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肽连接光敏剂对黑色素细胞的特异性靶向用于光动力疗法。

Specific Targeting of Melanotic Cells with Peptide Ligated Photosensitizers for Photodynamic Therapy.

机构信息

Experimental Dermatology Group, Institute of Medical Biology, A*STAR, 8- Biomedical Grove, Singapore, Singapore.

Clinical Research Unit for Skin, Allergy & Regeneration, A*STAR, Singapore, Singapore.

出版信息

Sci Rep. 2017 Nov 16;7(1):15750. doi: 10.1038/s41598-017-15142-w.

Abstract

A strategy combining covalent conjugation of photosensitizers to a peptide ligand directed to the melanocortin 1 (MC1) receptor with the application of sequential LED light dosage at near-IR wavelengths was developed to achieve specific cytotoxicity to melanocytes and melanoma (MEL) with minimal collateral damage to surrounding cells such as keratinocytes (KER). The specific killing of melanotic cells by targeted photodynamic therapy (PDT) described in this study holds promise as a potentially effective adjuvant therapeutic method to control benign skin hyperpigmentation or superficial melanotic malignancy such as Lentigo Maligna Melanoma (LMM).

摘要

一种将光敏剂通过共价键连接到针对黑色素皮质素 1 (MC1) 受体的肽配体上的策略,结合近红外波长下的顺序 LED 光剂量应用,旨在实现对黑色素细胞和黑色素瘤 (MEL) 的特异性细胞毒性,同时对周围细胞如角质形成细胞 (KER) 的最小附带损伤。本研究中描述的针对色素细胞的靶向光动力疗法 (PDT) 的特异性杀伤具有作为一种潜在有效的辅助治疗方法来控制良性皮肤色素沉着过度或浅表色素性恶性肿瘤如恶性雀斑样痣黑色素瘤 (LMM) 的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f6e/5691209/1a9a20e85601/41598_2017_15142_Fig1_HTML.jpg

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