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利用棒状、酸不稳定的载姜黄素聚合物纳米凝胶系统治疗全身炎症。

Exploitation of a rod-shaped, acid-labile curcumin-loaded polymeric nanogel system in the treatment of systemic inflammation.

机构信息

School of Pharmacy, College of Pharmacy, China Medical University, Taichung City 406040, Taiwan, ROC.

Department of Pharmacy, Chia Nan University of Pharmacy and Science, Tainan City 71710, Taiwan, ROC.

出版信息

Biomater Adv. 2022 Feb;133:112597. doi: 10.1016/j.msec.2021.112597. Epub 2021 Dec 8.

Abstract

Curcumin is proven to have potent anti-inflammatory activity, but its low water solubility and rapid degradation in physiological conditions limit its clinical use, particularly in intravenous drug delivery. In this study, we fabricated rod-shaped, acid-labile nanogels, using high biosafe and biocompatible polymers, for intravenous application in systemic inflammation treatment. The constituent polymers of the nanogels were prepared via the conjugation of vitamin B derivatives, including pyridoxal and pyridoxamine, onto poly(glutamate) with ester bonds. The aldehyde groups of the pyridoxal and amine groups of the pyridoxamine on the polymers enable crosslinking using a Schiff base during the solvent evaporation procedure for the preparation of the rod-shaped nanogels. Our study is the first to introduce this linkage, which is generated from two vitamin B derivatives into a nanogel system. It is also the first to fabricate a rod-shaped nanogel system via simple solvent evaporation. Under acidic conditions, such as those encountered in the endosomes and lysosomes within inflammatory macrophage cells spread in the whole body, imine bonds are cleaved and release payloads. The nanogel polymers were successfully synthesized and characterized, and the formation and disappearance of the Schiff base under neutral and acidic conditions were also confirmed using Fourier transform infrared spectroscopy. Following curcumin encapsulation, the long, rod-shaped nanogels were able to rapidly internalize into macrophage cells in static or adhere to cells under the flows, release their payloads in the acid milieus, and, thus, mitigate curcumin degradation. Consequently, curcumin-loaded, rod-shaped nanogels displayed exceptional anti-inflammatory activity both in vitro and in vivo, by efficiently inhibiting pro-inflammatory mediator secretion. These results demonstrate the feasibility of our acid-labile, rod-shaped nanogels for the treatment of systemic inflammation.

摘要

姜黄素已被证实具有很强的抗炎活性,但由于其在生理条件下的低水溶性和快速降解,限制了其在临床上的应用,特别是在静脉内给药。在这项研究中,我们使用高生物安全性和生物相容性的聚合物,制备了棒状、酸敏感的纳米凝胶,用于静脉内应用于全身炎症的治疗。纳米凝胶的组成聚合物是通过将维生素 B 衍生物,包括吡哆醛和吡哆胺,与聚(谷氨酸)通过酯键连接制备的。聚合物上的吡哆醛的醛基和吡哆胺的氨基在溶剂蒸发过程中能够通过席夫碱交联,用于制备棒状纳米凝胶。我们的研究首次将这种键合(由两种维生素 B 衍生物产生)引入纳米凝胶系统。这也是首次通过简单的溶剂蒸发制备棒状纳米凝胶系统。在酸性条件下,如全身扩散的炎症巨噬细胞细胞内的内体和溶酶体中遇到的条件,亚胺键被切断并释放出有效载荷。成功地合成和表征了纳米凝胶聚合物,并使用傅里叶变换红外光谱证实了中性和酸性条件下席夫碱的形成和消失。在姜黄素包封后,长棒状纳米凝胶能够在静态下迅速进入巨噬细胞内,或在流动下附着在细胞上,在酸性环境中释放其有效载荷,从而减轻姜黄素的降解。因此,负载姜黄素的棒状纳米凝胶在体外和体内都表现出了出色的抗炎活性,能够有效抑制促炎介质的分泌。这些结果证明了我们的酸敏感、棒状纳米凝胶用于治疗全身炎症的可行性。

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