in Balb/c mice showed no systemic dysfunction of vital organs post intravenous injection of IR/LNPs.

Enhanced Gold Nanoparticle aggregation with cancer cell DNA for improved radiation therapy and immune response in cancer treatment

In the United States, cancer is the second leading cause of death after heart disease and hundreds of thousands of people pass away each year due to this deadly disease. Many treatments for cancer are nonselective and do not provide long‐lasting immunity in case of recurrence. Gold nanoparticles can provide a more targeted radiation therapy and better effectiveness through heat generation and formation of reactive oxygen species via hydrolysis reaction which can cause DNA damage in the tumor. Unfortunately, gold particles have low photothermal transduction efficiency and must be aggregated to improve performance. To achieve this, positively charged gold nanoparticles were aggregated with MDA MB 231 cancer cell DNA to increase gold nanoparticle aggregation, to elicit higher photothermal efficiency, and to stimulate an immune response. In vitro analysis demonstrated DNA size and concentration dependent gold nanoparticle aggregation, which varied little in the pH range of 5.5 to 8.6. Furthermore, these aggregates elicited an immune response via delivery of DNA for direct transfection of antigen presenting cells. Tumor necrosis factor alpha released from mouse RAW macrophages increased in the presence of the cancer cell DNA aggregated gold particles. This work suggests that the promise of combination therapy using cancer cell DNA not only can improve photothermal therapy of gold nanoparticles, but also can elicit an immune response in cancer treatment.

A Sub-nL Chip Calorimeter and Its Application to the Measurement of the Photothermal Transduction Efficiency of Plasmonic Nanoparticles

Here, we introduce a microchip for differential measurements of aqueous samples in twin calorimetric arms with a sub-nL enclosed space. Each arm features a fluidic microchannel located in close proximity to a thin-film resistance thermometer and heater patterned on a low-stress SiN membrane held over a Si cavity with suspension beams. The chip exhibits a rapid response with a thermal time constant of less than 10 ms in atmosphere and a residual thermal conductance below <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"> <tex-math notation="LaTeX">$6{\mu }\text{W}{\cdot }\text{K}^{-1 }$ </tex-math></inline-formula> , one of the lowest reported and accounts for the excellent sensitivity registered in vacuum up to 11 <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"> <tex-math notation="LaTeX">$\text{V}{\cdot }\text{W}^{-1 }$ </tex-math></inline-formula> . These values are in good agreement with those ones predicted by modeling using finite element method, lumped-capacitance analysis, and calorimeter electrothermal circuit simulation together with the measurement system. Long suspension beams in each arm ensure uniform temperature maintained across its membrane as revealed by the fluorescence-based melting curve analysis. We share the specific heat capacity values of water, glycerin, and mineral oil accurately measured by the chip. Lastly, we demonstrate the chip calorimeter utility on the measurement of the photothermal transduction efficiency of plasmonic nanoparticles, which makes our study further unique in expanding the applications of chip calorimeters. [2021-0044]

Dual Plasmonic Au-Cu2-x S Nanocomposites: Design Strategies and Photothermal Properties.

Coupling two different materials to create a hybrid nanostructured system is a powerful strategy for achieving synergistically enhanced properties and advanced functionalities. In the case of Au and Cu2-x S, their combination on the nanoscale results in dual plasmonic Au-Cu2-x S nanocomposites that exhibit intense photon absorption in both the visible and the near-infrared spectral ranges. Their strong light-absorbing properties translate to superior photothermal transduction efficiency, making them attractive in photothermal-based applications. There are several nanostructure configurations that are possible for the Au-Cu2-x S system, and the successful fabrication of a particular architecture often requires a carefully planned synthetic strategy. In this Minireview, the different synthetic approaches that can be employed to produce rationally designed Au-Cu2-x S nanocomposites are presented, with a focus on the experimental protocols that can lead to heterodimer, core-shell, reverse core-shell, and yolk-shell configurations. The photothermal behavior of these materials is also discussed, providing a glimpse of their potential use as photothermally active agents in therapeutic and theranostic applications.

