GSH‐Responsive Shape‐Transformable Nanotheranostics for Dual‐Modal T1/T2 MRI‐Guided Enhanced PDT of Nasopharyngeal Carcinoma

Author:

Yang Qianyu1,Wu Gang2,Yang Yefeng3,Zhou Yang45,Song Jiali1,Gao Huile5ORCID,Huang Weiyuan1

Affiliation:

1. Department of Radiology Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) Haikou Hainan 570311 China

2. Department of Radiotherapy Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) Haikou Hainan 570311 China

3. Department of Respiratory Medicine Second Affiliated Hospital of Hainan Medical University Haikou Hainan 570100 China

4. Key Laboratory of Tropical Biological Resources of Ministry of Education School of Pharmaceutical Sciences Hainan University Haikou Hainan 570200 China

5. Key Laboratory of Drug Targeting and Drug Delivery Systems West China School of Pharmacy Sichuan University Chengdu Sichuan 610064 China

Abstract

AbstractBased on the properties of photodynamic therapy (PDT) and magnetic resonance imaging (MRI), combining them to construct multifunctional nanotheranostics can leverage strengths and avoid weaknesses for tumor diagnosis and treatment. However, certain problems remain unsolved, notably the short observation window caused by insufficient retention time. In this study, a GSH‐responsive shape‐transformable nanotheranostics Gd‐Ce6‐FFVLGGGC‐SS‐PEG are designed (abbreviated as GdCFS) by combining a single metal Gd with Ce6, and peptide (Phe‐Phe‐Val‐Leu‐Gly‐Gly‐Gly‐Cys) disulfide‐conjugated with polyethylene glycol (PEG) to perform dual‐modal T1/T2 MRI specifically at the tumor site. Due to its amphiphilic features, GdCFS can self‐assemble to spherical nanoparticles, while transforming to nanofibers (NFs) in the presence of intracellular overexpressed GSH stimuli. After NFs formation, the hydrophobic core of GdCFS is exposed, resulting in T1 positive contrast enhancement, whereas NFs can simultaneously achieve T2 negative contrast enhancement. Furthermore, GSH depletion can cause imbalance in intracellular redox state, ultimately improving PDT efficacy. GdCFS benefits from the shape‐transformation in terms of sufficient retention time, thus positively minimizing the toxicity risk. On the tumor model of nasopharyngeal carcinoma, in vivo and in vitro outcomes confirm that GdCFS can be a promising candidate for early diagnosis, real‐time monitoring, and precise treatment of tumors with great biocompatibility.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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