The molecularly imprinted polymer essentials: curation of anticancer, ophthalmic, and projected gene therapy drug delivery systems
Journal of Controlled Release, ISSN: 0168-3659, Vol: 287, Page: 24-34
2018
- 62Citations
- 85Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations62
- Citation Indexes62
- 62
- CrossRef58
- Captures85
- Readers85
- 85
Review Description
The development of polymeric materials as drug delivery systems has advanced from systems that rely on classical passive targeting to carriers that can sustain the precisely controlled release of payloads upon physicochemical triggers in desired microenvironment. Molecularly imprinted polymers (MIP), materials designed to capture specific molecules based on their molecular shape and charge distribution, are attractive candidates for fulfilling these purposes. In particular, drug-imprinted polymers coupled with active targeting mechanisms have been explored as potential drug delivery systems. In this review, we have curated important recent efforts in the development of drug-imprinted polymers in a variety of clinical applications, especially oncology and ophthalmology. MIP possesses properties that may complement the traditional delivery systems of these two disciplines, such as passive enhanced permeability and retention effect (EPR) in cancer tumors, and passive drug diffusion in delivering ophthalmic therapeutics. Furthermore, the prospects of MIP integration with the emerging gene therapies will be discussed.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168365918304899; http://dx.doi.org/10.1016/j.jconrel.2018.08.023; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85051663514&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/30110614; https://linkinghub.elsevier.com/retrieve/pii/S0168365918304899; https://dx.doi.org/10.1016/j.jconrel.2018.08.023
Elsevier BV
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