Shatabdi
Paul
ab,
Binduma
Yadav
bc,
Mahesh D.
Patil‡
a,
Anil Kumar
Pujari
ad,
Umesh
Singh
a,
Vikas
Rishi
c and
Jayeeta
Bhaumik
*ab
aCenter of Innovative and Applied Bioprocessing (CIAB), Department of Nanomaterials and Application Technology, Department of Biotechnology (DBT), Government of India, Sector 81 (Knowledge City), S.A.S. Nagar, 140306, Punjab, India. E-mail: jayeeta@ciab.res.in
bRegional Centre for Biotechnology, Department of Biotechnology (DBT), Government of India, Faridabad 121001, Haryana, India
cNational Agri-Food Biotechnology Institute (NABI), Department of Biotechnology (DBT), Government of India, Sector 81 (Knowledge City), S.A.S. Nagar, 140306, Punjab, India
dDepartment of Chemical Sciences, Indian Institute of Science Education and Research, Sector-81 (Knowledge City), S.A.S. Nagar, 140306, Mohali, Punjab, India
First published on 2nd January 2024
Currently, combinatorial therapy has evoked interest in cancer treatment, and may promote achieving a synergistic effect using cancer medicines. Laser-assisted and pH-responsive therapies have attracted significant attention, and their combination leads to high efficiency cancer treatment. Herein, we developed a chemo–phototherapeutic hydrogel comprised of doxorubicin (DOX, a chemotherapeutic drug) and zinc phthalocyanine (ZnPc, a phototherapeutic drug) for combinatorial and synergistic treatment of breast cancer. Firstly, we have developed carbon dots (CDs, size of ∼5 nm) utilizing lignin and folic acid as biocompatible sources. Then doxorubicin was loaded on the surface of the carbon dots via conjugation (DOX@CDs). Later on, zinc phthalocyanine and acrylic acid derivatives were utilized to develop a laser-responsive hydrogel (ZnPc-PP H). Afterward, doxorubicin-conjugated carbon dots were incorporated into the photoarchitectonic hydrogel to develop a chemo–phototherapeutic drug-loaded hydrogel (DOX@CDs–ZnPc-PP H). Subsequently, the in vitro pH-triggering experiments demonstrated that the hydrogel loaded with both DOX and ZnPc could release the drugs in an acidic environment. Interestingly, in vitro assays confirmed that DOX@CDs–ZnPc-PP H could effectively target breast cancer cells (MCF-7). Furthermore, the developed chemo–phototherapeutic hydrogel exhibited non-cytotoxic behavior. Owing to laser assisted reactive oxygen species generation from ZnPc present in the hydrogel, the growth of MCF-7 cells was significantly lowered. In conclusion, all experimental outcomes indicate that the photoarchitectonic hydrogel has the potential to be applied in synergistic chemo- and photodynamic therapy of cancer.
Doxorubicin (DOX) is a prominent cancer chemotherapeutic drug used to treat many types of carcinomas and soft tissue sarcomas.6 Like most anticancer chemotherapeutic drugs, DOX has systemic adverse effects because of the non-selective uptake of the drug by healthy non-cancerous tissues. The recent research efforts aim to improve the efficacy and selectivity of targeted drug delivery systems, which can selectively transport and release drugs at cancer sites.7,8 Next, to deliver chemotherapeutic drugs to tumor areas, nanoparticles are used.9 Recent developments in receptor-mediated targeted drug delivery methods using different targeting ligands, such as folic acid (FA), are noteworthy.10 Folic acid receptor-mediated uptake by endocytosis might be applied for drug delivery systems. In this context, carbon dots (CDs) that exhibit excellent biocompatibility, strong surface functionality, and improved cellular absorption have become potential drug delivery carriers.11,12 Extensive studies have been carried out on the preparation of CDs, and several approaches, including hydrothermal cracking, microwave-mediated synthesis, and oxidation of carbon nanotubes and graphite, have been developed.13 Hydrothermal methods have been the most extensively used of these techniques because they are easy to use and economically friendly, and they can be carried out under controlled reaction conditions.14 Recently, enhanced cellular absorption, strong surface activity, and outstanding biocompatibility make CDs an attractive alternative for improving the effectiveness of cancer treatment and reducing adverse side effects. Due to the prevalence of numerous functional groups, including NH2, OH, and COOH, that are present on the surface of CDs, it is feasible for CDs to interact with various drugs through covalent or electrostatic bonding.15 In this context, research has demonstrated that DOX conjugated carbon dots, compared to only DOX, are more effective in targeting cells, probably owing to the high receptor-mediated transport to the cancer sites.6,9 Hence, chemotherapeutic drug conjugated carbon dots would pave the way to deliver the drugs to the cancer sites.
