纳米载体
聚合物
纳米技术
定量蛋白质组学
化学
材料科学
生物物理学
药物输送
生物医学工程
蛋白质组学
生物化学
生物
医学
有机化学
基因
作者
Dheeraj K. Agrohia,Ritabrita Goswami,Teerapong Jantarat,Yağız Anıl Çiçek,Korndanai Thongsukh,Taewon Jeon,Jonathan M. Bell,Vincent M. Rotello,Richard W. Vachet
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-06-13
卷期号:18 (26): 16808-16818
标识
DOI:10.1021/acsnano.4c02344
摘要
Amidst the rapid growth of protein therapeutics as a drug class, there is an increased focus on designing systems to effectively deliver proteins to target organs. Quantitative monitoring of protein distributions in tissues is essential for optimal development of delivery systems; however, existing strategies can have limited accuracy, making it difficult to assess suborgan dosing. Here, we describe a quantitative imaging approach that utilizes metal-coded mass tags and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to quantify the suborgan distributions of proteins in tissues that have been delivered by polymeric nanocarriers. Using this approach, we measure nanomole per gram levels of proteins as delivered by guanidinium-functionalized poly(oxanorborneneimide) (PONI) polymers to various tissues, including the alveolar region of the lung. Due to the multiplexing capability of the LA-ICP-MS imaging, we are also able to simultaneously quantify protein and polymer distributions, obtaining valuable information about the relative excretion pathways of the protein cargo and carrier. This imaging approach will facilitate quantitative correlations between nanocarrier properties and protein cargo biodistributions.
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