Antibacterial Therapy by Ag+ Ions Complexed with Titan Yellow/Congo Red and Albumin during Anticancer Therapy of Urinary Bladder Cancer

According to the World Health Organization report, the increasing antibiotic resistance of microorganisms is one of the biggest global health problems. The percentage of bacterial strains showing multidrug resistance (MDR) to commonly used antibiotics is growing rapidly. Therefore, the search for alternative solutions to antibiotic therapy has become critical to combat this phenomenon. It is especially important as frequent and recurring infections can cause cancer. One example of this phenomenon is urinary tract infections that can contribute to the development of human urinary bladder carcinoma. This tumor is one of the most common malignant neoplasms in humans. It occurs almost three times more often in men than in women, and in terms of the number of cases, it is the fifth malignant neoplasm after prostate, lung, colon, and stomach cancer. The risk of developing the disease increases with age. Despite the improvement of its treatment methods, the current outcome in the advanced stages of this tumor is not satisfactory. Hence, there is an urgent need to introduce innovative solutions that will prove effective even in the advanced stage of the disease. In our study, a nanosystem based on ionic silver (Ag+) bound to a carrier—Titan yellow (TY) was analyzed. The possibility of binding the thus formed TY-Ag system to Congo red (CR) and albumin (BSA) was determined. TY-Ag binding to CR provides for better nanosystem solubility and enables its targeted intracellular transport and binding to immune complexes. The binding of TY-Ag or CR-TY-Ag to albumin also protects the system against the uncontrolled release of silver ions. It will also allow the delivery of silver in a targeted manner directly to the desired site in the case of intravenous administration of such a system. In this study, the MIC (Minimum Inhibitory Concentration) and MBC (Minimum Bactericidal Concentration) values of the TY-Ag or BSA-TY-Ag systems were determined in two reference strains (Escherichia coli and Staphylococcus aureus). The paper presents nanosystems with a size of about 40–50 nm, with an intense antibacterial effect obtained at concentrations of 0.019 mM. We have also discovered that TY-Ag free or complexed with BSA (with a minimal Ag+ dose of 15–20 μM) inhibited cancer cells proliferation. TY-Ag complex diminished migration and effectively inhibited the T24 cell viability and induced apoptosis. On the basis of the obtained results, it has been shown that the presented systems may have anti-inflammatory and antitumor properties at the same time. TY-Ag or BSA-TY-Ag are new potential drugs and may become in future important therapeutic compounds in human urinary bladder carcinoma treatment and/or potent antimicrobial factors as an alternative to antibiotics.

Abstract: According to the World Health Organization report, the increasing antibiotic resistance of microorganisms is one of the biggest global health problems. The percentage of bacterial strains showing multidrug resistance (MDR) to commonly used antibiotics is growing rapidly. Therefore, the search for alternative solutions to antibiotic therapy has become critical to combat this phenomenon. It is especially important as frequent and recurring infections can cause cancer. One example of this phenomenon is urinary tract infections that can contribute to the development of human urinary bladder carcinoma. This tumor is one of the most common malignant neoplasms in humans. It occurs almost three times more often in men than in women, and in terms of the number of cases, it is the fifth malignant neoplasm after prostate, lung, colon, and stomach cancer. The risk of developing the disease increases with age. Despite the improvement of its treatment methods, the current outcome in the advanced stages of this tumor is not satisfactory. Hence, there is an urgent need to introduce innovative solutions that will prove effective even in the advanced stage of the disease. In our study, a nanosystem based on ionic silver (Ag + ) bound to a carrier-Titan yellow (TY) was analyzed. The possibility of binding the thus formed TY-Ag system to Congo red (CR) and albumin (BSA) was determined. TY-Ag binding to CR provides for better nanosystem solubility and enables its targeted intracellular transport and binding to immune complexes. The binding of TY-Ag or CR-TY-Ag to albumin also protects the system against the uncontrolled release of silver ions. It will also allow the delivery of silver in a targeted manner directly to the desired site in the case of intravenous administration of such a system. In this study, the MIC (Minimum Inhibitory Concentration) and MBC (Minimum Bactericidal Concentration) values of the TY-Ag or BSA-TY-Ag systems were determined in two reference strains (Escherichia coli and Staphylococcus aureus). The paper presents nanosystems with a size of about 40-50 nm, with an intense antibacterial effect obtained at concentrations of 0.019 mM. We have also discovered that TY-Ag free or complexed with BSA (with a minimal Ag + dose of 15-20 µM) inhibited cancer cells proliferation. TY-Ag complex diminished migration and effectively inhibited the T24 cell viability and induced apoptosis. On the basis of the obtained results, it has been shown that the presented systems may have anti-inflammatory and antitumor properties at the same time. TY-Ag or BSA-TY-Ag are new potential drugs and may become in future important therapeutic compounds in human urinary bladder carcinoma treatment and/or potent antimicrobial factors as an alternative to antibiotics.

Introduction
According to the World Health Organization report, the increasing antibiotic resistance of microorganisms is one of the biggest global health problems [1,2]. It is a very dangerous phenomenon because frequent and recurring infections can cause many neoplastic diseases, including human urinary bladder carcinoma.
The percentage of bacterial strains showing multidrug resistance (MDR) to commonly used antibiotics is growing rapidly. Therefore, there is an urgent need to develop new drugs to combat them [3][4][5]. In the last five years, most strains of the Gram-negative Enterobacteriacae species (such as Klebsiella pneumoniae and Escherichia coli (E. coli) recorded in southern and south-eastern Europe were resistant to third-generation cephalosporins, fluoroquinolones, and aminoglycosides [6]. Methicillin-resistant Staphylococcus aureus (MRSA) strains, once associated mainly with hospital-acquired MRSA (HA MRSA), are now also responsible for the majority of community-acquired staph infections (CA MRSA). Genetic studies have shown that the strains causing these infections often have the SCCmec type IV chromosome, which is not usually found in hospital MRSA strains. Thus, we are dealing with a new threat, and not with infectious hospital strains that got into the outside community [7]. One of the causes of this problem is the frequent use of antibiotics, which increased significantly between 2010 and 2020 in the European community. Unfortunately, the mere supervision of alarm strains, their registration, as well as the system controlling the consumption of antibiotics is insufficient in the fight against multidrug resistance of microorganisms. In the case of patients with urothelial carcinoma, the statistics show that the use of antibiotics contributes to a worse survival rate than in those who do not receive antibiotics [8].
Bladder cancer is diagnosed in more than 430,000 patients worldwide every year, making it the ninth most common malignancy. Referring to the data for the United States from 2020 on the www.cancer.net portal, it is almost three times more prevalent in men than in women [9]. Unfortunately, the etiology and pathophysiology of bladder cancer remain unknown. It may be caused by genetic mutations and external risk factors, including tobacco smoking, carcinogen exposure, the chlorination of drinking water, and possibly cyclophosphamide [10]. Bladder cancer most often (approx. 90%) originates from the cells of the transitional epithelium lining the bladder. Depending on the degree of differentiation of this neoplasm, the following forms can be distinguished: well-differentiated tumors with low malignancy potential (G1), medium-grade (G2) neoplasms, poorly differentiated, high-grade (G3) neoplasms, and undifferentiated, anaplastic neoplasms [11]. The disease may also develop as a consequence of previous radiotherapy or frequent and recurrent urinary tract infections. Transient inflammation is considered to be a part of the body's immune defense against the pathogen, but persistent inflammation has the potential to contribute to the development of cancer of varying degrees of severity [12].
A long-term indwelling catheter use is also a risk factor for bladder cancer. Conversely, treatments for an already diagnosed bladder cancer are often associated with catheterization. Administration of drugs into the bladder also increases the risk of infection. Various types of intravesical chemotherapy are used. For example, thanks to the HIVEC system used immediately after the transurethral surgery to remove (resect) the tumor, the progression and recurrence of the disease are significantly reduced by about 2.5 times. Treatment is based on heating and recirculation of the chemotherapeutic between the apparatus and the inside of the bladder through the inserted catheter. Such action results in better penetration of the drug into cells, which results in greater effectiveness of the therapy. However, patients with HIVEC therapy exhibit symptoms of inflammation [13]. Finding a solution

