Chu Yanwu, Zhang Zhanjie, He Qianyuan, Chen Feng, Sheng Ziqian, Zhang Deng, Jin Honglin, Jiang Fagang, Guo Lianbo
Wuhan National Laboratory for Optoelectronics (WNLO), Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.
Cancer Center, Union Hospital, TongjiMedical College, Huazhong University of Science and Technology, Wuhan, Hubei 430022, China.
J Adv Res. 2020 May 16;24:353-361. doi: 10.1016/j.jare.2020.05.001. eCollection 2020 Jul.
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.
无机或无机-有机杂化纳米材料在生物医学领域具有巨大的应用潜力。生物半衰期是这些材料发挥作用的一个重要药代动力学参数。与作为金标准的电感耦合等离子体质谱法(ICP-MS)相比,激光诱导击穿光谱法(LIBS)是一种更快、更高效的元素检测方法。我们研究了一种使用LIBS定量代谢率的有效方法。通过静脉注射将纳米颗粒平台,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)注入小鼠体内以获取LIBS光谱。首先,使用多项式拟合方法校正光谱背景;同时通过洛伦兹拟合消除每个LIBS光谱的光谱干扰。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结果进行比较。通过LIBS和ICP-MS计算得到的MnO-BSA的半衰期分别为2.49小时和2.42小时。对于AlO(OH)-BSA,LIBS和ICP-MS检测到的半衰期分别为3.46小时和3.57小时。与ICP-MS相比,LIBS的相对误差在5%以内。结果表明,LIBS是一种用于高精度定量代谢率的有价值工具。