胰岛素样生长因子1定量吸收微采样分散监测。

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2025-09-15 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1648347
Xiaogang Li, Zeqing Zhao, Shi Chen, Ye Guo, Hui Pan, Xiao Yang
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引用次数: 0

摘要

本研究建立了一种新的胰岛素样生长因子1 (IGF-1)定量声学质谱(QAMS)检测方法。方法:采用Peptide C18色谱柱(1.8 μm, 50 mm), 0.1%甲酸/乙腈梯度洗脱,采用串联质谱法(sMRM)进行分离。结果:该方法的定量下限为10 ng/mL,线性动态范围为10 ~ 500 ng/mL。74对血浆标本的对比分析显示基质间相关性强,可量化偏倚。讨论:这些进展将QAMS定位为分散IGF-1监测的强大工具,在儿童生长障碍研究和资源有限的环境中尤其有价值。纵向稳定性验证和异构体区分仍然是未来优化的重点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quantitative absorptive micro-sampling for decentralized monitoring of insulin-like growth factor 1.

Quantitative absorptive micro-sampling for decentralized monitoring of insulin-like growth factor 1.

Quantitative absorptive micro-sampling for decentralized monitoring of insulin-like growth factor 1.

Introduction: This study establishes a novel quantitative acoustic mass spectrometry (QAMS) methodology for insulin-like growth factor 1 (IGF-1) detection.

Methods: Chromatographic separation utilized a Peptide C18 column (1.8 μm, 50 mm) with 0.1% formic acid/acetonitrile gradient elution, coupled to tandem mass spectrometry operated in scheduled multiple reaction monitoring (sMRM) mode.

Results: The method demonstrated a lower limit of quantification (LOQ) of 10 ng/mL with linear dynamic range spanning 10-500 ng/mL. Comparative analysis of 74 paired plasma specimens revealed strong inter-matrix correlation with quantifiable bias.

Discussion: These advancements position QAMS- as a robust tool for decentralized IGF-1 monitoring, particularly valuable in pediatric growth disorder studies and resource-limited settings. Longitudinal stability validation and isoform differentiation remain focal points for future optimization.

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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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