Characterization of TY-Ag Complexes with Protein (BSA-TY-Ag, BSA-CR-TY-Ag)
The characterization of the presented systems is the subject of this study. The size and stability of the resulting complexs were characterized by electrophoresis, gel filtration, UV-VIS spectrometry and DLS methods. The real effect of the added CR and BSA on the size of the systems and their effect on bacteria and neoplastic cells was assessed.
2.1.1. TY-Ag Complexes with CR and/or BSA in the Optimal Molar Ratio of TY-Ag = 1:0.5 (Agarose Gel Electrophoresis) The aim of the analysis was to show that ionic silver can bind to Titan yellow and then can form complexes with CR, which improves solubility (CR-TY-Ag), and with BSA, which provides a protective role. The binding efficiency of Ag + to TY at different molar ratios of TY-Ag (1:1.6 and 1:0.8) was compared in order to optimize the complex for further use in microbiological analyzes. It has been shown that a strong TY-silver complex is formed, which at a ratio of 1:0.8 has no excess silver, does not decay in electrophoresis, and does not travel to the cathode (-).
First, the complexes formed on the basis of the TY-Ag complex were analyzed in a molar ratio of 1:1.6 ( Figure 1). BSA complexed with TY (sample 4) travels faster than free albumin (sample 3) ( Figure 1C), and there is practically complete complexation of TY by BSA ( Figure 1A). The addition of CR to BSA (sample 5) or to BSA-TY (sample 6) causes an additional increase in the rate of albumin migration in the complexes thus formed ( Figure 1C). BSA complexes CR-TY (added in a molar ratio of 1:2), which is visible in sample 6. There is also an additional streak of the CR-TY complex migrating towards the anode (in the experiment where CR-TY was added in a ratio of 1:5, an excess of free TY migrating to the anode) ( Figure 1A). BSA complexes CR-TY-Ag very well ( Figure 1A, sample 10).
The characterization of the presented systems is the subject of this study. The size and stability of the resulting complexs were characterized by electrophoresis, gel filtration, UV-VIS spectrometry and DLS methods. The real effect of the added CR and BSA on the size of the systems and their effect on bacteria and neoplastic cells was assessed.
2.1.1. TY-Ag Complexes with CR and/or BSA in the Optimal Molar Ratio of TY-Ag = 1:0.5 (Agarose Gel Electrophoresis) The aim of the analysis was to show that ionic silver can bind to Titan yellow and then can form complexes with CR, which improves solubility (CR-TY-Ag), and with BSA, which provides a protective role. The binding efficiency of Ag + to TY at different molar ratios of TY-Ag (1:1.6 and 1:0.8) was compared in order to optimize the complex for further use in microbiological analyzes. It has been shown that a strong TY-silver complex is formed, which at a ratio of 1:0.8 has no excess silver, does not decay in electrophoresis, and does not travel to the cathode (-).
First, the complexes formed on the basis of the TY-Ag complex were analyzed in a molar ratio of 1:1.6 ( Figure 1). BSA complexed with TY (sample 4) travels faster than free albumin (sample 3) ( Figure 1C), and there is practically complete complexation of TY by BSA ( Figure 1A). The addition of CR to BSA (sample 5) or to BSA-TY (sample 6) causes an additional increase in the rate of albumin migration in the complexes thus formed ( Figure  1C). BSA complexes CR-TY (added in a molar ratio of 1:2), which is visible in sample 6. There is also an additional streak of the CR-TY complex migrating towards the anode (in the experiment where CR-TY was added in a ratio of 1:5, an excess of free TY migrating to the anode) ( Figure 1A). BSA complexes CR-TY-Ag very well ( Figure 1A, sample 10).
The TY-Ag complex ( Figure 1A, sample 7) is formed, which travels more slowly than the free TY (sample 1), due to the positive charge of the complexed silver.
When comparing samples 8 (CR-TY), 9 (CR-TY-Ag), and 10 (BSA-CR-TY-Ag), migration to the anode is clearly slowed down as the complexes are increased by adding further factors. This proves the formation of these complexes ( Figure 1A). Sample 10 shows the most effective silver binding (the dashed line in Figure 1B indicates the lowest amount of free silver in the sample).  The TY-Ag complex ( Figure 1A, sample 7) is formed, which travels more slowly than the free TY (sample 1), due to the positive charge of the complexed silver.
When comparing samples 8 (CR-TY), 9 (CR-TY-Ag), and 10 (BSA-CR-TY-Ag), migration to the anode is clearly slowed down as the complexes are increased by adding further factors. This proves the formation of these complexes ( Figure 1A). Sample 10 shows the most effective silver binding (the dashed line in Figure 1B indicates the lowest amount of free silver in the sample).
Then, the complexes formed on the basis of the TY-Ag complex were analyzed in a molar ratio of 1:0.8 ( Figure 2). Sample 1 shows a slight trace of unbound silver traveling towards the cathode, while the addition of CR in sample 2 completely binds the silver in the complex (CR-TY-Ag). CR increases the solubility of the TY-Ag complex ( Figure 2B). The complexed silver is visible in both sample 3 (BSA-TY-Ag) and sample 4 (BSA-CR-TY-Ag). Due to the positive charge of Ag + , it binds to TY or TY-CR in albumin ( Figure 2C). Nonprotein bound TY-Ag complexes (samples 3 and 4) can also be observed, migrating faster than BSA-TY-Ag and BSA-CR-TY-Ag to the anode ( Figure 2C). Albumin in these complexes travels to the anode faster than free BSA (sample 5) ( Figure 2C). Congo red does not bind Ag + -migration towards the cathode is visible (sample 6) ( Figure 2A). Then, the complexes formed on the basis of the TY-Ag complex were analyzed in a molar ratio of 1:0.8 ( Figure 2). Sample 1 shows a slight trace of unbound silver traveling towards the cathode, while the addition of CR in sample 2 completely binds the silver in the complex (CR-TY-Ag). CR increases the solubility of the TY-Ag complex ( Figure 2B) The complexed silver is visible in both sample 3 (BSA-TY-Ag) and sample 4 (BSA-CR-TY Ag). Due to the positive charge of Ag + , it binds to TY or TY-CR in albumin ( Figure 2C) Non-protein bound TY-Ag complexes (samples 3 and 4) can also be observed, migrating faster than BSA-TY-Ag and BSA-CR-TY-Ag to the anode ( Figure 2C). Albumin in thes complexes travels to the anode faster than free BSA (sample 5) ( Figure 2C). Congo red does not bind Ag + -migration towards the cathode is visible (sample 6) ( Figure 2A). As in the electrophoresis presented above, at the ratio TY-Ag = 1:0.8, slight traces o streaking excess silver were visible; therefore, the target ratio of TY-Ag = 1:0.5 was used in microbiological experiments. It ensures that the added silver is completely bound, and a strong complex is obtained that does not decompose under electrophoresis. Thereby i is certain that the administration of excess free silver in microbiological tests has been avoided.

