Anti-Adhesive And Antiproliferative Synergistic Surface Modification Of Intraocular Lens For Reduced Posterior Capsular Opacification

被引:62
作者
Han, Yuemei [1 ]
Tang, Junmei [1 ]
Xia, Jiayi [1 ]
Wang, Rui [1 ]
Qin, Chen [1 ]
Liu, Sihao [1 ]
Zhao, Xia [1 ]
Chen, Hao [1 ,2 ]
Lin, Quankui [1 ,2 ]
机构
[1] Wenzhou Med Univ, Sch Ophthalmol & Optometry, Eye Hosp, 270 Xueyuan Xi Rd, Wenzhou 325027, Peoples R China
[2] Chinese Acad Sci, Wenzhou Inst Biomat & Engn, Wenzhou 32500, Peoples R China
基金
中国国家自然科学基金;
关键词
surface modification; intraocular lens; posterior capsular opacification; drug-eluting coating; nanoparticle; POLYSACCHARIDE MULTILAYER; IN-VITRO; HEPARIN; BIOCOMPATIBILITY; NANOPARTICLES; PREVENTION; DOXORUBICIN; RELEASE; STENTS; IOL;
D O I
10.2147/IJN.S215802
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Posterior capsular opacification (PCO) is the main complication after intraocular lens (IOL) implantation in cataract surgery, which is the result of lens epithelial cell (LEC) adhesion, proliferation and migration on the IOL and at the lens capsule interface. Hydrophilic surface modification, such as surface heparinization, decreases the cell adhesion, which has been commercialized and used clinically. However, clinical long-term observation results show no significant difference between the pristine and heparinized IOLs. Methods: To prevent PCO over the long time span, we modified the IOLs with an antiproliferative drug-loaded hydrophilic coating. The antiproliferative drug doxorubicin (DOX)-incorporated chitosan (CHI) nanoparticle was fabricated by sodium tripolyphosphate (TPP) gelation. Such antiproliferative drug-loaded CHI-TPP-DOX nanoparticles (CTDNP) were used as one of the building blocks to prepare polyelectrolyte multilayer with heparin (HEP) via layer-by-layer assembly, obtaining (HEP/CTDNP)(n) multilayers. The assembly process was characterized by quartz crystal microbalance with dissipation (QCM-D). The drug release behavior of the coating was investigated by ultra-HPLC (UPLC). In vitro cell experiments were carried out to monitor the effects of multifunctional coatings on cellular adhesion, proliferation and migration. And the intraocular implantation was performed on rabbits to evaluate the in vivo PCO inhibitory effect of such surface-functionalized IOLs. Results: The positively charged CTDNP was successfully prepared by ionic gelation. The QCM-D results indicate the successful preparation of the (HEP/CTDNP)(n) multilayer film. Drug release profiles showed that surface-multifunctionalized IOL had drug-sustained release properties. In vitro cell culture results showed significant inhibition of adhesion, proliferation and migration of LECs after surface modification. The in vivo results showed that the IOLs with multifunctionalized surface can effectively reduce the posterior hyperplasia and Soemmering's ring (SR) formation. Conclusion: These findings suggested that such multifunctionalized drug-eluting IOLs can effectively reduce the posterior hyperplasia and SR formation when intraocular implantation has a major impact on reducing PCO incidence. Thus they have a great potential in improving patient vision recovery and maintenance.
引用
收藏
页码:9047 / 9061
页数:15
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