4.7 Article

Utilizing Laser Activation of Photothermal Plasmonic Nanoparticles to Induce On-Demand Drug Amorphization inside a Tablet

Journal

MOLECULAR PHARMACEUTICS
Volume 18, Issue 6, Pages 2254-2262

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.1c00077

Keywords

plasmonic nanoaggregates; near-IR laser irradiation; in situ drug amorphization; amorphous solid dispersions

Funding

  1. NordForsk (Nordic University Hub project) [85352]
  2. Independent Research Fund Denmark [DFF-7026-00052B]
  3. European Research Council (ERC) under the European Union [758705]
  4. Swedish Research Council [2016-03471]
  5. AT
  6. European Research Council (ERC) [758705] Funding Source: European Research Council (ERC)
  7. Swedish Research Council [2016-03471] Funding Source: Swedish Research Council

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Poor aqueous drug solubility is a major challenge in oral drug delivery, and a novel approach to overcome this challenge is drug amorphization inside a tablet. Utilizing photothermal plasmonic nanoparticles for on-demand drug amorphization is a promising new pharmaceutical application.
Poor aqueous drug solubility represents a major challenge in oral drug delivery. A novel approach to overcome this challenge is drug amorphization inside a tablet, that is, on-demand drug amorphization. The amorphous form is a thermodynamically instable, disordered solid-state with increased dissolution rate and solubility compared to its crystalline counterpart. During on-demand drug amorphization, the drug molecularly disperses into a polymer to form an amorphous solid at elevated temperatures inside a tablet. This study investigates, for the first time, the utilization of photothermal plasmonic nanoparticles for on-demand drug amorphization as a new pharmaceutical application. For this, near-IR photothermal plasmonic nanoparticles were tableted together with a crystalline drug (celecoxib) and a polymer (polyvinylpyrrolidone). The tablets were subjected to a near-IR laser at different intensities and durations to study the rate of drug amorphization under each condition. During laser irradiation, the plasmonic nanoparticles homogeneously heated the tablet. The temperature was directly related to the rate and degree of amorphization. Exposure times as low as 180 s at 1.12 W cm(-2) laser intensity with only 0.25 wt % plasmonic nanoparticles and up to 50 wt % drug load resulted in complete drug amorphization. Therefore, near-IR photothermal plasmonic nanoparticles are promising excipients for on-demand drug amorphization with laser irradiation.

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