Ultrasound-Triggered Smart Drug Release from Multifunctional Core−Shell Capsules One-Step Fabricated by Coaxial Electrospray Method

Langmuir ◽  
2011 ◽  
Vol 27 (3) ◽  
pp. 1175-1180 ◽  
Author(s):  
Yujia Jing ◽  
Yihua Zhu ◽  
Xiaoling Yang ◽  
Jianhua Shen ◽  
Chunzhong Li
2020 ◽  
Vol 320 ◽  
pp. 201-213 ◽  
Author(s):  
Xiaochen Liu ◽  
Wenxin Zhang ◽  
Yabing Wang ◽  
Yunong Chen ◽  
Jian Xie ◽  
...  

2017 ◽  
Vol 37 (5) ◽  
pp. 1366-1373 ◽  
Author(s):  
Yu Shang ◽  
Fuyuan Ding ◽  
Jian Liu ◽  
Ling Xiao ◽  
Hongbing Deng ◽  
...  

RSC Advances ◽  
2014 ◽  
Vol 4 (57) ◽  
pp. 30430-30439 ◽  
Author(s):  
Yang Cao ◽  
Bochu Wang ◽  
Yazhou Wang ◽  
Deshuai Lou

Immiscible and miscible liquids were utilized to fabricate PVP/PLGA and PCL/PLGA nanoparticles with a distinct core–shell structure by coaxial electrospray. Two different sequential drug release profiles from different nanoparticles were observed. The melanoma cells and endothelial cells can be sequentially targeted and killed by therapeutic agents released from nanoparticles.


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Yang Cao ◽  
Fengqiu Liu ◽  
Yuli Chen ◽  
Tao Yu ◽  
Deshuai Lou ◽  
...  

2014 ◽  
Vol 2 (28) ◽  
pp. 4481-4488 ◽  
Author(s):  
Gui-Yun Mao ◽  
Wen-Jing Yang ◽  
Fan-Xing Bu ◽  
Dong-Mei Jiang ◽  
Zhen-Jie Zhao ◽  
...  

Core@shell structured Fe3O4@C nanoparticles synthesized by one-pot hydrothermal method show good pH-response drug release property and magneto-thermal performance.


2013 ◽  
Vol 13 (9) ◽  
pp. 1369-1380 ◽  
Author(s):  
Guangyan Qing ◽  
Minmin Li ◽  
Lijing Deng ◽  
Ziyu Lv ◽  
Peng Ding ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1546
Author(s):  
Zhen Li ◽  
Shunqi Mei ◽  
Yajie Dong ◽  
Fenghua She ◽  
Puwang Li ◽  
...  

Core-shell nanofibers have great potential for bio-medical applications such as wound healing dressings where multiple drugs and growth factors are expected to be delivered at different healing phases. Compared to monoaxial nanofibers, core-shell nanofibers can control the drug release profile easier, providing sustainable and effective drugs and growth factors for wound healing. However, it is challenging to produce core-shell structured nanofibers with a high production rate at low energy consumption. Co-axial centrifugal spinning is an alternative method to address the above limitations to produce core-shell nanofibers effectively. In this study, a co-axial centrifugal spinning device was designed and assembled to produce core-shell nanofibers for controlling the release rate of ibuprofen and hEGF in inflammation and proliferation phases during the wound healing process. Core-shell structured nanofibers were confirmed by TEM. This work demonstrated that the co-axial centrifugal spinning is a high productivity process that can produce materials with a 3D environment mimicking natural tissue scaffold, and the specific drug can be loaded into different layers to control the drug release rate to improve the drug efficiency and promote wound healing.


Pharmaceutics ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 13
Author(s):  
Benzion Amoyav ◽  
Yoel Goldstein ◽  
Eliana Steinberg ◽  
Ofra Benny

Microfluidics research for various applications, including drug delivery, cell-based assays and biomedical research has grown exponentially. Despite this technology’s enormous potential, drawbacks include the need for multistep fabrication, typically with lithography. We present a one-step fabrication process of a microfluidic chip for drug dissolution assays based on a 3D printing technology. Doxorubicin porous and non-porous microspheres, with a mean diameter of 250µm, were fabricated using a conventional “batch” or microfluidic method, based on an optimized solid-in-oil-in-water protocol. Microspheres fabricated with microfluidics system exhibited higher encapsulation efficiency and drug content as compared with batch formulations. We determined drug release profiles of microspheres in varying pH conditions using two distinct dissolution devices that differed in their mechanical barrier structures. The release profile of the “V” shape barrier was similar to that of the dialysis sac test and differed from the “basket” barrier design. Importantly, a cytotoxicity test confirmed biocompatibility of the printed resin. Finally, the chip exhibited high durability and stability, enabling multiple recycling sessions. We show how the combination of microfluidics and 3D printing can reduce costs and time, providing an efficient platform for particle production while offering a feasible cost-effective alternative to clean-room facility polydimethylsiloxane-based chip microfabrication.


2013 ◽  
Vol 50 (7) ◽  
pp. 495-501 ◽  
Author(s):  
Keitaro Nakamura ◽  
Akihiro Kinoshita ◽  
Shu Watanabe ◽  
Naohito Uemura ◽  
Kiyoshi Takahashi

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