Albumin Complexes with TY and TY-Ag (UV/VIS Spectrophotometry)
The comparative analyzes of the UV/VIS spectra show that TY binds to BSA, as evi denced by the hypochromic effect at 392 nm wavelength, with a slight shift towards longe wavelengths and maintaining the unchanged maximum at 330 nm. Additionally, there i a maximum at 280 nm related to albumin complexation. The spectrum of TY-Ag or BSA TY-Ag differs markedly from the spectrum of free TY or BSA-TY complex (Figure 3). As in the electrophoresis presented above, at the ratio TY-Ag = 1:0.8, slight traces of streaking excess silver were visible; therefore, the target ratio of TY-Ag = 1:0.5 was used in microbiological experiments. It ensures that the added silver is completely bound, and a strong complex is obtained that does not decompose under electrophoresis. Thereby it is certain that the administration of excess free silver in microbiological tests has been avoided.

Albumin Complexes with TY and TY-Ag (UV/VIS Spectrophotometry)
The comparative analyzes of the UV/VIS spectra show that TY binds to BSA, as evidenced by the hypochromic effect at 392 nm wavelength, with a slight shift towards longer wavelengths and maintaining the unchanged maximum at 330 nm. Additionally, there is a maximum at 280 nm related to albumin complexation. The spectrum of TY-Ag or BSA-TY-Ag differs markedly from the spectrum of free TY or BSA-TY complex (Figure 3).

Albumin Complexes with TY and TY-Ag (Gel-filtration Chromatography on BioGel P-150)
The analysis shows that both TY and TY-Ag are bound to albumin and descend quickly (approx. 1 mL each) the column filled with BioGel P-150. The free TY descends more slowly, becoming smoother as it passes through the gel, and most of it is delayed by about 2.5-3 mL. This demonstrates the complexation of TY and the TY-Ag system by albumin (Figure 4).  The analysis shows that both TY and TY-Ag are bound to albumin and descend quickly (approx. 1 mL each) the column filled with BioGel P-150. The free TY descends more slowly, becoming smoother as it passes through the gel, and most of it is delayed by about 2.5-3 mL. This demonstrates the complexation of TY and the TY-Ag system by albumin ( Figure 4). The autocorrelation curves of TY-Ag relative to free TY were analyzed. A shift in the autocorrelation curve of the TY-Ag complex relative to the autocorrelation curve of free TY was observed, which proves the presence of large TY aggregates formed under the influence of bound silver.  The analysis shows that both TY and TY-Ag are bound to albumin and descend quickly (approx. 1 mL each) the column filled with BioGel P-150. The free TY descends more slowly, becoming smoother as it passes through the gel, and most of it is delayed by about 2.5-3 mL. This demonstrates the complexation of TY and the TY-Ag system by albumin ( Figure 4). The autocorrelation curves of TY-Ag relative to free TY were analyzed. A shift in the autocorrelation curve of the TY-Ag complex relative to the autocorrelation curve of free TY was observed, which proves the presence of large TY aggregates formed under the influence of bound silver. The autocorrelation curves of TY-Ag relative to free TY were analyzed. A shift in the autocorrelation curve of the TY-Ag complex relative to the autocorrelation curve of free TY was observed, which proves the presence of large TY aggregates formed under the influence of bound silver. This is also confirmed by the % intensity analysis. Visible polydisperse plot for free Titan yellow with two peaks (R H1 = 4.4 nm and R H2 = 26 nm) and monodisperse plot for the TY-Ag complex with one peak (R H = 41 nm). During the % mass analysis, there is a clear shift of the maximum for the TY-Ag complex (R H = 19.5 nm) compared to the free TY (R H = 2.4 nm). This proves the presence of TY-Ag aggregates ( Figure 5). This is also confirmed by the % intensity analysis. Visible polydisperse plot for free Titan yellow with two peaks (RH1 = 4.4 nm and RH2 = 26 nm) and monodisperse plot for the TY-Ag complex with one peak (RH = 41 nm). During the % mass analysis, there is a clear shift of the maximum for the TY-Ag complex (RH = 19.5 nm) compared to the free TY (RH = 2.4 nm). This proves the presence of TY-Ag aggregates ( Figure 5). The BSA-TY autocorrelation curves against free albumin were analyzed. No change in the BSA versus BSA-TY autocorrelation curves was observed. This proves that TY is bound to a small degree by BSA, or that the whole thing is hidden in the pocket of albumin. On the other hand, a shift in the autocorrelation curve of the BSA-TY-Ag complex with respect to the autocorrelation curve of free BSA and BSA-TY was observed. This proves the presence of large BSA-TY-Ag aggregates.
Intensities and masses were also analyzed. Identical results were obtained for the samples of free BSA and BSA-TY complexes (in both cases for % intensity RH = 5 nm, for % mass RH = 3.9 nm). It was concluded that no large aggregates were formed and that TY was likely to bind at the albumin-binding cleft, and there was no bridging of albumin molecules ( Figure 6). The BSA-TY autocorrelation curves against free albumin were analyzed. No change in the BSA versus BSA-TY autocorrelation curves was observed. This proves that TY is bound to a small degree by BSA, or that the whole thing is hidden in the pocket of albumin. On the other hand, a shift in the autocorrelation curve of the BSA-TY-Ag complex with respect to the autocorrelation curve of free BSA and BSA-TY was observed. This proves the presence of large BSA-TY-Ag aggregates.
Intensities and masses were also analyzed. Identical results were obtained for the samples of free BSA and BSA-TY complexes (in both cases for % intensity R H = 5 nm, for % mass R H = 3.9 nm). It was concluded that no large aggregates were formed and that TY was likely to bind at the albumin-binding cleft, and there was no bridging of albumin molecules ( Figure 6).
The autocorrelation curves of BSA-TY-Ag versus BSA-TY were also analyzed ( Figure 7). A shift in the autocorrelation curve of the BSA-TY-Ag complex relative to the BSA-TY autocorrelation curve was observed, which proves the presence of large aggregates formed due to the binding of the Ty-Ag complex with albumin.
The appearance of an additional maximum was registered on the % intensity plot for the samples of the BSA-TY-Ag complex (R H1 = 3.8 nm and R H2 = 49.8 nm) relative to the maximum for free BSA and BSA-TY (in both cases for % intensity, there is only one R H maximum = 5 nm). An additional maximum also appears in the % mass plot for the samples of the BSA-TY-Ag complex: R H1 = 3.6 nm and R H2 = 22.2 nm relative to the maximum for free BSA and BSA-TY (in both cases for % mass R H = 3.9 nm). This proves the presence of larger BSA-TY-Ag aggregates or the possibility of Ag + -mediated bridging of two albumin molecules (BSA-TY-Ag-TY-BSA). As a result, nanosystems containing albumin and silver are created, which are still relatively small.  The autocorrelation curves of BSA-TY-Ag versus BSA-TY were also analyzed ( Figure  7). A shift in the autocorrelation curve of the BSA-TY-Ag complex relative to the BSA-TY autocorrelation curve was observed, which proves the presence of large aggregates formed due to the binding of the Ty-Ag complex with albumin.   The autocorrelation curves of BSA-TY-Ag versus BSA-TY were also analyzed ( Figure  7). A shift in the autocorrelation curve of the BSA-TY-Ag complex relative to the BSA-TY autocorrelation curve was observed, which proves the presence of large aggregates formed due to the binding of the Ty-Ag complex with albumin.

