scholarly journals PEG-PCL Nanocapsules Containing Curcumin: Validation of HPLC Method for Analyzing Drug-loading Efficiency, Stability Testing and Cytotoxicity on NIH-3T3 Cell Line

Author(s):  
Loanda Aparecida Cabral Rudnik ◽  
Amanda Martinez Lyra ◽  
Fernanda Malaquias Barboza ◽  
Traudi Klein ◽  
Carla Cristine Kanunfre ◽  
...  
2013 ◽  
Vol 10 (10/11) ◽  
pp. 996 ◽  
Author(s):  
Chiao Hsi Chiang ◽  
Hossein Hosseinkhani ◽  
Wen Sheng Cheng ◽  
g Wei Chen ◽  
Chun Hsiang Wang ◽  
...  

2017 ◽  
Vol 156 ◽  
pp. 29-37 ◽  
Author(s):  
Yongpeng Hou ◽  
Chen Yao ◽  
Longbing Ling ◽  
Yawei Du ◽  
Ruiyu He ◽  
...  

2019 ◽  
Vol 10 (3) ◽  
pp. 035017 ◽  
Author(s):  
Uyen Vy Vo ◽  
Van Cuong Nguyen ◽  
Xuan Vu Duong Vo ◽  
Minh Khang Tan Vo ◽  
Hoang Ai Le Pham ◽  
...  

2020 ◽  
Vol 26 ◽  
pp. 720-723
Author(s):  
Christina Vincent ◽  
Kiran M.D ◽  
Jitha S. Jayan ◽  
Appukuttan Saritha

2011 ◽  
Vol 335-336 ◽  
pp. 1439-1442 ◽  
Author(s):  
Yu Yan Zhou ◽  
Gui Yu Li ◽  
Hong Xia Wang ◽  
Lei Tao ◽  
Jian Ping Liang

In the present paper, monodisperse poly(lactic acid) (PLA) microspheres (MS) containing the enrofloxacin (ENRO), were manufactured by using a modified solid in oil in water (S/O/W) emulsion solvent evaporation method. In order to prepare PLA microspheres with a higher drug loading efficiency by this modified technique, the test of stability and productivity of the primary emulsion was preliminary examined by change species or concentration of the oil-soluble surfactant and the ratio of water and organic solvent. Firstly, enrofloxacin polylactic acid microspheres (ENRO-PLA-MS) were producted, then the morphology and particle size distribution were estimated by scanning electron microscopy (SEM), its encapsulation efficiency and drug loading efficiency were assessed by High performance liquid chromatography (HPLC). In vivo conditions were simulated by an stable release buffer to obtain a detailed release and polymer degradation profile. Consequently, the ENRO-PLA-MS had a denser structure with a smooth, pore-free surface, the preparation of microspheres was simple, the prepared microspheres had excellent controlled drug release characteristics in vitro.


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