Synthesis of porous gadolinium oxide nanosheets for cancer therapy and magnetic resonance imaging
Introduction
Cancer is still a major life-threating disease to human health in the world [1]. Chemotherapy has been clinically accepted as one of the important strategies for cancer treatment [2], [3], [4]. However, there are several inevitable drawbacks in chemotherapeutic agents, including low cellular uptake efficiency and many side effects [5]. Compared with the conventional chemotherapy, nanomaterials-based drug delivery has become a promising approach for enhancing the efficacy of the chemotherapy [6], [7], [8], [9]. Recently, pH-responsive system has been approved as an efficient stimuli-responsive strategy for on demand drug delivery [10], [11]. Various nanomaterials have attracted much attention in drug delivery due to their high surface-to-volume ratio and favorable physico-chemical characteristics [12], [13]. Nanoporous structures have great potential in gas separation and storage, sensing and drug delivery, due to the beneficial properties such as large surface area, surface functionalities and adjustable compositions [14]. In drug delivery, the porous nanomaterials have also exhibited high efficacy to cancer cell death after anticancer drug delivery and release [15].
Lanthanide-based nanomaterials have attracted tremendous attention in diagnosis, imaging and therapy, owing to their unique physical properties [16], [17]. Gadolinium possesses unpaired 4f electrons and a huge electron magnetic moment, which has been used as magnetic resonance (MR) contrast agent for imaging [18]. Now, there are lots of gadolinium-based nanomaterials, such as GdF3, NaGdF4 and Gd2O3, have been investigated for various biomedical applications [19], [20], [21]. However, the porous gadolinium oxides nanosheets (NSs) have not been explored yet for biomedical applications.
Herein, we report the synthesis of porous Gd2O3 NSs through a two-step colloidal synthesis method. After surface modification by polyetherimide (PEI) & polyethylene glycol (PEG), the as-obtained porous Gd2O3 NSs were stable in the aqueous solution, showing a high doxorubicin (DOX) drug loading capacity (Fig. 1). Furthermore, the porous Gd2O3 NSs also exhibits promising pH-responsive drug release behavior and MR imaging applications.
Section snippets
Experimental
The porous Gd2O3 NSs were prepared by two-step colloidal synthesis method. Firstly, we synthesized Gd2O3 NSs using thermal decomposition with surfactant, followed by etching with tri-octyl phosphine oxide (TOPO) to obtain porous Gd2O3 NSs, and the synthesis details are delineated in the supplementary material (SI). The morphologies were characterized by a Transmission electron microscopy (TEM) (Hitachi HT7700, Japan). The crystal structure was characterized by X-ray diffraction (XRD) (Rigaku
Results and discussion
The Gd2O3 NSs were prepared by thermal decomposition (Fig. S1). The porous Gd2O3 NSs could be obtained through the acid etching of TOPO. The potential mechanism of etching is similar to acid etching [22]. In brief, TOPO contains weak acids such as alkylphosphonic acids which could etch gadolinium oxide to generate vacancies. Besides, alkylphosphonic acids can coordinate to the Gd cations and form gadolinium-phosphonate complexes, which can be dissolved into solution to produce porous gadolinium
Conclusions
In summary, we have successfully prepared the porous Gd2O3 NSs using a two-step colloidal synthesis method. The as-obtained porous NSs with a large surface area exhibit a promising pH-responsive drug release behavior, which can efficiently kill the cancer cells. Moreover, the porous Gd2O3 NSs also can be used as an efficient contrast agent. This work introduces a novel approach to constructing multifunctional platforms based on the porous Gd2O3 NSs, which perform an ascendant cancer therapy.
CRediT authorship contribution statement
Meng Luo: Investigation, Writing - orginal draft. Lingling Xu: Data curation. Jiale Xia: Formal analysis. Hongyang Zhao: Visualization. Yaping Du: Supervision. Bo Lei: Funding acquisition and supervision, writing - review & editing.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgements
This study was supported by National Natural Science Foundation of China (Grant No. 51872224), Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi’an Jiaotong University (Grant No. 2018LHM-KFKT004).
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