Drug delivery: Zapped with ultraviolet light, polymer particles shrink
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Light Switch When ultraviolet light shines on nanoparticles containing spiropyran (bottom left), the molecule converts into merocyanine, causing the nanoparticles to shrink (bottom right). The conversion reaction spontaneously reverses in the dark, or in visible light. The R group is a long alkyl chain. Credit: J. Am. Chem. Soc |
Many chemists think encapsulating cancer drugs inside nanoparticles could lead to more efficient and specific drug delivery. But these nanoparticles often struggle to penetrate inside a tumor or to release their drug payloads once they’re in place. Now researchers demonstrate a solution to both problems using polymer nanoparticles that expand and contract when excited by certain wavelengths of light (J. Am. Chem. Soc., DOI: 10.1021/ja211888a).
Daniel Kohane and his colleagues at Children’s Hospital Boston thought that a nanoparticle whose size changed on command would allow them to maximize the amount of drug they could load into the particles. They thought such a particle would also be small enough to squeeze through the extracellular matrix inside a tumor. Also upon shrinking, the particles would release the loaded drugs, like a squeezed water balloon.
To make such nanoparticles, the researchers use two materials: lipid-decorated versions of the polymer polyethylene glycol, and the photoactive molecule spiropyran to which they added long alkyl groups. When the researchers mix the materials with a small molecule such as a drug or fluorescent dye, the components assemble into particles that are about 150 nm in diameter. If they apply a pulse of ultraviolet light, spiropyran converts into a more-hydrophilic molecule called merocyanine. This chemical transformation causes the particles to shrink to about 40 nm in diameter. In visible light or in the dark, the reaction reverses, restoring the particles to the larger volume.
To test the nanoparticles’ ability to release drugs, the scientists placed dye-loaded particles in buffer and measured how much dye diffused into the liquid. In the absence of ultraviolet light, the spiropyran-based particles slowly bled out the payload, releasing about 7% of the total contents in an hour. But after the researchers hit the mixture with a 30-second pulse of UV light, the particles dumped about 29% of their contents within an hour. The team could repeat the drug-release spike by allowing the particles to expand for three hours and irradiating them with UV light again.
To see how well the particles could squeeze into tight spaces, the researchers added dye-loaded nanoparticles to one end of a capillary tube filled with collagen gel and watched the dye diffuse along the tube. The gel, they reasoned, mimicked the tight spaces in a tumor’s extracellular matrix. A 10-second pulse of UV light increased diffusion of the dye-containing particles through the gel by almost 50% compared to non-irradiated particles, from 8.3 to 12.1 mm, suggesting they also could penetrate deeper into biological tissues.
Kohane says the new particles could allow physicians and patients to control when or where drugs are released, like nanoscale patient-controlled morphine pumps. Now the researchers want to show that the nanoparticles are safe and effective in animals.
Warren Chan of the University of Toronto says using light to control nanoparticle size offers “a unique twist” on drug delivery. But he points out that neither UV nor visible light penetrates mammalian tissues effectively. As a result, he says, the researchers should tweak their design to respond to more biologically relevant near-infrared wavelengths.
- Chemical & Engineering News
- ISSN 0009-2347
- Copyright © 2012 American Chemical Society
- Fonte: C&EN