Microbiological Analysis
Analyzes were carried out to check whether the proposed silver-based system bound to the carrier in the form of TY or additionally bound to BSA can be used to effectively remove the bacterial film, with a simultaneous therapeutic effect on the tumor. The aim of the research was to determine the MIC and MBC of the analyzed systems.

No Inhibition of Bacterial Growth by free TY and Enhanced Inhibition of Bacterial
Growth upon Complexation of TY with Ag + . Escherichia coli (EC, ATCC ® 35218™) and Staphylococcus aureus (SA, ATCC ® 29213™) As a result of serial dilution of the samples, 4 samples were obtained in which the molar ratio of TY and silver was equal to 1:1 and the concentrations were as it shown in Table 1. Also 4 samples with analogous concentrations of free TY without silver were prepared. The zones of inhibition appearing after the addition of the TY-Ag complex were observed, while TY did not inhibit the growth of the analyzed bacterial strains (Figure 8).
Analyzes were carried out to check whether the proposed silver-based system bou to the carrier in the form of TY or additionally bound to BSA can be used to effective remove the bacterial film, with a simultaneous therapeutic effect on the tumor. The a of the research was to determine the MIC and MBC of the analyzed systems.

No Inhibition of Bacterial Growth by free TY and Enhanced Inhibition of Bacteria
Growth upon Complexation of TY with Ag + .Escherichia Coli (EC, ATCC ® 35218™) and Staphylococcus Aureus (SA, ATCC ® 29213™) As a result of serial dilution of the samples, 4 samples were obtained in which t molar ratio of TY and silver was equal to 1:1 and the concentrations were as it shown Table 1. Also 4 samples with analogous concentrations of free TY without silver were p pared. The zones of inhibition appearing after the addition of the TY-Ag complex we observed, while TY did not inhibit the growth of the analyzed bacterial strains (Figure

Determination of the Minimum Inhibitory Concentration (MIC) Value
The value of MIC = 0.019 mM (for E. coli and for S. aureus) was determined for the molar ratio of TY-Ag (1:0.5), where we can be sure that the silver is completely bound (well diffusion in agar experiment). The presence of albumin in the complex doubles the MIC value 0.039 mM for Gram-positive S. aureus, which has a thick bacterial envelope, and there is no increase in the MIC value for Gram-negative E. coli (Table 2, Figure 9).  The value of MIC = 0.019 mM (for E. coli and for S. aureus) was determined for the molar ratio of TY-Ag (1:0.5), where we can be sure that the silver is completely bound (well diffusion in agar experiment). The presence of albumin in the complex doubles the MIC value 0.039 mM for Gram-positive S. aureus, which has a thick bacterial envelope, and there is no increase in the MIC value for Gram-negative E. coli (Table 2, Figure 9).   (Table 3) for E. coli was determined as 0.036 mM and 0.07 mM, respectively, for TY-Ag and BSA-TY-Ag ( Figure 10A and B). For S. aureus the MBC in the concentration range assessed was not determined ( Figure 10C and D).   The complexes with the TY-Ag molar ratio of 1:0.5 were analyzed, which, according to the results of the electrophoresis, were characterized by the complete binding of AgNO 3 by TY. The concentration of silver in all analyzed samples was 4.7 mM, which was a value well above the MIC for both analyzed strains. Modified Kirby-Bauer method was used (agarose wells instead of disks).

Antibacterial Agents
Both in the case of E. coli and S. aureus, the influence of the presence of TY on the enlargement of growth inhibitory zones can be seen. Free AgNO 3 produces smaller zones of inhibition than the complexed Ag + . An increase in these zones was also observed after the addition of CR and after the addition of BSA. However, the simultaneous use of BSA and CR (quadruple complex: BSA-CR-TY-Ag) resulted in smaller zones than using CR and BSA alone, but still increased relative to the free Ag + . The use of CR and/or BSA has been shown to increase the solubility of TY-Ag and to provide protection, thus improving the antibacterial effect of silver against both Gram-positive bacteria as exemplified by S. aureus and Gram-negative bacteria as exemplified by E. coli (Figure 11). The complexes with the TY-Ag molar ratio of 1:0.5 were analyzed, which, according to the results of the electrophoresis, were characterized by the complete binding of AgNO3 by TY. The concentration of silver in all analyzed samples was 4.7 mM, which was a value well above the MIC for both analyzed strains. Modified Kirby -Bauer method was used (agarose wells instead of disks).
Both in the case of E. coli and S. aureus, the influence of the presence of TY on the enlargement of growth inhibitory zones can be seen. Free AgNO3 produces smaller zones of inhibition than the complexed Ag + . An increase in these zones was also observed after the addition of CR and after the addition of BSA. However, the simultaneous use of BSA and CR (quadruple complex: BSA-CR-TY-Ag) resulted in smaller zones than using CR and BSA alone, but still increased relative to the free Ag + . The use of CR and/or BSA has been shown to increase the solubility of TY-Ag and to provide protection, thus improving the antibacterial effect of silver against both Gram-positive bacteria as exemplified by S. aureus and Gram-negative bacteria as exemplified by E. coli (Figure 11). The results were statistically analyzed using the Student's T-test. Statistically significant differences (**p < 0.01; ***p < 0.001) in the size of growth inhibitory zones were observed between the AgNO3 samples and those to which the silver complexes were added.

Cell Analysis
The effect of TY-Ag or BSA-TY-Ag complexes on T24 cell proliferation (MTS), migration (scratch test) as well as viability/survival, and apoptosis induction (Caspase 3 assay -Cas 3, Flow cytometry) was assessed. The preliminary results obtained by us earlier on human U937 lymphoid cell line in which late apoptosis (73.65% of cells) and necrosis The results were statistically analyzed using the Student's T-test. Statistically significant differences (** p < 0.01; *** p < 0.001) in the size of growth inhibitory zones were observed between the AgNO 3 samples and those to which the silver complexes were added.

