NIR Laser Responsive Nanoparticles for Ovarian Cancer Targeted Combination Therapy with Dual-Modal Imaging Guidance

Abstract

Purpose

Multifunctional nanoparticles with targeted therapeutic function and diagnostic-imaging are of great interest in the domain of precision therapy. NIR laser responsive nanoparticles (PLGA-PEG-FA encapsulating Bi₂S₃, PFP, and Dox (designed as FBPD NPs)) are synthesized for ovarian cancer targeted combination therapy with CT/PA dual-modal imaging guidance (PA: photoacoustic; CT: X-ray computed tomography).

Methods and Results

The FBPD NPS prepared by the double emulsification method revealed excellent dispersity, great stability, outstanding optical properties. The temperature of FBPD NPs increased rapidly after laser irradiation, inducing liquid-to-gas conversion of perfluoropentane (PFP), and promoting the release of Dox up to 86.7%. These FBPD NPs demonstrated their outstanding imaging capability for both PA and CT imaging both in vitro and in vivo, providing the potential for therapeutic guidance and monitoring. Assisted by folic acid, these nanoparticles could highly enrich in ovarian tumor tissue and the accumulation peaked at 3 h after intravenous administration. The desirable photothermal-conversion efficiency of the nanoparticles combined with chemotherapy achieved highly efficient therapy, which was demonstrated both in vitro and in vivo.

Conclusion

We successfully constructed multifunctional theranostic FBPD NPs for highly efficient PTT/chemotherapy combined therapy with dual CT/PA imaging guidance/monitoring. The unique nanoparticles with multiple abilities pave an emerging way toward precise treatment of ovarian cancer.

Keywords:

• bismuth sulfide
• folic acid
• chemotherapy
• photothermal therapy

Introduction

Ovarian cancer is the deadliest gynecological malignancy and one of the main causes of cancer death among women.¹,² According to American Cancer Society (ACS), it is estimated that there are around 22,240 new diagnoses of ovarian cancer and 14,070 deaths every year. No obvious symptoms and the lack of specific screening method in the early stage of ovarian cancer leads to the lethality. Thus, ovarian cancer is usually diagnosed in the advanced stages (stage III and IV) and the five-year survival rate declines substantially (39% for stage III and 17% for stage IV).³ Although conventional treatments, including surgery, chemotherapy, radiotherapy, etc., have proved to be efficient, they are often associated with certain unignorable weaknesses, such as immune system depletion, high cost, patient nonadherence, tumor recurrence and drug resistance.^4–7 These clinical problems have accordingly heightened the need for more specific and effective tumor treatment. These potential therapeutic strategies should meet the rigorous demands of precise killing effect without damaging normal cells/tissues.⁸

Among all the traditional treatments, chemotherapy is the most commonly used method for tumor treatment.⁵,⁹ As one of the most widespread anthracycline anti-cancer drugs, doxorubicin (Dox), as an ordinary Food and Drug Administration (FDA) approved anti-cancer drug, kills tumor cells through a series of nuclear events, including DNA damage and apoptosis.¹⁰,¹¹ However, the clinical application of Dox remains challenging due to its low aqueous solubility, inadequate accumulation, and nonspecific distribution.¹² In the meanwhile, the systemic medication is always inevitably accompanied by various side effects, such as cardiac toxicity, gastrointestinal, and bone marrow suppression.¹³ In order to mitigate the aforementioned adverse effects, drugs are encapsulated by nanoparticles for precise delivery owing to their incomparable advantages such as non-toxicity and enhanced biocompatibility.¹⁴,¹⁵ More importantly, nanoparticles have been proved to boost drug solubility significantly and minimize the systematic toxicity of traditional antitumor agents, strengthening the therapeutic index ultimately.¹⁶ Poly lactic-co-glycolic acid (PLGA) is a widely used FDA-approved biodegradable material for anti-cancer drug delivery.¹⁷ The diameter of PLGA nanospheres was described to be small enough to enable passive tumor targeting through the increased permeation and retention (EPR) effect.¹⁸ Thus, in this study, a Dox-loaded PLGA nanoparticle (PLGA-Dox) is applied for ovarian cancer treatment. In order to enhance the efficiency of cancer treatment, folic acid (FA) was chosen as the target as it is imperative in DNA synthesis and replication, cell proliferation, survival, and growth.¹⁹ Noticeably, the FA receptor could be overexpressed in various tumor cells but rarely distributed in normal cells. Also, FA has been recognized to have several advantages such as lower molecular weight, immunogenicity, relatively high stability, and ease of modification.¹⁴,¹⁵,²⁰

In recent years, photothermal therapy (PTT) has been performed as an emerging cancer treatment. Heat generated from the assimilation of optical energy via light-assimilating agents accumulated in the tumor area of post-NIR irradiation to kill tumor cells/tissues.²¹,²² Compared with visible light and ultraviolet, NIR laser is a safe light because of the little hurt to healthy and deep penetration.²³ Despite the efficient tumor ablation of PTT, the application is limited by the possible tumor reoccurrence induced by deficient hyperthermia or asymmetrical heat delivery within tumor areas.²⁴ One probable approach to optimize their therapeutic effects is to combine PTT with other types of treatments. It was reported that PTT and chemo-drug synergistically enhance the antitumor effect to a great extent.^25–29 Due to the post-X-ray bombardment, the secondary electrons were distributed to enhance the EPR effect, and consequently, high-Z nanomaterials could optimize the passive tumor targeting. As the atomic number is positively related to the photoelectric interaction, Bi nanoparticles are better than other elements.³⁰ Therefore, we considered bismuth sulfide (Bi₂S₃) as a PTT agent on account of its outstanding biocompatibility and imaging performance. Furthermore, perfluoropentane (PFP), as a phase change material, would trigger the liquid–gas phase conversion and result in the generation of bubbles post laser irradiation, which could accelerate the tumor cell uptake of Dox.³¹

