Optimizing photodynamic therapy: Talaporfin-encapsulated silica nanoparticles for red blood cell disruption in cancer treatment

IF 4.7 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-08-01 Epub Date: 2025-02-24 DOI:10.1016/j.jphotochem.2025.116356
Ghaseb N. Makhadmeh , Tariq AlZoubi , Samer H. Zyoud , Mahmoud Al-Gharram , M.H.A. Mhareb , Osama Abu Noqta , Abdulsalam Abuelsamen
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Abstract

Photodynamic therapy (PDT) is a highly effective cancer treatment that combines a photosensitizer (PS), and light for targeted cancer cell destruction in present of oxygen. However, the delivery of photosensitizers remains a challenge due to degradation risks and systemic toxicity. This study investigates the encapsulation of Talaporfin, a second-generation chlorin-based photosensitizer, within silica nanoparticles (SiNPs) to enhance PDT efficacy and safety. The research focuses on using red blood cells (RBCs) as a model system, highlighting their critical role in the tumor microenvironment. By targeting and destroying RBCs in proximity to tumors, PDT can disrupt the oxygen supply, indirectly leading to cancer cell death. Talaporfin-encapsulated SiNPs (T-SiNPs) were synthesized via a microemulsion method and characterized for size, morphology, and stability. The photodynamic effects of encapsulated versus naked Talaporfin were evaluated under varying concentrations and light exposure times. Results revealed that T-SiNPs achieved higher therapeutic efficacy, requiring lower concentrations and shorter exposure durations. This enhanced performance is attributed to improved light absorption and ROS production due to reduced aggregation of Talaporfin within SiNPs. Additionally, mathematical equations were developed to correlate the concentrations of encapsulated and naked Talaporfin with the 50% mortality rate (t50) of RBCs. These equations provide a predictive framework for optimizing PDT protocols, enabling the determination of optimal drug concentrations and exposure times without extensive experimental trials. This study underscores the potential of silica nanoparticles as efficient carriers for photosensitizers, enhancing PDT outcomes by targeting both RBCs and cancer cells. The findings pave the way for innovative cancer therapies that leverage nanotechnology to achieve precise, effective, and safer treatments. Future applications of this approach may extend to broader therapeutic areas, further revolutionizing modern medicine.

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优化光动力疗法:塔拉波芬包封二氧化硅纳米颗粒用于癌症治疗中的红细胞破坏
光动力疗法(PDT)是一种非常有效的癌症治疗方法,它结合了光敏剂(PS)和光,在氧气存在的情况下靶向癌细胞破坏。然而,由于降解风险和全身毒性,光敏剂的递送仍然是一个挑战。本研究研究了第二代氯基光敏剂塔拉波芬(Talaporfin)在二氧化硅纳米颗粒(SiNPs)内的包封,以提高PDT的疗效和安全性。本研究重点使用红细胞(rbc)作为模型系统,强调其在肿瘤微环境中的关键作用。通过靶向和破坏肿瘤附近的红细胞,PDT可以破坏氧气供应,间接导致癌细胞死亡。采用微乳液法合成了talaporfin包封的SiNPs (T-SiNPs),并对其大小、形态和稳定性进行了表征。在不同浓度和光照时间下,对包封的塔拉波芬和光动力学效应进行了评价。结果表明,T-SiNPs具有较低浓度和较短暴露时间的治疗效果。这种增强的性能是由于sinp中Talaporfin的聚集减少,从而改善了光吸收和ROS的产生。此外,还建立了数学方程,将包封和裸塔拉波芬浓度与红细胞50%死亡率(t50)联系起来。这些方程为优化PDT方案提供了预测框架,无需大量实验试验即可确定最佳药物浓度和暴露时间。这项研究强调了二氧化硅纳米颗粒作为光敏剂的有效载体的潜力,通过靶向红细胞和癌细胞来提高PDT的效果。这些发现为利用纳米技术实现精确、有效和更安全的治疗方法的创新癌症疗法铺平了道路。这种方法的未来应用可能会扩展到更广泛的治疗领域,进一步革新现代医学。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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