ROS-generating, pH-responsive and highly tunable reduced graphene oxide-embedded microbeads showing intrinsic anticancer properties and multi-drug co-delivery capacity for combination cancer therapy

The development of effective carriers enabling combination cancer therapy is of practical importance due to its potential to enhance the effectiveness of cancer treatment. However, most of the reported carriers are monofunctional in nature. The carriers that can be applied to concomitantly mediate m...

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Bibliographic Details
Main Authors: Adilakshmi Boddu (Author), Sreekanth Reddy Obireddy (Author), Dahong Zhang (Author), K. S. V. Krishna Rao (Author), Wing-Fu Lai (Author)
Format: Book
Published: Taylor & Francis Group, 2022-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Adilakshmi Boddu  |e author 
700 1 0 |a Sreekanth Reddy Obireddy  |e author 
700 1 0 |a Dahong Zhang  |e author 
700 1 0 |a K. S. V. Krishna Rao  |e author 
700 1 0 |a Wing-Fu Lai  |e author 
245 0 0 |a ROS-generating, pH-responsive and highly tunable reduced graphene oxide-embedded microbeads showing intrinsic anticancer properties and multi-drug co-delivery capacity for combination cancer therapy 
260 |b Taylor & Francis Group,   |c 2022-12-01T00:00:00Z. 
500 |a 10.1080/10717544.2022.2100512 
500 |a 1521-0464 
500 |a 1071-7544 
520 |a The development of effective carriers enabling combination cancer therapy is of practical importance due to its potential to enhance the effectiveness of cancer treatment. However, most of the reported carriers are monofunctional in nature. The carriers that can be applied to concomitantly mediate multiple treatment modalities are highly deficient. This study fills this gap by reporting the design and fabrication of ROS-generating carbohydrate-based pH-responsive beads with intrinsic anticancer therapy and multidrug co-delivery capacity for combination cancer therapy. Sodium alginate (SA) microspheres and reduced graphene oxide (rGO)-embedded chitosan (CS) beads are developed via emulsion-templated ionic gelation for a combination therapy involving co-delivery of curcumin (CUR) and 5-fluororacil (5-FU). Drug-encapsulated microbeads are characterized by FTIR, DSC, TGA, XRD, and SEM. 5-FU and CUR-encapsulated microbeads are subjected to in vitro drug release studies at pH 6.8 and 1.2 at 37 °C. Various release kinetic parameters are evaluated. The results show that the Korsmeyer-Peppas model and non-Fickian release kinetics are best suited. The microspheres and microbeads are found to effectively act against MCF7 cells and show intrinsic anticancer capacity. These results indicate the promising performance of our beads in mediating combination drug therapy to improve the effectiveness of cancer treatment. 
546 |a EN 
690 |a Carbohydrate 
690 |a curcumin 
690 |a reduced graphene oxide 
690 |a anti-cancer 
690 |a chitosan 
690 |a sodium alginate 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Drug Delivery, Vol 29, Iss 1, Pp 2481-2490 (2022) 
787 0 |n https://www.tandfonline.com/doi/10.1080/10717544.2022.2100512 
787 0 |n https://doaj.org/toc/1071-7544 
787 0 |n https://doaj.org/toc/1521-0464 
856 4 1 |u https://doaj.org/article/f4cd6529e62a495c9b718b83120e9dbb  |z Connect to this object online.