Overall, with the rapid evolution of diagnostic-image technique, molecular imaging has been recognized as a burgeoning methods for accurate diagnosis guaranteed with high sensitivity and resolution. The establishment of multipurpose probes with the integrated function of cancer-targeting, imaging, and therapeutics are fundamental for accurate oncology.³² In contrast to other different imaging methods, X-ray computed tomography (CT) is a mainstream clinical diagnostic strategy with advantages such as high resolution, little depth limitation, and permitting for three-dimensional (3D) reconstruction.³³ Besides, various internal limitations of CT imaging, especially low soft-tissue contrast and limited approachability, are vital factors that hinder the use of CT for clinical diagnosis.³⁴,³⁵ The performance of precision diagnosis can be optimized by the integration of CT with other imaging strategies that can uncover their preponderances. Comparatively, photoacoustic (PA) imaging, a nonionizing imaging form, transforms photon energy into acoustic pressure waves to obtain pictures, offering comparatively deeper tissue penetration because of the less scattering of acoustic waves than light.⁸,³⁶ Therefore, the design and synthesis of a therapeutic agent have become a major area of interest to effectuate the dual-modal imaging-guided treatment and concurrently maximize the virtue, safety, and precision of cancer treatment.

Herein, we designed the FA-targeted multifunctional NPs loading with Dox, Bi₂S₃ and PFP to achieve an appealing tumor-targeted and dual-modal imaging-guided ovarian cancer combination therapy. In this nano-system, Bi₂S₃ was used as the imaging contrast agent and PTT agent, while Dox served as the chemotherapy drug for the treatment of ovarian cancer. PFP as a phase change material was further encapsulated in PLGA. After intravenous administration of FA-Bi₂S₃-PFP-Dox-PLGA NPs (described as FBPD NPs), these NPs availably accumulated into the tumor area assisted by active FA targeting after been injected into the mouse. Subsequently, the investigations in vitro and in vivo proved that the FBPD NPs manifest an excellent synergistic effect of PTT and chemotherapy with the guidance of CT and PA imaging, which considerably inhibited the tumor growth in mouse ovarian cancer models (Figure 1).

Figure 1 Schematic illustration of the multipurpose nanoplatform for availably CT/PA imaging-guided combination therapy to tumor cells/tissue.

Materials and Methods

Materials

Dox was purchased from Beijing Bailingwei Technology Co., Ltd. (Mw=579.99, China). Bi₂S₃ modified by oleic acid and PLGA-PEG-FA were obtained from Xi’an Ruixi Biological Technology Co., Ltd. (China). Perfluoropentane (PFP) was obtained from Strem Chemicals, Inc. (America). Cell Counting Kit-8 (CCK-8) was obtained from Dojindo (Japan). The 2-(4-Amidinophenyl)-6-indolecarbamidinedihydrochloride (DAPI) and Trypsin-EDTA solution (0.25% trypsin) were obtained from Beyotime Technology. Dichloromethane (CHCl₂) and isopropyl alcohol were obtained from Chongqing Chuan Dong Chemical Co., Ltd. (China). Poly (vinyl alcohol) (PVA), 1,1′-dioctadecyl-3,3,3′,3′- tetramethylindotricarbocyanine iodide (DiR) and Dialysis membrane (10000–12000Da) were obtained from Sigma-Aldrich Chemical Co., Ltd. (MW: 25000, America). McCoy’s 5A was obtained from Procell Life Science&Technology Co., Ltd.

Synthesis of FBPD NPs

PLGA-PEG-FA encapsulating Bi₂S₃, PFP, and Dox (designed as FBPD NPs) was manufactured by a double emulsion (water/oil/water: W/O/W) method.³⁷ First, 10 mg of Dox dissolved in 200 µL of double distilled water; Then 400 µL of PFP was added to the above solution, followed by a probe sonication under the ice bath (100 W, 1 min). And 200 µL of Bi₂S₃ and 50 mg PLGA-PEG-FA were dissolved in 3 mL of CHCl₂, which was mixed with the mixture prepared before. Immediately, the compound was emulsified with an ultrasonic probe to form the initial emulsion (100 W, 3 min, ice bath). For the second emulsion, 8 mL of PVA (w/v = 4%) was joined into the initial emulsion and mixed by probe sonication for 2 min (100 W, ice bath). Subsequently, the second emulsion was diluted in 10 mL of isopropyl alcohol solution (w/v=2%), and the as-prepared emulsion was stirred at an ice bath for 3 hours to volatilize CHCl₂ fully. Finally, the FBPD NPs were collected after the centrifugation (10,000 rpm, 5 min, 4°C). As for the preparation of FBP NPs or BPD NPs, the difference lies in the removal of FA or Dox. All operations were carried out in dark.

