- Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin, China
The rational design of the nanocarriers with active tumor targeting and specific chemotherapy for heat shock protein 90 (Hsp90) inhibition is attractive for combined chemo-photothermal therapy (PTT). Herein, a smart gold nanorod (GNR)-cored micelle (T-GNRAAG) was developed to encapsulate 17-allylamino-17-demethoxygeldanamycin (17-AAG, Hsp90 inhibitor) through a facile preparation approach. The characteristics of T-GNRAAG were evaluated both in vitro and in vivo. The designed nanoplatform possessed sufficient 17-AAG loading content and lactobionic acid-mediated active targeting for hepatoma cells. More importantly, the 808 nm laser irradiation not only initiated PTT for cell killing but also remotely triggered 17-AAG liberation within cancer cells via inducing the phase transition of poly(ɛ-caprolactone). All these features forcefully supported the effectiveness of T-GNRAAG in tumor growth inhibition. This work represents a proof-of-concept combinatorial chemo-PTT treatment.
Introduction
Photothermal therapy (PTT), which absorbs optical energy and then converts it to the thermal effect, has attracted great attention for cancer therapy because of its highly noninvasive nature, controllability, and repeatability (Abadeer and Murphy, 2016; Doughty et al., 2019; Xi et al., 2020; Zhang et al., 2021). Upon laser irradiation with deep penetration in the body, the tumoral cells would be specifically ablated by the raised temperature in tumor sites (Wang et al., 2019; Dong et al., 2020; Sun et al., 2021). Up to now, various nanoparticles with photothermal conversion have been proposed to serve as anticancer agents, such as gold nanorods (GNRs), gold nanoshells, carbon nanotubes, conjugated polymers, and small molecules (Jang et al., 2011; Chen et al., 2016; He et al., 2020a; He et al., 2020b; Li and Pu, 2020"). Except for the photothermal effect itself, phototherapeutic agents have been widely utilized in combination with chemotherapy for more advanced antitumor efficiency through distinct molecular mechanisms (Yang J-.C. et al., 2017; Xie et al., 2020; Yang et al., 2021). Even more interesting is that the photothermal effect could not only directly kill the cancer cells but also boost the chemotherapeutic agent liberation specifically in the irradiated area, thereby achieving locoregional and precise chemo-PTT. For instance, Liu et al. designed GNR-cored micelles (AuNR-M-DOX) to realize photo-triggered drug release for overcoming the multidrug resistance in MCF-7/ADR cells (Zhong et al., 2013). Tan et al. intercalated doxorubicin into a DNA immobilized on GNRs and particularly liberated it inside the cancer cells via photocontrollable thermal effect and DNA unwinding (Yi et al., 2017).
Despite great efforts, PTT has been found to be limited by overexpression of heat shock protein 90 (Hsp90) (Gao et al., 2019; Sun et al., 2019; Chen et al., 2020). During the PTT process, Hsp90 is usually upregulated in tumoral cells and is responsible for protecting the client proteins from stress-induced cellular damage (Whitesell and Lindquist, 2005; Lamb et al., 2006; Shan et al., 2021). The overexpression of Hsp90 will result in the heat resistance acquired by cancer cells and thus remarkably weaken PTT efficacy (Yang Y. et al., 2017; Li L. et al., 2020). Therefore, inhibiting the expression or function of Hsp90 is crucial for improving the efficiency of PTT (Lin et al., 2016; Long et al., 2018). Fortunately, 17-allylamino-17-demethoxygeldanamycin (17-AAG), one of the geldanamycin derivatives, has been widely studied as the Hsp90 inhibitor (Kamal et al., 2003; Saxena, et al., 2012; Liu Y. et al., 2019). 17-AAG specifically binds to the amino-terminal ATP binding pocket of Hsp90 in cancer cells and inhibits the stabilization between Hsp90 and its client proteins (Ferrario and Gomer, 2010; Hasenstein et al., 2012). Since most Hsp90 client proteins (e.g., EGFR and AKT) contribute to tumor growth, 17-AAG is obviously toxic to cancer cells (Modi et al., 2011; Rochani et al., 2016). However, its application as a chemotherapeutic agent remains a significant challenge owing to the rapid blood clearance and lack of targeting to tumor tissue in vivo (Waza et al., 2005).
