scholarly journals Engineered hyaluronic acid-based smart nanoconjugates for enhanced intracellular drug delivery

Author(s):  
Mukherjee Arjama ◽  
Sivaraj Mehnath ◽  
Mariappan Rajan ◽  
Murugaraj Jeyaraj
2010 ◽  
Vol 11 (3) ◽  
pp. 713-720 ◽  
Author(s):  
Anna Szarpak ◽  
Di Cui ◽  
Frédéric Dubreuil ◽  
Bruno G. De Geest ◽  
Liesbeth J. De Cock ◽  
...  

2016 ◽  
Vol 12 (2) ◽  
pp. 498-499 ◽  
Author(s):  
Yinan Zhong ◽  
Jian Zhang ◽  
Ru Cheng ◽  
Chao Deng ◽  
Fenghua Meng ◽  
...  

Polymer ◽  
2015 ◽  
Vol 76 ◽  
pp. 237-244 ◽  
Author(s):  
Lin Wang ◽  
Yin Wang ◽  
Qiao Jin ◽  
Fan Jia ◽  
Haibo Wang ◽  
...  

2018 ◽  
Vol 14 (5) ◽  
pp. 1826-1827
Author(s):  
Yi Zhang ◽  
Jianxun Ding ◽  
Zhiyu Zhang ◽  
Xuesi Chen

Author(s):  
Meena K. S. ◽  
Sonia K ◽  
Alamelu Bai S

In order to develop the efficiency and the specificity of anticancer drug delivery, we have designed an innovative nanocarrier. The nanocarrier system comprises of a multifunctional graphene oxide nanoparticle-based drug delivery system (GO-CS-M-DOX) as a novel platform for intracellular drug delivery of doxorubicin (DOX). Firstly, graphene oxide (GO) was synthesized by hummer’s method whose surface was functionalized by chitosan (CS) in order to obtain a more precise drug delivery, the system was then decorated with mannose (M). Further conjugation of an anti-cancer drug doxorubicin to the nanocarrier system resulted in GO-CS-M-DOX drug delivery system. The resultant conjugate was characterized for its physio-chemical properties and its biocompatibility was evaluated via hemolysis assay. The drug entrapment efficiency is as high as 90% and in vitro release studies of DOX under pH 5.3 is significantly higher than that under pH 7.4. The anticancer activity of the synthesized drug delivery system was studied by 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay against MCF-7 cell line. These results stated that the pH dependent multifunctional doxorubicin- chitosan functionalized graphene oxide based nanocarrier system, could lead to a promising and potential platform for intracellular delivery and cytotoxicity activity for variety of anticancer drugs.   


2019 ◽  
Vol 9 (1) ◽  
pp. 2-14
Author(s):  
Sahil Kumar ◽  
Bandna Sharma ◽  
Kiran Thakur ◽  
Tilak R. Bhardwaj ◽  
Deo N. Prasad ◽  
...  

Background: Many efforts have been explored in the last decade to treat colon cancer but nanoparticulate drug delivery systems are making a vital contribution in the improvement of drug delivery to colon cancer cells. Objective: In this review, we attempt to highlight recent advancements in the development of novel drug delivery systems of nanoparticles for the targeted drug delivery to colon. Polymers like Epithelial Cell Adhesion Molecule (EpCAM) aptamer chitosan, Hyaluronic Acid (HA), Chitosan (CS)– Carboxymethyl Starch (CMS), silsesquioxane capped mesoporous silica, Near IR (NIR) fluorescent Human Serum Albumin (HAS), poly(ethylene glycol)-conjugated hyaluronic acid etc. have been discussed by employing various anticancer drugs like doxorubicin, oxaliplatin, paclitaxel, 5-fluorouracil etc. Conclusion: These novel drug delivery systems have been determined to be more efficacious in terms of stability, sustained and targeted drug delivery, therapeutic efficacy, improved bioavailability and enhanced anticancer activity.


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