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用于甲氨蝶呤控释的新型复合聚合物微球:表征及体内抗纤维化研究

Novel, Blended Polymeric Microspheres for the Controlled Release of Methotrexate: Characterization and In Vivo Antifibrotic Studies.

作者信息

Nabai Layla, Ghahary Aziz, Jackson John

机构信息

BC Professional Fire Fighters' Burn & Wound Healing Research Lab, ICORD, The Blusson Spinal Cord Centre, 818 West 10th Ave, Vancouver, BC V5Z 1M9, Canada.

Faculty of Pharmaceutical Sciences, The University of British Columbia, 2045 Westbrook Mall, Vancouver, BC V6T 1Z3, Canada.

出版信息

Bioengineering (Basel). 2023 Feb 27;10(3):298. doi: 10.3390/bioengineering10030298.

Abstract

Low dose methotrexate (MTX) is known to effectively decrease type I collagen production in dermal fibroblasts, while increasing the matrix metalloproteinase-1 (MMP-1) production in vitro. For in vivo use as an antifibrotic agent on wounds, a linear and extended controlled release formulation of MTX is required. The objective of this study was to optimize the fabrication of MTX-loaded polymeric microspheres with such properties, and to test the efficacy for the prevention of fibrosis in vivo. Poly lactic-co-glycolic acid (PLGA), Poly (L-lactic acid) (PLLA) and the diblock copolymer, methoxypolyethylene glycol-block-poly (D, L-lactide) (MePEG-b-PDLLA), were used to fabricate microspheres, which were then characterized in terms of size, drug encapsulation efficiency, and in vitro release profiles. The optimized formulation (PLGA with diblock copolymer) showed high drug encapsulation efficiency (>80%), low burst release (~10%) and a gradual release of MTX. The amphipathic diblock copolymer is known to render the microsphere surface more biocompatible. In vivo, these microspheres were effective in reducing fibrotic tissue which was confirmed by quantitative measurement of type I collagen and α-smooth muscle actin expression, demonstrating that MTX can be efficiently encapsulated in PLGA microspheres to provide a delayed, gradual release in wound beds to reduce fibrosis in vivo.

摘要

已知低剂量甲氨蝶呤(MTX)可有效降低真皮成纤维细胞中I型胶原蛋白的生成,同时在体外增加基质金属蛋白酶-1(MMP-1)的生成。为了在体内用作伤口抗纤维化剂,需要一种线性且延长的MTX控释制剂。本研究的目的是优化具有此类特性的载MTX聚合物微球的制备,并测试其在体内预防纤维化的功效。使用聚乳酸-乙醇酸共聚物(PLGA)、聚(L-乳酸)(PLLA)和二嵌段共聚物甲氧基聚乙二醇-嵌段-聚(D,L-丙交酯)(MePEG-b-PDLLA)制备微球,然后对其尺寸、药物包封率和体外释放曲线进行表征。优化后的制剂(含二嵌段共聚物的PLGA)显示出高药物包封率(>80%)、低突释(~10%)和MTX的缓释。已知两亲性二嵌段共聚物可使微球表面具有更高的生物相容性。在体内,这些微球可有效减少纤维化组织,这通过对I型胶原蛋白和α-平滑肌肌动蛋白表达的定量测量得到证实,表明MTX可有效包封在PLGA微球中,在伤口床中实现延迟、缓释,以减少体内纤维化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/10045572/25ba8ed5aadc/bioengineering-10-00298-g001.jpg

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