Cell Analysis
The effect of TY-Ag or BSA-TY-Ag complexes on T24 cell proliferation (MTS), migration (scratch test) as well as viability/survival, and apoptosis induction (Caspase 3 assay-Cas 3, Flow cytometry) was assessed. The preliminary results obtained by us earlier on human U937 lymphoid cell line in which late apoptosis (73.65% of cells) and necrosis (about 25% of cells) was observed after 72 h, after using TY-Ag 1:0.8 (where the concentration of TY was 0.072 mM and concentration of Ag + was 0.057 mM [15] provided the basis for the analysis of the effect of these agents on bladder cancer cells.  It was observed that an Ag + concentration of 10 µM did not reduce cell proliferation in the presence of complexed TY (20 µM). BSA at these concentrations of TY and Ag + had practically no effect on proliferation. The combination of Ag + (10 µM) with TY at a higher concentration (

Induction of Apoptosis in T24 Cells by TY-Ag (Flow Cytometry)
Using the flow cytometry method (Annexin/propidium iodide), apoptosis was assessed in the tumor cells of the bladder cancer cell line T24 after the addition of the TY(20 µM)-Ag(15 µM) complex. A total of 48 h after the addition of the factor, TY-complexed silver, added at a concentration of 15µM, resulted in a nearly complete apoptosis of 96.6%. This result confirmed that this concentration, close to the MIC value = 0.019 mM (for both analyzed E. coli and S. aureus strains) for silver in the TY-Ag complex (1:0.5), can induce complete apoptosis of T24 cells (Figure 14). The T24 cell lines were treated with TY(20 µM)-Ag(1 µM) complex, and the cell migration was evaluated with a wound-healing test/scratch assay. A significant reduction in cell motility was observed upon exposure to TY(20 µM)-Ag(1 µM) (Figure 15). Optical images show scratch overgrowth with time for T24 cells ( Figure 15A). The photographs

Reduction of T24 Cell Migration by TY-Ag (Scratch Assay)
The T24 cell lines were treated with TY(20 µM)-Ag(1 µM) complex, and the cell migration was evaluated with a wound-healing test/scratch assay. A significant reduction in cell motility was observed upon exposure to TY(20 µM)-Ag(1 µM) (Figure 15). Optical images show scratch overgrowth with time for T24 cells ( Figure 15A). The photographs were captured immediately after wounding as well as 24 h later with the corresponding control  Figure 15B. The arrest of cell division may be the result of disturbances in the course of the ce cycle and/or induction of apoptosis and necrosis in cells. Therefore, in the next stage the study, the influence of the tested compounds on the course of the cell cycle in th cultures of T24 cells after 48 h of incubation was determined. Cytometric analysis showe that the tested compounds (except for taxol) caused a slight increase in the number of cel in the G1 phase while reducing the number of cells in the S and G2 phases of the cell cyc ( Figure 16).

