1. Introduction
Cervical cancer is the most common human papillomavirus (HPV)-associated cancer among women [
1,
2,
3], and is mainly caused by high-risk HPVs 16 and 18 [
4]. In recent years, the combination of screening programs and vaccination against HPV has greatly reduced cervical cancer incidence and mortality [
4]. However, the populational coverage remains low, and for women already infected, the vaccination will not cure them or treat precancer lesions. For cervical dysplasia, the therapeutic options available include surgery, radio and chemotherapy, increasing the risk of infertility [
5].
Moreover, endometrial cancer is the most common gynecologic cancer, with an increasing incidence worldwide. Patients that are diagnosed at an early stage present good prognosis and high survival rates, although when diagnosed at a late stage they have poor prognosis, mostly caused by tumor metastasis, which has low survival rates and limited treatment options [
6,
7,
8,
9]. Thus, improved treatment options for women that already present cervical and endometrial cancer are still necessary.
Aptamers are structured nucleic acids that have several advantages relative to antibodies, including chemical synthesis and stability, conformational flexibility, and an overall smaller size [
10]. Some aptamers have guanine (G)-rich tracts that can form G-quadruplex (G4) structures [
11]. AS1411 is a G4 DNA aptamer that exhibits high affinity for nucleolin, has antiproliferative properties, and induces apoptosis in cancer cells with reduced toxicity in normal ones [
12,
13,
14,
15]. Its biological effects are mainly caused by cell cycle arrest, inhibition of NF-κB signaling, induction of tumor suppressor gene expression, and reduction of bcl-2 expression [
12]. Indeed, AS1411 reached Phases 1 and 2 clinical trials [
16,
17] but demonstrated low potency (µM) and suboptimal pharmacology (rapid clearance from the body) [
16,
18]. To improve its malignant cell selectivity/accumulation and to increase its toxicity, AS1411 has been associated with nanoparticles, such as liposomes and gold nanoparticles (AuNPs) [
18,
19,
20,
21,
22]. Previously, Malik et al. reported that AS1411 bound to AuNPs (AS1411-AuNPs) had higher cellular uptake and improved antiproliferative/cytotoxic effects relative to unconjugated AS1411 or control sequences [
21]. These aptamer-conjugated nanoparticles could deliver ligands efficiently and selectively to cancer cells [
21,
23].
Since conjugation of the aptamer to the AuNPs improves cellular uptake, we hypothesized that AS1411-AuNPs may also be a promising drug carrier for cancer cells, taking advantage intrinsic anticancer potential/selectivity of the AS1411-AuNPs to improve the effects of some drugs. To study this possibility, we focused on Imiquimod (IQ;
Figure 1) and acridine orange derivative 10-(8-(4-iodobenzamide) octyl)-3,6-bis (dimethylamine) acridinium iodide (C
8;
Figure 1).
IQ is an imidazoquinoline that can modulate the immune response through TLR7/8 activation, increase the activation of the NF-κB signaling pathway, and cause proapoptotic activity by triggering the caspase pathway [
24]. It has proven anticancer and antiviral effects [
25], but its biological properties are sub-optimal. It is currently used in premalignant lesions caused by low-risk HPV infections [
26]. It has also been tested in patients with recurrent high-grade vulvar, vaginal or cervical intraepithelial neoplasia and demonstrated to be a potential anticancer drug for these situations [
27].
Similarly, C
8 is an acridine orange derivative that exerts anticancer effects. However, this ligand has high toxicity in both malignant and normal cell lines [
28]. C
8 can bind to nucleolin-targeted aptamers, and it can potentially stabilize G4 structures. Thus, it may be possible to add C
8 to AS1411 to improve its therapeutic index while also enhancing an overall supramolecular assembly with nanoparticles [
23,
29,
30].