To this end, we report a GNR platform capable of lactobionic acid (LA)-mediated targeting for hepatoma cells and light-controlled 17-AAG release for improving chemo-PTT efficiency (Figure 1). Because of its robust affinity to asialoglycoprotein receptor, which is overexpressed on hepatoma cells, LA has been considered as a promising ligand for targeted drug delivery to hepatocellular carcinoma (Liu H. et al., 2014; Zhang et al., 2019; Huang et al., 2020). With the help of LA moiety, the designed nanoparticles (T-GNRAAG) could achieve selective accumulation in HepG2 tumors after intravenous injection. Following internalization into tumoral cells via interaction between LA and asialoglycoprotein receptor, 808 nm laser irradiation would produce a mild PTT against HepG2 cells, and the raised temperature on the GNR surface would trigger the phase transition of the PCL component to liberate hydrophobic 17-AAG. Subsequently, 17-AAG could not only act as an Hsp90 inhibitor to induce cell cycle arrest and apoptosis but also sensitize cancer cells to PTT through regulating the pro-survival and angiogenic signaling pathways, hence realizing the synergistic chemo-PTT in the specific cells that underwent PTT (Georgakis et al., 2006; Li and Katoka, 2021; Zhu et al., 2021). The cascade-amplified chemo-PTT of T-GNRAAG and its benefits under 808 nm laser irradiation were evaluated on HepG2 tumor-bearing mice.
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FIGURE 1. Scheme of LA-targeted drug delivery and 808 nm laser-triggered AAG release for combined chemo-PTT.
Materials and Methods
Materials
Sodium borohydride, cetyltrimethyl ammonium bromide (CTAB), ascorbic acid, silver nitrate, and tetrachloroauric acid were purchased from Sinopharm Chemical Reagent Co., Ltd. CTAB-stabilized GNRs were synthesized according to reported methods (Li et al., 2013). LA functional poly(ethylene glycol)-poly(ɛ-caprolactone)-SH (LA-PEG-PCL-SH) and poly(ethylene glycol)-poly(ɛ-caprolactone)-SH (PEG-PCL-SH) were obtained from Xi’an Ruixi Biological Technology Co., Ltd. Cell Counting Kit-8 (CCK-8) was purchased from Abcam Co., Ltd. Dulbecco’s modified Eagle’s medium and fetal bovine serum were purchased from Life Technologies Corporation (Gibco, United States). All other reagents were purchased from Shanghai Aladdin Bio-Chem Technology Co., LTD., and used as received.
Preparation of 17-AAG-Loaded T-GNR
Typically, the CTAB-stabilized GNRs were washed and purified by centrifugation (14,500 rpm, 10 min) twice to remove excess CTAB. Then, the organic DMSO containing the LA-PEG-PCL-SH and PEG-PCL-SH copolymer (1:5, molar ratio) was slowly added into CTAB-stabilized GNR aqueous dispersion under vigorous stirring. After reacting for 6 h at room temperature, the T-GNR was purified through centrifugation and washing with ddH2O twice. Finally, the DMSO containing 17-AAG was mixed with T-GNR aqueous (phosphate buffer, 10 mM, pH 7.4) dispersion under mile stirring. After reaction for overnight, free 17-AAG was removed by dialysis against PB at 4°C in the dark (MWCO: 3,500 Da), and the obtained nanoparticles were denoted by T-GNRAAG. Meanwhile, the nontargeted GNRAAG was prepared following a similar method just only using PEG-PCL-SH for surface decoration.
