Singh-Moon Rajinder P, Roblyer Darren M, Bigio Irving J, Joshi Shailendra
Columbia University College of Physicians and Surgeons, Department of Anesthesiology, 630 West 168th Street, New York, New York 10032, United States.
Boston University, Department of Biomedical Engineering, 44 Cummington Street, Boston, Massachusetts 02215, United States.
J Biomed Opt. 2014 Sep;19(9):96003. doi: 10.1117/1.JBO.19.9.096003.
We present an application of spatial frequency-domain imaging (SFDI) to the wide-field imaging of drug delivery to brain tissue. Measurements were compared with values obtained by a previously validated variation of diffuse reflectance spectroscopy, the method of optical pharmacokinetics (OP). We demonstrate a crosscorrelation between the two methods for absorption extraction and drug concentration determination in both experimental tissue phantoms and freshly extracted rodent brain tissue. These methods were first used to assess intra-arterial (IA) delivery of cationic liposomes to brain tissue in Sprague Dawley rats under transient cerebral hypoperfusion. Results were found to be in agreement with previously published experimental data and pharmacokinetic models of IA drug delivery. We then applied the same scheme to evaluate IA mitoxantrone delivery to glioma-bearing rats. Good correlation was seen between OP and SFDI determined concentrations taken from normal and tumor averaged sites. This study shows the feasibility of mapping drug/tracer distributions and encourages the use of SFDI for spatial imaging of tissues for drug/tracer-tagged carrier deposition and pharmacokinetic studies.
我们展示了空间频域成像(SFDI)在脑组织药物递送宽场成像中的应用。将测量结果与通过先前验证的漫反射光谱变体——光药代动力学(OP)方法获得的值进行了比较。我们证明了在实验组织模型和新鲜提取的啮齿动物脑组织中,这两种用于吸收提取和药物浓度测定的方法之间存在互相关性。这些方法首先用于评估在短暂性脑灌注不足的情况下,阳离子脂质体经动脉(IA)递送至Sprague Dawley大鼠脑组织的情况。结果与先前发表的IA药物递送实验数据和药代动力学模型一致。然后,我们应用相同的方案来评估IA米托蒽醌递送至荷胶质瘤大鼠的情况。从正常和肿瘤平均部位获取的OP和SFDI测定浓度之间呈现出良好的相关性。本研究表明了绘制药物/示踪剂分布的可行性,并鼓励使用SFDI对组织进行空间成像,以研究药物/示踪剂标记载体的沉积和药代动力学。