The Characterization of FBPD NPs

Scanning electron microscopy (SEM, Hitachi S-3400N, Japan) and transmission electron microscopy (TEM, Hitachi H-7600, Japan) were used to characterize the morphology and structure of the FBPD NPs. The zeta potential, average diameter and the polydispersity index (PDI) were determined by Malvern Zetasizer Nano ZS instrument (Malvern Instruments, UK). A UV−vis spectrophotometer (UV-3600, Shimadzu, Japan) was used to assess the UV−vis absorption spectra. The concentration of Dox was determined by a standard curve method using a UV−vis spectrometer. The concentration of Bi₂S₃ was confirmed by inductively coupled plasma mass spectrometry (ICP-MS). The in vivo circulation half-life of the FBPD NPs was also confirmed by inductively coupled plasma mass spectrometry (ICP-MS).

The release of Dox in vitro under laser irradiation was assessed by dialysis.⁸ FBPD NPs were transferred into dialysis bags (MWCO:10,000 Da) that were placed into 50 mL PBS, with stirring (150 rpm) at 37°C. FBPD NPs were irradiated with laser (1.5 W, 10 min) or not before stirring. A 1 mL of dialysate was aliquoted from the flask at different points (1, 2, 3, 4, 6, 12, 24, and 48 h), and 1 mL fresh PBS was added to the flask to remain constant volume. All samples were stored in −20°C before measurement. The absorbance of Dox in the above solutions was measured by UV-Vis spectrophotometer.

Cell Culture

The human ovarian cancer SKOV-3 cell line was acquired from Procell Life Science & Technology Co., Ltd. The cells were cultivated in McCoy’s 5A medium and maintained in an incubator with 5% CO₂ at 37°C. When the cells were observed under the microscope to reach the logarithmic growth phase, 0.25% trypsin-EDTA was employed to harvest the cells for follow-up experiments.

In vitro Cytotoxicity Assay of FBPD NPs

The SKOV-3 cells were cultivated in 96-well culture plates at a density of 1×10⁴ cells/well in McCoy’s 5A medium at 37 °C in the condition of 5% CO_2, although the cells adhere to the plates. Then, fresh culture medium containing NPs at the concentration of 2 mg/mL was used to substitute the above culture medium. Incubation of 3 h later, the viability of cells was evaluated by the CCK-8 assay. Partial experimental group were treated by laser at an intensity of 1.5 W/cm2 for 5 min. Eight treatment groups were set up in this experiment: the control group (Control), the group subjected to laser only (Laser only), the group operated with FBP NPs (FBP NPs), the group operated with FBP NPs and laser (FBP NPs + laser), the group operated with BPD NPs (BPD NPs), the group operated with BPD NPs and laser (BPD NPs + laser), the group operated with FBPD NPs (FBPD NPs), and the group operated with FBPD NPs and laser (FBPD NPs + laser). Finally, the viability of the cells was assessed by a standard CCK-8 assay.

In vitro Targeting Ability of FBPD NPs

The cellular uptake effect of FBPD NPs was assessed by confocal laser scanning microscopy (CLSM) and flow cytometry. SKOV-3 cells in logarithmic growth were seeded into CLSM-exclusive culture dishes at a density of 1×10⁵ cells/well. After 24 h of culture, FBPD NPs and BPD NPs were added separately and incubated 0.5, 1, 2, 3, and 4 h, respectively. After co-incubation with nanoemulsions, the cells were washed with PBS, and fixed in paraformaldehyde (4%) for 15 min. After fixing the cells, SKOV-3 cells were incubated with DAPI fluorescein (300 μL) for 15 min. Ultimately, these fluorescence pictures were obtained through CLSM. Furthermore, the quantitative intracellular uptake of FBPD NPs and BPD NPs was analyzed with flow cytometry. In detail, the cells were digested with trypsin (0.25%) after incubation with FBPD NPs or BPD NPs, and then suspended in PBS immediately. Finally, the flow cytometry was used to assess the phagocytosis rate.

In vitro and in vivo CT Imaging

A clinical CT-imaging system (General Electric Company, America) was used to conduct CT-imaging. FBPD NPs dissolved in PBS at different concentrations (0, 1, 2, 3, 4 and 5 mg/mL) were placed in a 2 mL Eppendorf tube for CT imaging in vitro. The imaging parameters were set as follows: 170 mA, 80 kV, and 0.625 mm. The CT-signal intensities of ROI were measured. In the experiment of CT-imaging in vivo, SKOV-3 tumor-bearing mice were i.v. injected with FBPD NPs or BPD NPs solution (200 µL, 5 mg/mL). Then, CT imaging was conducted at different time points (0, 0.5, 1, 2, 3, 4, 6, and 24 h). Average CT signal intensity (SI) of the tumor area of the same slice was measured.

In vitro and in vivo PA Imaging

A Vevo LAZR Photoacoustic Imaging System (VisualSonics Inc., Toronto, Canada) was employed to obtain PA images. For in vitro PA imaging, different concentrations of FBPD NPs (0, 1, 2, 3, 4, and 5 mg/mL) were dissolved in PBS, which was used for PA signal inspection and to assess the linear relation of the PA signal as a function of FBPD NPs concentration. As for PA imaging in vivo, the images were surveyed using SKOV-3 tumor-bearing mice, which were configured into two groups (FBPD NPs and BPD NPs) (n=3). After i.v. injecting 200 µL (5 mg/mL) BPD NPs or FBPD NPs solution, the homologous PA images were recorded at different time points (0, 0.5, 1, 2, 3, 4, 6 and 24 h). Then, the PA signal intensity of each sample was analyzed by Vevo LAZR software.

