Glangchai Luz Cristal, Caldorera-Moore Mary, Shi Li, Roy Krishnendu
Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
J Control Release. 2008 Feb 11;125(3):263-72. doi: 10.1016/j.jconrel.2007.10.021. Epub 2007 Nov 4.
Our ability to precisely manipulate size, shape and composition of nanoscale carriers is essential for controlling their in-vivo transport, bio-distribution and drug release mechanism. Shape-specific, "smart" nanoparticles that deliver drugs or imaging agents to target tissues primarily in response to disease-specific or physiological signals could significantly improve therapeutic care of complex diseases. Current methods in nanoparticle synthesis do not allow such simultaneous control over particle size, shape and environmentally-triggered drug release, especially at the sub 100 nm range. We report here a high-throughput nanofabrication technique using synthetic and biological macromers (peptides) to produce highly monodisperse, enzymatically-triggered nanoparticles of precise sizes and shapes. Particles as small as 50 nm were fabricated on silicon wafers and harvested directly into aqueous buffers using a biocompatible, one-step release technique. We further demonstrate successful encapsulation and precisely controlled enzyme-triggered release of antibodies and nucleic acids from these nanoparticles, thus providing a potential means for disease-controlled delivery of biomolecules.
我们精确操控纳米级载体的尺寸、形状和组成的能力对于控制其体内运输、生物分布和药物释放机制至关重要。能够主要响应疾病特异性或生理信号将药物或成像剂递送至靶组织的形状特异性“智能”纳米颗粒,可显著改善复杂疾病的治疗护理。目前纳米颗粒合成方法无法同时控制颗粒尺寸、形状以及环境触发的药物释放,尤其是在低于100纳米的范围内。我们在此报告一种高通量纳米制造技术,该技术使用合成和生物大分子(肽)来生产具有精确尺寸和形状的高度单分散、酶触发的纳米颗粒。在硅片上制造出小至50纳米的颗粒,并使用生物相容性一步释放技术直接收集到水性缓冲液中。我们进一步证明了从这些纳米颗粒中成功封装并精确控制抗体和核酸的酶触发释放,从而为生物分子的疾病控制递送提供了一种潜在手段。