| Literature DB >> 29320614 |
Ruoning Wang1, Yue Han1, Bo Sun2,3, Ziqiang Zhao1, Yaw Opoku-Damoah1, Hao Cheng1, Huaqing Zhang1, Jianping Zhou1, Yang Ding1.
Abstract
The relevance of personalized medicine has inspired research for individually concerted diagnosis and therapy. Numerous efforts are devoted to designing drug particulates with capabilities of tumor penetrating and subcellular trafficking to concurrently discharge theranostics in response to multistimulations. In this study, a bioinspired particulate, formulated with whole components of native high-density lipoproteins (HDLs) and decorated with the tumor-penetrating peptide iRGD, is proposed to promote tumor penetration of HDLs (pHDLs) together with payloads. Specifically, paclitaxel (PTX), and the NIR fluorescent probe indocyanine green (ICG) are integrated into pHDLs (pHDL/PTX-ICG) for synergetic chemo-phototherapy. Inspired by lipoproteins, pHDLs are not only restored from naturally occurring materials but also possessed artificially endowed functions, leading to an enhanced cellular uptake, higher accumulation, and deep penetration into tumors without causing appreciable adverse effects, compared to reconstituted HDLs or lipid-based nanoparticles. After intravenous administration, pHDL/PTX-ICG performs a burst of intracellular drug release and imaging-guided precision chemo-phototherapy upon NIR irradiation that completely eradicates xenograft tumors. Neither recurrence nor significant toxicity is observed due to maneuvered regional photodynamic and photothermal therapy. Taken together, pHDL/PTX-ICG is proven to be a promising platform to achieve deep tumor penetration and imaging-guided chemo-phototherapy.Entities:
Keywords: burst intracellular drug release; deep tumor penetration; diagnosis; high-density lipoproteins; photodynamic and photothermal therapy
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Year: 2018 PMID: 29320614 DOI: 10.1002/smll.201703110
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281