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可注射纳米复合水凝胶增强腹腔内化疗药物和免疫检查点抑制剂共递送用于增强腹膜转移治疗。

Injectable Nanocomposite Hydrogels Improve Intraperitoneal Co-delivery of Chemotherapeutics and Immune Checkpoint Inhibitors for Enhanced Peritoneal Metastasis Therapy.

机构信息

School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen 518000, China.

Precise Genome Engineering Center, School of Life Sciences, Guangzhou University, Guangzhou 510006, China.

出版信息

ACS Nano. 2024 Jul 23;18(29):18963-18979. doi: 10.1021/acsnano.4c02312. Epub 2024 Jul 14.

Abstract

Intraperitoneal co-delivery of chemotherapeutic drugs (CDs) and immune checkpoint inhibitors (ICIs) brings hope to improve treatment outcomes in patients with peritoneal metastasis from ovarian cancer (OC). However, current intraperitoneal drug delivery systems face issues such as rapid drug clearance from lymphatic drainage, heterogeneous drug distribution, and uncontrolled release of therapeutic agents into the peritoneal cavity. Herein, we developed an injectable nanohydrogel by combining carboxymethyl chitosan (CMCS) with bioadhesive nanoparticles (BNPs) based on polylactic acid-hyperbranched polyglycerol. This system enables the codelivery of CD and ICI into the intraperitoneal space to extend drug retention. The nanohydrogel is formed by cross-linking of aldehyde groups on BNPs with amine groups on CMCS via reversible Schiff base bonds, with CD and ICI loaded separately into BNPs and CMCS network. BNP/CMCS nanohydrogel maintained the activity of the biomolecules and released drugs in a sustained manner over a 7 day period. The adhesive property, through the formation of Schiff bases with peritoneal tissues, confers BNPs with an extended residence time in the peritoneal cavity after being released from the nanohydrogel. In a mouse model, BNP/CMCS nanohydrogel loaded with paclitaxel (PTX) and anti-PD-1 antibodies (αPD-1) significantly suppressed peritoneal metastasis of OC compared to all other tested groups. In addition, no systemic toxicity of nanohydrogel-loaded PTX and αPD-1 was observed during the treatment, which supports potential translational applications of this delivery system.

摘要

腹腔内共递送化疗药物 (CDs) 和免疫检查点抑制剂 (ICIs) 为改善卵巢癌 (OC) 腹膜转移患者的治疗效果带来了希望。然而,目前的腹腔内药物输送系统面临着从淋巴引流中快速清除药物、药物分布不均匀以及治疗剂在腹腔内不受控制释放等问题。在此,我们基于聚乳酸-超支化聚甘油开发了一种可注射的纳米水凝胶,该水凝胶将羧甲基壳聚糖 (CMCS) 与生物黏附纳米颗粒 (BNPs) 结合在一起。该系统能够将 CD 和 ICI 共递送到腹腔内,以延长药物保留时间。纳米水凝胶是通过 BNPs 上的醛基与 CMCS 上的胺基之间的可逆席夫碱键交联形成的,CD 和 ICI 分别负载在 BNPs 和 CMCS 网络中。BNP/CMCS 纳米水凝胶保持了生物分子的活性,并在 7 天内以持续的方式释放药物。通过与腹膜组织形成席夫碱,BNP/CMCS 纳米水凝胶具有粘性,使其在从纳米水凝胶中释放后在腹腔内的停留时间延长。在小鼠模型中,与所有其他测试组相比,载紫杉醇 (PTX) 和抗 PD-1 抗体 (αPD-1) 的 BNP/CMCS 纳米水凝胶显著抑制了 OC 的腹膜转移。此外,在治疗过程中未观察到载纳米水凝胶的 PTX 和 αPD-1 的全身毒性,这支持了该输送系统的潜在转化应用。

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