scholarly journals Correction to “Thermosensitive Chitosan-Based Injectable Hydrogel as an Efficient Anticancer Drug Carrier”

ACS Omega ◽  
2020 ◽  
Vol 5 (38) ◽  
pp. 24973-24973
Author(s):  
Anam Ahsan ◽  
Muhammad Asim Farooq ◽  
Wen-xia Tian ◽  
Amna Parveen
ACS Omega ◽  
2020 ◽  
Vol 5 (32) ◽  
pp. 20450-20460 ◽  
Author(s):  
Anam Ahsan ◽  
Muhammad Asim Farooq ◽  
Amna Parveen

2016 ◽  
Vol 4 (14) ◽  
pp. 2412-2420 ◽  
Author(s):  
Aneeya K. Samantara ◽  
Santanu Maji ◽  
Arnab Ghosh ◽  
Bamaprasad Bag ◽  
Rupesh Dash ◽  
...  

A facile one-step approach has been developed for the synthesis of carbon quantum dots (CQDs) from Good’s buffer.


RSC Advances ◽  
2015 ◽  
Vol 5 (109) ◽  
pp. 89397-89406 ◽  
Author(s):  
Chun Xiang Cynthia Lin ◽  
Siddharth Jambhrunkar ◽  
Pei Yuan ◽  
Chun Hui Clayton Zhou ◽  
George Xiu Song Zhao

Multi-compartment periodic mesoporous organosilica materials show desirable properties as anticancer drug carrier with high loading capacity and slow release rate.


BioResources ◽  
2019 ◽  
Vol 14 (2) ◽  
pp. 3615-3629 ◽  
Author(s):  
Yanli Li ◽  
Yucheng Feng ◽  
Jun Jing ◽  
Fei Yang

A novel magnetic anticancer drug carrier based on cellulose, guar gum, and Fe3O4 hydrogel microspheres was synthesized by chemical crosslinking. These microspheres were crosslinked with epoxy chloropropane and loaded with 5-fluorouracil (5-fu). The effect of the ratio of cellulose to guar gum on bead size, drug loading, and in vitro release behaviors were investigated. The influence of the magnetic content on drug loading and in vitro release behaviors were also evaluated. The magnetic hydrogel microspheres were characterized via an optical microscope, Fourier transform infrared spectroscopy, swelling behavior analysis, vibrating sample magnetometer, and ultraviolet absorption spectroscopy. The results showed that as the ratio of cellulose to guar gum increased from 3:1 to 5:1, the particle size increased from 395 to 459 um. Moreover, the drug loading capacity, encapsulation efficiency, and in vitro release behavior were influenced by the ratio of cellulose/guar gum and Fe3O4 content. Finally, the Fe3O4 particle had an adsorption effect on the drug, thereby reducing the maximum cumulative release.


2020 ◽  
Vol 10 (23) ◽  
pp. 8755
Author(s):  
Hiroto Fujita ◽  
Yuka Kataoka ◽  
Masayasu Kuwahara

We have previously developed a bifunctional aptamer (bApt) binding to both human thrombin and camptothecin derivative (CPT1), and showed that bApt acts as a drug carrier under the phenomenon named selective oligonucleotide entrapment in fibrin polymers (SOEF), which enables efficient enrichment of CPT1 into fibrin gels, resulting in significant inhibition of tumor cell growth. However, although the derivative CPT1 exhibits anticancer activity, it is not an approved drug. In this study, we evaluated the binding properties of bApt to irinotecan, a camptothecin analog commonly used for anticancer drug therapy, in addition to unmodified camptothecin (CPT). Furthermore, we have revealed that irinotecan binds to bApt like CPT1 and is selectively concentrated on fibrin gels formed around the tumor cells under the SOEF phenomenon to suppress cell proliferation.


2017 ◽  
Vol 164 ◽  
pp. 309-316 ◽  
Author(s):  
Jeongwook Lee ◽  
Ki Chun Yoo ◽  
Jaehyoung Ko ◽  
Bowon Yoo ◽  
Joohuei Shin ◽  
...  

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