Cellular Uptake of Targeted Nanocarriers
HepG2 cells in 12-well plates (50,000 cells per well) were incubated with GNRAAG or T-GNRAAG for 4 h. After the incubation, the cells were washed with PBS twice and treated with 0.1% Triton X-100. The internalized 17-AAG and GNRs in cell lysis were detected by UV-vis spectrophotometry and inductively coupled plasma-mass spectrometry (ICP-MS), respectively. For the confocal laser scanning microscope (CLSM) observation, ICG was encapsulated in GNRs instead of 17-AAG because 17-AAG was difficult in a fluorescence imaging application. HepG2 cells were seeded and incubated with GNRICG or T-GNRICG for 4 h. Following 4 h of incubation, the cells were washed and fixed with 4% paraformaldehyde and then stained with Alexa Fluor® 488 phalloidin and DAPI sequentially following the standard protocol. The cells were then visualized and imaged on a Zeiss LSM 810 microscope.
Cell Killing of T-GNRAAG Under Laser Irradiation In Vitro
To determine the biocompatibility of GNRs, HepG2 cells were seeded in a 96-well plate (10,000 cells per well) and incubated with GNR or T-GNR for 72 h. The cell viabilities were analyzed using a standard CCK-8 assay. To study the combined chemo-PTT efficiency, HepG2 cells were seeded in a 96-well plate (5,000 cells per well). Then, the cells were incubated with free 17-AAG, GNR, T-GNR, GNRAAG, or T-GNRAAG for 24 h. Following the replacement of blank medium without drug or nanoparticles, the cells were exposed to an 808 nm laser (200 mW/cm2, 10 min). The cell viabilities were analyzed using a standard CCK-8 assay after further incubation for 48 h.
Pharmacokinetic and Tumor Targeting of T-GNRAAG In Vivo
To study the retention of T-GNRAAG in vivo, BALB/c mice were randomly divided into three groups (n = 4). The mice received i.v. injection of free 17-AAG, GNRAAG, or T-GNRAAG (equivalent [17-AAG] = 10 μg/g body weight). At a predetermined time point postinjection (0.17, 0.5, 1, 2, 4, 8, 12, 24, and 48 h), blood samples were collected from the retroorbital plexus. After the centrifugation (3,000 rpm, 10 min), the plasma was collected and 17-AAG concentration was detected using UV-vis spectrophotometry.
To investigate the distribution in different organs of T-GNRAAG in vivo, BALB/c nude mice bearing HepG2 tumor xenografts were treated with i.v. injection of free 17-AAG, GNRAAG or T-GNRAAG (equivalent [17-AAG] = 10 μg/g body weight). At a predetermined time point postinjection (12, 24, and 48 h), the major organs and tumor tissues were harvested, washed, and weighed, and the gold atom concentration was quantified by ICP-MS.
Antitumor Activity In Vivo
HepG2 tumor-bearing BALB/c nude mice were randomly divided into six groups (n = 5). On the day when the tumor volume reached ∼100 mm3, the mice were treated with PBS, free 17-AAG, GNR, T-GNR, or T-GNRAAG ([17-AAG] = 5.0 μg/g body weight) by i.v. injections. The tumor lesion was then exposed to an 808 nm laser (0.2 W/cm2, 10 min). The tumor size and mice body weight were monitored every 3 days. The tumor volume was calculated as 0.5 × length × width2. The blood sample was collected after the treatment (day 18) for ALT, AST, and BUN detection.
Results and Discussions
Preparation and Characterization of T-GNRAAG
To prepare T-GNR with hydrophobic 17-AAG loading, CTAB-stabilized GNRs were first modified and coated with both PEG-PCL-SH and LA-PEG-PCL-SH at a molar ratio of 5:1. The unconjugated copolymers were removed by centrifugation. Then, the hydrophobic 17-AAG was encapsulated into T-GNR hydrophobic–hydrophobic interactions. The drug loading content of 17-AAG was determined using UV-vis spectra as 6.73%, and it could be increased to ∼15% by raising the feeding ratio. The transmission electron microscopy observation (Figure 2A) revealed that T-GNRAAG was well dispersed with a uniform dimension of approximately 30 nm in length and 6 nm in width. In addition, the nontargeted GNRAAG was prepared following a similar route using only PEG-PCL-SH for surface modification. Owing to the protection and stabilization by the PEG component, both GNRAAG and T-GNRAAG maintained their stability even in PBS (pH 7.4) for 168 h (Figure 2B).