Herein we describe the synthesis and characterization of AS1411-AuNPs and their potential as drug carriers to selectively deliver IQ and C8 to nucleolin-positive cancer cells. The nanoparticles were characterized by different physico-chemical methods and the drug release kinetics assessed. Furthermore, their anticancer activity, cellular uptake and lysosomal trapping were evaluated. Finally, their potential to be incorporated in a gel formulation and their vaginal penetration profile was studied.
2. Materials and Methods
2.1. Oligonucleotides, Ligands and AuNPs
AS1411 was purchased from Eurogentec (Liège, Belgium) with HPLC-grade purification and a purity of 98%. The oligonucleotide had a regular DNA backbone (i.e., phosphodiester) and a 5′-Thiol C6 S-S modification (Thio-MC6-D). Stock solutions of 500 µM were prepared using Milli-Q water. Light-on LysoView™ 540 was purchased from Biotium (San Francisco, CA, USA), Hoechst 33342 from Thermo Scientific (Waltham, MA, USA) and IQ from Tokyo Chemical Industry (Zwijndrecht, Belgium). The ligands, C
8 [
31] and IQ were dissolved in DMSO to obtain a 10 mM and 5 mM stock solution, respectively, and further diluted in milli-Q water. Stabilized AuNPs (5 nm diameter) suspension in citrate buffer was purchased from Sigma-Aldrich (St. Louis, MO, USA) at concentration of 5.5 × 10
13 particles/mL.
2.2. Nanoparticles Synthesis
Functionalization of gold nanospheres with thiolated AS1411 was achieved using a method adapted from the one previously described in Malik et al. [
21] based on the original protocol of Mirkin et al. [
32]. This methodology was used since, the resulting nanoparticles were efficiently internalized and showed selectivity for cancer cells compared to non-malignant cells. Moreover, by using an in vivo model, the authors demonstrated that systemic administration of AS1411-AuNPs could completely inhibit tumor growth with no signs of toxicity [
32]. Since Malik et al. reached such interesting results, we decided to use a similar approach to improve the potential of IQ and C
8 and to increase the selectivity of this drugs towards malignant cells.
Thiolated oligonucleotides were first reduced by incubating with a filtrated solution of 10 mM tris-(2-carboxyethyl)-phosphine hydrochloride (TCEP, Pierce, Waltham, MA, USA; in a 100× molar excess) for 6 h at room temperature. Then, the oligonucleotides were added to 5 nm colloidal gold nanospheres to give a final oligonucleotide:gold nanoparticle ratio of 200:1. After overnight incubation on a rotator, filtrated solution of 20 mM KPi was added until reaching a final concentration of 10 mM. Four hours later, filtrated 3 M NaCl was added to the solution until reaching a final concentration of 100 mM and the solution was left in rotation for more 6 h. To finish, more filtrated NaCl solution was added (until reaching a final concentration of 300 mM) and it was incubated in rotation, at room temperature for an additional overnight.
The sample was inserted in a D-tube Dialyzer Maxi (Milipore, Burlington, MA, USA; MWCO 3.5 KDa). To remove the salts from the solution of aptamer functionalized AuNPs, dialysis was performed for 48 h and the H2O Milli Q was replaced two times a day.
Supramolecular assembly of C8 or IQ with AS1411-AuNPs was obtained after mixing both components. In case of AS1411-AuNPs with C8 the mixture was performed with a molar ratio of 15:1 and for AS1411-AuNPs with IQ with a molar ratio of 15:5.
2.3. Nanoparticles Characterization
Hydrodynamic size analysis and zeta potential of the aptamer-modified AuNPs were determined using Zetasizer Nano ZS equipment (Malvern Instruments, Worcestershire, UK). Particles were diluted in purified water for these measurements.
Additionally, the morphology was assessed through transmission electron microscopy (TEM) using a Hitachi-HT7700 (Krefeld, Germany). Samples were prepared by placing a drop of particles dispersed in purified water on nickel grid coated with carbon and allowing the samples to dry for 15 min. Images were captured at an accelerating voltage of 80 kV and with magnification of 100 k.
