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DC Field | Value | Language |
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dc.contributor.author | Rawal, Shruti | - |
dc.contributor.author | Patel, Mayur M. | - |
dc.date.accessioned | 2022-03-15T08:15:13Z | - |
dc.date.available | 2022-03-15T08:15:13Z | - |
dc.date.issued | 2019 | - |
dc.identifier.uri | http://10.1.7.192:80/jspui/handle/123456789/11005 | - |
dc.description | Journal of Controlled Release 301 (2019); 76-109 | en_US |
dc.description.abstract | Employing combination therapy has become obligatory in cancer cases exhibiting high tumor load, chemore sistant tumor population, and advanced disease stages. Realization of this fact has now led many of the com bination oncotherapies to become an integral part of anticancer regimens. Combination oncotherapy may encompass a combination of anticancer agents belonging to a similar therapeutic category or that of different therapeutic categories (e.g. chemotherapy + gene therapy). Differences in the physicochemical properties, pharmacokinetics and biodistribution pattern of different payloads are the major constraints that are faced by combination chemotherapy. Concordant efforts in the field of nanotechnology and oncology have emerged with several approaches to solve the major issues encountered by combination therapy. Unique colloidal behaviors of various types of nanoparticles and differential targeting strategies have accorded an unprecedented ability to optimize combination oncotherapeutic delivery. Nanocarrier based delivery of the various types of payloads such as chemotherapeutic agents and other anticancer therapeutics such as small interfering ribonucleic acid (siRNA), chemosensitizers, radiosensitizers, and antiangiogenic agents have been addressed in the present review. Various nano-delivery systems like liposomes, polymeric nanoparticles, polymerosomes, dendrimers, micelles, lipid based nanoparticles, prodrug based nanocarriers, polymer-drug conjugates, polymer-lipid hybrid nanoparticles, carbon nanotubes, nanosponges, supramolecular nanocarriers and inorganic nanoparticles (gold nanoparticles, silver nanoparticles, magnetic nanoparticles and mesoporous silica based nanoparticles) that have been extensively explored for the formulation of multidrug delivery is an imperative part of discussion in the review. The present review features the outweighing benefits of combination therapy over mono-oncotherapy and discusses several existent nano formulation strategies that facilitate a successful combination oncotherapy. Several obstacles that may impede in transforming nanotechnology-based combination oncotherapy from bench to bedside, and challenges associated therein have also been discussed in the present review. | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartofseries | IPFP0468; | - |
dc.subject | Targeted drug delivery | en_US |
dc.subject | Receptors | en_US |
dc.subject | Colloidal carriers | en_US |
dc.subject | Nanoparticulate system | en_US |
dc.subject | Prodrugs | en_US |
dc.subject | Angiogenesis | en_US |
dc.title | Threatening Cancer with Nanoparticle Aided Combination Oncotherapy | en_US |
dc.type | Faculty Papers | en_US |
Appears in Collections: | Faculty Papers |
Files in This Item:
File | Description | Size | Format | |
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IPFP0468.pdf | IPFP0468 | 2.69 MB | Adobe PDF | ![]() View/Open |
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