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载有黄花补血草生物大分子的壳聚糖-PEG 纳米载体与生物支架的设计,以诱导人脂肪来源干细胞向表皮角质细胞分化。

Design of bio-scaffold conjugated with chitosan-PEG nano-carriers containing bio-macromolecules of Verbascum sinuatum L. to differentiate human adipose-derived stem cells into dermal keratinocytes.

机构信息

Department of Chemical Engineering, Ayatollah Amoli Branch, Islamic Azad University, Amol 678, Iran.

Department of Chemical Engineering, Ayatollah Amoli Branch, Islamic Azad University, Amol 678, Iran.

出版信息

Int J Biol Macromol. 2024 Jan;255:127520. doi: 10.1016/j.ijbiomac.2023.127520. Epub 2023 Oct 19.

Abstract

Regenerative medicine and drug delivery systems provide promising approaches for the treatment of skin lesions. However, the design of engineered substrates containing therapeutic agents for cell proliferation and its differentiation into skin cells, with skin-like patterns, is the major challenge. Here, to overcome this problem, a hybrid scaffold conjugated with nanoparticles containing the extract of Verbascum sinuatum L. flowers (HE) was designed. To this end, (chitosan-PEG)-based nanocarriers (Chi-PEG) were first prepared in the volume ratios of 90:10, 80:20, 70:30, and 50:50 v/v. The results indicated that the 70:30 ratio possessed better physical/morphologic properties along with more suitable stability than other nanoparticles (encapsulation-efficiency:86.34 %, zeta-potential:21.2 mV, and PDI:0.30). Afterward, PCL-collagen biologic scaffold (PCL-Coll) were prepared by the lyophilization method, then conjugated with selected nanoparticles(Chi-PEG-HE). Notably, in addition to PCL-Coll/Chi-PEG-HE, two scaffolds of PCL-Coll and PCL-Coll/Chi-PEG were prepared to evaluate the role of conjugation in the release behavior of herbal bio-macromolecules. Based on the results, the conjugation process was led to a more stable release, compared to unconjugated nanoparticles. The mentioned process also created an integrated network along with better physicomechanical properties [modulus:12.31 MPa, tensile strength:4.44 MPa, smaller pore size(2 μm), and better swelling (100.27 %) with a symmetrical wettability on the surface]. PCL-Coll/Chi-PEG-HE scaffold was also resulted in higher expression levels of K10 and K14 keratinocytes with biomimetic patterns than PCL-Coll/Chi-PEG scaffold. This could be due to the active ingredients of V. sinuatum extract like alkaloids, flavonoids, and triterpenoids which imparts the wound healing (anti-inflammatory, anti-bacterial, anti-oxidant) properties to this scaffold. It seems that the use of bioactive materials like herbal extracts, in the form of encapsulated into polymeric nanocarriers, in the structure of engineered scaffolds can be a promising option for regenerating damaged skin without scarring. Hence, this study can provide innovative insights into the combination of two techniques of drug delivery and tissue engineering to design bio-scaffolds containing bioactive molecules with better therapeutic approaches.

摘要

再生医学和药物输送系统为治疗皮肤损伤提供了有前途的方法。然而,设计含有治疗剂的工程化基质以促进细胞增殖并将其分化为具有皮肤样形态的皮肤细胞是主要挑战。在这里,为了克服这个问题,设计了一种与含有毛地黄黄花提取物(HE)的纳米粒子缀合的杂化支架。为此,首先以 90:10、80:20、70:30 和 50:50 的体积比制备壳聚糖-PEG 为基础的纳米载体(Chi-PEG)。结果表明,70:30 比例的纳米粒子具有更好的物理/形态特性和更合适的稳定性,优于其他纳米粒子(包封效率:86.34%,Zeta 电位:21.2 mV,PDI:0.30)。随后,通过冷冻干燥法制备聚己内酯-胶原蛋白生物支架(PCL-Coll),然后与选定的纳米粒子(Chi-PEG-HE)缀合。值得注意的是,除了 PCL-Coll/Chi-PEG-HE 之外,还制备了 PCL-Coll 和 PCL-Coll/Chi-PEG 两种支架,以评估缀合在草药生物大分子释放行为中的作用。基于结果,与未缀合的纳米粒子相比,缀合过程导致更稳定的释放。该过程还创建了一个集成网络,同时具有更好的物理机械性能[模量:12.31 MPa,拉伸强度:4.44 MPa,较小的孔径(2 μm),更好的溶胀(100.27%),表面具有对称的润湿性]。与 PCL-Coll/Chi-PEG 支架相比,PCL-Coll/Chi-PEG-HE 支架还导致具有仿生图案的角蛋白 10 和角蛋白 14 角质形成细胞的表达水平更高。这可能是由于毛地黄黄花提取物中的活性成分,如生物碱、类黄酮和三萜类化合物,赋予了这种支架伤口愈合(抗炎、抗菌、抗氧化)的特性。似乎使用生物活性材料,如草药提取物,以封装到聚合物纳米载体中的形式,在工程化支架的结构中,可以成为一种有前途的选择,可用于再生无瘢痕的受损皮肤。因此,这项研究为药物输送和组织工程两种技术的结合提供了新的见解,可用于设计含有生物活性分子的生物支架,以提供更好的治疗方法。

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