Lai Jinping, Shah Birju P, Zhang Yixiao, Yang Letao, Lee Ki-Bum
Department of Chemistry and Chemical Biology, Institute for Advanced Materials, Devices and Nanotechnology (IAMDN), Rutgers University, Piscataway, New Jersey 08854, United States.
ACS Nano. 2015 May 26;9(5):5234-45. doi: 10.1021/acsnano.5b00641. Epub 2015 Apr 15.
Stimuli-responsive drug delivery vehicles have garnered immense interest in recent years due to unparalleled progress made in material science and nanomedicine. However, the development of stimuli-responsive devices with integrated real-time monitoring capabilities is still in its nascent stage because of the limitations of imaging modalities. In this paper, we describe the development of a polypeptide-wrapped mesoporous-silica-coated multicolor upconversion nanoparticle (UCNP@MSN) as an adenosine triphosphate (ATP)-responsive drug delivery system (DDS) for long-term tracking and real-time monitoring of drug release. Our UCNP@MSN with multiple emission peaks in UV-NIR wavelength range was functionalized with zinc-dipicolylamine analogue (TDPA-Zn(2+)) on its exterior surface and loaded with small-molecule drugs like chemotherapeutics in interior mesopores. The drugs remained entrapped within the UCNP-MSNs when the nanoparticles were wrapped with a compact branched polypeptide, poly(Asp-Lys)-b-Asp, because of multivalent interactions between Asp moieties present in the polypeptide and the TDPA-Zn(2+) complex present on the surface of UCNP-MSNs. This led to luminescence resonance energy transfer (LRET) from the UCNPs to the entrapped drugs, which typically have absorption in UV-visible range, ultimately resulting in quenching of UCNP emission in UV-visible range while retaining their strong NIR emission. Addition of ATP led to a competitive displacement of the surface bound polypeptide by ATP due to its higher affinity to TDPA-Zn(2+), which led to the release of the entrapped drugs and subsequent elimination of LRET. Monitoring of such ATP-triggered ratiometric changes in LRET allowed us to monitor the release of the entrapped drugs in real-time. Given these results, we envision that our proposed UCNP@MSN-polypeptide hybrid nanoparticle has great potential for stimuli-responsive drug delivery as well as for monitoring biochemical changes taking place in live cancer and stem cells.
近年来,由于材料科学和纳米医学取得了无与伦比的进展,刺激响应型药物递送载体引起了极大的关注。然而,由于成像方式的局限性,具有集成实时监测能力的刺激响应型装置的开发仍处于起步阶段。在本文中,我们描述了一种多肽包裹的介孔二氧化硅包覆的多色上转换纳米颗粒(UCNP@MSN)的开发,作为一种三磷酸腺苷(ATP)响应型药物递送系统(DDS),用于长期跟踪和实时监测药物释放。我们的UCNP@MSN在紫外-近红外波长范围内具有多个发射峰,其外表面用锌-二吡啶胺类似物(TDPA-Zn(2+))进行了功能化,并在内部介孔中装载了小分子药物,如化疗药物。当纳米颗粒用紧密分支的多肽聚(天冬氨酸-赖氨酸)-b-天冬氨酸包裹时,由于多肽中存在的天冬氨酸部分与UCNP-MSN表面存在的TDPA-Zn(2+)络合物之间的多价相互作用,药物被困在UCNP-MSNs内。这导致了从UCNPs到被困药物的发光共振能量转移(LRET),被困药物通常在紫外-可见光范围内有吸收,最终导致UCNP在紫外-可见光范围内的发射猝灭,同时保留其强烈的近红外发射。ATP的加入导致ATP因其对TDPA-Zn(2+)的更高亲和力而竞争性取代表面结合的多肽,从而导致被困药物的释放和随后LRET的消除。监测这种ATP触发的LRET比例变化使我们能够实时监测被困药物的释放。鉴于这些结果,我们设想我们提出的UCNP@MSN-多肽杂化纳米颗粒在刺激响应型药物递送以及监测活癌细胞和干细胞中发生的生化变化方面具有巨大潜力。