Next Article in Journal
Self-Adaptive Flask-like Nanomotors Based on Fe3O4 Nanoparticles to a Physiological pH
Previous Article in Journal
Quantum Transport of Dirac Fermions in HgTe Gapless Quantum Wells
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Nanomaterials
Volume 12
Issue 12
10.3390/nano12122048
nanomaterials-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Flower-like Composite Material Delivery of Co-Packaged Lenvatinib and Bufalin Prevents the Migration and Invasion of Cholangiocarcinoma

by
Zhouyu Ning
,
Yingke Zhao
,
Xia Yan
,
Yongqiang Hua
and
Zhiqiang Meng
*
Department of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China
*
Author to whom correspondence should be addressed.
Nanomaterials 2022, 12(12), 2048; https://doi.org/10.3390/nano12122048
Submission received: 7 May 2022 / Accepted: 20 May 2022 / Published: 15 June 2022
Browse Figures
Review Reports Versions Notes

Abstract

:
The co-delivery of multiple drugs using nanocarriers has been recognized as a promising strategy for cancer treatment to enhance therapeutic efficacy. In this study, a monodisperse mesoporous silica nanoparticle (mSiO2) is prepared and functionalized into high-efficiency loaded Lenvatinib and Bufalin for targeted delivery to Cholangiocarcinoma (CCA). mSiO2 was synthesized on solid silica nanoparticles by oil–water interface method, and highly monodisperse mSiO2 with uniform morphology was obtained. mSiO2 was then sequentially modified by polyethylene glycol (PEG) and the targeting molecule folic acid (FA). mSiO2-FA was designed as co-delivery system for Lenvatinib (Le) and Bufalin (Bu) to increase drug availability and highly target tumor cells. Compared with unfunctionalized mSiO2, mSiO2-FA can more efficiently enter human CCA cell lines (9810 cells) and enhance intracellular drug delivery. Moreover, drug-loaded mSiO2-FA (Le/Bu@mSiO2-FA) significantly inhibited the viability, migration and invasion of 9810 cells. In vivo, the nanocomplex significantly reduced the tumor load in CCA tumor-bearing mouse models compared to Le or Bu alone. The current work provides a useful strategy for highly targeted and multidrug-resistance reversal therapy for CCA.

1. Introduction

Morbidity and mortality of cholangiocarcinoma (CCA) have increased year by year [1]. Most patients are in advanced stage when they first visit the doctor, and the recurrence rate after CCA is high. Even after radical resection, the 5-year survival rate for CCA patients ranges from 22% to 44% [2]. Many studies have used gemcitabine combined with cisplatin and gemcitabine combined with albumin-bound paclitaxel as the first-line standard regimens for advanced or metastatic CCA [3,4]. CCA-targeted therapies targeting EGFR, RAS/RAF/MEK/MAPK, PI3K/Akt/mTOR signaling pathways, anti-angiogenic therapeutic targets, IDH1/2 mutations, HER2 amplification, FGFR2 fusion and NTRK fusion have made significant progress, but most of them are currently in the stage of research and development and clinical studies [5,6]. Targeted PD-1 therapy has been approved for advanced intrahepatic cholangiocarcinoma (ICC) in cases where there is a mismatch repair deficiency (d MMR) or high micro satellite instability (MSI-H). The efficacy of immune-checkpoint therapy in p MMR/MSS type ICC is not clear, and the predictive effect of TMB and PDL-1 expression state on the efficacy is not yet confirmed [7,8]. At present, CCA immunotherapy-related studies are mostly in the pre-clinical and clinical trial stage, and significant clinical benefits have not been obtained, which may be related to the heterogeneity and unique tumor microenvironment of CCA tumor rejection antigen (TRA). Therefore, finding novel strategies for ICC therapy is urgent.
Clinical studies confirmed that proper combinations of Chinese medicine (CM) and Western medicine (WM) could decrease toxicity and increase efficiency for promoting strengths and avoiding weaknesses [9,10,11]. Integrated Traditional and Western Medicine has shown some advantages in the treatment of CCA, especially in middle and advanced stage CCA [12,13]. Lenvatinib is a tyrosine kinase receptor (RTK) inhibitor that inhibits kinases including vascular endothelial growth factor receptor VEG-FR1 (FLT1), VEGFR2 (KDR), and VEGFR3 (FLT4) [14,15]. It also inhibits other RTKs associated with pathogenic tumor angiogenesis, tumor cell growth, and tumor development for normal cellular functions, including fibroblast growth factor receptors (FGFR) 1, 2, 3 and 4, KIT, platelet-derived growth factor receptor-α/β (PDGFR-α/β) and RET [16,17]. For advanced hepatic carcinoma (HCC) phase II trial results showed that Lenvatinib was superior in terms of overall survival, as well as significantly improved progression-free survival (PFS), time to tumor progression (TTP) and objective response rate (ORR), which is the first-line treatment for HCC [18]. However, CCA is highly desmoplastic and its tumor microenvironment is exceptionally rich, features that determine its resistance to the chemotherapeutic agent Lenvatinib, limiting the therapeutic efficacy of Lenvatinib [19,20]. In addition, the main bioactive component extracted from toad venom, Bufalin, has been proven to be an effective antitumor drug [21,22,23]. Bufalin effectively kills tumor cells by three mechanisms: inhibiting cell proliferation, promoting apoptosis, reversing tumor cell multidrug resistance, and inhibiting tumor vessel proliferation [24,25,26].
In recent years, multifunctional nanocomposites with simultaneous diagnostic, targeting and therapeutic functions have drawn much attention in cancer therapy and tumor suppression [27,28]. Nanomaterials have developed rapidly and nanotechnology has been applied in medical fields such as cancer and cardiovascular medicine [29]. The targeted drug delivery system has drawn more and more attention in cancer therapy over the past few decades. For a novel drug delivery system, drug design and development are crucial aspects [30]. Compared with the traditional single-drug treatment, the use of nanomaterials as carriers through the use of mixed drugs can greatly improve the efficacy of the drug [31,32]. Because of its unique and excellent properties in drug-delivery system, virus-like mesoporous silica nanoparticle has become a hot topic in the medical field nowadays [19,33].
Here, we successfully developed a controlled release nanocarrier system of mesoporous silica nanoparticles (mSiO2-FA) for co-delivery of Le and Bu (Figure 1). mSiO2 was synthesized on solid silica nanoparticles by oil–water interface method, and highly monodisperse mSiO2 with uniform morphology was obtained. mSiO2 was then sequentially modified by polyethylene glycol (PEG) and the targeting molecule folic acid (FA) to study the loading rate and release rate of the co-loaded Le and Bu. In vitro drug release experiments were conducted to study the release regularity of Le and Bu. In addition, the biological evaluation of human CCA cell lines (9810 cells) was carried out by mSiO2-FA analysis of cell uptake, cell viability, migration and invasion. Finally, we evaluated the in vivo anti-tumor effect of mSiO2-FA in the tumor-bearing mouse model.

