Roller Benjamin T, Munson Jennifer M, Brahma Barunashish, Santangelo Philip J, Pai S Balakrishna, Bellamkonda Ravi V
Wallace H Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory School of Medicine, Atlanta, GA, USA.
Drug Deliv Transl Res. 2015 Apr;5(2):116-24. doi: 10.1007/s13346-013-0139-x.
Aggressive surgical resection is the primary therapy for glioma. However, aggressive resection may compromise functional healthy brain tissue. Currently, there are no objective cues for surgeons to distinguish healthy tissue from tumor and determine tumor borders; surgeons skillfully rely on subjective means such as tactile feedback. This often results in incomplete resection and recurrence. The objective of the present study was to design, develop, and evaluate, in vitro and in vivo, a nanoencapsulated visible dye for intraoperative, visual delineation of tumor margins in an invasive tumor model. Liposomal nanocarriers containing Evans blue dye (nano-EB) were developed, characterized, and tested for safety in vitro and in vivo. 3RT1RT2A glioma cells were implanted into brains of Fischer 344 rats. Nano-EB or EB solution was injected via tail vein into tumor-bearing animals. To assess tumor staining, tissue samples were analyzed visibly and using fluorescence microscopy. Area, perimeter ratios, and Manders overlap coefficients were calculated to quantify extent of staining. Nano-EB clearly marked tumor margins in the invasive tumor model. Area ratio of nano-EB staining to tumor was 0.89 ± 0.05, perimeter ratio was 0.94 ± 0.04, Manders R was 0.51 ± 0.08, and M1 was 0.97 ± 0.06. Microscopic tumor border inspection under high magnification verified that nano-EB did not stain healthy tissue. Nano-EB clearly aids in distinguishing tumor tissue from healthy tissue in an invasive tumor model, while injection of unencapsulated EB results in false identification of healthy tissue as tumor due to diffusion of dye from the tumor into healthy tissue.
积极的手术切除是胶质瘤的主要治疗方法。然而,积极切除可能会损害功能正常的脑组织。目前,外科医生没有客观线索来区分健康组织和肿瘤组织并确定肿瘤边界;外科医生只能巧妙地依靠触觉反馈等主观方法。这往往导致切除不完全和肿瘤复发。本研究的目的是在体外和体内设计、开发并评估一种纳米封装的可见染料,用于在侵袭性肿瘤模型中术中视觉描绘肿瘤边缘。开发了含有伊文思蓝染料的脂质体纳米载体(纳米伊文思蓝),对其进行了表征,并在体外和体内测试了安全性。将3RT1RT2A胶质瘤细胞植入Fischer 344大鼠的脑内。通过尾静脉将纳米伊文思蓝或伊文思蓝溶液注射到荷瘤动物体内。为了评估肿瘤染色情况,对组织样本进行了肉眼分析和荧光显微镜分析。计算面积、周长比和曼德尔斯重叠系数以量化染色程度。纳米伊文思蓝在侵袭性肿瘤模型中清晰地标记了肿瘤边缘。纳米伊文思蓝染色与肿瘤的面积比为0.89±0.05,周长比为0.94±0.04,曼德尔斯R为0.51±0.08,M1为0.97±0.06。高倍显微镜下对肿瘤边界的检查证实纳米伊文思蓝未对健康组织染色。在侵袭性肿瘤模型中,纳米伊文思蓝明显有助于区分肿瘤组织和健康组织,而注射未封装的伊文思蓝会因染料从肿瘤扩散到健康组织而导致将健康组织误识别为肿瘤。