In vitro Photothermal Imaging and Photo-Induced Phase Change Experiment

In order to verify the PTT effect, the FBPD NPs at different concentrations (0, 1, 2, 3, 4, and 5 mg/mL) was exposed to an 808 nm laser (1.5 W/cm², 5 min), and the infrared thermal images and temperature were reserved by an infrared thermal imaging camera (Fotric 226, China). To further show the photothermal stability of Bi₂S₃, the NPs were irradiated by NIR laser (1.5 W/cm²) for 5 min (laser on), then naturally cooled to room temperature (laser off) for five cycles to indicate the cyclical temperature change of FBPD NPs. The infrared thermal images were also recorded. Furthermore, in the experiment of FBPD NPs photo-induced phase changed, the FBPD NPs were placed on an inverted fluorescence microscope post laser irradiation, and the changes before and after the irradiation were recorded.

Animal Model

All animals (female nude mice with the weight of 16–20 g and age of 6–8 W) were obtained from Chongqing Tengxin Biotechnology Co., Ltd. All the operation were executed under direction ratified by the Institutional Animal Care and Use Committee of Chongqing Medical University. To construct SKOV-3 tumor-bearing mice models, SKOV-3 cells were suspended into McCoy’s 5A medium and then injected subcutaneously to the flank of nude mice.

In vivo Targeting Ability of FBPD NPs

To study the distribution of FBPD NPs in vivo, six SKOV-3 tumor-bearing mice were divided into two groups: FBPD NPs group and BPD NPs group (n=3). Firstly, all the mice were injected with FBPD NPs or BPD NPs (200 µL, 5 mg/mL) intravenously; then, the fluorescence pictures were collected at certain moments (0, 0.5, 1, 2, 3, 4, 6, and 24 h) after injecting NPs by a fluorescence system (Fx7 Ir Spectra, Vilber Lourmat, France). The excitation and emission wavelengths of 748 nm and 780 nm.

In vivo Tumor Growth Inhibition of FBPD NPs

To further evaluate the in vivo chemotherapy/photothermal efficacy of FBPD NPs, eight groups were established as the in vivo experiment (n=5). When the tumor volume reached approximately 50–80 mm³, the SKOV-3 tumor-bearing mice were subjected to different treatments as follows: a. the group was i.v. injected with saline solution (200 µL) (control group); b. the group was treated with laser only (1.5 W/cm², 5 min) (Laser only); c. the group was i.v. injected with FBP NPs (200 µL, 5 mg/mL) (FBP NPs); d. the group was i.v. injected with FBP NPs (200 µL, 5 mg/mL) followed by 808 nm laser (1.5 W/cm², 5 min) 3 h later (FBP NPs + laser); e. the group was i.v. injected with BPD NPs (200 µL) at the concentration of 5 mg/mL (BPD NPs). f. the group was i.v. injected with BPD NPs (200 µL, 5 mg/mL) followed by 808 nm laser (1.5 W/cm², 5 min) 3 h later (BPD NPs + laser); g. the group was i.v. injected with FBPD NPs (200 µL, 5 mg/mL) (FBPD NPs); h. the group was i.v. injected with FBPD NPs (200 µL, 5 mg/mL) followed by 808 nm laser (1.5 W/cm², 5 min) 3 h later (FBPD NPs + laser). After various treatments, the changes in tumor-volume and the weight of each mouse were recorded every two days. The relative tumor volumes V/V₀ (V₀: the initial tumor volume before the treatment) were used to express the tumor-volume changes. The tumor tissues and the main organs (heart, liver, spleen, lung, and kidney) of one mouse of each group were collected after treatment, and then steeped in a 4% paraformaldehyde solution. Ultimately, the primary organs were stained with H&E, and the tumor were stained with H&E, TUNEL and PCNA for histopathological analysis.

Biosafety Assay of FBPD NPs

Twenty-five Balb/c mice were i.v. injected with FBPD NPs (5 mg/mL, 200 µL) and were divided into five groups (1, 3, 7, 14, and 28 days after the injection). Five Balb/c mice were injected with saline as the control group. Blood samples were used for the blood index including routine blood and biochemistry, and the major organs were used for H&E staining.

Statistical Analysis

All statistical analyses were executed with SPSS 20.0 software. Data were offered as mean ± standard deviation. The significance of the data is analyzed according to a Student’s t-test: *P < 0.01.