According to recent studies, combinatorial therapy can activate many cytotoxic pathways,16 resulting in a synergistic antitumor effect. Recently, using multimodal therapeutic nanomaterials in combinatorial cancer treatment has attracted interest.17 Combinational use of drugs has lately become a smart strategy to treat a complicated disease. The benefits of the combinational use of drugs include synergistic effects, low toxicity, dosage reduction, and reduced drug resistance.18–20 Combining targeted delivery systems, chemotherapy, and photodynamic therapy (PDT) result in effective cancer treatment.16,21 As a result, PDT in combination with chemotherapy has gained enormous interest in cancer therapy. Also, the combination of PDT and chemotherapy can improve the therapeutic efficacy of low-dose chemotherapy and thereby reduce the side effects and drug resistance.22–24 Furthermore, to avoid unwanted cytotoxicity, chemotherapeutic agents should be released in a controlled manner. Among the several stimuli, using a photosensitization process to produce reactive oxygen species (ROS) has attracted the most attention.25–27
In this context, using red laser capable of penetrating several centimeters into human soft tissue with minimal damage is a non-invasive external approach.28 Photodynamic therapy (PDT) is a photochemical approach in which a photosensitizer is applied that causes localized tumor tissue damage when the tissue is exposed to light.29,30 ROS, particularly singlet oxygen, are generated by the combined action of three individually nontoxic elements, including a photosensitizer, light with a particular wavelength, and oxygen, to cause cellular and tissue damage.31 Zinc phthalocyanine (ZnPc), a food and drug administration (FDA), USA-approved photosensitizer activatable by red laser, has been proven to be successful in treating cancers.32 Zinc phthalocyanine (ZnPc)-mediated photodynamic therapy (PDT) is effective as a unique therapeutic method in treating breast cancer in vitro.33,34 Owing to their strong absorption in the phototherapeutic window (650–800 nm) and high efficiency in generating ROS, zinc(II) phthalocyanines, second-generation photosensitizers for PDT, are highly promising imaging agents. Notably, phthalocyanine, one of the zinc(II) phthalocyanine derivatives, is currently undergoing phase II clinical trials to treat MCF-7 tumors.33 Light-responsive drugs, i.e., hydrophobic phthalocyanine macrocycles, could coordinate with a hydrophilic polymer to form a ZnPc–polymer-based hydrogel.
Furthermore, pH is important in most biological and many chemical systems. Precise monitoring of the physiological pH is highly recommended for treating various pathological and physiological conditions.35 A slight alteration in pH may indicate serious health issues, including cancer. Therefore, pH-responsive hydrogels are emerging as drug carriers to achieve the localized and site-specific sustained release of drugs in breast cancer.31,36,37 They have some significant features like possessing softness and resemblance to biological systems. Hydrogels have drawn a great deal of interest with a wide range of possible medical, pharmacological, and prosthetic uses.38,39 Hydrogels are three-dimensional hydrophilic polymer networks that hold a significant fraction of water.40 Hydrogels have capacity to absorb water and their swelling and permeability characteristics facilitate their direct biological use. These traits result in their rapid solubilization under pH stimuli, and their structure's weak mechanical strength allows them to undergo structural deformations.41,42 The crosslink density and distribution of a hydrogel network impact its mechanical properties, as structural heterogeneity may enhance its mechanical strength.43 Recent research on hydrogels has shown that two independently crosslinked biocompatible polymer networks can increase their mechanical strength. Therefore, two types of polymers have been considered, namely, poly(ethylene glycol) (PEG) and poly(acrylic acid) (PAA), where these two polymers were crosslinked to form a hydrogel.43 Non-linear PEG analogs, particularly PEGMA, are recognized to be biocompatible similar to linear PEG.44 Incorporating multifunctional nanoparticles into a hydrogel can produce an effective and smart delivery system. Therefore, incorporating nanoparticles into pH-responsive hydrogels, such as carbon dots (CDs), may result in an assembly with increased mechanical properties.
