Thermosensitive nanohydrogel of 5-fluorouracil for head and neck cancer: preparation, characterization and cytotoxicity assay

Introduction

The primary treatment for solid tumors is surgery followed by irradiation and/or systemic chemotherapy to kill malignant cells, which may remain even after surgery. Systemic chemotherapy has been shown to cause side effects upon administration as they are extensively transported to the whole body; a small fraction of it reaches the tumor site, whereas the rest is taken up by other healthy organs or normal tissues thereby getting damaged due to the nonspecific action of the cytotoxic agents. Due to their short period of activity, repeated injections are often required, which can lead to exacerbation of side effects and inconvenience to the patients. To overcome these obstacles, in this study, we developed controlled and targeted intratumoral injection. Such targeted delivery may be potentially more effective in maintaining therapeutic concentrations of drug, while reducing systemic drug levels and decreasing the side effects in healthy normal tissues. In recent years, an injectable in situ thermosensitive nanohydrogel has attracted considerable attention because it achieves targeted drug delivery and prolonged activity.^1,2 This in situ nanohydrogel exhibits sol phase to gel phase transition in response to temperature. At room temperature, various cytotoxic drugs can be easily incorporated into the solution by simple mixing, and this forms a gel in situ after administration under physiological conditions.

Among the many cytotoxic drugs used in clinics, 5-fluorouracil (5-FU) is an effective chemotherapeutic agent that is extensively employed in systemic chemotherapy for solid tumors such as head and neck cancer, breast cancer, colorectal cancer and brain tumor. After administration, 5-FU is rapidly metabolized in the body with an apparent terminal half-life of approximately 8–20 minutes as it is metabolized by dihydropyrimidine dehydrogenase.³ Therefore, continuous administration of 5-FU is required to maintain its therapeutic activity, which can be achieved by thermosensitive nanohydrogel.

Materials and methods

Methylcellulose (MC-METHOCEL A4C) was a gift from the Colorcon Asia Pvt. Ltd., Verna, Goa, India. Viscosity of 2% aqueous solution at 20°C was ~400 cP. 5-FU was purchased from the Zydus Cadila Healthcare Ltd., Ahmedabad, India. Trisodium citrate was purchased from the Merck Limited, Mumbai, India. Deionized water was used for the experiments.

Hydrogel was prepared by physical cross-linking method and three-level two-factor full factorial experimental design. Design Expert 9.0 was employed (Table 1). In this method, MC at 1%–2% concentration by weight of water was dissolved in deionized water by stirring gently at room temperature. A clear solution was achieved by storing it overnight in a refrigerator. Then, trisodium citrate (1%–5% w/v) was added to the MC solution.¹ This was mixed gently using magnetic stirrer until a clear solution was obtained, and its gelling time, temperature and viscosity were noted. Then, 5-FU was added and dissolved in MC hydrogel by stirring gently at room temperature. Nanohydrogel was prepared using tip probe-sonicator (Vibracell VCX-500; Sonics, Newtown, CT, USA). Different parameters of 5-FU-loaded nanohydrogel were checked (Table 2).

Table 1 Three-level two-factor full factorial design with observed response of methylcellulose (MC) hydrogel Note: Results are shown as mean (n=3) ± standard deviation.

Table 2 Characteristics of 5-FU-loaded nanohydrogel Abbreviations: 5-FU, 5-fluorouracil; WFI, water for injection.

Cytotoxicity of 5-FU-loaded nanohydrogel, drug solution and MC polymer against KB oral cancer cell line (purchased from National Centre for Cell Science (NCCS), Pune, Maharashtra, India) was investigated via 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide blue-indicator dye assay. Briefly, KB cells were seeded in 96-well plates and incubated for 24 hours for cell attachment. Following attachment, 5-FU drug solution, 5-FU nanohydrogel and MC polymer at a concentration ranging from 1 to 2,000 μg/mL were added.^4,5 Optical density was determined at 570 nm using ELISA plate reader (Bio-Tek, Winooski, VT, USA).

Results and discussion

Polymeric MC solution has a gelling temperature of 65°C–70°C. Addition of trisodium citrate reduces the gelling temperature to physiological temperature. This may be due to the interaction of trisodium citrate with water that ultimately breaks the intermolecular hydrogen bonding between water and MC molecules. This permits higher intramolecular cross-linking between MC chains resulting into gelation.

Results of MC hydrogel as per factorial design are given in Table 1. Based on the desirability value 0.96, batch F-8 was selected as optimized batch (Table 1). Results of 5-FU-loaded nanohydrogel are given in Table 2. It shows the sheer thinning viscosity of 37.27±0.32 cP which degrades within 2 days by the activity of cellular enzymes. Drug release by nanohydrogel indicates that it reduces the burst release and also releases the drug up to 24 hours. Sustained drug release of the formulation may be attributed to the pore size of nanohydrogel, which is also supported by lower swelling ratio of the formulation. It follows the Higuchi kinetic model for drug release. Korsmeyer–Peppas model n value (0.79) indicates a coupling of diffusion and erosion mechanisms, called anomalous diffusion. Results of cytotoxicity assay (Figure 1) indicate that IC₅₀ value of 5-FU drug solution and 5-FU nanohydrogel was found to be 250 μg/mL. Cytotoxicity assay shows that drug efficacy against cancer cells remained unchanged after incorporation in the nanohydrogel.

Figure 1 Cytotoxicity assay of 5-FU-loaded nanohydrogel, MC polymer and drug solution. Results are shown as mean (n=3) ± standard deviation. Abbreviations: 5-FU, 5-fluorouracil; MC, methylcellulose.

Conclusion

Biodegradable and thermosensitive 5-FU-loaded MC nanohydrogel synthesized by physical cross-linking method may be beneficial in efficiently targeting tumor site. Further in vivo pharmacokinetic and pharmacodynamic studies are needed to confirm this findings.

Acknowledgment

The authors are thankful to Prof. R.H. Parikh, Principal, Ramanbhai Patel College of Pharmacy, CHARUSAT, for providing facility for this research project.

Disclosure

The authors report no conflicts of interest in this work.

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