2. Materials and Methods

2.1. Materials

Tetraethyl orthosilicate (TEOS), ammonia water, ethanol, hexadecyltrimethylammonium bromide (CTAB), Triethanolamine (TEA), cyclohexane solution, ammonium nitrate (NH4NO3), N-Hydroxysuccinimide (NHS), 3-(ethyliminomethylideneamino)-N,N-dimethylpropan-1-amine,hydrochloride (EDC), PEG-COOH and FA, were purchased from Aladdin (Shanghai, China), Bufalin (Bu) and Lenvatinib (Le) were purchased from GLPBIO (Montclair, CA, USA), Fluorescein Isothiocyanate (FITC), 4′,6-diamidino-2-phenylindole (DAPI), and hematoxylin and eosin were acquired from Solarbio (Beijing, China), 9810 cells were detected by Cell Bank of Chinese Academy of Sciences (Shanghai, China), fluorescent sealing solution were purchased from Merck Millipore (Billerica, MA, USA). The Cell Counting Kit-8 (CCK-8) assay kit were purchased from Beyotime (Shanghai, China). Transwell chambers and Matrigel were obtained from Corning (Corning, NY, USA). Shanghai Model Organisms Center, Inc (Shanghai, China) provided us the BALB/c nude mice. Hematoxylin and eosin (H&E) were obtained from Sangon (Shanghai, China). Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ELISA kits were purchased from mlbio (Shanghai, China).

2.2. Preparation of Mesoporous Silica (mSiO2) Nanoparticles

Mesoporous silica nanoparticles (mSiO2) were synthesized by oil–water interface method. Briefly, 6 g CTAB and 0.18 g TEA were added to a single-mouth round-bottomed flask (100 mL) containing 60 mL water and stirred gently at 60 °C for 1 h. Then, 20 mL of cyclohexane solution with 20 v/v % TEOS was dropped onto the upper layer of CTAB aqueous solution and stirred at 60 °C for 12 h. After the reaction, the aqueous phase was extracted and centrifugated at a high speed (15,000 Revolutions Per Minute (rpm), 30 min), the supernatant was discarded, the products were added to 50 mL 0.6 wt. % ammonium nitrate (NH4NO3) ethanol solution, and the surfactant CTAB was extracted by reflux at 60 °C, and the extraction was repeated 3 times, for 12 h each time.

2.3. Modification of mSiO2

Ultrasonic dispersion of 20 mg amino mSiO2 into 20 mL ethanol was conducted. Then, 20 mg NHS, 15 mg EDC, and 10 mg PEG-COOH were added and stirred for 24 h, and mSiO2-PEG was obtained by centrifugation. mSiO2-PEG was again dispersed into 20 mL ethanol, and 10 mg NHS, 15 mg EDC, and 2.0 mg FA were added and stirred for 24 h. The obtained products were separated by centrifugation, washed with ethanol, and then dried in vacuum for subsequent research.

2.4. Drug Loading and Releasing

Bufalin (Bu) and Lenvatinib (Le) were simply loaded into mSiO2-FA. In short, 10 mg mSiO2-FA nanoparticles were dissolved with PBS (20 mL, pH 7.4) by the ultrasonic bath, but Bu, Le, or Bu and Le were diffused with 2 mL water. Then, the solution containing the drug was mixed with mSiO2-FA nanoparticle solution, and stirred for the next 24 h. Next, drug-loaded nanoparticles were acquired through ultracentrifugation at (12,000 rpm) and washed by H2O 3 times, 5 mL each time, to detach free and surface-attached drugs. To measure the drug content, the supernatant was collected totally. Meanwhile, the UV-vis absorption spectra of the supernatant collected after the first centrifugation procedure was measured to determine the loading capacity of Le and Bu on mSiO2-FA. Drug loading efficient (DLE) was calculated as follows: DLE% = (weight of drug loaded/weight of fed drug initially) × 100. Drug loading content (DLC) was calculated as follows: DLC% = weight of drug loaded/weight of whole nanoparticles × 100.
The release rates of Bu and Le containing PBS (pH =7.4) were studied by dialysis. mSiO2-FA carrying Bu and Le were dispersed in 2 mL, 0.1 mol/L PBS then put in the dialysis bag. The dialysis bag was immersed in the same PBS with 18 mL at 37 °C, and the released medium was mixed at 80 rpm for 32 h. Samples from multiple time intervals (0, 1, 2, 3, 4, 5, 8, 12, 36, and 72 h) were taken then replaced by the same amount of new PBS. The concentration of each drug in the sample was measured with UV-Vis spectroscopy.

2.5. Cell Culture and Transfection

Human CCA cell line (9810) was cultured in DMEM containing 10% FBS and 1% penicillin/streptomycin (Sigma, St. Louis, MO, USA). After 24 h, before the incubation in the 5% CO2 incubator at 37 °C, 1 mg/mL mSiO2-FA-FITC was added by 2 μL to each well. Meanwhile, mSiO2-FITC was also transfected as a control. After the 9810 cells were incubated for 1, 2, and 6 h respectively, they were fixed by 4% paraformaldehyde for 15 min. For staining, DAPI was added into each plate to co-incubate the cells. Subsequently, a drop of fluorescent sealing solution was added, and the cells were directly imaged with confocal laser scanning microscopy (CLSM, Leica, Wetzlar, Germany).

2.6. CCK-8 Assay

For detecting the effects of nanoparticles and concentrations on 9810 cell viability, we used the Cell Counting Kit-8 (CCK-8) assay kit. In brief, after seeding 9810 cells into 96-well plates (1 × 104 per well), they were incubated for 24 h with series concentrations of mSiO2-FA (0, 10, 20, 40, 80, 160, and 200 μg/mL), Le, Bu, Le/Bu, or Le/Bu@mSiO2-FA. After that, we added 10 µL of the CCK-8 solution into the medium with cell culture and incubated it for another 1 h. The absorbance was assessed at a wavelength of 450 nm using a microplate reader (Bio-Tek, Norcross, GA, USA).

2.7. Wound-Healing Assay

We used wound healing assay to assess cells migrating. Briefly, the 9810 were seeded in 6-well plates (2.5 × 105 per well). A sterile pipette tip was used to make a scratch after cells were attached to the well bottom, then the width of the original scratch was recorded. Fresh serum-free DMEM medium substituted the residual liquid in the wells, added with free mSiO2-FA nanoparticles, free Le, Le@mSiO2-FA, free Bu, Bu@mSiO2-FA, Le/Bu@mSiO2-FA (100 μg/mL), respectively. Cells were cultured at 37 °C for 24 h. The width of the scratch was then measured and recorded.

2.8. Apoptosis Analysis

Apoptosis analysis was performed using Annexin V-FITC Apoptosis Detection Kit (Beyotime, Shanghai) by the manufacturer’s instructions. In brief, 9810 cells were treated with free mSiO2-FA nanoparticles, free Le, Le@mSiO2-FA, free Bu, Bu@mSiO2-FA, free Le/Bu, Le/Bu@mSiO2-FA (100 μg/mL) for 48 h. Lastly, the cells were double stained with PI and Annexin V-FITC, and cell apoptosis was measured with flow cytometer (Thermo Fisher Scientific, Waltham, MA, USA).

2.9. Endocytosis Pathway Assay

To determine the endocytosis pathway of Le/Bu@mSiO2-FA nanoparticles, 9810 cells were inoculated on a 6-well plate at a density of 105 cells per well for 2 days at 37 °C and cultured with various specific inhibitors for various endocytosis for 1 h at 37 °C. Afterwards, the uptake study was performed in the presence of the inhibitor and Le/Bu@mSiO2-FA at concentration of 50 μg/mL for 2 h at 37 °C. The supernatant was taken and washed with cold HEPES 3 times and analyzed using flow cytometry.

