A polymer scaffold with drug-sustained release and antibacterial activity

2019 ◽  
Vol 69 (6) ◽  
pp. 398-405 ◽  
Author(s):  
Ping Wu ◽  
Shi Hu ◽  
Qin Liang ◽  
Wang Guo ◽  
Yang Xia ◽  
...  
Author(s):  
Nanjunda Reddy B H ◽  
Prdadipta Ranjan Rauta ◽  
Venkatalakshimi V ◽  
Swamy Sreenivasa

 Objective: The main objective of this work was to formulate and evaluate Closite-30B/nanoAg filled hydrogel composites which are further intentended to be used for the study of drug delivery,antibacterial, and anticancer activityMethods: In this study, Cloisite-30B (C-30B) clay dispersed biopolymer sodium alginate (SA)-grafted-poly (acrylamide [AAm]-co-lignosulfonic acid) hydrogel composites were synthesized by free radical in situ polymerization reaction technique using SA, AAm, and lignosulfonic acid biopolymers in different proportions in combination. which are subjected to invitro drug delivery and Minimum inhibitory concentration(MIC) method for antibacterial activity study by using Streptococcus faecalis (S.faecalis) and Escherichia coli (E. coli)bacteria. The biocompatibility of the prepared gels were determined by standard protocol HaCaT-cells and MCF-7 cell lines further the prepared hydrogel composites were characterized for particle size,encapsulation efficiency,swelling properties,compatibility studies by FTIR etc.Results: The formulated hydrogels were characterized by X-ray diffraction (XRD) to analyze the particles size and crystallinity. The presence of functional groups and their chemical interaction with the drug, C-30B, and silver nanoparticles (AgNPs) were confirmed by the FTIR spectroscopy. Furthermore, the presence of AgNPs in the matrix was confirmed by ultraviolet/visible spectroscopy. Thermogravimetric analysis was performed to find out the thermal degradation, thermal stability, and the percentage of weight loss at various temperatures. Swelling studies revealed that C-30B and AgNPs induced composites exhibited higher swelling ratio than pure hydrogels. The hydrogels with C-30B/AgNPs displayed excellent antibacterial activity against both Gram-positive and Gram-negative bacteria. Further, these hydrogel composites were loaded with the drug paclitaxel (PT), and drug release study showed that the sustained release of the drug from C-30B/Ag hydrogel matrix compared to rest of other samples. Hydrogel composites were cytocompatible in nature (with HaCaT cells) and the cell viability decreased (with MCF-7cells) with the presence of lignosulfonic acid as well as C-30B and AgNPs in the samples as evaluated through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide to its insoluble formazan assay.Conclusion: The synthesized hydrogel composites were successfully characterized and eavaluated for sustained release of paclitaxel drug delivery at different pHs and temperatures and it is found that C30B/Ag filled composites exhibits contolled release of drug with higher rate, especially at lower pH (pH2) and higher temperature (37oC) and the same formulations which exhibits better anitbcterial and anticancer activity compared to the virgin samples So the prepared C30B/AgNPs hydrogels composites used in drug dlivery for the effective treatment of cancer and used against bacterias and cancerous cells.


2020 ◽  
Vol 60 (12) ◽  
pp. 3231-3243
Author(s):  
Gabriella Onila do Nascimento Soares ◽  
Raíssa Ribeiro Lima Machado ◽  
Mariana Mendonça Diniz ◽  
Aline Bruna da Silva

2010 ◽  
Vol 76 (1) ◽  
pp. 362-365 ◽  
Author(s):  
Caixin Guo ◽  
Shaoqin Liu ◽  
Zhifei Dai ◽  
Chang Jiang ◽  
Wenyuan Li

2011 ◽  
Vol 311-313 ◽  
pp. 1751-1754
Author(s):  
Gui Yu Li ◽  
Xi Hong Lu ◽  
Xue Hu Li ◽  
Lei Tao ◽  
Jian Ping Liang

Drug was encapsulated in a novel copolymers of poly(lactic-co-glycolic acid) (PLGA) to investigate the sustained-release formulation of drug loaded polymer microspheres delivery system. Used a modified solid-in-oil-in-water (S/O/W) emulsion solvent evaporation method to prepare microspheres, its morphology and particle size distribution were estimated by scanning electron microscopy (SEM), the profile of in vitro drug release were assessed by High performance liquid chromatography (HPLC). Finally, an stable release buffer was utilized to obtain a detailed drug release profile, which was analyzed by HPLC also. Results showed that the microspheres morphology, encapsulation efficiency and the cumulative drug release efficiency were appropriate for veterinary medicine using. The modified preparation method was simple and optimized, PLGA microspheres with excellent controlled-release characteristics may serve as drug delivery carrier and may prolong the drug sustained-release effect.


2018 ◽  
Vol 57 (18) ◽  
pp. 1873-1881 ◽  
Author(s):  
Shunyu Chen ◽  
Zhi Luo ◽  
Linzhao Wu ◽  
Chunling Xie ◽  
Xiufeng Xiao

RSC Advances ◽  
2016 ◽  
Vol 6 (55) ◽  
pp. 49817-49823 ◽  
Author(s):  
Tonghe Zhu ◽  
Kui Yu ◽  
M. Aqeel Bhutto ◽  
Juan Wang ◽  
Wei Shen ◽  
...  

Herein, we report a facile method for the fabrication of flurbiprofen axetil (FA)-loaded core–sheath composite ultrafine fibers for drug sustained release.


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