Various stimuli-responsive hydrogels have been developed for ‘smart’ drug delivery.45,46 Although hydrogels and carbon dots are independently studied for drug delivery, no reports on integrating hydrogels and carbon dots to target cancer cells are available. Furthermore, combinatorial drugs to be administered can be enclosed in a hydrogel and delivered at tumor sites maintaining a high drug concentration in the tumor tissue for an extended period and lessening systemic toxic side effects.47 Therefore, our research focuses on developing a ZnPc-based hydrogel system using a biocompatible polymer. Initially, an integrated DOX conjugated CDs and ZnPc-PP hydrogel system was developed. The resulting chemo–phototherapeutic drug-loaded hydrogel system was utilized in red laser assisted drug delivery which released the therapeutic drugs in the cancer microenvironment. We demonstrate that DOX@CDs–ZnPc-PP H with a combinatorial dose of the chemo–phototherapy drugs elicits anticancer efficacy after a single treatment. Therefore, red laser assisted ROS-generation by the photoarchitectonic hydrogel with combined chemo–phototherapeutic drugs can be applied to destroy breast cancer cells as illustrated in Scheme 1. Finally, the cell viability assessment was conducted for the Michigan Cancer Foundation (MCF-7) breast cancer cell line to evaluate the anticancer potential of the material.
![]() | ||
Scheme 2 Schematic illustration of the carbon dots (CDs) (a) synthesis from lignin and folic acid as a coating via a hydrothermal method and (b) the conjugation of doxorubicin (DOX) on CDs (DOX@CDs). |
The high-resolution transmission electron microscopy (HR-TEM) images of CDs displayed black dots with an average size of ∼4.6 nm (Fig. 1(a)–(c)). The HR-TEM images also showed visible lattice fringes (Fig. 1(d)), which corresponded to the d-spacing of the carbon planes, with a lattice spacing of 0.21 nm (Fig. 1(e)). The standard atomic configurations seen in most CDs suggested a high degree of crystallinity.49 In this line, the crystalline character of the material is well demonstrated by the bright spots in the selected area electron diffraction (SAED) pattern (Fig. 1(e)). A broad single diffraction peak in the XRD pattern centred at angle of 25° is attributed to disordered carbon atoms with an amorphous surface structure (Fig. 1(f)).50,51 Furthermore, the analysis of the composition of CDs using EDS (energy-dispersive X-ray spectroscopy) revealed the uniform distribution of C, O, and N. The presence of N and C elements of the folic acid showed its successful embedding on the CDs (Fig. S2 and Table S1, ESI†).
Next, the UV-Vis absorption and FTIR spectra of the CDs were obtained to examine the assembly of the lignin–folic acid-based CDs. The CDs are developed via π–π stacking interactions, and their peaks are observed at 212 nm and 264 nm (Fig. 1(g)).52 Additionally, the FTIR spectra were used to confirm the formation of CDs (Fig. 1(h)). Importantly, a CO (acid) stretching frequency peak was observed in the fingerprint area in the range of 1750–1600 cm−1 and a broad absorption peak in the range of 3500–3000 cm−1 due to the –OH and –NH2 functional groups of folic acid which is retained in CDs. A similar FTIR pattern has been reported for CDs prepared hydrothermally from citric acid and ethylenediamine.39 Next, in the XRD pattern of the crystalline phase of CDs, peaks were observed at 11.08, 26.92, and 28.5 (Fig. 1(f)). However, lignin depicts amorphous nature (Fig. S3, ESI†). However, peaks present at 2θ of 11.12, 14.2, 16.1, 23.8, 27.1, and 28.5° with a slight shift for the CDs can be attributed to the formation of a folic acid layer and they were compared with the reported folic acid peaks40 for confirming that the lignin–folic acid carbon dot synthesis was accomplished.
Subsequently, to improve the targeted delivery of DOX, it was conjugated with the surface of CDs (DOX@CDs) using EDC–NHS coupling. For this, the conjugation reaction was carried out using the CDs. The carboxylic group of folic acid on the CDs can be coupled to the NH2 group of DOX to form an amide linkage between CDs and DOX as shown in Scheme 2(b). In a typical reaction, CDs (10 mL, 1 mg mL−1 water) and a solution of DOX (1 mL, 1 mg mL−1) were coupled. To activate the carboxylic acid group of CDs, aqueous solutions of the coupling reagent EDC (80 μL, 5 mg mL−1) and after some time NHS (80 μL, 5 mg mL−1) were added to generate a highly active ester center that was responsible for DOX conjugation. The reaction mixture was then agitated in the dark for 24 hours at a temperature of 37 °C and 150 rpm. Following the centrifugation and decantation procedures, DOX@CDS was purified (washing three times, 16000 rpm, 20 min). Furthermore, HR-TEM images confirmed the successful conjugation of DOX on the CDs, and the size of spherical-shaped DOX@CDs was ∼12 nm (Fig. 1(i)). The average particle size obtained for the distributed DOX conjugated CDs (DOX@CDs) displayed that the maximum size of nanoparticles was on the order of 12 nm (Fig. 1(j)); the zeta potential (ξ) values of the CDs and DOX@CDs were −22.12 mV and −9.03 mV, respectively (Fig. 1(k)). The decrease in the surface charge suggested that the conjugation of DOX on the surface of CDs was accomplished. The drug loading percentage of DOX@CDs was calculated to be 65 ± 1.2% (Table S2 and Fig. S4, S5, ESI†) using the standard plot of only DOX (Fig. S4, ESI†). UV-Vis absorption spectra revealed the red-shifting of the characteristic peak of DOX from 480 to 500 nm, corroborating the conjugation of DOX on CDs (Fig. 1(l)).
