Kidney-targeted therapies: A quantitative perspective
Journal of Controlled Release, ISSN: 0168-3659, Vol: 328, Page: 762-775
2020
- 16Citations
- 40Captures
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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
- Citations16
- Citation Indexes16
- CrossRef16
- 15
- Captures40
- Readers40
- 40
Review Description
Chronic and acute kidney disease constitute a worldwide health burden, but are still lacking efficient therapeutics. Current medication such as anti-inflammatory steroids causes systemic side effects, and is unable to stop the progression of the disease. Efforts have been devoted towards the development of renal-targeted therapies, however, no such approach has reached the clinic, yet. Here, we critically review the current status of renal-targeted drugs and delivery strategies. Specifically, we focus on the quantitative aspect of delivery by compiling information on kidney-to-liver ratios and also investigating to which degree the implementation of a targeting functionality increases the distribution of the drug to the kidney. As we show, two types of functional outcomes can be distinguished: (i) Targeting to the kidney goes along with an increase in kidney-to-liver ratio. This, we denote as direct targeting; (ii) the accumulation of the drug in the kidney increases, but the kidney-to-liver ratio remains unchanged, thereby the carrier leads to a general uptake enhancement. Overall, the most effective targeting was reached with receptor and transporter directed strategies. Reaching glomerular cells and the avoidance of liver accumulation for nanoparticulate formulations pose the greatest challenges.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168365920305381; http://dx.doi.org/10.1016/j.jconrel.2020.09.022; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85092476161&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/32931896; https://linkinghub.elsevier.com/retrieve/pii/S0168365920305381; https://dx.doi.org/10.1016/j.jconrel.2020.09.022
Elsevier BV
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