Results and Discussion

Design, Synthesis, and Characterization of FBPD NPs

The multipurpose FBPD NPs were synthesized following the strategy as shown in Figure 2A. The double-emulsion approach to synthesize FBPD NPs has been reported by our group before has been skillfully operated.³⁸ A series of characterizations have been conducted on the as-synthesized NPs. The TEM images (Figure 2C) showed that the FBPD NPs had a well-defined spherical shape, and the SEM image (Figure 2B) revealed that homogeneous size distribution of FBPD NPs. The mean hydrodynamic diameter of the FBPD NPs was 236.2 ± 33.17 nm (Figure 2D). The PDI values of the FBPD NPs were 0.147, demonstrating a narrow size distribution of these fabricated nanoparticles. The size range indicated that it could readily transport in the blood vessel and accumulate into tumor tissue via the representative enhanced permeability and retention (EPR) effect.³⁷ In addition, the zeta potential of FBPD NPs was (−7.99 ± 6.66) mV, a favorable negative potential. The negative zeta potential may facilitate the nanodroplets to repel each other and prevent aggregation in vivo. Furthermore, as has been proved recently, different drug delivery systems with a negatively charged surface are generally less toxic compared to the positively charged ones.³⁹ UV-spectra of Dox dispersed in saline at different concentrations (0, 25, 30, 35, 40, 45 and 50 µg/mL) and the corresponding relationship between concentrations of Dox and absorbance (Figure 2E and F). The EE and DL of Dox were calculated by UV spectrophotometry, the EE and DL of Bi₂S₃ were calculated by ICP-MS. The EE was (87.48 ± 0.19%) for Bi₂S₃ and (25.21 ± 3.05%) for DOX, respectively. The DL was (3.38 ± 0.07%) for Bi₂S₃ and (4.07 ± 0.49%) for DOX, respectively. The result displayed that FBPD NPs could carry oil-solute and soluble drugs. While these FBPD NPs could act as photothermal conversion agents for therapeutic tumor ablation, due to its excellent imaging performance, these FBPD NPs could be potentially used as contrast agents for CT and PA simultaneously, offering guidance for subsequent photothermal ablation and evaluating the potential of treatment results. To study the systemic circulation time of FBPD NPs, 200 μL of 5 mg∕mL FBPD NPs were injected into three mice. At various time points after the injection, 10 μL of blood was collected from the eye socket of the mice for ICP-MS analysis. As shown in Figure S1, the elimination half-life was calculated as 3.77 h for the FBPD NPs and the concentration of FBPD NPs in the body was only 3.5 μg/mL at 24 h, demonstrating that the FBPD NPs are excellent in vivo clearance and have the potential to be a good contrasting agent.

Figure 2 Morphology and characterization. (A) Schematic diagram for the fabrication of FBPD NPs. (B) SEM and (C) TEM of FBPD NPs. (D) Size distribution of FBPD NPs. (E) UV-spectra of Dox dispersed in saline in different concentrations (20, 25, 30, 35, 40, 45, 50 µg/mL) and (F) corresponding relationship between concentration of Dox and absorbance. (G) In vitro release of DOX in FBPD NPs with or without laser irradiation.

Different releasing behaviors were observed for Dox for FBPD NPs when in the presence and absence of laser irradiation (Figure 2G). The percentage of Dox released almost reached 46.2% at 4 h after laser irradiation, while the percentage of Dox released reached 49.7% at 48 h in the control group. This is probably due to the addition of phase-changing PFP into the FBPD NPs. The laser irradiation triggered the liquid–gas phase conversion and subsequently induced a faster release of Dox.

In vitro Cytotoxicity Assay of FBPD NPs

The cytotoxicity against SKOV-3 cells was assessed by the CCK-8 protocol. As shown in Figure 3, the cell viabilities of the FBPD NPs + Laser group was only 9.6%, demonstrating that the combination of PTT and drug-loaded nanoparticles with active targeting ability could significantly improve the killing efficiency. In addition, the cell viabilities of FBP NPs + laser group was 14.1%, ranking second to FBPD NPs + laser group. In contrast, the FBP NPs group exhibited 99% cell survival rate, demonstrating almost no killing effect on ovarian cancer cells. This result indicated that PTT is an efficient way for partial tumor remedy utilizing light-responsive nanoparticles and light source. Normally, NIR light-responsive nanoparticles including Bi₂S₃ are irradiated by an NIR laser producing heat, which triggers cancer cell death. However, in the absence of laser irradiation and chemotherapy drugs, FBP NPS did not cause damage to cells, indicating that Bi₂S₃ has a good biosecurity. Furthermore, the cell survival rate of BPD NPs group showed significantly higher than that of FBPD NPs group, approximately 1.9-fold than the latter group, demonstrating that FA could effectively increase the active targeting ability of nanoparticles and facilitate the efficient delivery of drugs into tumor cells, thus enhancing the therapeutic effect of tumor.

Figure 3 Relative cell viability of SKOV-3 cells after different treatments (n = 3, *p < 0.01).

In vitro Targeting Ability of FBPD NPs

Efficient cellular uptake of NPs the requirement to guarantee their therapeutic efficacy. Folate has been shown to increase the cellular uptake of nanocarrier systems by targeting the folate receptor.⁴⁰ Confocal microscopy and flow cytometry were used to investigate the intracellular uptake of FBPD NPs. As shown in CLSM images, NPs contained Dox present red fluorescence, and DAPI-labeled SKOV-3 cells exhibit blue fluorescence (Figure 4A). As expected, in the treatment group, numerous FBPD NPs with red fluorescence were internalized within the cells after 3 h of co-incubation. On the other hand, only a few BPD NPs assembled within the cells in the control group. Flow detection shows the same trend (Figure 4B). The intercellular uptake of FBPD NPs and BPD NPs was in a time-dependent manner within 3 h of incubation, indicating that both nanoparticles could enter the cells. But with the guidance of FA, intercellular uptake efficacy of FBPD NPs was much higher than that of BPD NPs. Especially after 3 h of incubation, the uptake of FBPD NPs by the SKOV-3 cells reached the peak. The results revealed that FBPD NPs could deliver Dox more efficiently into FA-receptor overexpressed cells.