Discussion
The prevention of infections is mainly associated with the use of antibiotics, the effectiveness of which is decreasing. In addition, frequent and recurring infections can cause cancer. For these reasons, finding an alternative, innovative therapy integrating antibacterial and anti-cancer treatment is the goal of scientific research [5,27,28].
Finding an agent that would combine the ability to minimize infections and anti-cancer activity seems to be very important. Such an agent could have practical applications in hospital treatments, and such attempts have long been made, but most involve alternative use of antibiotics. Various antibiotics are used in the treatment of neoplasms due to their antiproliferative, pro-apoptotic, and anti-epithelial-mesenchymal transition (EMT) abilities [29]. Yadav et al. described fluoroquinolones which have been used as antibiotics for over four decades. Recent research highlighted their use as pharmacological compounds with multifaceted implications. Repositioning of fluoroquinolones into anti-cancer molecules seems to be a highly plausible option owing to their profound immunomodulatory, pro-apoptotic, anti-proliferative, and anti-metastatic potential [30]. Research conducted by Kamat et al. described the use of antibiotics ciprofloxacin, trimethoprim-sulfamethoxazole, cefazolin, or nitrofurantoin in bladder tumor treatment [31]. However, the newest research showed that antibiotics could also induce cancer by disrupting the gut microbiota, which further promoted chronic inflammation, altered normal tissue metabolism, led to genotoxicity, and weakened the immune response, thereby adversely affecting cancer treatment [32,33].
Among non-antibiotic anti-infectious agents, silver has been known for a long time for its antibacterial and anti-inflammatory properties. Applied in the form of nanosilver, it is used in many areas of medicine. Plastic catheters coated with silver nanoparticles prevent biofilm formation by bacteria, including E. coli and S. aureus. It is used to produce disinfectants, in dental composites, or as bactericidal coatings [34]. Silver is even used to prevent HIV binding to host cells [35]. The antimicrobial effects of silver are mostly attributed to silver ions [36,37]. Silver nanoparticles (AgNPs) continuously release silver ions in an aqueous microenvironment [38,39]. Due to the larger surface of AgNPs, they show stronger and better bactericidal activity [40]. The main reasons for the bactericidal properties of AgNPs are the disruption of the integrity of the bacterial cell by binding to the basic cellular structures [41,42], especially to their -SH groups [43]. AgNPs also generate reactive oxygen species (ROS) and free radicals that damage the bacterial cell wall and inhibit respiratory enzymes [44], as well as disrupt DNA replication and destroy bacteria. Silver nanoparticles are biocidal against various Gram-positive and Gram-negative bacteria [45].
AgNPs exhibit anti-cancer properties against various cancer cell lines, such as MCF-7 breast cancer cells [46], HCT116 colon cancer cells [47,48], prostate cancer cells [49], HeLa cells [50], or lung carcinoma A549 cells [51]. AgNPs can be used to induce regression of bladder cancer through apoptosis under the influence of ROS-producing radicals [52,53]. However, there are reports on a higher toxicity profile of silver nanoparticles than gold nanoparticles for normal organs. It relates to the high ROS generation capacity [54]. This property of AgNPs has so far represented a significant limitation in the development of these nanoparticles as drug delivery systems. However, recent studies have shown their biocompatible nature after coupling or coating with polymers. In our research, we also assumed that the conjugation of silver with a supramolecular compound, in particular Titan yellow, and additionally with CR or with albumin, will increase its biocompatibility.
Titan yellow comprises symmetric polar groups and aromatic rings. Its halves are linked by a tri-azo bond capable of complexing metal ions, particularly silver and mercury. The silver-containing complex is more convenient due to its stability and formation in both neutral and slightly alkaline environments [15,55,56]. Thanks to this binding, Ag + becomes better available both for bacteria to fight them and for bladder cancer cells. Our research, based on electrophoretic methods, gel chromatography, and UV/VIS spectrophotometry, also showed that the TY-Ag system could additionally be bound by albumin or by Congo red. As a result, complexes were obtained that not only bound ionic silver but also provided protection and better solubility. The TY-Ag complexes and the triple complexes of BSA-TY-Ag or CR-TY-Ag represent systems of potential therapeutic value. Due to the very good solubility provided by CR, as well as the protective effect of albumin, these systems can reduce the accumulation of metals in the body by facilitating the removal of silver from the complex. There are examples in the literature of the interaction of silver nanoparticles with proteins. Although the capping proteins can increase the internalization of AgNPs into cells via endocytosis, regulate cellular uptake and bioavailability of AgNPs, they can also be responsible for the toxic activity of AgNPs [57]. The interaction of AgNPs with albumin has been described [58,59]. The silver complexes with TY or BSA-TY presented in this paper give an opportunity to create high-capacity systems. The pursuit of high payload combined with high targeting efficiency will increase the localization of cancer drugs, thus avoiding toxicity and side effects caused by drugs being distributed outside of the target.
Therefore, further studies are needed to understand the type of proteins and their precise role in the formation and bioactivity of nanoparticles.
Microbiological analyzes showing the effect of silver in various forms have been previously carried out on different bacterial strains [60]. Nevertheless, the MIC and MBC values after treatment with TY-Ag or BSA-TY-Ag in E. coli and S. aureus have been presented here for the first time. E. coli was selected because it is the main bacteria isolated from cases of urinary tract infections [23], whereas S. aureus, a facultative anaerobic Gram-positive coccus, was selected for use in this study because it is one of the facultative bacteria found in inflammation of the urinary bladder and it can develop resistance to antimicrobial agents. S. aureus may be a pathogen of the urinary tract among patients staying in long-term care facilities, wearing indwelling catheters, with urinary tract obstruction and/or malignant neoplasms [24].
Since our research has shown that free TY does not inhibit the growth of E. coli or S. aureus bacteria, while zones of growth inhibition are visible with the Ag + complex, TY can be considered a useful type of carrier for silver. The results obtained by us have shown that thanks to the complexation of Ag + with TY, a lower concentration of the administered silver can be used, which significantly reduces its toxicity and, additionally, provides protection. Additional protection is provided by albumin, which in the BSA-TY-Ag complex has increased the zones of inhibition of bacterial growth in both E. coli and S. aureus, as confirmed by our research. Additionally, the complexes with Congo red, which increases the solubility of the TY-Ag complex, increased the zones of inhibition of bacterial growth. The use of CR and/or BSA has been shown to increase the solubility of TY-Ag and to provide protection, thereby improving the antibacterial activity of silver in both Gram-positive bacteria, for example S. aureus, and Gram-negative bacteria, e.g., E. coli.
The relationship between the size of nanosystems and their antimicrobial efficacy (prokaryotic cells) is often analyzed in the literature. Similar to prokaryotic cells, in eukaryotic cells (antitumor efficacy), the size of AgNPs is a key factor determining their penetration into the cells by diffusion (translocation), endocytosis, or phagocytosis [61][62][63]. In recent times, it has been established that particle size is particularly important while other physicochemical parameters are under control. To confirm this, a systematic evaluation of the size-dependent biological profile and biodistribution of the three monodisperse drug-silica nanoconjugates at 20, 50, and 200 nm was performed in a previous study. This evaluation was performed through laboratory experiments in conjunction with mathematical modeling to determine the optimal size of the most effective anti-cancer drug delivery system. Thanks to this study, it was found that 50 nm drug-silica nanoconjugate particles exhibited the highest retention in cancer tissue over time, leading to deeper tissue penetration and effective internalization in cancer cells along with slower removal [64]. Silver in a nanometric scale (less than 100 nm) has different antibacterial properties compared with the bulk form of silver metal, like a large effective surface area of individual silver nanoparticles and strong toxicity to a wide range of microorganisms [65]. The analyzes carried out in this study with the use of DLS showed that the hydrodynamic diameter of the TY-Ag complex is about 40 nm, while the BSA-TY-Ag aggregate is about 40-50 nm. As a result, nanosystems containing albumin and silver are created, which are relatively small in size, which is very advantageous in the context of delivering silver to tissues.
Different silver-based nanosystems may give different MIC and MBC results for the tested bacterial strains. This variability may be due to the methodology used to prepare the silver nanoparticles and the size of the silver nanoparticles used. A study by Ayala-Núñez NV et al. estimated MIC, MBC of 10 nm silver nanoparticles at a concentration of 1.35 mg/mL against S. aureus. [66]. The authors indicated that the ultra-fine particle size caused it to function at a lower concentration. A commercially available 5 nm silver nanoparticle was used in that study. In a study by Agnihotri et al., silver nanoparticles smaller than 10 nm showed enhanced antimicrobial activity. They also concluded that compared to other sizes of silver nanoparticles, the 5 nm size has the fastest antibacterial activity [67].
Based on these results, we also conducted a MIC and MBC analysis of our test systems to determine the antimicrobial efficacy of our 50 nm nanosystems. MIC values for TY-Ag (1:0.5) were estimated at 0.019 mM (for E. coli and for S. aureus), and for BSA-TY-Ag at 0.019 mM for E. coli and 0.039 mM for S. aureus. MBC for TY-Ag (1:0.5) was found to be 0.036 mM (for E. coli) while the determination of MBC for S. aureus was impossible. MBC for BSA-TY-Ag was calculated as 0.07 mM(for E. coli), whereas the determination of MBC for S. aureus was impossible. It was reported that the activity of silver in AgNPs against Gram-negative bacteria was stronger than against Gram-positive bacteria [68][69][70][71], which was confirmed by the results of the present study. It is due to the presence of a thicker peptidoglycan cell wall in Gram-positive bacteria. However, there are works that contradict this statement [72][73][74] or show variable susceptibility within these bacterial groups [75,76]. The present results demonstrate the inhibitory effect of bound albumin on the activity of complexed silver in bacteria. The addition of BSA increases the MIC for S. aureus, also increases MBC for E.coli (for S. aureus, it was not possible to perform such an observation due to the inability to determine the MBC). BSA also provides protection in bladder cancer T24 cell culture (reduces the cytotoxic effect of the TY-Ag system). It can be treated as an advantage if we consider the system with albumin as a drug carrier that will prolong the action of silver, causing its gradual release. This protein may also play a protective role, e.g., when administered intravenously.
Comparing our results with the results of some research teams, we noticed low values of the above parameters (at the level of a few µM), much lower than those obtained with the use of biologically or chemically synthesized silver nanoparticles [77]. In our research, we obtained nanosystems with a size of about 40-50 nm, with an intense antibacterial effect obtained at concentrations of 3 µg/mL (19 µM). These results are comparable to the results of Wypij M. et al. They obtained nanoparticles AgNPs, which were spherical in shape, small in size (mean 13.2 nm), and exhibited antibacterial activity against both Gram-positive and Gram-negative bacteria (MIC of 8-128 µg/mL, MBC of 64-256 µg/mL). However, S. aureus was much less sensitive (MIC = 128 µg/mL and MBC = 256 µg/mL) than Gram-negative bacteria E. coli (MIC values of 8 µg/mL; MBC values 32 µg/mL), which is different from the results obtained by us [63]. Therefore, our findings are in line with these previously published data, which is extremely important due to the lower efficient doses of silver.
Despite the strong antimicrobial activity of AgNPs and a wide range of biomedical applications, their use as therapeutic agents is limited due to their cytotoxicity to mammalian cells [78].
According to [79], if the cell viability was reduced to <70% of the control, the agent would have a cytotoxicity potential. In our study, the viability of T24 cells after 24 h was higher than 70% when the cells were stimulated with TY ( The cell viability of both tested cell lines was significantly inhibited in the presence of AgNPs at a concentration of 16 µg/mL or higher, which gives similar results as those obtained for silver in our complex presented in this study on the cells of bladder cancer T24, with a significant degree of malignancy. AgNP concentration in the range of 16-64 µg/mL decreased the viability of RAW 264.7 cells from 42.2 to 14.2%, while in the case of MCF-7 cells, the viability of the measured cells decreased from 38 to 15.8% [63]. Based on these findings, we are aware that there is a need to search for concentrations of the tested TY-Ag complexes, which will be microbicidal, decrease in T24 cells proliferation, and will not be cytotoxic to normal cells at the same time. Our results show that the tested Ty-Ag complex can be considered as a potential antimicrobial agent, which exhibits antibacterial activity against Gram-negative and Gram-positive bacteria at doses being safe for healthy cells. It is worth noting that the conducted research also showed the inhibition of cell migration under the influence of TY-Ag, which may be of great importance when it comes to metastasis. In addition, studies have shown the cytostatic and cytotoxic effects of the system under study on neoplastic cells. It appears obvious that in order to effectively eradicate tumors, it is necessary to trigger apoptosis of cancer cells. Our preliminary results for TY-Ag on human U937 lymphoid cell line cells confirm the efficacy of Ag + complexed at 9.8 µg/mL. Late apoptosis (73.65% of cells) and necrosis (about 25% of cells) were demonstrated after 72 h, after using TY-Ag 1:0.8 (where concentration of TY was 0.072 mM and concentration of Ag + was 0.057 mM [15]. Zhou et al. described apoptosis of T24 cells induced by 48 h exposure to silver complexed in the Ag-SP-DNC complex (20 µM) at the level of 28.72% (early and late apoptosis together) [80]. Our results obtained for TY-Ag (1:0.8) showed a strong pro-apoptotic effect of this system (late apoptosis after 48 h affected 96.6% of cells) at concentrations of TY(20 µM)-Ag(15 µM), confirmed by a modified Cas3 test. It is worth noting that the activation of Caspase-3 by free TY at a concentration of 60 µM was at a negligible level close to the control sample one.
To summarize, we have demonstrated for the first time that TY-Ag complex regulates proliferation, survival, and migration of T24 urinary bladder cells as well as inhibits bacterial growth of two reference strains, E. coli and S. aureus, showing the high antibacterial activity in relatively low concentration (19 µM). TY-Ag complexes were characterized and analyzed for their antibacterial and cytotoxic activities. They can interact with protein, in particular albumin, which increases the biocompatibility and protects the system, or with Congo red, a supramolecular carrier that can provide for targeted transport. The TY-Ag complex is a promising compound for the treatment of bladder cancer as well as the treatment of bactericidal infections and could open up new avenues for new non-antibiotic treatment strategies for infections. TY and CR were dissolved in 0.05 M TRIS/HNO 3 /0.9% KNO 3 buffer, pH 8.2 to the appropriate concentration. It was boiled for 2 min at 100 • C to dissolve, then cooled. Initially, the molar ratio CR:TY = 1:2 (and 1:5-unpublished results) was calculated.