Next, the FTIR spectra of DOX@CDs revealed a distinctive intense absorption peak at 1800–1600 cm−1 with a significant shift that was attributed to the –CONH stretching vibrations of the amide linkage between CDs and DOX (Fig. 1(m)). The broad stretching peaks at 3500–3000 cm−1 were ascribed to –NH2 and –OH functional groups present in DOX and CDs. Also, the FTIR spectrum of DOX@CDs reflects that the the conjugation of DOX onto the surface of CDs was successfully achieved (Fig. 1(h)). In addition, the crystal structure of DOX@CDs was investigated by X-ray diffraction (XRD). In the case of only DOX, a clear crystalline phase was seen in its native phase. Nevertheless, the lowest degree of crystallinity was observed in DOX@CDs (Fig. S6, ESI†).
To endow ZnPc with laser-induced therapeutic ability, hydrogels were developed for pH-responsive sustained release of drugs. For this purpose, hydrogels were fabricated using biocompatible polymers PEGMA [poly(polyethylene glycol methyl ether methacrylate)] and PAA (polyacrylic acid) and zinc phthalocyanine using a chemical cross-linking reaction. Consequently, the weight ratio of PEGMA:
ZnPC
:
PAA was optimized (ESI,† Fig. S7). As shown in Scheme 3, the synthesized zinc phthalocyanine–poly(polyethylene glycol methyl ether methacrylate–polyacrylic acid) hydrogel (ZnPc-PP H) is a cross linked hydrogel with the ZnPc photosensitizer bonded between PEGMA and PAA. The light-responsiveness of drug ZnPcs allows it to interact with the PEGMA55 and PAA56 hydrogel via hydrogen bonding and co-ordination interactions.57 Potassium persulfate (KPS) has been introduced as a free radical initiator for cross-linking of PEGMA and PAA. Hence, ZnPc-PP H was developed upon step-wise addition of all the mentioned reagents under heating conditions (at 70 °C for 30 min). Transparency is the foremost requirement for photodynamic treatment because it allows light to pass through a hydrogel and excite a photosensitizer.35 Consequently, the transmittance of the newly developed hydrogel was recorded in the 200 to 700 nm wavelength range. ZnPc-PP H under red laser irradiation and the transmittance of red laser at different concentrations of ZnPc in the developed hydrogel of (i) 0.071 wt/vol%, (ii) 0.14 wt/vol%, (iii) 0.21 wt/vol%, (iv) 0.28 wt/vol%, and (v) 0.35 wt/vol% are illustrated in Fig. 2(a). This figure indicates that typically 5 mg of ZnPc-PP H would be effective for laser light-induced anticancer therapy. Further validation was done by measuring transmittance at different concentrations of ZnPc in the hydrogel. The results showed that 5 mg concentration of ZnPc in the hydrogel exhibited 90% of transmittance compared to 10, 15, 20, and 25 mg ZnPc (Fig. 2(b)).
