Design, fabrication, and evaluation of antimicrobial sponge microneedles for the transdermal delivery of insulin

被引:1
|
作者
Zhang, Xinyi [1 ,2 ]
Zhang, Yuelian [1 ,2 ]
Zheng, Huishan [1 ,2 ]
Yang, Xue [2 ]
Zou, Shiqi [2 ]
Chen, Jianmin [1 ,2 ,3 ,4 ]
机构
[1] Fujian Med Univ, Sch Pharm, Fujian, Peoples R China
[2] Putian Univ, Sch Pharm & Med Technol, Fujian 351100, Peoples R China
[3] Fujian Prov Univ, Putian Univ, Key Lab Pharmaceut Anal, Fujian, Peoples R China
[4] Fujian Prov Univ, Putian Univ, Lab Med, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Microneedles; Transdermal; Diabetes; Insulin; Antimicrobial; Safety; DISSOLVING MICRONEEDLES; DRUG; BARRIER; PATCHES;
D O I
10.1016/j.ejpb.2024.114586
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Transdermal drug delivery systems hold promise, but their effectiveness is often constrained by the skin's barrier. Microneedles (MNs) improve drug permeability by creating micro-channels in the skin, yet they continue to face challenges such as infection risks and safety concerns. To overcome these challenges, a novel antimicrobial sponge MNs (ASMNs@PVP-INS) modified with polyvinylpyrrolidone (PVP) for insulin (INS) delivery was designed. Mechanical testing demonstrated that these MNs possess excellent mechanical strength, capable of withstanding at least 0.11 N per needle without rupture. In vitro drug penetration tests revealed that the MNs consistently released over 75 % of INS within a 6 h. In an animal model, ASMNs@PVP-INS reduced initial blood glucose levels from 22.4 to 5.72 mmol/L, effectively maintaining glucose control for more than 6 h without inducing hypoglycemia. Additionally, agar diffusion assays indicated that INS loading did not compromise the antimicrobial properties of antimicrobial sponge MNs (ASMNs). Skin irritation tests showed that ASMNs@PVPINS exhibited mild irritation (PII < 0.6), with skin damage fully recovering within 8 h. Safety assessments indicated no significant toxicity to mice, with biochemical markers remaining within normal ranges, thereby confirming their good biocompatibility. In conclusion, ASMNs@PVP-INS hold promise as a novel drug delivery vehicle.
引用
收藏
页数:15
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