Journal of Nanomaterials
Volume 2018 (2018), Article ID 1357812, 5 pages
https://doi.org/10.1155/2018/1357812

Research Article

Synthesis of Folic Acid-Modified DOX@ZIF-8 Nanoparticles for Targeted Therapy of Liver Cancer

Jian Bi,¹ Yishan Lu,² Yan Dong,³ and Ping Gao³

¹Department of Gastroenterology, The First Affiliated Hospital of Dalian Medical University, Dalian 116011, China
²Queen Mary College, Nanchang University, Nanchang, Jiangxi 330031, China
³Department of Oncology, The First Affiliated Hospital of Dalian Medical University, Dalian 116011, China

Correspondence should be addressed to Yan Dong; dongyan100@aliyun.com and Ping Gao; gaopinggaoping2008@163.com

Received 14 March 2018; Revised 6 June 2018; Accepted 28 June 2018; Published 30 July 2018

Academic Editor: Ilaria Armentano

Copyright © 2018 Jian Bi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The effective chemotherapy treatment for liver cancer patients remains an urgent issue due to the difficulty in precisely delivering drugs to the tumor site. The targeted delivery of drugs by nanoparticles is a promising strategy to address this problem. However, the fabrication of drug targeted delivery nanosystem still remains a major challenge. In this study, a novel folic acid-functionalized (doxorubicin, DOX) DOX@ZIF-8 nanoparticles (DOX@ZIF-8-FA) were prepared as a liver cancer-targeted drug delivery system. The delivery nanosystem exhibited a high drug loading capacity (15.7 wt%) and presented excellent drug-sustained release performances and good pH-responsive properties. Compared with free DOX and DOX@ZIF-8 nanoparticles, the DOX@ZIF-8-FA nanoparticles displayed much higher anticancer efficiency in HepG2 cells, suggesting that the folic acid-functionalized DOX@ZIF-8 nanoparticles have promising applications in targeted treatment of cancer cells.

1. Introduction

Hepatocellular carcinoma (HCC) is the major form of liver cancer and is the third most common cause of cancer death worldwide [1]. Currently, chemotherapy is the major treatment method. However, advanced HCC often has a poor prognosis, and only a few chemotherapeutic drugs, such as sorafenib, demonstrate efficacy in increasing overall survival in advanced or metastatic HCC [2]. Due to the rapid development of drug resistance and low targeting ability, the effective course of chemotherapy for HCC often lasts for only a few months [3]. Thus, developing new strategies for targeted drug delivery and controllable drug release is vital.

With the rapid development of nanotechnology, nanoscaled materials such as mesoporous silica nanomaterials, metal nanoparticles, polymers, liposomes, and metal-organic-framework (MOF) materials [4–9] are used as drug vehicles for reducing side effects and enhancing therapeutic efficacy, which offers an alternative strategy to address the problem discussed above. Among these nanocarriers, zeolitic imidazolate framework (ZIF), a subclass of MOF, with large surface areas, high porosity, and high stability, has been extensively utilized in drug delivery. Recently, several studies showed that ZIF-8 possessed a remarkable drug loading capacity and a pH-triggered control of drug release property [10–16]. However, a major drawback is their lack of tumor targeting ability. Further study is needed to develop tumor targeting ligand-functionalized MOFs to achieve targeted drug delivery and enhance therapeutic efficacy.

In this study, we report the synthesis of a folic acid-modified (doxorubicin, DOX) DOX@ZIF-8 nanoparticles (abbreviated as DOX@ZIF-8-FA) for targeted treatment of human hepatocellular carcinoma HepG2 cells. The DOX@ZIF-8-FA nanoparticles were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and zeta potential meter. Their in vitro cytotoxicity and therapeutic efficacy in HepG2 cells were also investigated using MTT assays. Furthermore, we demonstrated that the DOX@ZIF-8-FA complex has a higher anticancer efficiency towards the HepG2 cell lines compared with doxorubicin in the absence of ZIF-8 nanoparticles. The proliferation of HepG2 cells was significantly decreased after DOX@ZIF-8-FA treatment.