![]() | ||
Scheme 3 Schematic illustration of fabrication of a pH-responsive combinatorial chemo–phototherapeutic hydrogel. |
Additionally, the UV-Vis absorption spectrum of ZnPc-PP H revealed the characteristic absorption peaks of ZnPc at ∼650 nm, PEGMA at ∼260 nm, and PAA at ∼340 nm. Furthermore, the formation of ZnPc-PP H was confirmed via a peak attributed to hydrogen bond and co-ordination interactions between PEGMA and PAA (Fig. 2(c)).53 Next, FTIR spectroscopy was employed to characterize ZnPC-PP H as shown in Fig. 2(d). The absorption peak at 700–500 cm−1 indicated the co-ordination of zinc with the oxygen atom present in the hydrogel. Also, a broad and slightly shifted absorption peak was observed at 1200–1000 cm−1 which confirms the hydrogen bond formation between the hydrogel and ZnPc. Additionally, the FTIR spectra of PEGMA and PAA were obtained, in which an ester (–CO) stretching peak was observed at 1750–1600 cm−1 attributing to PEGMA. An acid (–C
O) stretching peak at 1700–1650 cm−1 and a stretching peak at 3400–3000 cm−1 were observed and were attributed to the –OH functional group present in PAA. The reduction of –OH peak intensity was observed which confirms the hydrogen bonding of ZnPc with the hydrogel (Fig. 2(d)).
Furthermore, energy-dispersive X-ray spectroscopy (EDS) analysis confirmed the presence of the carbon, oxygen, and zinc elements (Fig. S8, ESI†). The presence of Zn, C, and O elements in the hydrogel indicates the presence of ZnPC, PEGMA, and PAA, respectively. The diffraction peaks positioned at 19°, 23.8°, 26.3°, and 28.5° in the XRD pattern may be attributed to the crystalline plane of ZnPc-PP H (Fig. S9, ESI†). The diffraction peaks of PEGMA at 23.3° and ZnPc (23.8°) indicate that the hydrogen and coordination interactions of ZnPc with PEGMA and PAA might decline due to the crystallinity of ZnPc-PP H. The peaks observed at 6.2°, 9.3°, 10.5°, 12.7°, 14.1°, 15.3°, 18.2°, 18.8°, 23.8°, 26.3°, 28.5°, and 30.5° confirmed the presence of ZnPc in the hydrogel.58 Furthermore, a peak with a 2θ value of 18.5 indicated the decline in crystallinity due to the grafting of polyacrylic acid onto the PEGMA chain.59,60 Moreover, the porous network structure of ZnPc-PP H (∼200 nm) was investigated using scanning electron microscopy (SEM) analysis (Fig. 2(e) and (f)). The 3D porous network could contribute to the fast adsorption of drugs, which is suitable for the pH-responsive slow and sustained release of drugs from the hydrogel.
To achieve the pH-triggered sustained release of a chemo–photodynamic therapeutic drug in breast cancer cells, DOX@CDs-loaded ZnPc-PP H was developed using a physical absorption approach, as displayed in Scheme 4. DOX@CDs incorporated ZnPc-PP H for dual drug delivery was fabricated in one step. To proceed, DOX@CDs–ZnPc-PP H was constructed through the π–π stacking61 of the aromatic rings of DOX and ZnPc, respectively, present in DOX@CDs and ZnPc-PP H, as depicted in Scheme 4. Briefly, a combinatorial chemo and phototherapeutic hydrogel was constructed. In this, DOX@CDs was made to absorb by the photoresponsive ZnPc-PP H drug at 25 °C for 8 h.
![]() | ||
Scheme 4 Construction of final chemo–phototherapeutic drug-loaded hydrogels; absorption of DOX@CDs with ZnPc-PP H. |
Subsequently, the final combinatorial drug was analyzed by UV-Vis and FTIR spectroscopy as shown in Fig. 3(a) and (b). To integrate DOX conjugated CDs (DOX@CDs) inside ZnPc-PP H, lyophilized ZnPc-PP H was incubated with the solutions of DOX@CDs until they were completely absorbed by the hydrogel. Furthermore, the UV-Vis absorption spectra of DOX@CDs in ZnPc-PP H in phosphate-buffered saline (PBS) revealed peaks at 260 nm and 340 nm corresponding to PEGMA and CDs, respectively. Next, the two peaks at 490 nm and 650 nm correspond to DOX and ZnPc (Fig. 3(a)). Since ZnPc has an excitation wavelength of 650 nm, herein a red laser was used for photodynamic treatment applications.31 Subsequently, FTIR spectroscopy was employed for the characterization of DOX@CDs–ZnPC-PP H as shown in Fig. 3(b). DOX@CDs–ZnPc-PP H was fabricated through the π–π stacking of the aromatic rings of DOX and ZnPc, respectively, present in DOX@CDs and ZnPc-PP H. The final formation of the combinatorial hydrogel (DOX@CDs–ZnPc-PP H) was confirmed from the characteristic peaks present in the FTIR spectra. Subsequently, no significant changes were observed in the characteristic peak in the fingerprint print region of the final formulation (DOX@CDs–ZnPcPP H). Notably, the characteristic absorption peaks of DOX@CDs and ZnPC-PP H were retained for the combinatorial hydrogel (Fig. 3(b)).62 To ensure that the porous structure of ZnPc-PP H was retained upon internalization of DOX@CDs, HR-TEM analysis was performed. It was noticed that DOX@CDs was entirely internalized in ZnPc-PP H, and the size of DOX@CDs was found to be ∼12 nm (Fig. 3(c)). The absorption of DOX@CDs in the developed hydrogels altered the surface charge (Fig. 3(d)). The resultant surface charge of DOX@CDs–ZnPc-PP H was measured at −14 mV, while the individual surface charges of ZnPc-PP H and DOX@CDs were measured at −5 mV and −9.03 mV, respectively. The swelling percentage of the prepared ZnPc-PP H was 90 wt% (Fig. S7, ESI†). Moreover, the pore size and volume of the hydrogel were studied through N2 adsorption–desorption isotherms obtained using the multipoint BET technique. The hydrogel showed a multimodal distribution of pores centered at 2.456 nm. Incorporating drugs into the hydrogels strongly led to a decreased pore size of 1.230 nm in agreement with BET data (Fig. S10, ESI†).
