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TCPP-异莲心碱纳米粒用于温和温度光热治疗。

TCPP-Isoliensinine Nanoparticles for Mild-Temperature Photothermal Therapy.

机构信息

Department of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 201620, People's Republic of China.

State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai, 200237, People's Republic of China.

出版信息

Int J Nanomedicine. 2021 Oct 5;16:6797-6806. doi: 10.2147/IJN.S317462. eCollection 2021.

Abstract

PURPOSE

Photothermal therapy (PTT) is promising for the treatment of tumors due to its advantages including minimally invasive, easy implementation and selective localized treatment. However, single PTT suffers from several limitations, such as constrained light penetration and low delivery efficiency, typically leading to heterogeneous heating and incomplete elimination of cancer cells. Therefore, combination of PTT with other therapies, eg, chemotherapy is desirable in order to achieve synergistic effects in cancer treatment.

METHODS

Here, we designed a new type of TCPP-Iso combined nanoparticle for synergetic therapy for breast cancer. Specifically, photothermal agent tetra(4-carboxyphenyl) porphine (TCPP) and anti-cancer drug isoliensinine (Iso) were encapsulated in PEG--PLGA polymeric nanoparticles through a precipitation process.

RESULTS

The obtained NPs displayed well-controlled size and high stability over time. Tuning TCPP-Iso/polymer ratio, or total concentration of drug and polymers led to increased hydrodynamic radius of NPs from 65 to 108 nm without disturbing the narrow size distribution. Besides, the formed NPs showed a consequently cumulative release of TCPP and of Iso. The temperature elevation ability of both TCPP NPs and TCPP-Iso NPs was TCPP-concentration dependent. Solutions of TCPP NPs that contained equivalent amount of TCPP with respect to TCPP-Iso NPs, presented the same trend and exhibited non-obvious difference in temperature elevation under certain laser power. The viability of MDA-MB-231 cells treated with TCPP-Iso NPs could be inhibited effectively at a relatively mild temperature (42-43°C) compared to the other groups, which may minimize heat damage to the surrounding healthy tissues.

CONCLUSION

The results indicate that the TCPP-Iso combined NPs showed hardly any toxicity to normal tissue cell line, but displayed an efficient synergistic effect for killing cancer cells under laser irradiation. Our study demonstrates that the successful combination of TCPP and Iso realized a synergistic therapy effect at a relatively mild temperature, and the insights obtained here shall be helpful for designing new combined PTT agents for cancer treatment.

摘要

目的

光热疗法(PTT)因其微创、易于实施和选择性局部治疗等优点,在肿瘤治疗中具有广阔的应用前景。然而,单一的 PTT 存在一些局限性,例如有限的光穿透和低的递送效率,通常导致不均匀的加热和不完全消除癌细胞。因此,为了在癌症治疗中达到协同效应,将 PTT 与其他疗法(如化疗)相结合是可取的。

方法

在这里,我们设计了一种新型 TCPP-Iso 联合纳米颗粒用于协同治疗乳腺癌。具体来说,通过沉淀过程将光热剂四(4-羧基苯基)卟啉(TCPP)和抗癌药物异莲心碱(Iso)包封在 PEG-PLGA 聚合物纳米颗粒中。

结果

所得到的 NPs 显示出良好的尺寸控制和长时间的高稳定性。通过调整 TCPP-Iso/聚合物的比例或药物和聚合物的总浓度,可以将 NPs 的水动力学半径从 65nm 增加到 108nm,而不会干扰其窄的尺寸分布。此外,形成的 NPs 表现出 TCPP 和 Iso 的持续累积释放。TCPP NPs 和 TCPP-Iso NPs 的升温能力均与 TCPP 浓度有关。含有与 TCPP-Iso NPs 中 TCPP 当量的 TCPP NPs 溶液,在一定激光功率下,呈现出相同的升温趋势,升温效果没有明显差异。与其他组相比,在相对温和的温度(42-43°C)下,用 TCPP-Iso NPs 处理的 MDA-MB-231 细胞的活力可以得到有效抑制,这可能最大限度地减少对周围健康组织的热损伤。

结论

结果表明,TCPP-Iso 联合纳米颗粒对正常组织细胞系几乎没有毒性,但在激光照射下对癌细胞表现出有效的协同杀伤作用。我们的研究表明,TCPP 和 Iso 的成功结合在相对温和的温度下实现了协同治疗效果,这里获得的见解将有助于设计用于癌症治疗的新型联合 PTT 试剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/201d/8502540/0b623b1ba66a/IJN-16-6797-g0001.jpg

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