2.4. Drug Release Kinetics Assay
Initially, a standard fluorescence curve was established with different concentrations of C8 solution in order to enable the determination of the exact amount of drug released by the AS1411-AuNPs, using the equipment Spectra MAX GEMINI EM (Molecular Devices, San Jose, CA, USA).
For drug release kinetics assay, 100 µL of AS1411-AuNPs with C8 at a final concentration of 5 µM were inserted in Slide-A-Lyzer (Thermo Fisher Scientific, Waltham, MA, USA; MWCO of 3.5 KDa). The dialysis device was inserted in an Eppendorf with 1 mL of buffer (20 mM KPi and 100 mM KCl) and, at different time points (0 min, 5 min, 15 min, 30 min, 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 12 h, 24 h and 48 h)., 100 µL of buffer solution was collected and, subsequently, replaced. The samples were in agitation under room temperature.
The fluorescence of the collected buffer (λex = 498 nm and λem = 530 nm) was measured, and the obtained value in each range was used to estimate the percentage of drug released.
2.5. Confocal Fluorescence Microscopy
For fluorescence confocal microscopy assays, human cervical cancer cells (HeLa; ref. CCL-2™, ATCC), human endometrial carcinoma cells (HEC-1-A; ref. HTB-112™, ATCC), and normal human dermal fibroblasts (NHDF; ref. PCS-201-012™, ATCC) were seeded at 5 × 104 cells/mL in a treated µ-slide 8 well (IBIDI, Gräfelfing, Germany) in 200 µL of medium and grown at 37 °C under a 95% air and 5% CO2 humidified atmosphere.
For the medium replacement assay, performed to determine if the nanoparticles are retained in the cell lines, HeLa, HEC-1-A and NHDF cells were treated with AS1411-AuNPs with IQ or C8. The day after, medium was replaced by new one without any treatment. Nuclei were stained with the 1 µM nuclear probe Hoechst 33342 for 15 min. The probe was washed off by rinsing with PBS three times and cells were imaged using a Zeiss AxioObserver LSM 710 microscope (Oberkochen, Germany).
For the LysoViewTM experiments, cells were treated with the nanoparticles assembled with IQ or C8 for 2 h. The cells were then washed three times with PBS and nuclei were stained with 1 µM of nuclear probe Hoechst 33,342 for 15 min. After that, the probe was washed off by rinsing with PBS three times. Then, LysoView was added to the wells and it was left for 30 min. The cells were washed three times with PBS and imaged using a Zeiss AxioObserver LSM 710 microscope with 405, 488 and 555 nm laser excitation for Hoechst 33342, drug (IQ or C8) and LysoViewTM 540, respectively.
For nucleolin immunocytochemistry, HeLa and HEC-1-A cells were firstly incubated with the nucleolin antibody (1:100) during 2 h and a secondary antibody (Alexa Fluor 647®, 1:1000) for 1 h. Nuclei were stained with the 1 µM nuclear probe Hoechst 33,342 for 15 min. The probe was washed off by rinsing with PBS three times. Then, cells were incubated with AS1411-AuNPs with IQ or C8 for 15 min, washed three times with PBS and then imaged using a Zeiss AxioObserver LSM 710 microscope.
2.6. Flow Cytometry
HeLa, HEC-1-A and NHDF cells were seeded in 12-well plates at a density of 50 × 104 cells/well and incubated overnight for cell adhesion. Then, cells were treated for 24 h with the AS1411-AuNPs with C8 and free C8 as control. After the incubation period, the wells were washed by rinsing with PBS three times and cells were then trypsinized, resuspended in PBS and analyzed in a BD FACSCanto™ II flow cytometry system (BD Life Sciences, Franklin Lakes, NJ, USA) to evaluate the uptake of the aptamer-ligand complexes. C8 fluorescence was used to monitor the cellular uptake of AS1411-AuNPs. Non-specific staining, doublets and debris were excluded.