Photothermal Effect of Superparamagnetic Fe3O4 Nanoparticles Irradiated by Near-Infrared Laser

Fe3O4 nanoparticles (NPs) have been widely used in biomedicine due to their unique magnetism, biocompatibility, and biodegradability. Magnetic hyperthermia of Fe3O4 NPs for cancer treatment has attracted more attention. However, it could interfere with magnetic field-sensitive devices of patients, such as pacemakers. Therefore, it is necessary to find a new method for clinical therapy. In this study, the superparamagnetic Fe3O4 NPs were fabricated. Visible-near-infrared absorption spectra indicated that the Fe3O4 NPs have near-infrared absorption. The influences of Fe3O4 NP concentrations, power density, and wavelength of near-infrared laser irradiation on the photothermal performance of Fe3O4 NPs were investigated. The results revealed that high concentrations, large power density, and short irradiation wavelength could improve the photothermal performance of Fe3O4 NPs. The temperature variation and the absorption intensity simultaneously determined the photothermal transduction efficiency of Fe3O4 NPs. The application of the photothermal performance of Fe3O4 NPs would provide a new opportunity for clinic cancer treatment.

Redox responsive nanoparticle encapsulating black phosphorus quantum dots for cancer theranostics

Effective cancer treatment puts high demands for cancer theranostics. For cancer diagnostics, optical coherence tomography (OCT) technology (including photothermal optical coherence tomography (PT-OCT)) has been widely investigated since it induces changes in optical phase transitions in tissue through environmental changes (such as temperature change for PT-OCT). In this report, redox responsive nanoparticle encapsulating black phosphorus quantum dots was developed as a robust PT-OCT agent. Briefly, black phosphorus quantum dots (BPQDs) are incorporated into cysteine-based poly-(disulfide amide) (Cys-PDSA) to form stable and biodegradable nanoagent. The excellent photothermal feature allows BPQD/Cys-PDSA nanoparticles (NPs) as a novel contrast agent for high-resolution PT-OCT bioimaging. The Cys-PDSA can rapidly respond to glutathione and effectively release BPQDs and drugs in vitro and in vivo. And the obtained NPs exhibit excellent near-infrared (NIR) photothermal transduction efficiency and drug delivery capacity that can serve as novel therapeutic platform, with very low chemo drug dosage and side effects. Both of the polymer and BPQD are degradable, indicating this platform is a rare PT-OCT agent that is completely biodegradable. Overall, our research highlights a biodegradable and biocompatible black phosphorus-based nanoagent for both cancer diagnosis and therapy.

Photothermal Transduction Efficiencies of Plasmonic Group 4 Metal Nitride Nanocrystals.

The photothermal transduction efficiencies of group 4 metal nitrides, TiN, ZrN, and HfN, at λ = 850 nm are reported, and the performance of these materials is compared to an Au nanorod benchmark. Transition metal nitride nanocrystals with an average diameter of ∼15 nm were prepared using a solid-state metathesis reaction. HfN exhibited the highest photothermal transduction efficiency of 65%, followed by ZrN (58%) and TiN (49%), which were all higher than those of the commercially purchased Au nanorods (43%). Computational studies performed using a finite element method showed HfN and Au to have the lowest and highest scattering cross section, respectively, which could be a contributing factor to the efficiency trends observed. Furthermore, the changes in temperature as a function of illumination intensity and solution concentration, as well as the cycling stability of the metal nitride solutions, were studied in detail.

Gold nanoparticle clusters for the investigation of therapeutic efficiency against prostate cancer under near-infrared irradiation

Gold particles have been widely used in the treatment of prostate cancer due to their unique optical properties, such as their light-heat conversion in response to near-infrared radiation. Due to well-defined synthesis mechanisms and simple manufacturing methods, gold particles have been fabricated in various sizes and shapes. However, the low photothermal transduction efficiency in their present form is a major obstacle to practical and therapeutic uses of these particles. In the current work, we present a silica-coated gold nanoparticle cluster to address the therapeutic limit of single gold nanoparticles (AuNPs) and use its photothermal effect for treatment against PC-3, a typical prostate cancer. Due to its specific nanostructure, this gold nanocluster showed three times higher photothermal transduction efficiency than free single AuNPs. Moreover, while free single particles easily clump and lose optical properties, this silica-coated cluster form remained stable for a longer time in a given medium. In photothermal tests under near-infrared radiation, the excellent therapeutic efficacy of gold nanoclusters, referred to as AuNC@SiO2, was observed in a preclinical sample. Only the samples with both injected nanoclusters followed by photothermal treatment showed completely degraded tumors after 15 days. Due to the unique intrinsic biocompatibility and higher therapeutic effect of these silica-coated gold nanoclusters, they may contribute to enhancement of therapeutic efficacy against prostate cancer.