2. Materials and Methods

2.1. Materials and Chemicals

Zinc nitrate hexahydrate (Zn(NO₃)₂·6H₂O), folic acid (FA), and ethanol were obtained from Sinopharm Chemical Reagent Co. Ltd. (Shanghai, China). 2-Methylimidazole was purchased from Alfa Aesar. Doxorubicin (DOX) was purchased from Huafeng United Technology Co. Ltd. (Beijing, China). The other chemicals in this experiment were of analytical grade and used without further purification.

2.2. Synthesis of DOX@ZIF-8 Nanoparticles

The DOX@ZIF-8 nanoparticles were prepared by optimizing the previously reported method [10]. In brief, 1.0 mL of DOX solution (DOX, 12 mg) was mixed with 200 μL of zinc nitrate solution (Zn(NO₃)₂·6H₂O, 50 mg). The mixture was shaken at room temperature for 2 min. Then, 2.5 g of an aqueous solution containing 0.5 g of 2-methylimidazole was added dropwise to the above solution under ultrasonication. Following 15 min ultrasonication, the DOX@ZIF-8 nanoparticles were collected, washed with ethanol and water, and then dispersed in water. The quantification of DOX loaded in ZIF-8 nanoparticles was measured by using UV/Vis spectroscopy with the absorbance at 479 nm. The supernatant was used to quantify the DOX concentration. Because the obtained DOX@ZIF-8 nanoparticles are insoluble in the aqueous solution, the percentage of loaded amount of DOX was determined by performing the subtraction of the amounts of their initial and remaining DOX in the aqueous solution. The quantification of DOX was performed using the calibration curve of DOX in phosphate buffer (pH = 7.4, Supplementary Figure S1). The loading amount was calculated as follows:

2.3. Synthesis of FA-Modified DOX@ZIF-8 (DOX@ZIF-8-FA) Nanoparticles

20 mg of DOX@ZIF-8 nanoparticles was dispersed in 1 mL of water, followed by adding 1.0 mL of FA solution (FA, 20 mg/mL, pH = 7.0). The mixture was applied to ultrasonic treatment at room temperature for 10 min. The obtained DOX@ZIF-8-FA nanoparticles were separated by centrifugation, washed with ethanol and water, and dissolved in water for further use.

2.4. In Vitro DOX Release from the DOX@ZIF-8-FA Nanoparticles

DOX release from the DOX@ZIF-8-FA nanoparticles analysis was performed in PBS buffer solution (pH = 7.4, 6.0, and 5.0, resp.) at 37°C. For each release study, 200 μg of DOX@ZIF-8-FA nanoparticles was dispersed in 200 μL of PBS buffer solution and incubated at 37°C. At a given time, the nanoparticles were collected by centrifugation; 200 μL of fresh PBS buffer solution was added for the next release experiment. The DOX content in the release solution was measured by an UV/Vis spectrophotometry with the absorbance at 479 nm. The released percentage of DOX was calculated by the ratio of the released amount of DOX to the total loaded amount of DOX.

2.5. Cell Culture and Proliferation Assays

Cells were maintained in DMEM (supplemented with 10% fetal bovine serum and 1% antibiotic/antimycotic agent) at 37°C in 5% CO₂ and 21% O₂. HepG2 cells were plated at a concentration of 5 × 10⁴ cells/mL in a 24-well plate and were treated with 25 nM free DOX, DOX@ZIF-8 nanoparticles, or DOX@ZIF-8-FA nanoparticles. Cell viability assays were performed using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reagent as previously described [17].

2.6. Statistical Analysis

Statistical analyses were performed by the Student -test (two-tailed) using Prism GraphPad software. Differences with were considered statistically significant. Data were represented as mean ± SEM.