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FIGURE 2. (A) Transmission electron microscope of GNRAAG and T-GNRAAG. The scale bar is 50 µm. (B) Change of hydrodynamic size in PBS solution (10 mM, pH 7.4). (C) Temperature change curves of GNRAAG and T-GNRAAG under 808 nm laser irradiation (1.0 W/cm2) at different concentrations. (D) IR thermal images of GNRAAG and T-GNRAAG (30 μg/ml) under laser irradiation (808 nm, 1.0 W/cm2).
To assess the photothermal activity of T-GNRAAG and GNRAAG, the temperature change of the T-GNRAAG and GNRAAG aqueous solution was monitored for 10 min, while the PBS was used as a negative control group. As displayed in Figure 2B, both the T-GNRAAG and GNRAAG groups exhibited laser power-dependent temperature elevation. The solution temperature was increased from 25.2°C to 55.1°C under 808 nm laser irradiation (1.0 W/cm2, 10 min) when the [T-GNRAAG] was 30 μg/ml. However, there was negligible temperature change for the PBS group, which could be attributed to the lower laser power we used. In addition, the IR thermal images further demonstrated the abovementioned results, and the temperature of the irradiated region of the T-GNRAAG and GNRAAG groups was ca. 30°C. According to the cooling curve (Supplementary Figure S1), the photothermal conversion efficiency of GNRAAG and T-GNRAAG calculated using the reported method was 39.7 and 42.7% at 808 nm (Liu S. et al., 2019), respectively, which is comparable to that of reported GNR (Almada et al., 2017).
808 nm Laser-Triggered 17-AAG Release
The hydrophobic 17-AAG was encapsulated and restrained in the amorphous PCL regions of micellar PEG-PCL outside the T-GNRAAG. Upon 808 nm laser irradiation, the PTT effect (∼60°C) would melt the hydrophobic PCL domain, leading to lower micellar stability and boosted 17-AAG diffusion (Zhong et al., 2013; Liu J. et al., 2014). To verify this assumption, we first measured the melting temperature (Tm) of GNRAAG and T-GNRAAG via differential scanning calorimetry. In comparison with bulk PCL homopolymer, whose Tm is ∼60°C (He et al., 2004), both GNRAAG and T-GNRAAG showed a slightly decreasing Tm (∼55°C, Supplementary Figure S2). The 17-AAG release profile was then evaluated by immersing the GNRAAG and T-GNRAAG in the aqueous solution at different temperatures. As illustrated in Figure 3A, a robust 17-AAG release behavior was observed when the temperature was above 55°C, which is consistent with the melting temperature (Tm) of GNR-cored micelles. Finally, the quantitative 17-AAG release under 808 nm laser exposure was studied at a 0.2 W/cm2 power density for 5 min. The pulsed laser irradiation led to 59.29 ± 3.35% and 64.42 ± 3.84% of 17-AAG release from GNRAAG and T-GNRAAG at 4 h, respectively (Figure 3B). In contrast, only ∼6.09% of total 17-AAG was detected from both nanocarriers without laser treatment. More importantly, the solution temperature of GNRAAG and T-GNRAAG was only increased by ∼5.7°C and was significantly lower than the Tm of PCL homopolymer. Collectively, the NIR irradiation is not enough to obviously warm the aqueous solution but could initiate a sufficient local photothermal effect (>55°C) on GNR surface and subsequently melt the coating PCL domain to boost 17-AAG release.
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FIGURE 3. (A) The 17-AAG release pattern from GNRAAG and T-GNRAAG in aqueous solutions at different temperatures. (B) 808 nm laser-stimulated pulsed 17-AAG release from GNRAAG and T-GNRAAG. The samples were irradiated with an 808 nm laser at specific time points indicated by the arrows.
