Designing lysate-based hydrogels for on-demand therapy.

IF 8.9
Journal of pharmaceutical analysis Pub Date : 2026-08-01 Epub Date: 2025-12-09 DOI:10.1016/j.jpha.2025.101514
Yang Lv, Siteng Tieng, Xiaoling Xu, Wei Chen
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引用次数: 0

Abstract

Hydrogels are three-dimensional hydrophilic networks formed via physical or chemical crosslinking. Owing to their structural mimicry of native extracellular matrices and tunable capacity for therapeutic cargo delivery, they have garnered substantial attention in biomedical engineering. Traditional hydrogels primarily function as passive scaffolds for drug encapsulation; however, recent advances have shifted toward integrating bioactive lysates that extract derived from cells or tissues are rich in growth factors, cytokines, and antigenic components to construct dynamic, multifunctional platforms. Lysate-based hydrogels combine the intrinsic bioactivity of lysate-derived factors (e.g., tumor-specific neoantigens or bacteria-derived pathogen-associated molecular patterns) with the spatiotemporal control afforded by hydrogel matrices. This synergy enables precise modulation of the tumor microenvironment, immune priming, and tissue regeneration. In this review, we highlight the emergence of lysate-based hydrogels, which hold significant guiding value for the entire field of bioengineering. This technology represents an innovation in both design concepts and therapeutic strategies, with potential applications across multiple related disciplines. By proposing strategies to exploit underexplored lysate sources (e.g., microbiota-derived components) and integrate stimuli-responsive materials, this work aims to advance lysate-based hydrogels as next-generation platforms for precision oncology, while balancing biological complexity with engineering reproducibility. Key challenges in the development of lysate-based hydrogels include determining the optimal dosage and composition of lysate-derived factors, as well as coordinating their interactions. The presence of multiple factors endows these hydrogels with pluripotent therapeutic effects, but potential crosstalk between factors may limit their efficacy. This area requires further in-depth exploration in future research.

为按需治疗设计基于裂解物的水凝胶。
水凝胶是通过物理或化学交联形成的三维亲水性网络。由于它们的结构模仿天然细胞外基质和可调节的治疗货物输送能力,它们在生物医学工程中获得了大量关注。传统的水凝胶主要作为药物包封的被动支架;然而,最近的进展已经转向整合从细胞或组织中提取的富含生长因子、细胞因子和抗原成分的生物活性裂解物,以构建动态的多功能平台。基于裂解液的水凝胶结合了裂解液衍生因子(例如,肿瘤特异性新抗原或细菌衍生的病原体相关分子模式)的内在生物活性与水凝胶基质提供的时空控制。这种协同作用能够精确调节肿瘤微环境、免疫启动和组织再生。在这篇综述中,我们重点介绍了裂解物基水凝胶的出现,它对整个生物工程领域具有重要的指导价值。这项技术代表了设计理念和治疗策略的创新,具有跨多个相关学科的潜在应用。通过提出利用未充分开发的裂解物来源(例如微生物群衍生成分)和整合刺激响应材料的策略,本工作旨在推进裂解物为基础的水凝胶作为下一代精确肿瘤学平台,同时平衡生物复杂性和工程可重复性。开发以裂解液为基础的水凝胶的关键挑战包括确定裂解液衍生因子的最佳剂量和组成,以及协调它们的相互作用。多种因素的存在使这些水凝胶具有多能性的治疗作用,但因素之间潜在的串扰可能会限制其疗效。这一领域需要在今后的研究中进一步深入探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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