2.10. Transwell Assay

In transwell chambers with 8 μm pore size and Matrigel coating, the invasion of 9810 cells was evaluated. A total of 3 × 104 9810 cells were suspended in 100 μL serum-free DMEM medium, then added to the upper chamber of a transwell plate. Subsequently, free Le, free Bu, Le/Bu, or Le/Bu@mSiO2-FA (100 μg/mL), respectively, were added. Besides, the lower chamber was added 800 μL DMEM medium including 80 μL FBS. Before cells in the lower chamber were fixed by methanol and then 0.2% crystal violet-stained, they were incubated 24 h at 37 °C with 5% CO2. The invaded cells were counted by utilizing a light microscope (Zeiss, Jena, Germany). To assess the migration of 9810 cells, all the procedures were identical to invasion assay, while the chamber was not covered by Matrigel and the incubation time was extended to 36 h.

2.11. Animal Experiments

BALB/c nude mice (male; 4–6 weeks; 18–22 g) were selected from Shanghai Model Organisms Center, Inc. The Ethics Committee in Fudan University Shanghai Cancer Center certified the animal experiment. We inoculated 9810 tumor cells (1 × 106) subcutaneously to the mice in their left armpit. When tumor volumes reached 40 mm3 in average, five groups were used to divide the tumor-bearing mice (n = 6 per group). In addition to the first group of the caudal vein injection of saline (as a control), the Le, Bu, Le/Bu, or Le/Bu@mSiO2-FA (10 mg/kg) were injected, respectively, into the other four group of mice. Every mouse was measured the body weight and all tumors were removed and photographed 21 days later. The long and short diameter sizes of tumors in nude mice were measured and recorded every day. Tumor volume size V = (tumor long diameter)/(tumor short diameter)2/2.

2.12. Histological Staining

The major organs (heart, spleen, kidney, lung, and liver) of the tumor-bearing mice in different groups of treating were collected, dehydrated, embedded, and stained with hematoxylin and eosin. We observed the histological changes under a light microscopy at 200× magnification (Olympus, Tokyo, Japan).

2.13. Measurement of Serum Biochemical Index in Blood

The blood serum biochemical index was used to evaluate the long-term accumulation of Le/Bu@mSiO2-FA nanoparticles and drugs. The blood was collected by extracting eyeballs from different mice. Blood samples were analyzed through the blood cell analyzer, then the serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were further detected.

2.14. Statistical Analysis

Statistical analyses were carried out with the SPSS 17.0 software (IBM, Armonk, NY, USA). We repeated every experiment independently by three times. All values are presented in the way of mean ± standard deviation (SD). Among them, values from multiple groups were compared via one-way ANOVA, and two groups were compared via Student’s t-test. p < 0.05 indicated statistical significance.

3. Results and Discussions

3.1. mSiO2-FA Synthesis and Characterization

The synthetic process of Le/Bu@mSiO2-FA was summarized in Figure 1. mSiO2 was synthesized on solid silica nanoparticles by oil–water interface method, and highly monodisperse mSiO2 with uniform morphology was obtained. mSiO2 was then sequentially modified by polyethylene glycol (PEG) and the targeting molecule folic acid (FA). The TEM and SEM images of the obtained mSiO2-FA show that the nanoparticles were monodisperse, spherical in shape with an average diameter of 115–120 nm (Figure 2A–D). The size distribution of Solid SiO2, mSiO2, and mSiO2-FA was detected by dynamic light scattering (DLS) assay, and the results showed that the particle size of the three groups did not change much, with a diameter of 120 ± 23 nm (Figure 2E). To detect the modification process, the charge of these nanoparticles on the surface was also measured (Figure 2F). The mSiO2 exhibited a strongly negative surface (−44.3 ± 0.2 mV). The charge of PEG-modified nanoparticles was −12.4 ± 0.42 mV. The final product mSiO2-FA had a negative surface too, the zeta potential of which was −10 ± 0.2 mV, showing that mSiO2-FA is physically stable, and the synthesis of Le/Bu@mSiO2-FA is successful. In order to determine the stability of mSiO2-FA nanoparticles under physiological conditions, the nanoparticles were placed in water (H2O), phosphate buffer (PBS) and culture medium for 12, 24, and 48 h, and then the size of nanoparticles was measured by dynamic light scattering. The results showed that the average size of mSiO2-FA nanoparticles stayed at about 120 nm; nevertheless, the incubation time was 48 h, illustrating that these nanoparticles were strongly stable (Figure 2G). In addition, the hemolysis ratio of mSiO2-FA with different concentrations was also tested in vitro (Figure 2H). The mSiO2-FA induced a hemolysis rate of less than 2.0% by contacting with erythrocytes in whole blood at 37 °C for 1 h (clinical requirements for biomedical materials are lower than 5.0% of hemolysis rate). Therefore, the mSiO2-FA was considered as a nonhemolytic material.

3.2. Drug Loading and Release of mSiO2-FA

Because of the mesoporous structure and large specific surface (Table 1) area of mSiO2, we used mSiO2 to load bufalin and Lenvatinib. In this study of Len loading ability of solutions with distinct drug concentration, DLE (~95.3%) was still high even when the concentration of Le achieved 100 μg/mL, illustrating a high affinity in Le with mSiO2-FA nanoparticles. Moreover, when Le concentration was more than 500 μg/mL, a relatively high concentration, it could lead to a DLC of about 40.3%, which is also relatively high. The results (Table 2) indicated that the DLE of Le was not interfered with by the Bu addition when Le was loaded. With the concentration increasing, the Bu loading ability raised to 39.2%, however, the drug loading efficiency decreased slightly when the Bu concentration was changed to 500 μg/mL (80.3%, compared with 89.3% in 250 μg/mL and DLC of 17.4%). In addition, in further studies, we selected mSiO2-FA nanoparticles loaded Le and Bu with DLC of 16.4% (DLE of 90.1%) and 17.4% (DLE of 89.3%), separately. Controlled drug release in tumor tissue is one of the keys of drug delivery system for tumor therapy. Tumors are known to have a pH (about 6) slightly lower than normal tissue and blood. In addition, the pH of normal human plasma is about 7.35–7.45. Therefore, we performed pH-stimulated drug release of Le/Bu@mSiO2-FA in vitro. The percentage of Bu and Le released by Le/Bu@mSiO2-FA nanoparticles under different pH conditions is shown in Figure 3. At physiological pH (~7.4), mSiO2-FA released about 33.47% Bu after 72 h, while in tumor cell environment (pH 5.5), up to 74.27% Bu could escape from the nanoparticles, suggesting that the dismantling of nanoparticles can greatly promote the release of Bu (Figure 3A). The release behavior of Le was similar to that of Bu, but the release rate was relatively slow (Figure 3B). In clinical use, sustained-release drugs can stabilize the concentration of the drug in the body, thus achieving a lasting effect and avoiding the side effects associated with the concentration of the drug. FA can also lead to more solid tumor deposition by enhancing permeability and retention. This property not only improves the targeting property of nanomaterials, but also enhances their sustained-release effect.

