Leibniz Institute of Polymer Research Dresden, Institute of Biofunctional Polymer Materials, Hohe Strasse 6, 01069, Dresden, Germany.
Max Planck Institute for Multidisciplinary Sciences, 37077, Göttingen, Germany.
Adv Sci (Weinh). 2023 Mar;10(7):e2206412. doi: 10.1002/advs.202206412. Epub 2022 Dec 29.
While autoregulative adaptation is a common feature of living tissues, only a few feedback-controlled adaptive biomaterials are available so far. This paper herein reports a new polymer hydrogel platform designed to release anti-inflammatory molecules in response to the inflammatory activation of human blood. In this system, anti-inflammatory peptide drugs, targeting either the complement cascade, a complement receptor, or cyclophilin A, are conjugated to the hydrogel by a peptide sequence that is cleaved by elastase released from activated granulocytes. As a proof of concept, the adaptive drug delivery from the gel triggered by activated granulocytes and the effect of the released drug on the respective inflammatory pathways are demonstrated. Adjusting the gel functionalization degree is shown to allow for tuning the drug release profiles to effective doses within a micromolar range. Feedback-controlled delivery of covalently conjugated drugs from a hydrogel matrix is concluded to provide valuable safety features suitable to equip medical devices with highly active anti-inflammatory agents without suppressing the general immunosurveillance.
虽然自动调节适应是活组织的共同特征,但到目前为止,只有少数反馈控制的适应性生物材料可用。本文报告了一种新的聚合物水凝胶平台,旨在响应人血液的炎症激活而释放抗炎分子。在该系统中,针对补体级联、补体受体或亲环素 A 的抗炎肽药物通过弹性蛋白酶从活化的粒细胞释放的肽序列连接到水凝胶上。作为概念验证,证明了由活化的粒细胞触发的凝胶的自适应药物释放以及释放的药物对各自炎症途径的作用。结果表明,通过调整凝胶的功能化程度,可以将药物释放曲线调整到微摩尔范围内的有效剂量。从水凝胶基质中进行共价连接药物的反馈控制递送被认为提供了有价值的安全特性,适合为医疗设备配备高活性抗炎剂,而不会抑制一般的免疫监视。