2.7. Cytotoxicity Assay
HeLa cancer cells were grown in DMEM medium supplemented with 10% fetal bovine serum and a 1% streptomycin–penicillin antibiotic. NHDF and HEC-1-A cells were grown in RPMI medium, supplemented with 10% fetal bovine serum (FBS), 1% streptomycin–penicillin antibiotic, 0.01 M HEPES, 0.02 M L-glutamine and 0.001 M sodium pyruvate. Upon confluence, cells were seeded into 48-well culture plates (2 × 104 cells/mL) in 250 µL of medium. Cells were treated with 200 µL of medium with different stimuli. Firstly, IC50 of IQ or C8 in the cell lines was determined. Then, cells were treated with different conditions: control, AS1411-AuNPs (15 µM), AS1411-AuNPs with IQ (15 µM:5 µM) or AS1411-AuNPs with C8 (15 µM:1 µM).
After 3 days of incubation under a controlled humidified atmosphere at 37 °C and 5% CO2, 50 μL of 5 mg/mL thiazolyl blue tetrazolium bromide (MTT) solution was added into each well and were further incubated for 1 h. The resulting formazan crystals were dissolved in 250 μL of DMSO and the optical density (OD) was recorded at 570 nm. Cell viability was determined using wells without compounds as the control.
2.8. Franz Cell Experiments
For the Franz cell experiments, the AS1411-AuNPs with C8 were incorporated in two different topical formulations. The difference between them was the propylene glycol percentage (8% or 10%). Gels were prepared by dissolving potassium sorbate (0.14% w/w, used as preservative) in sterile water (90.36% or 88.36%) and further dispersing 1.5% (w/w) of hydroxypropylmethyl cellulose (Methocel K100, DOW Chemical Company, Midland, MI, USA) using a helical stirrer (Heidolph RZR 2041, Heidolph Instruments GmbH & Co., Schwabach, Germany). Propylene glycol (8% or 10% w/w) was added under agitation. After the gel preparation, the nanoparticles (7.5 µM AS1411-AuNPs with 0.5 µM C8) were added.
Tissue permeation studies were performed in Static Franz Diffusion Vertical Cells (Model V6A-02, SES GMBH, Waldbrunn, Germany). The receptor chamber was filled with PBS (pH 7.4) up to 5 mL and magnetic stirring was maintained at 500 rpm at 37 °C. The diffusion area was 1.77 cm2 and on the donor chamber about 300 mg of each formulation was applied (weighted on an analytical balance on pre-filled syringes, before and after application on the chamber to determine the exact amount dispensed and available for diffusion). The interface between the two chambers was a vaginal porcine tissue and the total experiment time was 24 h, with samples (200 µL) being collected at different time points (0, 6, 12 and 24 h). The volume collected was replaced by pre-heated fresh PBS. Samples were quantified by high-performance liquid chromatography coupled to fluorescence detector (HPLC-FLD), described in the “Study of the Release Kinetics of C8” section.
The vaginal tissue was processed in order to quantify the C8 present in the sample. For that, the porcine vaginal tissue was sonicated in PBS (2 µL of PBS per mg of tissue) and the supernatant was collected and analyzed. Each formulation was tested in three different tissues (from different animals) in experiments performed in three independents days (n = 3).
Vaginal tissues used throughout the experiments were obtained from a local slaughterhouse (pigs up to 6 months old). The organs were transported to the lab and processed within 3 h from time of collection. The vagina was isolated with surgical scissors, opened longitudinally, washed with normal saline and wrapped in aluminum foil before being stored in zipped plastic bags, at −20 °C, for no more than 7 months. Immediately before the experiments, tissues were thawed in normal saline. Portions of epithelial vaginal tissue with controlled thickness were obtained by horizontally slicing the vagina with a manual dermatome up to a maximum of 300 µm (measured with an electronic digital micrometer (Vogel, model 231061).