3.3. Le/Bu@mSiO2-FA Weakens the Viability, Migration and Invasion of CCA In Vitro

Nanomaterials should be designed to enter cells rapidly and efficiently to realize a better therapeutic effect. Here, cell internalization of two types of FITC-labeled nanoparticles, mSiO2 and mSiO2-FA, were examined against 9810 cells by CLSM (Figure 4A). The relative uptake rate for each nanostructure was found to be quite different. After incubating for 1 h, the mSiO2 and mSiO2-FA nanoparticles obtained above were all able to penetrate the cell membrane of 9810 cells and accumulated throughout the cytosol. With the extension of time, the luminescence signal of mSiO2-FA nanoparticles entering 9810 cells was stronger than that of mSiO2 nanoparticles. It revealed that the internalization rate of mSiO2-FA nanoparticles is faster than that of mSiO2 nanoparticles. We further determined the relative uptake of mSiO2 and mSiO2-FA nanoparticles in 9810 cells after 6 h incubation (Figure 4B). The uptake of mSiO2-FA (32 μg/mg) in 9810 cells was significantly higher than that of mSiO2 (20 μg/mg). The results showed that, consistent with the results observed by the laser confocal microscope, the mSiO2-FA nanoparticles designed and synthesized by us could enter cells more efficiently and quickly, showing great application potential in the field of biomedicine. This is due to the use of FA here as a targeted agent in the drug delivery system. Folate receptor is a cell surface receptor that is overexpressed in various cancer cells. This receptor is closely related to folic acid (FA), the soluble form of the vitamin B [34]. FA can interact with folate receptors, resulting in cell internalization of anticancer drug loaded nanomaterials [35]. At present, the research on FA modified mesoporous silica surface as tumor cell targeting agent has been relatively mature [36,37,38,39,40,41,42,43].
In order to determine the endocytosis mechanism of mSiO2-FA nanoparticles composite by 9810 cells, the flow cytometry was performed (Figure 4C). Hypothermia or chlorpromazine, an inhibitor of endocytosis mediated by clathrin, obviously inhibited cellular uptake compared with the control experiment without inhibitor. While cells were pretreated by genistein (an inhibitor of endocytosis relied on caveolae), colchicine (an inhibitor of macropinocytosis relied on microtubule) and amiloride (an inhibitor of macropinocytosis), little or almost no inhibition was induced. This result showed that the cellular uptake pathway for vesicles was an endocytosis process that depended on energy and was mediated by clathrin. In 9810 cells, CCK-8 assay detected the cytotoxicity of various pharmaceutical preparations and vectors of increasing concentrations (0~200 µg/mL) for 48 h. With the increase of dose, all the cytotoxicity of pharmaceutical preparations to 9810 cells was enhanced (Figure 4D). The vector, mSiO2-FA, was nontoxic at a relatively high dose (200 µg/mL), proving that its biocompatibility was good. The killing potency of the free Lenvatinib or Bufalin to 9810 cells was very weak with low doses, as expected. Meanwhile, Lenvatinib@mSiO2-FA and Bufalin/Lenvatinib@mSiO2-FA were much more efficient compared with relevant groups (free Lenvatinib and free Bufalin/Lenvatinib combination) since cells could internalize the mSiO2-FA nanoparticles by clathrin-mediated energy-dependent endocytosis. Table 3 was the summary of the IC50 values (half maximal inhibitory concentration) which were calculated through the dose–response curve. The results indicated that the IC50 values of Bufalin/Lenvatinib@mSiO2-FA were much lower than free Lenvatinib, Lenvatinib@mSiO2-FA, Bufalin@mSiO2-FA and free drugs Bufalin/Lenvatinib combination, illustrating that Bufalin/Lenvatinib@mSiO2-FA had more efficiency for killing 9810 cells. The IC50 value of free Lenvatinib was 43.26 µg/mL. When the mSiO2-FA nanoparticles loaded Lenvatinib, the IC50 values reduced significantly, only around half of free Lenvatinib. A combination index (CI) is generally applied for analysis of the additive, synergistic or antagonistic effects of two drugs [44]. The CI could be obtained from the following formula: CI = C1/Cx1 + C2/Cx2, where C1 is the concentration of drug 1 required to induce a specific effect for combination therapy, Cx1 is the concentration of drug 1 generating the same influence independently; C2 is the concentration of drug 2 needed to reach the specific effect in combination therapy, Cx2 was the concentration of drug 2 achieving the identical influence individually. If CI > 1, it represents an antagonistic effect; if CI = 1, the two drugs show an additive effect; and if CI < 1, they have synergistic effects. Within our investigation, CI was calculated by IC50 values from Lenvatinib@mSiO2-FA, Bufalin@mSiO2-FA and Bufalin/Lenvatinib@mSiO2-FA. In 9810 cells, IC50 from Lenvatinib@mSiO2-FA and Bufalin@mSiO2-FA was 21.52 µg/mL and 22.17 µg/mL, separately (Table 3). For their combination therapy, Lenvatinib and Bufalin both had a concentration of 7.62 µg/mL, when the survival rate reached 50%. Consequently, nanogels delivered the Lenvatinib and Bufalin with the CI of 7.62/21.52 + 7.62/22.17 = 0.70 implying a synergistic effect. Cell apoptosis analysis was used to further verify the anti-cancer activity from our drug-loaded nanoparticles. In this study, the cells with Lenvatinib@mSiO2-FA and Bufalin/Lenvatinib@mSiO2-FA treatment had apoptosis rates of 51.28% and 80.26%, separately, while only 21.61% of cells were apoptotic after being treated with the same concentration of free Lenvatinib but the empty nanoparticles treated the cells with almost no apoptosis, which implies their biocompatibility (Figure 4E). These results confirmed that Bufalin/Lenvatinib@mSiO2-FA was more efficient at cytotoxicity than that of free Lenvatinib against 9810 cells.
To evaluate the effects of Le/Bu@mSiO2-FA nanoparticles on the collective migration of CCA cells, we performed a 2D scratch assay on the monolayers of 9810 cells. After the introduction of a “scratch” or “wound” into the cell culture, cancer cells collectively migrated into the empty space, and images were taken immediately and 24 h after scratching for 9810 in Figure 5A. The results showed that 9810 cells in the control group exhibited significantly different wound-healing abilities compared to those treated with either Le or Bu alone, while the Le and Bu combination treatment further reduced the wound-healing ability of cancer cells. Moreover, Le/Bu@mSiO2-FA nanoparticles treatment resulted in the lowest wound-healing ability of cancer cells. In order to examine the ability to migrate and invade for 9810 cells with treatments of the single Le or Bu, the Le and Bu combination, or Le/Bu@mSiO2-FA nanoparticles, the Transwell assay was performed. Both Le and Bu-exposed cells demonstrated a significant decrease in cell migration and invasion as compared to control group. Likewise, Le and Bu combination-exposed cells exhibited a decrease in cell migration and invasion as compared to the single Le or Bu-treated group, but to a higher extent than the Le/Bu@mSiO2-FA nanoparticles-exposed cells (Figure 5B). These results indicate that Le/Bu@mSiO2-FA nanoparticles can attenuate the migration and invasion of CCA cells.

3.4. Le/Bu@mSiO2-FA Inhibits the Tumor Growth of CCA In Vivo

Based on the above results, Le/Bu@mSiO2-FA could alleviate CCA migrating and invading in vitro, and the influence of Le/Bu@mSiO2-FA on CCA tumor growth in vivo was further explored. Orthotopic xenograft nude mice model of CCA was established by injecting 1 × 106 9810 cells into liver. The nude mice were injected into the caudal vein with single Le or Bu, Le/Bu, or Le/Bu@mSiO2-FA nanoparticles (100 μg/mL). Experimental mice show no significant change in body weight when they were treated with the drugs (Figure 6B), indicating that the treatments could be tolerated well and not lead to undesired effects on mice. Correspondingly, we detected the tumor size during the following 3 weeks after the treatments. Single Le or Bu slightly inhibits tumor growth of CCA, while the combination of Le and Bu further inhibits tumor growth. In contrast, Le/Bu@mSiO2-FA nanoparticles show significant anti-cancer effect (Figure 6A). Accordingly, tumor volume was monitored for 3 weeks after treatment. Le and Bu alone have little effect on tumor growth, which may be related to the poor retention effect of free Le and Bu on tumor. However, Le/Bu@mSiO2-FA group showed significant inhibitory effect (Figure 6C). To sum up, the results illustrate that Le/Bu@mSiO2-FA nanoparticles could inhibit the growth of tumors with high efficiency through their high DLC and targeted ability.