Figure 4 In vitro targeting ability. (A) Intracellular uptake of BPD NPs and FBPD NPs as observed by CLSM after various intervals of incubation. The scale bars are 100 µm. (B) Flow cytometry analysis of intracellular uptake of BPD NPs and FBPD NPs.

In vitro and in vivo CT Imaging

Based on deep tissue penetration and 3D structure imaging advantages, CT imaging is one of the most helpful diagnostic methods.⁴¹,⁴² The high atomic number of bismuth has strong X-ray absorption ability, which can significantly improve the contrast of CT imaging. Furthermore, bi-nanoparticles have the advantages of low toxicity, small particle size, long blood circulation time, and surface modification.⁴³ Therefore, the experiment investigated the CT contrast imaging both in vitro and in vivo of FBPD NPs. When in vitro, it has been found that as the concentration of FBPD NPs increased, the CT signal value also increased and showed a good linear relationship (Figure 5A). The CT imaging property in vivo was further evaluated on SKOV-3 tumor-bearing mice. As shown in Figure 5C, after i.v. injection of FBPD NPs or BPD NPs, the group of FBPD NPs showed a distinct bright effect within the tumor area. The CT signal intensities of the tumor regions were measured with Pacs software, and it showed that the CT signal value peaked at 3 h (Figure 5B). Furthermore, the pseudo-colored images were also recorded, it clearly indicated the increase of CT imaging. This result demonstrated that the targeted nanoparticles coated with Bi₂S₃ could effectively gather in the tumor area and efficiently enhance the effect of CT imaging.

Figure 5 In Vitro and In Vivo CT Imaging. (A) In vitro CT contrast images and CT values of FBPD NPs at different concentrations. (B) In vivo CT images of tumors on SKOV-3 tumor-bearing mice after i.v. injection of BPD NPs or FBPD NPs as recorded at different time points (0, 0.5, 1, 2, 3, 4, 6, and 24 h). The top row shows black and white images, and bottom row represents the pseudo-colored images. (C) Changes of CT-signal intensities within tumor regions at corresponding time points.

In vitro and in vivo PA Imaging

To evaluate the capability of FBPD NPs as a PA probe, PA images were obtained using FBPD NPs as the contrast agent both in vivo and in vitro. Compared with other imaging methods, PA imaging has very high sensitivity.²⁴ Bi₂S₃ has been used as a PA contrast agent because of its strong absorbance in the NIR region.⁴¹ While applied in vitro, PA imaging performance of FBPD NPs dispersed in PBS at different concentrations was recorded (Figure 6A). Furthermore, the PA signal intensities increased linearly with the concentration of NPs increased from 1 to 5 mg/mL, suggesting that FBPD NPs could efficiently transform the absorbed energy into heat and trigger ultrasonic wave subsequently. During the in vivo assessment, PA imaging of SKOV-3 tumor-bearing mice was conducted at different time points after i.v. injection of FBPD NPs or BPD NPs (Figure 6B), and the relevant quantitative analyses of PA intensities were executed (Figure 6C). Before i.v. injection, the tumor showed only a weak PA signal. The PA signal reached the maximum approximately 3 h after injection with FBPD NPs. The reason could be the actively tumor-targeting induced by FA modification tumor cells at 3 h, and specifically bind to the folate-receptor on the tumor surface resulting in a high degree of accumulation of FBPD NPs in the tumor. In contrast to the FBPD NPs injection, few PA signal was discovered after BPD NPs injection. These results demonstrated that FBPD NPs could be served as a excellent contrast agent for PA imaging, which achieves diagnostic-imaging guidance and monitoring during tumor therapy.

Figure 6 In vitro and in vivo PA imaging. (A) In vitro PA contrast images and PA values of FBPD NPs at different concentrations. (B) PA images of tumor regions in SKOV-3 bearing-mice after i.v. injections of BPD NPs or FBPD NPs at varied time intervals (0, 0.5, 1, 2, 3, 4, 6, and 24 h). (C) PA signal at tumor regions in SKOV-3 tumor-bearing mice.

Photothermal and Photo-Induced Phase Change Performance of FBPD NPs

To assess the photothermal performance of FBPD NPs, the temperature changes of FBPD NPs aqueous solution were recorded by an infrared thermal imaging camera after the NIR irradiation (808 nm). After laser irradiation at 1.5 W/cm² for 5 min, FBPD NPs showed a rapid temperature increase at all concentrations. FPBD NPs revealed a rapid temperature increase of more than 50°C at the maximum concentration of 5 mg/mL after the laser irradiation. Comparatively, the PBS did not show any obvious temperature rise as the given conditions (Figure 7A), indicating that the existence of FBPD NPs can effectively and quickly transform NIR light into thermal energy. During the laser on-off cycles, the maximum temperature of FBPD NPs did not drop significantly after the cycle, indicated that it has good thermal stability (Figure 7B).