Laser ablation in liquids for the assembly of Se@Au chain-oligomers with long-term stability for photothermal inhibition of tumor cells

For the potential use of Au nanoparticles (NPs) in photothermal therapy, it is important and effective to achieve the uniaxial assembly of Au NPs to allow enhanced absorption in the near infrared (NIR) region. Herein, we first presented the construction of amorphous selenium encapsulated gold (Se@Au) chain-oligomers by successive laser ablation of Au and Se targets in sodium chloride solution without other toxic precursors, stabilizers, or templating molecules. Se@Au chain-oligomers showed evidently enhanced NIR absorption and excellent photothermal transduction efficiency (η), which was higher than 47% at 808 nm. After being stored for 1 year, the Se@Au colloids still exhibited outstanding photothermal performance. The cytotoxicity assay demonstrated that there is negligible toxicity of Se@Au chain-oligomers in cells, but cell viability declined to only 1% in phototherapeutic experiments that were implemented in vitro. In intracellular Reactive Oxygen Species (ROS) generation measurements, Se@Au chain-oligomers could trigger a 35.9% increment of ROS upon laser irradiation. The possible synergetic effects between the anticancer function of Se and photothermal behaviors of Se@Au oligomers were intended to increase ROS level in cells. Therefore, such designed Se@Au chain-oligomers of high stability exhibit promising potential for their use as in vivo photothermal therapeutic agents.

Electrocatalytic synthesis of black tin oxide nanomaterial as photothermal agent for cancer therapy.

Photothermal therapy (PTT) is among the popular approach for treating solid tumours. The rapid killing of cancer cells under the influence of infrared radiation by a rapid increase in the temperature of the remote area now demands external agents with high photothermal transduction efficiency (PTE). Despite their improved PTE, black nanomaterials such as black phosphorus and titanium oxide are unable to meet the challenges in the physiological conditions. To address this major concern, we have developed black tin oxide (bSnO) with enhanced capabilities to respond in the physiological milieu. To make the synthesis cost-effective and eco-friendly, we have used electrochemical oxidation at 5 V and 100 mA to achieve ∼15 nm nanoparticle of bSnO. The as-synthesized bSnO exhibited high NIR absorption as well as high photothermal transduction efficiency. To circumvent the low aqueous solubility and photostability, bSnO was functionalized with polyethyleneimine (PEI). Upon exposure to 808 nm laser for ∼8-10 min, the temperature of the bSnO@PEI solution reached ∼58.5 °C. PTE of bSnO@PEI was calculated to be 51.2%. Owing to its high biological compatibility, tin offers relatively better stability when exposed to cancer cells in vitro and in vivo. In comparison to other black nanomaterials, bSnO@PEI was found to exhibit better response under NIR irradiance for non-invasive photothermal therapy of cancer.

A nanoscale photothermal agent based on a metal-organic coordination polymer as a drug-loading framework for effective combination therapy

