PEGylated Water-Soluble Organic Nanoparticles with Chlorin Derivative for Biocompatible Photodynamic Therapy In Vitro and In Vivo

被引:4
|
作者
Liu, Yang [1 ,2 ]
Lee, Min Seob [3 ]
Lee, Sang Hyeob [1 ,2 ]
Song, Hyeon Ho [1 ,2 ]
Baek, Bo Sun [1 ,2 ]
Lee, Woo Kyoung [1 ,2 ]
Kim, Yeon-Jeong [3 ,4 ]
Yoon, Il [1 ,2 ]
机构
[1] Inje Univ, Ctr Nano Mfg, 197 Injero, Gimhae 50834, Gyeongnam, South Korea
[2] Inje Univ, Dept Nanosci & Engn, 197 Injero, Gimhae 50834, Gyeongnam, South Korea
[3] Inje Univ, Lab Microbiol & Immunol, Coll Pharm, 197 Injero, Gimhae, Gyeongnam, South Korea
[4] Inje Univ, Inje Inst Pharmaceut Sci & Res, 197 Injero, Gimhae 50834, Gyeongnam, South Korea
基金
新加坡国家研究基金会;
关键词
biocompatible; chlorins; PEGylation; photodynamic therapy; water-soluble organic nanoparticles; PHOTOSENSITIZERS; DELIVERY; PEPTIDE; MICELLES; ENHANCE;
D O I
10.1002/cnma.202000535
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photodynamic therapy (PDT) is a non-invasive and highly selective therapeutic approach. Photosensitizers (PSs) are an essential ingredient in PDT. However, many PSs are hydrophobic and insoluble, seriously restraining their clinical use. In this study, we prepared biocompatible PSs using water-soluble organic nanoparticles (WSONs) with a chlorin derivative, pyropheophorbide a (PPa), and polyethylene glycol (PEG) to overcome the limited clinical applications of PDT. Among the PEGylated WSONs (WSON-PEGs), WSON-PEG 3400 and 2000 exhibited good water solubility and stability, with no aggregation in aqueous media, a high photoactivity, and low dark toxicity in vitro against A549 and HeLa cells. An in vivo application of WSON-PEG 3400 using A549 tumour-bearing BALB/c nude mice demonstrated a three-fold higher PDT efficacy compared with the control and drug only groups, without treatment-induced toxicity or toxic side effects. These results demonstrate that WSON-PEG (3400) is a biocompatible PS with a high PDT efficacy and reduced dark toxicity, suitable for use in clinical trials.
引用
收藏
页码:165 / 173
页数:9
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