药品
药物输送
体内
药理学
肾
靶向给药
医学
肾功能
肾脏疾病
毒性
毒品携带者
化学
生物
内科学
生物技术
有机化学
作者
Peng‐Fei Xu,Hailiang Zhang,Ruili Dang,Pei Jiang
出处
期刊:Protein and Peptide Letters
[Bentham Science Publishers]
日期:2018-05-31
卷期号:25 (6): 522-527
被引量:6
标识
DOI:10.2174/0929866525666180530123441
摘要
Due to their targeting ability and high degree of safety, Low Molecular Weight Proteins (LMWP) and peptides based kidney-targeted drug delivery systems raise lots of concerns for increasing renal effectiveness and reducing extra-renal toxicity. In general, the accumulation of drug-carrier conjugation in the kidney is associated with its size and charge. After accumulation, the drug need to quantitatively release from the carrier and regenerate the parent drug. Furthermore, the linkage between the drug and carrier can significantly influence the in vivo efficacy of the drug, it is important to employ a proper linkage to achieve a suitable balance between the drug stability in the circulation and intrarenal release rate. Now, most of developed drug-carrier conjugations are tested in vitro or in vivo, but not available in the clinical use. Although much future work remains to do, the prospects are exciting, and the success may be just around the corner.
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