Figure 7 Photothermal and Photo-induced Phase Change performance. (A) Plot of temperature change (ΔT) of PBS and FBPD NPs at different concentrations (0, 1, 2, 3, 4, and 5 mg/mL) as a function of irradiation duration using an 808 nm laser (1.50 W/cm²). (B) Cycled heating profiles of FBPD NPs (concentration: 100 μL, 5 mg/mL) irradiated by an 808 nm laser (1.50 W/cm²) for five laser on/off cycles. (C) The imaging of FBPD NPs under the optical microscope before an 808 nm laser (1.50 W/cm²). (D) The imaging of FBPD NPs under the optical microscope after an 808 nm laser (1.50 W/cm²).

In the experiment of photo-induced phase change, before laser irradiation, FBPD NPs did not change significantly under the optical microscope (Figure 7C); After exposed to laser irradiation, FBPD NPs undergone a liquid–gas phase change, and the volume of FBPD NPs increases significantly (Figure 7D). This result indicated that the NPs could easily transform into gas while heating to physiological temperature due to the lower boiling point of PFP.²¹ The PFP had eventuated a phase change after being heated, then resulted in increase in the size of the FBPD NPs, which was subsequently more helpful for the release of drugs and the thermal ablation effect in the tumor area.

In vivo Targeting Ability of FBPD NPs

To further verify the targeting efficiency in vivo, the SKOV-3 tumor-bearing mice model was created, and fluorescence pictures were executed at certain time points after the intravenous administration with DiR-labeled FBPD NPs or BPD NPs. After injection of DiR-stained FBPD NPs, strong fluorescence signals were observed in the tumor area, while only weak signals were found in tumors in mice treated with DiR-stained BPD NPs (Figure 8A). According to Figure 8B, the fluorescence intensities with tumor regions reached a peak at 3 hours after FBPD NPs administration. Furthermore, in order to determine the distribution of NPs in the body, main organs and tumors were collected 24 hours post-injection for excised fluorescence imaging (Figure 8C), and the relevant fluorescence intensities were quantified (Figure 8D). As shown, strong fluorescence signals highlighted the liver and spleen tissues in both two groups because of the phagocytosis of the reticuloendothelial system (RES). Moreover, the fluorescence intensity of the tumor in FBPD NPs group showed significantly stronger than that in BPD NPs group, approximately 1.96-fold than the latter group. These results revealed that FBPD NPs show an effectively selective accumulation in tumor.

Figure 8 In vivo targeting ability. (A) In vivo fluorescence imaging and tumor targeting of a mouse at 0, 0.5, 1, 2, 3, 4, 6, and 24 h post-injection of SKOV-3 tumor-bearing mice. (B) Quantitative fluorescence intensity of tumor tissue at different times (n = 3). (C) Bio-distribution of DiR-labeled BPD NPs or FBPD NPs in major organs excised from mice at 24 h post-injection. (D) Quantitative bio-distribution of BPD NPs or FBPD NPs in mice as determined by the average FL intensities of organs and tumors (n = 3).

In vivo Cytotoxicity Assay of FBPD NPs

The combination of PTT and chemotherapy, an efficient therapy for tumors, causes less damage to surrounding normal tissues. According to cytotoxicity assay in vivo, eight groups (control, laser only, FBP NPs group, FBP NPs + laser group, BPD NPs group, BPD NPs + laser group, FBPD NPs group, and FBPD NPs + laser group) were performed to evaluate the therapeutic efficacy. After conducting different treatments, the inhibitory effect on SKOV-3 tumor growth is shown in Figure 9B. The volumes of tumor and the weights of mice were measured every two days (Figure 9C and D); meanwhile, photographs of these mice were taken every two days for fourteen days after the therapy (Figure 9A). The effect of chemotherapy could be fully verified by comparing the FBPD NPs + Laser group and FBP NPs + Laser group. It is known that the tumor cells are difficult to eliminate completely by only relying on PTT because the heat of NIR light is reduced with the increase of tissues depth because of light scattering and absorption. Besides, tumors treated with FBP NPs showed no therapeutic effect. In contrast, in the FBP NPS + Laser group, tumor tissues were effectively ablated. These results demonstrated that upon laser irradiation, FBP NPs-mediated hyperthermia could ablate tumor cells/tissues. Generally, Bi₂S₃-based NIR light-responsive nanoparticles generate heat irradiated by an NIR light, resulting in cancer cell death. However, in the absence of laser irradiation and chemotherapy drugs, FBP NPS did not cause damage to tissues, indicating the biosafety of Bi₂S₃. At the same time, the weight of body is also an important factor to assess the nanoparticle toxicity. In vivo cytotoxicity assay, the body weight of the eight groups did not decrease during treatment, suggesting ignorable side effect of these synthetic nanoparticles. The result demonstrated that FA-loaded NPs could deliver Dox and Bi₂S₃ to the tumor area and specifically kill the tumor. Furthermore, it had been reported that hyperthermia at 41°C–45°C would incur a synergistic effect together with traditional therapeutic approaches such as chemotherapy in tumor treatment.⁴⁴ Moreover, the NIR laser which transforms optical energy to heat could penetrate tissue deeply owning to its feebleness absorbance by skin and tissue.⁴⁵ Our experimental results presented consistency with reported mechanisms.