The relative elastic and viscous characterization of hydrogels under continuous shear strain has been carried out to determine the linear viscoelastic region in the hydrogel.64 Higher strain causes the microstructural network of the hydrogel to be disrupted, which causes the stress response to become nonlinear.40 When DOX@CDs–ZnPc-PP H was subjected to shear strain, it was observed that its γc was higher than that of ZnPc-PP H, implying that the mechanical strength of the hydrogel has improved (Fig. 3(e) and (f)). This higher γc of DOX@CDs–ZnPc-PP H resulted from the increase in mechanical strength of ZnPc-PP H caused by the absorption of DOX@CDs, as shown in the TEM image (Fig. 3(c)). Reported literature also claimed that the introduction of nanoparticles increased the mechanical strength of a hydrogel which is in accordance with our present study.63 Furthermore, the continuous flow study results in Fig. S11a and b (ESI†) show that as the shear rate increases, the viscosity of ZnPc-PP H decreases. Meanwhile, DOX@CDs acts as an absorbing agent through the π–π stacking of the aromatic ring between DOX and ZnPc, respectively. Additionally, the presence of DOX@CDs and ZnPc-PP H leads to a more powerful interaction, resulting in a stable hydrogel (Fig. S11a and b, ESI†). The viscosity of both hydrogels was observed to decrease as the shear rate increased, implying that these hydrogels possessed significant shear-thinning capabilities, which enabled them to control the release of therapeutic drugs from them. Fig. S12a and b (ESI†) also show that Zn-PcPP H and DOX@CDs–ZnPc-PP H have larger G′ than G′′, signifying that they are shear-thinning hydrogel materials.
The viscoelastic behavior of the hydrogel was monitored to instantly observe an alteration in the storage modulus (G′) values obtained from the strain/amplitude sweep test of the hydrogel (Fig. S12a and b, ESI†). For around 6000 s at 37 °C, frequency-sweep measurements were performed on the developed hydrogels. For all hydrogels, it was found that the values of G′ increase as time increases. Variable angular frequency shear in the range of 0.1–100 rad s−1 was applied to the hydrogels at a constant amplitude (1%) in the frequency sweep test. It was observed that the hydrogels exhibited mechanical robustness across all the tested frequency ranges (Fig. S12a and b, ESI†). The higher value of G′ than G′′ indicates the elastic nature.40 The hydrogel showed higher values of G′ (1311 Pa), which limits its ability to move the chains across the hydrogel matrix. G′ values obtained from the frequency sweep test showed a similar trend to those obtained from the amplitude sweep test. Additionally, G′ and G′′ values of ZnPc-PP H indicate that high-frequency shear forces have disrupted the loose, impermanent ZnPc-PP H network created by either the carboxylic group or the ester group present gradually, demonstrating its propensity towards becoming a liquid, Fig. 3(e). Further, the incorporation of DOX@CDs into ZnPc-PP H significantly improves the mechanical strength of the hydrogel structure through the π–π stacking61 of the aromatic ring present in the hydrogel (DOX@CDs–ZnPc-PP H) as evidenced by the increase in the LVE region depicted Fig. 3(f). As a result, it is ascertained that ZnPc-PP H and DOX-loaded CDs–ZnPc-PP H are viable solutions for achieving pH-responsive and light-induced cancer treatment. This phenomenon implies that the rheological properties of the prepared hydrogel point to its ease of use as a drug carrier to the cancer sites.