Materials
AgNO 3 was prepared fresh in a dark tube. It was dissolved in 0.05 M Tris/HNO 3 /0.9% KNO 3 buffer, pH 8.2. Initially, the molar ratios of TY-Ag = 1:1.6 (samples with excess silver) or 1:0.8 (samples with all silver bound) or 1:0.5 (samples with completely bound silver used in microbiological experiments to completely eliminate free silver) were calculated. To prepare the TY-Ag complex, AgNO 3 solution was added to TY and incubated for 3 min.
To prepare complexes with albumin, a 10× excess of TY over BSA or a 10× excess of CR over BSA was initially calculated. Then, after addition of BSA and the buffer, the mixture was incubated for 10 min. Co-micelle CR-TY (both components with the same molar mass) was used at 12-fold excess over BSA.

Characterization of TY-Ag
Complexes with Protein or with CR (BSA-TY-Ag, BSA-CR-TY-Ag)

• Electrophoresis
Electrophoresis was performed in 1% agarose gel (0.06 M sodium barbital buffer pH 8.6). Proteins were fixed in the gel with picrate and then stained with bromophenol blue solution. CR was removed from the gel by reduction with sodium dithionite. The sodium dithionite also revealed the location of the silver after the separation. The differences in the speed of migration of individual complexes and the possibilities of silver binding depending on the molar ratio of TY-Ag (1:1.6 vs. 1:0.8) were assessed.

•
Assessment of TY and TY-Ag binding by BSA-Spectrophotometry The synthesis of the TY-Ag complex was observed visually by the color change of the TY from yellow to orange after adding AgNO 3 and spectroscopically using UV/VIS spectroscopy (CarryWinUV, Perlan, Agilent Technologies, Inc., Santa Clara, CA, USA) in a wavelength range from 200 to 800 nm, at a resolution of 1 nm. The TY without silver nitrate was used as the control sample. The spectra of TY, TY-Ag, as well as BSA-TY and BSA-TY-Ag, were compared, and on that basis, the formation of complexes was assessed.

•
Assessment of TY and TY-Ag binding by BSA -Gel filtration Chromatography Using the gel-filtration method, the speed at which the systems differing in molecular weights (TY and the BSA-TY complex in a molar ratio of 1:10) passed through the column filled with BioGel P-150 was compared. The separation was done in 0.01 M PBS pH 7.4 buffer. An 80µL sample was applied to the column filled with 4 mL of the BioGel P-150, then the separation was carried out. Spectrophotometric analysis of the migration rates of free TY, TY-Ag, and complexed with protein was performed. An observed low value of the elution volume indicates the formation of large and stable complexes.

• Microorganisms
In order to evaluate the effect of silver complexed with TY or with the CR-TY or with BSA-TY systems, screening tests were performed on two model reference strains: Gram-positive and Gram-negative bacteria. The complexes were tested using strains from the collection of the American Type Culture Collection (ATCC). In the case of S. aureus and E. coli, reference strains recommended by EUCAST (European Committee on Antimicrobial Susceptibility Testing) were chosen as control strains for susceptibility testing and as control strains in quality control. These strains are S. aureus (ATCC ® 29213™) and E. coli (ATCC ® 35218™)-a strain producing TEM-1β-lactamase, which causes resistance to all β-lactam antibiotics.