2.9. Study of the Release Kinetics of C8
A simple HPLC-FLD method was developed and validated according to the guiding principles of the Food and Drug Administration (
https://www.fda.gov/regulatory-information/search-fda-guidance-documents/analytical-procedures-and-methods-validation-drugs-and-biologics (accessed on 15 September 2020)). The assays were performed using a 1290 HPLC with a binary pump coupled to a 1260 FLD detector from Agilent Technologies (Soquimica, Lisbon, Portugal). For compound separation, a YMC-Triart PFP (5 μm, 4.6 i.d. × 150 mm) analytical column coupled to a Guard-c holder (4 × 10 mm) and a Triart PFP (5 μm, 3 × 10 mm) pre-column were used, all from YMC Europe GMBH (Solítica, Lisbon, Portugal). The mobile phase consisted of methanol/0.1% trifluoroacetic acid (9:1,
v/
v), operated in the isocratic mode with a flow of 0.5 mL/min, and the injection volume was 50 μL. The column and autosampler temperatures were set at 25 and 4 °C, respectively, and the analyte was detected at 498 and 530 nm as excitation and emission wavelengths, respectively. A calibration curve between 0.98 and 500 ng/mL was prepared with several successive dilutions of the analyte, using the mobile phase as solvent.
Figure S1 presents a chromatogram (the retention time of the analyte was 9.57 min).
2.10. Statistical Analysis
All data are expressed as mean ± SEM of at least three independent experiments. Statistical analysis was performed using unpaired two tailed Student’s t test. Values of p < 0.05 were considered significant. All statistical analysis was made using the GraphPad Prism 6.0 Software (GraphPad Sotware Inc, San Diego, CA, USA).
3. Results and Discussion
Citrate AuNPs were functionalized with thiolated AS1411 through a methodology based on increasing concentrations of salts. Then, AS1411-AuNPs were mixed with C
8 (molar ratio of 15:1) and IQ (molar ratio of 15:5). These ratios were defined in accordance with a previous report [
23], in which it was demonstrated that due to the binding strength of C
8 to AS1411, with this molar ratio there is no free C
8 in the solution, and with the IC
50 of each drug determined after 3 days of incubation (
Figure S2). Additionally, the molar ratios were chosen taking into account the in vitro experiments, in order to have the highest concentration to elicit significant cell toxicity and still suitable to observe any changes induced by the ligand complexation to the aptamer, as previously reported [
23].
The morphology of these aptamer-functionalized nanoparticles was analyzed by transmission electron microscopy (TEM) (
Figures S3 and S4). As observed in
Figure S3 and
Figure 2, the nanoparticles present a uniform size (
Figure S4) and are not aggregated. When IQ and C
8 were added, the nanoparticles with IQ (
Figure 2B) and with C
8 (
Figure 2C) also presented a uniform size (
Figure S4) and distribution, without any aggregation, as previously observed. In these images, the metallic core of the resulting nanoparticles can be observed (
Figure 2).
Dynamic light scattering (DLS) was performed to assess the size variation in each step of assembly, as presented in
Table 1. As expected, the starting AuNPs (citrate AuNPs) showed the smallest size. When AS1411 was attached to the surface of AuNPs an increment in size was obtained, from a hydrodynamic diameter of 12.00 ± 1.20 nm to 15.76 ± 1.64 nm. Finally, the hydrodynamic diameter increased to values ranging between 18.30 and 21.16 nm, when C
8 and IQ were supramolecularly associated with aptamer-functionalized AuNPs. Due to their small size, these nanoparticles, aside from the active targeting resulting from the coating with the AS1411 aptamer, also benefit from the enhanced permeability and retention (EPR) effect [
33].
Additionally, the Zeta potential of the particles was measured, and we verified that all of the nanoparticles presented a negative charge in the range of −24.00 to −41.30, and we observed more negative values for the AuNPs carrying the anti-cancer compounds. Since the surfaces of blood vessels and cells are negatively charged components, these nanoparticles can avoid nonspecific interactions [
34]. However, the G4 aptamer, which is more densely negatively charged than duplex DNA, can favor the interaction with positively charged pockets of proteins [
15], namely nucleolin.