Furthermore, it was observed that the hydrogels completely disintegrated within 24–72 h as illustrated in Fig. 4(a). This can be attributed to breaking of the H-bonds in the hydrogel at an acidic pH, which ultimately causes the hydrogel to degrade under low pH (5.5) conditions. The drug-incorporated hydrogels, however, exhibited high stability under neutral pH conditions. In conclusion, the developed hydrogel could be used as a pH-triggered release material for both therapeutics upon administration under acidic environmental conditions. Following this, a pH-stimuli response study of pH-subjected DOX@CDs–ZnPc-PP H was carried out using SEM (Fig. S14, ESI†). While the pores of the hydrogel were observed to be intact at neutral pH 7, acidic pH disrupted the structure of the hydrogels. The in vitro drug release profile was studied using pH-triggered drug release to evaluate the pH responsiveness of the developed hydrogel. Hydrogel development is mainly significant for prolonged nanocarrier-drug release increasing the efficiency of administration and effectiveness of therapeutic drugs delivered to the cancer sites. The benefits of nanocarrier–hydrogel composite materials in drug administration have been demonstrated to be combating the adverse side effects of drugs that, when supplied intravenously, can accumulate in healthy tissues.65 In this context, our designed drug delivery system was based on the pH-triggered drug release from the hydrogel system. The drug release experiments of DOX@CDs–ZnPC-PP H were carried out at 37 °C and at pHs 7.4 and 5.5. The drug release experiments revealed that DOX@CDs–ZnPC-PP H exhibited strong pH sensitivity (Fig. 4(b)). The cumulative release of DOX at pH 5.5 reached 58.35% within 24 h and 73.07% and 80.43% within 48 h and 72 h, respectively. While the cumulative release of DOX at 24 h, 48 h, and 72 h was 21.62, 23.32, and 26.48%, respectively, in PBS buffer at pH 7.4 (Fig. 4(a) and (b)).
Similarly, the release of ZnPc for 24, 48, and 72 h was found to be 38.62, 59.13, and 63.89%, respectively, at pH 5.5, while it was 5.8, 7.3, and 8.0% for 24, 48, and 72 h, respectively, in PBS at pH 7.4 (Fig. 4(b)). Various cumulative release curves demonstrated that under physiological conditions, DOX and ZnPc would not result in premature leakage. Drug release increases when the acidic environment prevails in the microenvironment of the tumor cell, and DOX release under acidic conditions is increased from 24 to 72 h compared to ZnPc. At the same time, prolonged incubation of the hydrogel under acidic conditions causes the disintegration of bonds, as revealed in SEM images (Fig. S14, ESI†). It should be noted that, the hydrogel is developed via optimization in such a way that it only gets triggered by a pH change making it a pH-responsive hydrogel. Furthermore, the hydrogel remains intact upon light exposure and does not release the probes until pH is regulated. To validate this, we monitored the in vitro release of DOX and ZnPc under 650 nm laser irradiation for 60 min. The light intensity was adjusted to 50 mW with a five-minute exposure time (“ON”), followed by another five-minute exposure time (“OFF”). The absorption spectra of ZnPc at 650 nm and DOX at 480 nm depicted no significant change under red laser irradiation (Fig. S15, ESI†). As shown in Fig. S15 (ESI†), ZnPc and DOX were not released under laser irradiation (650 nm) up to 60 min. However, the pH responsiveness of the hydrogel at acidic pH (5.5) increases, and the release of DOX and ZnPc from the hydrogel, demonstrating that the concentration of DOX and ZnPc increases considerably at acidic pH (Fig. 4(b)), compared to the unaltered concentration when irradiated (Fig. S15, ESI†). A similar finding has also been reported in the literature, where BTZ (bortezomib) was used for drug therapy, however ICG (indocyanine green) wrapped in supramolecular hydrogels was more light stable than free ICG for photodynamic therapy.66 Hence, the developed therapeutic hydrogel releasing DOX and ZnPc at acidic pH makes it a pH-responsive hydrogel. Thus, it can be concluded that the final drug delivery system DOX@CDs loaded ZnPC-PP H performed pH-sensitivity-triggered drug release efficiently, which avoids the cytotoxicity towards the normal cells.
