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一种用于缓解类风湿性关节炎的新型聚乳酸基持续释放透明质酸微球的制备

The Preparation of a Novel Poly(Lactic Acid)-Based Sustained HS Releasing Microsphere for Rheumatoid Arthritis Alleviation.

作者信息

Yu Yue, Wang Zhou, Ding Qian, Yu Xiangbin, Yang Qinyan, Wang Ran, Fang Yudong, Qi Wei, Liao Junyi, Hu Wei, Zhu Yizhun

机构信息

State Key Laboratory of Quality Research in Chinese Medicine & School of Pharmacy, Macau University of Science and Technology, Macau SAR 999078, China.

School of Pharmacy, Fujian Medical University, Fuzhou 350108, China.

出版信息

Pharmaceutics. 2021 May 18;13(5):742. doi: 10.3390/pharmaceutics13050742.

Abstract

Rheumatoid arthritis (RA) is a chronic, inflammatory autoimmune disease that mainly erodes joints and surrounding tissues, and if it is not treated in time, it can cause joint deformities and loss of function. S-propargyl-cysteine (SPRC) is an excellent endogenous hydrogen sulfide donor which can relieve the symptoms of RA through the promotion of HS release via the CSE/HS pathway in vivo. However, the instant release of HS in vivo could potentially limit its further clinical use. To solve this problem, in this study, a SPRC-loaded poly(lactic acid) (PLA) microsphere (SPRC@PLA) was prepared, which could release SPRC in vitro in a sustained manner, and further promote sustained in vivo HS release. Furthermore, its therapeutical effect on RA in rats was also studied. A spherical-like SPRC@PLA was successfully prepared with a diameter of approximately 31.61 μm, yielding rate of 50.66%, loading efficiency of 6.10% and encapsulation efficiency of 52.71%. The SPRC@PLA showed significant prolonged in vitro SPRC release, to 4 days, and additionally, an in vivo HS release around 3 days could also be observed. In addition, a better therapeutical effect and prolonged administration interval toward RA rats was also observed in the SPRC@PLA group.

摘要

类风湿关节炎(RA)是一种慢性炎症性自身免疫性疾病,主要侵蚀关节及周围组织,若不及时治疗,可导致关节畸形和功能丧失。S-炔丙基半胱氨酸(SPRC)是一种优良的内源性硫化氢供体,可通过体内CSE/HS途径促进硫化氢释放来缓解RA症状。然而,硫化氢在体内的即时释放可能会限制其进一步的临床应用。为解决这一问题,本研究制备了负载SPRC的聚乳酸(PLA)微球(SPRC@PLA),其可在体外持续释放SPRC,并进一步促进体内硫化氢的持续释放。此外,还研究了其对大鼠RA的治疗效果。成功制备了直径约为31.61μm的球形SPRC@PLA,产率为50.66%,载药效率为6.10%,包封率为52.71%。SPRC@PLA在体外SPRC释放显著延长至4天,此外,在体内还可观察到约3天的硫化氢释放。此外,在SPRC@PLA组中还观察到对RA大鼠有更好的治疗效果和延长给药间隔。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ae/8157395/0b767b8e3beb/pharmaceutics-13-00742-g001.jpg

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