3.5. mSiO2-FA Has Good Biological Safety

Studies have shown that nanoparticles with small particle size can be distributed in the brain, liver and other organs through the blood brain barrier and other biofilms, showing certain toxic effects [45]. In order to evaluate the biosafety of mSiO2-FA, the serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) from healthy mice treated with saline, Le, Bu, Le/Bu, and Le/BumSiO2-FA were determined by hematological analysis. The results showed that there was no obvious distinction in ALT and AST content among all groups (Figure 7A,B). Further, the toxic effects of mSiO2-FA on the main organs of mice were determined by H&E staining. The results showed that 3 days after mSiO2-FA was injected into mice, no obvious pathological changes such as inflammation were observed in the sections of the heart, liver, spleen, lung, kidney, etc. (Figure 7C). All the above results indicate that mSiO2-FA has good biological safety.

4. Conclusions

In conclusion, a new type of nanoparticle, mSiO2-FA, with high-loading Bufalin and Lenvatinib and targeted delivery to tumor tissue was synthesized by a simple method. Bufalin could be loaded into the nanoparticle with high DLE (89.3%) and DLC (17.4%), as could Lenvatinib, with DLE 90.1% and DLC 16.4%. Both drugs release slowly in addition to the high release level (within 72 h, 74.27% and 65.41%, separately). The mSiO2-FA nanoparticles loading Bufalin and Lenvatinib could achieve the combination chemotherapy with the synergistic effect from both drugs, the content of which could be modulated separately. Bufalin and Lenvatinib were released into 9810 cells with high efficiency and indicated effective antitumor activity in vitro. Moreover, we observed obvious suppression tumor growth and decreased side effects of drug-related multi-organ toxicity in vivo, because they had the benefits of extended blood circulation, advantageous tumor accumulation, and induced drug release. Consequently, this delivery system of nanoparticle can be expanded to wide combination therapy then be expected to be a potent tool for treating drug-resistant tumors.

Author Contributions

Data curation: Y.Z.; formal analysis: Y.H. and X.Y.; funding acquisition: Z.N. and Z.M.; investigation: Y.H.; methodology: Y.Z.; software: X.Y.; validation: Y.H.; visualization: X.Y.; writing—review and editing: Z.N. and Z.M. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China, international cooperation and exchange programme (No. 81820108032), and Beijing Heart and Courage Public Welfare Foundation (No. HYXH2021041).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Ethics Committee of Laboratory Animal Center, Fudan University Cancer Hospital (protocol code FUSCC-IACUC-S20210369 and date of approval: 1 March 2021).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in the article.

Conflicts of Interest

The authors report no conflict of interest in this work.