•
MIC determination. Well Diffusion in agar. Assay and growth conditions The minimum dilutions of the analyzed compounds that inhibited the growth of the microorganisms were denoted as minimum inhibitory concentration (MIC). The values of MIC for different kinds of complexes, TY-Ag and BSA-TY-Ag; for two kinds of strains, E. coli (EC, ATCC ® 35218™) and S. aureus (SA, ATCC ® 29213™) were determined with the method of well diffusion of compounds in agar. For this purpose, appropriate bacterial suspensions were prepared according to the following methodology presented by Gibała et al.: 0.5 optical density (OD) in McFarland scale was made to receive 1.5 × 10 8 CFU (colony forming units)/ mL solution, then the cell suspension was diluted to 10 6 CFU mL −1 . The prepared suspension was used for further studies, including the determination of MIC. The modified diffusion-disk screening method described by Gibała et al. was used to study the antimicrobial efficacy of TY-Ag (molar ratio 1:0.5) (or its complexes with BSA) by evaluating the visible growth of microorganisms in the agar [81]. Serial two-fold dilutions of the analyzed compounds in concentrations listed in Table 4 were used. . Cultures were carried out at 37 • C with 5% CO 2 content and 95% humidity, changing the medium every 24-48 h. Cells were grown until the culture area was completely covered. Cells were then passaged using 0.05% trypsin.

•
Treatments of the Cells The Titan yellow (TY) complexed with silver (TY-Ag) and TY-Ag in combination with albumin (BSA) were added at 24 h from seeding the cells on the plate. The combination of 3 concentrations of Ag + compound: 10 µM, 15 µM, and 20 µM and 2 concentrations of Titan Yellow (TY): 20 µM and 40 µM were analyzed in the cell proliferation assays. Then the selected concentrations were used for the evaluation of cell survival and migration.

•
Cell Proliferation Assays T24 cells were seeded on 24-well plates at a density of 15.25 × 10 3 cells/well. After 24 h growth at 37 • C in a humidified atmosphere (Day 0), the culture medium with the analyzed complexes (TY-Ag and BSA-TY-Ag) was added to the cells. The concentrations of TY of 40 µM and 20 µM were used for the preparation of the complexes with Ag + (in the molar ratio TY-Ag = 1:0.5) and additionally with albumin (in the molar ratio BSA-TY = 1:10). The incubation was continued for the next 24, 48, and 72 h at 37 • C in a humidified atmosphere. The MTS assay (Promega, Madison, WI, USA) was used to determine the influence of the Ag + complexes (TY-Ag or BSA-TY-Ag) on the proliferation of T24 cells. The absorbance was measured at 570 nm using an Epoch Microplate Spectrophotometer (BioTek Instruments Inc, Winooski, VT, USA). Four replicate wells were used for each experiment. The effect of TY-Ag or BSA-TY-Ag complexes was presented as the proliferation curves [82,83].

• Cell Survival Analysis
Caspase-3 Activity Assay: Apoptosis was analyzed by evaluation of the Caspase-3 activity. Briefly, cells were seeded and cultured on 24-well plates with TY-Ag in 4 concentrations of Ag + : 3.75 µM, 7.5 µM, 15 µM, and 30 µM complexed with TY (60 µM) for 24 and 48 h, then the cells were lysed in lysis buffer 0.05 M Tris/HCl, pH 7.6, 0.1 M NaCl, 0.001 M EDTA, 1% Triton X-100, and assayed for activity of Caspase-3 (DEVD-like caspase activity). An identical experiment was performed in parallel to estimate the cell number in each well (MTS). The amount of aminofluorocoumarin (AFC) released during incubation with Ac-DEVD-AFC was measured using a spectrofluorometer. For clarity of representation, fluorescent signal reflecting Caspase-3 activity was normalized to cell number (DEVD-like caspase activity/MTS cell number) and expressed as a fold increase in relation to untreated/control sample. The results show a single experiment performed in triplicates. The obtained data were averaged, and the standard deviation is represented in graphs by bars [84].
Flow cytometry: Apoptosis was analyzed with PE Annexin V Apoptosis Detection Kit I (BD Biosciences, San Jose, CA), following the manufacturer's instructions. Briefly, T24 cells (3 × 10 5 ) were seeded and cultured overnight on a six-well plate with TY and TY-Ag for 24 h. Approximately 1 × 10 5 cells were stained with Annexin V for 15 min at RT in the dark. After the incubation, 5µL of propidium iodide and 400 µL of buffer solution were added prior to the cytometric analysis alone. Fluorescence intensities of treated samples and controls were analyzed by flow cytometry on a BD FACSCantoTM (Becton Dickinson, New York, NY, USA). Experiments were performed at least twice.

•
Scratch Assay Confluent T24 cells were cultured with McCoy medium with 0.5% BSA for 24 h. Next, cells were treated with TY-Ag for 24 h. The control cells were cultured under identical conditions without TY and TY-Ag (non-treated cells). The monolayer was scratched with a pipette tip and washed with phosphate-buffered saline (PBS) to remove floating cells. The scrape was monitored and photographed after 24 h incubation. The pictures were analyzed using Image J software (National Institute of Health, Bethesda, MD, USA), as described previously [85].

• Cell Cycle Assay
Cell cycle analysis was performed with the PI/RNase Staining Buffer assay (Becton Dickinson, New York, NY, USA). In this method, PI enters the cell through damaged membranes and can integrate into double-stranded DNA producing a fluorescent signal when properly excited. PI can also integrate into double-stranded RNA, therefore cells are treated with RNAse (RNA digestion). The amount of PI attached to the cell correlates with the amount of DNA, and thus allowed for the quantification of cells at particular phases of the cell cycle. For this purpose, cells, after 48 h of incubation, were rinsed with PBS and then fixed with cold 70% ethanol for 2 h. The cells were then washed again with PBS and resuspended in staining buffer (PBS with 100 µg/mL RNase A, 50 µg/mL Propidium Iodide) for 15 min in the dark. Acquire data on a flow cytometer (Becton Dickinson, Canto, New York, NY, USA). The analysis of the cell cycle was carried out in the ModFit program.

Conclusions
To conclude, our results suggest that TY-Ag and BSA-TY-Ag, also with CR, are promising complexes in antimicrobial therapy and in the treatment of human urinary bladder carcinoma during inflammation and cancer.
The complexes can be effective in the removal of the bacterial film. TY-Ag or BSA-TY-Ag are new potential drugs and may become important therapeutic options in human urinary bladder carcinoma treatment or/and important antimicrobial agents as an alternative to antibiotics. Treatment of T24 cells with such inhibitors diminishes proliferation and migration of T24 cells and induces apoptosis. The ability to bind TY-Ag to BSA will protect the drug from uncontrolled release and ensure targeted delivery directly to the desired site when such a system is intravenously administered. Binding to CR will increase the solubility of the system as well as enable targeted transport using antigen-antibody systems. Based on our findings, it can be concluded that the TY-Ag complex may be a potential cytotoxic agent against cancer cells and bacteria. Considering the potential of these complexes, they may be recommended for biomedical applications after further in vivo/clinical studies.

Data Availability Statement:
The data presented in this stude are available on request from the corresponding author.