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通过离子凝胶化制备的用于肿瘤学应用的热响应性壳聚糖接枝聚(乙烯基己内酰胺)微凝胶

Thermoresponsive Chitosan-Grafted-Poly(-vinylcaprolactam) Microgels via Ionotropic Gelation for Oncological Applications.

作者信息

Marsili Lorenzo, Dal Bo Michele, Berti Federico, Toffoli Giuseppe

机构信息

Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127 Trieste, Italy.

Experimental and Clinical Pharmacology Unit, CRO National Cancer Institute IRCCS, Via Franco Gallini 2, 33081 Aviano, Italy.

出版信息

Pharmaceutics. 2021 Oct 11;13(10):1654. doi: 10.3390/pharmaceutics13101654.


DOI:10.3390/pharmaceutics13101654
PMID:34683947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8539247/
Abstract

Microgels can be considered soft, porous and deformable particles with an internal gel structure swollen by a solvent and an average size between 100 and 1000 nm. Due to their biocompatibility, colloidal stability, their unique dynamicity and the permeability of their architecture, they are emerging as important candidates for drug delivery systems, sensing and biocatalysis. In clinical applications, the research on responsive microgels is aimed at the development of "smart" delivery systems that undergo a critical change in conformation and size in reaction to a change in environmental conditions (temperature, magnetic fields, pH, concentration gradient). Recent achievements in biodegradable polymer fabrication have resulted in new appealing strategies, including the combination of synthetic and natural-origin polymers with inorganic nanoparticles, as well as the possibility of controlling drug release remotely. In this review, we provide a literature review on the use of dual and multi-responsive chitosan-grafted-poly-(-vinylcaprolactam) (CP) microgels in drug delivery and oncological applications.

摘要

微凝胶可被视为柔软、多孔且可变形的颗粒,其内部凝胶结构被溶剂溶胀,平均尺寸在100至1000纳米之间。由于其生物相容性、胶体稳定性、独特的动力学特性以及结构的渗透性,它们正成为药物递送系统、传感和生物催化的重要候选物。在临床应用中,对响应性微凝胶的研究旨在开发“智能”递送系统,该系统在环境条件(温度、磁场、pH值、浓度梯度)变化时会发生构象和尺寸的关键变化。可生物降解聚合物制造方面的最新成果带来了新的有吸引力的策略,包括合成聚合物与天然来源聚合物与无机纳米颗粒的组合,以及远程控制药物释放的可能性。在这篇综述中,我们提供了关于双响应和多响应壳聚糖接枝聚(N-乙烯基己内酰胺)(CP)微凝胶在药物递送和肿瘤学应用中的文献综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/e6ec234ec917/pharmaceutics-13-01654-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/651124b0ee1f/pharmaceutics-13-01654-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/7d5aec181fbd/pharmaceutics-13-01654-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/599eb0c2438b/pharmaceutics-13-01654-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/f7878f992847/pharmaceutics-13-01654-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/e6ec234ec917/pharmaceutics-13-01654-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/651124b0ee1f/pharmaceutics-13-01654-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/7d5aec181fbd/pharmaceutics-13-01654-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/599eb0c2438b/pharmaceutics-13-01654-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/f7878f992847/pharmaceutics-13-01654-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeed/8539247/e6ec234ec917/pharmaceutics-13-01654-g005.jpg

相似文献

[1]
Thermoresponsive Chitosan-Grafted-Poly(-vinylcaprolactam) Microgels via Ionotropic Gelation for Oncological Applications.

Pharmaceutics. 2021-10-11

[2]
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J Colloid Interface Sci. 2025-1-15

[3]
Chitosan-Based Biocompatible Copolymers for Thermoresponsive Drug Delivery Systems: On the Development of a Standardization System.

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[4]
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ACS Appl Bio Mater. 2022-7-18

[5]
Evaluation of cationic core-shell thermoresponsive poly(N-vinylcaprolactam)-based microgels as potential drug delivery nanocarriers.

Mater Sci Eng C Mater Biol Appl. 2019-6-7

[6]
Hydrophobic superparamagnetic FePt nanoparticles in hydrophilic poly(N-vinylcaprolactam) microgels: a new multifunctional hybrid system.

J Mater Chem B. 2017-2-14

[7]
Recent advances in cellulose microgels: Preparations and functionalized applications.

Adv Colloid Interface Sci. 2023-1

[8]
Biodegradable colloidal microgels with tunable thermosensitive volume phase transitions for controllable drug delivery.

J Colloid Interface Sci. 2015-7-15

[9]
Functional Microgels and Microgel Systems.

Acc Chem Res. 2017-2-10

[10]
Thermoresponsive microgels at the air-water interface: the impact of the swelling state on interfacial conformation.

Soft Matter. 2016-12-21

引用本文的文献

[1]
Synthesis and Physicochemical Properties of Thermally Sensitive Polymeric Derivatives of -vinylcaprolactam.

Polymers (Basel). 2024-7-5

[2]
Biopolymer Micro/Nanogel Particles as Smart Drug Delivery and Theranostic Systems.

Pharmaceutics. 2023-7-31

[3]
Chitosan as an Outstanding Polysaccharide Improving Health-Commodities of Humans and Environmental Protection.

Polymers (Basel). 2023-1-19

[4]
Immunogenicity of inactivated O157:H7 with Stx2B microparticle in mice.

Iran J Basic Med Sci. 2022-9

[5]
Chitosan-Based Biocompatible Copolymers for Thermoresponsive Drug Delivery Systems: On the Development of a Standardization System.

Pharmaceutics. 2021-11-5

本文引用的文献

[1]
Polydiacetylene-Nanoparticle-Functionalized Microgels for Topical Bacterial Infection Treatment.

ACS Macro Lett. 2019-5-21

[2]
Retraction: CuS nanocrystal@microgel nanocomposites for light-regulated release of dual-drugs and chemo-photothermal synergistic therapy .

RSC Adv. 2020-10-19

[3]
Characterization of Thermoresponsive Poly-N-Vinylcaprolactam Polymers for Biological Applications.

Polymers (Basel). 2021-8-8

[4]
Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine.

N Engl J Med. 2020-12-31

[5]
pH-Sensitive Biomaterials for Drug Delivery.

Molecules. 2020-11-30

[6]
Modulation of the volume phase transition temperature of thermo-responsive gels.

J Mech Behav Biomed Mater. 2021-2

[7]
On Going to a New Era of Microgel Exhibiting Volume Phase Transition.

Gels. 2020-8-17

[8]
Volume Phase Transition in Gels: Its Discovery and Development.

Gels. 2020-7-31

[9]
Novel amphiphilic chitosan micelles as carriers for hydrophobic anticancer drugs.

Mater Sci Eng C Mater Biol Appl. 2020-7

[10]
Emerging Prospects for Nanoparticle-Enabled Cancer Immunotherapy.

J Immunol Res. 2020

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