We investigated the release profile of C
8 from the AS1411-AuNPs in a buffer containing KPi (20 mM) and KCl (100 mM) over a period of 48 h. As seen in
Figure 3, C
8 was almost fully released from the nanoparticles during the first 12 h, suggesting that the drug can be efficiently released to the cancer cells. These results can be regarded as favorable, since the final goal is to produce a topical formulation to apply in the region of interest. Thus, the rapid release of the compound can be promoted in the region that we want to deliver it.
Then, we performed cellular studies for free compounds and the AS1411-AuNPs, carrying or not the anticancer drugs. Initially, the cellular uptake of free IQ was studied in HeLa, HEC-1-A and NHDF cells by confocal microscopy. As observed in
Figure S5, HeLa and HEC-1-A cells were able to better internalize free IQ, which is consistent with the fact that IQ already has some selectivity for cancer cells, which could be related to its modulatory effect in the NF-κB signaling pathway, which plays a fundamental role in tumorigenesis [
35,
36]. The same effect was not seen with C
8, which was internalized by all the cell lines (
Figure S6). However, when IQ was added to aptamer-conjugated nanoparticles, there was a higher uptake of the nanoparticles by the cancer cell lines relative to the free IQ and some greater internalization by NHDF cells (compare
Figure S5C and
Figure 4C). This is probably due to the fact that normal cells also internalize AS1411, as previously described [
12].
To determine whether the improved drug delivery was due to lysosomal entrapment, we used LysoViewTM 540 to observe lysosome localization. As observed in
Figure 4B,C, the AS1411-AuNPs colocalized with the lysosomotropic dye in HEC-1-A and NHDF cells, respectively (orange staining in the merge image). In HeLa cells, this colocalization was less pronounced, and a green coloration was observed in the merged image (
Figure 4A). Similar distribution of AS1411-AuNPs loaded with C
8 was observed in all cell lines (
Figure 5), with a green coloration, suggesting that the nanoparticles were outside the lysosomal compartment. Nevertheless, the conjugation with AS1411-AuNPs conferred a higher selectivity to C
8.
Previously, it has been reported that after lysosomal compartmentalization, the AS1411 aptamer can be eliminated from cells [
12]. The involvement of this mechanism would not have been observed in the previous images, as cells were constantly cultured in the same medium containing the AS1411-AuNPs. Taking this into account, a new experiment involving fresh medium replacement (without any addition of AS1411-AuNPs with IQ or C
8) was performed. The NHDF cells showed a residual internal fluorescence signal with the AS1411-AuNPs loaded with IQ (
Figure S7C) or C
8 (
Figure S8C). However, in HeLa cells (
Figures S7A and S8A) and HEC-1-A cells (
Figures S7B and S8B) the fluorescence from the nanoparticles remains inside the cells. Thus, it seems as though the efflux mechanism could remove nanoparticles from normal cells while the cancer cells retained the nanoparticles. These results are in accordance with previous ones obtained by Malik et al., where AS1411-AuNPs accumulated at higher levels in cancer cells than in normal cells [
21].
The internalization mechanism of the aptamer AS1411 is likely to be different in cancer cells from in normal cells, because HeLa and HEC-1-A cells present nucleolin on their surfaces [
29]. As was the case with free aptamer [
23], AS1411-AuNPs loaded with C
8 were internalized by nucleolin-positive cells (
Figure 6). After 15 min of incubation, almost all nanoparticles were internalized by the cells and localized in the cytoplasm compartment. Similar results were obtained with IQ, as shown in
Figure 7.
In normal cells (
Figure S9), nucleolin is not overexpressed and the cells did not internalize the compound as quickly as the cancer cells, showing a lower green fluorescence than the malignant cell lines.
