This review presented the unique characteristics of different types of cyclodextrin polymers by non-covalent host–guest interactions to synthesize an inclusion complex. Various cancers are treated with different types of modified cyclodextrins, along with the anticancer drug paclitaxel. PTX acts as a mitotic inhibitor, but due to its low dissolution and permeability in aqueous solutions, it causes considerable challenges for drug delivery system (DDS) designs. To enhance the solubility, it is reformulated with derivatives of cyclodextrins using freeze-drying and co-solvent lyophilization methods. The present supramolecular assemblies involve cyclodextrin as a key mediator, which is encapsulated with paclitaxel and their controlled release a...
The use of cytotoxic chemotherapic agents is the most common method for the treatment of metastatic ...
Since 1970s cyclodextrins (CDs) and their derivatives, in virtue of their peculiar inclusion propert...
Jong-Suep Baek,* Ju-Heon Kim,* Jeong-Sook Park, Cheong-Weon Cho College of Pharmacy and Institute o...
Effective anticancer therapy can be achieved by designing a targeted drug-delivery system with high ...
Background: Paclitaxel is a potent anticancer drug that is effective against a wide spectrum of canc...
Background: Paclitaxel is a potent anticancer drug that is effective against a wide spectrum of canc...
Background and Objective: Cyclodextrins have been of great interest as excellent candidates for fabr...
Amphiphilic cyclodextrins are biocompatible oligosaccharides that can be used for drug delivery espe...
Paclitaxel is effective against a wide range of cancers which are considered to be refractory to con...
Paclitaxel (PTX) is a chemotherapeutic agent that belongs to the taxane family and which was approve...
Drugs with low aqueous solubility and permeability possess substantial challenges in designing effec...
The uniqueness of paclitaxel’s antimitotic action mechanism has fueled research toward its applicati...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Paclitaxel is a microtubule inhibitor causing mitotic arrest and is widely used in cancer chemothera...
Copyright © 2012 Madhu S. Surapaneni et al. This is an open access article distributed under the Cre...
The use of cytotoxic chemotherapic agents is the most common method for the treatment of metastatic ...
Since 1970s cyclodextrins (CDs) and their derivatives, in virtue of their peculiar inclusion propert...
Jong-Suep Baek,* Ju-Heon Kim,* Jeong-Sook Park, Cheong-Weon Cho College of Pharmacy and Institute o...
Effective anticancer therapy can be achieved by designing a targeted drug-delivery system with high ...
Background: Paclitaxel is a potent anticancer drug that is effective against a wide spectrum of canc...
Background: Paclitaxel is a potent anticancer drug that is effective against a wide spectrum of canc...
Background and Objective: Cyclodextrins have been of great interest as excellent candidates for fabr...
Amphiphilic cyclodextrins are biocompatible oligosaccharides that can be used for drug delivery espe...
Paclitaxel is effective against a wide range of cancers which are considered to be refractory to con...
Paclitaxel (PTX) is a chemotherapeutic agent that belongs to the taxane family and which was approve...
Drugs with low aqueous solubility and permeability possess substantial challenges in designing effec...
The uniqueness of paclitaxel’s antimitotic action mechanism has fueled research toward its applicati...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Paclitaxel is a microtubule inhibitor causing mitotic arrest and is widely used in cancer chemothera...
Copyright © 2012 Madhu S. Surapaneni et al. This is an open access article distributed under the Cre...
The use of cytotoxic chemotherapic agents is the most common method for the treatment of metastatic ...
Since 1970s cyclodextrins (CDs) and their derivatives, in virtue of their peculiar inclusion propert...
Jong-Suep Baek,* Ju-Heon Kim,* Jeong-Sook Park, Cheong-Weon Cho College of Pharmacy and Institute o...