3. Results and Discussion

High-dispersion DOX@ZIF-8 nanoparticles were synthesized using the modified method developed by Zheng et al. (please see experimental section for details) [10]. As seen in SEM and TEM images (Figures 1(a) and 1(b)), the DOX@ZIF-8 nanoparticles are nearly spherical with a very coarse surface. The particle size was also measured from SEM images at three different regions. The data revealed that the obtained DOX@ZIF-8 nanoparticles have a wide particle size distribution with a diameter of 30–110 nm, which is smaller than Zheng and coworkers’ reported results [10]. This might be due to ultrasonication which could accelerate the reaction rate and produce more seed crystals at the early stage of the reaction, leading to the decrease of the particle sizes. The powder X-ray diffraction (PXRD) pattern of the DOX@ZIF-8 nanoparticles is shown in Figure 1(c). All of the sharp diffraction peaks can be indexed to the crystalline ZIF-8 particles, and no other peaks of impurity were observed in the PXRD patterns, suggesting high purity of the obtained DOX@ZIF-8 nanomaterials.

(a)

(b)

(c)

Figure 1: SEM image (a), TEM image (b), and XRD patterns (c) of DOX@ZIF-8 nanoparticles.

In order to endow this drug delivery system with tumor targeted ability, the DOX@ZIF-8 nanoparticles were integrated with folic acid, which has been widely used as a targeting ligand for treatment of folate receptor-overexpressing tumors including breast, lung, liver, and ovarian cancers [18, 19]. The surface functionalization of the particles was then investigated by zeta potential measurements. As revealed in Table 1, the zeta potential of the DOX@ZIF-8 nanoparticles and the DOX@ZIF-8-FA nanoparticles was +28.0 mV and −4.9 mV, respectively. The zeta potential of the DOX@ZIF-8-FA nanoparticles was lower than the DOX@ZIF-8 nanoparticles, which was due to the present of negative charged carboxyl groups on the nanoparticles’ surface by folic acid functionalization.

Table 1: Zeta potential of DOX@ZIF-8 nanoparticles and DOX @ ZIF-8-FA nanoparticles in ultrapure water.

Samples
Zeta potential (mV)

DOX@ZIF-8 nanoparticles
+28.0 ± 0.2

DOX@ZIF-8-FA nanoparticles
−4.9 ± 0.1

The release profiles of DOX from the DOX@ZIF-8-FA nanoparticles with 15.7 wt% DOX loading in different pH values of PBS buffer are shown in Figure 2. There was only 48.5% of DOX released during the test time in PBS buffer at pH 7.4, whereas the cumulative release of DOX was about 68.8% at pH 5.0 and 65.5% at pH 6.0, respectively, in 12 days, suggesting that the DOX@ZIF-8-FA drug delivery system possesses excellent drug-sustained release performances and good pH-responsive properties, which are similar to previously reported DOX-ZIF-8 drug delivery nanosystems [10, 12]. The pH-responsive drug release mechanism of the DOX@ZIF-8-FA nanosystem involves two possible factors [12, 20]: (1) the easy degradation of ZIF-8 nanoparticles in acidic environments and (2) the increased solubility of DOX at low pH due to the increased protonation of amino groups in DOX molecules.

Figure 2: Release kinetics of DOX from DOX@ZIF-8-FA nanoparticles in PBS buffer solution at different pH values.

It is very important to evaluate the biocompatibility of the ZIF-8 NPs for their potential bioapplications. Hence, we performed the standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay on HepG2 cells to investigate the cytotoxicity of the ZIF-8 nanoparticles. Figure 3 revealed the cytotoxic efficacy of the ZIF-8 NPs with the HepG2 cells. The results demonstrated that the ZIF-8 NPs have minimal toxicity at lower concentration and can be applied in the biomedical field with good biocompatibility.

Figure 3: In vitro cytotoxicity of empty ZIF-8 nanoparticles against HepG2 cells at different concentrations after 24 h. versus control. NS: No statistical significance versus control.