References

  1. Picarelli, H.; Oliveira, M.; Marta, G.N.; Solla, D.; Teixeira, M.J.; Figueiredo, E.G. Mortality, Morbidity, and Prognostic Factors in the Surgical Resection of Brain Metastases: A Contemporary Cohort Study. J. Neurol. Surg. A Cent. Eur. Neurosurg. 2020, 81, 279–289. [Google Scholar] [CrossRef] [PubMed]
  2. Narasimhan, G.; Rela, M. Surgery for Cholangiocarcinoma. In ECAB Clinical Update: Surgical Gastroenterology and Liver Transplantation, Surgery of the Liver; Elsevier: Amsterdam, The Netherlands, 2015; pp. 114–128. [Google Scholar]
  3. Bekaii-Saab, T.S.; Valle, J.W.; Cutsem, E.V.; Rimassa, L.; Vogel, A.J.F.O. FIGHT-302: First-line pemigatinib vs gemcitabine plus cisplatin for advanced cholangiocarcinoma with FGFR2 rearrangements. Future Oncol. 2020, 16, 2385–2399. [Google Scholar] [CrossRef]
  4. Pietge, H.; Sánchez-Velázquez, P.; Akhoundova, D.; Siebenhüner, A.; Samaras, P.J.O. Combination of HAI-FUDR and Systemic Gemcitabine and Cisplatin in Unresectable Cholangiocarcinoma: A Dose Finding Single Center Study. Oncology 2021, 99, 300–309. [Google Scholar] [CrossRef] [PubMed]
  5. Tannapfel, A.; Sommerer, F.; Benicke, M.; Katalinic, A.; Uhlmann, D.; Witzigmann, H.; Hauss, J.; Wittekind, C. Mutations of the gene in cholangiocarcinoma but not in hepatocellular carcinoma. Gut 2003, 52, 706–712. [Google Scholar] [CrossRef] [PubMed]
  6. Rizvi, S.; Gores, G.J. Molecular pathogenesis of cholangiocarcinoma. BMC Cancer 2014, 19, 185. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Goeppert, B.; Roessler, S.; Renner, M.; Singer, S.; Mehrabi, A.; Vogel, M.N.; Pathil, A.; Czink, E.; Köhler, B.; Springfeld, C.; et al. Mismatch repair deficiency is a rare but putative therapeutically relevant finding in non-liver fluke associated cholangiocarcinoma. Br. J. Cancer 2018, 120, 109–114. [Google Scholar] [CrossRef] [Green Version]
  8. Naganuma, A.; Sakuda, T.; Murakami, T.; Aihara, K.; Watanuki, Y.; Suzuki, Y.; Shibasaki, E.; Masuda, T.; Uehara, S.; Yasuoka, H.; et al. Microsatellite Instability-high Intrahepatic Cholangiocarcinoma with Portal Vein Tumor Thrombosis Successfully Treated with Pembrolizumab. Intern. Med. 2020, 59, 2261–2267. [Google Scholar] [CrossRef] [PubMed]
  9. Xing, Q.; Fu, L.; Yu, Z.; Zhou, X. Efficacy and Safety of Integrated Traditional Chinese Medicine and Western Medicine on the Treatment of Rheumatoid Arthritis: A Meta-Analysis. Evid.-Based Complement. Altern. Med. 2020, 2020, 4348709. [Google Scholar] [CrossRef] [PubMed]
  10. Lue, H.C.; Su, Y.C.; Lin, S.J.; Huang, Y.C.; Chang, Y.H.; Lin, I.H.; Yang, S.P. Taipei consensus on integrative traditional Chinese and Western Medicine. J. Formos. Med. Assoc. 2021, 120, 34–47. [Google Scholar] [CrossRef]
  11. Zhang, Y.; Lou, Y.; Wang, J.; Yu, C.; Shen, W. Research Status and Molecular Mechanism of the Traditional Chinese Medicine and Antitumor Therapy Combined Strategy Based on Tumor Microenvironment. Front. Immunol. 2020, 11, 609705. [Google Scholar] [CrossRef]
  12. Fu, Z.; Ma, K.; Dong, B.; Zhao, C.; Che, C.; Dong, C.; Zhang, R.; Wang, H.; Wang, X.; Liang, R. The synergistic antitumor effect of Huaier combined with 5-Florouracil in human cholangiocarcinoma cells. BMC Complement. Altern. Med. 2019, 19, 203. [Google Scholar] [CrossRef]
  13. Xiong, F.; Gong, J.; Wang, Q. Olaparib and Pembrolizumab Treatment for BRCA1-Mutated and PD-L1-Positive Intrahepatic Cholangiocarcinoma Recurrence and Metastasis: A Case Report. OncoTargets Ther. 2020, 13, 6385–6391. [Google Scholar] [CrossRef]
  14. Chen, W.X.; Li, G.X.; Hu, Z.N.; Zhu, P.; Zhang, B.X.; Ding, Z.Y. Significant response to anti-PD-1 based immunotherapy plus lenvatinib for recurrent intrahepatic cholangiocarcinoma with bone metastasis: A case report and literature review. Medicine 2019, 98, e17832. [Google Scholar] [CrossRef]
  15. Ogasawara, S.; Mihara, Y.; Kondo, R.; Kusano, H.; Akiba, J.; Yano, H. Antiproliferative Effect of Lenvatinib on Human Liver Cancer Cell Lines In Vitro and In Vivo. Anticancer Res. 2019, 39, 5973–5982. [Google Scholar] [CrossRef] [PubMed]
  16. Mei, J.; Tang, Y.H.; Wei, W.; Shi, M.; Zheng, L.; Li, S.H.; Guo, R.P. Hepatic Arterial Infusion Chemotherapy Combined with PD-1 Inhibitors Plus Lenvatinib Versus PD-1 Inhibitors Plus Lenvatinib for Advanced Hepatocellular Carcinoma. Front. Oncol. 2021, 11, 618206. [Google Scholar] [CrossRef]
  17. Hatanaka, T.; Kakizaki, S.; Nagashima, T.; Ueno, T.; Namikawa, M.; Tojima, H.; Takizawa, D.; Naganuma, A.; Arai, H.; Sato, K.; et al. A change in the timing for starting systemic therapies for hepatocellular carcinoma: The comparison of sorafenib and lenvatinib as the first-line treatment. Acta Gastroenterol. Belg. 2021, 84, 65–72. [Google Scholar] [CrossRef] [PubMed]
  18. Yamamoto, Y.; Matsui, J.; Matsushima, T.; Obaishi, H.; Miyazaki, K.; Nakamura, K.; Tohyama, O.; Semba, T.; Yamaguchi, A.; Hoshi, S.S.; et al. Lenvatinib, an angiogenesis inhibitor targeting VEGFR/FGFR, shows broad antitumor activity in human tumor xenograft models associated with microvessel density and pericyte coverage. Vasc. Cell 2014, 6, 18. [Google Scholar] [CrossRef] [Green Version]
  19. Zhao, Z.; Song, J.; Zhang, D.; Wu, F.; Tu, J.; Ji, J. Oxysophocarpine suppresses FGFR1-overexpressed hepatocellular carcinoma growth and sensitizes the therapeutic effect of lenvatinib. Life Sci. 2021, 264, 118642. [Google Scholar] [CrossRef]
  20. Rodriguez-Hernandez, M.A.; Chapresto-Garzon, R.; Cadenas, M.; Navarro-Villaran, E.; Negrete, M.; Gomez-Bravo, M.A.; Victor, V.M.; Padillo, F.J.; Muntane, J. Differential effectiveness of tyrosine kinase inhibitors in 2D/3D culture according to cell differentiation, p53 status and mitochondrial respiration in liver cancer cells. Cell Death Dis. 2020, 11, 339. [Google Scholar] [CrossRef] [PubMed]
  21. Takai, N.; Ueda, T.; Nishida, M.; Nasu, K.; Narahara, H. Bufalin induces growth inhibition, cell cycle arrest and apoptosis in human endometrial and ovarian cancer cells. Int. J. Mol. Med. 2008, 21, 637–643. [Google Scholar] [CrossRef]
  22. Huang, W.W.; Yang, J.S.; Pai, S.J.; Wu, P.P.; Chang, S.J.; Chueh, F.S.; Fan, M.J.; Chiou, S.M.; Kuo, H.M.; Yeh, C.C.; et al. Bufalin induces G0/G1 phase arrest through inhibiting the levels of cyclin D, cyclin E, CDK2 and CDK4, and triggers apoptosis via mitochondrial signaling pathway in T24 human bladder cancer cells. Mutat. Res. 2012, 732, 26–33. [Google Scholar] [CrossRef] [PubMed]
  23. Yin, J.Q.; Shen, J.N.; Su, W.W.; Wang, J.; Huang, G.; Jin, S.; Guo, Q.C.; Zou, C.Y.; Li, H.M.; Li, F.B. Bufalin induces apoptosis in human osteosarcoma U-2OS and U-2OS methotrexate300-resistant cell lines. Acta Pharmacol. Sin. 2007, 28, 712–720. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Sheng, X.; Sun, X.; Sun, K.; Sui, H.; Qin, J.; Li, Q. Inhibitory effect of bufalin combined with Hedgehog signaling pathway inhibitors on proliferation and invasion and metastasis of liver cancer cells. Int. J. Oncol. 2016, 49, 1513–1524. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Zhai, B.; Hu, F.; Yan, H.; Zhao, D.; Jin, X.; Fang, T.; Pan, S.; Sun, X.; Xu, L. Bufalin Reverses Resistance to Sorafenib by Inhibiting Akt Activation in Hepatocellular Carcinoma: The Role of Endoplasmic Reticulum Stress. PLoS ONE 2015, 10, e0138485. [Google Scholar] [CrossRef] [PubMed]
