Dextran sulfate-modified pH-sensitive layered double hydroxide nanocomposites for treatment of rheumatoid arthritis

被引:18
作者
Wang, Xiahui [1 ]
Yang, Bowen [2 ,3 ]
Xu, Xiaowen [1 ]
Su, Meiling [1 ]
Xi, Mingrong [2 ,3 ]
Yin, Zongning [1 ]
机构
[1] Sichuan Univ, West China Sch Pharm, Key Lab Drug Targeting & Drug Delivery Syst, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Dept Obstet & Gynecol, West China Univ Hosp 2, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, Key Lab Birth Defects & Related Dis Women & Child, Minist Educ, West China Univ Hosp 2, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Dextran sulfate; Rheumatoid arthritis; Layered double hydroxides; pH-sensitive; Scavenger receptor; Methotrexate; RESPONSIVE NANOCARRIERS; ANTIBACTERIAL ACTIVITY; INTERCALATION; NANOPARTICLES; DELIVERY; RELEASE;
D O I
10.1007/s13346-020-00832-2
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
To reduce the side effects of methotrexate and increase its anti-inflammatory effect, we developed a drug delivery system, dextran sulfate-modified methotrexate-loaded layered double hydroxide nanocomposites (LDH-MTX-DS), with both targeting and pH-sensitivity for the treatment of rheumatoid arthritis. The nanocomposites had a mean particle size of 303.1 +/- 8.07 nm, zeta potential of - 12.4 +/- 0.7 mV, encapsulation efficiency of 49.64%, and loading efficiency of 16.81%. In vitro release experiments demonstrated that the drug was released faster in PBS at pH 5.5 than at pH 7.4, which reflected the pH-sensitivity of this system. Cellular uptake assays displayed higher cellular uptake rate of the dextran sulfate-modified targeting carrier compared with that of a non-targeting carrier (P < 0.01), which indicated that the LDH-MTX-DS could actively target scavenger receptors on the surface of activated RAW 264.7 cells. In vivo pharmacodynamic experiments showed that, after the second (P < 0.001) and third (P < 0.05) administrations, the preparation group exhibited significantly improved therapeutic efficacy in adjuvant-induced arthritis (AIA) rats when compared with free MTX alone. These results indicated that this drug delivery system was promising in the treatment of rheumatoid arthritis.
引用
收藏
页码:1096 / 1106
页数:11
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