Nanofibrous polylactide composite scaffolds with electroactivity and sustained release capacity for tissue engineering

2016 ◽  
Vol 4 (14) ◽  
pp. 2477-2485 ◽  
Author(s):  
Jing Chen ◽  
Juan Ge ◽  
Baolin Guo ◽  
Kun Gao ◽  
Peter X. Ma

A conveniently fabricated electroactive nanofibrous composite scaffold serves as a sustained drug release system and promotes myoblast differentiation.

2019 ◽  
Vol 43 (4) ◽  
pp. 1827-1837 ◽  
Author(s):  
Ling Huang ◽  
Jian Chen ◽  
Xiufang Li ◽  
Hui Liu ◽  
Jianbing Li ◽  
...  

A long-term antibacterial and sustained drug release system was fabricated, in which the TNTs acted as the loading platform of NOR and then encapsulated with PMAA.


2001 ◽  
Vol 21 (2) ◽  
pp. 145-148 ◽  
Author(s):  
Ye Zhangqun ◽  
Chen Jie ◽  
Zhang Xu ◽  
Li Jiagui ◽  
Zhou Siwei ◽  
...  

2012 ◽  
Vol 20 (1) ◽  
pp. 303-308 ◽  
Author(s):  
Yong-Ha Kim ◽  
Il-Kug Kim ◽  
Tae-Gon Kim ◽  
Jun-Ho Lee ◽  
Young-Kook Lim ◽  
...  

2020 ◽  
Vol 12 ◽  
Author(s):  
Sagar R. Pardeshi ◽  
Harshal A. Mistari ◽  
Rakhi S. Jain ◽  
Pankaj R. Pardeshi ◽  
Rahul L. Rajput ◽  
...  

Background: Moxifloxacin is a BCS class I drug used in the treatment of bacterial conjunctivitis and keratitis. Despite its high water solubility, it possesses limited bioavailability due to anatomical and physiological constraints associated with the eyes which required multiple administrations to achieve a therapeutic effect. Objective: In order to prolong drug release and to improve antibacterial efficacy for the treatment of bacterial keratitis and conjunctivitis, moxifloxacin loaded nanoemulsion was developed. Methods: The concentration of oil (oleic acid), surfactant (tween 80), and cosurfactant (propylene glycol) were optimized by employing a 3-level 2-factorial design of experiment for the development of nanoemulsion. The developed nanoemulsion was characterized by particle size distribution, viscosity, refractive index, pH, drug content and release, transmission electron microscopy (TEM), and antibacterial study. The compatibility of the drug with the excipients was accessed by Fourier transform infrared spectroscopy (FTIR). Result: The average globule size was found to be 198.20 nm. The TEM study reveals the globules were nearly spherical and are well distributed. In vitro drug release profile for nanoemulsion shown sustained drug release (60.12% at the end of 6 h) compared to drug solution, where complete drug released within 2 h. The antibacterial effectiveness of the drug-loaded nanoemulsion was improved against S. aureus compared with the marketed formulation. Conclusion: The formulated sustained release nanoemulsion could be a promising alternative to eye drop with improved patient compliance by minimizing dosing frequency with improved antibacterial activity.


ACS Omega ◽  
2020 ◽  
Author(s):  
Shaoxin Deng ◽  
Cheng-Xing Cui ◽  
Lingyao Duan ◽  
Linfeng Hu ◽  
Xiaoxun Yang ◽  
...  

Pain ◽  
1986 ◽  
Vol 25 (1) ◽  
pp. 75-77 ◽  
Author(s):  
P. Schoeffler ◽  
E. Pichard ◽  
R. Ramboatiana ◽  
D. Joyon ◽  
J. P. Haberer

2007 ◽  
Vol 36 (4) ◽  
pp. 297-301 ◽  
Author(s):  
J.P. Zheng ◽  
L. Luan ◽  
H.Y. Wang ◽  
L.F. Xi ◽  
K.D. Yao

2021 ◽  
Vol 123 ◽  
pp. 111968
Author(s):  
Ye Liu ◽  
Yangying Si ◽  
Mingyu Di ◽  
Dejian Tang ◽  
Li Meng ◽  
...  

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