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可注射微颗粒集成水凝胶复合材料生物材料的合成与表征:体内生物相容性和炎性关节炎治疗。

Synthesis and characterization of an injectable microparticles integrated hydrogel composite biomaterial: In-vivo biocompatibility and inflammatory arthritis treatment.

机构信息

Department of Biosciences and Bioengineering, Indian Institute of Technology Bombay (IIT Bombay), Mumbai, India.

Center for Research in Nanotechnology & Science (CRNTS), IIT Bombay, Mumbai, India.

出版信息

Colloids Surf B Biointerfaces. 2021 May;201:111597. doi: 10.1016/j.colsurfb.2021.111597. Epub 2021 Feb 2.

Abstract

Polymeric hydrogels and microparticles have been widely used for localized drug delivery applications for the treatment of arthritis. Nonetheless, owing to initial burst drug release, non-specific biodistribution and low retention time at the target site in body, these polymeric drug delivery systems have been found with low in-vivo performance. Hence, the above limitations need to be resolved by designing a smart novel drug delivery system which is the current need in biomedicine. Herein, a novel localized injectable thermoresponsive microparticles embedded hydrogel composite drug delivery system has been developed for the treatment of inflammatory arthritis. In the current study, methotrexate (MTX) loaded alginate microparticles (MTX-Microparticles) are embedded into thermoreversible hydrogel matrix (MTX-MPs-H) prepared by physical blending of sodium hyaluronate and methylcellulose (SHMC). Microparticles-hydrogel composite system exhibited appropriate in-vitro thermoreversibility (sol at 4 °C and gel at 37 °C), biocompatibility (>80 %), hemocompatibility, and controlled drug release profile. The in-vivo biocompatibility studies for 10 days revealed that composite system is non-toxic in nature. The developed MTX-MPs-H composite drug delivery system effectively decreased the swelling/ inflammation of the arthritis affected paw in wistar rats in comparison to only alginate microparticles and pure MTX up to 30 days.

摘要

聚合物水凝胶和微球已广泛用于治疗关节炎的局部药物输送应用。然而,由于初始药物突释、非特异性生物分布和在体内靶部位的滞留时间短,这些聚合物药物输送系统的体内性能较低。因此,需要通过设计一种智能新型药物输送系统来解决上述限制,这是当前生物医学的需求。本文开发了一种新型局部可注射温敏性微球嵌入水凝胶复合药物输送系统,用于治疗炎症性关节炎。在本研究中,将甲氨蝶呤(MTX)负载的海藻酸钠微球(MTX-微球)嵌入到由透明质酸钠和甲基纤维素(SHMC)物理混合制备的温敏可逆水凝胶基质(MTX-MPs-H)中。微球-水凝胶复合体系表现出适当的体外温敏可逆性(4°C 时为溶胶,37°C 时为凝胶)、生物相容性(>80%)、血液相容性和控制药物释放特性。10 天的体内生物相容性研究表明,该复合体系在性质上是无毒的。与仅用海藻酸钠微球和纯 MTX 相比,所开发的 MTX-MPs-H 复合药物输送系统可有效减轻关节炎大鼠受影响爪子的肿胀/炎症,持续 30 天。

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