  26. Gu, W.; Liu, L.; Fang, F.F.; Huang, F.; Cheng, B.B.; Li, B. Reversal effect of bufalin on multidrug resistance in human hepatocellular carcinoma BEL-7402/5-FU cells. Oncol. Rep. 2014, 31, 216–222. [Google Scholar] [CrossRef] [Green Version]
  27. Zhao, J.; Yang, H.; Li, J.; Wang, Y.; Wang, X. Fabrication of pH-responsive PLGA(UCNPs/DOX) nanocapsules with upconversion luminescence for drug delivery. Sci. Rep. 2017, 7, 18014. [Google Scholar] [CrossRef] [Green Version]
  28. Tsompanas, M.A.; Bull, L.; Adamatzky, A.; Balaz, I. In silico optimization of cancer therapies with multiple types of nanoparticles applied at different times. Comput. Methods Programs Biomed. 2021, 200, 105886. [Google Scholar] [CrossRef]
  29. Decha, P.; Kanokwan, K.; Jiraporn, T.; Pichaya, J.; Pisittawoot, A. Phonopheresis Associated with Nanoparticle Gel from Phyllanthus amarus Relieves Pain by Reducing Oxidative Stress and Proinflammatory Markers in Adults with Knee Osteoarthritis. Chin. J. Integr. Med. 2019, 25, 691–695. [Google Scholar] [CrossRef]
  30. Li, B.; Han, L.; Cao, B.; Yang, X.; Zhu, X.; Yang, B.; Zhao, H.; Qiao, W. Use of magnoflorine-phospholipid complex to permeate blood-brain barrier and treat depression in the CUMS animal model. Drug Deliv. 2019, 26, 566–574. [Google Scholar] [CrossRef] [Green Version]
  31. Tang, L.; Zhu, Z.F.; Cao, L.P.; Shen, M.; Gao, Y.; Tu, C.J.; Zhang, Z.H.; Shan, W.G. Thermosensitive gel of polysaccharide from Ganoderma applanatum combined with paclitaxel for mice with 4T1 breast cancer. Zhongguo Zhong Yao Za Zhi 2020, 45, 2533–2539. [Google Scholar] [CrossRef]
  32. Gao, S.; Zheng, M.; Lin, Y.; Lin, K.; Zeng, J.; Xie, S.; Yu, Y.; Lin, J. Surface-enhanced Raman scattering analysis of serum albumin via adsorption-exfoliation on hydroxyapatite nanoparticles for noninvasive cancers screening. J. Biophotonics 2020, 13, e202000087. [Google Scholar] [CrossRef] [PubMed]
  33. Xu, D.; Song, X.; Zhou, J.; Ouyang, X.; Li, J.; Deng, D. Virus-like hollow mesoporous silica nanoparticles for cancer combination therapy. Colloids Surf. B Biointerfaces 2021, 197, 111452. [Google Scholar] [CrossRef]
  34. Xue, W.J.; Feng, Y.; Wang, F.; Guo, Y.B.; Li, P.; Wang, L.; Liu, Y.F.; Wang, Z.W.; Yang, Y.M.; Mao, Q.S. Asialoglycoprotein receptor-magnetic dual targeting nanoparticles for delivery of RASSF1A to hepatocellular carcinoma. Sci. Rep. 2016, 6, 22149. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Hao, N.; Li, L.; Zhang, Q.; Huang, X.; Li, L.J.M.; Materials, M. The shape effect of PEGylated mesoporous silica nanoparticles on cellular uptake pathway in Hela cells. Microporous Mesoporous Mater. 2012, 162, 14–23. [Google Scholar] [CrossRef]
  36. Al-Nadaf, A.H.; Dahabiyeh, L.A.; Jawarneh, S.; Bardaweel, S.; Mahmoud, N.N. Folic acid-hydrophilic polymer coated mesoporous silica nanoparticles target doxorubicin delivery. Pharm. Dev. Technol. 2021, 26, 582–591. [Google Scholar] [CrossRef]
  37. Li, Z.; Zhang, Y.; Zhu, C.; Guo, T.; Xia, Q.; Hou, X.; Liu, W.; Feng, N. Folic acid modified lipid-bilayer coated mesoporous silica nanoparticles co-loading paclitaxel and tanshinone IIA for the treatment of acute promyelocytic leukemia. Int. J. Pharm. 2020, 586, 119576. [Google Scholar] [CrossRef]
  38. Zhang, L.; Wei, F.; Al-Ammari, A.; Sun, D. An optimized mesoporous silica nanosphere-based carrier system with chemically removable Au nanoparticle caps for redox-stimulated and targeted drug delivery. Nanotechnology 2020, 31, 475102. [Google Scholar] [CrossRef]
  39. Song, Y.; Zhou, B.; Du, X.; Wang, Y.; Zhang, J.; Ai, Y.; Xia, Z.; Zhao, G. Folic acid (FA)-conjugated mesoporous silica nanoparticles combined with MRP-1 siRNA improves the suppressive effects of myricetin on non-small cell lung cancer (NSCLC). Biomed. Pharm. 2020, 125, 109561. [Google Scholar] [CrossRef]
  40. Sun, X.; Wang, N.; Yang, L.Y.; Ouyang, X.K.; Huang, F. Folic Acid and PEI Modified Mesoporous Silica for Targeted Delivery of Curcumin. Pharmaceutics 2019, 11, 430. [Google Scholar] [CrossRef] [Green Version]
  41. Park, J.; Park, S.S.; Jo, N.J.; Ha, C.S. Folic Acid-Polyethyleneimine Functionalized Mesoporous Silica Nanoparticles as a Controlled Release Nanocarrier. J. Nanosci. Nanotechnol. 2019, 19, 6217–6224. [Google Scholar] [CrossRef] [PubMed]
  42. Qu, W.; Meng, B.; Yu, Y.; Wang, S. Folic acid-conjugated mesoporous silica nanoparticles for enhanced therapeutic efficacy of topotecan in retina cancers. Int. J. Nanomed. 2018, 13, 4379–4389. [Google Scholar] [CrossRef] [Green Version]
  43. AbouAitah, K.; Swiderska-Sroda, A.; Farghali, A.A.; Wojnarowicz, J.; Stefanek, A.; Gierlotka, S.; Opalinska, A.; Allayeh, A.K.; Ciach, T.; Lojkowski, W. Folic acid-conjugated mesoporous silica particles as nanocarriers of natural prodrugs for cancer targeting and antioxidant action. Oncotarget 2018, 9, 26466–26490. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Li, P.; Yang, S.; Dou, M.; Chen, Y.; Zhang, J.; Zhao, X. Synergic effects of artemisinin and resveratrol in cancer cells. J. Cancer Res. Clin. Oncol. 2014, 140, 2065–2075. [Google Scholar] [CrossRef] [PubMed]
  45. Bharathala, S.; Kotarkonda, L.K.; Singh, V.P.; Singh, R.; Sharma, P. In silico and experimental studies of bovine serum albumin-encapsulated carbenoxolone nanoparticles with reduced cytotoxicity. Colloids Surf. B Biointerfaces 2021, 202, 111670. [Google Scholar] [CrossRef] [PubMed]
Nanomaterials 12 02048 g001 550
Figure 1. The synthesis process of Le/Bu@mSiO2-FA.
Figure 1. The synthesis process of Le/Bu@mSiO2-FA.
Nanomaterials 12 02048 g001
Nanomaterials 12 02048 g002 550
Figure 2. Characterization of mSiO2-FA. (A,B) TEM image of mSiO2-FA nanoparticles. Scale bars = 100 nm (A) and 20 nm (B) for TEM. (C,D) SEM image of mSiO2-FA nanoparticles. Scale bars = 1 μm and 100 nm for SEM. (E) Size distribution of the SiO2, mSiO2, and mSiO2-FA nanoparticles by Dynamic light scattering (DLS) assay. (F) Zeta potential of the mSiO2, mSiO2-FA, and Le/Bu@mSiO2-FA nanoparticles. (G) Size distributions of mSiO2-FA nanoparticles in different medium for different time. (H) Hemolysis test results of mSiO2-FA nanoparticles. TEM—Transmission Electron Microscope; SEM—Scanning Electronic Microscopy; Le/Bu—Lenvatinib and Bufalin combination.
Figure 2. Characterization of mSiO2-FA. (A,B) TEM image of mSiO2-FA nanoparticles. Scale bars = 100 nm (A) and 20 nm (B) for TEM. (C,D) SEM image of mSiO2-FA nanoparticles. Scale bars = 1 μm and 100 nm for SEM. (E) Size distribution of the SiO2, mSiO2, and mSiO2-FA nanoparticles by Dynamic light scattering (DLS) assay. (F) Zeta potential of the mSiO2, mSiO2-FA, and Le/Bu@mSiO2-FA nanoparticles. (G) Size distributions of mSiO2-FA nanoparticles in different medium for different time. (H) Hemolysis test results of mSiO2-FA nanoparticles. TEM—Transmission Electron Microscope; SEM—Scanning Electronic Microscopy; Le/Bu—Lenvatinib and Bufalin combination.
