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Half-life determination of inorganic-organic hybrid nanomaterials in mice using laser-induced breakdown spectroscopy

机译:激光诱导击穿光谱法测定小鼠中无机-有机杂化纳米材料的半衰期

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摘要

Inorganic or inorganic-organic hybrid nanomaterials have great potential for applications in the biomedical fields. Biological half-life is an essential pharmacokinetic parameter for these materials to function . Compared to inductively coupled plasma mass spectrometry (ICP-MS), which is the gold standard, laser-induced breakdown spectroscopy (LIBS) is a faster and more efficient elemental detection method. We investigated an efficient way to quantify the metabolic rate using LIBS. Nanoparticle platforms, such as manganese dioxide-bovine serum albumin (MnO -BSA) or boehmite-bovine serum albumin (AlO(OH)-BSA) were injected into mice through intravenous administration for LIBS spectrum acquisition. First, the spectral background was corrected using the polynomial fitting method; The spectral interference was eliminated by Lorentz fitting for each LIBS spectrum simultaneously. The support vector regression (SVR) was then used for LIBS quantitative analyses. Finally, the LIBS results were compared with the ICP-MS ones. The half-lives of MnO -BSA calculated by LIBS and ICP-MS were 2.49 and 2.42 h, respectively. For AlO(OH)-BSA, the half-lives detected by LIBS and ICP-MS were 3.46 and 3.57 h, respectively. The relative error of LIBS is within 5% compared to ICP-MS. The results demonstrate that LIBS is a valuable tool for quantifying the metabolic rates with a high degree of accuracy.
机译:无机或无机-有机杂化纳米材料在生物医学领域具有广阔的应用前景。生物半衰期是这些材料起作用的必不可少的药代动力学参数。与金标准电感耦合等离子体质谱(ICP-MS)相比,激光诱导击穿光谱(LIBS)是一种更快,更有效的元素检测方法。我们研究了一种使用LIBS量化代谢率的有效方法。通过静脉内给药将纳米颗粒平台,例如二氧化锰-牛血清白蛋白(MnO -BSA)或勃姆石-牛血清白蛋白(AlO(OH)-BSA)注射到小鼠中以获得LIBS光谱。首先,使用多项式拟合方法校正光谱背景;通过同时对每个LIBS频谱进行Lorentz拟合消除了频谱干扰。然后将支持向量回归(SVR)用于LIBS定量分析。最后,将LIBS结果与ICP-MS进行了比较。通过LIBS和ICP-MS计算得出的MnO -BSA的半衰期分别为2.49和2.42 h。对于AlO(OH)-BSA,通过LIBS和ICP-MS检测到的半衰期分别为3.46和3.57 h。与ICP-MS相比,LIBS的相对误差在5%以内。结果表明,LIBS是用于高度准确地定量代谢率的有价值的工具。

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