Cellular Internalization of HepG2 Cells
In order to measure the targeted delivery of LA-modified T-GNRAAG, HepG2 cell line (human hepatocarcinoma cell line) was chosen to study the active targeting for internalization. The HepG2 cells were incubated with different formulations for 4 h, and the intracellular gold atom and 17-AAG content were determined by ICP-MS and UV-vis spectrophotometry, respectively. As displayed in Figure 4A, the gold atom concentration in lysis of HepG2 cells incubated with T-GNRAAG for 4 h (196.64 ± 27.99 μg/mg protein) was significantly higher than that of GNRAAG (131.04 ± 17.82 μg/mg protein), indicating that LA ligands substantially recognized the receptor on the cellular membrane and improved the cellular internalization. Meanwhile, the UV-vis spectrophotometry results in Figure 4B further demonstrated more 17-AAG content in the T-GNRAAG group. In the presence of free LA, the internalization of T-GNRAAG was decreased to a level that was comparable to that of GNRAAG, further suggesting the receptor-mediated endocytosis pathway of LA-decorated nanoparticles by HepG2 cells. Because of the absence of asialoglycoprotein receptor, the cellular uptake of GNRAAG and T-GNRAAG was similar on Hela cells regardless of the presence of free LA (human cervical cancer cell line, Supplementary Figure S3). The advanced cellular uptake of T-GNR was further visualized using a CLSM. Because the fluorescence of 17-AAG is weak, ICG was used to replace 17-AAG for labeling the GNRs. As expected, there was a much greater ICG (red fluorescence) distribution localized inside the cytoplasm in the T-GNRICG group (Figure 4C).
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FIGURE 4. Quantitative cellular uptake of GNRAAG and T-GNRAAG on HepG2 cells detected by ICP-MS (A) and UV-vis spectrophotometry (B). (C) CLSM observation of internalization of GNRICG and T-GNRICG on HepG2 cells. DAPI (blue) and Alexa Fluor 488 phalloidin (green) were used to stain cell nuclei and F-actin, respectively.
Cell Killing Effect of T-GNRAAG Under Laser Irradiation
According to our design, T-GNRAAG would boost the antitumor activity via LA-promoted tumoral cell internalization. Then, the thermal effect generated from GNR under 808 nm laser irradiation liberated 17-AAG release and turned on subsequent Hsp90 inhibition and PTT-specific chemotherapy. The cytotoxicity of GNR and T-GNR without 17-AAG encapsulation was first measured on HepG2 cells through the CCK-8 assay. As shown in Figure 5A, insignificant cell viability change was observed even though the GNR concentration was 500 μM. Next, the HepG2 cells were incubated with free 17-AAG, GNR, T-GNR, GNRAAG, or T-GNRAAG and received 808 nm laser treatment (0.2 W/cm2) for 10 min. Because the client proteins of Hsp90 were highly associated with tumoral cell proliferation (Talaei et al., 2019), free 17-AAG showed substantial cell killing regardless of laser irradiation (Supplementary Figure S4). The IC50 value of free 17-AAG was 7.63 μg/ml (L-). Upon laser irradiation, the negligible cell death of both the GNR + L and T-GNR + L groups suggested that such mild photothermal effect by a lower power density (0.2 W/cm2) would not induce substantial damage against HepG2 cells (Zhong et al., 2013). More importantly, the significant difference between the GNRAAG + L and T-GNRAAG + L groups at both concentrations could be explained by the increased cellular uptake of T-GNRAAG (Figure 5B). Compared to the T-GNR + L group, wherein chemotherapy was absent, the T-GNRAAG + L group further exhibited more remarkable cell killing, with only 31.72 ± 4.45% of cell viability ([17-AAG] = 10.0 μM). To demonstrate the Hsp90 inhibition effect of 17-AAG, we analyzed the Hsp90 and its client protein (e.g., survivin and Akt) expression after the various treatments ([17-AAG] = 10 μM). As shown in Supplementary Figure S5, the expression of Hsp90, surviving, and Akt was elevated after PTT to enhance the thermal resistance but significantly decreased following incubation with free or released 17-AAG, which is in agreement with previous reports (Li et al., 2019; Sun et al., 2022). These results were consistent with both laser-activated drug release and cellular uptake experiments, verifying that the definitive cell killing efficacy of T-GNRAAG + L is a result of both LA-facilitated agent delivery and combination chemo-PTT effect.