Although AS1411 has been reported to bind to nucleolin, there have been additional reports that the initial uptake of AS1411 is nucleolin-independent [
12]. This mechanism could be associated with the absence of colocalization of AS1411-AuNPs with this protein in the confocal studies, since the nanoparticles were only in contact with the HeLa and HEC-1-A cells for 15 min. Other endocytic mechanisms were also proposed by Reyes-Reyes et al. for the internalization of AS1411, such as micropinocytosis [
12]. Contrarily, normal cells internalize AS1411 through other mechanisms, which lead to endosomal entrapment or lysosomal degradation, and consequently, cell death is not induced [
12]. Similar mechanisms may be happening in our experiments with AS1411-AuNPs carrying potential anticancer drugs, which can benefit from these cancer selective mechanisms. Overall, it is possible that nucleolin recognition may localize aptamers on the cells surface, followed by generic macropinocytosis, which would avoid endosomal capture and overall make this targeting mechanism more efficacious for functional drug delivery.
Flow cytometry studies were also performed to evaluate cellular uptake in normal and cancer cells, by following the native fluorescence of the compound. C
8 assembled with AS1411-AuNPs show higher internalization in HeLa cancer cells relative to normal cells, as shown in
Figure 8. Therefore, the AS1411-AuNPs were able to provide C
8 with selectivity towards the cervical cancer cell line and should improve the overall therapeutic index. In HEC-1-A cells, the internalization of C
8 is higher, which could suggest that AS1411-AuNPs are more selective for HeLa cervical cancer cells. The differences in fluorescence levels, when compared with the confocal microscopy experiment (
Figure 5), could be related to the different incubation times (2 h vs. 24 h).
The AS1411 aptamer exhibits antiproliferative activity against various cancer cell lines but requires several days for anticancer action to be observed. Previous results showed that the use of AS1411-nanoparticles can improve AS1411 uptake and decrease the time required for its action [
21]. We also find that nanoparticles at a final concentration of 15 µM, as seen in
Figure 9, are highly selective. In normal cells, they are not toxic, presenting a cellular viability of 85.00 ± 7.01%. In contrast, their toxicity is much higher in cancer cells, with a cellular viability of 37.34 ± 2.83% in HeLa cells and 30.50 ± 1.76% in HEC-1-A cells. Previously, it was found that at least 5 days of treatment was necessary to observe the antiproliferative effect of AS1411 [
14]. The present results were obtained after 3 days of treatment, demonstrating that the covalent bonding of AS1411 to AuNPs was able to decrease the time required for aptamer function.
IQ is usually used in lesions caused by low-risk HPC, but it has been suggested that it may also have anticancer effects in malignant cells resulting from high-grade HPV infections [
27]. Therefore, we evaluated the effect of IQ on the cellular viability of normal and cancer cells, in order to understand what nanoparticle concentrations might be used to treat various HPV lesions. As observed in
Figure S2A,C,E, cervical cancer cells have a higher sensitivity to IQ (with an IC
50 value of 4.22 µM) compared to normal cells (IC
50 of 7.41 µM) and to endometrial cancer cells (IC
50 of 25.77 µM). IQ at a concentration of 5 µM gave cell viabilities in HeLa, HEC-1-A and NHDF cells of 31.09 ± 3.10%, 36.33 ± 3.31% and 49.22 ± 3.24%, respectively. The higher toxicity in cancer cells is presumably due to their higher cellular uptake of IQ, as observed by confocal microscopy (
Figure S5).
The in vitro cytotoxic effects of the complex AS1411-AuNPs with IQ were finally tested on HeLa and HEC-1-A vs. NHDF cells, using an MTT assay. For the same 5 µM concentration of the drug, the AS1411-AuNPs with IQ (61.37 ± 4.33%,
Figure 9) showed lower cellular toxicity in non-malignant cells than the free IQ (49.22 ± 3.24%,
Figure S2E) (
p-value = 0.0506). Additionally, the nanoparticles with IQ were also able to increase the cytotoxicity linked to IQ (14.70 ± 1.91%,
Figure 9) in the cervical cancer line, relative to free IQ (31.09 ± 3.10%,
Figure S2A) (
p-value = 0.0046). Relative to the endometrial carcinoma cell line, AS1411-AuNPs with IQ (24.25 ± 3.90%,
Figure 9) showed a tendency to improve the cytotoxicity of IQ alone (36.33 ± 3.31%,
Figure S2C) (
p-value = 0.0730). Briefly, the complex was able to improve selectivity for cancer cells by decreasing the toxic effect in the non-malignant cell line.
