纳米载体
新陈代谢
化学
生物化学
有机化学
药物输送
作者
Wongsakorn Suchaoin,Andreas Bernkop‐Schnürch
出处
期刊:Nanomedicine
[Future Medicine]
日期:2017-01-17
卷期号:12 (3): 255-269
被引量:31
标识
DOI:10.2217/nnm-2016-0331
摘要
Pre-uptake metabolism within the GI tract is responsible for the poor oral bioavailability of numerous drugs. As nanocarriers function as a 'shield', protecting incorporated drugs from enzymatic attack, there is an increasing interest in utilizing them as a tool for overcoming drug degradation. Degradation of carriers resulting in the release of incorporated drugs, mucus permeation, enzyme inhibitory properties and their toxicity are crucial factors that must be taken into account when designing proper nanocarriers. The use of polymer- and lipid-based nanocarriers as protective vehicles are discussed within this review. Lipid-based carriers and novel mucopenetrating particles seem to have a great potential in avoiding metabolizing enzymes. Accordingly, nanocarriers are promising tools for improving the bioavailability of drugs, being sensitive to a pre-uptake metabolism.
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