Core-Shell Nanoparticles as an Efficient, Sustained, and Triggered Drug-Delivery System

被引:63
|
作者
Deshpande, Sonal [1 ]
Sharma, Sapna [1 ]
Koul, Veena [1 ,2 ]
Singh, Neetu [1 ,2 ]
机构
[1] Indian Inst Technol Delhi, Ctr Biomed Engn, New Delhi 110016, India
[2] All India Inst Med Sci, Biomed Engn Unit, New Delhi 110029, India
来源
ACS OMEGA | 2017年 / 2卷 / 10期
关键词
MESOPOROUS SILICA NANOPARTICLES; GOLD NANOPARTICLES; ANTICANCER DRUGS; RELEASE; NANOSPHERES; MICELLES; NANOGELS; CARRIERS;
D O I
10.1021/acsomega.7b01016
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
One of the challenges in designing a successful drug-delivery vehicle is the control over drug release. Toward this, a number of multifunctional nanoparticles with multiple triggers and complex chemistries have been developed. To achieve an efficient and maximum therapeutic effect, a trigger dependent drug-delivery system with sustained release is desirable. In this paper, we report the use of a combination of thermoresponsive gold core and polymeric shell nanoparticles that can provide a sustained, triggered release of doxorubicin, making the system more efficient compared to individual nanoparticles. The selection of the system was dependent on the best trigger applicable in biological systems and a component responsive to that trigger. Because of the best tissue penetration depth observed for radiofrequency (rf), we chose rf as a trigger. Whereas the gold nanoparticles (AuNPs) provided hyperthermia trigger on exposure to rf fields, the thermoresponsiveness was endowed by poly(N-isopropylacrylamide) (pNIPAm)-based polymer shells. AuNPs with three different compositions of shells, only pNIPAm and p(NIPAm-co-NIPMAm) with the ratio of NIPAm/N-(isopropylmethacrylamide) (NIPMAm) 1:1 (pNIPMAm(50)) and 1:3 (pNIPMAm(75)), were synthesized. We observed that the polymer coating on the AuNPs did not affect the heating efficiency of AuNPs by rf and exhibited a temperature-dependent release of the chemotherapeutic drug, doxorubicin. The nanoparticles were biocompatible, stable in biologically relevant media, and were able to show a burst as well as a sustained release, which was rf-dependent. Interestingly, we observed that when HeLa cells were treated with doxorubicin-loaded gold core-polymeric shell NPs and exposed to rf for varying times, the mixture of the two polymeric shell nanoparticles induced more cell death as compared to the cells treated with single nanoparticles, suggesting that such multi-nanoparticle systems can be more efficacious delivery systems instead of a single multicomponent system.
引用
收藏
页码:6455 / 6463
页数:9
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