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可注射系统及其在利用温敏性聚(γ-谷氨酸)基物理水凝胶输送生物分子方面的潜在应用。

Injectable system and its potential application for the delivery of biomolecules by using thermosensitive poly(γ-glutamic acid)-based physical hydrogel.

机构信息

School of Materials Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.

School of Materials Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.

出版信息

Int J Biol Macromol. 2018 Apr 15;110:457-464. doi: 10.1016/j.ijbiomac.2017.09.108. Epub 2017 Sep 29.

DOI:10.1016/j.ijbiomac.2017.09.108
PMID:28970167
Abstract

Poly (γ-glutamic acid) (PGA) is a natural biomaterial with numerous good properties such as non-toxicity, non-immunogenicity, and water holding. So, various forms of PGA-based materials have been developed for bio-applications, including sheet, cross-linked hydrogel, and nanoparticle except injectable hydrogel type. Considering inherent advantages of injectable system, injectable hydrogel based on PGA can broaden the bio-application range of PGA. In this study, a PGA-based injectable hydrogel system was prepared by physically mixing it with a small amount of chitosan with two different water solubility and molecular weight. The prepared hydrogel system showed a thermo-sensitivity through sol-gel transition behavior in the body temperature change. The mechanical properties and in vitro stability could be modulated by varying the ratio of two types of chitosan. In vitro protein (human bFGF) delivery using this injectable formulation showed a sustained release for ∼2 weeks while preserving its bioactivity. In addition, the in situ formation of this PGA-based hydrogel formulation upon subcutaneous injection was demonstrated in vivo. The hydrogel formed in vivo also showed a long term (∼2 weeks) stability without noticeable inflammatory response. Therefore, the present formulation can be applied as a promising injectable hydrogel system for tissue engineering or drug delivery.

摘要

聚(γ-谷氨酸)(PGA)是一种具有多种优良性能的天然生物材料,如无毒、无免疫原性和保水性。因此,已经开发出各种形式的 PGA 基材料用于生物应用,包括薄片、交联水凝胶和纳米颗粒,除了可注射水凝胶类型。考虑到可注射系统的固有优势,基于 PGA 的可注射水凝胶可以拓宽 PGA 的生物应用范围。在这项研究中,通过将少量具有两种不同水溶性和分子量的壳聚糖与 PGA 物理混合来制备 PGA 基可注射水凝胶系统。所制备的水凝胶系统通过在体温变化时的溶胶-凝胶转变行为表现出热敏感性。通过改变两种壳聚糖的比例可以调节机械性能和体外稳定性。使用这种可注射制剂进行体外蛋白质(人 bFGF)递送显示出约 2 周的持续释放,同时保持其生物活性。此外,还在体内证明了这种基于 PGA 的水凝胶制剂在皮下注射时的原位形成。体内形成的水凝胶也表现出长达 2 周的稳定性,没有明显的炎症反应。因此,该制剂可作为一种有前途的组织工程或药物输送的可注射水凝胶系统。

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