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FIGURE 5. (A) CCK-8 assay of GNR and T-GNR on HepG2 cells for 72 h. (B) Combined chemo-PTT effect of free 17-AAG, GNR, T-GNR, GNRAAG, or T-GNRAAG against HepG2 cells upon 808 nm laser irradiation. *p < 0.05.
Pharmacokinetic and Biodistribution of T-GNRAAG In Vivo
As expected, the nanocarriers with PEGylation would prolong the retention of chemotherapeutic agents in the bloodstream via reduced interaction with phagocytes. After systemic injection of different formulations, we collected the blood sample and measured the 17-AAG concentration in plasma at 0.17, 0.5, 1, 2, 4, 8, 12, 24, and 48 h. Because of the lower molecular weight, free 17-AAG was rapidly cleared from blood circulation even in the first 2 h (Figure 6A). The content of free 17-AAG was too low to be detected by UV-vis spectrophotometry at 48 h postinjection. On the other hand, both nanoparticular GNRAAG and T-GNRAAG maintained the 17-AAG concentration at 1.33 ± 0.28 and 0.70 ± 0.21 μg/ml at 48 h postinjection, respectively. Their difference after the 6 h time point could be attributed to the specific recognition and clearance of LA moiety. As shown in Figure 6B, we calculated their area under the curve (AUC0-t) based on a noncompartmental model, and GNRAAG and T-GNRAAG were found to increase 7.21- and 5.35-folds of AUC0-t than that of free 17-AAG (30.48 ± 1.34 μg/ml*h). Moreover, the t1/2 of GNRAAG and T-GNRAAG was prolonged to 22.45 ± 5.50 and 11.23 ± 1.99 h, respectively (Figure 6C).
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FIGURE 6. (A) Plasma 17-AAG concentration vs. time after systemic administration of free 17-AAG, GNRAAG, or T-GNRAAG (n = 4). The area under curve (B) and half-life (C) of free 17-AAG, GNRAAG, and T-GNRAAG. *p < 0.05 vs. GNRAAG. (D) Quantitative 17-AAG content in HepG2 tumors at 6, 12, and 24 h postinjection. (E) Quantitative 17-AAG content in major organs of tumor-bearing mice at 24 h postinjection.
Taking advantage of the LA targeting ligand, T-GNRAAG has more opportunities to interact and be internalized by hepatoma cells. To demonstrate its tumor enriching, HepG2 tumor-bearing BALB/c nude mice were treated with GNRAAG or T-GNRAAG through i.v. injection, and the GNR content in major tissues and tumors was quantitatively determined by ICP-MS at 6, 12, and 24 h postinjection. As shown in Figure 6D, the 17-AAG content of GNRAAG was 1.31 ± 0.25, 1.49 ± 0.16, and 1.41 ± 0.22 %ID/g at 6, 12, and 24 h postinjection, respectively. However, the T-GNRAAG group exhibited a more pronounced tumor accumulation, whereas the 17-AAG concentration maintained to ca. 2.12 %ID/g tumor at both 12 and 24 h postinjection. As shown in Figure 6E, both GNRAAG and T-GNRAAG are preferentially distributed in reticuloendothelial system organs (i.e., spleen and liver), which is in line with previous reports (Ernsting et al., 2013; Li X. et al., 2020).