Metallic materials are widely emerging as photothermal agents owing to their superior photothermal transduction efficiency and satisfactory photostability. In this study, an iron-based coordination polymer (Fe-CNP) loaded with doxorubicin (DOX) was assessed as a dual-function agent for photothermal therapy (PTT) and tumor-targeted chemotherapy. Fe-CNPs were synthesized by a one-step coordination reaction between Fe3+, hydrocaffeic acid, and dopamine-modified hyaluronic acid. A drug-loading method was developed to entrap DOX within Fe-CNPs through the formation of coordination bonds by Fe3+ and DOX (Scheme 1). DOX release was rapidly triggered in the cellular acidic environment and further enhanced by hyperpyrexia in the part of tumor, which will kill the remaining tumor cells after PTT. Animal experiments demonstrated complete inhibition of tumor growth without recurrence in 21 days after injection of DOX@Fe-CNPs with NIR laser irradiation. These results confirmed the enhanced anti-tumor efficiency of the chemo-photothermal nanosystem. Our work may reveal a photothermal coordination polymer as a drug-loading framework and highlight the development of metal-organic materials in combined chemo-photothermal therapy. Statement of SignificancePhotothermal therapy (PTT), which could directly act on tumors, has been considered as a promising treatment method for cancer. The combination of PTT with chemotherapy is attracting tremendous attention because such advanced application can achieve personalized precise medicine. Unfortunately, most PTT materials have photobleaching property, which results in reduced photothermal efficiency. Furthermore, their clinical applications also suffer from low loading capacity of chemotherapeutic drugs or nonbiodegradability in the biological system. In this study, we hypothesized that iron-based coordination polymers (Fe-CNPs) could function dually as agents to deliver both PTT and tumor-targeted chemotherapy by coordination loading of the chemotherapeutic drug doxorubicin (DOX). Our work may open up new avenues to rationally design versatile platforms for photothermal–chemotherapy to obtain synergistically enhanced therapeutic efficacy.

Multi-stimuli responsive nanosystem modified by tumor-targeted carbon dots for chemophototherapy synergistic therapy

In this work, a tumor-targeted and multi-stimuli responsive drug delivery system combining infrared thermal imaging of cells with thermo-chemotherapy was developed. Oxidized mesoporous carbon nanoparticles (MCNs-COOH) with high photothermal conversion ability (photothermal transduction efficiency η = 27.4%) in near-infrared (NIR) region were utilized to encapsulate doxorubicin (DOX). The outer surfaces of MCNs-COOH were capped with multifunctional carbon dots (CDHA) as simultaneous smart gatekeepers, a tumor targeting moiety and a fluorescent probe. NIR laser irradiation killed cancer cells through NIR-light induced hyperthermia, facilitated chemotherapeutic drug release and enhanced the sensitivity of tumor cells to drugs. The therapeutic efficacy in two-dimensional (2D) and three-dimensional (3D) cells demonstrated that MC-CDHA loading DOX (MC-CDHA/DOX) had good chemo-photothermal synergistic antitumor effects (combination index of CI = 0.448). The biodistribution and pharmacodynamics experiments of MC-CDHA/DOX in the 4T1 tumor model indicated that MCNs-COOH prolonged the residence time of DOX in tumor tissues and therefore actualized effective synergistic photothermal chemotherapy. By combining these excellent capabilities, the tumor-targeted and multi-stimuli responsive drug delivery system can be utilized as a visible nanoplatform for chemophotothermal synergistic therapy.

Effects of Nanoscale Structures on Photothermal Heating Behaviors of Surface-Modified Fe3O4 Nanoparticles

In this investigation, the photothermal heating of superparamagnetic Fe3O4 nanoparticles was carried out by irradiating with either 785[Formula: see text]nm or 808[Formula: see text]nm near infrared (NIR) lasers. The effects of nanoparticle configuration, arrangement, and surface coating on the photothermal heating behavior were investigated for different Fe3O4 nanoparticle systems. Depending on the preparation method, Fe3O4 nanoparticles with mean hydrodynamic diameter ranging from 30[Formula: see text]nm to 250[Formula: see text]nm were synthesized. Photothermal transduction efficiency is a measure of light to thermal energy conversion; the highest efficiency obtained was 56% by 785[Formula: see text]nm and 42% by 808[Formula: see text]nm light irradiation for poly(acrylic) acid (PAA) coated Fe3O4 samples. With this conversion efficiency, the PAA-coated Fe3O4 nanoparticles raised the solution temperature [Formula: see text] [Formula: see text]C above physiological temperature, which is sufficient for cancer therapeutics. Photothermal transduction efficiency was found to decrease as the particle hydrodynamic diameter increased. Nanoparticle absorption and scattering properties were found different due to surface modifications. UV-VIS-NIR absorption spectroscopy was carried out and results were analyzed using the Mie scattering theory. Experimental photothermal transduction efficiency was found to scale with the theoretical results for a particular wavelength. These results have significance in the design and development of the Fe3O4 nanoparticle systems for effective cancer therapy with NIR light.