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瘤内注射多西他赛:抑制淋巴结肿瘤细胞生长的创新治疗方法。

Intranodal delivery of modified docetaxel: Innovative therapeutic method to inhibit tumor cell growth in lymph nodes.

机构信息

Laboratory of Biomedical Engineering for Cancer, Graduate School of Biomedical Engineering, Tohoku University, Sendai, Miyagi, Japan.

Biomedical Engineering Cancer Research Center, Graduate School of Biomedical Engineering, Tohoku University, Sendai, Miyagi, Japan.

出版信息

Cancer Sci. 2022 Apr;113(4):1125-1139. doi: 10.1111/cas.15283. Epub 2022 Feb 14.

Abstract

Delivery of chemotherapeutic agents into metastatic lymph nodes (LNs) is challenging as they are unevenly distributed in the body. They are difficult to access via traditional systemic routes of drug administration, which produce significant adverse effects and result in low accumulation of drugs into the cancerous LN. To improve the survival rate of patients with LN metastasis, a lymphatic drug delivery system (LDDS) has been developed to target metastatic LN by delivering chemotherapy agents into sentinel LN (SLN) under ultrasound guidance. The LDDS is an advanced method that can be applied in the early stage of the progression of tumor cells in the SLN before tumor mass formation has occurred. Here we investigated the optimal physicochemical ranges of chemotherapeutic agents' solvents with the aim of increasing treatment efficacy using the LDDS. We found that an appropriate osmotic pressure range for drug administration was 700-3,000 kPa, with a viscosity < 40 mPa⋅s. In these physicochemical ranges, expansion of lymphatic vessels and sinuses, drug retention, and subsequent antitumor effects could be more precisely controlled. Furthermore, the antitumor effects depended on the tumor progression stage in the SLN, the injection rate, and the volumes of administered drugs. We anticipate these optimal ranges to be a starting point for developing more effective drug regimens to treat metastatic LN with the LDDS.

摘要

将化疗药物递送到转移性淋巴结 (LNs) 具有挑战性,因为它们在体内的分布不均匀。通过传统的全身药物给药途径很难到达这些淋巴结,因为这些途径会产生严重的不良反应,并导致药物在癌性 LN 中的积累量很低。为了提高 LN 转移患者的生存率,已经开发了一种淋巴药物递送系统 (LDDS),通过在超声引导下将化疗药物递送到前哨淋巴结 (SLN) 来靶向转移性 LN。LDDS 是一种先进的方法,可在肿瘤细胞在 SLN 中进展的早期阶段应用,即在肿瘤肿块形成之前。在这里,我们研究了化疗药物溶剂的最佳物理化学范围,以期通过 LDDS 提高治疗效果。我们发现,给药的适当渗透压范围为 700-3000kPa,粘度 < 40mPa⋅s。在这些物理化学范围内,可以更精确地控制淋巴管和窦的扩张、药物保留以及随后的抗肿瘤作用。此外,抗肿瘤作用取决于 SLN 中的肿瘤进展阶段、注射速度和给药药物的体积。我们期望这些最佳范围成为开发更有效的药物方案的起点,以通过 LDDS 治疗转移性 LN。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ff/8990862/fc16d425f03d/CAS-113-1125-g012.jpg

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