CuS Nanodot-Loaded Thermosensitive Hydrogel for Anticancer Photothermal Therapy

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Ji-jun Fu, Jian-ye Zhang, Song-pei Li, Ling-min Zhang, Zhong-xiao Lin, Lu Liang, Ai-ping Qin*, Xi-yong Yu*
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引用次数: 25

Abstract

The purpose of this research is to establish an injectable hydrogel encapsulating copper sulfide (CuS) nanodots for photothermal therapy against cancer. The CuS nanodots were prepared by one-pot synthesis, and the thermosensitive Pluronic F127 was used as the hydrogel matrix. The CuS nanodots and the hydrogel were characterized by morphous, particle size, serum stability, photothermal performance upon repeated 808 nm laser irradiation, and rheology features. The effects of the CuS nanodots and the hydrogel were evaluated qualitatively and quantitatively in 4T1 mouse breast cancer cells. The retention, photothermal efficacy, therapeutic effects, and systemic toxicity of the hydrogel were assessed in tumor bearing mouse model. The CuS nanodots with a diameter of about 8 nm exhibited satisfying serum stability, photoheat conversion ability, and repeated laser exposure stability. The hydrogel encapsulation did not negatively influence the above features of the photothermal agent. The nanodot-loaded hydrogel shows a phase transition at body temperature and, as a result, a long retention in vivo. The photothermal-agent-embedded hydrogel played a promising photothermal therapeutic effect in the tumor bearing mouse model with low systemic toxicity after peritumoral administration.

Abstract Image

用于抗癌光热治疗的cu纳米点负载热敏水凝胶
本研究的目的是建立一种可注射的水凝胶包封硫化铜纳米点用于光热治疗癌症。以热敏Pluronic F127为水凝胶基质,采用一锅法制备了cu纳米点。通过形貌、粒径、血清稳定性、808 nm激光反复照射下的光热性能和流变学特性对制备的cu纳米点和水凝胶进行了表征。对cu纳米点和水凝胶在4T1小鼠乳腺癌细胞中的作用进行了定性和定量评价。在荷瘤小鼠模型上评价水凝胶的滞留性、光热功效、治疗效果和全身毒性。直径约为8 nm的cu纳米点具有良好的血清稳定性、光热转换能力和重复激光曝光稳定性。水凝胶包封对光热剂的上述特性没有负面影响。纳米点负载的水凝胶在体温下表现出相变,从而在体内保持较长时间。光热剂包埋水凝胶在荷瘤小鼠模型中具有良好的光热治疗效果,瘤周给药后全身毒性低。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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