Figure 9 In vivo tumor growth inhibition. (A) Photographs of SKOV-3 tumor-bearing mice of eight groups taken during 14 d period after various treatments. (B) Photographs of tumors dissected from mice of eight groups after various treatments. (C) Time-dependent tumor volume curves of eight groups after various treatments (n = 5). (D) Time-dependent body weights of eight groups after various treatments (n = 5).

Hematoxylin-eosin (H&E) staining, proliferating cell nuclear antigen (PCNA) staining, and TdT-mediated dUTP Nick-End Labeling (TUNEL) staining on tumor slices better affirmed the synergistic PTT/chemotherapy effect (Figure 10A). As shown in the H&E-staining tumor sections, there were much more deformed nucleus in FBPD NPs + Laser group than tumor sections in other groups, prompting serious necrosis of tumor cells. The result of TUNEL and PCNA staining followed the parallel tendency. Representative apoptosis cells were prompted by brown nucleus in the TUNEL staining. PCNA staining on tumor slices showed the in vivo proliferative abilities of eight groups where proliferative tumor cells were stained into brown. The TUNEL and PCNA staining indicated that synergistic PTT + chemotherapy possessed the highest efficacy than other groups. In addition, heart, liver, spleen, lung, and kidney of mice were conducted H&E staining after the treatments to survey the relevant pathological toxicity. Insignificant negative effect was discovered during the treatment course for all groups, indicating no obvious histological damage in the treatment group (Figure 10B).

Figure 10 (A) H&E, TUNEL and PCNA staining on tumor sections from SKOV-3 tumor-bearing mice after various treatments. (B) H&E staining of the major organs (heart, liver, spleen, lung, and kidney) of SKOV-3 tumor-bearing mice after different treatments. The scale bars are 50 µm.

Biosafety Assay of FBPD NPs

In order to explored the short/long-term potential toxicity of FBPD NPs, a blood biochemical assay and H&E staining of major organs were verified on Balb/c mice. The result of blood biochemical revealed that negligible changes after different treatments (Figure 11A), indicating the satisfactory biocompatibility of FBPD NPs. In addition, no obvious damage to major tissues was discovered, suggesting the high therapeutic biosafety of FBPD NPs (Figure 11B).

Figure 11 Biosafety of FBPD NPs. (A) Assay of blood index after i.v. injection of FBPD NPs (n = 5). (B) Images of H&E stained slices of major organs (scale bar = 50 µm).

Conclusions

In summary, we successfully constructed multifunctional theranostic FBPD NPs for highly efficient PTT/chemotherapy combination therapy with dual CT/PA imaging guidance/monitoring. The cell/tissue growth inhibition was comprehensively confirmed both in vitro and in vivo. The thermal energy generated by laser irradiation and the DOX released after the phase changed exerted a strengthened therapeutic effect on tumor cells/tissues. Dox could be rapidly released under an on-site laser irradiation, thus with reduced toxicity to non-tumor regions. In vivo experiments showed that FBPD NPs after laser irradiation could effectively inhibit the growth of tumors, and the NPs effectively accumulated in tumor region assisted by FA guidance. Furthermore, these NPs enhanced CT/PA imaging both in vitro and in vivo, offering the potential for tumor treatment guidance/monitoring. Our study provided greats insights on using FBPD NPs as a multifunctional cancer theranostics nanoplatform.

Abbreviations

PTT, photothermal therapy; PFP, perfluoropentane; Dox, doxorubicin; FDA, Food and Drug Administration; PLGA, poly lactic-co-glycolic acid; EPR, enhanced permeation and retention; FA, folic acid; Bi₂S₃, bismuth sulfide; CT, computed tomography; 3D, three-dimensional; PA, photoacoustic; FBPD NPs, FA-Bi₂S₃-PFP-Dox-PLGA nanoparticles; FBP NPs, FA-Bi₂S₃-PFP-PLGA nanoparticles; BPD NPs, Bi₂S₃-PFP-PLGA nanoparticles; CCK-8, Cell Counting Kit-8; DAPI, 2-(4-Amidinophenyl)-6-indolecarbamidinedihydrochloride; DiR, 1,1′-dioctadecyl-3,3,3′,3′- tetramethylindotricarbocyanine iodide; CHCl_2, dichloromethane; PVA, poly (vinyl alcohol); SEM, scanning electron microscopy; TEM, transmission electron microscopy; ICP-MS, inductively coupled plasma mass spectrometry; EE, encapsulation efficiency; DL, drug loading; OD, optical density; CLSM, confocal laser scanning microscopy; H&E, Hematoxylin-eosin; TUNEL, TdT-mediated dUTP Nick-End Labeling; PCNA, proliferating cell nuclear antigen.

Data Sharing Statement

All data generated or analysed during this study are included in this published article.

Ethics Approval and Consent to Participate

All animal procedures were performed in accordance with the Guidelines for Care and Use of Laboratory Animals of Chongqing Medical University and approved by the Animal Ethics Committee of Chongqing Medical University.

Author Contributions

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agreed to be accountable for all aspects of the work.

Disclosure

The authors declare that they have no competing interests.

Additional information

Funding

This work was supported by the National Natural Science Foundation of China Youth Science Foundation Project (NO.81801717), Medical Science Cultivation Fund of the First Affiliated Hospital of Chongqing Medical University (PYJJ2018-15) and Chongqing Postgraduate Research and Innovation Project (Grant No: CYS18194).