A Facile Approach to Producing Liposomal J-Aggregates of Indocyanine Green with Diagnostic and Therapeutic Potential

IF 3.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Noah B Stern, Binita Shrestha, Tyrone Porter
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引用次数: 0

Abstract

Liposomal J-Aggregates of Indocyanine Green (L-JA) can serve as a biocompatible and biodegradable nanoparticle for photoacoustic imaging (PAI) and photothermal therapy (PTT). When compared to monomeric indocyanine green (IcG), L-JA is characterized by longer circulation, improved photostability, elevated absorption at longer wavelengths, and increased photoacoustic signal generation. However, the documented methods for the production of L-JA vary widely. An approach to efficiently form IcG J-aggregates (IcG-JA) directly in liposomes at elevated temperatures is developed. Aggregating within fully formed liposomes ensures particle uniformity and allows for control of J-aggregate size. L-JA has unique properties compared to IcG. L-JA provides significant contrast enhancement in photoacoustic images for up to 24 h after injection, while IcG and unencapsulated IcG-JA are cleared within an hour. L-JA allows for more accurate photoacoustic-based blood oxygen saturation (sO2) estimation and particle tracking compared to IcG. Furthermore, photothermal heating of L-JA with an 852 nm laser is demonstrated to be more effective at lower laser powers than conventional 808 nm lasers for the first time. The presented technique offers an avenue for formulating a multi-faceted contrast agent for photoacoustic imaging and photothermal therapy that offers significant advantages over other conventional agents.

Abstract Image

Abstract Image

生产具有诊断和治疗潜力的吲哚菁绿脂质体 J-聚集体的简便方法
吲哚菁绿(L-JA)的脂质体 J-聚集体可作为一种生物相容性和可生物降解的纳米粒子,用于光声成像(PAI)和光热治疗(PTT)。与单体吲哚菁绿(IcG)相比,L-JA 的特点是循环时间更长、光稳定性更好、在更长波长上的吸收率更高,并能产生更多的光声信号。然而,有文献记载的 L-JA 生产方法差别很大。本研究开发了一种在高温下直接在脂质体中有效形成 IcG J-聚合体(IcG-JA)的方法。在完全形成的脂质体中聚合可确保颗粒的均匀性,并可控制 J-聚合体的大小。与 IcG 相比,L-JA 具有独特的特性。L-JA 可在注射后 24 小时内明显增强光声图像的对比度,而 IcG 和未封装的 IcG-JA 会在一小时内被清除。与 IcG 相比,L-JA 能更准确地进行基于光声的血氧饱和度(sO2)估算和粒子追踪。此外,用 852 nm 激光对 L-JA 进行光热加热首次证明在较低激光功率下比传统的 808 nm 激光更有效。所介绍的技术为配制用于光声成像和光热治疗的多元造影剂提供了一种途径,这种造影剂与其他传统造影剂相比具有显著优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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