Similar experiments were performed with C
8, which has previously been demonstrated to be highly toxic in both normal and cancer cell lines [
23,
29,
30]. In accordance with these observations, the IC
50 values of free C
8 incubated with HeLa, HEC-1-A and NHDF cells for three days were 0.26 µM (
Figure S2B), 0.10 µM (
Figure S2D) and 0.27 µM (
Figure S2F), respectively. In previous studies we used C
8 at 1 µM [
23,
29,
30], so the same concentration was considered in this work to perform the association of C
8 to AS1411-AuNPs (15 µM) based on the supramolecular strategy. This concentration is high enough to elicit significant cell toxicity while still being suitable for observing any changes induced by the ligand complexation to the aptamer. Then, the resulting complex was incubated with HeLa, HEC-1-A and NHDF cells and their viability was evaluated to verify whether the AS1411-AuNPs could also improve the cancer selectivity of this drug. As observed in
Figure 9 and
Figure S2, the AS1411-AuNPs significantly improved the cancer selectivity of C
8. In fact, 1 µM of free C
8 strongly comprised the viability (<10%) of all cell lines to a similar extent; when carried by nanoparticles, C
8 is considerably more cytotoxic against tumoral cells than normal ones, as also observed for those carrying AS1411-AuNPs.
In brief, IQ addition to the AS1411-AuNPs seems to affect NHDF cells (85.66 ± 7.01% vs. 61.37 ± 4.33%; p = 0.0146), while on HEC-1A cells it has a minor impact (30.50 ± 1.76% vs. 24.25 ± 3.90%; p = 0.1944); however, on HeLa cells it appears to have a larger effect (37.34 ± 2.83% vs. 14.70 ± 1.91%; p < 0.0001). In the case of C8 addition to AS1411-AuNPs, it seems to be safer for NHDF cells (85.66 ± 7.01% vs. 71.31 ± 2.98%; p = 0.0604), exerting a minor impact on HeLa (37.34 ± 2.83% vs. 30.45 ± 1.31%; p = 0.0331), and was more effective on HEC-1A cells (30.50 ± 1.76% vs. 17.00 ± 2.48%; p = 0.0044). These results suggest that the conjugation of AS1411-AuNPs with C8 is more appropriate for use in the endometrial carcinoma cell line, while conjugation with IQ is more appropriate for application in cervical cancer cells.
Overall, MTT assay demonstrated that besides acting as a drug carrier, the AS141-AuNPs also presents an intrinsic therapeutic effect and can potentiate the drug anticancer effects.
The promising nanoparticles were formulated for topical application and their potential to permeate vaginal tissue was evaluated using Franz cells. Porcine vaginal tissue was used in Franz cells, and AS1411-AuNPs with C
8 were incorporated in topical formulations (hydroxypropyl methylcellulose gels) containing either 8% or 10% propylene glycol. As observed in
Table 2, both formulations containing the AS1411-AuNPs loaded with C
8 were retained in the vaginal tissue after 24 h but were not detected in the receptor chamber, as determined by HPLC-FLD analysis at different time points. However, these studies were performed only for 24 h, so the formulation may be able to permeate the tissue and reach the receptor chamber after longer exposure times; the formulation cannot permeate the tissue and reach the receptor chamber. Moreover, there is still a large amount of active compound in the donor chamber after 24 h (
Table 2). Nevertheless, the nanoparticle formulation containing 10% of propylene glycol seems to be better retained in the tissue compared to the 8% formulation. (
Table 2). These results suggest that the viscosity of the formulation could influence the retention of the nanoparticles in the vaginal tissue.