The present study examined the combinatorial effect of the chemotherapy and phototherapy using DOX@CDs incorporated DOX@CDs–ZnPc-PP H. Firstly, the effect of a red laser light intensity (650 nm) on the viability of MCF-7 cells was optimized in the range of 25–100 mW (Fig. S15 and Table S4, ESI†). The cell viabilities obtained upon exposure to 50 mW red laser and those of unexposed control cells (grown in the dark) were 96 and 99%, respectively. This indicates that the exposure to red laser is not toxic to the cell lines as the cell integrity is maintained. Furthermore, the therapeutic efficacy of the combinatorial chemo–phototherapeutic drugs was investigated using DOX@CDs–ZnPc-PP H, and the results are illustrated in Table 1 and Fig. 6(c), (d). After administration of chemo and phototherapeutic drugs, and irradiation with red laser at 650 nm (50 mW), cells treated with or without CDs remained highly viable.
S. no. | Probes | IC50 (μg mL−1) | ||
---|---|---|---|---|
Dark treatment | Light treatment | Fold of reduction | ||
1. | DOX | 10.65 ± 0.10 | 10.26 ± 0.22 | 1.03 |
2. | CDs | 20.96 ± 0.20 | 16.60 ± 0.20 | 1.26 |
3. | ZnPc | 12.90 ± 0.20 | 3.17 ± 0.10 | 4.06 |
4. | DOX@CDs | 8.90 ± 0.20 | 7.89 ± 0.11 | 1.12 |
5. | ZnPcPP H | 11.20 ± 0.20 | 3.82 ± 0.14 | 2.94 |
6. | DOX@CDs–ZnPc-PP H | 3.65 ± 0.10 | 1.06 ± 0.18 | 3.44 |
The IC50 values of only DOX and ZnPc for the dark treatment were 10.65 and 12.90 μg mL−1, and those for the laser treatment were found to be 10.26 and 3.17 μg mL−1, respectively. Notably, the chemo–photo therapeutic hydrogel (DOX@CDs–ZnPc-PP H), wherein the combinatorial drugs are loaded, exhibited an IC50 value of 3.65 μg mL−1 under dark conditions, showing its anticancer potential. However, DOX@CDs–ZnPc-PP H displayed a significant reduction in the cell viability (IC50: 1.06 μg mL−1) upon laser exposure. The treatment under laser irradiation using the chemo–photo therapeutic hydrogel achieved a significant fold reduction (3.44-fold), compared to dark, contributing to the synergistic anticancer effect. Notably, this therapeutic potential of dual drugs can be attributed to various plausible reasons. Firstly, the acidic environment of the MCF-7 cells triggers the release of DOX and ZnPc from the hydrogel. Secondly, DOX, a chemotherapeutic drug, displayed efficient and sustained anticancer ability. Thirdly, the red laser-responsive ZnPc-mediated generation of ROS in the vicinity of cancer cells can also be attributed to the therapeutic effect of the released drugs. Next, combinational use of drugs is a common strategy nowadays. The benefits of combinational use of drugs include synergistic effects, low toxicity, dosage reduction, and reduced drug resistance.52 As a result, PDT in combination with chemotherapy has aroused enormous interest in cancer therapy. Also, the combination of PDT and chemotherapy can improve the therapeutic efficacy of low-dose chemotherapy and thereby reduce the side effects and drug resistance.52 To provide more quantifiable information on the dual chemo and photo-therapeutic effect, the combination index (CI) was calculated using the concentration-dependent survival curves. Briefly, in combination therapy, the CI values could be more than 1, equal to 1, or lower than 1 to indicate antagonism, additivity, or synergism, respectively. In the present study, the CI < 1 (the CI value of dark treatment was 0.83 and the CI value of light treatment was found to be 0.84) suggested the synergistic cytotoxic effect owing to the PDT activity of ZnPc and the chemotherapeutic action of DOX at IC50 drug concentrations. The obtained value of CI < 1 suggested the synergistic cytotoxic effect exhibited by the combined ZnPc-mediated PDT and DOX-mediated chemotherapy against the MCF-7 cells. Consequently, the findings above demonstrate that DOX@CDs–ZnPc-PP H with a combinatorial dose of chemo–phototherapy drugs elicits anticancer efficacy after a single treatment.
![]() | (1) |
![]() | (2) |
Footnotes |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3ma00900a |
‡ Present address: Chemical Engineering & Process Development Division, CSIR-National Chemical Laboratory, Dr Homi Bhabha Road, Pune 411008, India. |
This journal is © The Royal Society of Chemistry 2024 |