Nanomaterials 12 02048 g002
Nanomaterials 12 02048 g003 550
Figure 3. (A) Bu release profiles of Le/Bu@mSiO2-FA in different conditions; (B) Le release profiles of Le/Bu@mSiO2-FA in different conditions. Le, Lenvatinib; Bu, Bufalin; Le/Bu, Lenvatinib and Bufalin combination.
Figure 3. (A) Bu release profiles of Le/Bu@mSiO2-FA in different conditions; (B) Le release profiles of Le/Bu@mSiO2-FA in different conditions. Le, Lenvatinib; Bu, Bufalin; Le/Bu, Lenvatinib and Bufalin combination.
Nanomaterials 12 02048 g003
Nanomaterials 12 02048 g004 550
Figure 4. (A) Confocal laser scanning microscopy (CLSM) images of the 9810 tumor cells incubated with the same concentration (100 mg/mL) of mSiO2 and mSiO2-FA for 1, 2, and 6 h. Blue indicates DAPI nuclear stain, green is FITC fluorescence. (B) Uptake of mSiO2 and mSiO2-FA nanoparticles in 9810 cells at 6 h. (C) Relative uptake efficiency of mSiO2-FA nanoparticles in 9810 cells in the presence of various endocytosis inhibitors. (D) In vitro cytotoxicity of mSiO2-FA, free Le, free drugs Bu-Le combination, Bu@mSiO2-FA, Le@mSiO2-FA, Bu/Le@ mSiO2-FA by CCK8 assay. (E) Cell apoptosis of mSiO2-FA, free Le, Le@mSiO2-FA, free Bu, Bu@mSiO2-FA, free drugs Bu-Le combination, Bu/Le@ mSiO2-FA by flow cytometry. N = 3. *** p < 0.001, **** p < 0.0001. CLSM—confocal laser scanning microscopy; Le—Lenvatinib; Bu—Bufalin; Le/Bu—Lenvatinib and Bufalin combination.
Figure 4. (A) Confocal laser scanning microscopy (CLSM) images of the 9810 tumor cells incubated with the same concentration (100 mg/mL) of mSiO2 and mSiO2-FA for 1, 2, and 6 h. Blue indicates DAPI nuclear stain, green is FITC fluorescence. (B) Uptake of mSiO2 and mSiO2-FA nanoparticles in 9810 cells at 6 h. (C) Relative uptake efficiency of mSiO2-FA nanoparticles in 9810 cells in the presence of various endocytosis inhibitors. (D) In vitro cytotoxicity of mSiO2-FA, free Le, free drugs Bu-Le combination, Bu@mSiO2-FA, Le@mSiO2-FA, Bu/Le@ mSiO2-FA by CCK8 assay. (E) Cell apoptosis of mSiO2-FA, free Le, Le@mSiO2-FA, free Bu, Bu@mSiO2-FA, free drugs Bu-Le combination, Bu/Le@ mSiO2-FA by flow cytometry. N = 3. *** p < 0.001, **** p < 0.0001. CLSM—confocal laser scanning microscopy; Le—Lenvatinib; Bu—Bufalin; Le/Bu—Lenvatinib and Bufalin combination.
Nanomaterials 12 02048 g004
Nanomaterials 12 02048 g005 550
Figure 5. (A) Scratch assay of 9810 cells (control, free Le treatment, free Bu treatment, Le/Bu combination treatment, and Le/Bu@mSiO2-FA treatment) at 0 and 24 h (N = 3). (B) The cell migration and invasion of 9810 cells treated with control, free Le, free Bu, Le/Bu combination, and Le/Bu@mSiO2-FA for 24 h was detected by Transwell assay (N = 3). The invading and migrating cell numbers were then quantified by counting and depicted as bar charts. *** p < 0.001, **** p < 0.0001. Le—Lenvatinib; Bu—Bufalin; Le/Bu—Lenvatinib and Bufalin combination.
Figure 5. (A) Scratch assay of 9810 cells (control, free Le treatment, free Bu treatment, Le/Bu combination treatment, and Le/Bu@mSiO2-FA treatment) at 0 and 24 h (N = 3). (B) The cell migration and invasion of 9810 cells treated with control, free Le, free Bu, Le/Bu combination, and Le/Bu@mSiO2-FA for 24 h was detected by Transwell assay (N = 3). The invading and migrating cell numbers were then quantified by counting and depicted as bar charts. *** p < 0.001, **** p < 0.0001. Le—Lenvatinib; Bu—Bufalin; Le/Bu—Lenvatinib and Bufalin combination.
Nanomaterials 12 02048 g005
Nanomaterials 12 02048 g006 550
Figure 6. (A) Photographs of excreted tumor after different treatments. (B) Body weight change of treated mice of different treatments during treatment periods. (C) Tumor volume statistics of each group of tumor-bearing mice. N = 3 of each group.
Figure 6. (A) Photographs of excreted tumor after different treatments. (B) Body weight change of treated mice of different treatments during treatment periods. (C) Tumor volume statistics of each group of tumor-bearing mice. N = 3 of each group.
Nanomaterials 12 02048 g006
Nanomaterials 12 02048 g007 550
Figure 7. (A,B) Hematological analysis of the function of liver and heart in heathy mice treated with saline, Le, Bu, Le/Bu, and Le/BumSiO2-FA. (C) H&E staining of the heart, liver, spleen, lung and kidney after treatment with saline, Le, Bu, Le/Bu, and Le/BumSiO2-FA. N = 3 of each group.
Figure 7. (A,B) Hematological analysis of the function of liver and heart in heathy mice treated with saline, Le, Bu, Le/Bu, and Le/BumSiO2-FA. (C) H&E staining of the heart, liver, spleen, lung and kidney after treatment with saline, Le, Bu, Le/Bu, and Le/BumSiO2-FA. N = 3 of each group.
Nanomaterials 12 02048 g007
Table
Table 1. Textural parameters of mSiO2. Data are presented as the mean ± standard deviation (SD; n = 3).
Table 1. Textural parameters of mSiO2. Data are presented as the mean ± standard deviation (SD; n = 3).
SampleSizeBET (m2/g)Dav.Pore (nm)Vpore (cm3/g)
mSiO2112.5 ± 3.9419.3 ± 1.45.8 ± 0.10.6 ± 0.1
Table
Table 2. Drugs loading data and characterization of the drug loaded mSiO2-FA nanoparticles.
Table 2. Drugs loading data and characterization of the drug loaded mSiO2-FA nanoparticles.
CodeLenvatinib
(μg/mL)		Bufalin
(μg/mL)		LenvatinibBufalinDDLS (nm)
DLE DLCDLEDLC
100////115
2100095.3%16.5%//121
3500091.6%40.3%//108
410050093.7%15.2%80.3%39.2%110
510025090.1%16.4%89.3%17.4%113
Table
Table 3. IC50 values of different various drug formulations in 9810 cells measured by CCK8 assay.
Table 3. IC50 values of different various drug formulations in 9810 cells measured by CCK8 assay.
Free LenvatinibLenvatinib@mSiO2-FABufalin@mSiO2-FALenvatinib/Bufalin Free DrugsLenvatinib/Bufalin@mSiO2-FA
IC50 (μg/mL)43.2621.5222.1732.147.62
SD a±1.89±1.26±2.03±1.49±1.06
a Data represent the mean of three separate experiments.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ning, Z.; Zhao, Y.; Yan, X.; Hua, Y.; Meng, Z. Flower-like Composite Material Delivery of Co-Packaged Lenvatinib and Bufalin Prevents the Migration and Invasion of Cholangiocarcinoma. Nanomaterials 2022, 12, 2048. https://doi.org/10.3390/nano12122048

AMA Style

Ning Z, Zhao Y, Yan X, Hua Y, Meng Z. Flower-like Composite Material Delivery of Co-Packaged Lenvatinib and Bufalin Prevents the Migration and Invasion of Cholangiocarcinoma. Nanomaterials. 2022; 12(12):2048. https://doi.org/10.3390/nano12122048

Chicago/Turabian Style

Ning, Zhouyu, Yingke Zhao, Xia Yan, Yongqiang Hua, and Zhiqiang Meng. 2022. "Flower-like Composite Material Delivery of Co-Packaged Lenvatinib and Bufalin Prevents the Migration and Invasion of Cholangiocarcinoma" Nanomaterials 12, no. 12: 2048. https://doi.org/10.3390/nano12122048

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop