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用于胰腺癌光动力治疗的新型吉西他滨-铼(I)双喹啉基配合物与液晶纳米颗粒的组合及制剂

Novel Gemcitabine-Re(I) Bisquinolinyl Complex Combinations and Formulations With Liquid Crystalline Nanoparticles for Pancreatic Cancer Photodynamic Therapy.

作者信息

Liew Hui Shan, Mai Chun-Wai, Zulkefeli Mohd, Madheswaran Thiagarajan, Kiew Lik Voon, Pua Lesley Jia Wei, Hii Ling Wei, Lim Wei Meng, Low May Lee

机构信息

School of Postgraduate Studies, International Medical University, Kuala Lumpur, Malaysia.

Centre for Cancer and Stem Cell Research, International Medical University, Kuala Lumpur, Malaysia.

出版信息

Front Pharmacol. 2022 Jul 6;13:903210. doi: 10.3389/fphar.2022.903210. eCollection 2022.

Abstract

With less than 10% of 5-year survival rate, pancreatic ductal adenocarcinoma (PDAC) is known to be one of the most lethal types of cancer. Current literature supports that gemcitabine is the first-line treatment of PDAC. However, poor cellular penetration of gemcitabine along with the acquired and intrinsic chemoresistance of tumor against it often reduced its efficacy and hence necessitates the administration of high gemcitabine dose during chemotherapy. Photodynamic therapy (PDT), a more selective and minimally invasive treatment, may be used synergistically with gemcitabine to reduce the doses utilized and dose-related side effects. This study reports the synergistic use of Re(I) bisquinolinyl complex, a transition metal complex photosensitizer with gemcitabine against PDAC. Re(I) bisquinolinyl complex was found to act synergistically with gemcitabine against PDAC at various ratios. With the aim to enhance cellular uptake and therapeutic efficiency, the Re(I) bisquinolinyl complex and gemcitabine were encapsulated into liquid crystalline nanoparticles (LCNPs) system. The formulations were found to produce homogeneous drug-loaded LCNPs (average size: 159-173 nm, zeta potential +1.06 to -10 mV). Around 70% of gemcitabine and 90% of the Re(I) bisquinolinyl complex were found to be entrapped efficiently in the formulated LCNPs. The release rate of gemcitabine or/and the Re(I) bisquinolinyl complex loaded into LCNPs was evaluated and the hydrophilic gemcitabine was released at a faster rate than the lipophilic Re(I) complex. LCNPs loaded with gemcitabine and Re(I) bisquinolinyl complex in a 1:1 ratio illustrated the best anti-cancer activity among the LCNP formulations (IC of BxPC3: 0.15 μM; IC of SW 1990: 0.76 μM) through apoptosis. The current findings suggest the potential use of transition metal-based photosensitizer as an adjunctive agent for gemcitabine-based chemotherapy against PDAC and the importance of nano-formulation in such application.

摘要

胰腺导管腺癌(PDAC)的5年生存率不到10%,是已知最致命的癌症类型之一。目前的文献支持吉西他滨是PDAC的一线治疗药物。然而,吉西他滨较差的细胞穿透性以及肿瘤对其获得性和内在的化疗耐药性常常降低其疗效,因此在化疗期间需要给予高剂量的吉西他滨。光动力疗法(PDT)是一种更具选择性和微创性的治疗方法,可与吉西他滨协同使用,以减少用药剂量和剂量相关的副作用。本研究报告了铼(I)双喹啉配合物(一种过渡金属配合物光敏剂)与吉西他滨协同用于治疗PDAC。发现铼(I)双喹啉配合物与吉西他滨以各种比例协同作用于PDAC。为了提高细胞摄取和治疗效率,将铼(I)双喹啉配合物和吉西他滨封装到液晶纳米颗粒(LCNPs)系统中。发现这些制剂可产生均匀的载药LCNPs(平均尺寸:159 - 173 nm,ζ电位 +1.06至 -10 mV)。发现约70%的吉西他滨和90%的铼(I)双喹啉配合物有效地包封在配制的LCNPs中。评估了负载到LCNPs中的吉西他滨或/和铼(I)双喹啉配合物的释放速率,亲水性的吉西他滨释放速率比亲脂性的铼(I)配合物快。以1:1比例负载吉西他滨和铼(I)双喹啉配合物的LCNPs在LCNP制剂中表现出最佳的抗癌活性(BxPC3的IC:0.15 μM;SW 1990的IC:0.76 μM),通过凋亡发挥作用。目前的研究结果表明,基于过渡金属的光敏剂作为基于吉西他滨的化疗辅助药物用于治疗PDAC具有潜在用途,以及纳米制剂在这种应用中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fc1/9299370/a20222ccb5e3/fphar-13-903210-g001.jpg

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