靶向胶质母细胞瘤的lintt1功能化杂化脂质-聚合物纳米颗粒

IF 3.7 Q1 CHEMISTRY, MEDICINAL
Antonella Rocchi, , , Valeria Sidorenko, , , Nicola d’Avanzo, , , Luca Marchetti, , , Jhalak Sethi, , , Luigi Ciriolo, , , Anna Maria Tolomeo, , , Maria Grazia Cifone, , , Paola Palumbo, , , Massimo Fresta, , , Tambet Teesalu*, , and , Christian Celia*, 
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引用次数: 0

摘要

多形性胶质母细胞瘤(GBM)是一种侵袭性脑肿瘤,治疗选择有限,预后差。我们开发了用肿瘤归巢c端规则肽LinTT1 (LinTT1-HLPNs)功能化的混合脂质-聚合物纳米颗粒(HLPNs)来提高GBM靶向性。体外研究表明,与游离药物相比,LinTT1-HLPNs选择性结合GBM细胞,显著提高了负载替莫唑胺(TMZ)的细胞毒性(LinTT1-HLPNs@TMZ)。在体内,浸润性和非浸润性GBM小鼠模型中静脉注射HLPNs均增强了肿瘤区域TMZ的积累,从而支持了LinTT1-HLPNs的选择性靶向和组织渗透。该纳米平台结合了混合脂质-聚合物纳米颗粒的优势和GBM特异性靶向策略,从而通过多步靶向方法提供了更好的药物传递和治疗效果,解决了GBM的关键挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LinTT1-Functionalized Hybrid Lipid–Polymer Nanoparticles for Glioblastoma Targeting

Glioblastoma multiforme (GBM) is an aggressive brain tumor with limited therapeutic options and a poor prognosis. We developed hybrid lipid-polymer nanoparticles (HLPNs) functionalized with tumor-homing C-end Rule peptide LinTT1 (LinTT1-HLPNs) to improve the GBM targeting. In vitro studies demonstrated that LinTT1-HLPNs bind selectively to GBM cells and significantly improved the cytotoxicity of the loaded temozolomide (TMZ) (LinTT1-HLPNs@TMZ) compared to that of the free drug. In vivo, intravenous injection of HLPNs in both infiltrative and noninfiltrative GBM murine models had an enhanced accumulation of TMZ in the tumor area, thus endorsing the selective targeting and tissue penetration of LinTT1-HLPNs. This nanoplatform combines the advantages of hybrid lipid–polymer nanoparticles with a GBM-specific targeting strategy, thus providing an improved drug delivery and therapeutic effect by a multistep targeting approach, which addresses the key challenge of GBM.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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