Finally, we have investigated the roles of DOX@ZIF-8-FA nanoparticles in the progression of the HCC cell line. The results showed that DOX@ZIF nanoparticles or DOX@ZIF-8-FA nanoparticles significantly inhibited the growth of HepG2 cells compared to equivalent concentration of free DOX alone (Figure 4). Moreover, DOX@ZIF-8-FA nanoparticles exerted a better inhibition function than the treatment with either DOX@ZIF nanoparticles at the DOX concentration of 7.5 μg/mL for 24 h (Figure 4). The concentrations causing 70% cell growth inhibition. The possible mechanism may be attributed to the targeting ligand (folic acid) on the particle surface to enhance cellular uptake of the nanoparticles into HepG2 cells, resulting a higher therapeutic effect. In addition, our results have shown that the cell morphology was destroyed after treated with DOX@ZIF nanoparticles or DOX@ZIF-8-FA nanoparticles compared to free DOX (Supplementary Figure S2).

Figure 4: MTT assay in HepG2 cells treated with DOX, DOX@ZIF-8 nanoparticles, or DOX@ZIF-8-FA nanoparticles at the equivalent concentration of free DOX after 24 h. versus DOX, versus DOX@ZIF-8.

4. Conclusions

In conclusion, we have reported a novel folic acid-modified DOX@ZIF-8 nanoparticles for targeted treatment of liver cancer. Doxorubicin hydrochloride (DOX), selected as a model drug, was efficiently entrapped in ZIF-8 nanoparticles. The low cytotoxicity, high drug capacity, and tumor targeting ability make it a promising targeted drug delivery system. MTT assay also showed that DOX@ZIF-8-FA nanoparticles displayed a higher therapeutic efficiency towards HepG2 cells than free DOX and DOX@ZIF-8 nanoparticles. These results indicated that the DOX@ZIF-8-FA nanoparticles are a promising drug delivery system for folate receptor-related liver cancer.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no competing interests.

Authors’ Contributions

Jian Bi and Ping Gao designed the experiments. Jian Bi, Yishan Lu, and Yan Dong performed the experiments. Jian Bi, Yan Dong, and Ping Gao analyzed the data. Jian Bi, Yan Dong, and Ping Gao contributed to the writing of the manuscript. Jian Bi, Yishan Lu, Yan Dong, and Ping Gao revised the manuscript. All authors reviewed the manuscript.

Acknowledgments

This work was supported by Natural Science Foundation of Liaoning Province, China (no. 20162225), and Education Department of Liaoning Province project (no. L2016019).

Supplementary Materials

Supplementary Figure S1: the calibration curve of DOX in PBS solution. Supplementary Figure S2: the cell morphology was destroyed after treated with DOX@ZIF nanoparticles, DOX@ZIF-8-FA nanoparticles, and free DOX. (Supplementary Materials)

References

A. Jemal, F. Bray, M. M. Center, J. Ferlay, E. Ward, and D. Forman, “Global cancer statistics,” CA: A Cancer Journal for Clinicians, vol. 61, no. 2, pp. 69–90, 2011.

B. Xie, D. H. Wang, and S. J. Spechler, “Sorafenib for treatment of hepatocellular carcinoma: a systematic review,” Digestive Diseases and Sciences, vol. 57, no. 5, pp. 1122–1129, 2012.

H. Y. Kim and J. W. Park, “Molecularly targeted therapies for hepatocellular carcinoma: sorafenib as a stepping stone,” Digestive Diseases, vol. 29, no. 3, pp. 303–309, 2011.

Z. Li, J. C. Barnes, A. Bosoy, J. F. Stoddart, and J. I. Zink, “Mesoporous silica nanoparticles in biomedical applications,” Chemical Society Reviews, vol. 41, no. 7, pp. 2590–2605, 2012.

