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原位制备载甲氨蝶呤和地塞米松的磷脂凝胶用于协同治疗类风湿关节炎。

In situ Preparation of a Phospholipid Gel Co-Loaded with Methotrexate and Dexamethasone for Synergistic Rheumatoid Arthritis Treatment.

机构信息

School of Pharmacy, North Sichuan Medical College, Nanchong, 637000, People's Republic of China.

Oncology Department of Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, People's Republic of China.

出版信息

Int J Nanomedicine. 2022 Nov 2;17:5153-5162. doi: 10.2147/IJN.S384772. eCollection 2022.

Abstract

BACKGROUND

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by arthrocele, cartilage damage and disability. Although several anti-RA drugs have been developed for long-term treatment, they require frequent local injection and lead to multiple adverse effects such as osteoporosis and myelosuppression.

PURPOSE

Reducing the amount and frequency of anti-RA drugs methotrexate (MTX) and dexamethasone sodium phosphate (DSP) by local injection of phospholipid-based phase separation gel (PPSG) coloaded the two drugs, which presented PPSG-(+).

METHODS

First, We characterized PPSG-(+). And we used UV spectrophotometry and high performance liquid chromatography (HPLC) to detect drug concentration, which can clarify the drug release in vitro and in vivo, respectively. We also injected PPSG-(+) into the joint cavity of healthy rabbits to prove the safety of PPSG-(+). Then, we injected PPSG-(+) into the joint cavity of RA modeled rabbits to demonstrate the effect in anti-RA of PPSG-(+) including the thickness of joints, tumor necrosis factor (TNF)-α and interleukin (IL)-1β detection, hematoxylin-eosin (H&E) staining and computed tomography (CT) of joints.

RESULTS

Suspended particles show a tight and uniform arrangement in PPSG-(+). The gel underwent a phase transition at 20 min in vitro and 8 h in vivo, and vesicular structures reflecting its degradation and phase transition were observed in vivo. PPSG-(+) released both drugs in a sustained and fixed ratio for more than 14 days, while it proved to be safe for intra-articular injection and did not induce inflammation in a rabbit. Eventually, PPSG-(+) showed a good anti-RA effect and its potency can be maintained for 3 weeks.

CONCLUSION

PPSG-(+) is a drug delivery system offering good biocompatibility and sustained release of MTX and DSP, leading to long-lasting anti-RA effect.

摘要

背景

类风湿性关节炎(RA)是一种慢性自身免疫性疾病,其特征为关节肿胀、软骨损伤和功能障碍。虽然已经开发了几种抗 RA 药物用于长期治疗,但它们需要频繁进行局部注射,并导致多种不良反应,如骨质疏松症和骨髓抑制。

目的

通过局部注射载药磷脂相分离凝胶(PPSG)减少抗 RA 药物甲氨蝶呤(MTX)和磷酸地塞米松钠(DSP)的用量和注射频率,制备 PPSG-(+)。

方法

首先对 PPSG-(+)进行了表征。我们使用紫外分光光度法和高效液相色谱法(HPLC)分别检测药物浓度,以阐明其体外和体内的药物释放情况。我们还将 PPSG-(+)注入健康兔的关节腔,以证明 PPSG-(+)的安全性。然后,我们将 PPSG-(+)注入 RA 造模兔的关节腔,以证明 PPSG-(+)在抗 RA 中的作用,包括关节厚度、肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1β检测、关节苏木精-伊红(H&E)染色和 CT。

结果

PPSG-(+)中的悬浮颗粒呈现出紧密均匀的排列。凝胶在体外 20 分钟和体内 8 小时发生相转变,体内观察到囊泡结构反映其降解和相转变。PPSG-(+)以持续和固定的比例释放两种药物超过 14 天,同时证明其关节内注射安全,不会引起兔炎症。最终,PPSG-(+)显示出良好的抗 RA 效果,其效力可维持 3 周。

结论

PPSG-(+)是一种具有良好生物相容性和 MTX 和 DSP 持续释放的药物传递系统,可实现持久的抗 RA 效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/481f/9637340/db1a1614ac1a/IJN-17-5153-g0001.jpg

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