Nguyen KhanhVan T, Anker Jeffrey N
Department of Chemistry, Center for Optical Materials Science and Engineering Technology (COMSET), SC BioCRAFT and Environmental Toxicology Program, Clemson University, Clemson SC 29634.
Sens Actuators B Chem. 2014 Dec 15;205:313-321. doi: 10.1016/j.snb.2014.08.073.
Alginate gels are widely used for drug delivery and implanted devices. The rate at which these gels break down is important for controlling drug release. Since the de-gelation may be different , monitoring this process is essential. However, it is challenging to monitor the gel through tissue due to optical scattering and tissue autofluorescence. Herein we describe a method to detect through tissue the chemically-induced changes in viscosity and de-gelation process of alginate gels using magnetically modulated optical nanoprobes (MagMOONs). The MagMOONs are fluorescent magnetic microspheres coated with a thin layer of opaque metal on one hemisphere. The metal layer prevents excitation and emission light from passing through one side of the MagMOONs, which creates orientation-dependent fluorescence intensity. The magnetic particles also align in an external magnetic field and give blinking signals when they rotate to follow an external modulated magnetic field. The blinking signals from these MagMOONs are distinguished from background autofluorescence and can be tracked on a single particle level in the absence of tissue, or for an ensemble average of particles blinking through tissue. When these MagMOONs are dispersed in calcium alginate gel, they become sensors for detecting gel degradation upon addition of either ammonium ion or alginate lyase. Our results show MagMOONs start blinking approximately 10 minutes after 2 mg/mL alginate lyase addition and this blinking is clearly detected even through up to 4 mm chicken breast. This approach can potentially be employed to detect bacterial biofilm formation on medical implants by sensing specific proteases that either activate a related function or regulate biofilm formation. It can also be applied to other biosensors and drug delivery systems based on enzyme-catalyzed breakdown of gel components.
海藻酸盐凝胶广泛应用于药物递送和植入式装置。这些凝胶的分解速率对于控制药物释放至关重要。由于脱胶过程可能不同,监测这一过程至关重要。然而,由于光散射和组织自发荧光,通过组织监测凝胶具有挑战性。在此,我们描述了一种使用磁调制光学纳米探针(MagMOONs)通过组织检测海藻酸盐凝胶化学诱导的粘度变化和脱胶过程的方法。MagMOONs是一种荧光磁性微球,在一个半球上涂有一层薄薄的不透明金属。金属层可防止激发光和发射光穿过MagMOONs的一侧,从而产生与方向相关的荧光强度。磁性颗粒也会在外部磁场中排列,并在它们旋转以跟随外部调制磁场时发出闪烁信号。这些MagMOONs发出的闪烁信号与背景自发荧光不同,在没有组织的情况下可以在单个颗粒水平上进行跟踪,或者对通过组织闪烁的颗粒进行整体平均跟踪。当这些MagMOONs分散在海藻酸钙凝胶中时,它们就成为了检测添加铵离子或海藻酸裂解酶后凝胶降解的传感器。我们的结果表明,在添加2mg/mL海藻酸裂解酶后约10分钟,MagMOONs开始闪烁,即使透过高达4mm厚的鸡胸肉也能清晰检测到这种闪烁。这种方法有可能通过检测激活相关功能或调节生物膜形成的特定蛋白酶来检测医疗植入物上的细菌生物膜形成。它还可以应用于基于凝胶成分酶催化分解的其他生物传感器和药物递送系统。