Effects of some process parameters on the niflumic acid controlled release polymeric microspheres: Optimization using designs of experiments

2019 ◽  
Vol 14 (2) ◽  
pp. e2283 ◽  
Author(s):  
Nedjma Assas ◽  
Zineb Elbahri ◽  
Milad Baitiche ◽  
Ferhat Djerboua
2013 ◽  
Vol 450 (1-2) ◽  
pp. 114-122 ◽  
Author(s):  
Aparna Saigal ◽  
Wai Kiong Ng ◽  
Reginald B.H. Tan ◽  
Sui Yung Chan

2014 ◽  
Vol 71 (7) ◽  
pp. 1625-1643 ◽  
Author(s):  
Keerti V. Phadke ◽  
Lata S. Manjeshwar ◽  
Tejraj M. Aminabhavi

2021 ◽  
Vol 11 (1) ◽  
pp. 171-182
Author(s):  
Payal D Borawake ◽  
Arumugam Kauslya ◽  
Jitendra V Shinde ◽  
Rajashree S Chavan

Numbers of developments are implemented in drug delivery system to achieve the goals of optimized efficacy, cost effectiveness of therapy. One of the latest, novel and highly evolving technologies is microsponge drug delivery system which gives controlled release and site specific delivery of active ingredients. They are highly cross linked, porous and polymeric microspheres with size range of 5-300µm. This system is emerging as valuable option for topical delivery of drugs due to characteristics like decreased side effects, improved stability, better formulation flexibility, superior product performance. It is having number of applications in oral, topical, ocular and biopharmaceuticals delivery. The current review describes microsponge technology and details of the formulation methods, evaluation, programmable release mechanisms and applications.   Keywords: Microsponges; Controlled release; Quasi emulsion solvent diffusion; Programmable drug release; Oral administration; Topical drug delivery.


2007 ◽  
Vol 342 (1-2) ◽  
pp. 82-86 ◽  
Author(s):  
Dongming Peng ◽  
Kelong Huang ◽  
Yanfei Liu ◽  
Suqin Liu

Author(s):  
Fatima Zohra BELMOKHTAR ◽  
Zineb ELBAHRI ◽  
Mohamed ELBAHRI

In the present paper, factorial designs of experiments (DOE) were built in the aim of preparing new solid optimized controlled release microparticles charged with the herbicide 2,4-D and, also investigating the influence of some process and encapsulation variables. Composed from mixtures of ethylcellulose (EC) / hydroxy propyl methyl cellulose (HPMC), cellulose acetate butyrate butyryle (CAB) / HPMC and pure CAB as biodegradable polymeric matrices, the microparticles were prepared by emulsification-solvent evaporation technique. Then, the effect of some parameters such as the stirring speed of emulsification, initial drug concentration and polymer concentration were studied. Depending on the selected variables, a large range of microparticles’ size was obtained; from 25 to 208 µm of d<sub>10</sub> and the 2,4-D content reached 69%. Also, different release profiles accompanied with a burst effect were obtained. Finaly, by modelling using Minitab 16.1 software, the main and interactive effects of these variables on the microparticles’ chacteristics (size, drug entrapment and drug release) were evaluated.


2008 ◽  
Vol 70 (3) ◽  
pp. 303 ◽  
Author(s):  
S Ravi ◽  
KK Peh ◽  
Yusrida Darwis ◽  
BKrishna Murthy ◽  
TRaghu Raj Singh ◽  
...  

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