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用于细胞内药物递送的刺激性响应性软纳米颗粒的应用。

Use of stimulatory responsive soft nanoparticles for intracellular drug delivery.

作者信息

Hughes Krystal A, Misra Bishal, Maghareh Maryam, Bobbala Sharan

机构信息

Department of Pharmaceutical Sciences, West Virginia University School of Pharmacy, Morgantown, WV 26505 USA.

Department of Clinical Pharmacy, West Virginia University School of Pharmacy, Morgantown, WV 26505 USA.

出版信息

Nano Res. 2023;16(5):6974-6990. doi: 10.1007/s12274-022-5267-5. Epub 2023 Jan 14.


DOI:10.1007/s12274-022-5267-5
PMID:36685637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9840428/
Abstract

Drug delivery has made tremendous advances in the last decade. Targeted therapies are increasingly common, with intracellular delivery highly impactful and sought after. Intracellular drug delivery systems have limitations due to imprecise and non-targeted release profiles. One way this can be addressed is through using stimuli-responsive soft nanoparticles, which contain materials with an organic backbone such as lipids and polymers. The choice of biomaterial is essential for soft nanoparticles to be responsive to internal or external stimuli. The nanoparticle must retain its integrity and payload in non-targeted physiological conditions while responding to particular intracellular environments where payload release is desired. Multiple internal and external factors could stimulate the intracellular release of drugs from nanoparticles. Internal stimuli include pH, oxidation, and enzymes, while external stimuli include ultrasound, light, electricity, and magnetic fields. Stimulatory responsive soft nanoparticulate systems specifically utilized to modulate intracellular delivery of drugs are explored in this review.

摘要

在过去十年中,药物递送取得了巨大进展。靶向治疗越来越普遍,细胞内递送具有高度影响力且备受追捧。由于释放曲线不精确和非靶向性,细胞内药物递送系统存在局限性。解决这一问题的一种方法是使用刺激响应性软纳米颗粒,其包含具有有机主链的材料,如脂质和聚合物。生物材料的选择对于软纳米颗粒对内部或外部刺激作出响应至关重要。纳米颗粒必须在非靶向生理条件下保持其完整性和载药量,同时对期望释放载药量的特定细胞内环境作出响应。多种内部和外部因素可刺激纳米颗粒在细胞内释放药物。内部刺激包括pH值、氧化和酶,而外部刺激包括超声、光、电和磁场。本文综述了专门用于调节细胞内药物递送的刺激响应性软纳米颗粒系统。

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本文引用的文献

[1]
Dendritic peptide-conjugated polymeric nanovectors for non-toxic delivery of plasmid DNA and enhanced non-viral transfection of immune cells.

iScience. 2022-6-8

[2]
Legumain/pH dual-responsive lytic peptide-paclitaxel conjugate for synergistic cancer therapy.

Drug Deliv. 2022-12

[3]
The development of a redox-sensitive curcumin conjugated chitosan oligosaccharide nanocarrier for the efficient delivery of docetaxel to glioma cells.

Ann Transl Med. 2022-3

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Tumor targetable and pH-sensitive polymer nanoparticles for simultaneously improve the Type 2 Diabetes Mellitus and malignant breast cancer.

Bioengineered. 2022-4

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Photo-Induced Drug Release from Polymeric Micelles and Liposomes: Phototriggering Mechanisms in Drug Delivery Systems.

Polymers (Basel). 2022-3-23

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Front Oncol. 2022-3-22

[7]
Redox-Responsive Crosslinked Mixed Micelles for Controllable Release of Caffeic Acid Phenethyl Ester.

Pharmaceutics. 2022-3-20

[8]
pH-Responsive Nanoparticles for Delivery of Paclitaxel to the Injury Site for Inhibiting Vascular Restenosis.

Pharmaceutics. 2022-2-27

[9]
Construction of pH-sensitive targeted micelle system co-delivery with curcumin and dasatinib and evaluation of anti-liver cancer.

Drug Deliv. 2022-12

[10]
A Nanosized Codelivery System Based on Intracellular Stimuli-Triggered Dual-Drug Release for Multilevel Chemotherapy Amplification in Drug-Resistant Breast Cancer.

Pharmaceutics. 2022-2-15

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