Tumor Growth Inhibition of T-GNRAAG
Inspired by the superior effect of T-GNRAAG in blood circulation and biodistribution, we conducted antitumor experiments of T-GNRAAG in vivo using HepG2 tumor-bearing mice. Mice were randomly divided into six groups with five in each group. For both the GNRAAG + L and T-GNRAAG + L groups, mice received three dose of nano-formulation via intravenous administration on day 0, followed by the 808 nm laser irradiation (0.2 W/cm2) for 10 min. During the laser irradiation, the mice that received an injection of T-GNR or T-GNRAAG exhibited the highest tumor temperature at ∼42°C (Supplementary Figure S6). However, a limited PT effect was observed in mice injected with nontargeting GNRAAG. As shown in Figures 7A and B, the tumor volume of mice treated with negative control groups grew rapidly, and the average tumor volume reached to ∼1,350 mm3 after 18 days. Owing to the moderate tumor accumulation, the GNR + L group showed partially tumor growth inhibition with a tumor inhibition rate (TIR) of 20.27%. With the help of LA-facilitated tumor enriching, the tumor volume in the T-GNR + L group was further decreased to about 950 mm3 on day 18 after the single laser irradiation (p > 0.05 vs. the GNR + L group). More importantly, the T-GNRAAG + L group exhibited the most substantial tumor growth inhibition with a TIR of 70.45%. The comparison between the T-GNR + L and T-GNRAAG + L groups suggested that the antitumor effect was induced by a combination of PTT and chemotherapy, indicating the distinctly advanced therapeutic efficacy of such treatment. Furthermore, there was no substantial body weight loss for mice in all the groups on day 18 (Figure 7C). Additionally, liver/kidney function (Figures 7D–F) and blood routine count evaluation (Supplementary Table S1) verified the biocompatibility and biosafety of T-GNRAAG + L in vivo.
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FIGURE 7. (A) Tumor growth in HepG2 tumor xenograft-bearing BALB/c nude mice received various formulations. The i.v. injections were performed on day 0 (n = 5). (B) The HepG2 tumor mass after the treatment (day 18). *p < 0.05. (C) Body weight change of the mice during the therapeutic window. ELISA examination of ALT (D), AST (E), and BUN (F) in the serum on day 18.
Conclusion
A targeted GNR has been developed for precise agent delivery and light-controlled drug release for combined chemo-PTT. After the LA modification, T-GNRAAG achieved more tumor enrichment via the LA-mediated targeting mechanism. Under 808 nm laser irradiation, T-GNRAAG not only achieved mild PTT for hepatocellular carcinoma but also accelerated the 17-AAG release for Hsp90 inhibition and PTT-specific chemotherapy via thermal-activated PCL phase transition. Considering the spatial directivity of the NIR laser, the combined chemo-PTT functioned within tumor regions, resulting in the advanced antitumor activity in vivo. Our work offers an attractive strategy for rational designing the remotely controlled nanocarriers for precise cancer therapy.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics Statement
The animal study was reviewed and approved by the Tianjin Medical University Animal Care and Use Committee.
Author Contributions
ZZ: conceptualization, investigation, writing–original draft, and writing–review and editing; CS: conceptualization, investigation, funding acquisition, supervision, and writing–review and editing.
Funding
This research was funded by the National Natural Science Foundation of China (82071907), Natural Science Foundation of Tianjin (18JCYBJC25100, 18JCQNJC80200), Health Science and Technology project of Tianjin (MS20022), Wu Jieping Medical Foundation Special Fund for Clinical Research (320.6750.2022-3-5), Tianjin Medical University General Hospital (ZYYFY2016041), and Tianjin Key Medical Discipline (Specialty) Construction Project.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmats.2022.931682/full#supplementary-material
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Keywords: lactobionic acid targeting ligand, gold nanorod, chemotherapy and photothermal therapy, on-demand drug release, Hsp90 inhibitor
Citation: Zhang Z and Sun C (2022) Lactobionic Acid-Navigated Gold Nanorods With Light-Triggered “on-Demand” Drug Release for Synergistic Photothermal-Chemotherapy. Front. Mater. 9:931682. doi: 10.3389/fmats.2022.931682
Received: 29 April 2022; Accepted: 01 June 2022;
Published: 06 July 2022.
Edited by:
Huaqiong Li, University of Chinese Academy of Sciences, ChinaReviewed by:
Junjie Li, Innovation Centre of NanoMedicine (iCONM), JapanChang-Ming Dong, Shanghai Jiao Tong University, China
Copyright © 2022 Zhang and Sun. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Chunyang Sun, chysun412@163.com