摘要
In recent years, many nanomaterials have been developed as drug carriers to overcome their low solubility. However, the poor drug loading (general <5%) requires excessive use of carrier materials which may induce side effects and inhibit their clinical translation. Herein, hydrophobic meso- tetraphenylporphyrin (TPP) photosensitizer (PS) molecules are firstly assembled into pure nanocrystals by solvent exchange. Secondly, amphiphilic multidentate polymer ligand, PEG-grafted poly (maleic anhydride-alt-1-octadecene) (C 18PMH-PEG), is modified on the nanocrystal surface to enhance their stability in saline. The as-prepared drug delivery system (DDS) by the two-step strategy significantly improves the drug loading (over 87%). The DDS shows high stability in saline and is engulfed by cancer cells. Further study demonstrates that the DDS is an effective photodynamic therapeutic agent of cancer cells while the free PS molecules quickly precipitate without obvious destruction of cancer cells.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 323-326 |
| 页数 | 4 |
| 期刊 | Materials Letters |
| 卷 | 122 |
| DOI | |
| 出版状态 | 已出版 - 1 5月 2014 |
| 已对外发布 | 是 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
学术指纹
探究 'Carrier-free photosensitizer nanocrystal for photodynamic therapy' 的科研主题。它们共同构成独一无二的指纹。引用此
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