P. Ghosh, G. Han, M. De, C. K. Kim, and V. M. Rotello, “Gold nanoparticles in delivery applications,” Advanced Drug Delivery Reviews, vol. 60, no. 11, pp. 1307–1315, 2008.

M. S. Yavuz, Y. Cheng, J. Chen et al., “Gold nanocages covered by smart polymers for controlled release with near-infrared light,” Nature Materials, vol. 8, no. 12, pp. 935–939, 2009.

A. Kumari, S. K. Yadav, and S. C. Yadav, “Biodegradable polymeric nanoparticles based drug delivery systems,” Colloids and Surfaces B: Biointerfaces, vol. 75, no. 1, pp. 1–18, 2010.

P. Horcajada, T. Chalati, C. Serre et al., “Porous metal–organic-framework nanoscale carriers as a potential platform for drug delivery and imaging,” Nature Materials, vol. 9, no. 2, pp. 172–178, 2010.

M.-X. Wu and Y.-W. Yang, “Metal–organic framework (MOF)-based drug/cargo delivery and cancer therapy,” Advanced Materials, vol. 29, no. 23, article 1606134, 2017.

H. Zheng, Y. Zhang, L. Liu et al., “One-pot synthesis of metal–organic frameworks with encapsulated target molecules and their applications for controlled drug delivery,” Journal of the American Chemical Society, vol. 138, no. 3, pp. 962–968, 2016.

H. Ren, L. Zhang, J. An et al., “Polyacrylic acid@zeolitic imidazolate framework-8 nanoparticles with ultrahigh drug loading capability for pH-sensitive drug release,” Chemical Communications, vol. 50, no. 8, pp. 1000–1002, 2014.

C.-Y. Sun, C. Qin, X.-L. Wang et al., “Zeolitic imidazolate framework-8 as efficient pH-sensitive drug delivery vehicle,” Dalton Transactions, vol. 41, no. 23, pp. 6906–6909, 2012.

I. B. Vasconcelos, T. G. da Silva, G. C. G. Militão et al., “Cytotoxicity and slow release of the anti-cancer drug doxorubicin from ZIF-8,” RSC Advances, vol. 2, no. 25, pp. 9437–9442, 2012.

X. Wang, D. Miao, X. Liang et al., “Nanocapsules engineered from polyhedral ZIF-8 templates for bone-targeted hydrophobic drug delivery,” Biomaterials Science, vol. 5, no. 4, pp. 658–662, 2017.

E. Shearier, P. Cheng, Z. Zhu, J. Bao, Y. H. Hu, and F. Zhao, “Surface defection reduces cytotoxicity of Zn(2-methylimidazole)₂ (ZIF-8) without compromising its drug delivery capacity,” RSC Advances, vol. 6, no. 5, pp. 4128–4135, 2016.

X. Cao, L. Dai, L. Wang, J. Liu, and J. Lei, “A surfactant template-assisted strategy for synthesis of ZIF-8 hollow nanospheres,” Materials Letters, vol. 161, pp. 682–685, 2015.

H. Zhang, S. K. Ramakrishnan, D. Triner et al., “Tumor-selective proteotoxicity of verteporfin inhibits colon cancer progression independently of YAP1,” Science Signaling, vol. 8, no. 397, p. ra98, 2015.

J. Sudimack and R. J. Lee, “Targeted drug delivery via the folate receptor,” Advanced Drug Delivery Reviews, vol. 41, no. 2, pp. 147–162, 2000.

Y. G. Assaraf, C. P. Leamon, and J. A. Reddy, “The folate receptor as a rational therapeutic target for personalized cancer treatment,” Drug Resistance Updates, vol. 17, no. 4-6, pp. 89–95, 2014.

Z. Liu, X. Sun, N. Nakayama-Ratchford, and H. Dai, “Supramolecular chemistry on water-soluble carbon nanotubes for drug loading and delivery,” ACS Nano, vol. 1, no. 1, pp. 50–56, 2007.