An in vitro assessment of the thermoreversible PLGA-PEG-PLGA copolymer: Implications for Descemet's membrane endothelial keratoplasty

被引:3
|
作者
Tint, Naing L. [1 ,2 ]
Cheng, Kelvin K. W. [2 ]
Dhillon, Amritpaul S. [3 ]
Keane, Pearse A. [4 ,5 ]
Alexander, Philip [3 ]
Kennedy, David [6 ]
Chau, David Y. S. [7 ]
Rose, Felicity R. A. J. [3 ]
Allan, Bruce D. S. [1 ,5 ]
机构
[1] Moorfields Eye Hosp NHS Fdn Trust, Cornea & External Eye Dis Serv, 162 City Rd, London, England
[2] NHS Lothian, Princess Alexandra Eye Pavil, Edinburgh, Midlothian, Scotland
[3] Univ Nottingham, Sch Pharm Nottingham, Nottingham Biodiscovery Inst, Div Regenerat Med & Cellular Therapies, Nottingham, Notts, England
[4] UCL, Inst Ophthalmol, London, England
[5] Moorfields Eye Hosp NHS Fdn Trust, NIHR Biomed Res Ctr Ophthalmol, London, England
[6] Moorfields Eye Hosp NHS Fdn Trust, Lions Eye Bank, London, England
[7] UCL, Div Biomat & Tissue Engn, Eastman Dent Inst, London, England
来源
关键词
Descemet's membrane; endothelial keratoplastybiodegradable polymers; endothelial keratoplasty; endothelium; thermoreversible; DRUG-DELIVERY; HYDROGEL; DMEK;
D O I
10.1111/ceo.14167
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background To explore the use of a thermoreversible copolymer gel coating to prevent donor tissue scrolling in Descemet's membrane endothelial keratoplasty (DMEK). Methods PLGA-PEG-PLGA triblock copolymer was synthesised via ring opening polymerisation. Two formulations were fabricated and gelation properties characterised using rheological analyses. Endothelial cytotoxicity of the copolymer was assessed using a Trypan Blue exclusion assay. Thickness of the copolymer gel coating on the endothelial surface was analysed using anterior segment optical coherence tomography (OCT) (RTVue-100, Optovue Inc.). Gold nanoparticles were added to the copolymer to aid visualisation using OCT. Prevention of Descemet membrane donor scrolling was represented via a novel, in vitro, immersion of copolymer coated donor graft material. Results Two different formulations of PLGA-PEG-PLGA copolymer were successfully fabricated and the desired peak gelling temperature of 24 degrees C was achieved by polymer blending. Application of 20%, 30% and 40% (wt/vol) polymer concentrations resulted in a statistically significant increase in polymer thickness on the endothelium (p < 0.001). There was no detectable endothelial cytotoxicity. The polymer was easy to apply to the endothelium and prevented scrolling of the DMEK graft. Conclusion This PLGA-PEG-PLGA thermoreversible copolymer gel could be exploited as a therapeutic aid for preventing DMEK graft scrolling.
引用
收藏
页码:58 / 66
页数:9
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