纳米载体
聚合物
纳米颗粒
材料科学
体内分布
药物输送
免疫原
肽
甲基丙烯酰胺
生物结合
纳米技术
共轭体系
共聚物
化学
组合化学
生物物理学
有机化学
体外
生物化学
单克隆抗体
免疫学
抗体
生物
丙烯酰胺
作者
Lucie Kracíková,Ladislav Androvič,Lucie Schindler,Gabriela Mixová,Michal Babič,Monika Paúrová,Marcela Filipová,Jiřina Hromádková,Dana Kaňková,Michal Pechar,Geoffrey M. Lynn,David Červený,Daniel Jirák,Richard Laga
标识
DOI:10.1016/j.eurpolymj.2022.111704
摘要
• Polymer-coated γ -Fe 2 O 3 particles are stable and well-defined biocompatible nanomaterials. • The polymer coating is removable in a reducing environment mimicking the cell interior. • The nanocarriers are designed to effectively deliver a big load of peptide immunogen. • The nanoparticle vaccines are detectable by magnetic resonance imaging in vivo. Diverse macromolecular delivery systems have been created to increase the stability and potency of peptide vaccines. However, many of them are insufficient in size and morphology to ensure efficient interaction between immunogens and immune cell receptors. Moreover, they are often released too slowly from the body after performing their desired function. To overcome these limitations, we have developed novel biocompatible polymer-colloidal carriers based on maghemite ( γ -Fe 2 O 3 ) nanoparticles coated with poly[ N -(2-hydroxypropyl)methacrylamide] (p(HPMA)) polymers. Various types of p(HPMA) polymers (semitelechelic homopolymers, statistical copolymers and di-block copolymers) are attached to the surface of the γ -Fe 2 O 3 particles via an iron-chelating deferoxamine group linked to the ends of their chains through stable or stimuli-responsive bonds. The resulting nanoparticles are stable and well-defined with negligible toxicity and of a suitable hydrodynamic size. They also feature a high number of binding sites for attaching peptide immunogens. Nanoparticles with polymers attached via reducible disulphide bonds exhibited rapid decoating upon incubation in the solutions, mimicking a reductive intracellular environment. In addition, we successfully conjugated a minimal peptide immunogen (V3) derived from the HIV-1 binding site to representative polymer-colloidal systems, demonstrating their suitability for vaccine delivery. Finally, the superparamagnetic properties of these nanoparticle vaccines enable their detection by MRI, which can be used to monitor biodistribution and pharmacokinetics.
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